id
stringlengths
13
13
task_type
stringclasses
6 values
pipeline
stringclasses
1 value
difficulty
stringclasses
3 values
num_hops
int64
1
5
question
stringlengths
94
258
context
stringlengths
41
511
reasoning_chain
dict
answer
stringlengths
1
511
modalities
listlengths
1
3
modality_data
listlengths
1
5
evidence
listlengths
1
5
metadata
stringlengths
49
912
path_confidence_score
float64
0.61
1
choices
listlengths
4
4
⌀
no_dise_00435
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in FGFR1 classified as Pathogenic or Likely Pathogenic for Hypogonadotropic hypogonadism.
NM_023110.3(FGFR1):c.670G>C (p.Asp224His) VARIANT_IN_GENE FGFR1 → NM_023110.3(FGFR1):c.670G>C (p.Asp224His) VARIANT_HAS_CLINICAL_SIGNIFICANCE Hypogonadotropic hypogonadism
{ "steps": [ { "hop": 1, "source_node_id": "FGFR1", "source_node_type": "GENE", "source_node_label": "FGFR1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_023110.3...
NM_023110.3(FGFR1):c.670G>C (p.Asp224His)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"FGFR1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"FGFR1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_023110.3(FGFR1):c.670G>C (p.Asp224His)", "text": "NM_023110.3(FGFR1):c.670G>C (p.Asp224His) VARIANT_IN_GENE FGFR1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:hypogonadotropic_hypogonadism", "text": "NM_023110.3(FGFR1...
{"gene": "FGFR1", "disease": "Hypogonadotropic hypogonadism", "pathogenic_variants": ["NM_023110.3(FGFR1):c.729C>A (p.Tyr243Ter)", "NM_023110.3(FGFR1):c.1716C>G (p.Tyr572Ter)", "NM_023110.3(FGFR1):c.1029G>A (p.Ala343=)", "NM_023110.3(FGFR1):c.670G>C (p.Asp224His)"]}
0.921954
null
no_dise_00294
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BRAF classified as Pathogenic or Likely Pathogenic for BRAF-related disorder.
NM_004333.6(BRAF):c.722C>T (p.Thr241Met) VARIANT_IN_GENE BRAF → NM_004333.6(BRAF):c.722C>T (p.Thr241Met) VARIANT_HAS_CLINICAL_SIGNIFICANCE BRAF-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "BRAF", "source_node_type": "GENE", "source_node_label": "BRAF", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004333.6(B...
NM_004333.6(BRAF):c.722C>T (p.Thr241Met)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BRAF\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BRAF\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_004333.6(BRAF):c.722C>T (p.Thr241Met)", "text": "NM_004333.6(BRAF):c.722C>T (p.Thr241Met) VARIANT_IN_GENE BRAF", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:braf_related_disorder", "text": "NM_004333.6(BRAF):c.722C>T (...
{"gene": "BRAF", "disease": "BRAF-related disorder", "pathogenic_variants": ["NM_004333.6(BRAF):c.1502A>C (p.Glu501Ala)", "NM_004333.6(BRAF):c.1403T>C (p.Phe468Ser)", "NM_004333.6(BRAF):c.722C>T (p.Thr241Met)"]}
0.921954
null
no_dise_00185
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in FAT4 classified as Pathogenic or Likely Pathogenic for Autosomal recessive FAT4-related disorders.
NM_001291303.3(FAT4):c.7504G>T (p.Glu2502Ter) VARIANT_IN_GENE FAT4 → NM_001291303.3(FAT4):c.7504G>T (p.Glu2502Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE Autosomal recessive FAT4-related disorders
{ "steps": [ { "hop": 1, "source_node_id": "FAT4", "source_node_type": "GENE", "source_node_label": "FAT4", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_001291303....
NM_001291303.3(FAT4):c.7504G>T (p.Glu2502Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"FAT4\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"FAT4\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_001291303.3(FAT4):c.7504G>T (p.Glu2502Ter)", "text": "NM_001291303.3(FAT4):c.7504G>T (p.Glu2502Ter) VARIANT_IN_GENE FAT4", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:autosomal_recessive_fat4_related_disorders", "text"...
{"gene": "FAT4", "disease": "Autosomal recessive FAT4-related disorders", "pathogenic_variants": ["NM_001291303.3(FAT4):c.7504G>T (p.Glu2502Ter)"]}
0.921954
null
no_dise_00345
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in FGFR1 classified as Pathogenic or Likely Pathogenic for Autosomal recessive FGFR1-related disorders.
NM_023110.3(FGFR1):c.1889T>G (p.Leu630Arg) VARIANT_IN_GENE FGFR1 → NM_023110.3(FGFR1):c.1889T>G (p.Leu630Arg) VARIANT_HAS_CLINICAL_SIGNIFICANCE Autosomal recessive FGFR1-related disorders
{ "steps": [ { "hop": 1, "source_node_id": "FGFR1", "source_node_type": "GENE", "source_node_label": "FGFR1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_023110.3...
NM_023110.3(FGFR1):c.1889T>G (p.Leu630Arg)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"FGFR1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"FGFR1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_023110.3(FGFR1):c.1889T>G (p.Leu630Arg)", "text": "NM_023110.3(FGFR1):c.1889T>G (p.Leu630Arg) VARIANT_IN_GENE FGFR1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:autosomal_recessive_fgfr1_related_disorders", "text": "N...
{"gene": "FGFR1", "disease": "Autosomal recessive FGFR1-related disorders", "pathogenic_variants": ["NM_023110.3(FGFR1):c.1889T>G (p.Leu630Arg)"]}
0.83666
null
no_dise_00571
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in NOTCH1 classified as Pathogenic or Likely Pathogenic for Adams-Oliver syndrome 5.
NM_017617.5(NOTCH1):c.3792_3793del (p.Cys1264_Glu1265delinsTer) VARIANT_IN_GENE NOTCH1 → NM_017617.5(NOTCH1):c.3792_3793del (p.Cys1264_Glu1265delinsTer) VARIANT_HAS_CLINICAL_SIGNIFICANCE Adams-Oliver syndrome 5
{ "steps": [ { "hop": 1, "source_node_id": "NOTCH1", "source_node_type": "GENE", "source_node_label": "NOTCH1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_017617...
NM_017617.5(NOTCH1):c.3792_3793del (p.Cys1264_Glu1265delinsTer)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"NOTCH1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"NOTCH1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_017617.5(NOTCH1):c.3792_3793del (p.Cys1264_Glu1265delinsTer)", "text": "NM_017617.5(NOTCH1):c.3792_3793del (p.Cys1264_Glu1265delinsTer) VARIANT_IN_GENE NOTCH1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:adams_oliver_synd...
{"gene": "NOTCH1", "disease": "Adams-Oliver syndrome 5", "pathogenic_variants": ["Single allele", "NM_017617.5(NOTCH1):c.1342del (p.Arg448fs)", "NM_017617.5(NOTCH1):c.1650C>A (p.Tyr550Ter)", "NM_017617.5(NOTCH1):c.3963del (p.Cys1322fs)", "NM_017617.5(NOTCH1):c.5164C>T (p.Gln1722Ter)", "NM_017617.5(NOTCH1):c.2157_2158in...
0.83666
null
no_dise_00192
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BRCA2 classified as Pathogenic or Likely Pathogenic for Breast-ovarian cancer, familial, susceptibility to, 2.
NM_000059.4(BRCA2):c.8786del (p.Ala2928_Leu2929insTer) VARIANT_IN_GENE BRCA2 → NM_000059.4(BRCA2):c.8786del (p.Ala2928_Leu2929insTer) VARIANT_HAS_CLINICAL_SIGNIFICANCE Breast-ovarian cancer, familial, susceptibility to, 2
{ "steps": [ { "hop": 1, "source_node_id": "BRCA2", "source_node_type": "GENE", "source_node_label": "BRCA2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000059.4...
NM_000059.4(BRCA2):c.8786del (p.Ala2928_Leu2929insTer)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BRCA2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BRCA2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_000059.4(BRCA2):c.8786del (p.Ala2928_Leu2929insTer)", "text": "NM_000059.4(BRCA2):c.8786del (p.Ala2928_Leu2929insTer) VARIANT_IN_GENE BRCA2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:breast_ovarian_cancer_familial_susce...
{"gene": "BRCA2", "disease": "Breast-ovarian cancer, familial, susceptibility to, 2", "pathogenic_variants": ["NM_000059.4(BRCA2):c.6577G>T (p.Glu2193Ter)", "NM_000059.4(BRCA2):c.4658del (p.Thr1553fs)", "NM_000059.4(BRCA2):c.6065C>A (p.Ser2022Ter)", "NM_000059.4(BRCA2):c.8108_8115delinsTATATAAATAAATAAATAAATATATATTTATTT...
0.83666
null
no_dise_00115
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in CHEK2 classified as Pathogenic or Likely Pathogenic for CHEK2-related cancer predisposition.
NM_007194.4(CHEK2):c.1461+1del VARIANT_IN_GENE CHEK2 → NM_007194.4(CHEK2):c.1461+1del VARIANT_HAS_CLINICAL_SIGNIFICANCE CHEK2-related cancer predisposition
{ "steps": [ { "hop": 1, "source_node_id": "CHEK2", "source_node_type": "GENE", "source_node_label": "CHEK2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_007194.4...
NM_007194.4(CHEK2):c.1461+1del
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"CHEK2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"CHEK2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_007194.4(CHEK2):c.1461+1del", "text": "NM_007194.4(CHEK2):c.1461+1del VARIANT_IN_GENE CHEK2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:chek2_related_cancer_predisposition", "text": "NM_007194.4(CHEK2):c.1461+1del VA...
{"gene": "CHEK2", "disease": "CHEK2-related cancer predisposition", "pathogenic_variants": ["NM_007194.4:c.(908+21_909-21)_(1095+21_1096-21)del", "NC_000022.11:g.(?_29092888)_(29095925_?)del", "NC_000022.11:g.(?_29120964)_(29121355_?)del", "NC_000022.11:g.(?_29105993)_(29108005_?)del", "NM_007194.4(CHEK2):c.1241del (p....
0.921954
null
no_dise_00374
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in DNMT3A classified as Pathogenic or Likely Pathogenic for EBV-positive nodal T- and NK-cell lymphoma.
NM_022552.5(DNMT3A):c.1319G>A (p.Trp440Ter) VARIANT_IN_GENE DNMT3A → NM_022552.5(DNMT3A):c.1319G>A (p.Trp440Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE EBV-positive nodal T- and NK-cell lymphoma
{ "steps": [ { "hop": 1, "source_node_id": "DNMT3A", "source_node_type": "GENE", "source_node_label": "DNMT3A", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_022552...
NM_022552.5(DNMT3A):c.1319G>A (p.Trp440Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"DNMT3A\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"DNMT3A\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_022552.5(DNMT3A):c.1319G>A (p.Trp440Ter)", "text": "NM_022552.5(DNMT3A):c.1319G>A (p.Trp440Ter) VARIANT_IN_GENE DNMT3A", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:ebv_positive_nodal_t_and_nk_cell_lymphoma", "text": "...
{"gene": "DNMT3A", "disease": "EBV-positive nodal T- and NK-cell lymphoma", "pathogenic_variants": ["NM_022552.5(DNMT3A):c.1319G>A (p.Trp440Ter)", "NM_022552.5(DNMT3A):c.2250del (p.Phe751fs)", "NM_022552.5(DNMT3A):c.754_760dup (p.Ala254fs)"]}
0.707107
null
no_dise_00163
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in AFP classified as Pathogenic or Likely Pathogenic for Alpha-fetoprotein deficiency.
NM_001134.3(AFP):c.883_884del (p.Leu295fs) VARIANT_IN_GENE AFP → NM_001134.3(AFP):c.883_884del (p.Leu295fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Alpha-fetoprotein deficiency
{ "steps": [ { "hop": 1, "source_node_id": "AFP", "source_node_type": "GENE", "source_node_label": "AFP", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_001134.3(AFP...
NM_001134.3(AFP):c.883_884del (p.Leu295fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"AFP\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"AFP\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_001134.3(AFP):c.883_884del (p.Leu295fs)", "text": "NM_001134.3(AFP):c.883_884del (p.Leu295fs) VARIANT_IN_GENE AFP", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:alpha_fetoprotein_deficiency", "text": "NM_001134.3(AFP):c...
{"gene": "AFP", "disease": "Alpha-fetoprotein deficiency", "pathogenic_variants": ["NM_001134.3(AFP):c.543G>A (p.Trp181Ter)", "NM_001134.3(AFP):c.883_884del (p.Leu295fs)"]}
0.707107
null
no_dise_00410
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in DCTN1 classified as Pathogenic or Likely Pathogenic for DCTN1-related disorder.
NM_004082.5(DCTN1):c.279+1G>T VARIANT_IN_GENE DCTN1 → NM_004082.5(DCTN1):c.279+1G>T VARIANT_HAS_CLINICAL_SIGNIFICANCE DCTN1-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "DCTN1", "source_node_type": "GENE", "source_node_label": "DCTN1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004082.5...
NM_004082.5(DCTN1):c.279+1G>T
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"DCTN1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"DCTN1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_004082.5(DCTN1):c.279+1G>T", "text": "NM_004082.5(DCTN1):c.279+1G>T VARIANT_IN_GENE DCTN1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:dctn1_related_disorder", "text": "NM_004082.5(DCTN1):c.279+1G>T VARIANT_HAS_CLINIC...
{"gene": "DCTN1", "disease": "DCTN1-related disorder", "pathogenic_variants": ["NM_004082.5(DCTN1):c.279+1G>T"]}
0.921954
null
no_dise_00070
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in VPS35 classified as Pathogenic or Likely Pathogenic for Parkinson disease 17.
NM_018206.6(VPS35):c.2146C>G (p.Gln716Glu) VARIANT_IN_GENE VPS35 → NM_018206.6(VPS35):c.2146C>G (p.Gln716Glu) VARIANT_HAS_CLINICAL_SIGNIFICANCE Parkinson disease 17
{ "steps": [ { "hop": 1, "source_node_id": "VPS35", "source_node_type": "GENE", "source_node_label": "VPS35", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_018206.6...
NM_018206.6(VPS35):c.2146C>G (p.Gln716Glu)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"VPS35\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"VPS35\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_018206.6(VPS35):c.2146C>G (p.Gln716Glu)", "text": "NM_018206.6(VPS35):c.2146C>G (p.Gln716Glu) VARIANT_IN_GENE VPS35", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:parkinson_disease_17", "text": "NM_018206.6(VPS35):c.214...
{"gene": "VPS35", "disease": "Parkinson disease 17", "pathogenic_variants": ["NM_018206.6(VPS35):c.2146C>G (p.Gln716Glu)"]}
0.83666
null
no_dise_00494
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BRCA1 classified as Pathogenic or Likely Pathogenic for Inherited ovarian cancer (without breast cancer).
NM_007294.4(BRCA1):c.5057A>G (p.His1686Arg) VARIANT_IN_GENE BRCA1 → NM_007294.4(BRCA1):c.5057A>G (p.His1686Arg) VARIANT_HAS_CLINICAL_SIGNIFICANCE Inherited ovarian cancer (without breast cancer)
{ "steps": [ { "hop": 1, "source_node_id": "BRCA1", "source_node_type": "GENE", "source_node_label": "BRCA1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_007294.4...
NM_007294.4(BRCA1):c.5057A>G (p.His1686Arg)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BRCA1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BRCA1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_007294.4(BRCA1):c.5057A>G (p.His1686Arg)", "text": "NM_007294.4(BRCA1):c.5057A>G (p.His1686Arg) VARIANT_IN_GENE BRCA1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:inherited_ovarian_cancer_without_breast_cancer", "text...
{"gene": "BRCA1", "disease": "Inherited ovarian cancer (without breast cancer)", "pathogenic_variants": ["NM_007294.4(BRCA1):c.2850_2851del (p.Arg951fs)", "NM_007294.4(BRCA1):c.135-1G>A", "NM_007294.4(BRCA1):c.5057A>G (p.His1686Arg)"]}
0.921954
null
no_dise_00412
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in ABL1 classified as Pathogenic or Likely Pathogenic for Leukemia, Philadelphia chromosome-positive, resistant to imatinib.
NM_005157.6(ABL1):c.706G>A (p.Glu236Lys) VARIANT_IN_GENE ABL1 → NM_005157.6(ABL1):c.706G>A (p.Glu236Lys) VARIANT_HAS_CLINICAL_SIGNIFICANCE Leukemia, Philadelphia chromosome-positive, resistant to imatinib
{ "steps": [ { "hop": 1, "source_node_id": "ABL1", "source_node_type": "GENE", "source_node_label": "ABL1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_005157.6(A...
NM_005157.6(ABL1):c.706G>A (p.Glu236Lys)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"ABL1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"ABL1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_005157.6(ABL1):c.706G>A (p.Glu236Lys)", "text": "NM_005157.6(ABL1):c.706G>A (p.Glu236Lys) VARIANT_IN_GENE ABL1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:leukemia_philadelphia_chromosome_positive_resistant_to_imati", ...
{"gene": "ABL1", "disease": "Leukemia, Philadelphia chromosome-positive, resistant to imatinib", "pathogenic_variants": ["NM_005157.6(ABL1):c.757T>C (p.Tyr253His)", "NM_005157.6(ABL1):c.706G>A (p.Glu236Lys)", "NM_005157.6(ABL1):c.707A>T (p.Glu236Val)"]}
0.707107
null
no_dise_00157
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in PDE10A classified as Pathogenic or Likely Pathogenic for Infantile-onset generalized dyskinesia with orofacial involvement.
NM_001385079.1(PDE10A):c.1799T>G (p.Phe600Cys) VARIANT_IN_GENE PDE10A → NM_001385079.1(PDE10A):c.1799T>G (p.Phe600Cys) VARIANT_HAS_CLINICAL_SIGNIFICANCE Infantile-onset generalized dyskinesia with orofacial involvement
{ "steps": [ { "hop": 1, "source_node_id": "PDE10A", "source_node_type": "GENE", "source_node_label": "PDE10A", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_001385...
NM_001385079.1(PDE10A):c.1799T>G (p.Phe600Cys)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"PDE10A\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"PDE10A\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_001385079.1(PDE10A):c.1799T>G (p.Phe600Cys)", "text": "NM_001385079.1(PDE10A):c.1799T>G (p.Phe600Cys) VARIANT_IN_GENE PDE10A", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:infantile_onset_generalized_dyskinesia_with_orofaci...
{"gene": "PDE10A", "disease": "Infantile-onset generalized dyskinesia with orofacial involvement", "pathogenic_variants": ["NM_001385079.1(PDE10A):c.1799T>G (p.Phe600Cys)", "NM_001385079.1(PDE10A):c.1144G>C (p.Ala382Pro)", "NM_001385079.1(PDE10A):c.686del (p.Gly229fs)", "NM_001385079.1(PDE10A):c.193_200dup (p.Pro68fs)"...
0.921954
null
no_dise_00198
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in DNMT3A classified as Pathogenic or Likely Pathogenic for Hydrocephalus, nonsyndromic, autosomal recessive 2.
GRCh37/hg19 2p23.3(chr2:25437125-25487783)x1 VARIANT_IN_GENE DNMT3A → GRCh37/hg19 2p23.3(chr2:25437125-25487783)x1 VARIANT_HAS_CLINICAL_SIGNIFICANCE Hydrocephalus, nonsyndromic, autosomal recessive 2
{ "steps": [ { "hop": 1, "source_node_id": "DNMT3A", "source_node_type": "GENE", "source_node_label": "DNMT3A", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "GRCh37/hg...
GRCh37/hg19 2p23.3(chr2:25437125-25487783)x1
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"DNMT3A\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"DNMT3A\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "GRCh37/hg19 2p23.3(chr2:25437125-25487783)x1", "text": "GRCh37/hg19 2p23.3(chr2:25437125-25487783)x1 VARIANT_IN_GENE DNMT3A", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:hydrocephalus_nonsyndromic_autosomal_recessive_2", ...
{"gene": "DNMT3A", "disease": "Hydrocephalus, nonsyndromic, autosomal recessive 2", "pathogenic_variants": ["GRCh37/hg19 2p23.3(chr2:25437125-25487783)x1"]}
0.83666
null
no_dise_00601
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BRCA2 classified as Pathogenic or Likely Pathogenic for Breast-ovarian cancer, familial, susceptibility to, 1.
NM_000059.4(BRCA2):c.2234_2235del (p.Lys745fs) VARIANT_IN_GENE BRCA2 → NM_000059.4(BRCA2):c.2234_2235del (p.Lys745fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Breast-ovarian cancer, familial, susceptibility to, 1
{ "steps": [ { "hop": 1, "source_node_id": "BRCA2", "source_node_type": "GENE", "source_node_label": "BRCA2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000059.4...
NM_000059.4(BRCA2):c.2234_2235del (p.Lys745fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BRCA2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BRCA2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_000059.4(BRCA2):c.2234_2235del (p.Lys745fs)", "text": "NM_000059.4(BRCA2):c.2234_2235del (p.Lys745fs) VARIANT_IN_GENE BRCA2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:breast_ovarian_cancer_familial_susceptibility_to_1",...
{"gene": "BRCA2", "disease": "Breast-ovarian cancer, familial, susceptibility to, 1", "pathogenic_variants": ["NM_000059.4(BRCA2):c.2234_2235del (p.Lys745fs)", "NM_000059.4(BRCA2):c.1094del (p.Pro365fs)", "NM_000059.4(BRCA2):c.4361_4368delinsTCAGAT (p.Pro1454fs)"]}
0.83666
null
no_dise_00018
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in KMT2C classified as Pathogenic or Likely Pathogenic for KMT2C-related disorder.
NM_170606.3(KMT2C):c.14245C>T (p.Pro4749Ser) VARIANT_IN_GENE KMT2C → NM_170606.3(KMT2C):c.14245C>T (p.Pro4749Ser) VARIANT_HAS_CLINICAL_SIGNIFICANCE KMT2C-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "KMT2C", "source_node_type": "GENE", "source_node_label": "KMT2C", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_170606.3...
NM_170606.3(KMT2C):c.14245C>T (p.Pro4749Ser)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"KMT2C\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"KMT2C\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_170606.3(KMT2C):c.14245C>T (p.Pro4749Ser)", "text": "NM_170606.3(KMT2C):c.14245C>T (p.Pro4749Ser) VARIANT_IN_GENE KMT2C", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:kmt2c_related_disorder", "text": "NM_170606.3(KMT2C)...
{"gene": "KMT2C", "disease": "KMT2C-related disorder", "pathogenic_variants": ["NM_170606.3(KMT2C):c.8026C>T (p.Gln2676Ter)", "NM_170606.3(KMT2C):c.10449dup (p.Gln3484fs)", "NM_170606.3(KMT2C):c.14245C>T (p.Pro4749Ser)", "NM_170606.3(KMT2C):c.4272del (p.His1424fs)"]}
0.83666
null
no_dise_00384
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BRAF classified as Pathogenic or Likely Pathogenic for Paediatric disorders.
NM_004333.6(BRAF):c.1729C>A (p.Leu577Ile) VARIANT_IN_GENE BRAF → NM_004333.6(BRAF):c.1729C>A (p.Leu577Ile) VARIANT_HAS_CLINICAL_SIGNIFICANCE Paediatric disorders
{ "steps": [ { "hop": 1, "source_node_id": "BRAF", "source_node_type": "GENE", "source_node_label": "BRAF", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004333.6(B...
NM_004333.6(BRAF):c.1729C>A (p.Leu577Ile)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BRAF\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BRAF\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_004333.6(BRAF):c.1729C>A (p.Leu577Ile)", "text": "NM_004333.6(BRAF):c.1729C>A (p.Leu577Ile) VARIANT_IN_GENE BRAF", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:paediatric_disorders", "text": "NM_004333.6(BRAF):c.1729C>A...
{"gene": "BRAF", "disease": "Paediatric disorders", "pathogenic_variants": ["NM_004333.6(BRAF):c.1729C>A (p.Leu577Ile)"]}
0.83666
null
no_dise_00278
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in MSH2 classified as Pathogenic or Likely Pathogenic for Uterine corpus cancer.
NM_000251.2(MSH2):c.2459-2_2472del VARIANT_IN_GENE MSH2 → NM_000251.2(MSH2):c.2459-2_2472del VARIANT_HAS_CLINICAL_SIGNIFICANCE Uterine corpus cancer
{ "steps": [ { "hop": 1, "source_node_id": "MSH2", "source_node_type": "GENE", "source_node_label": "MSH2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000251.2(M...
NM_000251.2(MSH2):c.2459-2_2472del
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"MSH2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"MSH2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_000251.2(MSH2):c.2459-2_2472del", "text": "NM_000251.2(MSH2):c.2459-2_2472del VARIANT_IN_GENE MSH2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:uterine_corpus_cancer", "text": "NM_000251.2(MSH2):c.2459-2_2472del VARIA...
{"gene": "MSH2", "disease": "Uterine corpus cancer", "pathogenic_variants": ["NM_000251.2(MSH2):c.2459-2_2472del"]}
0.707107
null
no_dise_00277
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BRCA2 classified as Pathogenic or Likely Pathogenic for BRCA2-related cancer predisposition.
NM_000059.4(BRCA2):c.6052del (p.Ser2018fs) VARIANT_IN_GENE BRCA2 → NM_000059.4(BRCA2):c.6052del (p.Ser2018fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE BRCA2-related cancer predisposition
{ "steps": [ { "hop": 1, "source_node_id": "BRCA2", "source_node_type": "GENE", "source_node_label": "BRCA2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000059.4...
NM_000059.4(BRCA2):c.6052del (p.Ser2018fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BRCA2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BRCA2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_000059.4(BRCA2):c.6052del (p.Ser2018fs)", "text": "NM_000059.4(BRCA2):c.6052del (p.Ser2018fs) VARIANT_IN_GENE BRCA2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:brca2_related_cancer_predisposition", "text": "NM_000059...
{"gene": "BRCA2", "disease": "BRCA2-related cancer predisposition", "pathogenic_variants": ["NM_000059.4:c.(1_67+1)del", "NM_000059.4(BRCA2):c.5112_5119delinsG (p.Ile1705fs)", "NM_000059.4(BRCA2):c.8754+1152_9256del", "NM_000059.4(BRCA2):c.8633-6_8635del", "NM_000059.4(BRCA2):c.8469_8478delinsTA (p.Gln2823fs)", "NM_000...
0.921954
null
no_dise_00180
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in CHEK2 classified as Pathogenic or Likely Pathogenic for Congenital heart defects, multiple types, 3.
NM_007194.4(CHEK2):c.409C>T (p.Arg137Ter) VARIANT_IN_GENE CHEK2 → NM_007194.4(CHEK2):c.409C>T (p.Arg137Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE Congenital heart defects, multiple types, 3
{ "steps": [ { "hop": 1, "source_node_id": "CHEK2", "source_node_type": "GENE", "source_node_label": "CHEK2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_007194.4...
NM_007194.4(CHEK2):c.409C>T (p.Arg137Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"CHEK2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"CHEK2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_007194.4(CHEK2):c.409C>T (p.Arg137Ter)", "text": "NM_007194.4(CHEK2):c.409C>T (p.Arg137Ter) VARIANT_IN_GENE CHEK2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:congenital_heart_defects_multiple_types_3", "text": "NM_00...
{"gene": "CHEK2", "disease": "Congenital heart defects, multiple types, 3", "pathogenic_variants": ["NM_007194.4(CHEK2):c.409C>T (p.Arg137Ter)"]}
0.921954
null
no_dise_00122
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in CBL classified as Pathogenic or Likely Pathogenic for Inborn genetic diseases.
NM_005188.4(CBL):c.1166A>C (p.Lys389Thr) VARIANT_IN_GENE CBL → NM_005188.4(CBL):c.1166A>C (p.Lys389Thr) VARIANT_HAS_CLINICAL_SIGNIFICANCE Inborn genetic diseases
{ "steps": [ { "hop": 1, "source_node_id": "CBL", "source_node_type": "GENE", "source_node_label": "CBL", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_005188.4(CBL...
NM_005188.4(CBL):c.1166A>C (p.Lys389Thr)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"CBL\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"CBL\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_005188.4(CBL):c.1166A>C (p.Lys389Thr)", "text": "NM_005188.4(CBL):c.1166A>C (p.Lys389Thr) VARIANT_IN_GENE CBL", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:inborn_genetic_diseases", "text": "NM_005188.4(CBL):c.1166A>C ...
{"gene": "CBL", "disease": "Inborn genetic diseases", "pathogenic_variants": ["NM_005188.4(CBL):c.1166A>C (p.Lys389Thr)"]}
0.921954
null
no_dise_00593
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in RET classified as Pathogenic or Likely Pathogenic for Medullary thyroid carcinoma.
NM_020975.6(RET):c.2671T>G (p.Ser891Ala) VARIANT_IN_GENE RET → NM_020975.6(RET):c.2671T>G (p.Ser891Ala) VARIANT_HAS_CLINICAL_SIGNIFICANCE Medullary thyroid carcinoma
{ "steps": [ { "hop": 1, "source_node_id": "RET", "source_node_type": "GENE", "source_node_label": "RET", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_020975.6(RET...
NM_020975.6(RET):c.2671T>G (p.Ser891Ala)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"RET\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"RET\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_020975.6(RET):c.2671T>G (p.Ser891Ala)", "text": "NM_020975.6(RET):c.2671T>G (p.Ser891Ala) VARIANT_IN_GENE RET", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:medullary_thyroid_carcinoma", "text": "NM_020975.6(RET):c.2671...
{"gene": "RET", "disease": "Medullary thyroid carcinoma", "pathogenic_variants": ["NM_020975.6(RET):c.2671T>G (p.Ser891Ala)"]}
0.921954
null
no_dise_00428
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in ANXA11 classified as Pathogenic or Likely Pathogenic for Amyotrophic lateral sclerosis type 23.
NM_145868.2(ANXA11):c.744+1G>A VARIANT_IN_GENE ANXA11 → NM_145868.2(ANXA11):c.744+1G>A VARIANT_HAS_CLINICAL_SIGNIFICANCE Amyotrophic lateral sclerosis type 23
{ "steps": [ { "hop": 1, "source_node_id": "ANXA11", "source_node_type": "GENE", "source_node_label": "ANXA11", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_145868...
NM_145868.2(ANXA11):c.744+1G>A
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"ANXA11\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"ANXA11\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_145868.2(ANXA11):c.744+1G>A", "text": "NM_145868.2(ANXA11):c.744+1G>A VARIANT_IN_GENE ANXA11", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:amyotrophic_lateral_sclerosis_type_23", "text": "NM_145868.2(ANXA11):c.744+1G>A...
{"gene": "ANXA11", "disease": "Amyotrophic lateral sclerosis type 23", "pathogenic_variants": ["NM_145868.2(ANXA11):c.744+1G>A", "NM_145868.2(ANXA11):c.118G>T (p.Asp40Tyr)", "NM_145868.2(ANXA11):c.112G>A (p.Gly38Arg)", "NM_145868.2(ANXA11):c.119A>G (p.Asp40Gly)"]}
0.83666
null
no_dise_00580
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in CREBBP classified as Pathogenic or Likely Pathogenic for Inborn genetic diseases.
NM_004380.3(CREBBP):c.90del (p.Phe30fs) VARIANT_IN_GENE CREBBP → NM_004380.3(CREBBP):c.90del (p.Phe30fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Inborn genetic diseases
{ "steps": [ { "hop": 1, "source_node_id": "CREBBP", "source_node_type": "GENE", "source_node_label": "CREBBP", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004380...
NM_004380.3(CREBBP):c.90del (p.Phe30fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"CREBBP\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"CREBBP\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_004380.3(CREBBP):c.90del (p.Phe30fs)", "text": "NM_004380.3(CREBBP):c.90del (p.Phe30fs) VARIANT_IN_GENE CREBBP", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:inborn_genetic_diseases", "text": "NM_004380.3(CREBBP):c.90de...
{"gene": "CREBBP", "disease": "Inborn genetic diseases", "pathogenic_variants": ["NM_004380.3(CREBBP):c.3G>T (p.Met1Ile)", "NM_004380.3(CREBBP):c.1948T>C (p.Tyr650His)", "NM_004380.3(CREBBP):c.6271A>T (p.Lys2091Ter)", "NM_004380.3(CREBBP):c.4495C>G (p.Leu1499Val)", "NM_004380.3(CREBBP):c.3625C>T (p.Gln1209Ter)", "NM_00...
0.83666
null
no_dise_00594
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in NF1 classified as Pathogenic or Likely Pathogenic for Developmental defect during embryogenesis.
NM_001042492.3(NF1):c.3053_3054insTTCAACTAATTGTTGTTGAAA (p.Leu1018delinsPheSerThrAsnCysCysTer) VARIANT_IN_GENE NF1 → NM_001042492.3(NF1):c.3053_3054insTTCAACTAATTGTTGTTGAAA (p.Leu1018delinsPheSerThrAsnCysCysTer) VARIANT_HAS_CLINICAL_SIGNIFICANCE Developmental defect during embryogenesis
{ "steps": [ { "hop": 1, "source_node_id": "NF1", "source_node_type": "GENE", "source_node_label": "NF1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_001042492.3(...
NM_001042492.3(NF1):c.3053_3054insTTCAACTAATTGTTGTTGAAA (p.Leu1018delinsPheSerThrAsnCysCysTer)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"NF1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"NF1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_001042492.3(NF1):c.3053_3054insTTCAACTAATTGTTGTTGAAA (p.Leu1018delinsPheSerThrAsnCysCysTer)", "text": "NM_001042492.3(NF1):c.3053_3054insTTCAACTAATTGTTGTTGAAA (p.Leu1018delinsPheSerThrAsnCysCysTer) VARIANT_IN_GENE NF1", "confidence": 1 }, { "source_...
{"gene": "NF1", "disease": "Developmental defect during embryogenesis", "pathogenic_variants": ["NM_001042492.3(NF1):c.3053_3054insTTCAACTAATTGTTGTTGAAA (p.Leu1018delinsPheSerThrAsnCysCysTer)"]}
0.83666
null
no_dise_00222
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in TARDBP classified as Pathogenic or Likely Pathogenic for Frontotemporal dementia.
NM_007375.4(TARDBP):c.1129T>C (p.Ser377Pro) VARIANT_IN_GENE TARDBP → NM_007375.4(TARDBP):c.1129T>C (p.Ser377Pro) VARIANT_HAS_CLINICAL_SIGNIFICANCE Frontotemporal dementia
{ "steps": [ { "hop": 1, "source_node_id": "TARDBP", "source_node_type": "GENE", "source_node_label": "TARDBP", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_007375...
NM_007375.4(TARDBP):c.1129T>C (p.Ser377Pro)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"TARDBP\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"TARDBP\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_007375.4(TARDBP):c.1129T>C (p.Ser377Pro)", "text": "NM_007375.4(TARDBP):c.1129T>C (p.Ser377Pro) VARIANT_IN_GENE TARDBP", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:frontotemporal_dementia", "text": "NM_007375.4(TARDBP...
{"gene": "TARDBP", "disease": "Frontotemporal dementia", "pathogenic_variants": ["NM_007375.4(TARDBP):c.1129T>C (p.Ser377Pro)"]}
0.83666
null
no_dise_00463
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BRIP1 classified as Pathogenic or Likely Pathogenic for Inherited ovarian cancer (without breast cancer).
NM_032043.3(BRIP1):c.2244C>G (p.Tyr748Ter) VARIANT_IN_GENE BRIP1 → NM_032043.3(BRIP1):c.2244C>G (p.Tyr748Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE Inherited ovarian cancer (without breast cancer)
{ "steps": [ { "hop": 1, "source_node_id": "BRIP1", "source_node_type": "GENE", "source_node_label": "BRIP1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_032043.3...
NM_032043.3(BRIP1):c.2244C>G (p.Tyr748Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BRIP1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BRIP1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_032043.3(BRIP1):c.2244C>G (p.Tyr748Ter)", "text": "NM_032043.3(BRIP1):c.2244C>G (p.Tyr748Ter) VARIANT_IN_GENE BRIP1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:inherited_ovarian_cancer_without_breast_cancer", "text":...
{"gene": "BRIP1", "disease": "Inherited ovarian cancer (without breast cancer)", "pathogenic_variants": ["NM_032043.3(BRIP1):c.688del (p.Ser230fs)", "NM_032043.3(BRIP1):c.1888dup (p.Thr630fs)", "NM_032043.3(BRIP1):c.2244C>G (p.Tyr748Ter)", "NM_032043.3(BRIP1):c.1495C>T (p.Gln499Ter)", "NM_032043.3(BRIP1):c.918+1G>A", "...
0.921954
null
no_dise_00394
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in KDM6A classified as Pathogenic or Likely Pathogenic for Kabuki syndrome 1.
NM_001291415.2(KDM6A):c.133dup (p.Glu45fs) VARIANT_IN_GENE KDM6A → NM_001291415.2(KDM6A):c.133dup (p.Glu45fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Kabuki syndrome 1
{ "steps": [ { "hop": 1, "source_node_id": "KDM6A", "source_node_type": "GENE", "source_node_label": "KDM6A", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_00129141...
NM_001291415.2(KDM6A):c.133dup (p.Glu45fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"KDM6A\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"KDM6A\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_001291415.2(KDM6A):c.133dup (p.Glu45fs)", "text": "NM_001291415.2(KDM6A):c.133dup (p.Glu45fs) VARIANT_IN_GENE KDM6A", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:kabuki_syndrome_1", "text": "NM_001291415.2(KDM6A):c.133...
{"gene": "KDM6A", "disease": "Kabuki syndrome 1", "pathogenic_variants": ["NM_001291415.2(KDM6A):c.133dup (p.Glu45fs)"]}
0.83666
null
no_dise_00488
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BCHE classified as Pathogenic or Likely Pathogenic for BCHE Newfoundland.
BCHE Newfoundland VARIANT_IN_GENE BCHE → BCHE Newfoundland VARIANT_HAS_CLINICAL_SIGNIFICANCE BCHE Newfoundland
{ "steps": [ { "hop": 1, "source_node_id": "BCHE", "source_node_type": "GENE", "source_node_label": "BCHE", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "BCHE Newfound...
BCHE Newfoundland
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BCHE\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BCHE\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "BCHE Newfoundland", "text": "BCHE Newfoundland VARIANT_IN_GENE BCHE", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:bche_newfoundland", "text": "BCHE Newfoundland VARIANT_HAS_CLINICAL_SIGNIFICANCE BCHE Newfoundland", "c...
{"gene": "BCHE", "disease": "BCHE Newfoundland", "pathogenic_variants": ["BCHE Newfoundland"]}
0.707107
null
no_dise_00466
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in TARDBP classified as Pathogenic or Likely Pathogenic for FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED.
NM_007375.4(TARDBP):c.787A>G (p.Lys263Glu) VARIANT_IN_GENE TARDBP → NM_007375.4(TARDBP):c.787A>G (p.Lys263Glu) VARIANT_HAS_CLINICAL_SIGNIFICANCE FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
{ "steps": [ { "hop": 1, "source_node_id": "TARDBP", "source_node_type": "GENE", "source_node_label": "TARDBP", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_007375...
NM_007375.4(TARDBP):c.787A>G (p.Lys263Glu)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"TARDBP\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"TARDBP\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_007375.4(TARDBP):c.787A>G (p.Lys263Glu)", "text": "NM_007375.4(TARDBP):c.787A>G (p.Lys263Glu) VARIANT_IN_GENE TARDBP", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:frontotemporal_dementia_with_tdp43_inclusions_tardbp_relate...
{"gene": "TARDBP", "disease": "FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED", "pathogenic_variants": ["NM_007375.4(TARDBP):c.787A>G (p.Lys263Glu)"]}
0.707107
null
no_dise_00584
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BRAF classified as Pathogenic or Likely Pathogenic for LEOPARD syndrome 3.
NM_004333.6(BRAF):c.1801A>C (p.Lys601Gln) VARIANT_IN_GENE BRAF → NM_004333.6(BRAF):c.1801A>C (p.Lys601Gln) VARIANT_HAS_CLINICAL_SIGNIFICANCE LEOPARD syndrome 3
{ "steps": [ { "hop": 1, "source_node_id": "BRAF", "source_node_type": "GENE", "source_node_label": "BRAF", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004333.6(B...
NM_004333.6(BRAF):c.1801A>C (p.Lys601Gln)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BRAF\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BRAF\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_004333.6(BRAF):c.1801A>C (p.Lys601Gln)", "text": "NM_004333.6(BRAF):c.1801A>C (p.Lys601Gln) VARIANT_IN_GENE BRAF", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:leopard_syndrome_3", "text": "NM_004333.6(BRAF):c.1801A>C (...
{"gene": "BRAF", "disease": "LEOPARD syndrome 3", "pathogenic_variants": ["NM_004333.6(BRAF):c.1801A>C (p.Lys601Gln)", "NM_004333.6(BRAF):c.1802A>T (p.Lys601Ile)"]}
0.921954
null
no_dise_00592
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in CDH1 classified as Pathogenic or Likely Pathogenic for Malignant tumor of breast.
NC_000016.9:g.(68771367_68772199)_(68772315_68835572)del VARIANT_IN_GENE CDH1 → NC_000016.9:g.(68771367_68772199)_(68772315_68835572)del VARIANT_HAS_CLINICAL_SIGNIFICANCE Malignant tumor of breast
{ "steps": [ { "hop": 1, "source_node_id": "CDH1", "source_node_type": "GENE", "source_node_label": "CDH1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NC_000016.9:g...
NC_000016.9:g.(68771367_68772199)_(68772315_68835572)del
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"CDH1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"CDH1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NC_000016.9:g.(68771367_68772199)_(68772315_68835572)del", "text": "NC_000016.9:g.(68771367_68772199)_(68772315_68835572)del VARIANT_IN_GENE CDH1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:malignant_tumor_of_breast", "...
{"gene": "CDH1", "disease": "Malignant tumor of breast", "pathogenic_variants": ["NC_000016.9:g.(68771367_68772199)_(68772315_68835572)del", "NM_004360.5(CDH1):c.2440-2_*1del", "NC_000016.9:g.(68857530_68862076)_(68863701_68867192)dup"]}
0.83666
null
no_dise_00485
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in CTNNA1 classified as Pathogenic or Likely Pathogenic for Craniosynostosis syndrome.
NM_001903.5(CTNNA1):c.2572_2586dup (p.Ser858_Lys862dup) VARIANT_IN_GENE CTNNA1 → NM_001903.5(CTNNA1):c.2572_2586dup (p.Ser858_Lys862dup) VARIANT_HAS_CLINICAL_SIGNIFICANCE Craniosynostosis syndrome
{ "steps": [ { "hop": 1, "source_node_id": "CTNNA1", "source_node_type": "GENE", "source_node_label": "CTNNA1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_001903...
NM_001903.5(CTNNA1):c.2572_2586dup (p.Ser858_Lys862dup)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"CTNNA1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"CTNNA1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_001903.5(CTNNA1):c.2572_2586dup (p.Ser858_Lys862dup)", "text": "NM_001903.5(CTNNA1):c.2572_2586dup (p.Ser858_Lys862dup) VARIANT_IN_GENE CTNNA1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:craniosynostosis_syndrome", "...
{"gene": "CTNNA1", "disease": "Craniosynostosis syndrome", "pathogenic_variants": ["NM_001903.5(CTNNA1):c.2572_2586dup (p.Ser858_Lys862dup)"]}
0.707107
null
no_dise_00272
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in RAD51D classified as Pathogenic or Likely Pathogenic for Familial ovarian cancer.
NM_002878.4(RAD51D):c.536dup (p.Asp180fs) VARIANT_IN_GENE RAD51D → NM_002878.4(RAD51D):c.536dup (p.Asp180fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Familial ovarian cancer
{ "steps": [ { "hop": 1, "source_node_id": "RAD51D", "source_node_type": "GENE", "source_node_label": "RAD51D", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_002878...
NM_002878.4(RAD51D):c.536dup (p.Asp180fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"RAD51D\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"RAD51D\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_002878.4(RAD51D):c.536dup (p.Asp180fs)", "text": "NM_002878.4(RAD51D):c.536dup (p.Asp180fs) VARIANT_IN_GENE RAD51D", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:familial_ovarian_cancer", "text": "NM_002878.4(RAD51D):c....
{"gene": "RAD51D", "disease": "Familial ovarian cancer", "pathogenic_variants": ["NM_002878.4(RAD51D):c.547C>T (p.Gln183Ter)", "NM_002878.4(RAD51D):c.748del (p.His250fs)", "NM_002878.4(RAD51D):c.536dup (p.Asp180fs)", "NM_002878.4(RAD51D):c.144+1G>A"]}
0.83666
null
no_dise_00006
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in PMS2 classified as Pathogenic or Likely Pathogenic for PMS2-related disorder.
NM_000535.7(PMS2):c.1438G>T (p.Gly480Ter) VARIANT_IN_GENE PMS2 → NM_000535.7(PMS2):c.1438G>T (p.Gly480Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE PMS2-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "PMS2", "source_node_type": "GENE", "source_node_label": "PMS2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000535.7(P...
NM_000535.7(PMS2):c.1438G>T (p.Gly480Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"PMS2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"PMS2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_000535.7(PMS2):c.1438G>T (p.Gly480Ter)", "text": "NM_000535.7(PMS2):c.1438G>T (p.Gly480Ter) VARIANT_IN_GENE PMS2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:pms2_related_disorder", "text": "NM_000535.7(PMS2):c.1438G>...
{"gene": "PMS2", "disease": "PMS2-related disorder", "pathogenic_variants": ["NM_000535.7(PMS2):c.1438G>T (p.Gly480Ter)"]}
0.707107
null
no_dise_00343
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in RET classified as Pathogenic or Likely Pathogenic for Abnormality of the digestive system.
NM_020975.6(RET):c.960del (p.Asp322fs) VARIANT_IN_GENE RET → NM_020975.6(RET):c.960del (p.Asp322fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Abnormality of the digestive system
{ "steps": [ { "hop": 1, "source_node_id": "RET", "source_node_type": "GENE", "source_node_label": "RET", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_020975.6(RET...
NM_020975.6(RET):c.960del (p.Asp322fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"RET\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"RET\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_020975.6(RET):c.960del (p.Asp322fs)", "text": "NM_020975.6(RET):c.960del (p.Asp322fs) VARIANT_IN_GENE RET", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:abnormality_of_the_digestive_system", "text": "NM_020975.6(RET):c....
{"gene": "RET", "disease": "Abnormality of the digestive system", "pathogenic_variants": ["NM_020975.6(RET):c.960del (p.Asp322fs)"]}
0.83666
null
no_dise_00368
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in RAD51D classified as Pathogenic or Likely Pathogenic for Deleterious RAD51D Gene Mutation.
NM_002878.4(RAD51D):c.620C>A (p.Ser207Ter) VARIANT_IN_GENE RAD51D → NM_002878.4(RAD51D):c.620C>A (p.Ser207Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE Deleterious RAD51D Gene Mutation
{ "steps": [ { "hop": 1, "source_node_id": "RAD51D", "source_node_type": "GENE", "source_node_label": "RAD51D", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_002878...
NM_002878.4(RAD51D):c.620C>A (p.Ser207Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"RAD51D\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"RAD51D\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_002878.4(RAD51D):c.620C>A (p.Ser207Ter)", "text": "NM_002878.4(RAD51D):c.620C>A (p.Ser207Ter) VARIANT_IN_GENE RAD51D", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:deleterious_rad51d_gene_mutation", "text": "NM_002878.4...
{"gene": "RAD51D", "disease": "Deleterious RAD51D Gene Mutation", "pathogenic_variants": ["NM_002878.4(RAD51D):c.564_567del (p.Val189fs)", "NM_002878.4(RAD51D):c.620C>A (p.Ser207Ter)"]}
0.83666
null
no_dise_00226
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in PFN1 classified as Pathogenic or Likely Pathogenic for PAGET DISEASE OF BONE 7, EARLY-ONSET.
PFN1, 4-BP DEL, 318TGAC VARIANT_IN_GENE PFN1 → PFN1, 4-BP DEL, 318TGAC VARIANT_HAS_CLINICAL_SIGNIFICANCE PAGET DISEASE OF BONE 7, EARLY-ONSET
{ "steps": [ { "hop": 1, "source_node_id": "PFN1", "source_node_type": "GENE", "source_node_label": "PFN1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "PFN1, 4-BP DE...
PFN1, 4-BP DEL, 318TGAC
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"PFN1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"PFN1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "PFN1, 4-BP DEL, 318TGAC", "text": "PFN1, 4-BP DEL, 318TGAC VARIANT_IN_GENE PFN1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:paget_disease_of_bone_7_early_onset", "text": "PFN1, 4-BP DEL, 318TGAC VARIANT_HAS_CLINICAL_SIG...
{"gene": "PFN1", "disease": "PAGET DISEASE OF BONE 7, EARLY-ONSET", "pathogenic_variants": ["NM_005022.4(PFN1):c.325+10T>C", "PFN1, 1-BP DEL, 324G", "PFN1, 4-BP DEL, 318TGAC"]}
0.707107
null
no_dise_00242
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in POLD1 classified as Pathogenic or Likely Pathogenic for Immunodeficiency 120.
NM_002691.4(POLD1):c.[2052G>C;2816C>G] VARIANT_IN_GENE POLD1 → NM_002691.4(POLD1):c.[2052G>C;2816C>G] VARIANT_HAS_CLINICAL_SIGNIFICANCE Immunodeficiency 120
{ "steps": [ { "hop": 1, "source_node_id": "POLD1", "source_node_type": "GENE", "source_node_label": "POLD1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_002691.4...
NM_002691.4(POLD1):c.[2052G>C;2816C>G]
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"POLD1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"POLD1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_002691.4(POLD1):c.2052G>C (p.Gln684His)", "text": "NM_002691.4(POLD1):c.[2052G>C;2816C>G] VARIANT_IN_GENE POLD1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:immunodeficiency_120", "text": "NM_002691.4(POLD1):c.[2052G>...
{"gene": "POLD1", "disease": "Immunodeficiency 120", "pathogenic_variants": ["NM_002691.4(POLD1):c.[2052G>C;2816C>G]"]}
0.707107
null
no_dise_00610
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in NLRP3 classified as Pathogenic or Likely Pathogenic for Pericardial effusion.
NM_001243133.2(NLRP3):c.1799A>G (p.Gln600Arg) VARIANT_IN_GENE NLRP3 → NM_001243133.2(NLRP3):c.1799A>G (p.Gln600Arg) VARIANT_HAS_CLINICAL_SIGNIFICANCE Pericardial effusion
{ "steps": [ { "hop": 1, "source_node_id": "NLRP3", "source_node_type": "GENE", "source_node_label": "NLRP3", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_00124313...
NM_001243133.2(NLRP3):c.1799A>G (p.Gln600Arg)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"NLRP3\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"NLRP3\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_001243133.2(NLRP3):c.1799A>G (p.Gln600Arg)", "text": "NM_001243133.2(NLRP3):c.1799A>G (p.Gln600Arg) VARIANT_IN_GENE NLRP3", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:pericardial_effusion", "text": "NM_001243133.2(NLR...
{"gene": "NLRP3", "disease": "Pericardial effusion", "pathogenic_variants": ["NM_001243133.2(NLRP3):c.1799A>G (p.Gln600Arg)"]}
0.707107
null
no_dise_00276
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in NF1 classified as Pathogenic or Likely Pathogenic for Neurofibromatosis-Noonan syndrome.
NM_001042492.3(NF1):c.6452_6453del (p.Leu2151fs) VARIANT_IN_GENE NF1 → NM_001042492.3(NF1):c.6452_6453del (p.Leu2151fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Neurofibromatosis-Noonan syndrome
{ "steps": [ { "hop": 1, "source_node_id": "NF1", "source_node_type": "GENE", "source_node_label": "NF1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_001042492.3(...
NM_001042492.3(NF1):c.6452_6453del (p.Leu2151fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"NF1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"NF1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_001042492.3(NF1):c.6452_6453del (p.Leu2151fs)", "text": "NM_001042492.3(NF1):c.6452_6453del (p.Leu2151fs) VARIANT_IN_GENE NF1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:neurofibromatosis_noonan_syndrome", "text": "N...
{"gene": "NF1", "disease": "Neurofibromatosis-Noonan syndrome", "pathogenic_variants": ["NM_001042492.3(NF1):c.6452_6453del (p.Leu2151fs)"]}
0.83666
null
no_dise_00105
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BCL11B classified as Pathogenic or Likely Pathogenic for Combined immunodeficiency.
NM_138576.4(BCL11B):c.1323T>G (p.Asn441Lys) VARIANT_IN_GENE BCL11B → NM_138576.4(BCL11B):c.1323T>G (p.Asn441Lys) VARIANT_HAS_CLINICAL_SIGNIFICANCE Combined immunodeficiency
{ "steps": [ { "hop": 1, "source_node_id": "BCL11B", "source_node_type": "GENE", "source_node_label": "BCL11B", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_138576...
NM_138576.4(BCL11B):c.1323T>G (p.Asn441Lys)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BCL11B\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BCL11B\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_138576.4(BCL11B):c.1323T>G (p.Asn441Lys)", "text": "NM_138576.4(BCL11B):c.1323T>G (p.Asn441Lys) VARIANT_IN_GENE BCL11B", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:combined_immunodeficiency", "text": "NM_138576.4(BCL1...
{"gene": "BCL11B", "disease": "Combined immunodeficiency", "pathogenic_variants": ["NM_138576.4(BCL11B):c.1323T>G (p.Asn441Lys)"]}
0.707107
null
no_dise_00285
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in APC classified as Pathogenic or Likely Pathogenic for Inherited polyposis and early onset colorectal cancer - germline testing.
NM_000038.6(APC):c.4175C>G (p.Ser1392Ter) VARIANT_IN_GENE APC → NM_000038.6(APC):c.4175C>G (p.Ser1392Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE Inherited polyposis and early onset colorectal cancer - germline testing
{ "steps": [ { "hop": 1, "source_node_id": "APC", "source_node_type": "GENE", "source_node_label": "APC", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000038.6(APC...
NM_000038.6(APC):c.4175C>G (p.Ser1392Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"APC\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"APC\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_000038.6(APC):c.4175C>G (p.Ser1392Ter)", "text": "NM_000038.6(APC):c.4175C>G (p.Ser1392Ter) VARIANT_IN_GENE APC", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:inherited_polyposis_and_early_onset_colorectal_cancer_germli", ...
{"gene": "APC", "disease": "Inherited polyposis and early onset colorectal cancer - germline testing", "pathogenic_variants": ["NM_000038.6(APC):c.4175C>G (p.Ser1392Ter)"]}
0.83666
null
no_dise_00066
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in DDX41 classified as Pathogenic or Likely Pathogenic for DDX41-related hematologic malignancy predisposition syndrome.
NM_016222.4(DDX41):c.1586_1587del (p.Thr529fs) VARIANT_IN_GENE DDX41 → NM_016222.4(DDX41):c.1586_1587del (p.Thr529fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE DDX41-related hematologic malignancy predisposition syndrome
{ "steps": [ { "hop": 1, "source_node_id": "DDX41", "source_node_type": "GENE", "source_node_label": "DDX41", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_016222.4...
NM_016222.4(DDX41):c.1586_1587del (p.Thr529fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"DDX41\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"DDX41\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_016222.4(DDX41):c.1586_1587del (p.Thr529fs)", "text": "NM_016222.4(DDX41):c.1586_1587del (p.Thr529fs) VARIANT_IN_GENE DDX41", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:ddx41_related_hematologic_malignancy_predisposition_...
{"gene": "DDX41", "disease": "DDX41-related hematologic malignancy predisposition syndrome", "pathogenic_variants": ["NM_016222.4(DDX41):c.1301del (p.Pro434fs)", "NM_016222.4(DDX41):c.2T>C (p.Met1Thr)", "NM_016222.4(DDX41):c.1621_1621+10del", "NM_016222.4(DDX41):c.547T>A (p.Phe183Ile)", "NM_016222.4(DDX41):c.434+1G>T",...
0.921954
null
no_dise_00324
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in DCTN1 classified as Pathogenic or Likely Pathogenic for Perry syndrome.
NM_004082.5(DCTN1):c.279+1G>C VARIANT_IN_GENE DCTN1 → NM_004082.5(DCTN1):c.279+1G>C VARIANT_HAS_CLINICAL_SIGNIFICANCE Perry syndrome
{ "steps": [ { "hop": 1, "source_node_id": "DCTN1", "source_node_type": "GENE", "source_node_label": "DCTN1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004082.5...
NM_004082.5(DCTN1):c.279+1G>C
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"DCTN1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"DCTN1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_004082.5(DCTN1):c.279+1G>C", "text": "NM_004082.5(DCTN1):c.279+1G>C VARIANT_IN_GENE DCTN1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:perry_syndrome", "text": "NM_004082.5(DCTN1):c.279+1G>C VARIANT_HAS_CLINICAL_SIGNI...
{"gene": "DCTN1", "disease": "Perry syndrome", "pathogenic_variants": ["NM_004082.5(DCTN1):c.626dup (p.Leu210fs)", "NM_004082.5(DCTN1):c.279+1G>C"]}
0.921954
null
no_dise_00387
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in KIF5A classified as Pathogenic or Likely Pathogenic for Spastic Paraglegia 10.
NM_004984.4(KIF5A):c.1550_1554del (p.Asp517fs) VARIANT_IN_GENE KIF5A → NM_004984.4(KIF5A):c.1550_1554del (p.Asp517fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Spastic Paraglegia 10
{ "steps": [ { "hop": 1, "source_node_id": "KIF5A", "source_node_type": "GENE", "source_node_label": "KIF5A", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004984.4...
NM_004984.4(KIF5A):c.1550_1554del (p.Asp517fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"KIF5A\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"KIF5A\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_004984.4(KIF5A):c.1550_1554del (p.Asp517fs)", "text": "NM_004984.4(KIF5A):c.1550_1554del (p.Asp517fs) VARIANT_IN_GENE KIF5A", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:spastic_paraglegia_10", "text": "NM_004984.4(KIF...
{"gene": "KIF5A", "disease": "Spastic Paraglegia 10", "pathogenic_variants": ["NM_004984.4(KIF5A):c.1550_1554del (p.Asp517fs)", "NM_004984.4(KIF5A):c.404_407del (p.Tyr135fs)", "NM_004984.4(KIF5A):c.2549_2562dup (p.Arg855fs)"]}
0.83666
null
no_dise_00398
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in KIF5A classified as Pathogenic or Likely Pathogenic for Hereditary spastic paraplegia.
NM_004984.4(KIF5A):c.868G>C (p.Asp290His) VARIANT_IN_GENE KIF5A → NM_004984.4(KIF5A):c.868G>C (p.Asp290His) VARIANT_HAS_CLINICAL_SIGNIFICANCE Hereditary spastic paraplegia
{ "steps": [ { "hop": 1, "source_node_id": "KIF5A", "source_node_type": "GENE", "source_node_label": "KIF5A", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004984.4...
NM_004984.4(KIF5A):c.868G>C (p.Asp290His)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"KIF5A\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"KIF5A\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_004984.4(KIF5A):c.868G>C (p.Asp290His)", "text": "NM_004984.4(KIF5A):c.868G>C (p.Asp290His) VARIANT_IN_GENE KIF5A", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:hereditary_spastic_paraplegia", "text": "NM_004984.4(KIF5A...
{"gene": "KIF5A", "disease": "Hereditary spastic paraplegia", "pathogenic_variants": ["NM_004984.4(KIF5A):c.868G>C (p.Asp290His)"]}
0.83666
null
no_dise_00235
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in RET classified as Pathogenic or Likely Pathogenic for Multiple endocrine neoplasia, type 2.
NM_020975.6(RET):c.1522+2T>C VARIANT_IN_GENE RET → NM_020975.6(RET):c.1522+2T>C VARIANT_HAS_CLINICAL_SIGNIFICANCE Multiple endocrine neoplasia, type 2
{ "steps": [ { "hop": 1, "source_node_id": "RET", "source_node_type": "GENE", "source_node_label": "RET", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_020975.6(RET...
NM_020975.6(RET):c.1522+2T>C
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"RET\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"RET\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_020975.6(RET):c.1522+2T>C", "text": "NM_020975.6(RET):c.1522+2T>C VARIANT_IN_GENE RET", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:multiple_endocrine_neoplasia_type_2", "text": "NM_020975.6(RET):c.1522+2T>C VARIANT_HA...
{"gene": "RET", "disease": "Multiple endocrine neoplasia, type 2", "pathogenic_variants": ["NM_020975.6(RET):c.206del (p.Gly69fs)", "NM_020975.6(RET):c.1341del (p.Asn448fs)", "NM_020975.6(RET):c.758dup (p.Val254fs)", "NM_020975.6(RET):c.2715C>A (p.Tyr905Ter)", "NM_020975.6(RET):c.668_669dup (p.Ser224Ter)", "NM_020975.6...
0.83666
null
no_dise_00332
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in MET classified as Pathogenic or Likely Pathogenic for Papillary renal cell carcinoma type 1.
NM_000245.4(MET):c.3562G>T (p.Val1188Leu) VARIANT_IN_GENE MET → NM_000245.4(MET):c.3562G>T (p.Val1188Leu) VARIANT_HAS_CLINICAL_SIGNIFICANCE Papillary renal cell carcinoma type 1
{ "steps": [ { "hop": 1, "source_node_id": "MET", "source_node_type": "GENE", "source_node_label": "MET", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000245.4(MET...
NM_000245.4(MET):c.3562G>T (p.Val1188Leu)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"MET\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"MET\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_000245.4(MET):c.3562G>T (p.Val1188Leu)", "text": "NM_000245.4(MET):c.3562G>T (p.Val1188Leu) VARIANT_IN_GENE MET", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:papillary_renal_cell_carcinoma_type_1", "text": "NM_000245.4...
{"gene": "MET", "disease": "Papillary renal cell carcinoma type 1", "pathogenic_variants": ["NM_000245.4(MET):c.3562G>T (p.Val1188Leu)"]}
0.707107
null
no_dise_00478
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in PFN1 classified as Pathogenic or Likely Pathogenic for Amyotrophic lateral sclerosis type 18.
NM_005022.4(PFN1):c.318_319dup (p.Asp107fs) VARIANT_IN_GENE PFN1 → NM_005022.4(PFN1):c.318_319dup (p.Asp107fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Amyotrophic lateral sclerosis type 18
{ "steps": [ { "hop": 1, "source_node_id": "PFN1", "source_node_type": "GENE", "source_node_label": "PFN1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_005022.4(P...
NM_005022.4(PFN1):c.318_319dup (p.Asp107fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"PFN1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"PFN1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_005022.4(PFN1):c.318_319dup (p.Asp107fs)", "text": "NM_005022.4(PFN1):c.318_319dup (p.Asp107fs) VARIANT_IN_GENE PFN1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:amyotrophic_lateral_sclerosis_type_18", "text": "NM_005...
{"gene": "PFN1", "disease": "Amyotrophic lateral sclerosis type 18", "pathogenic_variants": ["NM_005022.4(PFN1):c.318_319dup (p.Asp107fs)"]}
0.921954
null
no_dise_00301
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in ERG classified as Pathogenic or Likely Pathogenic for Neurofibromatosis, type 1.
t(21;22)(q21;q12) VARIANT_IN_GENE ERG → t(21;22)(q21;q12) VARIANT_HAS_CLINICAL_SIGNIFICANCE Neurofibromatosis, type 1
{ "steps": [ { "hop": 1, "source_node_id": "ERG", "source_node_type": "GENE", "source_node_label": "ERG", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "t(21;22)(q21;q1...
t(21;22)(q21;q12)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"ERG\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"ERG\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "t(21;22)(q21;q12)", "text": "t(21;22)(q21;q12) VARIANT_IN_GENE ERG", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:neurofibromatosis_type_1", "text": "t(21;22)(q21;q12) VARIANT_HAS_CLINICAL_SIGNIFICANCE Neurofibromatosis, t...
{"gene": "ERG", "disease": "Neurofibromatosis, type 1", "pathogenic_variants": ["t(21;22)(q21;q12)"]}
0.707107
null
no_dise_00089
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in CBL classified as Pathogenic or Likely Pathogenic for Cardiovascular phenotype.
NM_005188.4(CBL):c.1109_1111dup (p.Leu370_Tyr371insLeu) VARIANT_IN_GENE CBL → NM_005188.4(CBL):c.1109_1111dup (p.Leu370_Tyr371insLeu) VARIANT_HAS_CLINICAL_SIGNIFICANCE Cardiovascular phenotype
{ "steps": [ { "hop": 1, "source_node_id": "CBL", "source_node_type": "GENE", "source_node_label": "CBL", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_005188.4(CBL...
NM_005188.4(CBL):c.1109_1111dup (p.Leu370_Tyr371insLeu)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"CBL\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"CBL\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_005188.4(CBL):c.1109_1111dup (p.Leu370_Tyr371insLeu)", "text": "NM_005188.4(CBL):c.1109_1111dup (p.Leu370_Tyr371insLeu) VARIANT_IN_GENE CBL", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:cardiovascular_phenotype", "text...
{"gene": "CBL", "disease": "Cardiovascular phenotype", "pathogenic_variants": ["NM_005188.4(CBL):c.1109_1111dup (p.Leu370_Tyr371insLeu)"]}
0.83666
null
no_dise_00554
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BIN1 classified as Pathogenic or Likely Pathogenic for Myopathy, centronuclear, 2.
NM_139343.3(BIN1):c.105G>T (p.Lys35Asn) VARIANT_IN_GENE BIN1 → NM_139343.3(BIN1):c.105G>T (p.Lys35Asn) VARIANT_HAS_CLINICAL_SIGNIFICANCE Myopathy, centronuclear, 2
{ "steps": [ { "hop": 1, "source_node_id": "BIN1", "source_node_type": "GENE", "source_node_label": "BIN1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_139343.3(B...
NM_139343.3(BIN1):c.105G>T (p.Lys35Asn)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BIN1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BIN1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_139343.3(BIN1):c.105G>T (p.Lys35Asn)", "text": "NM_139343.3(BIN1):c.105G>T (p.Lys35Asn) VARIANT_IN_GENE BIN1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:myopathy_centronuclear_2", "text": "NM_139343.3(BIN1):c.105G>T ...
{"gene": "BIN1", "disease": "Myopathy, centronuclear, 2", "pathogenic_variants": ["NM_139343.3(BIN1):c.1713G>A (p.Trp571Ter)", "NM_139343.3(BIN1):c.451G>A (p.Asp151Asn)", "NM_139343.3(BIN1):c.105G>T (p.Lys35Asn)", "NM_139343.3(BIN1):c.166-2_220+3del", "NM_139343.3(BIN1):c.433C>T (p.Arg145Cys)", "NM_139343.3(BIN1):c.172...
0.707107
null
no_dise_00087
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in REST classified as Pathogenic or Likely Pathogenic for Autosomal dominant nonsyndromic hearing loss 27.
NM_005612.5(REST):c.983-2247C>G VARIANT_IN_GENE REST → NM_005612.5(REST):c.983-2247C>G VARIANT_HAS_CLINICAL_SIGNIFICANCE Autosomal dominant nonsyndromic hearing loss 27
{ "steps": [ { "hop": 1, "source_node_id": "REST", "source_node_type": "GENE", "source_node_label": "REST", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_005612.5(R...
NM_005612.5(REST):c.983-2247C>G
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"REST\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"REST\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_005612.5(REST):c.983-2247C>G", "text": "NM_005612.5(REST):c.983-2247C>G VARIANT_IN_GENE REST", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:autosomal_dominant_nonsyndromic_hearing_loss_27", "text": "NM_005612.5(REST):c....
{"gene": "REST", "disease": "Autosomal dominant nonsyndromic hearing loss 27", "pathogenic_variants": ["NM_005612.5(REST):c.983-2247C>G"]}
0.707107
null
no_dise_00450
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in PSEN1 classified as Pathogenic or Likely Pathogenic for Early-onset autosomal dominant Alzheimer disease.
NM_000021.4(PSEN1):c.856C>G (p.Leu286Val) VARIANT_IN_GENE PSEN1 → NM_000021.4(PSEN1):c.856C>G (p.Leu286Val) VARIANT_HAS_CLINICAL_SIGNIFICANCE Early-onset autosomal dominant Alzheimer disease
{ "steps": [ { "hop": 1, "source_node_id": "PSEN1", "source_node_type": "GENE", "source_node_label": "PSEN1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000021.4...
NM_000021.4(PSEN1):c.856C>G (p.Leu286Val)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"PSEN1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"PSEN1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_000021.4(PSEN1):c.856C>G (p.Leu286Val)", "text": "NM_000021.4(PSEN1):c.856C>G (p.Leu286Val) VARIANT_IN_GENE PSEN1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:early_onset_autosomal_dominant_alzheimer_disease", "text":...
{"gene": "PSEN1", "disease": "Early-onset autosomal dominant Alzheimer disease", "pathogenic_variants": ["NM_000021.4(PSEN1):c.856C>G (p.Leu286Val)", "NM_000021.4(PSEN1):c.498TAT[1] (p.Ile168del)"]}
0.921954
null
no_dise_00541
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in KMT2D classified as Pathogenic or Likely Pathogenic for Neurodevelopmental abnormality.
NM_003482.4(KMT2D):c.7762del (p.His2588fs) VARIANT_IN_GENE KMT2D → NM_003482.4(KMT2D):c.7762del (p.His2588fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Neurodevelopmental abnormality
{ "steps": [ { "hop": 1, "source_node_id": "KMT2D", "source_node_type": "GENE", "source_node_label": "KMT2D", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_003482.4...
NM_003482.4(KMT2D):c.7762del (p.His2588fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"KMT2D\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"KMT2D\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_003482.4(KMT2D):c.7762del (p.His2588fs)", "text": "NM_003482.4(KMT2D):c.7762del (p.His2588fs) VARIANT_IN_GENE KMT2D", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:neurodevelopmental_abnormality", "text": "NM_003482.4(KM...
{"gene": "KMT2D", "disease": "Neurodevelopmental abnormality", "pathogenic_variants": ["NM_003482.4(KMT2D):c.7762del (p.His2588fs)"]}
0.83666
null
no_dise_00026
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in MSH6 classified as Pathogenic or Likely Pathogenic for Breast and/or ovarian cancer.
NM_000179.3(MSH6):c.3917_3938dup (p.Ile1313_Gln1314insTer) VARIANT_IN_GENE MSH6 → NM_000179.3(MSH6):c.3917_3938dup (p.Ile1313_Gln1314insTer) VARIANT_HAS_CLINICAL_SIGNIFICANCE Breast and/or ovarian cancer
{ "steps": [ { "hop": 1, "source_node_id": "MSH6", "source_node_type": "GENE", "source_node_label": "MSH6", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000179.3(M...
NM_000179.3(MSH6):c.3917_3938dup (p.Ile1313_Gln1314insTer)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"MSH6\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"MSH6\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_000179.3(MSH6):c.3917_3938dup (p.Ile1313_Gln1314insTer)", "text": "NM_000179.3(MSH6):c.3917_3938dup (p.Ile1313_Gln1314insTer) VARIANT_IN_GENE MSH6", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:breast_and_or_ovarian_cancer"...
{"gene": "MSH6", "disease": "Breast and/or ovarian cancer", "pathogenic_variants": ["NM_000179.3(MSH6):c.3917_3938dup (p.Ile1313_Gln1314insTer)"]}
0.83666
null
no_dise_00609
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in CDKN2A classified as Pathogenic or Likely Pathogenic for Acute lymphoid leukemia.
NM_000077.5(CDKN2A):c.151-6_151delinsC VARIANT_IN_GENE CDKN2A → NM_000077.5(CDKN2A):c.151-6_151delinsC VARIANT_HAS_CLINICAL_SIGNIFICANCE Acute lymphoid leukemia
{ "steps": [ { "hop": 1, "source_node_id": "CDKN2A", "source_node_type": "GENE", "source_node_label": "CDKN2A", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000077...
NM_000077.5(CDKN2A):c.151-6_151delinsC
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"CDKN2A\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"CDKN2A\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_000077.5(CDKN2A):c.151-6_151delinsC", "text": "NM_000077.5(CDKN2A):c.151-6_151delinsC VARIANT_IN_GENE CDKN2A", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:acute_lymphoid_leukemia", "text": "NM_000077.5(CDKN2A):c.151-6_...
{"gene": "CDKN2A", "disease": "Acute lymphoid leukemia", "pathogenic_variants": ["NM_000077.5(CDKN2A):c.174_185delinsGG (p.Val59fs)", "NM_000077.5(CDKN2A):c.151-6_151delinsC"]}
0.83666
null
no_dise_00312
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in POLD1 classified as Pathogenic or Likely Pathogenic for Carcinoma of pancreas.
NM_002691.4(POLD1):c.3148del (p.Arg1050fs) VARIANT_IN_GENE POLD1 → NM_002691.4(POLD1):c.3148del (p.Arg1050fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Carcinoma of pancreas
{ "steps": [ { "hop": 1, "source_node_id": "POLD1", "source_node_type": "GENE", "source_node_label": "POLD1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_002691.4...
NM_002691.4(POLD1):c.3148del (p.Arg1050fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"POLD1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"POLD1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_002691.4(POLD1):c.3148del (p.Arg1050fs)", "text": "NM_002691.4(POLD1):c.3148del (p.Arg1050fs) VARIANT_IN_GENE POLD1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:carcinoma_of_pancreas", "text": "NM_002691.4(POLD1):c.31...
{"gene": "POLD1", "disease": "Carcinoma of pancreas", "pathogenic_variants": ["NM_002691.4(POLD1):c.3148del (p.Arg1050fs)"]}
0.707107
null
no_dise_00127
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in TARDBP classified as Pathogenic or Likely Pathogenic for Amyotrophic lateral sclerosis type 10.
NM_007375.4(TARDBP):c.991C>A (p.Gln331Lys) VARIANT_IN_GENE TARDBP → NM_007375.4(TARDBP):c.991C>A (p.Gln331Lys) VARIANT_HAS_CLINICAL_SIGNIFICANCE Amyotrophic lateral sclerosis type 10
{ "steps": [ { "hop": 1, "source_node_id": "TARDBP", "source_node_type": "GENE", "source_node_label": "TARDBP", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_007375...
NM_007375.4(TARDBP):c.991C>A (p.Gln331Lys)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"TARDBP\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"TARDBP\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_007375.4(TARDBP):c.991C>A (p.Gln331Lys)", "text": "NM_007375.4(TARDBP):c.991C>A (p.Gln331Lys) VARIANT_IN_GENE TARDBP", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:amyotrophic_lateral_sclerosis_type_10", "text": "NM_007...
{"gene": "TARDBP", "disease": "Amyotrophic lateral sclerosis type 10", "pathogenic_variants": ["NM_007375.4(TARDBP):c.1123A>G (p.Ser375Gly)", "NM_007375.4(TARDBP):c.1035C>A (p.Asn345Lys)", "NM_007375.4(TARDBP):c.1028A>G (p.Gln343Arg)", "NM_007375.4(TARDBP):c.506A>G (p.Asp169Gly)", "NM_007375.4(TARDBP):c.991C>A (p.Gln33...
0.707107
null
no_dise_00335
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BCL11B classified as Pathogenic or Likely Pathogenic for BCL11B-related disorder.
NM_138576.4(BCL11B):c.2595del (p.Tyr866fs) VARIANT_IN_GENE BCL11B → NM_138576.4(BCL11B):c.2595del (p.Tyr866fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE BCL11B-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "BCL11B", "source_node_type": "GENE", "source_node_label": "BCL11B", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_138576...
NM_138576.4(BCL11B):c.2595del (p.Tyr866fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BCL11B\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BCL11B\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_138576.4(BCL11B):c.2595del (p.Tyr866fs)", "text": "NM_138576.4(BCL11B):c.2595del (p.Tyr866fs) VARIANT_IN_GENE BCL11B", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:bcl11b_related_disorder", "text": "NM_138576.4(BCL11B):...
{"gene": "BCL11B", "disease": "BCL11B-related disorder", "pathogenic_variants": ["NM_138576.4(BCL11B):c.756_765del (p.Gly253fs)", "NM_138576.4(BCL11B):c.2435_2436insAA (p.Val813fs)", "NM_138576.4(BCL11B):c.997G>A (p.Glu333Lys)", "NM_138576.4(BCL11B):c.2595del (p.Tyr866fs)", "NM_138576.4(BCL11B):c.1158C>A (p.Asn386Lys)"...
0.83666
null
no_dise_00372
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in SOD1 classified as Pathogenic or Likely Pathogenic for Motor neuron disease.
NM_000454.5(SOD1):c.112G>A (p.Gly38Arg) VARIANT_IN_GENE SOD1 → NM_000454.5(SOD1):c.112G>A (p.Gly38Arg) VARIANT_HAS_CLINICAL_SIGNIFICANCE Motor neuron disease
{ "steps": [ { "hop": 1, "source_node_id": "SOD1", "source_node_type": "GENE", "source_node_label": "SOD1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000454.5(S...
NM_000454.5(SOD1):c.112G>A (p.Gly38Arg)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"SOD1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"SOD1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_000454.5(SOD1):c.112G>A (p.Gly38Arg)", "text": "NM_000454.5(SOD1):c.112G>A (p.Gly38Arg) VARIANT_IN_GENE SOD1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:motor_neuron_disease", "text": "NM_000454.5(SOD1):c.112G>A (p.G...
{"gene": "SOD1", "disease": "Motor neuron disease", "pathogenic_variants": ["NM_000454.5(SOD1):c.280G>C (p.Gly94Arg)", "NM_000454.5(SOD1):c.302A>G (p.Glu101Gly)", "NM_000454.5(SOD1):c.112G>A (p.Gly38Arg)", "NM_000454.5(SOD1):c.437C>A (p.Ala146Asp)"]}
0.921954
null
no_dise_00074
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BRAF classified as Pathogenic or Likely Pathogenic for Noonan syndrome 1.
NM_004333.6(BRAF):c.741T>A (p.Phe247Leu) VARIANT_IN_GENE BRAF → NM_004333.6(BRAF):c.741T>A (p.Phe247Leu) VARIANT_HAS_CLINICAL_SIGNIFICANCE Noonan syndrome 1
{ "steps": [ { "hop": 1, "source_node_id": "BRAF", "source_node_type": "GENE", "source_node_label": "BRAF", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004333.6(B...
NM_004333.6(BRAF):c.741T>A (p.Phe247Leu)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BRAF\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BRAF\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_004333.6(BRAF):c.741T>A (p.Phe247Leu)", "text": "NM_004333.6(BRAF):c.741T>A (p.Phe247Leu) VARIANT_IN_GENE BRAF", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:noonan_syndrome_1", "text": "NM_004333.6(BRAF):c.741T>A (p.Ph...
{"gene": "BRAF", "disease": "Noonan syndrome 1", "pathogenic_variants": ["NM_004333.6(BRAF):c.741T>A (p.Phe247Leu)"]}
0.707107
null
no_dise_00034
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BRAF classified as Pathogenic or Likely Pathogenic for Cardio-facio-cutaneous syndrome.
NM_004333.6(BRAF):c.721A>C (p.Thr241Pro) VARIANT_IN_GENE BRAF → NM_004333.6(BRAF):c.721A>C (p.Thr241Pro) VARIANT_HAS_CLINICAL_SIGNIFICANCE Cardio-facio-cutaneous syndrome
{ "steps": [ { "hop": 1, "source_node_id": "BRAF", "source_node_type": "GENE", "source_node_label": "BRAF", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004333.6(B...
NM_004333.6(BRAF):c.721A>C (p.Thr241Pro)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BRAF\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BRAF\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_004333.6(BRAF):c.721A>C (p.Thr241Pro)", "text": "NM_004333.6(BRAF):c.721A>C (p.Thr241Pro) VARIANT_IN_GENE BRAF", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:cardio_facio_cutaneous_syndrome", "text": "NM_004333.6(BRAF):...
{"gene": "BRAF", "disease": "Cardio-facio-cutaneous syndrome", "pathogenic_variants": ["NM_004333.6(BRAF):c.1783T>C (p.Phe595Leu)", "NM_004333.6(BRAF):c.785A>C (p.Gln262Pro)", "NM_004333.6(BRAF):c.1743T>A (p.Asn581Lys)", "NM_004333.6(BRAF):c.1720C>T (p.His574Tyr)", "NM_004333.6(BRAF):c.1460T>G (p.Val487Gly)", "NM_00433...
0.921954
null
no_dise_00256
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in NOTCH1 classified as Pathogenic or Likely Pathogenic for Familial thoracic aortic aneurysm and aortic dissection.
NM_017617.5(NOTCH1):c.742G>C (p.Gly248Arg) VARIANT_IN_GENE NOTCH1 → NM_017617.5(NOTCH1):c.742G>C (p.Gly248Arg) VARIANT_HAS_CLINICAL_SIGNIFICANCE Familial thoracic aortic aneurysm and aortic dissection
{ "steps": [ { "hop": 1, "source_node_id": "NOTCH1", "source_node_type": "GENE", "source_node_label": "NOTCH1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_017617...
NM_017617.5(NOTCH1):c.742G>C (p.Gly248Arg)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"NOTCH1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"NOTCH1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_017617.5(NOTCH1):c.742G>C (p.Gly248Arg)", "text": "NM_017617.5(NOTCH1):c.742G>C (p.Gly248Arg) VARIANT_IN_GENE NOTCH1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:familial_thoracic_aortic_aneurysm_and_aortic_dissection", ...
{"gene": "NOTCH1", "disease": "Familial thoracic aortic aneurysm and aortic dissection", "pathogenic_variants": ["NM_017617.5(NOTCH1):c.4348G>T (p.Glu1450Ter)", "NM_017617.5(NOTCH1):c.1896del (p.Thr633fs)", "NM_017617.5(NOTCH1):c.3129C>G (p.Tyr1043Ter)", "NM_017617.5(NOTCH1):c.3909_3919del (p.Cys1304fs)", "NM_017617.5(...
0.83666
null
no_dise_00029
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in PALB2 classified as Pathogenic or Likely Pathogenic for Inherited breast cancer and ovarian cancer.
NM_024675.4(PALB2):c.2730T>A (p.Tyr910Ter) VARIANT_IN_GENE PALB2 → NM_024675.4(PALB2):c.2730T>A (p.Tyr910Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE Inherited breast cancer and ovarian cancer
{ "steps": [ { "hop": 1, "source_node_id": "PALB2", "source_node_type": "GENE", "source_node_label": "PALB2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_024675.4...
NM_024675.4(PALB2):c.2730T>A (p.Tyr910Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"PALB2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"PALB2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_024675.4(PALB2):c.2730T>A (p.Tyr910Ter)", "text": "NM_024675.4(PALB2):c.2730T>A (p.Tyr910Ter) VARIANT_IN_GENE PALB2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:inherited_breast_cancer_and_ovarian_cancer", "text": "NM...
{"gene": "PALB2", "disease": "Inherited breast cancer and ovarian cancer", "pathogenic_variants": ["NM_024675.4(PALB2):c.764_767dup (p.Ser256delinsArgTer)", "NM_024675.4(PALB2):c.1486_1487del (p.Glu495_Asp496insTer)", "NM_024675.4(PALB2):c.2556del (p.Gly853fs)", "NM_024675.4(PALB2):c.1458del (p.Val487fs)", "NM_024675.4...
0.921954
null
no_dise_00103
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in ACTB classified as Pathogenic or Likely Pathogenic for Dystonia 22, juvenile-onset.
GRCh37/hg19 7p22.1(chr7:5521357-5569119)x1 VARIANT_IN_GENE ACTB → GRCh37/hg19 7p22.1(chr7:5521357-5569119)x1 VARIANT_HAS_CLINICAL_SIGNIFICANCE Dystonia 22, juvenile-onset
{ "steps": [ { "hop": 1, "source_node_id": "ACTB", "source_node_type": "GENE", "source_node_label": "ACTB", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "GRCh37/hg19 7...
GRCh37/hg19 7p22.1(chr7:5521357-5569119)x1
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"ACTB\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"ACTB\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "GRCh37/hg19 7p22.1(chr7:5521357-5569119)x1", "text": "GRCh37/hg19 7p22.1(chr7:5521357-5569119)x1 VARIANT_IN_GENE ACTB", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:dystonia_22_juvenile_onset", "text": "GRCh37/hg19 7p22.1(...
{"gene": "ACTB", "disease": "Dystonia 22, juvenile-onset", "pathogenic_variants": ["GRCh37/hg19 7p22.1(chr7:5521357-5569119)x1"]}
0.707107
null
no_dise_00121
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in DNMT3A classified as Pathogenic or Likely Pathogenic for Heyn-Sproul-Jackson syndrome.
NM_022552.5(DNMT3A):c.916T>C (p.Trp306Arg) VARIANT_IN_GENE DNMT3A → NM_022552.5(DNMT3A):c.916T>C (p.Trp306Arg) VARIANT_HAS_CLINICAL_SIGNIFICANCE Heyn-Sproul-Jackson syndrome
{ "steps": [ { "hop": 1, "source_node_id": "DNMT3A", "source_node_type": "GENE", "source_node_label": "DNMT3A", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_022552...
NM_022552.5(DNMT3A):c.916T>C (p.Trp306Arg)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"DNMT3A\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"DNMT3A\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_022552.5(DNMT3A):c.916T>C (p.Trp306Arg)", "text": "NM_022552.5(DNMT3A):c.916T>C (p.Trp306Arg) VARIANT_IN_GENE DNMT3A", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:heyn_sproul_jackson_syndrome", "text": "NM_022552.5(DNM...
{"gene": "DNMT3A", "disease": "Heyn-Sproul-Jackson syndrome", "pathogenic_variants": ["NM_022552.5(DNMT3A):c.1092dup (p.Tyr365fs)", "NM_022552.5(DNMT3A):c.1012_1014+3del", "NM_022552.5(DNMT3A):c.988T>C (p.Trp330Arg)", "NM_022552.5(DNMT3A):c.916T>C (p.Trp306Arg)", "NM_022552.5(DNMT3A):c.905G>C (p.Gly302Ala)"]}
0.83666
null
no_dise_00626
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in SPTLC2 classified as Pathogenic or Likely Pathogenic for Hereditary neuropathy or pain disorder.
NM_004863.4(SPTLC2):c.547C>T (p.Arg183Trp) VARIANT_IN_GENE SPTLC2 → NM_004863.4(SPTLC2):c.547C>T (p.Arg183Trp) VARIANT_HAS_CLINICAL_SIGNIFICANCE Hereditary neuropathy or pain disorder
{ "steps": [ { "hop": 1, "source_node_id": "SPTLC2", "source_node_type": "GENE", "source_node_label": "SPTLC2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004863...
NM_004863.4(SPTLC2):c.547C>T (p.Arg183Trp)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"SPTLC2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"SPTLC2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_004863.4(SPTLC2):c.547C>T (p.Arg183Trp)", "text": "NM_004863.4(SPTLC2):c.547C>T (p.Arg183Trp) VARIANT_IN_GENE SPTLC2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:hereditary_neuropathy_or_pain_disorder", "text": "NM_00...
{"gene": "SPTLC2", "disease": "Hereditary neuropathy or pain disorder", "pathogenic_variants": ["NM_004863.4(SPTLC2):c.547C>T (p.Arg183Trp)"]}
0.921954
null
no_dise_00076
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in PSEN1 classified as Pathogenic or Likely Pathogenic for Telangiectasia, hereditary hemorrhagic, type 1.
NM_000021.4(PSEN1):c.308T>A (p.Val103Asp) VARIANT_IN_GENE PSEN1 → NM_000021.4(PSEN1):c.308T>A (p.Val103Asp) VARIANT_HAS_CLINICAL_SIGNIFICANCE Telangiectasia, hereditary hemorrhagic, type 1
{ "steps": [ { "hop": 1, "source_node_id": "PSEN1", "source_node_type": "GENE", "source_node_label": "PSEN1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000021.4...
NM_000021.4(PSEN1):c.308T>A (p.Val103Asp)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"PSEN1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"PSEN1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_000021.4(PSEN1):c.308T>A (p.Val103Asp)", "text": "NM_000021.4(PSEN1):c.308T>A (p.Val103Asp) VARIANT_IN_GENE PSEN1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:telangiectasia_hereditary_hemorrhagic_type_1", "text": "NM...
{"gene": "PSEN1", "disease": "Telangiectasia, hereditary hemorrhagic, type 1", "pathogenic_variants": ["NM_000021.4(PSEN1):c.308T>A (p.Val103Asp)"]}
0.83666
null
no_dise_00106
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BIN1 classified as Pathogenic or Likely Pathogenic for Inborn genetic diseases.
NM_139343.3(BIN1):c.91C>T (p.Gln31Ter) VARIANT_IN_GENE BIN1 → NM_139343.3(BIN1):c.91C>T (p.Gln31Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE Inborn genetic diseases
{ "steps": [ { "hop": 1, "source_node_id": "BIN1", "source_node_type": "GENE", "source_node_label": "BIN1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_139343.3(B...
NM_139343.3(BIN1):c.91C>T (p.Gln31Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BIN1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BIN1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_139343.3(BIN1):c.91C>T (p.Gln31Ter)", "text": "NM_139343.3(BIN1):c.91C>T (p.Gln31Ter) VARIANT_IN_GENE BIN1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:inborn_genetic_diseases", "text": "NM_139343.3(BIN1):c.91C>T (p.G...
{"gene": "BIN1", "disease": "Inborn genetic diseases", "pathogenic_variants": ["NM_139343.3(BIN1):c.91C>T (p.Gln31Ter)"]}
0.83666
null
no_dise_00283
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in FGFR1 classified as Pathogenic or Likely Pathogenic for Pfeiffer syndrome.
NM_023110.3(FGFR1):c.1946del (p.His649fs) VARIANT_IN_GENE FGFR1 → NM_023110.3(FGFR1):c.1946del (p.His649fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Pfeiffer syndrome
{ "steps": [ { "hop": 1, "source_node_id": "FGFR1", "source_node_type": "GENE", "source_node_label": "FGFR1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_023110.3...
NM_023110.3(FGFR1):c.1946del (p.His649fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"FGFR1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"FGFR1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_023110.3(FGFR1):c.1946del (p.His649fs)", "text": "NM_023110.3(FGFR1):c.1946del (p.His649fs) VARIANT_IN_GENE FGFR1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:pfeiffer_syndrome", "text": "NM_023110.3(FGFR1):c.1946del ...
{"gene": "FGFR1", "disease": "Pfeiffer syndrome", "pathogenic_variants": ["NM_023110.3(FGFR1):c.570del (p.Trp190fs)", "NM_023110.3(FGFR1):c.74del (p.Pro25fs)", "NM_023110.3(FGFR1):c.494del (p.Leu165fs)", "NM_023110.3(FGFR1):c.831dup (p.Lys278Ter)", "NM_023110.3(FGFR1):c.1231C>T (p.Gln411Ter)", "NM_023110.3(FGFR1):c.188...
0.83666
null
no_dise_00556
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in PALB2 classified as Pathogenic or Likely Pathogenic for PALB2-related disorder.
NM_024675.4(PALB2):c.2053A>T (p.Lys685Ter) VARIANT_IN_GENE PALB2 → NM_024675.4(PALB2):c.2053A>T (p.Lys685Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE PALB2-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "PALB2", "source_node_type": "GENE", "source_node_label": "PALB2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_024675.4...
NM_024675.4(PALB2):c.2053A>T (p.Lys685Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"PALB2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"PALB2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_024675.4(PALB2):c.2053A>T (p.Lys685Ter)", "text": "NM_024675.4(PALB2):c.2053A>T (p.Lys685Ter) VARIANT_IN_GENE PALB2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:palb2_related_disorder", "text": "NM_024675.4(PALB2):c.2...
{"gene": "PALB2", "disease": "PALB2-related disorder", "pathogenic_variants": ["NM_024675.4(PALB2):c.2053A>T (p.Lys685Ter)", "NM_024675.4(PALB2):c.454A>T (p.Lys152Ter)", "NM_024675.4(PALB2):c.934del (p.Ser312fs)", "NM_024675.4(PALB2):c.1553C>G (p.Ser518Ter)", "NM_024675.4(PALB2):c.2835-1G>A", "NM_024675.4(PALB2):c.3507...
0.707107
null
no_dise_00361
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in TUBA4A classified as Pathogenic or Likely Pathogenic for Amyotrophic lateral sclerosis type 22.
NM_006000.3(TUBA4A):c.959G>A (p.Arg320His) VARIANT_IN_GENE TUBA4A → NM_006000.3(TUBA4A):c.959G>A (p.Arg320His) VARIANT_HAS_CLINICAL_SIGNIFICANCE Amyotrophic lateral sclerosis type 22
{ "steps": [ { "hop": 1, "source_node_id": "TUBA4A", "source_node_type": "GENE", "source_node_label": "TUBA4A", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_006000...
NM_006000.3(TUBA4A):c.959G>A (p.Arg320His)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"TUBA4A\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"TUBA4A\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_006000.3(TUBA4A):c.959G>A (p.Arg320His)", "text": "NM_006000.3(TUBA4A):c.959G>A (p.Arg320His) VARIANT_IN_GENE TUBA4A", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:amyotrophic_lateral_sclerosis_type_22", "text": "NM_006...
{"gene": "TUBA4A", "disease": "Amyotrophic lateral sclerosis type 22", "pathogenic_variants": ["NM_006000.3(TUBA4A):c.190del (p.Arg64fs)", "NM_006000.3(TUBA4A):c.433A>C (p.Thr145Pro)", "NM_006000.3(TUBA4A):c.1220G>A (p.Trp407Ter)", "NM_006000.3(TUBA4A):c.959G>A (p.Arg320His)", "NM_006000.3(TUBA4A):c.313C>T (p.Arg105Cys...
0.707107
null
no_dise_00429
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in MTOR classified as Pathogenic or Likely Pathogenic for MTOR-related disorder.
NM_004958.4(MTOR):c.6306C>A (p.Asp2102Glu) VARIANT_IN_GENE MTOR → NM_004958.4(MTOR):c.6306C>A (p.Asp2102Glu) VARIANT_HAS_CLINICAL_SIGNIFICANCE MTOR-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "MTOR", "source_node_type": "GENE", "source_node_label": "MTOR", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004958.4(M...
NM_004958.4(MTOR):c.6306C>A (p.Asp2102Glu)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"MTOR\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"MTOR\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_004958.4(MTOR):c.6306C>A (p.Asp2102Glu)", "text": "NM_004958.4(MTOR):c.6306C>A (p.Asp2102Glu) VARIANT_IN_GENE MTOR", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:mtor_related_disorder", "text": "NM_004958.4(MTOR):c.6306...
{"gene": "MTOR", "disease": "MTOR-related disorder", "pathogenic_variants": ["NM_004958.4(MTOR):c.6306C>A (p.Asp2102Glu)"]}
0.83666
null
no_dise_00059
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in PSEN1 classified as Pathogenic or Likely Pathogenic for Alzheimer disease 4.
NM_000021.4(PSEN1):c.869-1624_956-2452del VARIANT_IN_GENE PSEN1 → NM_000021.4(PSEN1):c.869-1624_956-2452del VARIANT_HAS_CLINICAL_SIGNIFICANCE Alzheimer disease 4
{ "steps": [ { "hop": 1, "source_node_id": "PSEN1", "source_node_type": "GENE", "source_node_label": "PSEN1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000021.4...
NM_000021.4(PSEN1):c.869-1624_956-2452del
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"PSEN1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"PSEN1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_000021.4(PSEN1):c.869-1624_956-2452del", "text": "NM_000021.4(PSEN1):c.869-1624_956-2452del VARIANT_IN_GENE PSEN1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:alzheimer_disease_4", "text": "NM_000021.4(PSEN1):c.869-16...
{"gene": "PSEN1", "disease": "Alzheimer disease 4", "pathogenic_variants": ["NM_000021.4(PSEN1):c.869-1624_956-2452del"]}
0.707107
null
no_dise_00509
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in CDKN2A classified as Pathogenic or Likely Pathogenic for Hereditary cancer-predisposing syndrome.
NM_000077.5(CDKN2A):c.189del (p.Leu64fs) VARIANT_IN_GENE CDKN2A → NM_000077.5(CDKN2A):c.189del (p.Leu64fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Hereditary cancer-predisposing syndrome
{ "steps": [ { "hop": 1, "source_node_id": "CDKN2A", "source_node_type": "GENE", "source_node_label": "CDKN2A", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000077...
NM_000077.5(CDKN2A):c.189del (p.Leu64fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"CDKN2A\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"CDKN2A\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_000077.5(CDKN2A):c.189del (p.Leu64fs)", "text": "NM_000077.5(CDKN2A):c.189del (p.Leu64fs) VARIANT_IN_GENE CDKN2A", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:hereditary_cancer_predisposing_syndrome", "text": "NM_00007...
{"gene": "CDKN2A", "disease": "Hereditary cancer-predisposing syndrome", "pathogenic_variants": ["NM_000077.5(CDKN2A):c.171_172delinsTT (p.Arg58Ter)", "NM_000077.5(CDKN2A):c.328_329insA (p.Trp110Ter)", "NM_000077.5(CDKN2A):c.135_138del (p.Arg46fs)", "NM_000077.5(CDKN2A):c.98_150+1488del", "NM_000077.5(CDKN2A):c.274del ...
0.921954
null
no_dise_00060
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in FGFR1 classified as Pathogenic or Likely Pathogenic for Hartsfield-Bixler-Demyer syndrome.
NM_023110.3(FGFR1):c.1601TGA[1] (p.Met535del) VARIANT_IN_GENE FGFR1 → NM_023110.3(FGFR1):c.1601TGA[1] (p.Met535del) VARIANT_HAS_CLINICAL_SIGNIFICANCE Hartsfield-Bixler-Demyer syndrome
{ "steps": [ { "hop": 1, "source_node_id": "FGFR1", "source_node_type": "GENE", "source_node_label": "FGFR1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_023110.3...
NM_023110.3(FGFR1):c.1601TGA[1] (p.Met535del)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"FGFR1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"FGFR1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_023110.3(FGFR1):c.1601TGA[1] (p.Met535del)", "text": "NM_023110.3(FGFR1):c.1601TGA[1] (p.Met535del) VARIANT_IN_GENE FGFR1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:hartsfield_bixler_demyer_syndrome", "text": "NM_02...
{"gene": "FGFR1", "disease": "Hartsfield-Bixler-Demyer syndrome", "pathogenic_variants": ["NM_023110.3(FGFR1):c.1881G>C (p.Arg627Ser)", "NM_023110.3(FGFR1):c.1996T>C (p.Trp666Arg)", "NM_023110.3(FGFR1):c.1869C>G (p.Asp623Glu)", "NM_023110.3(FGFR1):c.1921G>A (p.Asp641Asn)", "NM_023110.3(FGFR1):c.1604T>A (p.Met535Lys)", ...
0.921954
null
no_dise_00464
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in MSH6 classified as Pathogenic or Likely Pathogenic for MSH6-related disorder.
NM_000179.3(MSH6):c.1993G>T (p.Glu665Ter) VARIANT_IN_GENE MSH6 → NM_000179.3(MSH6):c.1993G>T (p.Glu665Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE MSH6-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "MSH6", "source_node_type": "GENE", "source_node_label": "MSH6", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000179.3(M...
NM_000179.3(MSH6):c.1993G>T (p.Glu665Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"MSH6\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"MSH6\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_000179.3(MSH6):c.1993G>T (p.Glu665Ter)", "text": "NM_000179.3(MSH6):c.1993G>T (p.Glu665Ter) VARIANT_IN_GENE MSH6", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:msh6_related_disorder", "text": "NM_000179.3(MSH6):c.1993G>...
{"gene": "MSH6", "disease": "MSH6-related disorder", "pathogenic_variants": ["NM_000179.3(MSH6):c.160_196dup (p.Pro66fs)", "NM_000179.3(MSH6):c.1993G>T (p.Glu665Ter)"]}
0.921954
null
no_dise_00155
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in DDX41 classified as Pathogenic or Likely Pathogenic for Inborn genetic diseases.
NM_016222.4(DDX41):c.325C>T (p.Gln109Ter) VARIANT_IN_GENE DDX41 → NM_016222.4(DDX41):c.325C>T (p.Gln109Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE Inborn genetic diseases
{ "steps": [ { "hop": 1, "source_node_id": "DDX41", "source_node_type": "GENE", "source_node_label": "DDX41", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_016222.4...
NM_016222.4(DDX41):c.325C>T (p.Gln109Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"DDX41\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"DDX41\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_016222.4(DDX41):c.325C>T (p.Gln109Ter)", "text": "NM_016222.4(DDX41):c.325C>T (p.Gln109Ter) VARIANT_IN_GENE DDX41", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:inborn_genetic_diseases", "text": "NM_016222.4(DDX41):c.32...
{"gene": "DDX41", "disease": "Inborn genetic diseases", "pathogenic_variants": ["NM_016222.4(DDX41):c.304A>T (p.Lys102Ter)", "NM_016222.4(DDX41):c.622C>T (p.Gln208Ter)", "NM_016222.4(DDX41):c.116del (p.Leu39fs)", "NM_016222.4(DDX41):c.1233_1234dup (p.Val412fs)", "NM_016222.4(DDX41):c.1504C>T (p.Gln502Ter)", "NM_016222....
0.83666
null
no_dise_00004
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in FUS classified as Pathogenic or Likely Pathogenic for Amyotrophic lateral sclerosis 6, autosomal recessive.
NM_004960.4(FUS):c.1551C>G (p.His517Gln) VARIANT_IN_GENE FUS → NM_004960.4(FUS):c.1551C>G (p.His517Gln) VARIANT_HAS_CLINICAL_SIGNIFICANCE Amyotrophic lateral sclerosis 6, autosomal recessive
{ "steps": [ { "hop": 1, "source_node_id": "FUS", "source_node_type": "GENE", "source_node_label": "FUS", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004960.4(FUS...
NM_004960.4(FUS):c.1551C>G (p.His517Gln)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"FUS\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"FUS\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_004960.4(FUS):c.1551C>G (p.His517Gln)", "text": "NM_004960.4(FUS):c.1551C>G (p.His517Gln) VARIANT_IN_GENE FUS", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:amyotrophic_lateral_sclerosis_6_autosomal_recessive", "text": ...
{"gene": "FUS", "disease": "Amyotrophic lateral sclerosis 6, autosomal recessive", "pathogenic_variants": ["NM_004960.4(FUS):c.1551C>G (p.His517Gln)"]}
0.707107
null
no_dise_00511
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in BRCA1 classified as Pathogenic or Likely Pathogenic for Breast and/or ovarian cancer.
NM_007294.4(BRCA1):c.53T>A (p.Met18Lys) VARIANT_IN_GENE BRCA1 → NM_007294.4(BRCA1):c.53T>A (p.Met18Lys) VARIANT_HAS_CLINICAL_SIGNIFICANCE Breast and/or ovarian cancer
{ "steps": [ { "hop": 1, "source_node_id": "BRCA1", "source_node_type": "GENE", "source_node_label": "BRCA1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_007294.4...
NM_007294.4(BRCA1):c.53T>A (p.Met18Lys)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"BRCA1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"BRCA1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_007294.4(BRCA1):c.53T>A (p.Met18Lys)", "text": "NM_007294.4(BRCA1):c.53T>A (p.Met18Lys) VARIANT_IN_GENE BRCA1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:breast_and_or_ovarian_cancer", "text": "NM_007294.4(BRCA1):c.5...
{"gene": "BRCA1", "disease": "Breast and/or ovarian cancer", "pathogenic_variants": ["NM_007294.4(BRCA1):c.5332_5332+6delinsT", "NM_007294.4(BRCA1):c.3690dup (p.Phe1231fs)", "NM_007294.4(BRCA1):c.5116G>C (p.Gly1706Arg)", "NM_007294.4(BRCA1):c.53T>A (p.Met18Lys)"]}
0.921954
null
no_dise_00496
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in PMS2 classified as Pathogenic or Likely Pathogenic for Hereditary cancer-predisposing syndrome.
NM_000535.7(PMS2):c.2175-2A>C VARIANT_IN_GENE PMS2 → NM_000535.7(PMS2):c.2175-2A>C VARIANT_HAS_CLINICAL_SIGNIFICANCE Hereditary cancer-predisposing syndrome
{ "steps": [ { "hop": 1, "source_node_id": "PMS2", "source_node_type": "GENE", "source_node_label": "PMS2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000535.7(P...
NM_000535.7(PMS2):c.2175-2A>C
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"PMS2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"PMS2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_000535.7(PMS2):c.2175-2A>C", "text": "NM_000535.7(PMS2):c.2175-2A>C VARIANT_IN_GENE PMS2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:hereditary_cancer_predisposing_syndrome", "text": "NM_000535.7(PMS2):c.2175-2A>C VA...
{"gene": "PMS2", "disease": "Hereditary cancer-predisposing syndrome", "pathogenic_variants": ["NM_000535.7(PMS2):c.674_677dup (p.Asn226fs)", "NM_000535.7(PMS2):c.860_864del (p.Arg287fs)", "NM_000535.7(PMS2):c.1456dup (p.Asp486fs)", "NM_000535.7(PMS2):c.1240dup (p.Asp414fs)", "NM_000535.7(PMS2):c.2309T>A (p.Leu770Ter)"...
0.83666
null
no_dise_00040
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in FUS classified as Pathogenic or Likely Pathogenic for Tremor, hereditary essential, 4.
NM_004960.4(FUS):c.1561C>G (p.Arg521Gly) VARIANT_IN_GENE FUS → NM_004960.4(FUS):c.1561C>G (p.Arg521Gly) VARIANT_HAS_CLINICAL_SIGNIFICANCE Tremor, hereditary essential, 4
{ "steps": [ { "hop": 1, "source_node_id": "FUS", "source_node_type": "GENE", "source_node_label": "FUS", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004960.4(FUS...
NM_004960.4(FUS):c.1561C>G (p.Arg521Gly)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"FUS\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"FUS\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_004960.4(FUS):c.1561C>G (p.Arg521Gly)", "text": "NM_004960.4(FUS):c.1561C>G (p.Arg521Gly) VARIANT_IN_GENE FUS", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:tremor_hereditary_essential_4", "text": "NM_004960.4(FUS):c.15...
{"gene": "FUS", "disease": "Tremor, hereditary essential, 4", "pathogenic_variants": ["NM_004960.4(FUS):c.1441C>T (p.Arg481Ter)", "NM_004960.4(FUS):c.1573C>A (p.Pro525Thr)", "NM_004960.4(FUS):c.1500dup (p.Gly501fs)", "NM_004960.4(FUS):c.1509_1510dup (p.Gly504fs)", "NM_004960.4(FUS):c.1394-2del", "NM_004960.4(FUS):c.868...
0.921954
null
no_dise_00595
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in MSH6 classified as Pathogenic or Likely Pathogenic for Lynch-like syndrome.
NM_000179.3(MSH6):c.1372C>A (p.His458Asn) VARIANT_IN_GENE MSH6 → NM_000179.3(MSH6):c.1372C>A (p.His458Asn) VARIANT_HAS_CLINICAL_SIGNIFICANCE Lynch-like syndrome
{ "steps": [ { "hop": 1, "source_node_id": "MSH6", "source_node_type": "GENE", "source_node_label": "MSH6", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000179.3(M...
NM_000179.3(MSH6):c.1372C>A (p.His458Asn)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"MSH6\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"MSH6\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_000179.3(MSH6):c.1372C>A (p.His458Asn)", "text": "NM_000179.3(MSH6):c.1372C>A (p.His458Asn) VARIANT_IN_GENE MSH6", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:lynch_like_syndrome", "text": "NM_000179.3(MSH6):c.1372C>A ...
{"gene": "MSH6", "disease": "Lynch-like syndrome", "pathogenic_variants": ["NM_000179.3(MSH6):c.1372C>A (p.His458Asn)"]}
0.707107
null
no_dise_00025
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in NOTCH1 classified as Pathogenic or Likely Pathogenic for NOTCH1-related disorder.
NM_017617.5(NOTCH1):c.5078T>C (p.Phe1693Ser) VARIANT_IN_GENE NOTCH1 → NM_017617.5(NOTCH1):c.5078T>C (p.Phe1693Ser) VARIANT_HAS_CLINICAL_SIGNIFICANCE NOTCH1-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "NOTCH1", "source_node_type": "GENE", "source_node_label": "NOTCH1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_017617...
NM_017617.5(NOTCH1):c.5078T>C (p.Phe1693Ser)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"NOTCH1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"NOTCH1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_017617.5(NOTCH1):c.5078T>C (p.Phe1693Ser)", "text": "NM_017617.5(NOTCH1):c.5078T>C (p.Phe1693Ser) VARIANT_IN_GENE NOTCH1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:notch1_related_disorder", "text": "NM_017617.5(NOTC...
{"gene": "NOTCH1", "disease": "NOTCH1-related disorder", "pathogenic_variants": ["NM_017617.5(NOTCH1):c.3170del (p.Gln1057fs)", "NM_017617.5(NOTCH1):c.5078T>C (p.Phe1693Ser)", "NM_017617.5(NOTCH1):c.2436del (p.Tyr813fs)", "NM_017617.5(NOTCH1):c.4315_4318dup (p.Ile1440fs)", "NM_017617.5(NOTCH1):c.2536C>T (p.Gln846Ter)",...
0.707107
null
no_dise_00420
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in RET classified as Pathogenic or Likely Pathogenic for Pheochromocytoma.
NM_020975.6(RET):c.1996A>G (p.Lys666Glu) VARIANT_IN_GENE RET → NM_020975.6(RET):c.1996A>G (p.Lys666Glu) VARIANT_HAS_CLINICAL_SIGNIFICANCE Pheochromocytoma
{ "steps": [ { "hop": 1, "source_node_id": "RET", "source_node_type": "GENE", "source_node_label": "RET", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_020975.6(RET...
NM_020975.6(RET):c.1996A>G (p.Lys666Glu)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"RET\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"RET\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_020975.6(RET):c.1996A>G (p.Lys666Glu)", "text": "NM_020975.6(RET):c.1996A>G (p.Lys666Glu) VARIANT_IN_GENE RET", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:pheochromocytoma", "text": "NM_020975.6(RET):c.1996A>G (p.Lys6...
{"gene": "RET", "disease": "Pheochromocytoma", "pathogenic_variants": ["NM_020975.6(RET):c.1996A>G (p.Lys666Glu)"]}
0.921954
null
no_dise_00012
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in RAD51D classified as Pathogenic or Likely Pathogenic for Malignant tumor of breast.
NM_002878.4(RAD51D):c.738+402_*1465del VARIANT_IN_GENE RAD51D → NM_002878.4(RAD51D):c.738+402_*1465del VARIANT_HAS_CLINICAL_SIGNIFICANCE Malignant tumor of breast
{ "steps": [ { "hop": 1, "source_node_id": "RAD51D", "source_node_type": "GENE", "source_node_label": "RAD51D", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_002878...
NM_002878.4(RAD51D):c.738+402_*1465del
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"RAD51D\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"RAD51D\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_002878.4(RAD51D):c.738+402_*1465del", "text": "NM_002878.4(RAD51D):c.738+402_*1465del VARIANT_IN_GENE RAD51D", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:malignant_tumor_of_breast", "text": "NM_002878.4(RAD51D):c.738+...
{"gene": "RAD51D", "disease": "Malignant tumor of breast", "pathogenic_variants": ["NM_002878.4(RAD51D):c.738+402_*1465del"]}
0.83666
null
no_dise_00013
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in DCTN1 classified as Pathogenic or Likely Pathogenic for Amyotrophic lateral sclerosis type 1.
NM_004082.5(DCTN1):c.3823C>T (p.Arg1275Cys) VARIANT_IN_GENE DCTN1 → NM_004082.5(DCTN1):c.3823C>T (p.Arg1275Cys) VARIANT_HAS_CLINICAL_SIGNIFICANCE Amyotrophic lateral sclerosis type 1
{ "steps": [ { "hop": 1, "source_node_id": "DCTN1", "source_node_type": "GENE", "source_node_label": "DCTN1", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004082.5...
NM_004082.5(DCTN1):c.3823C>T (p.Arg1275Cys)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"DCTN1\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"DCTN1\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_004082.5(DCTN1):c.3823C>T (p.Arg1275Cys)", "text": "NM_004082.5(DCTN1):c.3823C>T (p.Arg1275Cys) VARIANT_IN_GENE DCTN1", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:amyotrophic_lateral_sclerosis_type_1", "text": "NM_004...
{"gene": "DCTN1", "disease": "Amyotrophic lateral sclerosis type 1", "pathogenic_variants": ["NM_004082.5(DCTN1):c.175G>C (p.Gly59Arg)", "NM_004082.5(DCTN1):c.175G>A (p.Gly59Ser)", "NM_004082.5(DCTN1):c.3823C>T (p.Arg1275Cys)", "NM_004082.5(DCTN1):c.232T>C (p.Tyr78His)"]}
0.83666
null
no_dise_00159
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in FAT4 classified as Pathogenic or Likely Pathogenic for Van Maldergem syndrome.
NM_001291303.3(FAT4):c.6700C>T (p.Arg2234Ter) VARIANT_IN_GENE FAT4 → NM_001291303.3(FAT4):c.6700C>T (p.Arg2234Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE Van Maldergem syndrome
{ "steps": [ { "hop": 1, "source_node_id": "FAT4", "source_node_type": "GENE", "source_node_label": "FAT4", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_001291303....
NM_001291303.3(FAT4):c.6700C>T (p.Arg2234Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"FAT4\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"FAT4\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_001291303.3(FAT4):c.6700C>T (p.Arg2234Ter)", "text": "NM_001291303.3(FAT4):c.6700C>T (p.Arg2234Ter) VARIANT_IN_GENE FAT4", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:van_maldergem_syndrome", "text": "NM_001291303.3(FA...
{"gene": "FAT4", "disease": "Van Maldergem syndrome", "pathogenic_variants": ["NM_001291303.3(FAT4):c.6700C>T (p.Arg2234Ter)"]}
0.921954
null
no_dise_00354
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in CREBBP classified as Pathogenic or Likely Pathogenic for CREBBP-related disorder.
NM_004380.3(CREBBP):c.3054del (p.Arg1018fs) VARIANT_IN_GENE CREBBP → NM_004380.3(CREBBP):c.3054del (p.Arg1018fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE CREBBP-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "CREBBP", "source_node_type": "GENE", "source_node_label": "CREBBP", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004380...
NM_004380.3(CREBBP):c.3054del (p.Arg1018fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"CREBBP\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"CREBBP\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Br...
[ { "source_db": "ClinVar", "source_id": "NM_004380.3(CREBBP):c.3054del (p.Arg1018fs)", "text": "NM_004380.3(CREBBP):c.3054del (p.Arg1018fs) VARIANT_IN_GENE CREBBP", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:crebbp_related_disorder", "text": "NM_004380.3(CREBBP...
{"gene": "CREBBP", "disease": "CREBBP-related disorder", "pathogenic_variants": ["NM_004380.3(CREBBP):c.2064_2077del (p.Gly689fs)", "NM_004380.3(CREBBP):c.5948dup (p.Gly1984fs)", "NM_004380.3(CREBBP):c.4944del (p.Ile1649fs)", "NM_004380.3(CREBBP):c.223C>T (p.Arg75Ter)", "NM_004380.3(CREBBP):c.4890+1G>A", "NM_004380.3(C...
0.707107
null
no_dise_00520
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in AXIN2 classified as Pathogenic or Likely Pathogenic for AXIN2-related attenuated familial adenomatous polyposis.
NM_004655.4(AXIN2):c.2062_2063del (p.Leu688fs) VARIANT_IN_GENE AXIN2 → NM_004655.4(AXIN2):c.2062_2063del (p.Leu688fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE AXIN2-related attenuated familial adenomatous polyposis
{ "steps": [ { "hop": 1, "source_node_id": "AXIN2", "source_node_type": "GENE", "source_node_label": "AXIN2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_004655.4...
NM_004655.4(AXIN2):c.2062_2063del (p.Leu688fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"AXIN2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"AXIN2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_004655.4(AXIN2):c.2062_2063del (p.Leu688fs)", "text": "NM_004655.4(AXIN2):c.2062_2063del (p.Leu688fs) VARIANT_IN_GENE AXIN2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:axin2_related_attenuated_familial_adenomatous_polypo...
{"gene": "AXIN2", "disease": "AXIN2-related attenuated familial adenomatous polyposis", "pathogenic_variants": ["NM_004655.4(AXIN2):c.2062_2063del (p.Leu688fs)", "NM_004655.4(AXIN2):c.1989G>A (p.Trp663Ter)", "NM_004655.4(AXIN2):c.2041C>T (p.Gln681Ter)", "NM_004655.4(AXIN2):c.1647T>G (p.Tyr549Ter)", "NM_004655.4(AXIN2):...
0.921954
null
no_dise_00206
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in KDM6A classified as Pathogenic or Likely Pathogenic for KDM6A-related disorder.
NM_001291415.2(KDM6A):c.1083_1084del (p.Leu361_Tyr362insTer) VARIANT_IN_GENE KDM6A → NM_001291415.2(KDM6A):c.1083_1084del (p.Leu361_Tyr362insTer) VARIANT_HAS_CLINICAL_SIGNIFICANCE KDM6A-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "KDM6A", "source_node_type": "GENE", "source_node_label": "KDM6A", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_00129141...
NM_001291415.2(KDM6A):c.1083_1084del (p.Leu361_Tyr362insTer)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"KDM6A\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"KDM6A\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_001291415.2(KDM6A):c.1083_1084del (p.Leu361_Tyr362insTer)", "text": "NM_001291415.2(KDM6A):c.1083_1084del (p.Leu361_Tyr362insTer) VARIANT_IN_GENE KDM6A", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:kdm6a_related_disorder",...
{"gene": "KDM6A", "disease": "KDM6A-related disorder", "pathogenic_variants": ["NM_001291415.2(KDM6A):c.2605del (p.Ser869fs)", "NM_001291415.2(KDM6A):c.1083_1084del (p.Leu361_Tyr362insTer)"]}
0.83666
null
no_dise_00325
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in GRN classified as Pathogenic or Likely Pathogenic for GRN-related disorder.
NM_002087.4(GRN):c.347C>A (p.Ser116Ter) VARIANT_IN_GENE GRN → NM_002087.4(GRN):c.347C>A (p.Ser116Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE GRN-related disorder
{ "steps": [ { "hop": 1, "source_node_id": "GRN", "source_node_type": "GENE", "source_node_label": "GRN", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_002087.4(GRN...
NM_002087.4(GRN):c.347C>A (p.Ser116Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"GRN\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"GRN\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_002087.4(GRN):c.347C>A (p.Ser116Ter)", "text": "NM_002087.4(GRN):c.347C>A (p.Ser116Ter) VARIANT_IN_GENE GRN", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:grn_related_disorder", "text": "NM_002087.4(GRN):c.347C>A (p.Ser...
{"gene": "GRN", "disease": "GRN-related disorder", "pathogenic_variants": ["NM_002087.4(GRN):c.1535del (p.Pro512fs)", "NM_002087.4(GRN):c.347C>A (p.Ser116Ter)", "NM_002087.4(GRN):c.1429_1430dup (p.Asp477fs)", "NM_002087.4(GRN):c.388_391del (p.Gln130fs)", "NM_002087.4(GRN):c.900_901dup (p.Ser301fs)"]}
0.83666
null
no_dise_00289
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in FAT4 classified as Pathogenic or Likely Pathogenic for Hennekam lymphangiectasia-lymphedema syndrome 2.
NM_001291303.3(FAT4):c.14610del (p.Lys4871fs) VARIANT_IN_GENE FAT4 → NM_001291303.3(FAT4):c.14610del (p.Lys4871fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Hennekam lymphangiectasia-lymphedema syndrome 2
{ "steps": [ { "hop": 1, "source_node_id": "FAT4", "source_node_type": "GENE", "source_node_label": "FAT4", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_001291303....
NM_001291303.3(FAT4):c.14610del (p.Lys4871fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"FAT4\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"FAT4\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_001291303.3(FAT4):c.14610del (p.Lys4871fs)", "text": "NM_001291303.3(FAT4):c.14610del (p.Lys4871fs) VARIANT_IN_GENE FAT4", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:hennekam_lymphangiectasia_lymphedema_syndrome_2", "...
{"gene": "FAT4", "disease": "Hennekam lymphangiectasia-lymphedema syndrome 2", "pathogenic_variants": ["NM_001291303.3(FAT4):c.13588C>T (p.Gln4530Ter)", "NM_001291303.3(FAT4):c.7204A>C (p.Arg2402=)", "NM_001291303.3(FAT4):c.1195del (p.Leu399fs)", "NM_001291303.3(FAT4):c.7035TGGAAC[3] (p.2346GT[3])", "NM_001291303.3(FAT...
0.83666
null
no_dise_00067
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in REST classified as Pathogenic or Likely Pathogenic for Inborn genetic diseases.
NM_005612.5(REST):c.2515G>T (p.Glu839Ter) VARIANT_IN_GENE REST → NM_005612.5(REST):c.2515G>T (p.Glu839Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE Inborn genetic diseases
{ "steps": [ { "hop": 1, "source_node_id": "REST", "source_node_type": "GENE", "source_node_label": "REST", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_005612.5(R...
NM_005612.5(REST):c.2515G>T (p.Glu839Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"REST\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"REST\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_005612.5(REST):c.2515G>T (p.Glu839Ter)", "text": "NM_005612.5(REST):c.2515G>T (p.Glu839Ter) VARIANT_IN_GENE REST", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:inborn_genetic_diseases", "text": "NM_005612.5(REST):c.2515...
{"gene": "REST", "disease": "Inborn genetic diseases", "pathogenic_variants": ["NM_005612.5(REST):c.2515G>T (p.Glu839Ter)"]}
0.83666
null
no_dise_00171
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in MSH6 classified as Pathogenic or Likely Pathogenic for Hereditary cancer-predisposing syndrome.
NM_000179.3(MSH6):c.3901_3911dup (p.Leu1305fs) VARIANT_IN_GENE MSH6 → NM_000179.3(MSH6):c.3901_3911dup (p.Leu1305fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Hereditary cancer-predisposing syndrome
{ "steps": [ { "hop": 1, "source_node_id": "MSH6", "source_node_type": "GENE", "source_node_label": "MSH6", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000179.3(M...
NM_000179.3(MSH6):c.3901_3911dup (p.Leu1305fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"MSH6\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"MSH6\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_...
[ { "source_db": "ClinVar", "source_id": "NM_000179.3(MSH6):c.3901_3911dup (p.Leu1305fs)", "text": "NM_000179.3(MSH6):c.3901_3911dup (p.Leu1305fs) VARIANT_IN_GENE MSH6", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:hereditary_cancer_predisposing_syndrome", "text":...
{"gene": "MSH6", "disease": "Hereditary cancer-predisposing syndrome", "pathogenic_variants": ["NM_000179.3(MSH6):c.2549dup (p.Tyr850Ter)", "NM_000179.3(MSH6):c.3034G>T (p.Glu1012Ter)", "NM_000179.3(MSH6):c.3108dup (p.Phe1037fs)", "NM_000179.3(MSH6):c.2799del (p.Phe933fs)", "NM_000179.3(MSH6):c.3215dup (p.Pro1073fs)", ...
0.921954
null
no_dise_00355
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in PALB2 classified as Pathogenic or Likely Pathogenic for Inherited ovarian cancer (without breast cancer).
NM_024675.4(PALB2):c.2727_2728del (p.Thr911fs) VARIANT_IN_GENE PALB2 → NM_024675.4(PALB2):c.2727_2728del (p.Thr911fs) VARIANT_HAS_CLINICAL_SIGNIFICANCE Inherited ovarian cancer (without breast cancer)
{ "steps": [ { "hop": 1, "source_node_id": "PALB2", "source_node_type": "GENE", "source_node_label": "PALB2", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_024675.4...
NM_024675.4(PALB2):c.2727_2728del (p.Thr911fs)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"PALB2\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"PALB2\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brai...
[ { "source_db": "ClinVar", "source_id": "NM_024675.4(PALB2):c.2727_2728del (p.Thr911fs)", "text": "NM_024675.4(PALB2):c.2727_2728del (p.Thr911fs) VARIANT_IN_GENE PALB2", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:inherited_ovarian_cancer_without_breast_cancer", ...
{"gene": "PALB2", "disease": "Inherited ovarian cancer (without breast cancer)", "pathogenic_variants": ["NM_024675.4(PALB2):c.2727_2728del (p.Thr911fs)"]}
0.921954
null
no_dise_00530
disease_reasoning
noncoding_regulatory
medium
2
According to ClinVar, name a variant in ATM classified as Pathogenic or Likely Pathogenic for Breast cancer, susceptibility to.
NM_000051.4(ATM):c.3973G>T (p.Glu1325Ter) VARIANT_IN_GENE ATM → NM_000051.4(ATM):c.3973G>T (p.Glu1325Ter) VARIANT_HAS_CLINICAL_SIGNIFICANCE Breast cancer, susceptibility to
{ "steps": [ { "hop": 1, "source_node_id": "ATM", "source_node_type": "GENE", "source_node_label": "ATM", "edge_relation": "VARIANT_IN_GENE", "edge_evidence_type": "curated", "edge_confidence": 1, "edge_source_db": "ClinVar", "target_node_id": "NM_000051.4(ATM...
NM_000051.4(ATM):c.3973G>T (p.Glu1325Ter)
[ "expression" ]
[ "{\"family\": \"transcriptomic\", \"tag\": \"expression\", \"anchor_node_id\": \"ATM\", \"source_db\": \"GTEx\", \"payload\": {\"gene\": \"ATM\", \"tissues\": [\"Adipose_Subcutaneous\", \"Adipose_Visceral_Omentum\", \"Adrenal_Gland\", \"Artery_Aorta\", \"Artery_Coronary\", \"Artery_Tibial\", \"Bladder\", \"Brain_Am...
[ { "source_db": "ClinVar", "source_id": "NM_000051.4(ATM):c.3973G>T (p.Glu1325Ter)", "text": "NM_000051.4(ATM):c.3973G>T (p.Glu1325Ter) VARIANT_IN_GENE ATM", "confidence": 1 }, { "source_db": "ClinVar", "source_id": "DISEASE:breast_cancer_susceptibility_to", "text": "NM_000051.4(ATM):...
{"gene": "ATM", "disease": "Breast cancer, susceptibility to", "pathogenic_variants": ["NM_000051.4(ATM):c.3973G>T (p.Glu1325Ter)"]}
0.921954
null