question stringlengths 84 268 | answer stringlengths 6 879 | reference_sequence stringlengths 4.1k 4.1k | mutated_sequence stringlengths 4.1k 4.1k | cleaned_pathogenicity stringclasses 2
values | __index_level_0__ int64 67 343k |
|---|---|---|---|---|---|
Is the genetic mutation found on chromosome 2 at position 47799294, within the gene MSH6 (mutS homolog 6), considered benign or pathogenic? If pathogenic, specify the associated disease(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CCTAAAAGACATTCATCTATAACTAAGCTCAGTTTCATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATC... | CCTAAAAGACATTCATCTATAACTAAGCTCAGTTTCATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATC... | pathogenic | 35,852 |
Determine whether the variant at chromosome 2, position 47799307, in gene MSH6 (mutS homolog 6) is benign or pathogenic. If pathogenic, identify the relevant disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CATCTATAACTAAGCTCAGTTTCATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATT... | CATCTATAACTAAGCTCAGTTTCATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATT... | pathogenic | 35,855 |
Variant on chromosome 2, at position 47799315, affecting MSH6 (mutS homolog 6): is it benign or pathogenic? If pathogenic, specify the associated disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | ACTAAGCTCAGTTTCATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATAT... | ACTAAGCTCAGTTTCATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATAT... | pathogenic | 35,857 |
Gene MSH6 (mutS homolog 6) variant at chromosome 2, position 47799321—is it benign or pathogenic? If pathogenic, what are the associated condition(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CTCAGTTTCATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTC... | CTCAGTTTCATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTC... | pathogenic | 35,859 |
Benign or pathogenic: chromosome 2, position 47799327, gene MSH6 (mutS homolog 6) variant? Disease(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TTCATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCA... | TTCATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCA... | pathogenic | 35,862 |
Does the genetic variant at chromosome 2, position 47799329, impacting gene MSH6 (mutS homolog 6), appear benign or pathogenic? If pathogenic, name the associated disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAAC... | CATGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAAC... | pathogenic | 35,865 |
For chromosome 2, position 47799331, gene MSH6 (mutS homolog 6): benign or pathogenic mutation? If pathogenic, what are the associated disease(s)? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5', 'Mismatch_repair_cancer_syndrome_3'] | TGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAG... | TGTTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAG... | pathogenic | 35,867 |
Is the genetic mutation found on chromosome 2 at position 47799333, within the gene MSH6 (mutS homolog 6), considered benign or pathogenic? If pathogenic, specify the associated disease(s). | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | TTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCT... | TTTTGTTCCTTTTTCAATAGATAAGATAGGGAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCT... | pathogenic | 35,869 |
Gene MSH6 (mutS homolog 6) variant at chromosome 2, position 47799363—is it benign or pathogenic? If pathogenic, what are the associated condition(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | GAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAA... | GAATGAGCAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAA... | pathogenic | 35,881 |
Gene MSH6 (mutS homolog 6) variant at chromosome 2, position 47799370—is it benign or pathogenic? If pathogenic, what are the associated condition(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | CAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTA... | CAAGTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTA... | pathogenic | 35,885 |
Assess the clinical significance (benign or pathogenic) of the variant at chromosome 2, position 47799373, gene MSH6 (mutS homolog 6). What disease(s) is it linked to if pathogenic? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5', 'MSH6-related_disorder'] | GTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATC... | GTTAATAAAGTGGGTATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATC... | pathogenic | 35,886 |
Mutation at chromosome 2, position 47799388, within MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, indicate the disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | ATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTG... | ATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTG... | pathogenic | 35,892 |
Is the genetic variant on chromosome 2, position 47799388, gene MSH6 (mutS homolog 6), benign or pathogenic? If pathogenic, what disease(s) is indicated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | ATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTG... | ATTTTAATTTTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTG... | pathogenic | 35,893 |
Variant in gene MSH6 (mutS homolog 6), located at chromosome 2 position 47799397: benign or pathogenic? What disease(s) does it cause if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCAC... | TTAAGGTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCAC... | pathogenic | 35,897 |
Evaluate if the mutation on chromosome 2 at position 47799402 in MSH6 (mutS homolog 6) is benign or pathogenic. Disease name(s) if pathogenic? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | GTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGT... | GTTGAAACTAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGT... | pathogenic | 35,901 |
Evaluate if the mutation on chromosome 2 at position 47799410 in MSH6 (mutS homolog 6) is benign or pathogenic. Disease name(s) if pathogenic? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGC... | TAAGGATCATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGC... | pathogenic | 35,904 |
For chromosome 2, position 47799417, gene MSH6 (mutS homolog 6): benign or pathogenic mutation? If pathogenic, what are the associated disease(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | CATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTT... | CATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTT... | pathogenic | 35,908 |
A genetic alteration at chromosome 2, position 47799418, in gene MSH6 (mutS homolog 6)—benign or pathogenic? If pathogenic, which disease(s) is involved? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | ATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTG... | ATAACATTATCAGAGGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTG... | pathogenic | 35,909 |
Clinical impact (benign or pathogenic) of the variant at chromosome 2, location 47799432, gene MSH6 (mutS homolog 6): what disease(s) if pathogenic? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | GGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCA... | GGTCTAGAACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCA... | pathogenic | 35,917 |
Mutation at chromosome 2, position 47799440, within MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, indicate the disease(s). | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | ACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTT... | ACTGGATGGCAGCTACAGAGATCATTTAGCCTAATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTT... | pathogenic | 35,921 |
Variant chromosome 2, position 47799472, gene MSH6 (mutS homolog 6): benign or pathogenic? Disease(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | AATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCA... | AATACTGGTTTAACAAATAATCCGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCA... | pathogenic | 35,932 |
The genetic variant at chromosome 2, position 47799494, affecting gene MSH6 (mutS homolog 6): benign or pathogenic? Disease name(s) if pathogenic? | pathogenic; ['Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | CGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATA... | CGGGAGATCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATA... | pathogenic | 35,938 |
Assess the variant on chromosome 2, position 47799501, impacting MSH6 (mutS homolog 6): is it benign or pathogenic? If pathogenic, specify the associated condition(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5', 'MSH6-related_disorder'] | TCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAA... | TCCGTGATATGTGAATGTGCTAGGCCTGAGATGAGACAGCCAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAA... | pathogenic | 35,942 |
The chromosome 2, position 47799541 genetic variant in gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, indicate disease(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTA... | CAATTGTGGAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTA... | pathogenic | 35,953 |
Regarding the variant found on chromosome 2 at position 47799549 in gene MSH6 (mutS homolog 6): is it benign or pathogenic? If pathogenic, identify the disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | GAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGA... | GAAGAGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGA... | pathogenic | 35,957 |
Considering the variant on chromosome 2, location 47799553, involving gene MSH6 (mutS homolog 6), would you classify it as benign or pathogenic? What disease(s), if any, does a pathogenic variant indicate? | pathogenic; ['Carcinoma_of_colon', 'Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | AGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCAC... | AGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCAC... | pathogenic | 35,959 |
Mutation at chromosome 2, position 47799553, within MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, indicate the disease(s). | pathogenic; ['Breast_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCAC... | AGCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCAC... | pathogenic | 35,960 |
Classify the chromosome 2 variant at position 47799554 affecting gene MSH6 (mutS homolog 6) as benign or pathogenic. If pathogenic, which disease(s) is associated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | GCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACT... | GCAAACACTAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACT... | pathogenic | 35,961 |
The mutation impacting MSH6 (mutS homolog 6) on chromosome 2 at position 47799562: benign or pathogenic? Name the associated disease(s) if pathogenic. | pathogenic; ['Lynch_syndrome'] | TAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGT... | TAGAACCAGTATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGT... | pathogenic | 35,968 |
A mutation at chromosome position 47799572 on chromosome 2 in gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, which disease(s) is it linked to? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | ATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTAC... | ATAAGTTGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTAC... | pathogenic | 35,972 |
Benign or pathogenic: chromosome 2, position 47799578, gene MSH6 (mutS homolog 6) variant? Disease(s) if pathogenic? | pathogenic; ['Lynch_syndrome', 'Mismatch_repair_cancer_syndrome_1'] | TGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTC... | TGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTC... | pathogenic | 35,975 |
A genetic alteration at chromosome 2, position 47799578, in gene MSH6 (mutS homolog 6)—benign or pathogenic? If pathogenic, which disease(s) is involved? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTC... | TGCTTACTGCTTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTC... | pathogenic | 35,976 |
Gene mutation in MSH6 (mutS homolog 6) at chromosome 2, position 47799588—is it benign or pathogenic? If pathogenic, specify the disease(s). | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | TTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAA... | TTTCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAA... | pathogenic | 35,981 |
Variant in MSH6 (mutS homolog 6), chromosome 2, position 47799590—is this benign or pathogenic? If pathogenic, what disease(s) is linked? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAAT... | TCTTATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAAT... | pathogenic | 35,982 |
Is the variant located on chromosome 2 at position 47799594, gene MSH6 (mutS homolog 6), benign or pathogenic? If pathogenic, specify the disease(s) linked. | pathogenic; ['Carcinoma_of_colon', 'Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | ATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTT... | ATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTT... | pathogenic | 35,984 |
Assess the variant on chromosome 2, position 47799594, impacting MSH6 (mutS homolog 6): is it benign or pathogenic? If pathogenic, specify the associated condition(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | ATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTT... | ATGCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTT... | pathogenic | 35,985 |
Assess the clinical significance (benign or pathogenic) of the variant at chromosome 2, position 47799596, gene MSH6 (mutS homolog 6). What disease(s) is it linked to if pathogenic? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | GCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGC... | GCTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGC... | pathogenic | 35,986 |
A genetic variant on chromosome 2, position 47799597, affects the gene MSH6 (mutS homolog 6). Is this variant benign or pathogenic? If pathogenic, what disease(s) does it cause? | pathogenic; ['Lynch_syndrome', 'Lynch_syndrome_1'] | CTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCA... | CTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCA... | pathogenic | 35,989 |
Variant in MSH6 (mutS homolog 6), chromosome 2, position 47799597—is this benign or pathogenic? If pathogenic, what disease(s) is linked? | pathogenic; ['Lynch_syndrome'] | CTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCA... | CTATTAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCA... | pathogenic | 35,990 |
The genetic variant at chromosome 2, position 47799601, affecting gene MSH6 (mutS homolog 6): benign or pathogenic? Disease name(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | TAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTC... | TAATGAGCATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTC... | pathogenic | 35,991 |
Considering the genetic mutation at chromosome 2, position 47799609, impacting MSH6 (mutS homolog 6): is it clinically benign or pathogenic? Name the associated disease(s) if pathogenic. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | ATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGC... | ATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGC... | pathogenic | 35,995 |
The genetic variant at chromosome 2, position 47799609, affecting gene MSH6 (mutS homolog 6): benign or pathogenic? Disease name(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | ATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGC... | ATATCGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGC... | pathogenic | 35,996 |
Variant at chromosome 2, position 47799613, gene MSH6 (mutS homolog 6): clinically benign or pathogenic? If pathogenic, specify the disease(s) involved. | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5', 'MSH6-related_disorder'] | CGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGC... | CGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGC... | pathogenic | 35,998 |
Determine whether the variant at chromosome 2, position 47799613, in gene MSH6 (mutS homolog 6) is benign or pathogenic. If pathogenic, identify the relevant disease(s). | pathogenic; ['Lynch_syndrome'] | CGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGC... | CGCCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGC... | pathogenic | 35,999 |
Evaluate if the mutation on chromosome 2 at position 47799615 in MSH6 (mutS homolog 6) is benign or pathogenic. Disease name(s) if pathogenic? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | CCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCAT... | CCTCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCAT... | pathogenic | 36,001 |
Assess the variant on chromosome 2, position 47799617, impacting MSH6 (mutS homolog 6): is it benign or pathogenic? If pathogenic, specify the associated condition(s). | pathogenic; ['Endometrial_carcinoma', 'Gastric_cancer', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | TCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTC... | TCCTGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTC... | pathogenic | 36,003 |
A genetic variant on chromosome 2, position 47799620, affects the gene MSH6 (mutS homolog 6). Is this variant benign or pathogenic? If pathogenic, what disease(s) does it cause? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome'] | TGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCT... | TGATATTTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCT... | pathogenic | 36,004 |
Variant at chromosome position 47799626, chromosome 2, gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, what condition(s) does it relate to? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | TTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATT... | TTATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATT... | pathogenic | 36,005 |
Evaluate this variant at chromosome 2, position 47799628, gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, what are the disease connection(s)? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | ATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTT... | ATGATATATGGTCATGCCAACAGCTTTGTCATAAATAGAACTCCCATGGCAGCAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTT... | pathogenic | 36,006 |
Variant in gene MSH6 (mutS homolog 6), located at chromosome 2 position 47799680: benign or pathogenic? What disease(s) does it cause if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | CAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTC... | CAATCACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTC... | pathogenic | 36,019 |
Benign or pathogenic: chromosome 2, position 47799684, gene MSH6 (mutS homolog 6) variant? Disease(s) if pathogenic? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1', 'Lynch_syndrome_5'] | CACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTT... | CACTTAATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTT... | pathogenic | 36,022 |
A genetic variant on chromosome 2, position 47799689, affects the gene MSH6 (mutS homolog 6). Is this variant benign or pathogenic? If pathogenic, what disease(s) does it cause? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | AATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCA... | AATCTTGTAGTTAGAGGTGGGGTCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCA... | pathogenic | 36,023 |
The mutation in gene MSH6 (mutS homolog 6) at chromosome 2, position 47799711—clinically benign or pathogenic? If pathogenic, identify the related disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACC... | TCTCACCATGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACC... | pathogenic | 36,031 |
Variant in gene MSH6 (mutS homolog 6), located at chromosome 2 position 47799719: benign or pathogenic? What disease(s) does it cause if pathogenic? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGC... | TGTTGCCGAGCTGGCCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGC... | pathogenic | 36,034 |
The mutation in gene MSH6 (mutS homolog 6) at chromosome 2, position 47799733—clinically benign or pathogenic? If pathogenic, identify the related disease(s). | pathogenic; ['Endometrial_carcinoma', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGC... | CCTTGAACTTCTGGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGC... | pathogenic | 36,040 |
Assess the clinical significance (benign or pathogenic) of the variant at chromosome 2, position 47799745, gene MSH6 (mutS homolog 6). What disease(s) is it linked to if pathogenic? | pathogenic; ['Lynch_syndrome_5'] | GGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGG... | GGGCTCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGG... | pathogenic | 36,046 |
Variant on chromosome 2, at position 47799749, affecting MSH6 (mutS homolog 6): is it benign or pathogenic? If pathogenic, specify the associated disease(s). | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch-like_syndrome', 'Lynch_syndrome_5'] | TCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAG... | TCAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAG... | pathogenic | 36,048 |
For chromosome 2, position 47799750, gene MSH6 (mutS homolog 6): benign or pathogenic mutation? If pathogenic, what are the associated disease(s)? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGA... | CAGCGATTTTCTCCACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGA... | pathogenic | 36,050 |
Regarding the variant at chromosome 2 and position 47799763, affecting gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, what are the associated illness(es)? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | CACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCT... | CACAGGCACCTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCT... | pathogenic | 36,057 |
Is the chromosome 2, position 47799772 variant in MSH6 (mutS homolog 6) clinically benign or pathogenic? If pathogenic, what condition(s) is associated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | CTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATT... | CTGCTACTGTGCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATT... | pathogenic | 36,060 |
Clinical classification of chromosome 2, position 47799782, gene MSH6 (mutS homolog 6): benign or pathogenic? Disease(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | GCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTT... | GCTCGGTGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTT... | pathogenic | 36,065 |
Is the genetic change at chromosome 2, position 47799788, within gene MSH6 (mutS homolog 6) benign or pathogenic? Name the disease(s) if pathogenic. | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | TGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGG... | TGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGG... | pathogenic | 36,069 |
The chromosome 2, position 47799788 genetic variant in gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, indicate disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | TGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGG... | TGCAGCACTTTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGG... | pathogenic | 36,070 |
Regarding the variant found on chromosome 2 at position 47799797 in gene MSH6 (mutS homolog 6): is it benign or pathogenic? If pathogenic, identify the disease(s). | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5', 'MSH6-related_disorder'] | TTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCT... | TTGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCT... | pathogenic | 36,075 |
Is the genetic change at chromosome 2, position 47799798, within gene MSH6 (mutS homolog 6) benign or pathogenic? Name the disease(s) if pathogenic. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome', 'Lynch_syndrome_5'] | TGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTG... | TGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTG... | pathogenic | 36,077 |
Is the chromosome 2, position 47799798 variant in MSH6 (mutS homolog 6) clinically benign or pathogenic? If pathogenic, what condition(s) is associated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch-like_syndrome'] | TGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTG... | TGTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTG... | pathogenic | 36,078 |
A genetic variant at chromosome 2, position 47799799, affecting gene MSH6 (mutS homolog 6)—is it benign or pathogenic? If pathogenic, identify the associated disorder(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | GTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGC... | GTGTTTTTGAACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGC... | pathogenic | 36,079 |
Evaluate if the mutation on chromosome 2 at position 47799809 in MSH6 (mutS homolog 6) is benign or pathogenic. Disease name(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | ACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACA... | ACATAACCTCAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACA... | pathogenic | 36,082 |
Is chromosome 2, position 47799818, gene MSH6 (mutS homolog 6) variant benign or pathogenic? If pathogenic, what condition(s) is it related to? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCA... | CAAGATGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCA... | pathogenic | 36,087 |
Is the genetic variant on chromosome 2, position 47799823, gene MSH6 (mutS homolog 6), benign or pathogenic? If pathogenic, what disease(s) is indicated? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5', 'MSH6-related_disorder'] | TGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGAT... | TGTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGAT... | pathogenic | 36,092 |
A genetic variant at chromosome 2, position 47799824, affecting gene MSH6 (mutS homolog 6)—is it benign or pathogenic? If pathogenic, identify the associated disorder(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | GTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATT... | GTTATTGTCTTCATAGTAAAACAAAAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATT... | pathogenic | 36,093 |
Regarding the variant at chromosome 2 and position 47799848, affecting gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, what are the associated illness(es)? | pathogenic; ['Lynch_syndrome_5'] | AAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAG... | AAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAG... | pathogenic | 36,100 |
Variant in gene MSH6 (mutS homolog 6), located at chromosome 2 position 47799848: benign or pathogenic? What disease(s) does it cause if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | AAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAG... | AAGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAG... | pathogenic | 36,101 |
Gene mutation in MSH6 (mutS homolog 6) at chromosome 2, position 47799849—is it benign or pathogenic? If pathogenic, specify the disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | AGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGA... | AGATGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGA... | pathogenic | 36,102 |
Does the chromosome 2 mutation at position 47799852 within gene MSH6 (mutS homolog 6) classify as benign or pathogenic? If pathogenic, indicate the related illness(es). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACT... | TGAGGCTTAGAACTGGATCACTTTGCCTGTCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACT... | pathogenic | 36,104 |
Regarding the variant found on chromosome 2 at position 47799881 in gene MSH6 (mutS homolog 6): is it benign or pathogenic? If pathogenic, identify the disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAA... | TCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAA... | pathogenic | 36,115 |
A genetic variant at chromosome 2, position 47799881, affecting gene MSH6 (mutS homolog 6)—is it benign or pathogenic? If pathogenic, identify the associated disorder(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | TCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAA... | TCTCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAA... | pathogenic | 36,116 |
Chromosome 2, position 47799883, gene MSH6 (mutS homolog 6): benign or pathogenic variant? If pathogenic, what are the linked illness(es)? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | TCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATG... | TCTTCTTACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATG... | pathogenic | 36,119 |
Is the genetic change at chromosome 2, position 47799889, within gene MSH6 (mutS homolog 6) benign or pathogenic? Name the disease(s) if pathogenic. | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGT... | TACCTCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGT... | pathogenic | 36,121 |
Is the genetic variant on chromosome 2, position 47799893, gene MSH6 (mutS homolog 6), benign or pathogenic? If pathogenic, what disease(s) is indicated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAA... | TCCTCCCAGTTCAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAA... | pathogenic | 36,122 |
Does the variant on chromosome 2 at location 47799904 affecting gene MSH6 (mutS homolog 6) have a clinical significance of benign or pathogenic? If pathogenic, what disease(s) is associated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | CAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGAT... | CAAAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGAT... | pathogenic | 36,131 |
Is the chromosome 2, position 47799906 variant in MSH6 (mutS homolog 6) clinically benign or pathogenic? If pathogenic, what condition(s) is associated? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGT... | AAATGCTTGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGT... | pathogenic | 36,133 |
The mutation in gene MSH6 (mutS homolog 6) at chromosome 2, position 47799913—clinically benign or pathogenic? If pathogenic, identify the related disease(s). | pathogenic; ['Endometrial_carcinoma', 'Lynch_syndrome', 'Lynch_syndrome_5'] | TGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGA... | TGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGA... | pathogenic | 36,134 |
Assess the variant on chromosome 2, position 47799913, impacting MSH6 (mutS homolog 6): is it benign or pathogenic? If pathogenic, specify the associated condition(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGA... | TGCATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGA... | pathogenic | 36,135 |
A mutation at chromosome position 47799916 on chromosome 2 in gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, which disease(s) is it linked to? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | ATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAG... | ATCTCTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAG... | pathogenic | 36,139 |
Assess the clinical significance (benign or pathogenic) of the variant at chromosome 2, position 47799920, gene MSH6 (mutS homolog 6). What disease(s) is it linked to if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTT... | CTTAATAGCTAGCATTCCCTTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTT... | pathogenic | 36,141 |
A genetic variant on chromosome 2, position 47799939, affects the gene MSH6 (mutS homolog 6). Is this variant benign or pathogenic? If pathogenic, what disease(s) does it cause? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | TTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGT... | TTGGATTTTGCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGT... | pathogenic | 36,146 |
Considering the variant on chromosome 2, location 47799948, involving gene MSH6 (mutS homolog 6), would you classify it as benign or pathogenic? What disease(s), if any, does a pathogenic variant indicate? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | GCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTT... | GCACATGAGCTCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTT... | pathogenic | 36,148 |
The mutation impacting MSH6 (mutS homolog 6) on chromosome 2 at position 47799958: benign or pathogenic? Name the associated disease(s) if pathogenic. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | TCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAA... | TCAAACTCAAGCCTCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAA... | pathogenic | 36,152 |
Evaluate this variant at chromosome 2, position 47799971, gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, what are the disease connection(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATT... | TCAGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATT... | pathogenic | 36,154 |
The mutation impacting MSH6 (mutS homolog 6) on chromosome 2 at position 47799973: benign or pathogenic? Name the associated disease(s) if pathogenic. | pathogenic; ['Hereditary_nonpolyposis_colon_cancer', 'Lynch_syndrome_5'] | AGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAA... | AGCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAA... | pathogenic | 36,157 |
Gene mutation in MSH6 (mutS homolog 6) at chromosome 2, position 47799974—is it benign or pathogenic? If pathogenic, specify the disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | GCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAG... | GCACAATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAG... | pathogenic | 36,159 |
Determine whether the variant at chromosome 2, position 47799978, in gene MSH6 (mutS homolog 6) is benign or pathogenic. If pathogenic, identify the relevant disease(s). | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAA... | AATCTTTTTTATAGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAA... | pathogenic | 36,162 |
Is the genetic mutation found on chromosome 2 at position 47799990, within the gene MSH6 (mutS homolog 6), considered benign or pathogenic? If pathogenic, specify the associated disease(s). | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTA... | AGTTTTAGTCTTTTAGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTA... | pathogenic | 36,165 |
The mutation in gene MSH6 (mutS homolog 6) at chromosome 2, position 47800004—clinically benign or pathogenic? If pathogenic, identify the related disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | AGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATC... | AGCCAGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATC... | pathogenic | 36,169 |
The mutation impacting MSH6 (mutS homolog 6) on chromosome 2 at position 47800008: benign or pathogenic? Name the associated disease(s) if pathogenic. | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCAT... | AGAGTCGACTTACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCAT... | pathogenic | 36,172 |
Variant chromosome 2, position 47800019, gene MSH6 (mutS homolog 6): benign or pathogenic? Disease(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | ACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTAT... | ACCCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTAT... | pathogenic | 36,175 |
Determine if the mutation at chromosome 2, position 47800021 in gene MSH6 (mutS homolog 6) is benign or pathogenic. If pathogenic, what disease(s) is associated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGA... | CCCCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGA... | pathogenic | 36,176 |
Is the genetic change at chromosome 2, position 47800023, within gene MSH6 (mutS homolog 6) benign or pathogenic? Name the disease(s) if pathogenic. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | CCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATG... | CCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATG... | pathogenic | 36,177 |
Gene MSH6 (mutS homolog 6) variant at chromosome 2, position 47800023—is it benign or pathogenic? If pathogenic, what are the associated condition(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | CCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATG... | CCCATACCCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATG... | pathogenic | 36,180 |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.