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 |
|---|---|---|---|---|---|
Considering the genetic mutation at chromosome 2, position 47466734, impacting MSH2 (mutS homolog 2): is it clinically benign or pathogenic? Name the associated disease(s) if pathogenic. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | AGTATGTTGAAAGCAACATAAATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTA... | AGTATGTTGAAAGCAACATAAATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTA... | pathogenic | 34,364 |
Regarding the variant at chromosome 2 and position 47466735, affecting gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, what are the associated illness(es)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | GTATGTTGAAAGCAACATAAATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTAT... | GTATGTTGAAAGCAACATAAATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTAT... | pathogenic | 34,365 |
Is the genetic mutation found on chromosome 2 at position 47466740, within the gene MSH2 (mutS homolog 2), considered benign or pathogenic? If pathogenic, specify the associated disease(s). | pathogenic; ['Lynch_syndrome'] | TTGAAAGCAACATAAATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGT... | TTGAAAGCAACATAAATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGT... | pathogenic | 34,366 |
Considering the variant on chromosome 2, location 47466742, involving gene MSH2 (mutS homolog 2), 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_1'] | GAAAGCAACATAAATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAA... | GAAAGCAACATAAATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAA... | pathogenic | 34,367 |
Clinical significance of chromosome 2, position 47466746, gene MSH2 (mutS homolog 2): benign or pathogenic? Name the disease(s) if pathogenic. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | GCAACATAAATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATAC... | GCAACATAAATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATAC... | pathogenic | 34,370 |
Clinical impact (benign or pathogenic) of the variant at chromosome 2, location 47466755, gene MSH2 (mutS homolog 2): what disease(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | ATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTT... | ATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTT... | pathogenic | 34,374 |
A mutation at chromosome position 47466755 on chromosome 2 in gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, which disease(s) is it linked to? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | ATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTT... | ATAGCACTCAAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTT... | pathogenic | 34,375 |
Does the chromosome 2 mutation at position 47466764 within gene MSH2 (mutS homolog 2) classify as benign or pathogenic? If pathogenic, indicate the related illness(es). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | AAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTA... | AAATTGAGACAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTA... | pathogenic | 34,379 |
Regarding the variant at chromosome 2 and position 47466773, affecting gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, what are the associated illness(es)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome'] | CAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTG... | CAGAAACTGTAACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTG... | pathogenic | 34,383 |
Gene mutation in MSH2 (mutS homolog 2) at chromosome 2, position 47466783—is it benign or pathogenic? If pathogenic, specify the disease(s). | pathogenic; ['Lynch_syndrome'] | AACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTGCTGTTGTTAA... | AACTGTAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTGCTGTTGTTAA... | pathogenic | 34,387 |
A genetic variant at chromosome 2, position 47466788, affecting gene MSH2 (mutS homolog 2)—is it benign or pathogenic? If pathogenic, identify the associated disorder(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | TAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTGCTGTTGTTAACACTG... | TAGTATAAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTGCTGTTGTTAACACTG... | pathogenic | 34,389 |
Gene MSH2 (mutS homolog 2) variant at chromosome 2, position 47466794—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_1'] | AAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTGCTGTTGTTAACACTGCAGTGA... | AAGAAGCATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTGCTGTTGTTAACACTGCAGTGA... | pathogenic | 34,392 |
The mutation in gene MSH2 (mutS homolog 2) at chromosome 2, position 47466801—clinically benign or pathogenic? If pathogenic, identify the related disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | ATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTGCTGTTGTTAACACTGCAGTGAAATGCAT... | ATTAGGCTGGGAATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTGCTGTTGTTAACACTGCAGTGAAATGCAT... | pathogenic | 34,393 |
Benign or pathogenic: chromosome 2, position 47466813, gene MSH2 (mutS homolog 2) variant? Disease(s) if pathogenic? | benign | ATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTGCTGTTGTTAACACTGCAGTGAAATGCATATATAAGCAAAC... | ATTGGGAAACACGAGTTCTAGTTGCAGCTTGGAAACTTTTTCTGAAGCTCTTTACAAATTACTTAATTTCTCTGGTTTTCACCACATTGTTCTATAGCATTAACATGTTGGATTCATTGCTTTAATTCTTAGACCTACGTGTCATCAGAAATGCCATTACACTTTGAGGATTTGAGCCTTATTTTAAATAAAGTTGTGATCCTCATGGCAGCCTAGGTTTACATGTGTTAAATAAACAGTATTCTGTAAATACCATTGTCTTTCATGTTTAGTGATGTTGCTGTTGTTAACACTGCAGTGAAATGCATATATAAGCAAAC... | benign | 34,405 |
Gene mutation in MSH2 (mutS homolog 2) at chromosome 2, position 47470946—is it benign or pathogenic? If pathogenic, specify the disease(s). | benign | AGTATTTTTTTCTTATTTTATTCTCATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAG... | AGTATTTTTTTCTTATTTTATTCTCATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAG... | benign | 34,416 |
Clinical classification of chromosome 2, position 47470947, gene MSH2 (mutS homolog 2): benign or pathogenic? Disease(s) if pathogenic? | benign | GTATTTTTTTCTTATTTTATTCTCATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGG... | GTATTTTTTTCTTATTTTATTCTCATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGG... | benign | 34,418 |
Mutation at chromosome 2, position 47470965, within MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, indicate the disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome'] | ATTCTCATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCC... | ATTCTCATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCC... | pathogenic | 34,431 |
Mutation at chromosome 2, position 47470968, within MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, indicate the disease(s). | pathogenic; ['Lynch_syndrome'] | CTCATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGC... | CTCATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGC... | pathogenic | 34,433 |
Considering the variant on chromosome 2, location 47470968, involving gene MSH2 (mutS homolog 2), would you classify it as benign or pathogenic? What disease(s), if any, does a pathogenic variant indicate? | pathogenic; ['Hereditary_cancer-predisposing_syndrome'] | CTCATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGC... | CTCATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGC... | pathogenic | 34,434 |
The mutation in gene MSH2 (mutS homolog 2) at chromosome 2, position 47470970—clinically benign or pathogenic? If pathogenic, identify the related disease(s). | pathogenic; ['Lynch_syndrome'] | CATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCC... | CATCTTCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCC... | pathogenic | 34,439 |
Does the variant impacting MSH2 (mutS homolog 2) on chromosome 2, position 47470975, classify as benign or pathogenic? If pathogenic, what disease(s) is it associated with? | pathogenic; ['Hereditary_cancer-predisposing_syndrome'] | TCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCT... | TCCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCT... | pathogenic | 34,441 |
The chromosome 2, position 47470976 genetic variant in gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, indicate disease(s). | pathogenic; ['Gastric_cancer', 'Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome', 'Lynch_syndrome_1', 'Uterine_corpus_cancer'] | CCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTC... | CCTTGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTC... | pathogenic | 34,442 |
Determine if the mutation at chromosome 2, position 47470979 in gene MSH2 (mutS homolog 2) is benign or pathogenic. If pathogenic, what disease(s) is associated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | TGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAA... | TGAGTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAA... | pathogenic | 34,443 |
Does the variant on chromosome 2 at location 47470982 affecting gene MSH2 (mutS homolog 2) 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_1'] | GTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTT... | GTATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTT... | pathogenic | 34,444 |
Considering the genetic mutation at chromosome 2, position 47470984, impacting MSH2 (mutS homolog 2): is it clinically benign or pathogenic? Name the associated disease(s) if pathogenic. | pathogenic; ['Lynch_syndrome'] | ATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTA... | ATTGTTTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTA... | pathogenic | 34,447 |
Considering the variant on chromosome 2, location 47470989, involving gene MSH2 (mutS homolog 2), would you classify it as benign or pathogenic? What disease(s), if any, does a pathogenic variant indicate? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1'] | TTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTT... | TTATTTCAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTT... | pathogenic | 34,450 |
Assess the variant on chromosome 2, position 47470995, impacting MSH2 (mutS homolog 2): is it benign or pathogenic? If pathogenic, specify the associated condition(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | CAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTC... | CAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTC... | pathogenic | 34,453 |
Variant at chromosome position 47470995, chromosome 2, gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, what condition(s) does it relate to? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | CAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTC... | CAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTC... | pathogenic | 34,455 |
Variant at chromosome 2, position 47470995, gene MSH2 (mutS homolog 2): clinically benign or pathogenic? If pathogenic, specify the disease(s) involved. | pathogenic; ['Lynch_syndrome'] | CAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTC... | CAACCTCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTC... | pathogenic | 34,456 |
Considering the genetic mutation at chromosome 2, position 47471000, impacting MSH2 (mutS homolog 2): is it clinically benign or pathogenic? Name the associated disease(s) if pathogenic. | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | TCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATT... | TCTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATT... | pathogenic | 34,458 |
A genetic variant at chromosome 2, position 47471001, affecting gene MSH2 (mutS homolog 2)—is it benign or pathogenic? If pathogenic, identify the associated disorder(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome'] | CTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTG... | CTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTG... | pathogenic | 34,459 |
Mutation found at chromosome 2 position 47471001, gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, indicate the relevant disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1'] | CTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTG... | CTTTTTTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTG... | pathogenic | 34,460 |
Considering the genetic mutation at chromosome 2, position 47471006, impacting MSH2 (mutS homolog 2): is it clinically benign or pathogenic? Name the associated disease(s) if pathogenic. | pathogenic; ['Lynch_syndrome'] | TTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAA... | TTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAA... | pathogenic | 34,462 |
Gene MSH2 (mutS homolog 2) variant at chromosome 2, position 47471006—is it benign or pathogenic? If pathogenic, what are the associated condition(s)? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | TTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAA... | TTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAA... | pathogenic | 34,463 |
Is the variant located on chromosome 2 at position 47471006, gene MSH2 (mutS homolog 2), benign or pathogenic? If pathogenic, specify the disease(s) linked. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1'] | TTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAA... | TTTTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAA... | pathogenic | 34,464 |
Regarding the variant at chromosome 2 and position 47471008, affecting gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, what are the associated illness(es)? | pathogenic; ['Lynch_syndrome'] | TTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATA... | TTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATA... | pathogenic | 34,466 |
Does the genetic variant at chromosome 2, position 47471008, impacting gene MSH2 (mutS homolog 2), appear benign or pathogenic? If pathogenic, name the associated disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | TTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATA... | TTTTTTTTTTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATA... | pathogenic | 34,467 |
Is the variant located on chromosome 2 at position 47471016, gene MSH2 (mutS homolog 2), benign or pathogenic? If pathogenic, specify the disease(s) linked. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | TTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAG... | TTTTTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAG... | pathogenic | 34,471 |
Variant chromosome 2, position 47471019, gene MSH2 (mutS homolog 2): benign or pathogenic? Disease(s)? | pathogenic; ['Lynch_syndrome'] | TTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTT... | TTGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTT... | pathogenic | 34,472 |
Determine whether the variant at chromosome 2, position 47471020, in gene MSH2 (mutS homolog 2) is benign or pathogenic. If pathogenic, identify the relevant disease(s). | pathogenic; ['Lynch_syndrome', 'Uterine_corpus_cancer'] | TGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTC... | TGGAGAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTC... | pathogenic | 34,473 |
Mutation found at chromosome 2 position 47471024, gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, indicate the relevant disease(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | GAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGA... | GAAGGGTTTGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGA... | pathogenic | 34,477 |
Gene MSH2 (mutS homolog 2) variant at chromosome 2, position 47471032—is it benign or pathogenic? If pathogenic, what are the associated condition(s)? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | TGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGACATTTTCC... | TGGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGACATTTTCC... | pathogenic | 34,480 |
Determine if the mutation at chromosome 2, position 47471041 in gene MSH2 (mutS homolog 2) is benign or pathogenic. If pathogenic, what disease(s) is associated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | CGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGACATTTTCCTGGCCGGGC... | CGCTCAGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGACATTTTCCTGGCCGGGC... | pathogenic | 34,484 |
The mutation in gene MSH2 (mutS homolog 2) at chromosome 2, position 47471046—clinically benign or pathogenic? If pathogenic, identify the related disease(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | AGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGACATTTTCCTGGCCGGGCATGGT... | AGGCTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGACATTTTCCTGGCCGGGCATGGT... | pathogenic | 34,486 |
Benign or pathogenic: chromosome 2, position 47471049, gene MSH2 (mutS homolog 2) variant? Disease(s) if pathogenic? | pathogenic; ['Lynch_syndrome_1'] | CTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGACATTTTCCTGGCCGGGCATGGTGGC... | CTGGAGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGACATTTTCCTGGCCGGGCATGGTGGC... | pathogenic | 34,490 |
Does the variant on chromosome 2 at location 47471053 affecting gene MSH2 (mutS homolog 2) 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_1'] | AGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGACATTTTCCTGGCCGGGCATGGTGGCTTAC... | AGTGCAGTGGCACAATTTTGGCCCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCCACCTCAGCCACCCAAGTAGCTGGGACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTCCACCTGCCTTGCCCTCCCAAAGTTCTGGGATTACAGGATTACAGATGCTGTGCCCGGCCCAACCTCTAATTTTAATTTTCTCTTCAAATTGTTCAATAAGATTTAGTTTCAAGACATTTTCCTGGCCGGGCATGGTGGCTTAC... | pathogenic | 34,494 |
Regarding the variant found on chromosome 2 at position 47474913 in gene MSH2 (mutS homolog 2): is it benign or pathogenic? If pathogenic, identify the disease(s). | benign | GTAATGGATCACTTTAATAATTTTCTATCATACAATTAAGTCATAAAAGGTCATGCTATTAAGAGCCAGTTATGTGACATGCCAAGTATAGACTCTTAATTAAGATGCTTTGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGG... | GTAATGGATCACTTTAATAATTTTCTATCATACAATTAAGTCATAAAAGGTCATGCTATTAAGAGCCAGTTATGTGACATGCCAAGTATAGACTCTTAATTAAGATGCTTTGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGG... | benign | 34,514 |
Variant in MSH2 (mutS homolog 2), chromosome 2, position 47475005—is this benign or pathogenic? If pathogenic, what disease(s) is linked? | benign | CTCTTAATTAAGATGCTTTGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCC... | CTCTTAATTAAGATGCTTTGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCC... | benign | 34,517 |
Does the variant impacting MSH2 (mutS homolog 2) on chromosome 2, position 47475007, classify as benign or pathogenic? If pathogenic, what disease(s) is it associated with? | benign | CTTAATTAAGATGCTTTGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTG... | CTTAATTAAGATGCTTTGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTG... | benign | 34,518 |
Gene mutation in MSH2 (mutS homolog 2) at chromosome 2, position 47475007—is it benign or pathogenic? If pathogenic, specify the disease(s). | benign | CTTAATTAAGATGCTTTGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTG... | CTTAATTAAGATGCTTTGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTG... | benign | 34,519 |
Chromosome 2, position 47475020, gene MSH2 (mutS homolog 2): benign or pathogenic variant? If pathogenic, what are the linked illness(es)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | CTTTGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTT... | CTTTGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTT... | pathogenic | 34,524 |
Variant at chromosome position 47475023, chromosome 2, gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, what condition(s) does it relate to? | pathogenic; ['Lynch_syndrome'] | TGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCT... | TGGTTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCT... | pathogenic | 34,527 |
Clinical significance of chromosome 2, position 47475026, gene MSH2 (mutS homolog 2): benign or pathogenic? Name the disease(s) if pathogenic. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | TTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTT... | TTTGCTTTTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTT... | pathogenic | 34,530 |
Chromosome 2, position 47475033, gene MSH2 (mutS homolog 2): Is this mutation clinically benign or pathogenic? If pathogenic, identify the related disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | TTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACT... | TTTATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACT... | pathogenic | 34,534 |
The genetic variant at chromosome 2, position 47475036, affecting gene MSH2 (mutS homolog 2): benign or pathogenic? Disease name(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1'] | ATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATA... | ATTTATTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATA... | pathogenic | 34,536 |
Is chromosome 2, position 47475041, gene MSH2 (mutS homolog 2) variant benign or pathogenic? If pathogenic, what condition(s) is it related to? | pathogenic; ['Lynch_syndrome'] | TTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTT... | TTTATTTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTT... | pathogenic | 34,539 |
The mutation impacting MSH2 (mutS homolog 2) on chromosome 2 at position 47475046: benign or pathogenic? Name the associated disease(s) if pathogenic. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | TTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCT... | TTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCT... | pathogenic | 34,543 |
A genetic variant at chromosome 2, position 47475046, affecting gene MSH2 (mutS homolog 2)—is it benign or pathogenic? If pathogenic, identify the associated disorder(s). | pathogenic; ['Lynch_syndrome'] | TTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCT... | TTATTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCT... | pathogenic | 34,544 |
Does the variant on chromosome 2 at location 47475049 affecting gene MSH2 (mutS homolog 2) have a clinical significance of benign or pathogenic? If pathogenic, what disease(s) is associated? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | TTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGT... | TTTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGT... | pathogenic | 34,547 |
Mutation at chromosome 2, position 47475050, within MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, indicate the disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome', 'Lynch_syndrome_1'] | TTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTC... | TTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTC... | pathogenic | 34,548 |
Evaluate if the mutation on chromosome 2 at position 47475050 in MSH2 (mutS homolog 2) is benign or pathogenic. Disease name(s) if pathogenic? | pathogenic; ['Carcinoma_of_colon', 'Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1', 'MSH2-related_disorder'] | TTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTC... | TTTTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTC... | pathogenic | 34,551 |
Evaluate if the mutation on chromosome 2 at position 47475052 in MSH2 (mutS homolog 2) is benign or pathogenic. Disease name(s) if pathogenic? | pathogenic; ['Lynch_syndrome'] | TTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAG... | TTCAGATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAG... | pathogenic | 34,552 |
The genetic variant at chromosome 2, position 47475057, affecting gene MSH2 (mutS homolog 2): benign or pathogenic? Disease name(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | ATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGC... | ATGGGGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGC... | pathogenic | 34,554 |
The chromosome 2, position 47475061 genetic variant in gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, indicate disease(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | GGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGC... | GGTCTTACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGC... | pathogenic | 34,560 |
The genetic variant at chromosome 2, position 47475067, affecting gene MSH2 (mutS homolog 2): benign or pathogenic? Disease name(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | ACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTT... | ACCATGTTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTT... | pathogenic | 34,564 |
Assess the variant on chromosome 2, position 47475073, impacting MSH2 (mutS homolog 2): is it benign or pathogenic? If pathogenic, specify the associated condition(s). | pathogenic; ['Lynch_syndrome'] | TTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGT... | TTGCCCAGGCTTTAGTGCAGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGT... | pathogenic | 34,571 |
Clinical classification of chromosome 2, position 47475091, gene MSH2 (mutS homolog 2): benign or pathogenic? Disease(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colon_cancer', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1'] | AGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCA... | AGTGATGCGATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCA... | pathogenic | 34,574 |
Benign or pathogenic: chromosome 2, position 47475100, gene MSH2 (mutS homolog 2) variant? Disease(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1'] | ATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCA... | ATCATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCA... | pathogenic | 34,579 |
A genetic variant on chromosome 2, position 47475102, affects the gene MSH2 (mutS homolog 2). Is this variant benign or pathogenic? If pathogenic, what disease(s) does it cause? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | CATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACT... | CATGACTCACTGCAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACT... | pathogenic | 34,581 |
Variant in gene MSH2 (mutS homolog 2), located at chromosome 2 position 47475114: benign or pathogenic? What disease(s) does it cause if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | CAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTC... | CAGCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTC... | pathogenic | 34,587 |
The mutation in gene MSH2 (mutS homolog 2) at chromosome 2, position 47475116—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_1'] | GCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTT... | GCCTCAACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTT... | pathogenic | 34,589 |
Is the chromosome 2, position 47475121 variant in MSH2 (mutS homolog 2) clinically benign or pathogenic? If pathogenic, what condition(s) is associated? | pathogenic; ['Lynch_syndrome'] | AACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGG... | AACCTCCTAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGG... | pathogenic | 34,590 |
Gene MSH2 (mutS homolog 2) variant at chromosome 2, position 47475128—is it benign or pathogenic? If pathogenic, what are the associated condition(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | TAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTAT... | TAGGTTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTAT... | pathogenic | 34,598 |
The genetic variant at chromosome 2, position 47475132, affecting gene MSH2 (mutS homolog 2): benign or pathogenic? Disease name(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | TTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCT... | TTCAAGGGATTCTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCT... | pathogenic | 34,604 |
Evaluate this variant at chromosome 2, position 47475143, gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, what are the disease connection(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | CTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGG... | CTCCCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGG... | pathogenic | 34,608 |
Determine if the mutation at chromosome 2, position 47475146 in gene MSH2 (mutS homolog 2) is benign or pathogenic. If pathogenic, what disease(s) is associated? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | CCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAG... | CCCACTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAG... | pathogenic | 34,610 |
Is the genetic mutation found on chromosome 2 at position 47475150, within the gene MSH2 (mutS homolog 2), considered benign or pathogenic? If pathogenic, specify the associated disease(s). | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms'] | CTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTG... | CTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTG... | pathogenic | 34,614 |
Mutation at chromosome 2, position 47475150, within MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, indicate the disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome'] | CTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTG... | CTTAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTG... | pathogenic | 34,615 |
For chromosome 2, position 47475152, gene MSH2 (mutS homolog 2): benign or pathogenic mutation? If pathogenic, what are the associated disease(s)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | TAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAA... | TAGCCTCCCAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAA... | pathogenic | 34,618 |
Mutation found at chromosome 2 position 47475160, gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, indicate the relevant disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | CAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAA... | CAAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAA... | pathogenic | 34,620 |
Gene mutation in MSH2 (mutS homolog 2) at chromosome 2, position 47475161—is it benign or pathogenic? If pathogenic, specify the disease(s). | pathogenic; ['Lynch_syndrome'] | AAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAA... | AAGTAGCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAA... | pathogenic | 34,621 |
Is the genetic change at chromosome 2, position 47475166, within gene MSH2 (mutS homolog 2) benign or pathogenic? Name the disease(s) if pathogenic. | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | GCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGT... | GCTTGGGACTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGT... | pathogenic | 34,624 |
Chromosome 2, position 47475174, gene MSH2 (mutS homolog 2): benign or pathogenic variant? If pathogenic, what are the linked illness(es)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1'] | CTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGC... | CTACTACATGTAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGC... | pathogenic | 34,628 |
Evaluate if the mutation on chromosome 2 at position 47475184 in MSH2 (mutS homolog 2) is benign or pathogenic. Disease name(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | TAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGT... | TAGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGT... | pathogenic | 34,633 |
Gene MSH2 (mutS homolog 2) variant at chromosome position 47475185 on chromosome 2: benign or pathogenic? If pathogenic, what disease(s) is it associated with? | pathogenic; ['Lynch_syndrome'] | AGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTA... | AGTAGTGCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTA... | pathogenic | 34,635 |
Is chromosome 2, position 47475191, gene MSH2 (mutS homolog 2) variant benign or pathogenic? If pathogenic, what condition(s) is it related to? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | GCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCAC... | GCCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCAC... | pathogenic | 34,638 |
Evaluate this variant at chromosome 2, position 47475192, gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, what are the disease connection(s)? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | CCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACA... | CCACCACACCTGGTTAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACA... | pathogenic | 34,639 |
The chromosome 2, position 47475206 genetic variant in gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, indicate disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome_1'] | TAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGC... | TAATTTTTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGC... | pathogenic | 34,644 |
Assess the clinical significance (benign or pathogenic) of the variant at chromosome 2, position 47475212, gene MSH2 (mutS homolog 2). What disease(s) is it linked to if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1'] | TTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTG... | TTTTTTAATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTG... | pathogenic | 34,646 |
A mutation at chromosome position 47475218 on chromosome 2 in gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, which disease(s) is it linked to? | pathogenic; ['Lynch_syndrome_1'] | AATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGC... | AATTATCTTTTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGC... | pathogenic | 34,649 |
Variant chromosome 2, position 47475227, gene MSH2 (mutS homolog 2): benign or pathogenic? Disease(s)? | pathogenic; ['Hereditary_nonpolyposis_colorectal_neoplasms', 'Lynch_syndrome', 'Lynch_syndrome_1'] | TTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGG... | TTGTGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGG... | pathogenic | 34,653 |
Is the genetic mutation found on chromosome 2 at position 47475230, within the gene MSH2 (mutS homolog 2), considered benign or pathogenic? If pathogenic, specify the associated disease(s). | pathogenic; ['Lynch_syndrome'] | TGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGG... | TGGAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGG... | pathogenic | 34,654 |
Regarding the variant at chromosome 2 and position 47475232, affecting gene MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, what are the associated illness(es)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | GAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGAT... | GAGATGAAGTCTCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGAT... | pathogenic | 34,658 |
Considering the variant on chromosome 2, location 47475243, involving gene MSH2 (mutS homolog 2), 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', 'Lynch_syndrome_1'] | TCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTC... | TCACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTC... | pathogenic | 34,664 |
Evaluate if the mutation on chromosome 2 at position 47475245 in MSH2 (mutS homolog 2) is benign or pathogenic. Disease name(s) if pathogenic? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome_1'] | ACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAG... | ACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAG... | pathogenic | 34,666 |
Gene mutation in MSH2 (mutS homolog 2) at chromosome 2, position 47475245—is it benign or pathogenic? If pathogenic, specify the disease(s). | pathogenic; ['Lynch_syndrome'] | ACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAG... | ACTCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAG... | pathogenic | 34,667 |
A genetic alteration at chromosome 2, position 47475247, in gene MSH2 (mutS homolog 2)—benign or pathogenic? If pathogenic, which disease(s) is involved? | pathogenic; ['Lynch_syndrome'] | TCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGA... | TCTGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGA... | pathogenic | 34,669 |
Mutation at chromosome 2, position 47475249, within MSH2 (mutS homolog 2): benign or pathogenic? If pathogenic, indicate the disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Hereditary_nonpolyposis_colorectal_neoplasms'] | TGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGAGT... | TGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGAGT... | pathogenic | 34,670 |
Chromosome 2, position 47475249, gene MSH2 (mutS homolog 2): benign or pathogenic variant? If pathogenic, what are the linked illness(es)? | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome'] | TGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGAGT... | TGTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGAGT... | pathogenic | 34,672 |
Is the genetic mutation found on chromosome 2 at position 47475250, within the gene MSH2 (mutS homolog 2), considered benign or pathogenic? If pathogenic, specify the associated disease(s). | pathogenic; ['Hereditary_cancer-predisposing_syndrome', 'Lynch_syndrome'] | GTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGAGTT... | GTTGCCCAGGCCAGACTCAAGCAGTCTTCCTGCCTTGGCCTCCGAAAGTGTTGGGATTACAGGCGTGAGCCACCCTGCCCAGCCTAGTTTTCTTTTTTTTACTATAAACTTATTCTTGTCAGTATGCTAGCAATTTTACAAGTTTTAAAGTAGTTATAGCAAGTACTTCACTCATGTTTAATTCTTAAAGGCTTCTATTGCTATATAATAGGGTAGTCTGAATTCTTCAAAAGTGTACTGAGGCCAGGTGCAGTAGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGAGTT... | pathogenic | 34,673 |
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