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 |
|---|---|---|---|---|---|
The mutation in gene MSH6 (mutS homolog 6) at chromosome 2, position 47800030—clinically benign or pathogenic? If pathogenic, identify the related disease(s). | pathogenic; ['Lynch_syndrome'] | CCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTAC... | CCACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTAC... | pathogenic | 36,185 |
Does the variant impacting MSH6 (mutS homolog 6) on chromosome 2, position 47800032, classify as benign or pathogenic? If pathogenic, what disease(s) is it associated with? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | ACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACAT... | ACTCTGCTTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACAT... | pathogenic | 36,187 |
Located at chromosome 2 position 47800039, the variant affecting gene MSH6 (mutS homolog 6)—benign or pathogenic? If pathogenic, which disease(s) does it relate to? | pathogenic; ['Familial_cancer_of_breast', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | TTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAA... | TTCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAA... | pathogenic | 36,189 |
Is chromosome 2, position 47800040, gene MSH6 (mutS homolog 6) variant benign or pathogenic? If pathogenic, what condition(s) is it related to? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | TCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAA... | TCCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAA... | pathogenic | 36,191 |
The genetic variant at chromosome 2, position 47800041, affecting gene MSH6 (mutS homolog 6): benign or pathogenic? Disease name(s) if pathogenic? | pathogenic; ['Carcinoma_of_colon', 'Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1', 'Lynch_syndrome_5'] | CCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAA... | CCTTCATAATGCTGCTTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAA... | pathogenic | 36,193 |
Is the genetic variant on chromosome 2, position 47800056, 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', 'Inherited_MMR_deficiency_(Lynch_syndrome)', 'Lynch_syndrome', 'Lynch_syndrome_5'] | TTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACAC... | TTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACAC... | pathogenic | 36,198 |
Clinical impact (benign or pathogenic) of the variant at chromosome 2, location 47800056, gene MSH6 (mutS homolog 6): what disease(s) if pathogenic? | pathogenic; ['Colorectal_cancer', 'Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch-like_syndrome', 'Lynch_syndrome_5', 'Mismatch_repair_cancer_syndrome_3'] | TTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACAC... | TTTCCCTGGGCAGAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACAC... | pathogenic | 36,200 |
Gene MSH6 (mutS homolog 6) variant at chromosome 2, position 47800068—is it benign or pathogenic? If pathogenic, what are the associated condition(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome', 'Lynch_syndrome_5', 'MSH6-related_disorder'] | GAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGA... | GAGAATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGA... | pathogenic | 36,204 |
Chromosome 2, position 47800071, gene MSH6 (mutS homolog 6): benign or pathogenic variant? If pathogenic, what are the linked illness(es)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | AATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATA... | AATCCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATA... | pathogenic | 36,206 |
Does the variant on chromosome 2 at location 47800074 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'] | CCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTG... | CCTTGCCCTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTG... | pathogenic | 36,207 |
Gene MSH6 (mutS homolog 6) variant at chromosome position 47800081 on chromosome 2: benign or pathogenic? If pathogenic, what disease(s) is it associated with? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTG... | CTTCTTGTATTATGTCACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTG... | pathogenic | 36,209 |
Is the genetic mutation found on chromosome 2 at position 47800097, 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'] | ACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTA... | ACTTTGTGGGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTA... | pathogenic | 36,214 |
Does the genetic variant at chromosome 2, position 47800105, impacting gene MSH6 (mutS homolog 6), appear benign or pathogenic? If pathogenic, name the associated disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome'] | GGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGAC... | GGGTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGAC... | pathogenic | 36,217 |
Evaluate the clinical significance of the mutation at chromosome 2, position 47800107 in gene MSH6 (mutS homolog 6): benign or pathogenic? What disease(s) does a pathogenic variant suggest? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | GTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGT... | GTTGGTGTCTGCTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGT... | pathogenic | 36,219 |
Variant at chromosome 2, position 47800118, gene MSH6 (mutS homolog 6): clinically benign or pathogenic? If pathogenic, specify the disease(s) involved. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome'] | CTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACAC... | CTACACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACAC... | pathogenic | 36,222 |
A genetic variant on chromosome 2, position 47800121, 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', 'Lynch_syndrome_5', 'Mismatch_repair_cancer_syndrome_3'] | CACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTA... | CACTTACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTA... | pathogenic | 36,223 |
Is the variant located on chromosome 2 at position 47800126, gene MSH6 (mutS homolog 6), benign or pathogenic? If pathogenic, specify the disease(s) linked. | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | ACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGT... | ACAGCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGT... | pathogenic | 36,225 |
A mutation at chromosome position 47800129 on chromosome 2 in gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, which disease(s) is it linked to? | pathogenic; ['Carcinoma_of_colon', 'Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5', 'MSH6-related_disorder', 'Mismatch_repair_cancer_syndrome_1', 'Mismatch_repair_cancer_syndrome_3'] | GCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAG... | GCAAGTCCAGAGATTTTTTTTCCACCACGTTTGCAGGAGAACTATTGGCATGGAAAATGACAATTGTTTTAATGTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAG... | pathogenic | 36,227 |
Evaluate if the mutation on chromosome 2 at position 47800202 in MSH6 (mutS homolog 6) is benign or pathogenic. Disease name(s) if pathogenic? | pathogenic; ['Lynch_syndrome'] | GTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCAT... | GTCAAGTGAAACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCAT... | pathogenic | 36,246 |
Gene MSH6 (mutS homolog 6) variant at chromosome position 47800211 on chromosome 2: benign or pathogenic? If pathogenic, what disease(s) is it associated with? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5', 'MSH6-related_disorder', 'Mismatch_repair_cancer_syndrome_1'] | AACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTG... | AACTGAAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTG... | pathogenic | 36,251 |
The genetic variant at chromosome 2, position 47800216, 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'] | AAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTA... | AAGTTGATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTA... | pathogenic | 36,254 |
Variant at chromosome position 47800221, 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_5'] | GATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAAT... | GATGTTCATTGAGAGGTTTCTAATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAAT... | pathogenic | 36,257 |
Is the genetic change at chromosome 2, position 47800242, within gene MSH6 (mutS homolog 6) benign or pathogenic? Name the disease(s) if pathogenic. | pathogenic; ['Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGG... | AATTTCTAGAGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGG... | pathogenic | 36,262 |
Variant chromosome 2, position 47800251, gene MSH6 (mutS homolog 6): benign or pathogenic? Disease(s)? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTAT... | AGGTGGGTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTAT... | pathogenic | 36,265 |
The genetic variant at chromosome 2, position 47800257, affecting gene MSH6 (mutS homolog 6): benign or pathogenic? Disease name(s) if pathogenic? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | GTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTC... | GTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTC... | pathogenic | 36,269 |
Variant at chromosome position 47800257, 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_5'] | GTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTC... | GTTCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTC... | pathogenic | 36,272 |
A genetic variant on chromosome 2, position 47800259, 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', 'Lynch_syndrome_5'] | TCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAA... | TCTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAA... | pathogenic | 36,273 |
Clinically, how would you classify the variant at chromosome 2, position 47800260, gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, specify the associated illness(es). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAA... | CTTTTTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAA... | pathogenic | 36,274 |
Variant in gene MSH6 (mutS homolog 6), located at chromosome 2 position 47800264: benign or pathogenic? What disease(s) does it cause if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | TTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAAT... | TTTTGGCATATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAAT... | pathogenic | 36,275 |
The genetic variant at chromosome 2, position 47800272, affecting gene MSH6 (mutS homolog 6): benign or pathogenic? Disease name(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTT... | TATGAAGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTT... | pathogenic | 36,278 |
Is the chromosome 2, position 47800277 variant in MSH6 (mutS homolog 6) clinically benign or pathogenic? If pathogenic, what condition(s) is associated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | AGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACT... | AGTTGCAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACT... | pathogenic | 36,281 |
Variant in gene MSH6 (mutS homolog 6), located at chromosome 2 position 47800282: benign or pathogenic? What disease(s) does it cause if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | CAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTT... | CAGCATATTAAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTT... | pathogenic | 36,284 |
Variant in gene MSH6 (mutS homolog 6), located at chromosome 2 position 47800291: benign or pathogenic? What disease(s) does it cause if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | AAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGG... | AAGAGAATTTACAGTAGTACAGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGG... | pathogenic | 36,289 |
Does the variant on chromosome 2 at location 47800311 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', 'Lynch_syndrome_5'] | AGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGT... | AGATGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGT... | pathogenic | 36,296 |
Mutation found at chromosome 2 position 47800314, gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, indicate the relevant disease(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTT... | TGGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTT... | pathogenic | 36,300 |
Does the chromosome 2 mutation at position 47800315 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'] | GGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTT... | GGGGTTATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTT... | pathogenic | 36,301 |
Gene MSH6 (mutS homolog 6) variant at chromosome position 47800320 on chromosome 2: benign or pathogenic? If pathogenic, what disease(s) is it associated with? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATA... | TATCCCATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATA... | pathogenic | 36,304 |
Considering the variant on chromosome 2, location 47800326, 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; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | ATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTT... | ATCCACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTT... | pathogenic | 36,310 |
Is the genetic variant on chromosome 2, position 47800329, 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', 'Lynch_syndrome_5'] | CACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCT... | CACAACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCT... | pathogenic | 36,312 |
Is the genetic mutation found on chromosome 2 at position 47800333, within the gene MSH6 (mutS homolog 6), considered benign or pathogenic? If pathogenic, specify the associated disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | ACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCC... | ACTTATGATGGGGTTACATAAACTAAAAACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCC... | pathogenic | 36,314 |
Evaluate the clinical significance of the mutation at chromosome 2, position 47800361 in gene MSH6 (mutS homolog 6): benign or pathogenic? What disease(s) does a pathogenic variant suggest? | pathogenic; ['Lynch_syndrome'] | ACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAG... | ACGTGTTTAATACACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAG... | pathogenic | 36,321 |
Gene MSH6 (mutS homolog 6) variant at chromosome position 47800373 on chromosome 2: benign or pathogenic? If pathogenic, what disease(s) is it associated with? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAG... | CACCTACCCCACCGAATATTGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAG... | pathogenic | 36,324 |
Mutation at chromosome 2, position 47800392, within MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, indicate the disease(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAG... | TGTAGCTTGGGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAG... | pathogenic | 36,334 |
Clinical impact (benign or pathogenic) of the variant at chromosome 2, location 47800401, gene MSH6 (mutS homolog 6): what disease(s) if pathogenic? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | GGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGA... | GGCGTAGCCTAACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGA... | pathogenic | 36,337 |
The genetic variant at chromosome 2, position 47800411, 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_5', 'likely other unspecified diseases'] | AACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCT... | AACCTATCTCAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCT... | pathogenic | 36,341 |
Variant at chromosome 2, position 47800420, gene MSH6 (mutS homolog 6): clinically benign or pathogenic? If pathogenic, specify the disease(s) involved. | pathogenic; ['Hereditary_nonpolyposis_colon_cancer', 'Lynch_syndrome_5'] | CAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAA... | CAGACGTGCTCAGAACACTTAAATGTTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAA... | pathogenic | 36,343 |
A genetic alteration at chromosome 2, position 47800445, 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'] | TTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAA... | TTAGCCTAAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAA... | pathogenic | 36,348 |
Evaluate this variant at chromosome 2, position 47800452, 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'] | AAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAA... | AAAGTTGGGCAAGATCATCTAACACAAAGCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAA... | pathogenic | 36,352 |
Classify the chromosome 2 variant at position 47800480 affecting gene MSH6 (mutS homolog 6) as benign or pathogenic. If pathogenic, which disease(s) is associated? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | GCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGT... | GCCTATTTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGT... | pathogenic | 36,360 |
Determine whether the variant at chromosome 2, position 47800486, in gene MSH6 (mutS homolog 6) is benign or pathogenic. If pathogenic, identify the relevant disease(s). | pathogenic; ['Carcinoma_of_colon', 'Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATT... | TTTATAATAAGGAATTGCCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATT... | pathogenic | 36,363 |
Located at chromosome 2 position 47800503, the variant affecting gene MSH6 (mutS homolog 6)—benign or pathogenic? If pathogenic, which disease(s) does it relate to? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGA... | CCTATCTCATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGA... | pathogenic | 36,369 |
Regarding the variant found on chromosome 2 at position 47800510 in gene MSH6 (mutS homolog 6): is it benign or pathogenic? If pathogenic, identify the disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | CATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAG... | CATGTAATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAG... | pathogenic | 36,372 |
Evaluate this variant at chromosome 2, position 47800516, gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, what are the disease connection(s)? | pathogenic; ['Lynch_syndrome', 'Lynch_syndrome_5'] | ATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGAC... | ATTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGAC... | pathogenic | 36,373 |
Regarding the variant at chromosome 2 and position 47800517, 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', 'Mismatch_repair_cancer_syndrome_3'] | TTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACA... | TTCATCGAATACTGTACTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACA... | pathogenic | 36,374 |
A genetic alteration at chromosome 2, position 47800533, in gene MSH6 (mutS homolog 6)—benign or pathogenic? If pathogenic, which disease(s) is involved? | pathogenic; ['Lynch_syndrome_5'] | CTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAG... | CTAAAAATGAAAAACAGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAG... | pathogenic | 36,381 |
Does the chromosome 2 mutation at position 47800548 within gene MSH6 (mutS homolog 6) classify as benign or pathogenic? If pathogenic, indicate the related illness(es). | pathogenic; ['Carcinoma_of_colon', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5', 'Mismatch_repair_cancer_syndrome_3', 'Ovarian_carcinoma'] | AGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAG... | AGTGGCTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAG... | pathogenic | 36,388 |
A genetic variant on chromosome 2, position 47800553, affects the gene MSH6 (mutS homolog 6). Is this variant benign or pathogenic? If pathogenic, what disease(s) does it cause? | pathogenic; ['Familial_cancer_of_breast', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | CTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTG... | CTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTG... | pathogenic | 36,389 |
Chromosome 2, position 47800553, gene MSH6 (mutS homolog 6): benign or pathogenic variant? If pathogenic, what are the linked illness(es)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | CTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTG... | CTGCACGGGTACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTG... | pathogenic | 36,390 |
Is chromosome 2, position 47800562, gene MSH6 (mutS homolog 6) variant benign or pathogenic? If pathogenic, what condition(s) is it related to? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | TACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGG... | TACCATTATAAAGTCAAAAAATCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGG... | pathogenic | 36,391 |
Clinical classification of chromosome 2, position 47800583, gene MSH6 (mutS homolog 6): benign or pathogenic? Disease(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGA... | TCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGA... | pathogenic | 36,395 |
Determine if the mutation at chromosome 2, position 47800583 in gene MSH6 (mutS homolog 6) is benign or pathogenic. If pathogenic, what disease(s) is associated? | pathogenic; ['Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGA... | TCATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGA... | pathogenic | 36,396 |
Is the genetic variant on chromosome 2, position 47800585, gene MSH6 (mutS homolog 6), benign or pathogenic? If pathogenic, what disease(s) is indicated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | ATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAAC... | ATAAGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAAC... | pathogenic | 36,397 |
Does the chromosome 2 mutation at position 47800588 within gene MSH6 (mutS homolog 6) classify as benign or pathogenic? If pathogenic, indicate the related illness(es). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGC... | AGTTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGC... | pathogenic | 36,398 |
Chromosome 2, position 47800590, gene MSH6 (mutS homolog 6): benign or pathogenic variant? If pathogenic, what are the linked illness(es)? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCC... | TTGAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCC... | pathogenic | 36,399 |
Clinically, how would you classify the variant at chromosome 2, position 47800592, gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, specify the associated illness(es). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome', 'Lynch_syndrome_5'] | GAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTG... | GAACTGTCTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTG... | pathogenic | 36,400 |
Mutation at chromosome 2, position 47800599, within MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, indicate the disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | CTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGT... | CTTACATTATGGTTTTCCAAATTTTGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGT... | pathogenic | 36,401 |
Regarding the variant at chromosome 2 and position 47800623, affecting gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, what are the associated illness(es)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGT... | TGATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGT... | pathogenic | 36,410 |
Is the variant located on chromosome 2 at position 47800625, gene MSH6 (mutS homolog 6), benign or pathogenic? If pathogenic, specify the disease(s) linked. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Mismatch_repair_cancer_syndrome_3'] | ATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGA... | ATTTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGA... | pathogenic | 36,411 |
Classify the chromosome 2 variant at position 47800627 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'] | TTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACT... | TTGTTTTTAAATACTCTTTCCTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACT... | pathogenic | 36,414 |
Gene MSH6 (mutS homolog 6) variant at chromosome 2, position 47800647—is it benign or pathogenic? If pathogenic, what are the associated condition(s)? | pathogenic; ['Lynch_syndrome_5'] | CTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAG... | CTTGCCTGGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAG... | pathogenic | 36,422 |
Evaluate this variant at chromosome 2, position 47800654, gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, what are the disease connection(s)? | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch-like_syndrome', 'Lynch_syndrome_5', 'MSH6-related_disorder'] | GGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGC... | GGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGC... | pathogenic | 36,425 |
Considering the variant on chromosome 2, location 47800654, 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; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | GGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGC... | GGCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGC... | pathogenic | 36,426 |
Does the genetic variant at chromosome 2, position 47800655, impacting gene MSH6 (mutS homolog 6), appear benign or pathogenic? If pathogenic, name the associated disease(s). | pathogenic; ['Lynch_syndrome'] | GCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCT... | GCAGGTAGGCACAACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCT... | pathogenic | 36,427 |
Assess the clinical significance (benign or pathogenic) of the variant at chromosome 2, position 47800667, gene MSH6 (mutS homolog 6). What disease(s) is it linked to if pathogenic? | pathogenic; ['Carcinoma_of_colon', 'Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAA... | AACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAA... | pathogenic | 36,433 |
A genetic variant on chromosome 2, position 47800667, affects the gene MSH6 (mutS homolog 6). Is this variant benign or pathogenic? If pathogenic, what disease(s) does it cause? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAA... | AACTTACGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAA... | pathogenic | 36,434 |
Benign or pathogenic: chromosome 2, position 47800673, gene MSH6 (mutS homolog 6) variant? Disease(s) if pathogenic? | pathogenic; ['Hereditary_nonpolyposis_colon_cancer', 'Lynch_syndrome_5'] | CGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCT... | CGTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCT... | pathogenic | 36,437 |
A genetic variant at chromosome 2, position 47800674, affecting gene MSH6 (mutS homolog 6)—is it benign or pathogenic? If pathogenic, identify the associated disorder(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | GTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTC... | GTAACAGATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTC... | pathogenic | 36,438 |
A mutation at chromosome position 47800680 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', 'Lynch_syndrome_5'] | GATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCAC... | GATAAGAGTGAAGAAGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCAC... | pathogenic | 36,441 |
Is the chromosome 2, position 47800694 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'] | AGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTA... | AGATAATGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTA... | pathogenic | 36,446 |
Gene MSH6 (mutS homolog 6) variant at chromosome 2, position 47800700—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'] | TGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTT... | TGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTT... | pathogenic | 36,448 |
Variant chromosome 2, position 47800708, gene MSH6 (mutS homolog 6): benign or pathogenic? Disease(s)? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAA... | AGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAA... | pathogenic | 36,451 |
Is chromosome 2, position 47800720, gene MSH6 (mutS homolog 6) variant benign or pathogenic? If pathogenic, what condition(s) is it related to? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | AAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACT... | AAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACT... | pathogenic | 36,458 |
Does the variant impacting MSH6 (mutS homolog 6) on chromosome 2, position 47800720, classify as benign or pathogenic? If pathogenic, what disease(s) is it associated with? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | AAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACT... | AAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACT... | pathogenic | 36,459 |
Determine if the mutation at chromosome 2, position 47800720 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'] | AAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACT... | AAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACT... | pathogenic | 36,460 |
Gene mutation in MSH6 (mutS homolog 6) at chromosome 2, position 47800731—is it benign or pathogenic? If pathogenic, specify the disease(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTT... | AAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTT... | pathogenic | 36,463 |
Does the chromosome 2 mutation at position 47800738 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'] | AAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCC... | AAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCC... | pathogenic | 36,466 |
Variant at chromosome position 47800738, 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', 'Uterine_corpus_cancer'] | AAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCC... | AAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCC... | pathogenic | 36,467 |
Gene MSH6 (mutS homolog 6) variant at chromosome 2, position 47800747—is it benign or pathogenic? If pathogenic, what are the associated condition(s)? | pathogenic; ['Lynch_syndrome'] | GGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAAT... | GGCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAAT... | pathogenic | 36,471 |
Is chromosome 2, position 47800748, 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_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | GCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATT... | GCGAAGTAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATT... | pathogenic | 36,473 |
The mutation impacting MSH6 (mutS homolog 6) on chromosome 2 at position 47800754: benign or pathogenic? Name the associated disease(s) if pathogenic. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAAT... | TAGCCGCCAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAAT... | pathogenic | 36,475 |
Chromosome 2, position 47800761, gene MSH6 (mutS homolog 6): Is this mutation clinically benign or pathogenic? If pathogenic, identify the related disease(s). | pathogenic; ['Breast_and/or_ovarian_cancer', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_5'] | CAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGC... | CAAATAAAAAAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGC... | pathogenic | 36,481 |
Chromosome 2, position 47800770, gene MSH6 (mutS homolog 6): Is this mutation clinically benign or pathogenic? If pathogenic, identify the related disease(s). | pathogenic; ['Endometrial_carcinoma', 'Hereditary_cancer-predisposing_syndrome'] | AAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAG... | AAACGAAGGGTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAG... | pathogenic | 36,484 |
Evaluate this variant at chromosome 2, position 47800779, gene MSH6 (mutS homolog 6): benign or pathogenic? If pathogenic, what are the disease connection(s)? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | GTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGG... | GTCATATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGG... | pathogenic | 36,488 |
Is the genetic variant on chromosome 2, position 47800784, 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'] | ATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATG... | ATCAGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATG... | pathogenic | 36,490 |
Variant at chromosome 2, position 47800787, gene MSH6 (mutS homolog 6): clinically benign or pathogenic? If pathogenic, specify the disease(s) involved. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACA... | AGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACA... | pathogenic | 36,492 |
Is the variant located on chromosome 2 at position 47800787, gene MSH6 (mutS homolog 6), benign or pathogenic? If pathogenic, specify the disease(s) linked. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | AGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACA... | AGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACA... | pathogenic | 36,493 |
Clinical significance of chromosome 2, position 47800787, gene MSH6 (mutS homolog 6): benign or pathogenic? Name the disease(s) if pathogenic. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | AGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACA... | AGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACA... | pathogenic | 36,494 |
Does the variant on chromosome 2 at location 47800787 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'] | AGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACA... | AGATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACA... | pathogenic | 36,495 |
Variant in gene MSH6 (mutS homolog 6), located at chromosome 2 position 47800788: benign or pathogenic? What disease(s) does it cause if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_5'] | GATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACAG... | GATTCTGAGAGTGACATTGGTGGCTCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACAG... | pathogenic | 36,496 |
Gene mutation in MSH6 (mutS homolog 6) at chromosome 2, position 47800812—is it benign or pathogenic? If pathogenic, specify the disease(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_5'] | TCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACAGTAGTCGCCCTACTGTTTGGTATCA... | TCTGATGTGGAATTTAAGCCAGACACTAAGGAGGAAGGAAGCAGTGATGAAATAAGCAGTGGAGTGGGGGATAGTGAGAGTGAAGGCCTGAACAGCCCTGTCAAAGTTGCTCGAAAGCGGAAGAGAATGGTGACTGGAAATGGCTCTCTTAAAAGGAAAAGCTCTAGGAAGGAAACGCCCTCAGCCACCAAACAAGCAACTAGCATTTCATCAGAAACCAAGAATACTTTGAGAGCTTTCTCTGCCCCTCAAAATTCTGAATCCCAAGCCCACGTTAGTGGAGGTGGTGATGACAGTAGTCGCCCTACTGTTTGGTATCA... | pathogenic | 36,504 |
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