ID stringlengths 13 17 | question stringlengths 88 1.13k | answer stringlengths 6 156 | reference_sequence stringlengths 4.1k 4.1k | variant_sequence stringlengths 4.1k 4.1k |
|---|---|---|---|---|
Task1_train_42900 | A variant affecting Chromosome 14 has been observed. Determine if it's benign or associated with disease. | Benign | TTAACATGAATATCCAAAGTTACCTCGGCAATAAAACATTTATGCTTTTGGGTTTGCTCCAGGTTTGATCAAGTACTGAAAGGCAGGCCTCTCGCTCTCTGTGGATCATATAAATGATGTAAAGATGGAATTTTGTGAGTATCTTAACAGTGACGCTAATAATACAATAAATTATCCTAATTTTAAAGTCATTATATTGCTAAATTTAAAATATTGATAGTGGCTTACCCAGCCAAATATTCTGAACTTTAACAAGGATATTTGAGGACACAGAAATAAGCCTGCTGGACCAATAGTTTCTAGAAAATTGTTAGCAAAAT... | TTAACATGAATATCCAAAGTTACCTCGGCAATAAAACATTTATGCTTTTGGGTTTGCTCCAGGTTTGATCAAGTACTGAAAGGCAGGCCTCTCGCTCTCTGTGGATCATATAAATGATGTAAAGATGGAATTTTGTGAGTATCTTAACAGTGACGCTAATAATACAATAAATTATCCTAATTTTAAAGTCATTATATTGCTAAATTTAAAATATTGATAGTGGCTTACCCAGCCAAATATTCTGAACTTTAACAAGGATATTTGAGGACACAGAAATAAGCCTGCTGGACCAATAGTTTCTAGAAAATTGTTAGCAAAAT... |
Task1_train_42901 | A change on Chromosome 14 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AAGATGGAATTTTGTGAGTATCTTAACAGTGACGCTAATAATACAATAAATTATCCTAATTTTAAAGTCATTATATTGCTAAATTTAAAATATTGATAGTGGCTTACCCAGCCAAATATTCTGAACTTTAACAAGGATATTTGAGGACACAGAAATAAGCCTGCTGGACCAATAGTTTCTAGAAAATTGTTAGCAAAATATCTAAGTTATTTATCTTGTCTCAACTCCTGATTTAGAAAATATCAGAAAGATCTTTCTGTTCTCTGCACATCCTGAGGTGACTCTTTTATTCATTATTTAATTTATGGAAAAGCAAGATA... | AAGATGGAATTTTGTGAGTATCTTAACAGTGACGCTAATAATACAATAAATTATCCTAATTTTAAAGTCATTATATTGCTAAATTTAAAATATTGATAGTGGCTTACCCAGCCAAATATTCTGAACTTTAACAAGGATATTTGAGGACACAGAAATAAGCCTGCTGGACCAATAGTTTCTAGAAAATTGTTAGCAAAATATCTAAGTTATTTATCTTGTCTCAACTCCTGATTTAGAAAATATCAGAAAGATCTTTCTGTTCTCTGCACATCCTGAGGTGACTCTTTTATTCATTATTTAATTTATGGAAAAGCAAGATA... |
Task1_train_42902 | This alteration occurs on Chromosome 14. Is it associated with a disease or is it a benign variant? | Benign | CTTAACAGTGACGCTAATAATACAATAAATTATCCTAATTTTAAAGTCATTATATTGCTAAATTTAAAATATTGATAGTGGCTTACCCAGCCAAATATTCTGAACTTTAACAAGGATATTTGAGGACACAGAAATAAGCCTGCTGGACCAATAGTTTCTAGAAAATTGTTAGCAAAATATCTAAGTTATTTATCTTGTCTCAACTCCTGATTTAGAAAATATCAGAAAGATCTTTCTGTTCTCTGCACATCCTGAGGTGACTCTTTTATTCATTATTTAATTTATGGAAAAGCAAGATAATGAAGGGACAAATTATAAAG... | CTTAACAGTGACGCTAATAATACAATAAATTATCCTAATTTTAAAGTCATTATATTGCTAAATTTAAAATATTGATAGTGGCTTACCCAGCCAAATATTCTGAACTTTAACAAGGATATTTGAGGACACAGAAATAAGCCTGCTGGACCAATAGTTTCTAGAAAATTGTTAGCAAAATATCTAAGTTATTTATCTTGTCTCAACTCCTGATTTAGAAAATATCAGAAAGATCTTTCTGTTCTCTGCACATCCTGAGGTGACTCTTTTATTCATTATTTAATTTATGGAAAAGCAAGATAATGAAGGGACAAATTATAAAG... |
Task1_train_42903 | Located on Chromosome 14, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ATTATATTGCTAAATTTAAAATATTGATAGTGGCTTACCCAGCCAAATATTCTGAACTTTAACAAGGATATTTGAGGACACAGAAATAAGCCTGCTGGACCAATAGTTTCTAGAAAATTGTTAGCAAAATATCTAAGTTATTTATCTTGTCTCAACTCCTGATTTAGAAAATATCAGAAAGATCTTTCTGTTCTCTGCACATCCTGAGGTGACTCTTTTATTCATTATTTAATTTATGGAAAAGCAAGATAATGAAGGGACAAATTATAAAGTTTAGGACTTAATTTCTAGCAAAAATAAAGGCACATGGCTTTATTACT... | ATTATATTGCTAAATTTAAAATATTGATAGTGGCTTACCCAGCCAAATATTCTGAACTTTAACAAGGATATTTGAGGACACAGAAATAAGCCTGCTGGACCAATAGTTTCTAGAAAATTGTTAGCAAAATATCTAAGTTATTTATCTTGTCTCAACTCCTGATTTAGAAAATATCAGAAAGATCTTTCTGTTCTCTGCACATCCTGAGGTGACTCTTTTATTCATTATTTAATTTATGGAAAAGCAAGATAATGAAGGGACAAATTATAAAGTTTAGGACTTAATTTCTAGCAAAAATAAAGGCACATGGCTTTATTACT... |
Task1_train_42904 | A mutation has occurred on Chromosome 14. What is the medical relevance of this mutation? | Benign | TGTTTTCCTCTCTCTGTCCCTTTCATTACTCACTTTGCACCTTCAGGAGAAGTGACATTTAAAAAAAAAGAAAAGATAAAAATAAAATCAATGTTTTTGTGGACTAAGAACTCACATAGATTTAGTGGTGAATATATTAGGAACTGTTTCTTACAAATATGTTGGAAATTATCTGTGAAATTTATTTACCATGCTTTCCCTGTGGCTAATTGTTTTTCTGCAAGGTTTTTGTTTGTTTGTTGTTTTTAATGTCAATGAAAGTAGTCTAAGCTCAAAGAAGCAGCTCGGTCTTGTGCATTTTGATTTTGGGTCAAAGTCTG... | TGTTTTCCTCTCTCTGTCCCTTTCATTACTCACTTTGCACCTTCAGGAGAAGTGACATTTAAAAAAAAAGAAAAGATAAAAATAAAATCAATGTTTTTGTGGACTAAGAACTCACATAGATTTAGTGGTGAATATATTAGGAACTGTTTCTTACAAATATGTTGGAAATTATCTGTGAAATTTATTTACCATGCTTTCCCTGTGGCTAATTGTTTTTCTGCAAGGTTTTTGTTTGTTTGTTGTTTTTAATGTCAATGAAAGTAGTCTAAGCTCAAAGAAGCAGCTCGGTCTTGTGCATTTTGATTTTGGGTCAAAGTCTG... |
Task1_train_42905 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTCTGTCCCTTTCATTACTCACTTTGCACCTTCAGGAGAAGTGACATTTAAAAAAAAAGAAAAGATAAAAATAAAATCAATGTTTTTGTGGACTAAGAACTCACATAGATTTAGTGGTGAATATATTAGGAACTGTTTCTTACAAATATGTTGGAAATTATCTGTGAAATTTATTTACCATGCTTTCCCTGTGGCTAATTGTTTTTCTGCAAGGTTTTTGTTTGTTTGTTGTTTTTAATGTCAATGAAAGTAGTCTAAGCTCAAAGAAGCAGCTCGGTCTTGTGCATTTTGATTTTGGGTCAAAGTCTGTGAATCTGAGT... | CTCTGTCCCTTTCATTACTCACTTTGCACCTTCAGGAGAAGTGACATTTAAAAAAAAAGAAAAGATAAAAATAAAATCAATGTTTTTGTGGACTAAGAACTCACATAGATTTAGTGGTGAATATATTAGGAACTGTTTCTTACAAATATGTTGGAAATTATCTGTGAAATTTATTTACCATGCTTTCCCTGTGGCTAATTGTTTTTCTGCAAGGTTTTTGTTTGTTTGTTGTTTTTAATGTCAATGAAAGTAGTCTAAGCTCAAAGAAGCAGCTCGGTCTTGTGCATTTTGATTTTGGGTCAAAGTCTGTGAATCTGAGT... |
Task1_train_42906 | This alteration on Chromosome 14 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGATCAAATACTATATATGTGCTACTTTAATTGAAAAAAATATAAGGCAAATTATCCTCTTAACAATCAAAAAAGTTAAAGGTATCTTGTTAAAATTTTTCTGAAGAGTCCCATATGTTAAAGCTATCATTTACTCTTTTCTTGGAGTTGTATTTGATTCTTGAAAATATATCTTCTTTGGTGATGGTGTTCTAAAGGAAACAAACCAACTCTCGGAAAATGGGTAAATAATTATGTTTGAAATAACACCTTTGATTCTCTTGTATCTTGTTTTTTTGAATATTTGGAGGCTATTATTTTACATGGACTAAAGAAAGATC... | TGATCAAATACTATATATGTGCTACTTTAATTGAAAAAAATATAAGGCAAATTATCCTCTTAACAATCAAAAAAGTTAAAGGTATCTTGTTAAAATTTTTCTGAAGAGTCCCATATGTTAAAGCTATCATTTACTCTTTTCTTGGAGTTGTATTTGATTCTTGAAAATATATCTTCTTTGGTGATGGTGTTCTAAAGGAAACAAACCAACTCTCGGAAAATGGGTAAATAATTATGTTTGAAATAACACCTTTGATTCTCTTGTATCTTGTTTTTTTGAATATTTGGAGGCTATTATTTTACATGGACTAAAGAAAGATC... |
Task1_train_42907 | This alteration occurs on Chromosome 14. Is it associated with a disease or is it a benign variant? | Benign | GTATAGAGAAACAACAGTGAGCCCAGGGGACCGGTACTCAGCACACCAAGGACCTGCACCGGCACCGGCCTCTGAGTTCCCTCAGTTTTTATTGATTATTATATTCATTATTTCAGCAAAAAGGAATGTAGTAGGAGAGCACGGTGATAATAAGGAGAAGGTCAGCAAAAAACATGTGAGCAGAAGAATCTATGTCATAATTAAGTTCAAGGGAAGGTACTATGCCTGGATGTGCACGTAGGCCAGATATATAGTTCTCTCCACCCAAGTATCTCAGTGAAGTAAAGAATAACAAGGCAGCATTACTGCCAACATGTCTC... | GTATAGAGAAACAACAGTGAGCCCAGGGGACCGGTACTCAGCACACCAAGGACCTGCACCGGCACCGGCCTCTGAGTTCCCTCAGTTTTTATTGATTATTATATTCATTATTTCAGCAAAAAGGAATGTAGTAGGAGAGCACGGTGATAATAAGGAGAAGGTCAGCAAAAAACATGTGAGCAGAAGAATCTATGTCATAATTAAGTTCAAGGGAAGGTACTATGCCTGGATGTGCACGTAGGCCAGATATATAGTTCTCTCCACCCAAGTATCTCAGTGAAGTAAAGAATAACAAGGCAGCATTACTGCCAACATGTCTC... |
Task1_train_42908 | A sequence alteration has been identified on Chromosome 14. Is it disease-inducing or harmless? | Benign | GGTGTGAGCCACCACGCCTGGCCGTATTTTTCTTTTTGTGACAGGGTCTCACTCTGATGGAGTGCAGAGGCACGATCTCAGCTCACAGCAACCTCCACCTCCTGGGTTCAAGTGATTCTTGTGCCTTGGCCTCCTGAGTAACTGGGATTACAGGCACATACAACCATGCCCATCTAATTTTTGTATTTTTTGGTAGAGGCAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAATGATCTCCCCACTTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACCACGTCTGGTCCATGTATAT... | GGTGTGAGCCACCACGCCTGGCCGTATTTTTCTTTTTGTGACAGGGTCTCACTCTGATGGAGTGCAGAGGCACGATCTCAGCTCACAGCAACCTCCACCTCCTGGGTTCAAGTGATTCTTGTGCCTTGGCCTCCTGAGTAACTGGGATTACAGGCACATACAACCATGCCCATCTAATTTTTGTATTTTTTGGTAGAGGCAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAATGATCTCCCCACTTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACCACGTCTGGTCCATGTATAT... |
Task1_train_42909 | Consider this mutation on Chromosome 14. Is this a benign change or a disease-causing variant? | Benign | CTCTTCTGAGAATGCCAATTACCATATTGACTAAAGTTGAAAGTCGTGTCAGAAGTTGGGAAAACCAGAAGGTTTGTTCCGCTTTCAATGGCTTGGCTCCTCACCTCTCATCTGGGTAGTTCTTTTTTTTTTTTTTTAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTCTCGGCTCACTGCAAGCTCCGCCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCCCGCCGCCACACCTGGCTAACTTTTTGTATTTTTTAGTAGAGACAGGGTTTCACTATG... | CTCTTCTGAGAATGCCAATTACCATATTGACTAAAGTTGAAAGTCGTGTCAGAAGTTGGGAAAACCAGAAGGTTTGTTCCGCTTTCAATGGCTTGGCTCCTCACCTCTCATCTGGGTAGTTCTTTTTTTTTTTTTTTAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTCTCGGCTCACTGCAAGCTCCGCCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCCCGCCGCCACACCTGGCTAACTTTTTGTATTTTTTAGTAGAGACAGGGTTTCACTATG... |
Task1_train_42910 | A genomic variant on Chromosome 14 is under review. What is the biological outcome — benign or pathogenic? | Benign | TGGAGCATCCCCTGGCTTCATGCAAAGTAACTTCAAATCTGCTTTGGCCAAGATGAGAAAGTGACCATCAGGAGCCCAATCCAGACTTGTCAGCACCCCTAAGTCCTCCTGTAGAATTCGGTTCAGGTGAAGACTAGCTCAAAAAAGTACATGGACAGAGAAAGATCCTATTTTAGTTAACCTTTCTCAGGCTCCTCAATCCCACATGAATTCCTCAGGAATGAAGTACAAAGCAAAATGTATCACCTTCCCTGAAAATCCTGTTCCACTTTCTGGTTTTTGTTTTTTAACATTAGTATTCATCGGTGCCATCCCATTAC... | TGGAGCATCCCCTGGCTTCATGCAAAGTAACTTCAAATCTGCTTTGGCCAAGATGAGAAAGTGACCATCAGGAGCCCAATCCAGACTTGTCAGCACCCCTAAGTCCTCCTGTAGAATTCGGTTCAGGTGAAGACTAGCTCAAAAAAGTACATGGACAGAGAAAGATCCTATTTTAGTTAACCTTTCTCAGGCTCCTCAATCCCACATGAATTCCTCAGGAATGAAGTACAAAGCAAAATGTATCACCTTCCCTGAAAATCCTGTTCCACTTTCTGGTTTTTGTTTTTTAACATTAGTATTCATCGGTGCCATCCCATTAC... |
Task1_train_42911 | A variant on Chromosome 14 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TGGATTTTCAGAGGGTAAATTCTGCCCCTCCTTGATTGTCATACCTGCCAAGTTCTCAGGTCCAACAGGTAAACTGTCCCATTGGCAGTGCCCACAGCTGCTCTTTGCCCATTGGTGGAGAAGGCCACAGCAGTAGGGGATGAGGAAACTGCCAGAGACAGGCTGGAGCTAGAGAAAGAGTAGGAAGAAAGGGAGGAAATAAACGAGAGAATGCAAACAGGAGTTGATTTATGTGCTTCTGTGCCTGGATCCCTCTCCAGTGTTTCTGGTCATCCTTATTCCTCAGTTTCAGAAAGAGCTGCAGCTTGCTCTCTGGTGGG... | TGGATTTTCAGAGGGTAAATTCTGCCCCTCCTTGATTGTCATACCTGCCAAGTTCTCAGGTCCAACAGGTAAACTGTCCCATTGGCAGTGCCCACAGCTGCTCTTTGCCCATTGGTGGAGAAGGCCACAGCAGTAGGGGATGAGGAAACTGCCAGAGACAGGCTGGAGCTAGAGAAAGAGTAGGAAGAAAGGGAGGAAATAAACGAGAGAATGCAAACAGGAGTTGATTTATGTGCTTCTGTGCCTGGATCCCTCTCCAGTGTTTCTGGTCATCCTTATTCCTCAGTTTCAGAAAGAGCTGCAGCTTGCTCTCTGGTGGG... |
Task1_train_42912 | This mutation is located on Chromosome 14. Is it associated with a disease or is it a benign polymorphism? | Benign | AACAGGTAAACTGTCCCATTGGCAGTGCCCACAGCTGCTCTTTGCCCATTGGTGGAGAAGGCCACAGCAGTAGGGGATGAGGAAACTGCCAGAGACAGGCTGGAGCTAGAGAAAGAGTAGGAAGAAAGGGAGGAAATAAACGAGAGAATGCAAACAGGAGTTGATTTATGTGCTTCTGTGCCTGGATCCCTCTCCAGTGTTTCTGGTCATCCTTATTCCTCAGTTTCAGAAAGAGCTGCAGCTTGCTCTCTGGTGGGCTTACTAGGGTCTGGGGTCAAGGTCTTACCTTTGCTGATTTTTCATGGTCCGGGGTTTATTAA... | AACAGGTAAACTGTCCCATTGGCAGTGCCCACAGCTGCTCTTTGCCCATTGGTGGAGAAGGCCACAGCAGTAGGGGATGAGGAAACTGCCAGAGACAGGCTGGAGCTAGAGAAAGAGTAGGAAGAAAGGGAGGAAATAAACGAGAGAATGCAAACAGGAGTTGATTTATGTGCTTCTGTGCCTGGATCCCTCTCCAGTGTTTCTGGTCATCCTTATTCCTCAGTTTCAGAAAGAGCTGCAGCTTGCTCTCTGGTGGGCTTACTAGGGTCTGGGGTCAAGGTCTTACCTTTGCTGATTTTTCATGGTCCGGGGTTTATTAA... |
Task1_train_42913 | This mutation on Chromosome 14 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GATGAGAACTGACCTGCTCATACAGCGTGAAGAGCCTCAGGTGATCGGTGACCAAGCGCAGGTAGAGCGGCCGGCCTGATTCCCGCTTCACCAGCAGCAGTCGCATCTGGCAAGACTCAGGACTCAGGGTGGGGTCCAGGAGGGCTGCCCGCAGCCAGCCCTCTGCCCCAGCACCAGCCCCTCTGCCAGGCAGCTCCTCCTCTGAGAGTCCCCAGCAGACGCCAGGTCCATGGCATCATCCCAGGACACAAACCATCCCTCTCCTACGCTGCTCTGCCCAGCCAGCCCTGCCAGAAAACCCCTGTGGCTCGGCCTACCCC... | GATGAGAACTGACCTGCTCATACAGCGTGAAGAGCCTCAGGTGATCGGTGACCAAGCGCAGGTAGAGCGGCCGGCCTGATTCCCGCTTCACCAGCAGCAGTCGCATCTGGCAAGACTCAGGACTCAGGGTGGGGTCCAGGAGGGCTGCCCGCAGCCAGCCCTCTGCCCCAGCACCAGCCCCTCTGCCAGGCAGCTCCTCCTCTGAGAGTCCCCAGCAGACGCCAGGTCCATGGCATCATCCCAGGACACAAACCATCCCTCTCCTACGCTGCTCTGCCCAGCCAGCCCTGCCAGAAAACCCCTGTGGCTCGGCCTACCCC... |
Task1_train_42914 | Mutation context: Chromosome 14. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TGGATGGAAGATTCAAAGCCGGGTGACGTGAATCCAGATTCTATGCTCTTAAATGCTACGTACAATACCTTATTTGTCCAAAAGTAAAAAGATTTTGTTTGGTTTGTTTTTAAAACTTCCTGTGAAAGGTATATATTTCATAATGTTTTTAACTCACTTATCCAACTTTACTGACATGTCACCCGGCAGTAAAGTACAATACCAGCTGGGTGTGGTGGCTCACATCTGTAATTCCAGCACTTTGGGAGGTCAAGGCAGGTGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTAC... | TGGATGGAAGATTCAAAGCCGGGTGACGTGAATCCAGATTCTATGCTCTTAAATGCTACGTACAATACCTTATTTGTCCAAAAGTAAAAAGATTTTGTTTGGTTTGTTTTTAAAACTTCCTGTGAAAGGTATATATTTCATAATGTTTTTAACTCACTTATCCAACTTTACTGACATGTCACCCGGCAGTAAAGTACAATACCAGCTGGGTGTGGTGGCTCACATCTGTAATTCCAGCACTTTGGGAGGTCAAGGCAGGTGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTAC... |
Task1_train_42915 | This genomic variant is located on Chromosome 14. Can you determine its pathogenicity and name any linked disease? | Benign | GAAAGGAAAGAAAAAAAGAAAAGGAAAATAAAAGAAAAAAGAAAAGGGGATTAGGAAGTGAGAAATAAGAGCTAGGTTGTATCCCTACCTTCCCCTTCCAACTGGGGAGGGGACCTGGTTCAAGTACTCCACCACCAACCTCCCCTCCACACCATTATTAACCTTCCCCTAACTCTTGAATTTTTACCTTCTTTTCCTGAAGGACATGGTCAGTAGGCTCTGGATGAGATTCAGAGTCTCCAGAGGTGAGCTTCACGGCCAGATCCTCCACCTCCTCCTCCTCTCCCAAGCTCAGACTATAAGAAGGCATTTGGGTCTCT... | GAAAGGAAAGAAAAAAAGAAAAGGAAAATAAAAGAAAAAAGAAAAGGGGATTAGGAAGTGAGAAATAAGAGCTAGGTTGTATCCCTACCTTCCCCTTCCAACTGGGGAGGGGACCTGGTTCAAGTACTCCACCACCAACCTCCCCTCCACACCATTATTAACCTTCCCCTAACTCTTGAATTTTTACCTTCTTTTCCTGAAGGACATGGTCAGTAGGCTCTGGATGAGATTCAGAGTCTCCAGAGGTGAGCTTCACGGCCAGATCCTCCACCTCCTCCTCCTCTCCCAAGCTCAGACTATAAGAAGGCATTTGGGTCTCT... |
Task1_train_42916 | This variant lies on Chromosome 14. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AAATGATGAGTTCATGTCCTTTGTAGGGACATGGATGAGATTGGAAATCATCATTCTCAGTAAACTATCGCAAGGACAAAAAAACCAAACACCGCATGTTCTCACTCATAGGTGGGAATTGAACAATGAGAACACGTGGACACAGGAAGGGGAACATCACACTCTGGAGAATGTTGTGGGGTGGGGGGAGGGGGGAAGGATAGCATTAGGAGATATACCTAATGCTAAATGACGAGTTAATGGGTGCAGCACACCAGCATGGCACATGTATACATATGTAACTAACCTGCACATTGGGCACATGTACCCTAAAACTTAAA... | AAATGATGAGTTCATGTCCTTTGTAGGGACATGGATGAGATTGGAAATCATCATTCTCAGTAAACTATCGCAAGGACAAAAAAACCAAACACCGCATGTTCTCACTCATAGGTGGGAATTGAACAATGAGAACACGTGGACACAGGAAGGGGAACATCACACTCTGGAGAATGTTGTGGGGTGGGGGGAGGGGGGAAGGATAGCATTAGGAGATATACCTAATGCTAAATGACGAGTTAATGGGTGCAGCACACCAGCATGGCACATGTATACATATGTAACTAACCTGCACATTGGGCACATGTACCCTAAAACTTAAA... |
Task1_train_42917 | A genomic variant on Chromosome 14 is under review. What is the biological outcome — benign or pathogenic? | Benign | CATGGCATGCCCCACTTCTTTCTGTTTCAAATGCATTCCCCCTTCTCTAATGGGTGAGACTCTAGGCAGCCTTTAAGATCCAGTTCAAAATACACCCATCGGATGACACCTTTCCTAACAGAAGCCTTCCTGAGCAGAGTTCACTGCTCTATCCTCTGGGCTCTCGCAAGACTCGTCCATACATGTAAGTCCACTCAAAATTTGTATTTGTTTATGTCTATCTGCTGGTCAGGAGCTCTCTGACCTCTGTATCTTGGTGCCTCCTACAGTGCCTGCCACACAGTAGGTAATTAATAACTGTGTGAGGGAGAAAGAAGAGA... | CATGGCATGCCCCACTTCTTTCTGTTTCAAATGCATTCCCCCTTCTCTAATGGGTGAGACTCTAGGCAGCCTTTAAGATCCAGTTCAAAATACACCCATCGGATGACACCTTTCCTAACAGAAGCCTTCCTGAGCAGAGTTCACTGCTCTATCCTCTGGGCTCTCGCAAGACTCGTCCATACATGTAAGTCCACTCAAAATTTGTATTTGTTTATGTCTATCTGCTGGTCAGGAGCTCTCTGACCTCTGTATCTTGGTGCCTCCTACAGTGCCTGCCACACAGTAGGTAATTAATAACTGTGTGAGGGAGAAAGAAGAGA... |
Task1_train_42918 | Consider a variant on Chromosome 14. Determine its clinical classification and disease relevance. | Benign | TCTGTTTTTCCACTGTGGGCCTCTCCCTCCTTGGCCTCTGCCCCCATCATCTTTCCCACACAACACTCCTGCCACATGGCCCTGGGGGGCCCGTCAGGCCTCTCAGGCCCCTGTGCCGTGCATGTCCATGTGGGAGCTTCTGCCTCAGAAGGAAACCAAGAGGTTCTCAGGGGCAGCCTGTGGTGTCTCGCTGGGAAACGCTAGACCAGGCCTACAAAGTTACCCGGGAGAGAATATTGTTAAGAAGGTTTAGGCATCCCAGGGGTGGGAGAGGAGAAAGGAGCAAGTTCCAGGAAAAAAAGGGCTGAACGATTTACAGT... | TCTGTTTTTCCACTGTGGGCCTCTCCCTCCTTGGCCTCTGCCCCCATCATCTTTCCCACACAACACTCCTGCCACATGGCCCTGGGGGGCCCGTCAGGCCTCTCAGGCCCCTGTGCCGTGCATGTCCATGTGGGAGCTTCTGCCTCAGAAGGAAACCAAGAGGTTCTCAGGGGCAGCCTGTGGTGTCTCGCTGGGAAACGCTAGACCAGGCCTACAAAGTTACCCGGGAGAGAATATTGTTAAGAAGGTTTAGGCATCCCAGGGGTGGGAGAGGAGAAAGGAGCAAGTTCCAGGAAAAAAAGGGCTGAACGATTTACAGT... |
Task1_train_42919 | A mutation has occurred on Chromosome 14. What is the medical relevance of this mutation? | Benign | AAGCTGTTTAAGAACTCCATGCTGCTTTGACCAACTGAGGCATGCGTGCCTTTCCCAAAGGGCAGGTGTTGTTCATATGACTTTCCACTGTCTTTTAAGCAGTAGGTAGTGGCCTGGTGCTTCCCAAGTAGTAAACATCAATGACAGATTTCAAATATATATTGTCTGAGAAAATCTGCATTCCTCAAAACAAGCTAAGCCATCTCAGCTCCCATATCATCAATCAACCTATAGTTCAGAGCCAACCCTGAAAGGGCTCACAGCCACTTGTATTCACCTCTTACTCATTACTATACCCTAGGATTTTAAGTGACAGATTC... | AAGCTGTTTAAGAACTCCATGCTGCTTTGACCAACTGAGGCATGCGTGCCTTTCCCAAAGGGCAGGTGTTGTTCATATGACTTTCCACTGTCTTTTAAGCAGTAGGTAGTGGCCTGGTGCTTCCCAAGTAGTAAACATCAATGACAGATTTCAAATATATATTGTCTGAGAAAATCTGCATTCCTCAAAACAAGCTAAGCCATCTCAGCTCCCATATCATCAATCAACCTATAGTTCAGAGCCAACCCTGAAAGGGCTCACAGCCACTTGTATTCACCTCTTACTCATTACTATACCCTAGGATTTTAAGTGACAGATTC... |
Task1_train_42920 | A variant was discovered on Chromosome 14. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TCAGAGCCAACCCTGAAAGGGCTCACAGCCACTTGTATTCACCTCTTACTCATTACTATACCCTAGGATTTTAAGTGACAGATTCGCAACCATTAAGTAGGAATATTTCCTAGGGAAATAAAAGCAGTGATATGAGTATGCTTAAATTCAAAAGCCTAGTGAGAATTTTATGATTATGAAAAATTTAAATCCCCTCTCCATCTAGTGCTATCATAAATGAAAATAGACTTTTGGAGTGGTTTTCCTTCTAGGAGTCCCAGAAGCACTTCAGTTCCCAGTCACTCCTCTAATGGGCAGTAGCTATGTGACTTTGGACAAGT... | TCAGAGCCAACCCTGAAAGGGCTCACAGCCACTTGTATTCACCTCTTACTCATTACTATACCCTAGGATTTTAAGTGACAGATTCGCAACCATTAAGTAGGAATATTTCCTAGGGAAATAAAAGCAGTGATATGAGTATGCTTAAATTCAAAAGCCTAGTGAGAATTTTATGATTATGAAAAATTTAAATCCCCTCTCCATCTAGTGCTATCATAAATGAAAATAGACTTTTGGAGTGGTTTTCCTTCTAGGAGTCCCAGAAGCACTTCAGTTCCCAGTCACTCCTCTAATGGGCAGTAGCTATGTGACTTTGGACAAGT... |
Task1_train_42921 | This variant is present on Chromosome 14. Is the change likely to result in a pathogenic outcome? | Benign | TCTTATTAGTCCCTCCAGGTCACCTCTACTTCATCTGTCCGATACCTGTGGAAAAACAGAAGAAACATGGTGGAGAGCGAGCCCTTAACATCCTTCATTCTTCTCTGCCCTCATGTTCCTGGACTCTTCCCTGCTGTTTTTGTCTATGTCCCAATAATCTACCCTCACCAAGAGGTGAATCACTCACCTCTGTGTAACCCCAGAATCACTGAGTGGGGTCCTGTGTCCAGCCCGAAACATCTCCCAGCCAGCCTGGGCTATCATCGCTCCATTGTCAATACAGAATCTGGGATGCAAGAGAGATGAAAATTGGGATCTAA... | TCTTATTAGTCCCTCCAGGTCACCTCTACTTCATCTGTCCGATACCTGTGGAAAAACAGAAGAAACATGGTGGAGAGCGAGCCCTTAACATCCTTCATTCTTCTCTGCCCTCATGTTCCTGGACTCTTCCCTGCTGTTTTTGTCTATGTCCCAATAATCTACCCTCACCAAGAGGTGAATCACTCACCTCTGTGTAACCCCAGAATCACTGAGTGGGGTCCTGTGTCCAGCCCGAAACATCTCCCAGCCAGCCTGGGCTATCATCGCTCCATTGTCAATACAGAATCTGGGATGCAAGAGAGATGAAAATTGGGATCTAA... |
Task1_train_42922 | A variant on Chromosome 14 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GTGGCTCCGTTGACCAGCCCCCAACCTACCTGATCCAACTGCTTCCCTGAGGGTAGCCTGGTGTATTGTGCAATCATGTCTGGTTTCCCGGGCTCTGCTTTCCAAGTAAAAAATTTCCTGTGAAAGCTTGGTTAGTTGTGTTCAGCTCTGTCACACCTCATTGCCACCTCTGAAAGCAACGTTTGGTCTTCCCAGATGGATGTGAGAGAACTGGACTTGGAACTGGGAGAAAAGTAACACGGGTTGATTCTTGCTAGTGTAGGGGTTCTGGGTAAGTGCCCTGAGGTTTCTGAAGAGCAAAGATCCTCGGTGGAGAGAAA... | GTGGCTCCGTTGACCAGCCCCCAACCTACCTGATCCAACTGCTTCCCTGAGGGTAGCCTGGTGTATTGTGCAATCATGTCTGGTTTCCCGGGCTCTGCTTTCCAAGTAAAAAATTTCCTGTGAAAGCTTGGTTAGTTGTGTTCAGCTCTGTCACACCTCATTGCCACCTCTGAAAGCAACGTTTGGTCTTCCCAGATGGATGTGAGAGAACTGGACTTGGAACTGGGAGAAAAGTAACACGGGTTGATTCTTGCTAGTGTAGGGGTTCTGGGTAAGTGCCCTGAGGTTTCTGAAGAGCAAAGATCCTCGGTGGAGAGAAA... |
Task1_train_42923 | This genomic variant is located on Chromosome 14. Can you determine its pathogenicity and name any linked disease? | Benign | GAATTGGCCCACACAATTACTGAGGCTGAGAAGCCCCACAATTTGCCATCTGCAAGCTGGGAAGCTGGTGATGGAGTTCCAGTCCAAACCCAAAGGTTCGAGAATCTGGAGAGCCAGTGTCATAAGTTCTAGTCTGAATATAAAGGTCCAAGAACCAGAAGCACTGATGTCCAAGGGCAGGAGAAGATGGACGTCTCAGTTCAAGCAGAGAGAGTCCATTTGCCCTTGCTCTGCCTTTTTGTTCCATTTAGGCCCTTAACAGATTGGACGATGCCCACCTGCATGGGTGAGGGAGATCTTTACTCAGTCTATGGATTAAA... | GAATTGGCCCACACAATTACTGAGGCTGAGAAGCCCCACAATTTGCCATCTGCAAGCTGGGAAGCTGGTGATGGAGTTCCAGTCCAAACCCAAAGGTTCGAGAATCTGGAGAGCCAGTGTCATAAGTTCTAGTCTGAATATAAAGGTCCAAGAACCAGAAGCACTGATGTCCAAGGGCAGGAGAAGATGGACGTCTCAGTTCAAGCAGAGAGAGTCCATTTGCCCTTGCTCTGCCTTTTTGTTCCATTTAGGCCCTTAACAGATTGGACGATGCCCACCTGCATGGGTGAGGGAGATCTTTACTCAGTCTATGGATTAAA... |
Task1_train_42924 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ATGCTCCTGGCCCAAAAAGAGCTAGCTATTCTGGGTCTTTGTTTTCTCTTCTGGTGAGGGATGATATGAGTACTCAATTTGAAGTAGGCAGCATTTACTTTTTCTTACACATTAAAGAAAACTCTCCCAGAGTTTAAATAGTTAGGCTCTGAGGCTGACATGACTCTCAGCCAGAGCTGGAAATCTACTGTCGGAAAGAAGTTATTCAAATCTGAACTAAATTTGAACAAGAGGAGACTGCTTAGACTACTCTACTGTGGATGGAGTCCACCCTTCTTTTTGATGAGTGGGTGGTAGCATCAGACTCACTATGTGGAGCT... | ATGCTCCTGGCCCAAAAAGAGCTAGCTATTCTGGGTCTTTGTTTTCTCTTCTGGTGAGGGATGATATGAGTACTCAATTTGAAGTAGGCAGCATTTACTTTTTCTTACACATTAAAGAAAACTCTCCCAGAGTTTAAATAGTTAGGCTCTGAGGCTGACATGACTCTCAGCCAGAGCTGGAAATCTACTGTCGGAAAGAAGTTATTCAAATCTGAACTAAATTTGAACAAGAGGAGACTGCTTAGACTACTCTACTGTGGATGGAGTCCACCCTTCTTTTTGATGAGTGGGTGGTAGCATCAGACTCACTATGTGGAGCT... |
Task1_train_42925 | A genomic change on Chromosome 14 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CTTCACAGACCTTTGCTGAATGAATGAATGAATAAATAAATAAATAAATAAATAAATAAATAAATAAATATTTGTTTCCAAGATTTCCAAAGGGATTTCCATGAATAGGAATCCCTTTTCAAATGTCCAATAAACTAGACAAAATTTACTACAAAGTTTGGTTCTTGGTAGATACAACAATATTTGGCATTTGGCATTCTTTTTTTTTTTTTTTTTAGATGGAGTTTTGCTCTTTCGCCCAGGCTGGAGTGAAGTGGCACGATCTTGGCTCGCTGCAAACCTCCGCCCCCTGGGTTCAGTGATTCTCCTGCCTCCTTATA... | CTTCACAGACCTTTGCTGAATGAATGAATGAATAAATAAATAAATAAATAAATAAATAAATAAATAAATATTTGTTTCCAAGATTTCCAAAGGGATTTCCATGAATAGGAATCCCTTTTCAAATGTCCAATAAACTAGACAAAATTTACTACAAAGTTTGGTTCTTGGTAGATACAACAATATTTGGCATTTGGCATTCTTTTTTTTTTTTTTTTTAGATGGAGTTTTGCTCTTTCGCCCAGGCTGGAGTGAAGTGGCACGATCTTGGCTCGCTGCAAACCTCCGCCCCCTGGGTTCAGTGATTCTCCTGCCTCCTTATA... |
Task1_train_42926 | A genetic alteration is present on Chromosome 14. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGGAGTGAAGTGGCACGATCTTGGCTCGCTGCAAACCTCCGCCCCCTGGGTTCAGTGATTCTCCTGCCTCCTTATATAATGCCTCCTTATATAATGAAATTATATGAAATTACCCTTTTTGGTAGCTGGGATTAAAGGCGCCCGCCACCACGCCCGGCTAATTTTTGTGTTTTTGTAGAGGCGGGGTTTCGCCATGTTGGCCAGACTGGTCTAGGAACTCCTGACCTCAGGTGATCAGCCTGTCTCGGCCTTCCAAAGGGCTAGGATTACAGGCGTGAGCCACCGTGTCCAGCCTATGTGGCATTCTTAACTCTTTAATA... | TGGAGTGAAGTGGCACGATCTTGGCTCGCTGCAAACCTCCGCCCCCTGGGTTCAGTGATTCTCCTGCCTCCTTATATAATGCCTCCTTATATAATGAAATTATATGAAATTACCCTTTTTGGTAGCTGGGATTAAAGGCGCCCGCCACCACGCCCGGCTAATTTTTGTGTTTTTGTAGAGGCGGGGTTTCGCCATGTTGGCCAGACTGGTCTAGGAACTCCTGACCTCAGGTGATCAGCCTGTCTCGGCCTTCCAAAGGGCTAGGATTACAGGCGTGAGCCACCGTGTCCAGCCTATGTGGCATTCTTAACTCTTTAATA... |
Task1_train_42927 | This alteration occurs on Chromosome 14. Is it associated with a disease or is it a benign variant? | Benign | AAAACAAAAGAAGATTTCACACAACAGATACAAGAATGTAAAAAGATGAACAAATGAATGAAACATAATCCAATGACAAAACGAGTGGAGATGTCTTTATCAATGTACTAAAGTGCACACTAGAAGAATACAGTAAATGCTATTACTCATGAAATCCCTCACTGATCTGCTTTCCCAACAGCACCTGGAATTACCACAGAGAAGTAATTAAGTCCCTTTATTAAATTTGCTTCACCTCTTTTTCCTCTAGCATTAAATGTAAATTTTTCTAACAAGCATGTACAAAAATATACAGATAATCTATTTTTATTTCATTTTAT... | AAAACAAAAGAAGATTTCACACAACAGATACAAGAATGTAAAAAGATGAACAAATGAATGAAACATAATCCAATGACAAAACGAGTGGAGATGTCTTTATCAATGTACTAAAGTGCACACTAGAAGAATACAGTAAATGCTATTACTCATGAAATCCCTCACTGATCTGCTTTCCCAACAGCACCTGGAATTACCACAGAGAAGTAATTAAGTCCCTTTATTAAATTTGCTTCACCTCTTTTTCCTCTAGCATTAAATGTAAATTTTTCTAACAAGCATGTACAAAAATATACAGATAATCTATTTTTATTTCATTTTAT... |
Task1_train_42928 | A variant found on Chromosome 14 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GGGCAAAAAGGAAATCAAACATCTGCCCTTCCTCCCACAACCTCTTTACTTCCCTCTCTTCCTAACACTGTATCTCACATCTACAGCTGCAGGCACACAGATATGACATACAGCTTGATATCTTTATGTGCAAAGGCAAAAGATGGCTATGGATATAGGAGGTGGCATTTAAAAGAACAATATCCATGTTTGATACTGCTTTCATTATCAATAATGAAAAGGTAGCCTTTCAGCAGAACAAAGTAAGGTACAGGTCGTTTGGAAGCCATTTCAGTCATTCACACAGTGTGATCCACCATTACGAAGCAGAATTTGAAATC... | GGGCAAAAAGGAAATCAAACATCTGCCCTTCCTCCCACAACCTCTTTACTTCCCTCTCTTCCTAACACTGTATCTCACATCTACAGCTGCAGGCACACAGATATGACATACAGCTTGATATCTTTATGTGCAAAGGCAAAAGATGGCTATGGATATAGGAGGTGGCATTTAAAAGAACAATATCCATGTTTGATACTGCTTTCATTATCAATAATGAAAAGGTAGCCTTTCAGCAGAACAAAGTAAGGTACAGGTCGTTTGGAAGCCATTTCAGTCATTCACACAGTGTGATCCACCATTACGAAGCAGAATTTGAAATC... |
Task1_train_42929 | A variant was discovered on Chromosome 14. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CTTTGATGTTTGTAGCCTTTGCTCGAGGCTACTGTTTGAGTGAGCCCAAGTGTTCCAGATGAAACGATACAGGGACAAGTTCACATAATAAGGCTGTTCCCCATCACCACCTCGGCTACCAATCAGCTGGAGCCCTGCAGCTCCCCCTACTATTCCTTTCTCCACTGCTGTAGATTTCCAGGGCTCTGAGAAAAGGAGGAGGACGCAGACTCTGCTCTTCAGATCCACATGCTGATCCCCACTACAATCAGTGACCTGAACTCAGAGTCCAAGTAGGGTAAGAAGGGCTCTGCTGAGGTTGCTCGGGGGACAGCCAGGAA... | CTTTGATGTTTGTAGCCTTTGCTCGAGGCTACTGTTTGAGTGAGCCCAAGTGTTCCAGATGAAACGATACAGGGACAAGTTCACATAATAAGGCTGTTCCCCATCACCACCTCGGCTACCAATCAGCTGGAGCCCTGCAGCTCCCCCTACTATTCCTTTCTCCACTGCTGTAGATTTCCAGGGCTCTGAGAAAAGGAGGAGGACGCAGACTCTGCTCTTCAGATCCACATGCTGATCCCCACTACAATCAGTGACCTGAACTCAGAGTCCAAGTAGGGTAAGAAGGGCTCTGCTGAGGTTGCTCGGGGGACAGCCAGGAA... |
Task1_train_42930 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AAATGGTATTGTGTTTTAAATATCAAATTGCAATTGTTCATTGCTGGTATATAAGAAAGCAACTGACTTTTGTATATTAACCTTGTATCCTGCAACCTTGCTATAAACAGACATTATGTTTATTCTGCAGACATTTGGAGCCATAAAAGCATGGGGCAAGAGTGTTGTACTATTATATCTTGTTCAAAAAAAGACTAATCTGGAAGTAATATGTAGAATGGATTGGAAGGAGAAAAAAACAAGGCAAGGAGTCCATGTGGGAGGCTTTTATGTGAGCCCTCCATAAGACAATGAGTTTCTGAATAAGGGTGTTGCAGTAC... | AAATGGTATTGTGTTTTAAATATCAAATTGCAATTGTTCATTGCTGGTATATAAGAAAGCAACTGACTTTTGTATATTAACCTTGTATCCTGCAACCTTGCTATAAACAGACATTATGTTTATTCTGCAGACATTTGGAGCCATAAAAGCATGGGGCAAGAGTGTTGTACTATTATATCTTGTTCAAAAAAAGACTAATCTGGAAGTAATATGTAGAATGGATTGGAAGGAGAAAAAAACAAGGCAAGGAGTCCATGTGGGAGGCTTTTATGTGAGCCCTCCATAAGACAATGAGTTTCTGAATAAGGGTGTTGCAGTAC... |
Task1_train_42931 | Given this context: Chromosome 14 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TGCAACCTATAAGACTTGGGATGAGGTGGAGAGGGTATGGAAGGCTTAGATCAAACGTCCTGAGTGAGACAGGACCAGATTGTCCCCAGTACAAAATAGCTGGGAAGCAGCTACCATAGACTTTCCTATTTTGGATTAGACCAACCCCAAGCACATGAACTAAGACTATCCGTAGCTCTTGGATTAGTCATGCCATTGAAGAGGAGGAGAAGACGCCACTGGGCTGTGCCTGGCAGGGAGTCTGGAGTTTCTGGTTTCCAAGCTCAGGAAGGCGTGAACCAGGGGAGGGGCCTCCATGCAGGGGGAGGGCTAGAAGCTGG... | TGCAACCTATAAGACTTGGGATGAGGTGGAGAGGGTATGGAAGGCTTAGATCAAACGTCCTGAGTGAGACAGGACCAGATTGTCCCCAGTACAAAATAGCTGGGAAGCAGCTACCATAGACTTTCCTATTTTGGATTAGACCAACCCCAAGCACATGAACTAAGACTATCCGTAGCTCTTGGATTAGTCATGCCATTGAAGAGGAGGAGAAGACGCCACTGGGCTGTGCCTGGCAGGGAGTCTGGAGTTTCTGGTTTCCAAGCTCAGGAAGGCGTGAACCAGGGGAGGGGCCTCCATGCAGGGGGAGGGCTAGAAGCTGG... |
Task1_train_42932 | A mutation on Chromosome 14 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GCCCCAGAACAAGCTGGAGGAAAAGGAGCCGGGTCACAGCTGGTGCCATTCCTCCTGCTGGTAGAGTTAAGGTGGTTGGGGGCAGCAGTGGGCCTGAAGTGGCTGTCTGCCACATCCCAGAGCCTCCAGCATTCCCAACCCAACAGTACTTTAGAGATCATCTCACCCATAACCAAGTTCTCATGACCCAGAAAGAGGAGATGCTTGCCCAAGGCCACCCAGACAACCAGCCACCTTCAGCCAGCCCTGCTCCCCTGGTCCACCACAGAATCTCAGCCTCTGCAGAGTCCGTGAGCTACATTTGCAGAATAAGAGCTCTA... | GCCCCAGAACAAGCTGGAGGAAAAGGAGCCGGGTCACAGCTGGTGCCATTCCTCCTGCTGGTAGAGTTAAGGTGGTTGGGGGCAGCAGTGGGCCTGAAGTGGCTGTCTGCCACATCCCAGAGCCTCCAGCATTCCCAACCCAACAGTACTTTAGAGATCATCTCACCCATAACCAAGTTCTCATGACCCAGAAAGAGGAGATGCTTGCCCAAGGCCACCCAGACAACCAGCCACCTTCAGCCAGCCCTGCTCCCCTGGTCCACCACAGAATCTCAGCCTCTGCAGAGTCCGTGAGCTACATTTGCAGAATAAGAGCTCTA... |
Task1_train_42933 | A mutation on Chromosome 14 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGGCCATTTTTGCCTTTTTTGTTCAGTGATATATCCCAAGTATCTTGACACTTAGTAGATGCTCGATAAATGTTTGTTGACCACATGAATGAAGCATGCCCAAGATTCTGAGATTGCCTACTACTTACAGGTAAATTCTGAAAACAAAAATATTCCTCATCTCAGTTTTACAGGCCTTCTCACCCACAGAGGGTGATGCTTCTCTGCCTTGGTGTCTCGGTTCTCCTGAGTGTCATATTCCAAGCTCACAAGAGCTTGGAGTAGCACTGACCCAGATGCTCCACACAGCTGTAACCACCACAAGGAACAGGACATACAAG... | TGGCCATTTTTGCCTTTTTTGTTCAGTGATATATCCCAAGTATCTTGACACTTAGTAGATGCTCGATAAATGTTTGTTGACCACATGAATGAAGCATGCCCAAGATTCTGAGATTGCCTACTACTTACAGGTAAATTCTGAAAACAAAAATATTCCTCATCTCAGTTTTACAGGCCTTCTCACCCACAGAGGGTGATGCTTCTCTGCCTTGGTGTCTCGGTTCTCCTGAGTGTCATATTCCAAGCTCACAAGAGCTTGGAGTAGCACTGACCCAGATGCTCCACACAGCTGTAACCACCACAAGGAACAGGACATACAAG... |
Task1_train_42934 | Consider a variant on Chromosome 14. Determine its clinical classification and disease relevance. | Benign | CATAATTGTGGGTGATGGCACCTCCACCTAAGATGGGGAGCCCTGGATGGTGGGTCTTATGGGAAGGGATTTGCAGGATGGCTGTGTGGAAATCTCCCTCATCCCCTCGAGTTCTCAGCCATAAGCTCAGTCCCCTGATAGCCCAGAAGCCTGTCTTTTCTCTCCTGGGAAAGATCTATGCAATCACCCCAACTCACGAGCACCCGGAACAGCCCTGATCAGGGGCATTCACAACAAATTCTCCCTGGATCTCCAAAGCCAAGGTCTCAGAGCGGGAGTGTTGAGCGCCCTGCCAGGTTTGTGCACTCTGGCCCAGCCCC... | CATAATTGTGGGTGATGGCACCTCCACCTAAGATGGGGAGCCCTGGATGGTGGGTCTTATGGGAAGGGATTTGCAGGATGGCTGTGTGGAAATCTCCCTCATCCCCTCGAGTTCTCAGCCATAAGCTCAGTCCCCTGATAGCCCAGAAGCCTGTCTTTTCTCTCCTGGGAAAGATCTATGCAATCACCCCAACTCACGAGCACCCGGAACAGCCCTGATCAGGGGCATTCACAACAAATTCTCCCTGGATCTCCAAAGCCAAGGTCTCAGAGCGGGAGTGTTGAGCGCCCTGCCAGGTTTGTGCACTCTGGCCCAGCCCC... |
Task1_train_42935 | This variant is found on Chromosome 14. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CATATGAATATAGACCCCTGACTGCTAGGTGACTTCCTCTTGTACACACACCCCAGAATTTGGCCCTTTGCCCATTTCTTCCCAAATGTACCGGCAACTAATTTCTCCTCAGGACTATTAACTAAAAACAGACCCCGTATGTCTGCCTTGCCTTATCTGCTATCCCCCAAAACACACACACAGCAGCCTCCTTGGCTCTTCCTGCTCCCGCAGGCCTGATCTACAGACACTGGGGCTGTCCGTCCTGCTGGACCTTCGTCAGGCACCTCCACTGCCTCCAGCACTCATTCCTGCCTTGAGCCAACTTCAGGTAACCACCC... | CATATGAATATAGACCCCTGACTGCTAGGTGACTTCCTCTTGTACACACACCCCAGAATTTGGCCCTTTGCCCATTTCTTCCCAAATGTACCGGCAACTAATTTCTCCTCAGGACTATTAACTAAAAACAGACCCCGTATGTCTGCCTTGCCTTATCTGCTATCCCCCAAAACACACACACAGCAGCCTCCTTGGCTCTTCCTGCTCCCGCAGGCCTGATCTACAGACACTGGGGCTGTCCGTCCTGCTGGACCTTCGTCAGGCACCTCCACTGCCTCCAGCACTCATTCCTGCCTTGAGCCAACTTCAGGTAACCACCC... |
Task1_train_42936 | This genomic variant is located on Chromosome 14. Can you determine its pathogenicity and name any linked disease? | Benign | GGGGAAAGGTCACCTCAGGGCCGGTGCAAAAGCGGGGGCCAAGACTTTCTGTTTCCTAGGATTTCTTCATATTGGCTTCCTCTAAGCCAATATCCTAGAGATGGGTTGCATCTCCTCCTGTTTGCTTACCTGCTTGTTAGCTGTTTCCCCAACTGTTTAAAAACAAGATTTGGAGTCTAACGTGCTCAGCTTGAGTTCTAGTTCTGCCATGTGTAAGATGTTGGACAAGTCATGAAGCTCCTCTGAGTTCCCAAGTCCTCATCTATAGAATGCGGATGGTAACAATTAACTCACAACGTGGTCAGAAAGATCAAGTGAAT... | GGGGAAAGGTCACCTCAGGGCCGGTGCAAAAGCGGGGGCCAAGACTTTCTGTTTCCTAGGATTTCTTCATATTGGCTTCCTCTAAGCCAATATCCTAGAGATGGGTTGCATCTCCTCCTGTTTGCTTACCTGCTTGTTAGCTGTTTCCCCAACTGTTTAAAAACAAGATTTGGAGTCTAACGTGCTCAGCTTGAGTTCTAGTTCTGCCATGTGTAAGATGTTGGACAAGTCATGAAGCTCCTCTGAGTTCCCAAGTCCTCATCTATAGAATGCGGATGGTAACAATTAACTCACAACGTGGTCAGAAAGATCAAGTGAAT... |
Task1_train_42937 | This is a variant located on Chromosome 14. Is this mutation a likely cause of disease or not? | Benign | CCCTTCTCCAGGAGCGCCTGGCCCAGGCACGGGAGGCCCTGGCTCTGGAGGAGAATGCCACCTCCCAGAAGGTGCTGGATATCTTTGAACAGCGGCTGGAGCAGGTTGAGAGTGGCCTCCATCGGGCCCTGCGGCTACAGCGCTTCTTCCAGCAGGTGCATGCAGAGCCTTTTCCTTCTGTGCCCCCCCATTTCCATTTATTCACTTCCTTTCTGCCTGGAGAGGCTAATCAAGTTGTTAAAAGTGGAGGCTGAGGGGCCCATCTCCTAGGTTTTTGCTCTTAGCTCTGCCACCTCCTTGCTGAATGGCATGGGGCAAGA... | CCCTTCTCCAGGAGCGCCTGGCCCAGGCACGGGAGGCCCTGGCTCTGGAGGAGAATGCCACCTCCCAGAAGGTGCTGGATATCTTTGAACAGCGGCTGGAGCAGGTTGAGAGTGGCCTCCATCGGGCCCTGCGGCTACAGCGCTTCTTCCAGCAGGTGCATGCAGAGCCTTTTCCTTCTGTGCCCCCCCATTTCCATTTATTCACTTCCTTTCTGCCTGGAGAGGCTAATCAAGTTGTTAAAAGTGGAGGCTGAGGGGCCCATCTCCTAGGTTTTTGCTCTTAGCTCTGCCACCTCCTTGCTGAATGGCATGGGGCAAGA... |
Task1_train_42938 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | ATGCACAGTACGTGAAGCACCGACACAAACTGGAGAATGGTCTGGCTGCGCTCAGTCCCTTAAGCAAGGTAACTTTTTCTCCAACCTTCAGGAGAAAAGTAGAGAGGCCAGAAAGACCTAAAAACCCACCCAACAAATCCCTCAGGGCAAAAAACTGGATATGCCCAGGAACATCACCTACCAATCATCTCCTAGAATTGCCGAGGGTGGGACAAGCACCGGACTGGTGAGGCCAGGTTCTTATCCAGTCCACCTGAGGGACTGGGCAGGACTCCTGTTTCCTCTGGGCCTCTATTTCCACAGCTGGTAAATGGGGGCAA... | ATGCACAGTACGTGAAGCACCGACACAAACTGGAGAATGGTCTGGCTGCGCTCAGTCCCTTAAGCAAGGTAACTTTTTCTCCAACCTTCAGGAGAAAAGTAGAGAGGCCAGAAAGACCTAAAAACCCACCCAACAAATCCCTCAGGGCAAAAAACTGGATATGCCCAGGAACATCACCTACCAATCATCTCCTAGAATTGCCGAGGGTGGGACAAGCACCGGACTGGTGAGGCCAGGTTCTTATCCAGTCCACCTGAGGGACTGGGCAGGACTCCTGTTTCCTCTGGGCCTCTATTTCCACAGCTGGTAAATGGGGGCAA... |
Task1_train_42939 | This variant is present on Chromosome 14. Is the change likely to result in a pathogenic outcome? | Benign | CAGGGCTCCTTGAAGCAGCGGCCGCACACCGGACACGCATGATCGAAGGAGGCCTTGTGCTTACGCATGTGGCCCTTGAGAAACCAAGACTGTGTAAAGCTCTGGCCGCACACTTGGCAGCGGAACTCCGGAGGCGCTGGGGGCTCCTCGGGAGCGGCAGGAGCTGGGGTCGGGGTTGCCTCACGTTCGGGCTCCGGCTCCGGCTCCGGCTGGGGGACTGATCTGGGTTCGGGCTGGGGTGGAGGCTGAGGCTGAGGCTGAGGCGGAGGCGCAGCGGAGGTGGCCGCCAGGGGACGCTCGGGAGCCCCGTGGGCCGTCAG... | CAGGGCTCCTTGAAGCAGCGGCCGCACACCGGACACGCATGATCGAAGGAGGCCTTGTGCTTACGCATGTGGCCCTTGAGAAACCAAGACTGTGTAAAGCTCTGGCCGCACACTTGGCAGCGGAACTCCGGAGGCGCTGGGGGCTCCTCGGGAGCGGCAGGAGCTGGGGTCGGGGTTGCCTCACGTTCGGGCTCCGGCTCCGGCTCCGGCTGGGGGACTGATCTGGGTTCGGGCTGGGGTGGAGGCTGAGGCTGAGGCTGAGGCGGAGGCGCAGCGGAGGTGGCCGCCAGGGGACGCTCGGGAGCCCCGTGGGCCGTCAG... |
Task1_train_42940 | This mutation occurs on Chromosome 14. Does this change lead to a known medical condition, or is it benign? | Benign | AAGGTCTCTCCATTTATTTAGATCTTCTCTAACTTTTCTCAGGAACGTTTTATGATTTCCAGTATATGGAAATGACAACATTTTTGTGAAAGAATTGTTTTCTTAATTTCATTTTTGGATTGTTTCTTGCCAATATATAAAAATATAATTAATTTTTCTATATTTTTTATATGCTGTAATTTTACTGAACTTGGTTATTAGTTCCAGTGGAGTTTTTTAATAGATTACTTGGAACTTTCTATATTCAGGATCATGTTATCTACAAATAAACTCAATTTTTCTTCTCCCTTTCCAATCTAGATGCTTTGTTTGTTTTAATG... | AAGGTCTCTCCATTTATTTAGATCTTCTCTAACTTTTCTCAGGAACGTTTTATGATTTCCAGTATATGGAAATGACAACATTTTTGTGAAAGAATTGTTTTCTTAATTTCATTTTTGGATTGTTTCTTGCCAATATATAAAAATATAATTAATTTTTCTATATTTTTTATATGCTGTAATTTTACTGAACTTGGTTATTAGTTCCAGTGGAGTTTTTTAATAGATTACTTGGAACTTTCTATATTCAGGATCATGTTATCTACAAATAAACTCAATTTTTCTTCTCCCTTTCCAATCTAGATGCTTTGTTTGTTTTAATG... |
Task1_train_42941 | The following genetic variant occurs on Chromosome 14. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CACCATATTTCAAAACATATGGGATGCAGGCTAAATAGAATTTGAAAAAATTTGTCTTAAATGCCTATATTTAAAAAGAAGACAGCCAGTGCGGTGGCTCATGCCTGTAATCCCTGCATTTTGGGAGGCCGAAGTGGGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGACATGGTGGCTCATACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGTGGTGAGCCGAGATCAC... | CACCATATTTCAAAACATATGGGATGCAGGCTAAATAGAATTTGAAAAAATTTGTCTTAAATGCCTATATTTAAAAAGAAGACAGCCAGTGCGGTGGCTCATGCCTGTAATCCCTGCATTTTGGGAGGCCGAAGTGGGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGACATGGTGGCTCATACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGTGGTGAGCCGAGATCAC... |
Task1_train_42942 | Consider a variant on Chromosome 14. Determine its clinical classification and disease relevance. | Benign | TCCATTGTGGATCAGCACTCTTCAGAGTTGGTGATTTTTTTTTTTTGAGATGGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACCGCAACCTCCGCCTCTCAGATTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCACCACGTGCAGCTAATTACAGACAGGGTTTCTCCATGTTAGTCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCGCCCACCTCAGCCCGGCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCAAAGGGCCGATT... | TCCATTGTGGATCAGCACTCTTCAGAGTTGGTGATTTTTTTTTTTTGAGATGGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACCGCAACCTCCGCCTCTCAGATTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCACCACGTGCAGCTAATTACAGACAGGGTTTCTCCATGTTAGTCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCGCCCACCTCAGCCCGGCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCAAAGGGCCGATT... |
Task1_train_42943 | Consider this mutation on Chromosome 14. Is this a benign change or a disease-causing variant? | Benign | GCACATATACAGGGGTGTGTAGACAAGTGGGATAGAAAAAGCAAATATTAAAATTGTTATTTATATTTGTCACCCATTTAAACATACATATTTTGTTTTATAATGACAATTTATTAGTACAAAAACAAGTCTATATATAATTTTTTTAAATGCACACAAATACTATTGGGGTAGTGGCTCAACTTTTTTTTTTTTTTTTTTTTTTTTTTTACTAAGATAAGGGTGTAATCACTGCAATAAAATAAAGACAGGTATCACAATGGCCCTGCCCTCAAAGAGTTACAGTGTACTGGGGACAGAAGGCTAATCTTTTTAAAGTG... | GCACATATACAGGGGTGTGTAGACAAGTGGGATAGAAAAAGCAAATATTAAAATTGTTATTTATATTTGTCACCCATTTAAACATACATATTTTGTTTTATAATGACAATTTATTAGTACAAAAACAAGTCTATATATAATTTTTTTAAATGCACACAAATACTATTGGGGTAGTGGCTCAACTTTTTTTTTTTTTTTTTTTTTTTTTTTACTAAGATAAGGGTGTAATCACTGCAATAAAATAAAGACAGGTATCACAATGGCCCTGCCCTCAAAGAGTTACAGTGTACTGGGGACAGAAGGCTAATCTTTTTAAAGTG... |
Task1_train_42944 | This genomic variant is located on Chromosome 14. Can you determine its pathogenicity and name any linked disease? | Benign | TACGGGAGCATCTGGGAACAACTGATGTTCTTCAGCTCAGTGAAATAAAGCAGTGTGGGGAGTATCCACTTCGATAGACATTACTCTGTGATAGACATTACTATTTGCCTCTCCCCTTCATCACTCAAAATACTATTTTCTTGAGTCCTTACATGATATATGGTCAGGCAATGCCAAGAAATGTTAATACTTGCCTAAGTAGGTTATTATTATTATTATTATTATTTTTTTTTTGAGGCAGAGTCTCACTCTGTTGCCCAGGGTAGAGTGCACTGGTGTGATCTTGGCTCACTGCAACCTCTGCCTCCTAGGTTCAAGTG... | TACGGGAGCATCTGGGAACAACTGATGTTCTTCAGCTCAGTGAAATAAAGCAGTGTGGGGAGTATCCACTTCGATAGACATTACTCTGTGATAGACATTACTATTTGCCTCTCCCCTTCATCACTCAAAATACTATTTTCTTGAGTCCTTACATGATATATGGTCAGGCAATGCCAAGAAATGTTAATACTTGCCTAAGTAGGTTATTATTATTATTATTATTATTTTTTTTTTGAGGCAGAGTCTCACTCTGTTGCCCAGGGTAGAGTGCACTGGTGTGATCTTGGCTCACTGCAACCTCTGCCTCCTAGGTTCAAGTG... |
Task1_train_42945 | This mutation on Chromosome 14 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TATCACCTCAGTTTACTGAGTCAATAAGCTAGAGTCCTCCTCTGTAGAAATAATAGAGAATTGCTTCTCAAATTTATAACATTAATTAAACCTTAGTGGGAAGATTAAATTCACACTTGATCCAACTCTGACCATGGTGATAAATAACTACAGAATTTCACATTTCTGGATTATTTTTCCCCAGCCCAAAATGAGGATCTGAAGCTTGAAGTCACCAACATACTTCAGAAGCATAAACAGGAAGTAGAGCTCCTCCAAAATGCAGCCACAATTTCCCAACCTCCTGACAGGCAATCTGAACCAGCCACTCACCCAGCTGT... | TATCACCTCAGTTTACTGAGTCAATAAGCTAGAGTCCTCCTCTGTAGAAATAATAGAGAATTGCTTCTCAAATTTATAACATTAATTAAACCTTAGTGGGAAGATTAAATTCACACTTGATCCAACTCTGACCATGGTGATAAATAACTACAGAATTTCACATTTCTGGATTATTTTTCCCCAGCCCAAAATGAGGATCTGAAGCTTGAAGTCACCAACATACTTCAGAAGCATAAACAGGAAGTAGAGCTCCTCCAAAATGCAGCCACAATTTCCCAACCTCCTGACAGGCAATCTGAACCAGCCACTCACCCAGCTGT... |
Task1_train_42946 | A variant found on Chromosome 14 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GGTGGTGGTGTAACACACAATCTCTCTCTCTCTCTCTCATTCTTTCTCTCTTGCTCCTCTCCCCTGTCCCTCTCTCCTAGTCACTGTTTCCTCAAAGCAGTTTTAGTCGGATAATAGAACTTCATCACTCATCTCCTGTTATTCTTGTCAGTGATTTCTCTCTTAAAAGCTCTAAAATCTTTGTTGCAATTTGAGGATGCTGACAGTGACAGGGCAGCTGGCTGGACACTGAATGCAAGTTTCATATTGTGGTGCCTCCTATACTTAGTGTAGTCACTGCTGACCAGAGCCTGGTCTCAGGCTTGTTTGTCAAGACACTT... | GGTGGTGGTGTAACACACAATCTCTCTCTCTCTCTCTCATTCTTTCTCTCTTGCTCCTCTCCCCTGTCCCTCTCTCCTAGTCACTGTTTCCTCAAAGCAGTTTTAGTCGGATAATAGAACTTCATCACTCATCTCCTGTTATTCTTGTCAGTGATTTCTCTCTTAAAAGCTCTAAAATCTTTGTTGCAATTTGAGGATGCTGACAGTGACAGGGCAGCTGGCTGGACACTGAATGCAAGTTTCATATTGTGGTGCCTCCTATACTTAGTGTAGTCACTGCTGACCAGAGCCTGGTCTCAGGCTTGTTTGTCAAGACACTT... |
Task1_train_42947 | Here is a genetic alteration on Chromosome 14. Based on the data, is it a benign variant or a cause of disease? | Benign | TCAGGCTGGTCTTCAACTCCCGACCTCAGGTGAACCTCCCACCTGAGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGCGCCTGGCTGAACAAACTTTTTCAAGCTCTGTAATGCTGTCTAGTATCTGTCTTTACTAAAGGCCTGTTGTTTCTTAGTGCATGACTACATAGATATCTGATTATAAACTGAGACCTTAACACTCCCCCATCATTCTCTCACTTCTTTTAAACACTGGACACAAGTTAGAGAGATTTCCACACCAGATCATGACAAACACAAATTTCTTGGATTTTTTTTTTCCTCCCAATGTGGA... | TCAGGCTGGTCTTCAACTCCCGACCTCAGGTGAACCTCCCACCTGAGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGCGCCTGGCTGAACAAACTTTTTCAAGCTCTGTAATGCTGTCTAGTATCTGTCTTTACTAAAGGCCTGTTGTTTCTTAGTGCATGACTACATAGATATCTGATTATAAACTGAGACCTTAACACTCCCCCATCATTCTCTCACTTCTTTTAAACACTGGACACAAGTTAGAGAGATTTCCACACCAGATCATGACAAACACAAATTTCTTGGATTTTTTTTTTCCTCCCAATGTGGA... |
Task1_train_42948 | A variant on Chromosome 14 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CATAAAAACTACAGGTCAGAAGACACAGTACAACTCACTTTGTTCATCATCCTATCTGTCTTGATGCAATCTTTTTTGTTATTTTTAGACAGGGTCTCGCTGTATTGCCCAGGCTAGAGTGCAGTGGCTATTCACAGGCACAACACTACTGCTGATCAGCAAGGGAGTGCTGCCCTGCTCCGTTTCCAACCTGGGCCAATTCATCCCTCCTTAGGCAACCTGGTGGTCCCTTGCTCCTGGGAGGTCACCATATTGATGTCAAACTTAGTGCAGACACCTGATTGGCATAGCACACCACAGCCCAGAACTCCTAGGCTCAA... | CATAAAAACTACAGGTCAGAAGACACAGTACAACTCACTTTGTTCATCATCCTATCTGTCTTGATGCAATCTTTTTTGTTATTTTTAGACAGGGTCTCGCTGTATTGCCCAGGCTAGAGTGCAGTGGCTATTCACAGGCACAACACTACTGCTGATCAGCAAGGGAGTGCTGCCCTGCTCCGTTTCCAACCTGGGCCAATTCATCCCTCCTTAGGCAACCTGGTGGTCCCTTGCTCCTGGGAGGTCACCATATTGATGTCAAACTTAGTGCAGACACCTGATTGGCATAGCACACCACAGCCCAGAACTCCTAGGCTCAA... |
Task1_train_42949 | A variant has been detected on Chromosome 14. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTTGGCCTTCAAAAACCAATGGACATTGGTAAGACTATAGATGGAAAAAAAAAAAAAGTGGACATTATTTCATAACTACCATTCTTCATATGGGGTGGCATATCCACTTTTTATAATTCTTCATGACCACTTCACTCAGAATACAGATGATTTTGCCCAGATACTTTTTTTTCTCATGCTTCCCTTACAATTGGTGCAATACCCAAGTACAGAAGGTCATAAGTCGGCTTGGTTAATAGAACAAGATATGGGCATTAATATTAAAAAACTGTGCTCCAAAATATCAAAATGGTATCCTTTATTGACTCTGAAAGCAGTAG... | CTTGGCCTTCAAAAACCAATGGACATTGGTAAGACTATAGATGGAAAAAAAAAAAAAGTGGACATTATTTCATAACTACCATTCTTCATATGGGGTGGCATATCCACTTTTTATAATTCTTCATGACCACTTCACTCAGAATACAGATGATTTTGCCCAGATACTTTTTTTTCTCATGCTTCCCTTACAATTGGTGCAATACCCAAGTACAGAAGGTCATAAGTCGGCTTGGTTAATAGAACAAGATATGGGCATTAATATTAAAAAACTGTGCTCCAAAATATCAAAATGGTATCCTTTATTGACTCTGAAAGCAGTAG... |
Task1_train_42950 | A variant was discovered on Chromosome 14. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCATGATCCGCCCGCCTTGACCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCCAGCCTGCATTCCTGTTTTTTTAATGGTTTTGGAGGGTAGCAGTAGAGATGGGGTCTCACTATGTTGCCCAGTCTAGTCTTGAACTCCTGGGCTACAGTTACCCTCCTACCTCGGCTTCCCAAAGTGCTCGGATTACAGGTGTGAGCCACTGTGCCTAGCCTATAATGATCATTTTAATGTTTCCCATGCACTCATTTAGTTTGAACCTTCACAGCAACCCA... | TCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCATGATCCGCCCGCCTTGACCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCCAGCCTGCATTCCTGTTTTTTTAATGGTTTTGGAGGGTAGCAGTAGAGATGGGGTCTCACTATGTTGCCCAGTCTAGTCTTGAACTCCTGGGCTACAGTTACCCTCCTACCTCGGCTTCCCAAAGTGCTCGGATTACAGGTGTGAGCCACTGTGCCTAGCCTATAATGATCATTTTAATGTTTCCCATGCACTCATTTAGTTTGAACCTTCACAGCAACCCA... |
Task1_train_42951 | This is a variant located on Chromosome 14. Is this mutation a likely cause of disease or not? | Benign | CTCTTCTGAATCACCTCTCACTGATATTGCCTTCTCACCTCCACTCTCTGAGCCTCTCCCTGCCAGGGAATCTTCATCAGTCACATCTTCCTCTTCTTCCTCATCCTCCTCTTCCTCCTCCTCAGACAACTCCTCTTCCGGTGATGGCTGCTGGGACTGCTGCTGGGGGAAACTCCGTGCCCCGGAGACTGTAGATTGCTCGGAGCCATTCTCCTGAGCAGCTCCTCCACCTTCAGGGAGTGCAGTACCACCGTTGGGGATCTGGCCCCCCAGGTGCATCCGGACATGCTGCTGCAGAGTGACAGCATTGGTGAACTTCT... | CTCTTCTGAATCACCTCTCACTGATATTGCCTTCTCACCTCCACTCTCTGAGCCTCTCCCTGCCAGGGAATCTTCATCAGTCACATCTTCCTCTTCTTCCTCATCCTCCTCTTCCTCCTCCTCAGACAACTCCTCTTCCGGTGATGGCTGCTGGGACTGCTGCTGGGGGAAACTCCGTGCCCCGGAGACTGTAGATTGCTCGGAGCCATTCTCCTGAGCAGCTCCTCCACCTTCAGGGAGTGCAGTACCACCGTTGGGGATCTGGCCCCCCAGGTGCATCCGGACATGCTGCTGCAGAGTGACAGCATTGGTGAACTTCT... |
Task1_train_42952 | A variant was discovered on Chromosome 14. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GTGATGGCTGCTGGGACTGCTGCTGGGGGAAACTCCGTGCCCCGGAGACTGTAGATTGCTCGGAGCCATTCTCCTGAGCAGCTCCTCCACCTTCAGGGAGTGCAGTACCACCGTTGGGGATCTGGCCCCCCAGGTGCATCCGGACATGCTGCTGCAGAGTGACAGCATTGGTGAACTTCTTCTGGCAGATGGGGCAGGAATTCTGTGCCCGGGCAGCTGGACTGGCCTTGTGGCCCACGAAATGTGCACGCAGATTACCCCTGGTGGAGAAGGCTCTGCCACACACTTTGCATTTGAAGGGCCTCTCACCTCCATGTTGG... | GTGATGGCTGCTGGGACTGCTGCTGGGGGAAACTCCGTGCCCCGGAGACTGTAGATTGCTCGGAGCCATTCTCCTGAGCAGCTCCTCCACCTTCAGGGAGTGCAGTACCACCGTTGGGGATCTGGCCCCCCAGGTGCATCCGGACATGCTGCTGCAGAGTGACAGCATTGGTGAACTTCTTCTGGCAGATGGGGCAGGAATTCTGTGCCCGGGCAGCTGGACTGGCCTTGTGGCCCACGAAATGTGCACGCAGATTACCCCTGGTGGAGAAGGCTCTGCCACACACTTTGCATTTGAAGGGCCTCTCACCTCCATGTTGG... |
Task1_train_42953 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GTGCAGTGATATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTCACGCGATTCTCCTTCCTCAGCCTCCTGAGTAGCTGAAATTACAAGCACGTGCCACTACGCCTGGCTAAATTTTTTTTTTTTTGAGATGGAGTTTCGAGCCCAGGCTGGAGTACAATGGCGTAATCTCAGCTCACCGCAACCTCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCGCCACCATGCCCGGCTAATTTTGTATTTTTAGTAGACACACGGTTTCTCTATGTTGGTCAGGCTGATC... | GTGCAGTGATATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTCACGCGATTCTCCTTCCTCAGCCTCCTGAGTAGCTGAAATTACAAGCACGTGCCACTACGCCTGGCTAAATTTTTTTTTTTTTGAGATGGAGTTTCGAGCCCAGGCTGGAGTACAATGGCGTAATCTCAGCTCACCGCAACCTCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCGCCACCATGCCCGGCTAATTTTGTATTTTTAGTAGACACACGGTTTCTCTATGTTGGTCAGGCTGATC... |
Task1_train_42954 | Chromosome 14 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CACCATGCCTGGCCCCAGAAATAGTAATTTTTAAAAAATTGCTTTTTAAGAAAATTTTATTTCAATAGTTTTTGGAGTACAGGTGGTTTTTGGTTACATGGATAAGTTCTTTAGTGGTGATTTCTGAGATTTTGGTGCACCCATAACCCAAGCAGTGTACACTGTACCCAATATGTAGTCTTTTATCTTTCACCCCTGTGTTAGTCAGGGGTCTCTTTGTTTTTTTTTTTTTTATTTTTTTATTTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCGCC... | CACCATGCCTGGCCCCAGAAATAGTAATTTTTAAAAAATTGCTTTTTAAGAAAATTTTATTTCAATAGTTTTTGGAGTACAGGTGGTTTTTGGTTACATGGATAAGTTCTTTAGTGGTGATTTCTGAGATTTTGGTGCACCCATAACCCAAGCAGTGTACACTGTACCCAATATGTAGTCTTTTATCTTTCACCCCTGTGTTAGTCAGGGGTCTCTTTGTTTTTTTTTTTTTTATTTTTTTATTTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCGCC... |
Task1_train_42955 | A genomic change on Chromosome 14 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGAGATGGAGGCGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAAAACGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCACGGCACTCCAGCCTGGGCGGCAGGGCGACACTCCATCTCAAAAAAAAAAAAAAAAAAAAAATTCAGCAGCAAATATTGATTTCTGTGTCTGCTCGTAGTTATTAGGCAATAGAGGCAGA... | GGAGATGGAGGCGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAAAACGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCACGGCACTCCAGCCTGGGCGGCAGGGCGACACTCCATCTCAAAAAAAAAAAAAAAAAAAAAATTCAGCAGCAAATATTGATTTCTGTGTCTGCTCGTAGTTATTAGGCAATAGAGGCAGA... |
Task1_train_42956 | This alteration occurs on Chromosome 14. Is it associated with a disease or is it a benign variant? | Benign | AGATGAAGTCTGGTACTGTCACCTAGGCTGGAGTGCAGTGGTGCAATCTCCGCTCACTGCAACCTCTACCTCCTGGGTTCAAGCAATTATCCTGCCTCAGCCTCCCAAGTAGTTGGGATTACAGGTGCATGCCACTATGCCTGGCTAACTTTTTATATTTTTAGTAGAGATGGGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAACTCCTGACTTCGTGATCTGCCCACCTCGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCGGTAGGAGATAAATTCTTGACTGTAATACGTGACAGACTGGGG... | AGATGAAGTCTGGTACTGTCACCTAGGCTGGAGTGCAGTGGTGCAATCTCCGCTCACTGCAACCTCTACCTCCTGGGTTCAAGCAATTATCCTGCCTCAGCCTCCCAAGTAGTTGGGATTACAGGTGCATGCCACTATGCCTGGCTAACTTTTTATATTTTTAGTAGAGATGGGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAACTCCTGACTTCGTGATCTGCCCACCTCGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCGGTAGGAGATAAATTCTTGACTGTAATACGTGACAGACTGGGG... |
Task1_train_42957 | Here is a mutation located on Chromosome 14. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGGAGAATGGTGTGAACCTGGAAGGCGGAGCTTGCAGTGAGCCGAGACCATGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCCGTCTCGAAAAAAATTTTTTTTTTTTGATTTAGTGGAGAGCAAAAATGAACATCTTATTTTACTTTATTTTACAGGTCAAGGACCATAAAAGAAGCCTGAGAGGGAATAGATAGGCTTTGACTGGGTCAGGAAAGTTTTCTTAAAGGTAGTGTTCTTTGAAATAGTCAAAGACAAAGTGAAGGATGAATAGTATTTTTTTCTTCACCTTTAAGTTCATGGATAAGTGTGCAG... | AGGAGAATGGTGTGAACCTGGAAGGCGGAGCTTGCAGTGAGCCGAGACCATGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCCGTCTCGAAAAAAATTTTTTTTTTTTGATTTAGTGGAGAGCAAAAATGAACATCTTATTTTACTTTATTTTACAGGTCAAGGACCATAAAAGAAGCCTGAGAGGGAATAGATAGGCTTTGACTGGGTCAGGAAAGTTTTCTTAAAGGTAGTGTTCTTTGAAATAGTCAAAGACAAAGTGAAGGATGAATAGTATTTTTTTCTTCACCTTTAAGTTCATGGATAAGTGTGCAG... |
Task1_train_42958 | This mutation is located on Chromosome 14. Is it associated with a disease or is it a benign polymorphism? | Benign | TGTGGCATGGTGGTTTACAGCACAGATCGTCAGGTATTAAGCCCAGACCTCCACAGGTGTAGAGTGGGTCCACGTGTTCTCATTATTCAGCTCCCACTTATAAATGGGAACATGTGATGTTTGGTTTTCTGTTCCTGCATTAGTTTGCTGAGGATAATGGCTTCCAAGTCTATCCATGTCCCTGCAAAGGACATGATCTTGTTCCTTTTTATGGCTGCATAATATTTCATGGTGTTATGTACCACATTTTCTTTATTCATTCTATCATTGATGGGCATTTAGGCTGATTCCATGACTTTGCTATTGTAAACAGTGCTGCA... | TGTGGCATGGTGGTTTACAGCACAGATCGTCAGGTATTAAGCCCAGACCTCCACAGGTGTAGAGTGGGTCCACGTGTTCTCATTATTCAGCTCCCACTTATAAATGGGAACATGTGATGTTTGGTTTTCTGTTCCTGCATTAGTTTGCTGAGGATAATGGCTTCCAAGTCTATCCATGTCCCTGCAAAGGACATGATCTTGTTCCTTTTTATGGCTGCATAATATTTCATGGTGTTATGTACCACATTTTCTTTATTCATTCTATCATTGATGGGCATTTAGGCTGATTCCATGACTTTGCTATTGTAAACAGTGCTGCA... |
Task1_train_42959 | This mutation on Chromosome 14 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | ACAGATCGTCAGGTATTAAGCCCAGACCTCCACAGGTGTAGAGTGGGTCCACGTGTTCTCATTATTCAGCTCCCACTTATAAATGGGAACATGTGATGTTTGGTTTTCTGTTCCTGCATTAGTTTGCTGAGGATAATGGCTTCCAAGTCTATCCATGTCCCTGCAAAGGACATGATCTTGTTCCTTTTTATGGCTGCATAATATTTCATGGTGTTATGTACCACATTTTCTTTATTCATTCTATCATTGATGGGCATTTAGGCTGATTCCATGACTTTGCTATTGTAAACAGTGCTGCAATGAGCATACATGTACATGTA... | ACAGATCGTCAGGTATTAAGCCCAGACCTCCACAGGTGTAGAGTGGGTCCACGTGTTCTCATTATTCAGCTCCCACTTATAAATGGGAACATGTGATGTTTGGTTTTCTGTTCCTGCATTAGTTTGCTGAGGATAATGGCTTCCAAGTCTATCCATGTCCCTGCAAAGGACATGATCTTGTTCCTTTTTATGGCTGCATAATATTTCATGGTGTTATGTACCACATTTTCTTTATTCATTCTATCATTGATGGGCATTTAGGCTGATTCCATGACTTTGCTATTGTAAACAGTGCTGCAATGAGCATACATGTACATGTA... |
Task1_train_42960 | A variant was discovered on Chromosome 14. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CAGAAATTTTGCTTGCTGCTATGAAAAAAATAAGCAAACATCACAACGTTGTTCCGTTATAGTTTTACCAGCTACAATCTTAATGGCTACGTTGAAGCATTGTGTTGTTGACAGACAATATGACAATTTTGCACGTGTTCCTCTGTATGGCTGATTCCTGCACAAGCAGTTCCATTTGGGCTCATTGGAAAGATATTTAGATATTTCTCCTTATTGTCTGCCATTGCCTATAATAAAAGGGCATTTATTTTACATAAATTTTATAATTCTTGTGTCACTTGAATATCCTTCCTAACACATTTCCTAGCAAATAAAAATTT... | CAGAAATTTTGCTTGCTGCTATGAAAAAAATAAGCAAACATCACAACGTTGTTCCGTTATAGTTTTACCAGCTACAATCTTAATGGCTACGTTGAAGCATTGTGTTGTTGACAGACAATATGACAATTTTGCACGTGTTCCTCTGTATGGCTGATTCCTGCACAAGCAGTTCCATTTGGGCTCATTGGAAAGATATTTAGATATTTCTCCTTATTGTCTGCCATTGCCTATAATAAAAGGGCATTTATTTTACATAAATTTTATAATTCTTGTGTCACTTGAATATCCTTCCTAACACATTTCCTAGCAAATAAAAATTT... |
Task1_train_42961 | Chromosome 14 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GCCATTGCCTATAATAAAAGGGCATTTATTTTACATAAATTTTATAATTCTTGTGTCACTTGAATATCCTTCCTAACACATTTCCTAGCAAATAAAAATTTTCCTCCTAAAAATCATGATGTAGACCTTGTGGCTCACAGGTTTATTGATCATACACTCACTGAGTGCCTAGGAAATCCCAGCTGCATTTAAGCATGCCTTTTTTAGCGATGATGTGAGAACAAACTGATGATTTCCAATGTGTCATGCTCTTTTGTAAACATGAATATGAGATGCCGTTATCTGGGATATCCTCTTCATATCCCAGTTGATTCACCACA... | GCCATTGCCTATAATAAAAGGGCATTTATTTTACATAAATTTTATAATTCTTGTGTCACTTGAATATCCTTCCTAACACATTTCCTAGCAAATAAAAATTTTCCTCCTAAAAATCATGATGTAGACCTTGTGGCTCACAGGTTTATTGATCATACACTCACTGAGTGCCTAGGAAATCCCAGCTGCATTTAAGCATGCCTTTTTTAGCGATGATGTGAGAACAAACTGATGATTTCCAATGTGTCATGCTCTTTTGTAAACATGAATATGAGATGCCGTTATCTGGGATATCCTCTTCATATCCCAGTTGATTCACCACA... |
Task1_train_42962 | This variant lies on Chromosome 14. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CCTATAATAAAAGGGCATTTATTTTACATAAATTTTATAATTCTTGTGTCACTTGAATATCCTTCCTAACACATTTCCTAGCAAATAAAAATTTTCCTCCTAAAAATCATGATGTAGACCTTGTGGCTCACAGGTTTATTGATCATACACTCACTGAGTGCCTAGGAAATCCCAGCTGCATTTAAGCATGCCTTTTTTAGCGATGATGTGAGAACAAACTGATGATTTCCAATGTGTCATGCTCTTTTGTAAACATGAATATGAGATGCCGTTATCTGGGATATCCTCTTCATATCCCAGTTGATTCACCACATTCCATT... | CCTATAATAAAAGGGCATTTATTTTACATAAATTTTATAATTCTTGTGTCACTTGAATATCCTTCCTAACACATTTCCTAGCAAATAAAAATTTTCCTCCTAAAAATCATGATGTAGACCTTGTGGCTCACAGGTTTATTGATCATACACTCACTGAGTGCCTAGGAAATCCCAGCTGCATTTAAGCATGCCTTTTTTAGCGATGATGTGAGAACAAACTGATGATTTCCAATGTGTCATGCTCTTTTGTAAACATGAATATGAGATGCCGTTATCTGGGATATCCTCTTCATATCCCAGTTGATTCACCACATTCCATT... |
Task1_train_42963 | Given this variant on Chromosome 14, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCAGAAGCAGAAGCCTCTATGCTTCCTGCACAGTCTGCAGAATCATGAGCCAATTAAACCTCTTTTCTTTATAAATTACTGAGTCTCAGGTATCTATAGCAATGCAAGAATAGACCAATACACCTGGTGTGGAAAATAGATTCCCTCAAAAGAATGGAGGGTTGTTACAATACTAAGGACAAGGTTTCCGTGGAAAAAGTAAAGAAAGTTAGGAACAGTGAAACTGCTTGCTCTATATTTCTGTTTAGACTTCAGGTAGAGTCAGTTAGATGAATGGGCCAAAAGAACCAGGAAAAGGAGGAAGATGCAGCTTGATCACA... | CCAGAAGCAGAAGCCTCTATGCTTCCTGCACAGTCTGCAGAATCATGAGCCAATTAAACCTCTTTTCTTTATAAATTACTGAGTCTCAGGTATCTATAGCAATGCAAGAATAGACCAATACACCTGGTGTGGAAAATAGATTCCCTCAAAAGAATGGAGGGTTGTTACAATACTAAGGACAAGGTTTCCGTGGAAAAAGTAAAGAAAGTTAGGAACAGTGAAACTGCTTGCTCTATATTTCTGTTTAGACTTCAGGTAGAGTCAGTTAGATGAATGGGCCAAAAGAACCAGGAAAAGGAGGAAGATGCAGCTTGATCACA... |
Task1_train_42964 | A variant on Chromosome 14 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATGAAGGATTTGATAATTGTATGAGGAATGGGTGAGATAACTGAAGATCCTTAGAATGGAGAAATTTCATATATGTAAAAGCACACATTATATATATACATATATTTATGTATTGAGTTGAGATTCTTAATCATAGCTGTCTGTAAATATTTAAGGGTGTGAGATGTGAATAAATAATTAGATTTAGTCTCTATAACTCCAGCAGACTAGTGAGTACAAATCACAGGAAAGGGGCTTTCCTCCTGGAAATGAGAAAGTCTTGGTTTCCCAGGTACCATTTCTCATGATCAGTATTTTACTGTCAGTTTTCTATTTGTACT... | ATGAAGGATTTGATAATTGTATGAGGAATGGGTGAGATAACTGAAGATCCTTAGAATGGAGAAATTTCATATATGTAAAAGCACACATTATATATATACATATATTTATGTATTGAGTTGAGATTCTTAATCATAGCTGTCTGTAAATATTTAAGGGTGTGAGATGTGAATAAATAATTAGATTTAGTCTCTATAACTCCAGCAGACTAGTGAGTACAAATCACAGGAAAGGGGCTTTCCTCCTGGAAATGAGAAAGTCTTGGTTTCCCAGGTACCATTTCTCATGATCAGTATTTTACTGTCAGTTTTCTATTTGTACT... |
Task1_train_42965 | A variant has been detected on Chromosome 14. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CACATTCAATTTTAAAAGTTATATATTTTTTTAAATAAATTTTCCAAGACTGTGGCGACTGCCATCTTGGGTTGCTCCTTCTTTGGTTTTTACAGTTACTGAGAAATGGCTTTTGTGATTTCTGCCACTTGCAACGTACTCTTAGAGAAAGGGATTTCGATATTAGTATATTCTCTTTCATTCTATTTCCTATGAAGTTGTTGGTGGGAATAGAAAAGACCTGCCCAAGCCATCATTGATGGATACTGGCTACATGGTCCTTGAGTAGAAAAGAGCCTGCATCCTTCATGGCCTCCAGCCACAAGCTTCTGCAAGGAAAC... | CACATTCAATTTTAAAAGTTATATATTTTTTTAAATAAATTTTCCAAGACTGTGGCGACTGCCATCTTGGGTTGCTCCTTCTTTGGTTTTTACAGTTACTGAGAAATGGCTTTTGTGATTTCTGCCACTTGCAACGTACTCTTAGAGAAAGGGATTTCGATATTAGTATATTCTCTTTCATTCTATTTCCTATGAAGTTGTTGGTGGGAATAGAAAAGACCTGCCCAAGCCATCATTGATGGATACTGGCTACATGGTCCTTGAGTAGAAAAGAGCCTGCATCCTTCATGGCCTCCAGCCACAAGCTTCTGCAAGGAAAC... |
Task1_train_42966 | With a mutation on Chromosome 14, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GCCATCTTGGGTTGCTCCTTCTTTGGTTTTTACAGTTACTGAGAAATGGCTTTTGTGATTTCTGCCACTTGCAACGTACTCTTAGAGAAAGGGATTTCGATATTAGTATATTCTCTTTCATTCTATTTCCTATGAAGTTGTTGGTGGGAATAGAAAAGACCTGCCCAAGCCATCATTGATGGATACTGGCTACATGGTCCTTGAGTAGAAAAGAGCCTGCATCCTTCATGGCCTCCAGCCACAAGCTTCTGCAAGGAAACAAAGCATGTTATGAACAAGAGGAGGAACAGTAGTTGTTTGTGCTTCTTTCTCTGTAGACA... | GCCATCTTGGGTTGCTCCTTCTTTGGTTTTTACAGTTACTGAGAAATGGCTTTTGTGATTTCTGCCACTTGCAACGTACTCTTAGAGAAAGGGATTTCGATATTAGTATATTCTCTTTCATTCTATTTCCTATGAAGTTGTTGGTGGGAATAGAAAAGACCTGCCCAAGCCATCATTGATGGATACTGGCTACATGGTCCTTGAGTAGAAAAGAGCCTGCATCCTTCATGGCCTCCAGCCACAAGCTTCTGCAAGGAAACAAAGCATGTTATGAACAAGAGGAGGAACAGTAGTTGTTTGTGCTTCTTTCTCTGTAGACA... |
Task1_train_42967 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TCATTATTACTTTTACCATTATGGATTCAAGTCATTCTTTTTATACTTCTAAATTTTATTTCAGTGGGAATATTGGAAAGATAAGACGAGAATACATATGCTTCTTAGGAATTTTGAATCAGAAGCACATCCTAGTAACATTTAAATGTTCAAACTGGCTATATGATTTTGTCTTACACATAAAAAATCTATAGGCAGAATCAAGGAATAGATCAGAAGTGCAAGGGAGAACTGATTTCAGGCTGGCGTGAGTGAACAGAGTACACAGAAAGGAGGGATTTTGTTCTGACCTTGTGAAAAGAATCCTTGTTGGCCAGGTT... | TCATTATTACTTTTACCATTATGGATTCAAGTCATTCTTTTTATACTTCTAAATTTTATTTCAGTGGGAATATTGGAAAGATAAGACGAGAATACATATGCTTCTTAGGAATTTTGAATCAGAAGCACATCCTAGTAACATTTAAATGTTCAAACTGGCTATATGATTTTGTCTTACACATAAAAAATCTATAGGCAGAATCAAGGAATAGATCAGAAGTGCAAGGGAGAACTGATTTCAGGCTGGCGTGAGTGAACAGAGTACACAGAAAGGAGGGATTTTGTTCTGACCTTGTGAAAAGAATCCTTGTTGGCCAGGTT... |
Task1_train_42968 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TGAGCATTACTCTACATTGTCAAAAAATAATAATTAGAATAGGGAAGCTAAGGGTAACATGTCCTCAAGTGGTTGATAGTTCATAAAGGTGTGAGAAAATCTTTTCTGGACCAACACATTGACAATGAGTTAGGTAATATTCAATGAAATAATCATAGGGTTGGGAATTTTGTCCAGGGGATGGCCATACCTAAGGCATAGTTAATATGTGGAATACTATGATCCATATGAGTGGTCATATTTAGACCATTACATTCAGTTCTTAATGCTATACTCAAAAGGCCAAATATTGACCTAAATTATCTGTCACCAAAAGGAGG... | TGAGCATTACTCTACATTGTCAAAAAATAATAATTAGAATAGGGAAGCTAAGGGTAACATGTCCTCAAGTGGTTGATAGTTCATAAAGGTGTGAGAAAATCTTTTCTGGACCAACACATTGACAATGAGTTAGGTAATATTCAATGAAATAATCATAGGGTTGGGAATTTTGTCCAGGGGATGGCCATACCTAAGGCATAGTTAATATGTGGAATACTATGATCCATATGAGTGGTCATATTTAGACCATTACATTCAGTTCTTAATGCTATACTCAAAAGGCCAAATATTGACCTAAATTATCTGTCACCAAAAGGAGG... |
Task1_train_42969 | A variant on Chromosome 14 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GGAATACTATGATCCATATGAGTGGTCATATTTAGACCATTACATTCAGTTCTTAATGCTATACTCAAAAGGCCAAATATTGACCTAAATTATCTGTCACCAAAAGGAGGGAAACTCATCCAATAAAGGATTTGAGAATTATATTGTATGAGGAATGAGTGAGAAAAGAGAAAATCCTTAGAATGGAGAAGTTTTACATATGTAAAAACACACATTTTATGTATACATATCTATATTTATATGTTTTAGTTGCTATTTTTCATCATAACTGTCCTTACATACTTAAGGGTGCAAGATGTGAATAAGAAATTATATTCAGT... | GGAATACTATGATCCATATGAGTGGTCATATTTAGACCATTACATTCAGTTCTTAATGCTATACTCAAAAGGCCAAATATTGACCTAAATTATCTGTCACCAAAAGGAGGGAAACTCATCCAATAAAGGATTTGAGAATTATATTGTATGAGGAATGAGTGAGAAAAGAGAAAATCCTTAGAATGGAGAAGTTTTACATATGTAAAAACACACATTTTATGTATACATATCTATATTTATATGTTTTAGTTGCTATTTTTCATCATAACTGTCCTTACATACTTAAGGGTGCAAGATGTGAATAAGAAATTATATTCAGT... |
Task1_train_42970 | A mutation on Chromosome 14 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGCTCACGTATTTTTTTCTAGCTTCTAAAGTGCCTTTCATACATGGAACTTTGTCTTCATTAGGAAATTTATTTCAATAGCGTCAAGACATCAAATAATTTATGTATTTGGTGTCCATTTTTATAAAGATACATGAAATATATGAGAAGGTTAAGAAGAGGTAAAGGAGGTTAAGGAACCTCATCGGCTCCATTATATTTGGAAGTTGTGACCTGTGTTAAAGCATTGACTATCACTGTTTATATTTATCATAATTTGGCATGCAAAAATGAGAGTCACAATTTCAGCCACTTGCATTAATTTTACTTCTAAGAGATTGA... | TGCTCACGTATTTTTTTCTAGCTTCTAAAGTGCCTTTCATACATGGAACTTTGTCTTCATTAGGAAATTTATTTCAATAGCGTCAAGACATCAAATAATTTATGTATTTGGTGTCCATTTTTATAAAGATACATGAAATATATGAGAAGGTTAAGAAGAGGTAAAGGAGGTTAAGGAACCTCATCGGCTCCATTATATTTGGAAGTTGTGACCTGTGTTAAAGCATTGACTATCACTGTTTATATTTATCATAATTTGGCATGCAAAAATGAGAGTCACAATTTCAGCCACTTGCATTAATTTTACTTCTAAGAGATTGA... |
Task1_train_42971 | A change on Chromosome 14 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TAGCGTCAAGACATCAAATAATTTATGTATTTGGTGTCCATTTTTATAAAGATACATGAAATATATGAGAAGGTTAAGAAGAGGTAAAGGAGGTTAAGGAACCTCATCGGCTCCATTATATTTGGAAGTTGTGACCTGTGTTAAAGCATTGACTATCACTGTTTATATTTATCATAATTTGGCATGCAAAAATGAGAGTCACAATTTCAGCCACTTGCATTAATTTTACTTCTAAGAGATTGAATTTTATAATAGAGTCGGGTAGTTATTACATAAAAAGTTTTGCGTTATTCCTTTTCAACTTTGAGTTTAATACATTA... | TAGCGTCAAGACATCAAATAATTTATGTATTTGGTGTCCATTTTTATAAAGATACATGAAATATATGAGAAGGTTAAGAAGAGGTAAAGGAGGTTAAGGAACCTCATCGGCTCCATTATATTTGGAAGTTGTGACCTGTGTTAAAGCATTGACTATCACTGTTTATATTTATCATAATTTGGCATGCAAAAATGAGAGTCACAATTTCAGCCACTTGCATTAATTTTACTTCTAAGAGATTGAATTTTATAATAGAGTCGGGTAGTTATTACATAAAAAGTTTTGCGTTATTCCTTTTCAACTTTGAGTTTAATACATTA... |
Task1_train_42972 | A variant was discovered on Chromosome 14. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ATTATTTTGTGGTATATTCCTTCCATGCTTAGTTTGTTGAGGGTTTTTATCATAAAGTGATGTTGGACTTTATTGAAAGCTGACTGCATCTATTGACATGATCATATGGTTTTGCTTTTAATTCTGTTTCTGTGGTGAATCACATTTATTGATTCGTCTATGTTGAACAAACCTTGCACCCCAGGAATGAAGCCTACTTGACCTTGAATTAACTTTTTGATGTACTGCTGGATTCAGTTTGCTAGTATTTTTGTTGAGGATTTTTACGTTTAAGTTTGTCAGGGATATTGACTGATATTTTCTTTTTTCATTGTGTCTCT... | ATTATTTTGTGGTATATTCCTTCCATGCTTAGTTTGTTGAGGGTTTTTATCATAAAGTGATGTTGGACTTTATTGAAAGCTGACTGCATCTATTGACATGATCATATGGTTTTGCTTTTAATTCTGTTTCTGTGGTGAATCACATTTATTGATTCGTCTATGTTGAACAAACCTTGCACCCCAGGAATGAAGCCTACTTGACCTTGAATTAACTTTTTGATGTACTGCTGGATTCAGTTTGCTAGTATTTTTGTTGAGGATTTTTACGTTTAAGTTTGTCAGGGATATTGACTGATATTTTCTTTTTTCATTGTGTCTCT... |
Task1_train_42973 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | TTCTTGTAAATTTGTTTGAGTTCATTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGATTGCAAAAATTTTCTCCCATTCTGTAGGTTGCCTGTTCACTCTGATGGTAGTTTCTTTTGCTGTGCAGAAGCTCTTTAGTTTAATTAGATCTCATTTGTCAATTTTGTCTTTTGTTGCCATTGCTTTTGGTGTTTTAGACATGAAGTCCTTGCCCATGCCTATGTCCTGAATGGTATTGCCTAGGTTTTCTTCTAGGGAGTTTATGGTTTTAGGTCTAACATGTAAGTCTTTAATCCATCTGGAATTAATTTTCGT... | TTCTTGTAAATTTGTTTGAGTTCATTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGATTGCAAAAATTTTCTCCCATTCTGTAGGTTGCCTGTTCACTCTGATGGTAGTTTCTTTTGCTGTGCAGAAGCTCTTTAGTTTAATTAGATCTCATTTGTCAATTTTGTCTTTTGTTGCCATTGCTTTTGGTGTTTTAGACATGAAGTCCTTGCCCATGCCTATGTCCTGAATGGTATTGCCTAGGTTTTCTTCTAGGGAGTTTATGGTTTTAGGTCTAACATGTAAGTCTTTAATCCATCTGGAATTAATTTTCGT... |
Task1_train_42974 | A mutation has occurred on Chromosome 14. What is the medical relevance of this mutation? | Benign | AGTAAATTATCTCCTACTCTGTTTCAATTCACGTGTCTCTTTCATTCAATGCATCTATGCATTTATCCATTCATCTACCTAACTAGTATCTGTATTTATTCTAGTCTAACAGAGTGGAAAACATCACTTTGGAAGTCAACACTTTTTTGAATTATACATGTTATCCTTCAAGCCCACATTAACTTCTGTAGTATAACTTTACAAGGTTTTCACCCACATACAGCCCAATATCCAGTCACACTAATCTGTGCCTAAAATTCCCTTATCCATTCTTTTTATGGGGAAATCTATCATGGTTTGTGGCCCAGTTCAAGCATCTC... | AGTAAATTATCTCCTACTCTGTTTCAATTCACGTGTCTCTTTCATTCAATGCATCTATGCATTTATCCATTCATCTACCTAACTAGTATCTGTATTTATTCTAGTCTAACAGAGTGGAAAACATCACTTTGGAAGTCAACACTTTTTTGAATTATACATGTTATCCTTCAAGCCCACATTAACTTCTGTAGTATAACTTTACAAGGTTTTCACCCACATACAGCCCAATATCCAGTCACACTAATCTGTGCCTAAAATTCCCTTATCCATTCTTTTTATGGGGAAATCTATCATGGTTTGTGGCCCAGTTCAAGCATCTC... |
Task1_train_42975 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | TTGGCTCACTACAACCTCCGCCTCCCAGGTTCAAGCGATTCTCATGTCCCAGCCTCCCAAGTAACTGGGACTACAGGCACAAGCCACCATGCCCAGCTAATTATTTGTATTTTTAGTAGAGATGGGATTTCACCATGTTGACCAGGCTGGTCTTGACTTCCTGGCCTCAGATGATCTTCCCACCTCAGCCTCCCAAAGGGCTGGAATTACAGGCGTGAGCCACCACGCCCAGCTTCAAGGTTTCTTTAGTACTTTTTCCACTATCTATCCCATCAGTGTTTGGGTTCCTTGAGGATTTTTTTAAGTCCCTATTCTCTTCT... | TTGGCTCACTACAACCTCCGCCTCCCAGGTTCAAGCGATTCTCATGTCCCAGCCTCCCAAGTAACTGGGACTACAGGCACAAGCCACCATGCCCAGCTAATTATTTGTATTTTTAGTAGAGATGGGATTTCACCATGTTGACCAGGCTGGTCTTGACTTCCTGGCCTCAGATGATCTTCCCACCTCAGCCTCCCAAAGGGCTGGAATTACAGGCGTGAGCCACCACGCCCAGCTTCAAGGTTTCTTTAGTACTTTTTCCACTATCTATCCCATCAGTGTTTGGGTTCCTTGAGGATTTTTTTAAGTCCCTATTCTCTTCT... |
Task1_train_42976 | A genomic change on Chromosome 14 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AAAAAGAAAATGCATATGCATTGTATTTTCCCATTTAAGATATTAACAAATAGTCATATGGCCAATCTGACTATCTTTACTAATGACTGTATGCAATGGCTGAAACAATCCTCTCGGTACACAAGATTTTGTGATATTTGAATACATACTATACTCACACCACAACATCTATATCCTTAAATCACTATACCAATGCACAAACAGTTTACATATCAATTCATGATTATGTGTTCACATCTTTCTGTCTAGTAACTGCTGGGGTTACAAGAGTGAAAAAAAAAGCACAACCTTTTCCACAAGGAACTTGTAGATGAGCCCAA... | AAAAAGAAAATGCATATGCATTGTATTTTCCCATTTAAGATATTAACAAATAGTCATATGGCCAATCTGACTATCTTTACTAATGACTGTATGCAATGGCTGAAACAATCCTCTCGGTACACAAGATTTTGTGATATTTGAATACATACTATACTCACACCACAACATCTATATCCTTAAATCACTATACCAATGCACAAACAGTTTACATATCAATTCATGATTATGTGTTCACATCTTTCTGTCTAGTAACTGCTGGGGTTACAAGAGTGAAAAAAAAAGCACAACCTTTTCCACAAGGAACTTGTAGATGAGCCCAA... |
Task1_train_42977 | This sequence variant lies on Chromosome 14. Is it clinically significant, and what condition might it cause if any? | Benign | AATGATTTCCAGCTAACATCGGTCTCAAGTTTTATTCATTTTATCAATTAGCAATTGTTAACTGGTTGCCTGCTGAGTTCTGCATAAATGTTACATGCTGGGAAAAAAAGAGCTATGGAAAAATACATATCTTCTTTGACTAAATTGTAGTCTAGTTAGTTATGTAGGCAGCTAATCAGACAGAGTAAAGTGAAATGAGGCCAACCTTGGGAAAGCAAAGGGAGGTATGAAGGCATATGGAAAGTCCCACCCCCATCTTAGCCTTAGAGGTGAGTCAGGGGCAGCCTGTAGTATGTCTTGCCTATGCTGAGACCTAAAGA... | AATGATTTCCAGCTAACATCGGTCTCAAGTTTTATTCATTTTATCAATTAGCAATTGTTAACTGGTTGCCTGCTGAGTTCTGCATAAATGTTACATGCTGGGAAAAAAAGAGCTATGGAAAAATACATATCTTCTTTGACTAAATTGTAGTCTAGTTAGTTATGTAGGCAGCTAATCAGACAGAGTAAAGTGAAATGAGGCCAACCTTGGGAAAGCAAAGGGAGGTATGAAGGCATATGGAAAGTCCCACCCCCATCTTAGCCTTAGAGGTGAGTCAGGGGCAGCCTGTAGTATGTCTTGCCTATGCTGAGACCTAAAGA... |
Task1_train_42978 | A change on Chromosome 14 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCACAAGGTCAGGAGTTCAAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATATAAAAAAAAAATTAGCTGGGCGTGATGATGCGCACCTATAGTCCCAGCTACTTGGGAGACTGAGGCAGGAGAATCACTTGAATCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGTGACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAGTTACATCAATTAAGGGGCAAGATGCTAATTAA... | GTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCACAAGGTCAGGAGTTCAAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATATAAAAAAAAAATTAGCTGGGCGTGATGATGCGCACCTATAGTCCCAGCTACTTGGGAGACTGAGGCAGGAGAATCACTTGAATCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGTGACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAGTTACATCAATTAAGGGGCAAGATGCTAATTAA... |
Task1_train_42979 | This variant is found on Chromosome 14. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TGAAGCATGTCTGACCCCCACTTCCCATTCTGGCCTGAACCAATCTCTCAAGTTGAATTTTAAGAGAGCCCTGGCCAAGAAGGAAGTCCACTCAGATGGTTGCGGGGGGCTGGGGGGCCTTAGAATTTTATTTTTGATCTACAGTTTCCTAGAATCACCTATAATAAACTATTTACACACAAATTATTGTGTCGAAGCTGACTTTTAGGGATCCAAAACCAAGATACAGGAATTCAAATCATGAGACAAGGGTGAAGATTATCCAGAAGAAATGTTGGTGCCCCTTCTCTTATTGCTACCAAGCTGAGCTTTGCAGCACA... | TGAAGCATGTCTGACCCCCACTTCCCATTCTGGCCTGAACCAATCTCTCAAGTTGAATTTTAAGAGAGCCCTGGCCAAGAAGGAAGTCCACTCAGATGGTTGCGGGGGGCTGGGGGGCCTTAGAATTTTATTTTTGATCTACAGTTTCCTAGAATCACCTATAATAAACTATTTACACACAAATTATTGTGTCGAAGCTGACTTTTAGGGATCCAAAACCAAGATACAGGAATTCAAATCATGAGACAAGGGTGAAGATTATCCAGAAGAAATGTTGGTGCCCCTTCTCTTATTGCTACCAAGCTGAGCTTTGCAGCACA... |
Task1_train_42980 | The following genetic variant occurs on Chromosome 14. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CCTCCTTCCCTCCAGTCTCCTGAAGGTGTCTCCATTGGCCAAACCAAATGGGATGGAGAGCCGGTGGATGCTGCCAATTAAGGTCAGGCTCAGAGTAAGAAGTAGAGTGGATGTGCAGAGGCAAACAGACTCAGTCTCAACTGCAATGCCACTTCCTCTTCAGGGAAGCCTTCCCTGACCTCCTGACCAAACCTGGCCTCTGTAACATGCTCCCATAGTCCTTCTGCTTCTGCAGAATATTTATAGCTGCAATGGAGGGATAAATTATGCAAATTATTAAGTGATGACTGGCTCTCATGCTAGAACATAAGCTCCATGAA... | CCTCCTTCCCTCCAGTCTCCTGAAGGTGTCTCCATTGGCCAAACCAAATGGGATGGAGAGCCGGTGGATGCTGCCAATTAAGGTCAGGCTCAGAGTAAGAAGTAGAGTGGATGTGCAGAGGCAAACAGACTCAGTCTCAACTGCAATGCCACTTCCTCTTCAGGGAAGCCTTCCCTGACCTCCTGACCAAACCTGGCCTCTGTAACATGCTCCCATAGTCCTTCTGCTTCTGCAGAATATTTATAGCTGCAATGGAGGGATAAATTATGCAAATTATTAAGTGATGACTGGCTCTCATGCTAGAACATAAGCTCCATGAA... |
Task1_train_42981 | This genomic variant is located on Chromosome 14. Can you determine its pathogenicity and name any linked disease? | Benign | ATGTCCAGAGTCATTCAGTGAGGCAGGGATATTGCTGGGAGCAGAACCAAGGTCTCAAGATTTTCAGCCCAAAGTTCCTGCTATAAGAACATACTGCATCCCCAAATGAGGACAAGATGTCAAAGTGAGTATCAGCTAGAATGAACTTCAGGATTGTCCCATATTTAGCATATAAATGAGCCACCCTCTAGCCCACTATGCCAGAAACAAAAAAAATCCTGGCATATCACAGGACCATGAATTTCCCACACCAAAAGGAGCCTCCAGGGAAGATTTAAGGCAAGAGCCAGGAGGGATTATGGCTGCCTTCTGATCTGGGG... | ATGTCCAGAGTCATTCAGTGAGGCAGGGATATTGCTGGGAGCAGAACCAAGGTCTCAAGATTTTCAGCCCAAAGTTCCTGCTATAAGAACATACTGCATCCCCAAATGAGGACAAGATGTCAAAGTGAGTATCAGCTAGAATGAACTTCAGGATTGTCCCATATTTAGCATATAAATGAGCCACCCTCTAGCCCACTATGCCAGAAACAAAAAAAATCCTGGCATATCACAGGACCATGAATTTCCCACACCAAAAGGAGCCTCCAGGGAAGATTTAAGGCAAGAGCCAGGAGGGATTATGGCTGCCTTCTGATCTGGGG... |
Task1_train_42982 | A variant has been detected on Chromosome 14. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GGGGAGGGCAGGGACATTTGCACAGCATTTCTGGATAAATTAGATCCAAATAATCAAATCAAAGACTCTCAGCTCAGAAAGTAATTAAAGATCTCCTCACCCACCTCTTTAATTTTGCAAATGAAGACAGTGAAACTCAGAGAGGTTATGAACTTGCTCAAGGTCACACAACTGATCCTGATATCAAGGTCCAGGGCAAAGCCAAGACAGCTCATAGTTCTCACCAGCCCAGACCCAAGGGAGAAAAAAACATCATAGTCCTTGGCCACGGCAGCATCATTTGCATCCCAAACATTCTTTACCCAAGACTTAATGAACTC... | GGGGAGGGCAGGGACATTTGCACAGCATTTCTGGATAAATTAGATCCAAATAATCAAATCAAAGACTCTCAGCTCAGAAAGTAATTAAAGATCTCCTCACCCACCTCTTTAATTTTGCAAATGAAGACAGTGAAACTCAGAGAGGTTATGAACTTGCTCAAGGTCACACAACTGATCCTGATATCAAGGTCCAGGGCAAAGCCAAGACAGCTCATAGTTCTCACCAGCCCAGACCCAAGGGAGAAAAAAACATCATAGTCCTTGGCCACGGCAGCATCATTTGCATCCCAAACATTCTTTACCCAAGACTTAATGAACTC... |
Task1_train_42983 | A genomic change on Chromosome 14 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTCTATTCTCCAAATTTATTCCCACTGATTCCCTTTCATGAATGCTCTGCTCCAGGAAAACTAGGTATCTCCCTCCCTTGAATATTTACACATGCCCACACCTGTACCCTGTGTCCATACATCAGACATCCTGGACCCACCACCTAAAACAGGCTTGCACAGGTGACAAAATTTGGCCTCATCATCTCTCAGCCTTGAGACCCAGCACAGGCATCACCAGATTTAGTTTCATAGGAAGAGCATGAAAAATCATATCATTTTTTAATTAAGCAGGCCAAGGTAAGAGATCCATCAGACAAAGAAGCAAAGTAGGAAGGAGA... | TTCTATTCTCCAAATTTATTCCCACTGATTCCCTTTCATGAATGCTCTGCTCCAGGAAAACTAGGTATCTCCCTCCCTTGAATATTTACACATGCCCACACCTGTACCCTGTGTCCATACATCAGACATCCTGGACCCACCACCTAAAACAGGCTTGCACAGGTGACAAAATTTGGCCTCATCATCTCTCAGCCTTGAGACCCAGCACAGGCATCACCAGATTTAGTTTCATAGGAAGAGCATGAAAAATCATATCATTTTTTAATTAAGCAGGCCAAGGTAAGAGATCCATCAGACAAAGAAGCAAAGTAGGAAGGAGA... |
Task1_train_42984 | This mutation is located on Chromosome 14. Is it associated with a disease or is it a benign polymorphism? | Benign | GACATGGCTAATACTGCAAGAAGGGAGTTAGGTTAGTGGTAAAACCTTTCTAATAGGTTTTTGAACAGTGAAAATGAGCTGTCAGGAGTAGTTGCCAGGGCACTTTCTCTAGAGAGTTTTTGAAAGGAGATAGACACCCTGCTATCAGAGGTGATTGGAGTGCAGCCCTGCCTCGAGGCAGGAGGAGAAATGAGAGAACCTCTTAAAGCCTCTTTCCAGCCCCCAGAGCCTGTCTCCATGAAAAAGGCCCAGGCTCATTAATGCAGAGCTGCATCCTCCAGGACACAGGGGGTTGCTGGGTTGTTAAGTTTGGAACCTTT... | GACATGGCTAATACTGCAAGAAGGGAGTTAGGTTAGTGGTAAAACCTTTCTAATAGGTTTTTGAACAGTGAAAATGAGCTGTCAGGAGTAGTTGCCAGGGCACTTTCTCTAGAGAGTTTTTGAAAGGAGATAGACACCCTGCTATCAGAGGTGATTGGAGTGCAGCCCTGCCTCGAGGCAGGAGGAGAAATGAGAGAACCTCTTAAAGCCTCTTTCCAGCCCCCAGAGCCTGTCTCCATGAAAAAGGCCCAGGCTCATTAATGCAGAGCTGCATCCTCCAGGACACAGGGGGTTGCTGGGTTGTTAAGTTTGGAACCTTT... |
Task1_train_42985 | This sequence change occurs on Chromosome 14. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGGTAAAGAACATTTACTTGCAGTGTCCTGTTTCAAATATTGTGTGCATTGAGCACAGAGGACACAAGAATGAACCCAAGCAGAAAACTAAAGAAAAGAAATCAATAAAACCACTGAAGAAAACCAGTTGCCCTTATCTTGCCTGTCTCTGATAATGAATGTGCCTTCCCTGCTCATTCCTCACTTTGGTTCTCAAATTTTCCAGGGAATTAGCAAAGAACTGGTAGGGTTGGGTTAGTCTTGGTCTAATTTGGTTAGTCATCTCTGGATAACAAGTCTCCTTTTTAGGAAGTGCCAGGGGATTTTTTGTAATGCCAATA... | AGGTAAAGAACATTTACTTGCAGTGTCCTGTTTCAAATATTGTGTGCATTGAGCACAGAGGACACAAGAATGAACCCAAGCAGAAAACTAAAGAAAAGAAATCAATAAAACCACTGAAGAAAACCAGTTGCCCTTATCTTGCCTGTCTCTGATAATGAATGTGCCTTCCCTGCTCATTCCTCACTTTGGTTCTCAAATTTTCCAGGGAATTAGCAAAGAACTGGTAGGGTTGGGTTAGTCTTGGTCTAATTTGGTTAGTCATCTCTGGATAACAAGTCTCCTTTTTAGGAAGTGCCAGGGGATTTTTTGTAATGCCAATA... |
Task1_train_42986 | With a mutation on Chromosome 14, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TGTCCATGTGGACACTCTGTGTGACTCGGATCCAGGATCTGCTCTTTCAGCCCCTCCATTTATCGCAAAAGGGATGATGATTAATTCCTCCATGCCTAGACTTCACTTTAGACATCACCTCAGAGAGGCCTGTCTTACCCAGCCAATCTAACAAGCCATCAAACACAGCCACTGCCTGGCTGCTCTCTACCCTGTTATTTAGCCTGATTTTAATTCACACACTTTCATCACTTAACATTATACTATCTGTGTATTTATTGTTTGCCTTCTTCTAGACCGTAGACACCAGGAGGACGGGGACAGTGTCTAAGTGGCTCTCA... | TGTCCATGTGGACACTCTGTGTGACTCGGATCCAGGATCTGCTCTTTCAGCCCCTCCATTTATCGCAAAAGGGATGATGATTAATTCCTCCATGCCTAGACTTCACTTTAGACATCACCTCAGAGAGGCCTGTCTTACCCAGCCAATCTAACAAGCCATCAAACACAGCCACTGCCTGGCTGCTCTCTACCCTGTTATTTAGCCTGATTTTAATTCACACACTTTCATCACTTAACATTATACTATCTGTGTATTTATTGTTTGCCTTCTTCTAGACCGTAGACACCAGGAGGACGGGGACAGTGTCTAAGTGGCTCTCA... |
Task1_train_42987 | This variant lies on Chromosome 14. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACCTCCAAATTAAAAGCGGCAAAGAGATAAGGTTGAACTAGACGTACATGGGGATAAAAAGTATAAAAGGTACATGGGAATGAAAGGATAAAAAGGCTAAAAAAATTAAGTACCTCTAACTCAGCCCCTGTTGCCATTTCTCAGAGTCTTGTGTTCTGTGGCATTGCGCTTTCTAGACCAACAGTGTCCAATAGAACTTTCTGTGGCAATGGAAATGTCCTGTCAATCTGCACTGTCCCATACAATAGCCACCAGCTACATGTGGCTATTGAGCTCTTGAAATGAAGTTTCCATTTTTAATTGAAAACATTTTATTTCAC... | ACCTCCAAATTAAAAGCGGCAAAGAGATAAGGTTGAACTAGACGTACATGGGGATAAAAAGTATAAAAGGTACATGGGAATGAAAGGATAAAAAGGCTAAAAAAATTAAGTACCTCTAACTCAGCCCCTGTTGCCATTTCTCAGAGTCTTGTGTTCTGTGGCATTGCGCTTTCTAGACCAACAGTGTCCAATAGAACTTTCTGTGGCAATGGAAATGTCCTGTCAATCTGCACTGTCCCATACAATAGCCACCAGCTACATGTGGCTATTGAGCTCTTGAAATGAAGTTTCCATTTTTAATTGAAAACATTTTATTTCAC... |
Task1_train_42988 | Consider this mutation on Chromosome 14. Is this a benign change or a disease-causing variant? | Benign | ATACAATAGCCACCAGCTACATGTGGCTATTGAGCTCTTGAAATGAAGTTTCCATTTTTAATTGAAAACATTTTATTTCACATTGACTAATTTTTATTTCAACAGCCACATGTAGCTAGAGACTATTATACCAGACAGAGCAGCCTAGATCTTCTCCAGTCTGACACCCACCAGCCCCAGGACTTGAGTGAGTGTTTAACCAGGACTCAAAGTTGGGTTTCTGCCCCACAAGGCCACCCCCTTTCCTCTTTAAAGCCAACCTGCATCTGGTGGCCCCTGATCCCCTGCCTTGAGGATCGGCACTTCCAGACTCCTCTCCC... | ATACAATAGCCACCAGCTACATGTGGCTATTGAGCTCTTGAAATGAAGTTTCCATTTTTAATTGAAAACATTTTATTTCACATTGACTAATTTTTATTTCAACAGCCACATGTAGCTAGAGACTATTATACCAGACAGAGCAGCCTAGATCTTCTCCAGTCTGACACCCACCAGCCCCAGGACTTGAGTGAGTGTTTAACCAGGACTCAAAGTTGGGTTTCTGCCCCACAAGGCCACCCCCTTTCCTCTTTAAAGCCAACCTGCATCTGGTGGCCCCTGATCCCCTGCCTTGAGGATCGGCACTTCCAGACTCCTCTCCC... |
Task1_train_42989 | A variant on Chromosome 14 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTGACCTCTGAGTGCAACTGGAGTCACAGCCACTCAGGAGAAAGGGCAGGCTATGCAAGCACGTGCTTCAGGAGCATCCTGGTGAGGTCTTCAGCTCTGACAGAGCAACCCCTCTGCTGCTACCCTCACTGGGGGCAGCCATCTGAGTCTTAAGGAGTTGCTTATTTTTTAGGTCCAAACATAAAATTCAACTCCCCTGGGATCACGTATACAGACAGGCCTATAGCACCTTATTATCAGGTACCATCCTAGTGTGGAAGTCCCCTGGCCTGTGTGCTCTGTGGGATGGGAATGTCCCTTGTCATCAATGTGTCCCCAGG... | TTGACCTCTGAGTGCAACTGGAGTCACAGCCACTCAGGAGAAAGGGCAGGCTATGCAAGCACGTGCTTCAGGAGCATCCTGGTGAGGTCTTCAGCTCTGACAGAGCAACCCCTCTGCTGCTACCCTCACTGGGGGCAGCCATCTGAGTCTTAAGGAGTTGCTTATTTTTTAGGTCCAAACATAAAATTCAACTCCCCTGGGATCACGTATACAGACAGGCCTATAGCACCTTATTATCAGGTACCATCCTAGTGTGGAAGTCCCCTGGCCTGTGTGCTCTGTGGGATGGGAATGTCCCTTGTCATCAATGTGTCCCCAGG... |
Task1_train_42990 | A mutation located on Chromosome 14 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TCTGAGTCTTAAGGAGTTGCTTATTTTTTAGGTCCAAACATAAAATTCAACTCCCCTGGGATCACGTATACAGACAGGCCTATAGCACCTTATTATCAGGTACCATCCTAGTGTGGAAGTCCCCTGGCCTGTGTGCTCTGTGGGATGGGAATGTCCCTTGTCATCAATGTGTCCCCAGGAACTAGAACAGTGCCTGGCACACAACAGATGCCGTTAAATGAATAAGTGAATGACTCCTGCAGTTAGGCTCTGGGTGGGGGGAGCTGAGTGTGAGGAGTGGGGAGTACAGGAGAAAGGAAAGTGGGGATTAGTAGAGGAAG... | TCTGAGTCTTAAGGAGTTGCTTATTTTTTAGGTCCAAACATAAAATTCAACTCCCCTGGGATCACGTATACAGACAGGCCTATAGCACCTTATTATCAGGTACCATCCTAGTGTGGAAGTCCCCTGGCCTGTGTGCTCTGTGGGATGGGAATGTCCCTTGTCATCAATGTGTCCCCAGGAACTAGAACAGTGCCTGGCACACAACAGATGCCGTTAAATGAATAAGTGAATGACTCCTGCAGTTAGGCTCTGGGTGGGGGGAGCTGAGTGTGAGGAGTGGGGAGTACAGGAGAAAGGAAAGTGGGGATTAGTAGAGGAAG... |
Task1_train_42991 | An alteration has been detected on Chromosome 14. Is it pathogenic, and if so, what disease is involved? | Benign | TGATTAAGCGCTTGCTTAGTACAGGGCAGACCCTCGAGACTTATGCTCAGGCCAGTGTCTCCTGGGAGGGAAGGAGGTGGGGAGGCCGTATTTGCCCCCACACAGAGCTAGGGCTGATTCTCTGAGGGACCCCCCCCCAATAGCACCTCCCCCCTTACCCTGATGCTTGTCCATTAGGTGATGGCCCTAATGGACGCCTTGATGGACACGTCCGGGACCCAGGGACCCGGAGACCAGGAATCTGCTGGTCTCAGGGAGCCGCAGAACCTGAAACCCAAAAATACCAGGCTTGATCGCCTGCTCTTCGGTAGTGTCGCCAT... | TGATTAAGCGCTTGCTTAGTACAGGGCAGACCCTCGAGACTTATGCTCAGGCCAGTGTCTCCTGGGAGGGAAGGAGGTGGGGAGGCCGTATTTGCCCCCACACAGAGCTAGGGCTGATTCTCTGAGGGACCCCCCCCCAATAGCACCTCCCCCCTTACCCTGATGCTTGTCCATTAGGTGATGGCCCTAATGGACGCCTTGATGGACACGTCCGGGACCCAGGGACCCGGAGACCAGGAATCTGCTGGTCTCAGGGAGCCGCAGAACCTGAAACCCAAAAATACCAGGCTTGATCGCCTGCTCTTCGGTAGTGTCGCCAT... |
Task1_train_42992 | This mutation occurs on Chromosome 14. Does this change lead to a known medical condition, or is it benign? | Benign | CCAAATGCAAGTGATGGTGGCTGACTCCCCTGATATAGCTAGCTCTGAATAAGTGGCATCTGTGCTCATTTAAGTAGTCTTCATTTATGTCCACAGAACTCTGCAGCAGTTCCTTAGGTATGCATGTGTCCTTCTGACCAGTTCCACGCAGAGCATAGGGGTTAATTTAGCAAAGTGGATGCTGCAGCACTGGCGGCCAAGCAAGACAAGAAATTAAACCTCAGAGATTCTGATGATATTGAAAAGCTGGTTTGCACTGAGCTGAACCACAGGCCCAGAGTGGGTCCAAGTAAGCATCCCAGACAGTGTTTGGGCACCAA... | CCAAATGCAAGTGATGGTGGCTGACTCCCCTGATATAGCTAGCTCTGAATAAGTGGCATCTGTGCTCATTTAAGTAGTCTTCATTTATGTCCACAGAACTCTGCAGCAGTTCCTTAGGTATGCATGTGTCCTTCTGACCAGTTCCACGCAGAGCATAGGGGTTAATTTAGCAAAGTGGATGCTGCAGCACTGGCGGCCAAGCAAGACAAGAAATTAAACCTCAGAGATTCTGATGATATTGAAAAGCTGGTTTGCACTGAGCTGAACCACAGGCCCAGAGTGGGTCCAAGTAAGCATCCCAGACAGTGTTTGGGCACCAA... |
Task1_train_42993 | This genomic variant is located on Chromosome 14. Can you determine its pathogenicity and name any linked disease? | Benign | TGTCCACAGAACTCTGCAGCAGTTCCTTAGGTATGCATGTGTCCTTCTGACCAGTTCCACGCAGAGCATAGGGGTTAATTTAGCAAAGTGGATGCTGCAGCACTGGCGGCCAAGCAAGACAAGAAATTAAACCTCAGAGATTCTGATGATATTGAAAAGCTGGTTTGCACTGAGCTGAACCACAGGCCCAGAGTGGGTCCAAGTAAGCATCCCAGACAGTGTTTGGGCACCAAGAATTCAGACTAGGAATGCAGTTAAAAACAGATTCTTGGCTGGGCGCAGTGGCTCATGCCTCTAATCCCAGCACTTTGGGAGGCCGA... | TGTCCACAGAACTCTGCAGCAGTTCCTTAGGTATGCATGTGTCCTTCTGACCAGTTCCACGCAGAGCATAGGGGTTAATTTAGCAAAGTGGATGCTGCAGCACTGGCGGCCAAGCAAGACAAGAAATTAAACCTCAGAGATTCTGATGATATTGAAAAGCTGGTTTGCACTGAGCTGAACCACAGGCCCAGAGTGGGTCCAAGTAAGCATCCCAGACAGTGTTTGGGCACCAAGAATTCAGACTAGGAATGCAGTTAAAAACAGATTCTTGGCTGGGCGCAGTGGCTCATGCCTCTAATCCCAGCACTTTGGGAGGCCGA... |
Task1_train_42994 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | CATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCACGCGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCACCACTGCACTCCATCCTGGGCGACAGAGTGAGACTCCGTCTCAAAACAAAAACAAAACAGATTCTTTCCAGGTGTATGGAGCCAGAAAAGGGGAGAAGCTATGCCTTGTGGAGAGATAATGAACTTTGTAGTCAAGCTGCTTTTTGGTCACAAGAATCTAAGACCTTCTCAAGATAGCTCAATAAAAAGG... | CATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCACGCGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCACCACTGCACTCCATCCTGGGCGACAGAGTGAGACTCCGTCTCAAAACAAAAACAAAACAGATTCTTTCCAGGTGTATGGAGCCAGAAAAGGGGAGAAGCTATGCCTTGTGGAGAGATAATGAACTTTGTAGTCAAGCTGCTTTTTGGTCACAAGAATCTAAGACCTTCTCAAGATAGCTCAATAAAAAGG... |
Task1_train_42995 | This alteration occurs on Chromosome 14. Is it associated with a disease or is it a benign variant? | Benign | CTAAAAATACAAAAATTAGCCAGGCATGGTGGCACGCGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCACCACTGCACTCCATCCTGGGCGACAGAGTGAGACTCCGTCTCAAAACAAAAACAAAACAGATTCTTTCCAGGTGTATGGAGCCAGAAAAGGGGAGAAGCTATGCCTTGTGGAGAGATAATGAACTTTGTAGTCAAGCTGCTTTTTGGTCACAAGAATCTAAGACCTTCTCAAGATAGCTCAATAAAAAGGGATTTCAT... | CTAAAAATACAAAAATTAGCCAGGCATGGTGGCACGCGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCACCACTGCACTCCATCCTGGGCGACAGAGTGAGACTCCGTCTCAAAACAAAAACAAAACAGATTCTTTCCAGGTGTATGGAGCCAGAAAAGGGGAGAAGCTATGCCTTGTGGAGAGATAATGAACTTTGTAGTCAAGCTGCTTTTTGGTCACAAGAATCTAAGACCTTCTCAAGATAGCTCAATAAAAAGGGATTTCAT... |
Task1_train_42996 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TTCAAGAAACAGAACACCCAAGCAACAGACTTAGAGTCTAAACAGTAAAGACCTTTAATCATCTTTTTTTTTTTTTTTTTGAGATGGAGTCTGTCGCCCAGGCTAGAGTGAGGTGGCTCCACCTCGGCTCACTGCAACCTCCACCTCCCGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTACAGGTATGCACCACCACGCCCGCCTAGTTATTTTGTTTTTTTGTTTTTTGTATTTTTAGTAGAGACAGGATTTCACCATGTTGGCCAGGCTGGTCTCGATCTCTTGACCTAGTTATCGAGACCA... | TTCAAGAAACAGAACACCCAAGCAACAGACTTAGAGTCTAAACAGTAAAGACCTTTAATCATCTTTTTTTTTTTTTTTTTGAGATGGAGTCTGTCGCCCAGGCTAGAGTGAGGTGGCTCCACCTCGGCTCACTGCAACCTCCACCTCCCGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTACAGGTATGCACCACCACGCCCGCCTAGTTATTTTGTTTTTTTGTTTTTTGTATTTTTAGTAGAGACAGGATTTCACCATGTTGGCCAGGCTGGTCTCGATCTCTTGACCTAGTTATCGAGACCA... |
Task1_train_42997 | A variant found on Chromosome 14 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TTTTTAGTAGAAATGGGGTTTCACCATGTTGGCCAGGATGGTCTCGACCTCCTGATCTCGTGATCCACCCACCTCGGCCTCCCAAAGTACTGGGATTACAGACCTGAGCCACCGCGCCCGGCCTGCACGTGAGCTTTTCATCTGGAAACTTGTCCCCTCATGGTCAGTCCTCACACCACCCCACTTACAGAAGAAAAAAATGGAAAGGTGAAGTCTCCTCTGGAAGCTTCGTCTTTTTATCTGGGAGGAAAATATTTCCCAGAAGCTGCCTTCTTTTAATTTCTGTCAGACTCTAGACTACCCTCAAATTTCACTGGACC... | TTTTTAGTAGAAATGGGGTTTCACCATGTTGGCCAGGATGGTCTCGACCTCCTGATCTCGTGATCCACCCACCTCGGCCTCCCAAAGTACTGGGATTACAGACCTGAGCCACCGCGCCCGGCCTGCACGTGAGCTTTTCATCTGGAAACTTGTCCCCTCATGGTCAGTCCTCACACCACCCCACTTACAGAAGAAAAAAATGGAAAGGTGAAGTCTCCTCTGGAAGCTTCGTCTTTTTATCTGGGAGGAAAATATTTCCCAGAAGCTGCCTTCTTTTAATTTCTGTCAGACTCTAGACTACCCTCAAATTTCACTGGACC... |
Task1_train_42998 | Assess the clinical impact of this variant found on Chromosome 14. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGTCTCAAACTCCTGACCTCAAGTGATCCACCCGCCTTGTCCTCCCAAAGTGCTGTGATTACAGGCATGAGCCACCACGCCCAGCCAATAGGAGATTTTTTTTTTAAGGTCAAGGGCATCTCCACTCAGAATTCCTCTGTGCTTACCAAAATGTGAAACCCCAAAATTTGAGACAGGTCTCAGTTAATTTAAAAAGTTTATTTTGCCAAGGTTGGGGATGTGCCTGTGACACAGTCTCAGGAAGTCCTGAAGACATGTGCCCAAGGTGGTCCGGGCGTAGCTTGGTTTTATACATTTTAGGGAGACATGAAAATGTAAGA... | GGTCTCAAACTCCTGACCTCAAGTGATCCACCCGCCTTGTCCTCCCAAAGTGCTGTGATTACAGGCATGAGCCACCACGCCCAGCCAATAGGAGATTTTTTTTTTAAGGTCAAGGGCATCTCCACTCAGAATTCCTCTGTGCTTACCAAAATGTGAAACCCCAAAATTTGAGACAGGTCTCAGTTAATTTAAAAAGTTTATTTTGCCAAGGTTGGGGATGTGCCTGTGACACAGTCTCAGGAAGTCCTGAAGACATGTGCCCAAGGTGGTCCGGGCGTAGCTTGGTTTTATACATTTTAGGGAGACATGAAAATGTAAGA... |
Task1_train_42999 | Located on Chromosome 14, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGTGAAACCCCAAAATTTGAGACAGGTCTCAGTTAATTTAAAAAGTTTATTTTGCCAAGGTTGGGGATGTGCCTGTGACACAGTCTCAGGAAGTCCTGAAGACATGTGCCCAAGGTGGTCCGGGCGTAGCTTGGTTTTATACATTTTAGGGAGACATGAAAATGTAAGAAGTCACATTAGTTCTGTCCAGAAAGGCAGAGACAGCTCAAAGCAAGGCCCCCTCACTGGGGGCCCCCAGGTCACATGTAGGTGAGAGACAGATGGTTGCATTATTTTGAGTTTCTGACAAGTCTTTCCAGAAGAGGTAGTCAGAATATGCA... | TGTGAAACCCCAAAATTTGAGACAGGTCTCAGTTAATTTAAAAAGTTTATTTTGCCAAGGTTGGGGATGTGCCTGTGACACAGTCTCAGGAAGTCCTGAAGACATGTGCCCAAGGTGGTCCGGGCGTAGCTTGGTTTTATACATTTTAGGGAGACATGAAAATGTAAGAAGTCACATTAGTTCTGTCCAGAAAGGCAGAGACAGCTCAAAGCAAGGCCCCCTCACTGGGGGCCCCCAGGTCACATGTAGGTGAGAGACAGATGGTTGCATTATTTTGAGTTTCTGACAAGTCTTTCCAGAAGAGGTAGTCAGAATATGCA... |
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