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_44800 | A change on Chromosome 16 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTGCTGGGAAGTCCTCCTTTTTTCCCAAAGGAGGAGGGAAAACATATTAACCTCCACTCCCAAATGCCTTGGGCTCCCACAGCCCTGCAGGGGAAGCAGAACTGTCTCCACTGACAGAAATGGAAATTGAGGCTCACAGGGGCCTGACTGCCCACAGTTCACAGCTGGAAACAGCTCGGAGACCCCCAAGCCCTCACTCCCAACCTCCAGGCTTCCTATGTCCACAAAGCTGCTACTGGGAATACCCAGGAGCCTGGGACTATCAGTGTTAAGAAAGAGCTCTGGTCCCTCCCACAAATGACAAATCAAAACCCAAACCC... | CTGCTGGGAAGTCCTCCTTTTTTCCCAAAGGAGGAGGGAAAACATATTAACCTCCACTCCCAAATGCCTTGGGCTCCCACAGCCCTGCAGGGGAAGCAGAACTGTCTCCACTGACAGAAATGGAAATTGAGGCTCACAGGGGCCTGACTGCCCACAGTTCACAGCTGGAAACAGCTCGGAGACCCCCAAGCCCTCACTCCCAACCTCCAGGCTTCCTATGTCCACAAAGCTGCTACTGGGAATACCCAGGAGCCTGGGACTATCAGTGTTAAGAAAGAGCTCTGGTCCCTCCCACAAATGACAAATCAAAACCCAAACCC... |
Task1_train_44801 | Given a variant located on Chromosome 16, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GTGTAGCTGTGGCAGGCCAGGTCTCACTAACACCAGCCTCCATTACAACTGTCTCAGCACTGACTGAGTAGTTAGGTTAAATATTAAAAGCTAATTGAACCAGTGCTCTTGTAGCAGGATGAGCCGCAGACGAAACCCCTCAGACACAGAGTTAAAGAAGGAAGCGGTTTATTCGGCCAGGAGCATCAGCAAGACTGCTGTCTCAAGAGCCGAGCTCCCCGAGTGAGCAATTCCTGTCCCTTTTAAGGGCTCACAACTCTAAGGGGGTCCACGTGAGAGGGTCGTGATCGATTGAGCAAGCAGGGGGTAGGTGACAGGGG... | GTGTAGCTGTGGCAGGCCAGGTCTCACTAACACCAGCCTCCATTACAACTGTCTCAGCACTGACTGAGTAGTTAGGTTAAATATTAAAAGCTAATTGAACCAGTGCTCTTGTAGCAGGATGAGCCGCAGACGAAACCCCTCAGACACAGAGTTAAAGAAGGAAGCGGTTTATTCGGCCAGGAGCATCAGCAAGACTGCTGTCTCAAGAGCCGAGCTCCCCGAGTGAGCAATTCCTGTCCCTTTTAAGGGCTCACAACTCTAAGGGGGTCCACGTGAGAGGGTCGTGATCGATTGAGCAAGCAGGGGGTAGGTGACAGGGG... |
Task1_train_44802 | A variant was discovered on Chromosome 16. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TTGTCCAATCAGAGCAGAAGCTCCAAAAGGGAGGATGCACTTCTTTGTCTTTGTACCACTCTGCTCCCATGTACCCTGTGATCTCTAAATAGGAGTTCCATGTTCATGCAAAGACCCTTGAGTACACAGAGCTAACCATGTTATCCCTACCTATATCCTAACATGTAGAAGGTGATGTCCCATCAAAGGCACAGAAGGGATGTGGGAAGACAGAACAGGGGAAACAGCAGGCTCTTCTTACTAGCCAGGAATATCCACTGTTGGCTGCCTCTTCGTCTTCTGTAATTCGGCCCTCATAGGGGCCAAAGTGCAGACCCAGT... | TTGTCCAATCAGAGCAGAAGCTCCAAAAGGGAGGATGCACTTCTTTGTCTTTGTACCACTCTGCTCCCATGTACCCTGTGATCTCTAAATAGGAGTTCCATGTTCATGCAAAGACCCTTGAGTACACAGAGCTAACCATGTTATCCCTACCTATATCCTAACATGTAGAAGGTGATGTCCCATCAAAGGCACAGAAGGGATGTGGGAAGACAGAACAGGGGAAACAGCAGGCTCTTCTTACTAGCCAGGAATATCCACTGTTGGCTGCCTCTTCGTCTTCTGTAATTCGGCCCTCATAGGGGCCAAAGTGCAGACCCAGT... |
Task1_train_44803 | A variant affecting Chromosome 16 has been observed. Determine if it's benign or associated with disease. | Benign | TACATTAAGGTCTTAAGGAATCTCAAATCCACAGATGGGGAAATCGTAGACCCAATCCAAGTTGCTTTCTCCAGTTTGGGCAGATTGACTGTTTTTACTTCTAAACTCTCCTAACCAAGCAGTAGAAGAGGAAATGAGCTTTGCACTTCTATTTTATAATTATGGTACATTATTTTATCTACTTGATGCTGTCTCTGGTCAGTGACATATGGGAAAGATCAGGGCAACTAAACAGCTCTCTCAAACCCGCTCCAGAATCGAGACAAAGAAGTAGATACATTTTGGTATAAGAGGATCATATAGTATGATGAAATGTACAT... | TACATTAAGGTCTTAAGGAATCTCAAATCCACAGATGGGGAAATCGTAGACCCAATCCAAGTTGCTTTCTCCAGTTTGGGCAGATTGACTGTTTTTACTTCTAAACTCTCCTAACCAAGCAGTAGAAGAGGAAATGAGCTTTGCACTTCTATTTTATAATTATGGTACATTATTTTATCTACTTGATGCTGTCTCTGGTCAGTGACATATGGGAAAGATCAGGGCAACTAAACAGCTCTCTCAAACCCGCTCCAGAATCGAGACAAAGAAGTAGATACATTTTGGTATAAGAGGATCATATAGTATGATGAAATGTACAT... |
Task1_train_44804 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCAGCCTCTGCAGCCATTTTCAGATAATACAATCTGTGGAGGGTAAACCTAGAAAGAAAAGCAGGTGATGCATCATACCAGGCCTTGTAAGCCACACTTTGTTATTTTTTTTTTTAAGACACAGAGGCCGGGCGTGGTGGCTCAAGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGTAGGCGGA... | CCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCAGCCTCTGCAGCCATTTTCAGATAATACAATCTGTGGAGGGTAAACCTAGAAAGAAAAGCAGGTGATGCATCATACCAGGCCTTGTAAGCCACACTTTGTTATTTTTTTTTTTAAGACACAGAGGCCGGGCGTGGTGGCTCAAGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGTAGGCGGA... |
Task1_train_44805 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | CCAGCCGCCCCTACTGGGAAGTGAGGAGCCCCTCTGCCAGGCCAGCCGCCCCGTCCGGGAGGGAGGTGGGGGGGGGGGTCAGCCCCCAACCCGGCCAGCCGCCCCATCCGGGAGGTGAGGGGCGCCTCTGCCCAGCCACCCCTACTGGGAAGTGAGGAGCCCCTCTGCCAGGCCAGCCGCCCCGTCCGGGAGGGAGGTGGGGGGGTCAGCCCCCCGCCCGGCCAGCCGCCCCGCCCGGGAGGTGAGGGGCGCCTCTGCCCGGCCGCCCCTACTGGGAAGTGAGGAGCCCCTCTGCCCGGCCACCACCCTGTCTGGGAGGT... | CCAGCCGCCCCTACTGGGAAGTGAGGAGCCCCTCTGCCAGGCCAGCCGCCCCGTCCGGGAGGGAGGTGGGGGGGGGGGTCAGCCCCCAACCCGGCCAGCCGCCCCATCCGGGAGGTGAGGGGCGCCTCTGCCCAGCCACCCCTACTGGGAAGTGAGGAGCCCCTCTGCCAGGCCAGCCGCCCCGTCCGGGAGGGAGGTGGGGGGGTCAGCCCCCCGCCCGGCCAGCCGCCCCGCCCGGGAGGTGAGGGGCGCCTCTGCCCGGCCGCCCCTACTGGGAAGTGAGGAGCCCCTCTGCCCGGCCACCACCCTGTCTGGGAGGT... |
Task1_train_44806 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TAACTTCCACAGTGACATCTGATGGGGCACCAAGGAATACAGTTTGAAAACCATTAGCTCTCACTAAAGACAAGCTAGGGAAGTCTAAAGAGAGAATAACCTACTGAAGGTCACATGGTCAGTCGGTTAATGGCCGACAAGAGTCCAGCATTTTCCCAGCACCTGACTCTGCTTTACCCCATGTACTGGTCAGATGTCAGTGTTCTGTGTTCTTAGAATGAGCAGGTCTTGGTCCTTACAACAGTAACTTCAAGCTTTCATAGGAGGAAAAAGTTCCAAGAAAAAGGAAAATTACATTTTACCTGGCAAAACTGATTTTG... | TAACTTCCACAGTGACATCTGATGGGGCACCAAGGAATACAGTTTGAAAACCATTAGCTCTCACTAAAGACAAGCTAGGGAAGTCTAAAGAGAGAATAACCTACTGAAGGTCACATGGTCAGTCGGTTAATGGCCGACAAGAGTCCAGCATTTTCCCAGCACCTGACTCTGCTTTACCCCATGTACTGGTCAGATGTCAGTGTTCTGTGTTCTTAGAATGAGCAGGTCTTGGTCCTTACAACAGTAACTTCAAGCTTTCATAGGAGGAAAAAGTTCCAAGAAAAAGGAAAATTACATTTTACCTGGCAAAACTGATTTTG... |
Task1_train_44807 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCTGTCTGCCACCGTCCTGTTGGCTAAGTCCCTTTTCTTAACCACATATAGGAAGATGTTAGAGGCTACATTCATTCCAAAAGGTCACAGCCTAGTAACTGATACTACCACTGAAGGAAAACTATCTTTTAAACCTGAGAAACATCTTCAGACTCCATCATGAATGAATCCAAATTGAAAAAAACAAAAGCTGTGCTCACTCTACACCAGTTCCTACATCACTAACTGCCGTGTTAAAGTAATTTAACTGGCACCTAACAGAAATCATCTGCCACTTTGTAAAAGTCATAGACTCATAAGAATCTAGAGCTGGAAGACCG... | GCTGTCTGCCACCGTCCTGTTGGCTAAGTCCCTTTTCTTAACCACATATAGGAAGATGTTAGAGGCTACATTCATTCCAAAAGGTCACAGCCTAGTAACTGATACTACCACTGAAGGAAAACTATCTTTTAAACCTGAGAAACATCTTCAGACTCCATCATGAATGAATCCAAATTGAAAAAAACAAAAGCTGTGCTCACTCTACACCAGTTCCTACATCACTAACTGCCGTGTTAAAGTAATTTAACTGGCACCTAACAGAAATCATCTGCCACTTTGTAAAAGTCATAGACTCATAAGAATCTAGAGCTGGAAGACCG... |
Task1_train_44808 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TTTTTTTTTTAACTATCAGTGTATCTTTAAAAGTCACCCTTACGGTGATTAAATTGCACTAACATTCCCAACTTATTCTCATTTGTGAAATACATCAATATCAGTGTCCTGTAAGAATCATCCTGTGACCTAGCTCGACTGGCTGCCGTGTGCTGTGGCTCAAGGTCTGTGTCCATGTAACTAGCAGAGGGGTGTGTGTGTGAATGCTTTCAGCCTCCAGAAAGGTCTAGCTCACACCTCACTCAAACCTATTTTTGTGGTTCATGGTCTCAGTAATACATTGAAGGTTCCCAGAGTTCAAGCGTAGTGGTCACACGTAA... | TTTTTTTTTTAACTATCAGTGTATCTTTAAAAGTCACCCTTACGGTGATTAAATTGCACTAACATTCCCAACTTATTCTCATTTGTGAAATACATCAATATCAGTGTCCTGTAAGAATCATCCTGTGACCTAGCTCGACTGGCTGCCGTGTGCTGTGGCTCAAGGTCTGTGTCCATGTAACTAGCAGAGGGGTGTGTGTGTGAATGCTTTCAGCCTCCAGAAAGGTCTAGCTCACACCTCACTCAAACCTATTTTTGTGGTTCATGGTCTCAGTAATACATTGAAGGTTCCCAGAGTTCAAGCGTAGTGGTCACACGTAA... |
Task1_train_44809 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | ACACGTAACTTGAGACCGTTTCTTCTCTTCATAAGTGAATCTTACTAGGAATTGGGAGAGTGGAAGACCGATTATTGGTCAGGGAGCCAAGCCTACTTTACCTGAGGAGAACCTGAGTAATGCCCCATTGTGAAGGAGGGTGTGGATATGGAGGGAGTGATGGGACATATTTTTTCCCCCTTTCATCTCACACATTAAACATGTCCCCAGCCAATTTTCATAGTTTCCTCATACCTCAGACACCTTAAACTCATTTTTTTTTCTTTTTGTAGAGACAGGTTATCTCTGTTGCCCAGGCTGGTCTCAAACTCCTGGCCTCA... | ACACGTAACTTGAGACCGTTTCTTCTCTTCATAAGTGAATCTTACTAGGAATTGGGAGAGTGGAAGACCGATTATTGGTCAGGGAGCCAAGCCTACTTTACCTGAGGAGAACCTGAGTAATGCCCCATTGTGAAGGAGGGTGTGGATATGGAGGGAGTGATGGGACATATTTTTTCCCCCTTTCATCTCACACATTAAACATGTCCCCAGCCAATTTTCATAGTTTCCTCATACCTCAGACACCTTAAACTCATTTTTTTTTCTTTTTGTAGAGACAGGTTATCTCTGTTGCCCAGGCTGGTCTCAAACTCCTGGCCTCA... |
Task1_train_44810 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GTGGTTTTTTTTTTGTAGAGACAGGGCTTCCATATGTTGGCTGGTCTCAAGTGATCCTCCCGCCTCGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGTCACCGCACCTGGCCCAAACTCATTTTTTATGTTCCTGCACACATCATTCCCTTATCCAAACCATTCATTCATCCAAATCTTGACAACCCCTCCTGAGGCAAAAGCTAACGTGACCCATCCATTCAGCACATCTCTGCTGGGTTTGCCAGGTCTCGTCTTCACAGTAGCCCCTTTGGGGGTGACTGAATAGATGGAGTTAAGACTGTATGGGAAGTGGGTG... | GTGGTTTTTTTTTTGTAGAGACAGGGCTTCCATATGTTGGCTGGTCTCAAGTGATCCTCCCGCCTCGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGTCACCGCACCTGGCCCAAACTCATTTTTTATGTTCCTGCACACATCATTCCCTTATCCAAACCATTCATTCATCCAAATCTTGACAACCCCTCCTGAGGCAAAAGCTAACGTGACCCATCCATTCAGCACATCTCTGCTGGGTTTGCCAGGTCTCGTCTTCACAGTAGCCCCTTTGGGGGTGACTGAATAGATGGAGTTAAGACTGTATGGGAAGTGGGTG... |
Task1_train_44811 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CATTCATCCAAATCTTGACAACCCCTCCTGAGGCAAAAGCTAACGTGACCCATCCATTCAGCACATCTCTGCTGGGTTTGCCAGGTCTCGTCTTCACAGTAGCCCCTTTGGGGGTGACTGAATAGATGGAGTTAAGACTGTATGGGAAGTGGGTGTGCTTATTGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCACTTGAGTCCAGGGGTTCAAGGCTAGTCTGAGCAACAAAGACTGTACACACTCCTCAATTCAGAGGGGACCCATTTTCTTGAGGTCACTAACCTAGCCCCTCGCCACTGAGTTTATCTTGGT... | CATTCATCCAAATCTTGACAACCCCTCCTGAGGCAAAAGCTAACGTGACCCATCCATTCAGCACATCTCTGCTGGGTTTGCCAGGTCTCGTCTTCACAGTAGCCCCTTTGGGGGTGACTGAATAGATGGAGTTAAGACTGTATGGGAAGTGGGTGTGCTTATTGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCACTTGAGTCCAGGGGTTCAAGGCTAGTCTGAGCAACAAAGACTGTACACACTCCTCAATTCAGAGGGGACCCATTTTCTTGAGGTCACTAACCTAGCCCCTCGCCACTGAGTTTATCTTGGT... |
Task1_train_44812 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | TTCTTGAGGTCACTAACCTAGCCCCTCGCCACTGAGTTTATCTTGGTCCTCCAATCCTCTCATTTTAGAATTGTGCAGGCCTCTCGGGCACAGCAGTCTCATGGCCAGAGGCAGAGCCAGGGCTGGACTGGATTCTTTTCCAAGCTGCTGTCCTTTCCAAGATACCTCAAGAAAAAAACATTAAAAGACGAAATAACTCTTGAAGGGGGTTATACGTACCATGTAATGCTTTTTCCACTCACATGGTTTCAACTTTGGGCTTATTTGCCAAAATCTAGGATGGAAAAGTCCAGTTATGAACATGTTCCTCCTGGCTGGAT... | TTCTTGAGGTCACTAACCTAGCCCCTCGCCACTGAGTTTATCTTGGTCCTCCAATCCTCTCATTTTAGAATTGTGCAGGCCTCTCGGGCACAGCAGTCTCATGGCCAGAGGCAGAGCCAGGGCTGGACTGGATTCTTTTCCAAGCTGCTGTCCTTTCCAAGATACCTCAAGAAAAAAACATTAAAAGACGAAATAACTCTTGAAGGGGGTTATACGTACCATGTAATGCTTTTTCCACTCACATGGTTTCAACTTTGGGCTTATTTGCCAAAATCTAGGATGGAAAAGTCCAGTTATGAACATGTTCCTCCTGGCTGGAT... |
Task1_train_44813 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TTGGTCCTCCAATCCTCTCATTTTAGAATTGTGCAGGCCTCTCGGGCACAGCAGTCTCATGGCCAGAGGCAGAGCCAGGGCTGGACTGGATTCTTTTCCAAGCTGCTGTCCTTTCCAAGATACCTCAAGAAAAAAACATTAAAAGACGAAATAACTCTTGAAGGGGGTTATACGTACCATGTAATGCTTTTTCCACTCACATGGTTTCAACTTTGGGCTTATTTGCCAAAATCTAGGATGGAAAAGTCCAGTTATGAACATGTTCCTCCTGGCTGGATTTGATCTTGAAGACACTAAACCCAATTTCAGAGCATATTTAA... | TTGGTCCTCCAATCCTCTCATTTTAGAATTGTGCAGGCCTCTCGGGCACAGCAGTCTCATGGCCAGAGGCAGAGCCAGGGCTGGACTGGATTCTTTTCCAAGCTGCTGTCCTTTCCAAGATACCTCAAGAAAAAAACATTAAAAGACGAAATAACTCTTGAAGGGGGTTATACGTACCATGTAATGCTTTTTCCACTCACATGGTTTCAACTTTGGGCTTATTTGCCAAAATCTAGGATGGAAAAGTCCAGTTATGAACATGTTCCTCCTGGCTGGATTTGATCTTGAAGACACTAAACCCAATTTCAGAGCATATTTAA... |
Task1_train_44814 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGGTTCCAGCCTTCCAGAGGAAGCCAATCACGACAGCTATGGCTGCAGAGAAACTGGAAAGTCCTCAGGAAGAGGACGGAGAGTTGCAACTCCTGGGCAAAGGGCTTCAGGTTGAGCAGGGGAACAAACTGAATATATTCCAGGCTATAAGGGACATGGAGGAGCTGCTTCTCCAGCAGTCTCCTGGTCAGCTGGTGAAGGCGCTGCCACTCCTGAGGGCTGCACCAAGGCATGACTTGCACCAGGGCCACCAGAAAGCCTTTGCTGAACAGTCTGACCTCCTCAGGATTGCCCACGTCCACCACCAAGAGAGACAGCAT... | TGGTTCCAGCCTTCCAGAGGAAGCCAATCACGACAGCTATGGCTGCAGAGAAACTGGAAAGTCCTCAGGAAGAGGACGGAGAGTTGCAACTCCTGGGCAAAGGGCTTCAGGTTGAGCAGGGGAACAAACTGAATATATTCCAGGCTATAAGGGACATGGAGGAGCTGCTTCTCCAGCAGTCTCCTGGTCAGCTGGTGAAGGCGCTGCCACTCCTGAGGGCTGCACCAAGGCATGACTTGCACCAGGGCCACCAGAAAGCCTTTGCTGAACAGTCTGACCTCCTCAGGATTGCCCACGTCCACCACCAAGAGAGACAGCAT... |
Task1_train_44815 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | ATTAGAAGCAATGCCGACCTGTCCATCCTGATATCCCATCTCCTTAACTTCAACTAAGCAACCTCAACTAAAGGCACATAAAACCAGCGGCTTCGCAAACATGTGCCATCTCCGCACTGGCTCTTCAGTTTTACTATGTAGCTCCTCCTCTCATCTACCTGTGGATATCCTATCTTTAGACGTCAACTCGAATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATATTTTTAAAAATTAGCCGGGTGTTGTGGTACGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCGGGA... | ATTAGAAGCAATGCCGACCTGTCCATCCTGATATCCCATCTCCTTAACTTCAACTAAGCAACCTCAACTAAAGGCACATAAAACCAGCGGCTTCGCAAACATGTGCCATCTCCGCACTGGCTCTTCAGTTTTACTATGTAGCTCCTCCTCTCATCTACCTGTGGATATCCTATCTTTAGACGTCAACTCGAATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATATTTTTAAAAATTAGCCGGGTGTTGTGGTACGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCGGGA... |
Task1_train_44816 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CGCACTGGCTCTTCAGTTTTACTATGTAGCTCCTCCTCTCATCTACCTGTGGATATCCTATCTTTAGACGTCAACTCGAATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATATTTTTAAAAATTAGCCGGGTGTTGTGGTACGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCGGGAGGCTGAGCTTACAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGCGACAGAGCAAGACTCCACCTCAAAAAAAAAAAAAAAAAAAAAAGTCAACTCGAATACAAGGTC... | CGCACTGGCTCTTCAGTTTTACTATGTAGCTCCTCCTCTCATCTACCTGTGGATATCCTATCTTTAGACGTCAACTCGAATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATATTTTTAAAAATTAGCCGGGTGTTGTGGTACGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCGGGAGGCTGAGCTTACAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGCGACAGAGCAAGACTCCACCTCAAAAAAAAAAAAAAAAAAAAAAGTCAACTCGAATACAAGGTC... |
Task1_train_44817 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AGGGAGACAGGCGACGACTCACAGAAATAAAAATCACTCCCTGGGAAAAGCCTAGTGTACTGGGCACCCCGGGGAGGGTGACAGATGTGGGTCTGGGGGGAGACAGGATTGCAGCCAGCTCTGAAGCAGCTGGGGCCAGTTGGGTAGCCTCCACCAAGGGCATTTGGAACTTGGCACTAGGGTGAAATCTTCAGGCTCTTCCCTTAAGTTAAAGAGACATATAAAAATGTTACCAGCATGGGCGGCAAGAGCATTGCCTGTGGGAAACACAGCCAATCTTTGCTAAGGAATAAGTGTAATTGATCAAAACAGATGACTTG... | AGGGAGACAGGCGACGACTCACAGAAATAAAAATCACTCCCTGGGAAAAGCCTAGTGTACTGGGCACCCCGGGGAGGGTGACAGATGTGGGTCTGGGGGGAGACAGGATTGCAGCCAGCTCTGAAGCAGCTGGGGCCAGTTGGGTAGCCTCCACCAAGGGCATTTGGAACTTGGCACTAGGGTGAAATCTTCAGGCTCTTCCCTTAAGTTAAAGAGACATATAAAAATGTTACCAGCATGGGCGGCAAGAGCATTGCCTGTGGGAAACACAGCCAATCTTTGCTAAGGAATAAGTGTAATTGATCAAAACAGATGACTTG... |
Task1_train_44818 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | AAATCACTCCCTGGGAAAAGCCTAGTGTACTGGGCACCCCGGGGAGGGTGACAGATGTGGGTCTGGGGGGAGACAGGATTGCAGCCAGCTCTGAAGCAGCTGGGGCCAGTTGGGTAGCCTCCACCAAGGGCATTTGGAACTTGGCACTAGGGTGAAATCTTCAGGCTCTTCCCTTAAGTTAAAGAGACATATAAAAATGTTACCAGCATGGGCGGCAAGAGCATTGCCTGTGGGAAACACAGCCAATCTTTGCTAAGGAATAAGTGTAATTGATCAAAACAGATGACTTGATGGACCTTCCAACTGTGCTTTTAGCAAAG... | AAATCACTCCCTGGGAAAAGCCTAGTGTACTGGGCACCCCGGGGAGGGTGACAGATGTGGGTCTGGGGGGAGACAGGATTGCAGCCAGCTCTGAAGCAGCTGGGGCCAGTTGGGTAGCCTCCACCAAGGGCATTTGGAACTTGGCACTAGGGTGAAATCTTCAGGCTCTTCCCTTAAGTTAAAGAGACATATAAAAATGTTACCAGCATGGGCGGCAAGAGCATTGCCTGTGGGAAACACAGCCAATCTTTGCTAAGGAATAAGTGTAATTGATCAAAACAGATGACTTGATGGACCTTCCAACTGTGCTTTTAGCAAAG... |
Task1_train_44819 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AGGCGTGAGCCACCATGCCCAGCCTGAGCAAAATTCTTAATTTAATATAGTCAAATTTATGAAACCTGCAAAGTTCTCCCAAAGCCACAAACATTGTTTTTTATTTGTTTGTTTGTTTGTTTGTTTTTAGTTGGAGTCTCATTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAACCTTGGCTCACTGCAACGTTCGCTTCTTCCCAGGTTCAAGTGATTCTCCTGCCTCAGTCTCCAAAGTAGCTGTGGTTACAGGCACCCACCACCACGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGATGGCCAGGC... | AGGCGTGAGCCACCATGCCCAGCCTGAGCAAAATTCTTAATTTAATATAGTCAAATTTATGAAACCTGCAAAGTTCTCCCAAAGCCACAAACATTGTTTTTTATTTGTTTGTTTGTTTGTTTGTTTTTAGTTGGAGTCTCATTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAACCTTGGCTCACTGCAACGTTCGCTTCTTCCCAGGTTCAAGTGATTCTCCTGCCTCAGTCTCCAAAGTAGCTGTGGTTACAGGCACCCACCACCACGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGATGGCCAGGC... |
Task1_train_44820 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCCCAGCCTGAGCAAAATTCTTAATTTAATATAGTCAAATTTATGAAACCTGCAAAGTTCTCCCAAAGCCACAAACATTGTTTTTTATTTGTTTGTTTGTTTGTTTGTTTTTAGTTGGAGTCTCATTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAACCTTGGCTCACTGCAACGTTCGCTTCTTCCCAGGTTCAAGTGATTCTCCTGCCTCAGTCTCCAAAGTAGCTGTGGTTACAGGCACCCACCACCACGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGATGGCCAGGCTGGTCTCGAACTGCTG... | GCCCAGCCTGAGCAAAATTCTTAATTTAATATAGTCAAATTTATGAAACCTGCAAAGTTCTCCCAAAGCCACAAACATTGTTTTTTATTTGTTTGTTTGTTTGTTTGTTTTTAGTTGGAGTCTCATTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAACCTTGGCTCACTGCAACGTTCGCTTCTTCCCAGGTTCAAGTGATTCTCCTGCCTCAGTCTCCAAAGTAGCTGTGGTTACAGGCACCCACCACCACGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGATGGCCAGGCTGGTCTCGAACTGCTG... |
Task1_train_44821 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | TTAGTTGGAGTCTCATTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAACCTTGGCTCACTGCAACGTTCGCTTCTTCCCAGGTTCAAGTGATTCTCCTGCCTCAGTCTCCAAAGTAGCTGTGGTTACAGGCACCCACCACCACGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGATGGCCAGGCTGGTCTCGAACTGCTGACCTCAAGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACCGTGCCCGGCTGAGTTTTCAAATCTTATTCATTTCCAGGTGTCCTTTCAG... | TTAGTTGGAGTCTCATTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAACCTTGGCTCACTGCAACGTTCGCTTCTTCCCAGGTTCAAGTGATTCTCCTGCCTCAGTCTCCAAAGTAGCTGTGGTTACAGGCACCCACCACCACGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGATGGCCAGGCTGGTCTCGAACTGCTGACCTCAAGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACCGTGCCCGGCTGAGTTTTCAAATCTTATTCATTTCCAGGTGTCCTTTCAG... |
Task1_train_44822 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCCCTGCCCTGACCTGCCTTCAGCTCTCAGGCAGTAGCACCGTGCTGCTGGACTCAGGGCTGCAGGCAGGCTCTTACCTGAATGGGCTCAGAGCCCAAGGCCTGCAGCACTCGGGGGCTGATCTCATCTGTACCTGCAACTCAGATGGCGGGGAGGGAAGTCAGTGGAGGCAATGGGGGACCAGGATGGTGACGAAAGGTCTGAGTGCTGGAAAGTCAGGGGCTCACCAAGCCGAGTGCTGATGAAGAGCCTGGGTACACTCTGAGGGTAATTATCCTTCTTGCCCTTGAAGATCTCACTAGCCACGGCCTTCTGCTGCA... | CCCCTGCCCTGACCTGCCTTCAGCTCTCAGGCAGTAGCACCGTGCTGCTGGACTCAGGGCTGCAGGCAGGCTCTTACCTGAATGGGCTCAGAGCCCAAGGCCTGCAGCACTCGGGGGCTGATCTCATCTGTACCTGCAACTCAGATGGCGGGGAGGGAAGTCAGTGGAGGCAATGGGGGACCAGGATGGTGACGAAAGGTCTGAGTGCTGGAAAGTCAGGGGCTCACCAAGCCGAGTGCTGATGAAGAGCCTGGGTACACTCTGAGGGTAATTATCCTTCTTGCCCTTGAAGATCTCACTAGCCACGGCCTTCTGCTGCA... |
Task1_train_44823 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CCAAGGCCTGCAGCACTCGGGGGCTGATCTCATCTGTACCTGCAACTCAGATGGCGGGGAGGGAAGTCAGTGGAGGCAATGGGGGACCAGGATGGTGACGAAAGGTCTGAGTGCTGGAAAGTCAGGGGCTCACCAAGCCGAGTGCTGATGAAGAGCCTGGGTACACTCTGAGGGTAATTATCCTTCTTGCCCTTGAAGATCTCACTAGCCACGGCCTTCTGCTGCAGCTGAGGAGACAAGGGGGGTGAGGAGAGTGTCATGGTGGGGAGCACCATCTTGGGGGGGCAGAGCCAGCCTTAGGACCTGAGACAGCCTCCCTC... | CCAAGGCCTGCAGCACTCGGGGGCTGATCTCATCTGTACCTGCAACTCAGATGGCGGGGAGGGAAGTCAGTGGAGGCAATGGGGGACCAGGATGGTGACGAAAGGTCTGAGTGCTGGAAAGTCAGGGGCTCACCAAGCCGAGTGCTGATGAAGAGCCTGGGTACACTCTGAGGGTAATTATCCTTCTTGCCCTTGAAGATCTCACTAGCCACGGCCTTCTGCTGCAGCTGAGGAGACAAGGGGGGTGAGGAGAGTGTCATGGTGGGGAGCACCATCTTGGGGGGGCAGAGCCAGCCTTAGGACCTGAGACAGCCTCCCTC... |
Task1_train_44824 | A sequence alteration has been identified on Chromosome 17. Is it disease-inducing or harmless? | Benign | CAATGCGGTGCTGTGGCTCGCTAGGTCTTCGCCCCCATCCCGCCCCCTCCCAAAGCCCCAGCTCCAGGAGCCCCCCGCAACCCCAGGCGCTTGTCTCACCTGGCTCGGTACACAGGTAGGAGTAAAAGCCCTCTGACTTGAGCATGATGAGCAGCGAGCCCCAGCCCAGGAGGACTGCCGAGAAGAGGAGGTTCTCCAGCACGGCCGTGCAGGCCATCCACCAGCGGCGCCGATGGGCAGTGGCCAGGGTGGGCGCCATGGTGCGGCGCGGCGCGGCTCCGGCTCCGGCTCCGGCTCTGCACCACCTGCGCACAGAACTC... | CAATGCGGTGCTGTGGCTCGCTAGGTCTTCGCCCCCATCCCGCCCCCTCCCAAAGCCCCAGCTCCAGGAGCCCCCCGCAACCCCAGGCGCTTGTCTCACCTGGCTCGGTACACAGGTAGGAGTAAAAGCCCTCTGACTTGAGCATGATGAGCAGCGAGCCCCAGCCCAGGAGGACTGCCGAGAAGAGGAGGTTCTCCAGCACGGCCGTGCAGGCCATCCACCAGCGGCGCCGATGGGCAGTGGCCAGGGTGGGCGCCATGGTGCGGCGCGGCGCGGCTCCGGCTCCGGCTCCGGCTCTGCACCACCTGCGCACAGAACTC... |
Task1_train_44825 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CAGCCTGGGCAACAGAGCAAAACTTCGTCTCAAAAAGAAAAAAAAAAAAAAAAAAAGAAGCTGAGGAACAGTATGCTTAGTATGCTAAAATTTTTTGTTTAAAATATTTGTTGACATGTACACAGAAAAACATCTGAAAGAAAGCACCTCAACTGTTGATGAGACTCTCTGAGCACTGAGATAGAAGGGGCTGCCCCTGGCCGGGCGCGGTGGCTCATGCCTATAATCCCAACACTCTGGGAGGCCGAAGCTGTGGAGCCCTTGAGTTTGGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCCACCAAA... | CAGCCTGGGCAACAGAGCAAAACTTCGTCTCAAAAAGAAAAAAAAAAAAAAAAAAAGAAGCTGAGGAACAGTATGCTTAGTATGCTAAAATTTTTTGTTTAAAATATTTGTTGACATGTACACAGAAAAACATCTGAAAGAAAGCACCTCAACTGTTGATGAGACTCTCTGAGCACTGAGATAGAAGGGGCTGCCCCTGGCCGGGCGCGGTGGCTCATGCCTATAATCCCAACACTCTGGGAGGCCGAAGCTGTGGAGCCCTTGAGTTTGGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCCACCAAA... |
Task1_train_44826 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | AGAAAAACATCTGAAAGAAAGCACCTCAACTGTTGATGAGACTCTCTGAGCACTGAGATAGAAGGGGCTGCCCCTGGCCGGGCGCGGTGGCTCATGCCTATAATCCCAACACTCTGGGAGGCCGAAGCTGTGGAGCCCTTGAGTTTGGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCCACCAAAAAATACAAAAATTAGCCGGGCATGGTGGCGGGCGCTTGTAATCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCGGGGAGACAGAGGTGGCAGTGAGCCGAGATCATACCACT... | AGAAAAACATCTGAAAGAAAGCACCTCAACTGTTGATGAGACTCTCTGAGCACTGAGATAGAAGGGGCTGCCCCTGGCCGGGCGCGGTGGCTCATGCCTATAATCCCAACACTCTGGGAGGCCGAAGCTGTGGAGCCCTTGAGTTTGGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCCACCAAAAAATACAAAAATTAGCCGGGCATGGTGGCGGGCGCTTGTAATCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCGGGGAGACAGAGGTGGCAGTGAGCCGAGATCATACCACT... |
Task1_train_44827 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTCTGGTGGCCTGGAGATGGGTACAACATTCTCATACTCAGGTTCCTCCTGCCTTTCCTCTTCAGCCTGCTTCTGGGGATCCTGTTCTGGGGAGCCACAGCCAGAGACTGGCTCCTGGGCTCTCCTTGAACTCTCGGTGCCAGCCCCCAGCCCCCGGACCGCTTCCTCTGGTCTGACTGCCATAGGCCCTGTGGCCCCAGGAAGCCCAGCTTTTGGGGCTGAGTTGGGGCTCTGGCCGACAGAGCCAGAGGCAAGGCCAGGGCTGCCCTTTTTCCGATTCAGGGCCTGGCGCGGAGGCTTAGGGATGGCCCTCTTGACCT... | TTCTGGTGGCCTGGAGATGGGTACAACATTCTCATACTCAGGTTCCTCCTGCCTTTCCTCTTCAGCCTGCTTCTGGGGATCCTGTTCTGGGGAGCCACAGCCAGAGACTGGCTCCTGGGCTCTCCTTGAACTCTCGGTGCCAGCCCCCAGCCCCCGGACCGCTTCCTCTGGTCTGACTGCCATAGGCCCTGTGGCCCCAGGAAGCCCAGCTTTTGGGGCTGAGTTGGGGCTCTGGCCGACAGAGCCAGAGGCAAGGCCAGGGCTGCCCTTTTTCCGATTCAGGGCCTGGCGCGGAGGCTTAGGGATGGCCCTCTTGACCT... |
Task1_train_44828 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | TTTATTTTATAGCTTGACACACAGCAGGCCCTGACACAGCCGCGGCTACAGTTTCACCCCCGTAAGAATAAACAGACCCAGCCAAGACAGGAACTTGAAGAATGAATGTGGAGAGGCAGTGTTGTCAGGCAGAATGGATGGCAGGCAAGGCAAGGGGAGTGGTGAGATCCAGGGAGAAGGGCGCAGGCTGGACAGCGGCCATGGGACACAGCCAGAGCAGGTCAGCAGGCCCTAGAAGCGGCCAGGCTAGGGAGGCTCAAGGGGTGACCGGGTTGGGGTGACAGCCTCAGTCTGAGACAATGGGCTCAGAGGGTGACCAG... | TTTATTTTATAGCTTGACACACAGCAGGCCCTGACACAGCCGCGGCTACAGTTTCACCCCCGTAAGAATAAACAGACCCAGCCAAGACAGGAACTTGAAGAATGAATGTGGAGAGGCAGTGTTGTCAGGCAGAATGGATGGCAGGCAAGGCAAGGGGAGTGGTGAGATCCAGGGAGAAGGGCGCAGGCTGGACAGCGGCCATGGGACACAGCCAGAGCAGGTCAGCAGGCCCTAGAAGCGGCCAGGCTAGGGAGGCTCAAGGGGTGACCGGGTTGGGGTGACAGCCTCAGTCTGAGACAATGGGCTCAGAGGGTGACCAG... |
Task1_train_44829 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ATCCCAGCCCCGCCGGCCTGGCACCCCGGAAGCCGTCGCCAGCAGGGCCGTGGCTGGGCTCAGCCCCGCGCTGCCCCCGGGCGGCCTGGAGGAGATGGCCCAGGGCAGCGGGGGGCGGGAAGGCGCTCTCAGAACCCCGGCCGGGGGCTGGCATTCCCCGCCAAGCCCAGACATGCAGGAGCTGCTCCGGAGCGTGGAGAGGGACCTGAGCATCGATCCCAGGCAGCTGGCTCCGGCCCCGGGGGGCACCCACGTGGTGGCCCTAGTGCCTGCGCGCTGGCTGGCCAGCCTCCGCGATCGCCGGCTGCCCCTGGGACCCT... | ATCCCAGCCCCGCCGGCCTGGCACCCCGGAAGCCGTCGCCAGCAGGGCCGTGGCTGGGCTCAGCCCCGCGCTGCCCCCGGGCGGCCTGGAGGAGATGGCCCAGGGCAGCGGGGGGCGGGAAGGCGCTCTCAGAACCCCGGCCGGGGGCTGGCATTCCCCGCCAAGCCCAGACATGCAGGAGCTGCTCCGGAGCGTGGAGAGGGACCTGAGCATCGATCCCAGGCAGCTGGCTCCGGCCCCGGGGGGCACCCACGTGGTGGCCCTAGTGCCTGCGCGCTGGCTGGCCAGCCTCCGCGATCGCCGGCTGCCCCTGGGACCCT... |
Task1_train_44830 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGAGACCCCCTCTCTAAAAATATATATAAAGGCCGAGCGTGGTGTCTCACCCCTGTAATCCCAGCACTTTGGGGGGCCAAGGCGGGTGGATCACGAGGTCAGGAGTTTGAGACCCACCTGGCCAACATGGTGAAACCCCGTCTCCACTAAAAATACAAAATCTTCGCTGGGCATGGCAGCAGGTGCCTGCAATCCCAGGTTCTCGGGAGGCTGCAATCCCAGGTTCTCAGGAGGCTGAGGCGGGAGAATTGCTTGAACCCAGGAAGCGGAGGTTGCAGTGAGCTGAGATCACGCCATTGTACTGCAGCCTAGGCGACAGA... | TGAGACCCCCTCTCTAAAAATATATATAAAGGCCGAGCGTGGTGTCTCACCCCTGTAATCCCAGCACTTTGGGGGGCCAAGGCGGGTGGATCACGAGGTCAGGAGTTTGAGACCCACCTGGCCAACATGGTGAAACCCCGTCTCCACTAAAAATACAAAATCTTCGCTGGGCATGGCAGCAGGTGCCTGCAATCCCAGGTTCTCGGGAGGCTGCAATCCCAGGTTCTCAGGAGGCTGAGGCGGGAGAATTGCTTGAACCCAGGAAGCGGAGGTTGCAGTGAGCTGAGATCACGCCATTGTACTGCAGCCTAGGCGACAGA... |
Task1_train_44831 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AAAATATATATAAAGGCCGAGCGTGGTGTCTCACCCCTGTAATCCCAGCACTTTGGGGGGCCAAGGCGGGTGGATCACGAGGTCAGGAGTTTGAGACCCACCTGGCCAACATGGTGAAACCCCGTCTCCACTAAAAATACAAAATCTTCGCTGGGCATGGCAGCAGGTGCCTGCAATCCCAGGTTCTCGGGAGGCTGCAATCCCAGGTTCTCAGGAGGCTGAGGCGGGAGAATTGCTTGAACCCAGGAAGCGGAGGTTGCAGTGAGCTGAGATCACGCCATTGTACTGCAGCCTAGGCGACAGAGCAAGACTCTGTCTCA... | AAAATATATATAAAGGCCGAGCGTGGTGTCTCACCCCTGTAATCCCAGCACTTTGGGGGGCCAAGGCGGGTGGATCACGAGGTCAGGAGTTTGAGACCCACCTGGCCAACATGGTGAAACCCCGTCTCCACTAAAAATACAAAATCTTCGCTGGGCATGGCAGCAGGTGCCTGCAATCCCAGGTTCTCGGGAGGCTGCAATCCCAGGTTCTCAGGAGGCTGAGGCGGGAGAATTGCTTGAACCCAGGAAGCGGAGGTTGCAGTGAGCTGAGATCACGCCATTGTACTGCAGCCTAGGCGACAGAGCAAGACTCTGTCTCA... |
Task1_train_44832 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CACCCAGCACCGCAAGAGCGTCTTCTTCGTGGGCCAGCTTGAGGCCCCGCAGCACGTGGTGAGCTGTGACGGGGCTGTGCACGTCTGGGACCCCTTCACAGGTGAGCGGGCCCAGGTGAGGCCTGTTCTCTTCCTGCTCCTGCGCCCCACCAGGCCTCCAGGAAGGGGGCCCGAGGGTGGGGCTGTAATGCTGCGGAGTTTGGGGAGACCCAGCGAGGCCGCCTAGGAGAACAGTTAGGGCTTCGAATCTGTTAGACTTGAGTCTGAATTGGCTCCACCGGCTTACTTGCTGAGTGACCTTGAGCAAGTTCCTGCTGCTG... | CACCCAGCACCGCAAGAGCGTCTTCTTCGTGGGCCAGCTTGAGGCCCCGCAGCACGTGGTGAGCTGTGACGGGGCTGTGCACGTCTGGGACCCCTTCACAGGTGAGCGGGCCCAGGTGAGGCCTGTTCTCTTCCTGCTCCTGCGCCCCACCAGGCCTCCAGGAAGGGGGCCCGAGGGTGGGGCTGTAATGCTGCGGAGTTTGGGGAGACCCAGCGAGGCCGCCTAGGAGAACAGTTAGGGCTTCGAATCTGTTAGACTTGAGTCTGAATTGGCTCCACCGGCTTACTTGCTGAGTGACCTTGAGCAAGTTCCTGCTGCTG... |
Task1_train_44833 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGAGGAGGGAGCTGCCTCCCTGGCTGAGGGGTCTGGGATTTATTCAGGAGGCCTGTCACTCCCCAGCCTCTTCTGGGACTTGAAAAACTGGAGCCTGTTCTTGGCAAGAAGATTCTAATGCCCAGGTCGGAGTCGGGGCCCTGGCCAAGGGCTCTTGTGTGGGATGGGGGTGGGGCCGGGGGGACCAAAGGATCCTCCAGAAGGGTTGGCCCCAAGATGGGGGTGGGCTGGAGGTAGCTGAGACCTGCTCTGACTTATCCTCCTGAGACCAACACCTGCCCTTCCCAGAGCCAGCCTGGAGCAGAGGCCTGTGATGCTCC... | GGAGGAGGGAGCTGCCTCCCTGGCTGAGGGGTCTGGGATTTATTCAGGAGGCCTGTCACTCCCCAGCCTCTTCTGGGACTTGAAAAACTGGAGCCTGTTCTTGGCAAGAAGATTCTAATGCCCAGGTCGGAGTCGGGGCCCTGGCCAAGGGCTCTTGTGTGGGATGGGGGTGGGGCCGGGGGGACCAAAGGATCCTCCAGAAGGGTTGGCCCCAAGATGGGGGTGGGCTGGAGGTAGCTGAGACCTGCTCTGACTTATCCTCCTGAGACCAACACCTGCCCTTCCCAGAGCCAGCCTGGAGCAGAGGCCTGTGATGCTCC... |
Task1_train_44834 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CTCCCAAAGTGCTAGGATTACAGGCGTGAGCCCCCATGCCCGGCCACACTGCTAGAAACTTTAAAAGCATCTCATTCGGTTACGTGTCCGCCTGCAGTGGGACAGGTAGTATGACTCCACCCCACTGTGAGGAAGTGGAGGAGCAGTGGGGTCAGTCACACGCCTGGCAGGATGGCCAGGAGCCCCATTGTCTGCCTTAGGAGCACCTGCTGGCCCCACCCCCACTTAGCTTCGGGGCTTTCTGTCCTCATGCTCTTCCCTTCCCTTTTCTGTAGGTGGCTCATTTCCCCTTTAAGAACAACATGAGCTTTGTGGTCCTT... | CTCCCAAAGTGCTAGGATTACAGGCGTGAGCCCCCATGCCCGGCCACACTGCTAGAAACTTTAAAAGCATCTCATTCGGTTACGTGTCCGCCTGCAGTGGGACAGGTAGTATGACTCCACCCCACTGTGAGGAAGTGGAGGAGCAGTGGGGTCAGTCACACGCCTGGCAGGATGGCCAGGAGCCCCATTGTCTGCCTTAGGAGCACCTGCTGGCCCCACCCCCACTTAGCTTCGGGGCTTTCTGTCCTCATGCTCTTCCCTTCCCTTTTCTGTAGGTGGCTCATTTCCCCTTTAAGAACAACATGAGCTTTGTGGTCCTT... |
Task1_train_44835 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | TGGCTCACACCTGTAATCCCAGCAGTGTGGGAGGCGGAGCAGGATGATCCCTTGAATCCAGGAGTTTGAGACCAGCATAGGCAACATAGTGAGACCCCTGTCTCTACAAAAAAGCAAAAATTACCAGGCGTGGTGGCAAGTGCTTGTGGTACTACCTACTTGGGAAGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGATTAAGACTGCAGTGAGGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCGGAGGTGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAA... | TGGCTCACACCTGTAATCCCAGCAGTGTGGGAGGCGGAGCAGGATGATCCCTTGAATCCAGGAGTTTGAGACCAGCATAGGCAACATAGTGAGACCCCTGTCTCTACAAAAAAGCAAAAATTACCAGGCGTGGTGGCAAGTGCTTGTGGTACTACCTACTTGGGAAGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGATTAAGACTGCAGTGAGGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCGGAGGTGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAA... |
Task1_train_44836 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AAGGCCGGGAGTTTGATACCAACCTGACCAACATAGTGAAATCCCGTCTCTACTAAAAATACAAAATTAGCCAGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATCACTTGAACCCGGAAGGCGGAGGTTGCCGTAAGCCAAGATCGCGCCATTGCGCTCCAGCCTGGGCAACAAGAGTGAAACTCCATCTCAAAAACAAAACAAAACAAAACAAAACAAAACAAAACCAACAACTCAGAAGGAGGCATATGTGTTATAAAGTCTTTACTACAACTTTGATTTTATTAGTGGTTGG... | AAGGCCGGGAGTTTGATACCAACCTGACCAACATAGTGAAATCCCGTCTCTACTAAAAATACAAAATTAGCCAGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATCACTTGAACCCGGAAGGCGGAGGTTGCCGTAAGCCAAGATCGCGCCATTGCGCTCCAGCCTGGGCAACAAGAGTGAAACTCCATCTCAAAAACAAAACAAAACAAAACAAAACAAAACAAAACCAACAACTCAGAAGGAGGCATATGTGTTATAAAGTCTTTACTACAACTTTGATTTTATTAGTGGTTGG... |
Task1_train_44837 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | CACCACCACGCCTGGCTAGTTTTTTGTATTTTTAGTAAAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACATCAGGTGATCCGCCCACCTTAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATACCTGGCCAGCAAAACCTCTTTAACTTGTGTTCCATGGGCTCCTTTTCTGTGGGTCAAAATCCTCCTGGAACCCTACAATGCAGGCCCTACAGGGGTGGGTGGTAAGTCCAACAAACAGGATTTCATCTTCTGGAGCTCCTGGATTTCATCGTCCCATGGGCCACAGTGCAGCGA... | CACCACCACGCCTGGCTAGTTTTTTGTATTTTTAGTAAAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACATCAGGTGATCCGCCCACCTTAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATACCTGGCCAGCAAAACCTCTTTAACTTGTGTTCCATGGGCTCCTTTTCTGTGGGTCAAAATCCTCCTGGAACCCTACAATGCAGGCCCTACAGGGGTGGGTGGTAAGTCCAACAAACAGGATTTCATCTTCTGGAGCTCCTGGATTTCATCGTCCCATGGGCCACAGTGCAGCGA... |
Task1_train_44838 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | GAGAGAGACTCTGTCTCACAAAAGAAAAAGAAAAAAAAAAAAAAAAGAAAACCAATAGAAAGGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCGCTTTGGGTGGTCGAGGCAGGTAGGTCGCTTGAGGCCAGGAGATCGAGACCAGCCTGGCCAACATGGAGAACATGGCCAACTCGTCTCTACTAAAAATACAAAGATTAGCTGGGCATGGTGGTGCATGCCTGTAATCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATTGCTTGAGTCTGGGAGGTTGAGGCTGTGGTAAGCAGAGATCGTGCCACTGCACTCA... | GAGAGAGACTCTGTCTCACAAAAGAAAAAGAAAAAAAAAAAAAAAAGAAAACCAATAGAAAGGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCGCTTTGGGTGGTCGAGGCAGGTAGGTCGCTTGAGGCCAGGAGATCGAGACCAGCCTGGCCAACATGGAGAACATGGCCAACTCGTCTCTACTAAAAATACAAAGATTAGCTGGGCATGGTGGTGCATGCCTGTAATCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATTGCTTGAGTCTGGGAGGTTGAGGCTGTGGTAAGCAGAGATCGTGCCACTGCACTCA... |
Task1_train_44839 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | GTAATCTCAGCATTTTGGGAGGCCAAAGCAGGTGGATCACCTGAAGCCAGGAGTTCAAGTCCCACCTGGCCAACATGGCAAAACCCCGTCTCTACTAACAACACAAAAAAATTAGCCAGGCATGGTGGCGCATGCTTGTAATCTCAGCTACTTGGGAGGCTGAGCATGAGAATCATTTGAACCTGGGAGGTGGAGGCTACAGTGAGCTGAGATTGCGCCACTGCACTCCAGCCTGGGAAAGAGCAAGACTCTGTCTCAAAAAAAAAATAAATAAATAAAGTAAAATAAAAAATAAATTTTTTTTCAGCAATATGGACTTT... | GTAATCTCAGCATTTTGGGAGGCCAAAGCAGGTGGATCACCTGAAGCCAGGAGTTCAAGTCCCACCTGGCCAACATGGCAAAACCCCGTCTCTACTAACAACACAAAAAAATTAGCCAGGCATGGTGGCGCATGCTTGTAATCTCAGCTACTTGGGAGGCTGAGCATGAGAATCATTTGAACCTGGGAGGTGGAGGCTACAGTGAGCTGAGATTGCGCCACTGCACTCCAGCCTGGGAAAGAGCAAGACTCTGTCTCAAAAAAAAAATAAATAAATAAAGTAAAATAAAAAATAAATTTTTTTTCAGCAATATGGACTTT... |
Task1_train_44840 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GACTTTTTAAAGAATTTCAAAAGAATTTTTACAAACAGCCAGGCACGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATGGTGAAACCCCGTCTCTGCTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGGCGTGAACCTGGGAGGCAGAGCTTGCAGTGAGCTGAGATCACGCCACTGCACCCCAGCCTGGGGGTGACAGAGTGAGACTCCGTCTCAAAAAAAAAAAAA... | GACTTTTTAAAGAATTTCAAAAGAATTTTTACAAACAGCCAGGCACGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATGGTGAAACCCCGTCTCTGCTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGGCGTGAACCTGGGAGGCAGAGCTTGCAGTGAGCTGAGATCACGCCACTGCACCCCAGCCTGGGGGTGACAGAGTGAGACTCCGTCTCAAAAAAAAAAAAA... |
Task1_train_44841 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | TTGTAGCAGTAGAAAGTAGTTTTCTAAATATATAAGTAGCCTCCTGGGCAGGAGAAGCTGGAAACAGTCTGATTTGCTGGCAGGTGTACTGGAAGCACTGGGAGGTGATGCCTGCTTGTGAGCGCCGTGGAGCTTTGGGACACAGCAGAAGGCACACAGTTGTGACCTCGATATGGGAGTGGTTTTGTGGGAAATGGGTTCTGACTGTGCAGATTCTCTATTTGCTTTATTTAAACTAAACAAAACCATGACGATGAGACAAAATTCCTATGCCATGGAAGTACGACAGTCTTGATAGCTGTTAATCAGTCCATTCGTTT... | TTGTAGCAGTAGAAAGTAGTTTTCTAAATATATAAGTAGCCTCCTGGGCAGGAGAAGCTGGAAACAGTCTGATTTGCTGGCAGGTGTACTGGAAGCACTGGGAGGTGATGCCTGCTTGTGAGCGCCGTGGAGCTTTGGGACACAGCAGAAGGCACACAGTTGTGACCTCGATATGGGAGTGGTTTTGTGGGAAATGGGTTCTGACTGTGCAGATTCTCTATTTGCTTTATTTAAACTAAACAAAACCATGACGATGAGACAAAATTCCTATGCCATGGAAGTACGACAGTCTTGATAGCTGTTAATCAGTCCATTCGTTT... |
Task1_train_44842 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTCCCCTCCCCTTCCCCCTCCCCTGCTCCCCCTCCCCTCCCCTGCTCCCCATCCCCCTCCCCAGTTTCCCCATCCCCTCCCCTGCTGCCCCATTCCCCTCCCCTACTCCCCCTTCCCCCTCCCCTGCTCCCCCCTCCCCTGCTGCCCCCTCCCCTCCTCCCCCACTCCCCTGCTGCCCCATCCCCCTCCCCTGCTGCTGCCCCATCCCCCTCCCCTGCTGCTGCCCTCCCTCCCCTGCTGCCCCATCTTGTTGCCACAGACTCACTTCCCTGCTCCCACCGTCTTGCCCCTTGGGGATGCTCTCTGGGGCTCAGGCCAAT... | CTCCCCTCCCCTTCCCCCTCCCCTGCTCCCCCTCCCCTCCCCTGCTCCCCATCCCCCTCCCCAGTTTCCCCATCCCCTCCCCTGCTGCCCCATTCCCCTCCCCTACTCCCCCTTCCCCCTCCCCTGCTCCCCCCTCCCCTGCTGCCCCCTCCCCTCCTCCCCCACTCCCCTGCTGCCCCATCCCCCTCCCCTGCTGCTGCCCCATCCCCCTCCCCTGCTGCTGCCCTCCCTCCCCTGCTGCCCCATCTTGTTGCCACAGACTCACTTCCCTGCTCCCACCGTCTTGCCCCTTGGGGATGCTCTCTGGGGCTCAGGCCAAT... |
Task1_train_44843 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCGAGTGCCTCTTCTGCTGCCCTAAACCACACTTAGCCTCCTTTCCACCCCTGCAGGTATCTTGGAGATGGCCGCTTCCATCTGGAGTCTGTCATGATTGCCAACCCCAATGTCCCCGCTTACCGGTATGGGCTGGGCCGGGCTGGGCTGACCAGCTGGTGAGGGGTGAGATTCCCTGCCACTGAGGTCCTCAATTGGTTGCATCCCCATTTCCTGGCCACTAAGCCACCAGCCCTAAGGGTCTGAGGCACTTGGGCCCTGGATCTGGGCATTAGCCCCAGGGCTGCTGTTGCCTACCCGTCTCCTGGGGTTTACACGGA... | GCGAGTGCCTCTTCTGCTGCCCTAAACCACACTTAGCCTCCTTTCCACCCCTGCAGGTATCTTGGAGATGGCCGCTTCCATCTGGAGTCTGTCATGATTGCCAACCCCAATGTCCCCGCTTACCGGTATGGGCTGGGCCGGGCTGGGCTGACCAGCTGGTGAGGGGTGAGATTCCCTGCCACTGAGGTCCTCAATTGGTTGCATCCCCATTTCCTGGCCACTAAGCCACCAGCCCTAAGGGTCTGAGGCACTTGGGCCCTGGATCTGGGCATTAGCCCCAGGGCTGCTGTTGCCTACCCGTCTCCTGGGGTTTACACGGA... |
Task1_train_44844 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AATGGAGAGTGAGAGGAAAAAGAGAGTGTGAGAGGAGGGGGAAGAGGCCTGGAGAACAGGAAAAAATAACCTAAAACATCAGAGGATAGGGAAGGTATTCAAAAAAAGTTCAAATAAAGAAGAAATAGAGAGGCAGGCAGGCTGTGGGCAGAAAGAAACAGAGCAGGATGAAGAGGGGAGCTGTAGGAACACGGGCAGGCCCAAGCCAGTGGTGCTGAAGCAATGGGCAGGTCAACTCACTGCGAGGGCAGATCCAGGGATGTGGGAGGAGGATTCCAGGTGTCCGGGTAGCCGAGCATCCAATCTGACCAGACTTTGAC... | AATGGAGAGTGAGAGGAAAAAGAGAGTGTGAGAGGAGGGGGAAGAGGCCTGGAGAACAGGAAAAAATAACCTAAAACATCAGAGGATAGGGAAGGTATTCAAAAAAAGTTCAAATAAAGAAGAAATAGAGAGGCAGGCAGGCTGTGGGCAGAAAGAAACAGAGCAGGATGAAGAGGGGAGCTGTAGGAACACGGGCAGGCCCAAGCCAGTGGTGCTGAAGCAATGGGCAGGTCAACTCACTGCGAGGGCAGATCCAGGGATGTGGGAGGAGGATTCCAGGTGTCCGGGTAGCCGAGCATCCAATCTGACCAGACTTTGAC... |
Task1_train_44845 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | ATTGCCAGTAATTTATGGTCCCAAGGAAGCAACTGGTGTAGGGAAGGCTCAGAACCCAAGAAAAGGGCAGTTTTTTTGTCGATATTCTGTTCTAAAACATAGTATTTCAGGTAGTAAAAATCCATCGTAACTACAGAATGCTGAAGCCTTTATCCTGAGGACAAAAAGATGACAGTTTACCTCATCCAAGAGCTCCAAAAGTCTGTTCCGAATCTGTTCTGGGTTCTCAACATTCGGATCCTTGACAAGTTGCCTGAACTTCTCAATCACCTGATAGAAAGCATTCTTCCACAGGATCTGATCCACATTCTGATTATCAG... | ATTGCCAGTAATTTATGGTCCCAAGGAAGCAACTGGTGTAGGGAAGGCTCAGAACCCAAGAAAAGGGCAGTTTTTTTGTCGATATTCTGTTCTAAAACATAGTATTTCAGGTAGTAAAAATCCATCGTAACTACAGAATGCTGAAGCCTTTATCCTGAGGACAAAAAGATGACAGTTTACCTCATCCAAGAGCTCCAAAAGTCTGTTCCGAATCTGTTCTGGGTTCTCAACATTCGGATCCTTGACAAGTTGCCTGAACTTCTCAATCACCTGATAGAAAGCATTCTTCCACAGGATCTGATCCACATTCTGATTATCAG... |
Task1_train_44846 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | GAAGCCTTTATCCTGAGGACAAAAAGATGACAGTTTACCTCATCCAAGAGCTCCAAAAGTCTGTTCCGAATCTGTTCTGGGTTCTCAACATTCGGATCCTTGACAAGTTGCCTGAACTTCTCAATCACCTGATAGAAAGCATTCTTCCACAGGATCTGATCCACATTCTGATTATCAGAGAACTCAATATCTAATAGAATACAGCGCTCATATAGCTGCAGCAGTTCAGCTCTGGAATAAAATACATGCAACTTCCAGCTCCAAATACACCACAGAAAAAGCTAGACTCAAGTTTTGAGATTCCTGCAAATTAACCACCT... | GAAGCCTTTATCCTGAGGACAAAAAGATGACAGTTTACCTCATCCAAGAGCTCCAAAAGTCTGTTCCGAATCTGTTCTGGGTTCTCAACATTCGGATCCTTGACAAGTTGCCTGAACTTCTCAATCACCTGATAGAAAGCATTCTTCCACAGGATCTGATCCACATTCTGATTATCAGAGAACTCAATATCTAATAGAATACAGCGCTCATATAGCTGCAGCAGTTCAGCTCTGGAATAAAATACATGCAACTTCCAGCTCCAAATACACCACAGAAAAAGCTAGACTCAAGTTTTGAGATTCCTGCAAATTAACCACCT... |
Task1_train_44847 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | TATCCTGAGGACAAAAAGATGACAGTTTACCTCATCCAAGAGCTCCAAAAGTCTGTTCCGAATCTGTTCTGGGTTCTCAACATTCGGATCCTTGACAAGTTGCCTGAACTTCTCAATCACCTGATAGAAAGCATTCTTCCACAGGATCTGATCCACATTCTGATTATCAGAGAACTCAATATCTAATAGAATACAGCGCTCATATAGCTGCAGCAGTTCAGCTCTGGAATAAAATACATGCAACTTCCAGCTCCAAATACACCACAGAAAAAGCTAGACTCAAGTTTTGAGATTCCTGCAAATTAACCACCTCCCCTGGC... | TATCCTGAGGACAAAAAGATGACAGTTTACCTCATCCAAGAGCTCCAAAAGTCTGTTCCGAATCTGTTCTGGGTTCTCAACATTCGGATCCTTGACAAGTTGCCTGAACTTCTCAATCACCTGATAGAAAGCATTCTTCCACAGGATCTGATCCACATTCTGATTATCAGAGAACTCAATATCTAATAGAATACAGCGCTCATATAGCTGCAGCAGTTCAGCTCTGGAATAAAATACATGCAACTTCCAGCTCCAAATACACCACAGAAAAAGCTAGACTCAAGTTTTGAGATTCCTGCAAATTAACCACCTCCCCTGGC... |
Task1_train_44848 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | TCCCATGGAGATGTCCGGAAGCTCTTAAGGCCTCTGTATTTCTGAAATCTAGAATATTGAAGATTTTTAAAGACATTAAGTCAGATTTATATGGTGCTATATAGACTCAAGTCACTGCTAAAATGGCTAAGGAGCTAGCTGAAAAGAACTCCAATCATCCTCTCTCCAAACAACCCAACAGCTTAAACCAAGACGACACTCCGAACAGCTTATAACAAGTTCTATCGGAACCAAACCCAAGCTTCTCACTGACAAAAAAGATGCTTGGTAATGGCCTGATACAGTTCAGATGTGTCTCCCTGCCCCAATCTCATACTGAA... | TCCCATGGAGATGTCCGGAAGCTCTTAAGGCCTCTGTATTTCTGAAATCTAGAATATTGAAGATTTTTAAAGACATTAAGTCAGATTTATATGGTGCTATATAGACTCAAGTCACTGCTAAAATGGCTAAGGAGCTAGCTGAAAAGAACTCCAATCATCCTCTCTCCAAACAACCCAACAGCTTAAACCAAGACGACACTCCGAACAGCTTATAACAAGTTCTATCGGAACCAAACCCAAGCTTCTCACTGACAAAAAAGATGCTTGGTAATGGCCTGATACAGTTCAGATGTGTCTCCCTGCCCCAATCTCATACTGAA... |
Task1_train_44849 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CGCCCCGGGCAGGAGCCGAGGGACGGGGAGGGGAATTTTGGAAGGAAGCCAGGGTATCTCCCTGGCCTGCCCTTGGCTTGCCCTTACCCCTTGCCTCACCACAGGTATGGGGAAGAGGAGCTTTTCTTCCTGCTCCCCCGTCTTTCCCAGGCTCAGATGCCGTTTCCCTTTGTGGCCTAGGTGCAGTGGAGGCTTGCCTCTTGCATCAGCTGAGACGCCGTGCCGCTGGCTTCCTGCGCAGTGACAAGATGGCAGCCCTGTTCACCAAGGTGGGGAAGACGTGCCCAGTGGCGGGGGAGATTTGCCACAAGGTACAGGAG... | CGCCCCGGGCAGGAGCCGAGGGACGGGGAGGGGAATTTTGGAAGGAAGCCAGGGTATCTCCCTGGCCTGCCCTTGGCTTGCCCTTACCCCTTGCCTCACCACAGGTATGGGGAAGAGGAGCTTTTCTTCCTGCTCCCCCGTCTTTCCCAGGCTCAGATGCCGTTTCCCTTTGTGGCCTAGGTGCAGTGGAGGCTTGCCTCTTGCATCAGCTGAGACGCCGTGCCGCTGGCTTCCTGCGCAGTGACAAGATGGCAGCCCTGTTCACCAAGGTGGGGAAGACGTGCCCAGTGGCGGGGGAGATTTGCCACAAGGTACAGGAG... |
Task1_train_44850 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGCCGAGGGACGGGGAGGGGAATTTTGGAAGGAAGCCAGGGTATCTCCCTGGCCTGCCCTTGGCTTGCCCTTACCCCTTGCCTCACCACAGGTATGGGGAAGAGGAGCTTTTCTTCCTGCTCCCCCGTCTTTCCCAGGCTCAGATGCCGTTTCCCTTTGTGGCCTAGGTGCAGTGGAGGCTTGCCTCTTGCATCAGCTGAGACGCCGTGCCGCTGGCTTCCTGCGCAGTGACAAGATGGCAGCCCTGTTCACCAAGGTGGGGAAGACGTGCCCAGTGGCGGGGGAGATTTGCCACAAGGTACAGGAGCTGCAGCAACAAG... | AGCCGAGGGACGGGGAGGGGAATTTTGGAAGGAAGCCAGGGTATCTCCCTGGCCTGCCCTTGGCTTGCCCTTACCCCTTGCCTCACCACAGGTATGGGGAAGAGGAGCTTTTCTTCCTGCTCCCCCGTCTTTCCCAGGCTCAGATGCCGTTTCCCTTTGTGGCCTAGGTGCAGTGGAGGCTTGCCTCTTGCATCAGCTGAGACGCCGTGCCGCTGGCTTCCTGCGCAGTGACAAGATGGCAGCCCTGTTCACCAAGGTGGGGAAGACGTGCCCAGTGGCGGGGGAGATTTGCCACAAGGTACAGGAGCTGCAGCAACAAG... |
Task1_train_44851 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | GGCTGTCTCTGTCTCCACAGTGGGACCCTGTGCCTTGGAATACACTAAGCTCAAGACAGCCGATCACTACTGGACTGACCCCTCTGCTGATGAGCTGGTCCAGCGGCACCGCATCCGGGGTCCACCTACTCGCCAGGACTCCCCTGCAAAGCGCCCAGCCCTGGGGGTAGGTGCCCCCTCCCCACCCTTTGGGCTCATCTGGGCTATGCCCATGGGCCTGTAGGGACGGGAAACCGGCCTCTCTACGGGACAGGCCTTGGAGATGCCCCAAGGTAGCGGCTGCCTCAGAAGAGCCTTCTCCGCACAATAAAACTTAACAC... | GGCTGTCTCTGTCTCCACAGTGGGACCCTGTGCCTTGGAATACACTAAGCTCAAGACAGCCGATCACTACTGGACTGACCCCTCTGCTGATGAGCTGGTCCAGCGGCACCGCATCCGGGGTCCACCTACTCGCCAGGACTCCCCTGCAAAGCGCCCAGCCCTGGGGGTAGGTGCCCCCTCCCCACCCTTTGGGCTCATCTGGGCTATGCCCATGGGCCTGTAGGGACGGGAAACCGGCCTCTCTACGGGACAGGCCTTGGAGATGCCCCAAGGTAGCGGCTGCCTCAGAAGAGCCTTCTCCGCACAATAAAACTTAACAC... |
Task1_train_44852 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | TAAAGTCTCTGGAAATGTTTCTAAGGGGTTATAGCGAATAAAGAAACATTTATTCAAGAAAATCTACTAAAATAAATGAATGGATAAATAAATAAATTTAGGCAAATAGGCAAATTCACAAAAAAAGAATCCACAAATCATAAGGATCAACTGTAGTTACTATTTTCTGAGTTAATTCTGGTATCAAGACAGCAAACCCAATTACAAAGTGCCAGATTTTTTTAAATTACCGAAGTCTGTGTATTAAAGAAAAAGGTAATGAAATGCGTTAAACTAAAAAGGCAGGTGAAGACACAAAGTTTGGAGGCATTCATTCTGTG... | TAAAGTCTCTGGAAATGTTTCTAAGGGGTTATAGCGAATAAAGAAACATTTATTCAAGAAAATCTACTAAAATAAATGAATGGATAAATAAATAAATTTAGGCAAATAGGCAAATTCACAAAAAAAGAATCCACAAATCATAAGGATCAACTGTAGTTACTATTTTCTGAGTTAATTCTGGTATCAAGACAGCAAACCCAATTACAAAGTGCCAGATTTTTTTAAATTACCGAAGTCTGTGTATTAAAGAAAAAGGTAATGAAATGCGTTAAACTAAAAAGGCAGGTGAAGACACAAAGTTTGGAGGCATTCATTCTGTG... |
Task1_train_44853 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CAGCATAGATTAAATGTAAGGAGAGGTTTGGTTTTTGTTTGTTTTGAGTCGGAGTCTCGCTTACTTTTTCTTTTGAATTTTAAAAAAGAAGAGTGAGAGTACGTCTTTACTCTCTCAGAACACAGTAAGTTTTGATCTTAGTTTTTACTAGGATGCCTACAGTAGTTGTTTAGAAACACTAATTACCATGAGTTTGGTCGGGACACAATGAACAGTGTGTCAAGGGTTGAGGCAACATCAGGGCAGATAATTACAGTGTATTGTGAGAAGTGGTAAATACGTGTATGTATGAAGTACTATGAAGTCACAGAAGAGGTGGT... | CAGCATAGATTAAATGTAAGGAGAGGTTTGGTTTTTGTTTGTTTTGAGTCGGAGTCTCGCTTACTTTTTCTTTTGAATTTTAAAAAAGAAGAGTGAGAGTACGTCTTTACTCTCTCAGAACACAGTAAGTTTTGATCTTAGTTTTTACTAGGATGCCTACAGTAGTTGTTTAGAAACACTAATTACCATGAGTTTGGTCGGGACACAATGAACAGTGTGTCAAGGGTTGAGGCAACATCAGGGCAGATAATTACAGTGTATTGTGAGAAGTGGTAAATACGTGTATGTATGAAGTACTATGAAGTCACAGAAGAGGTGGT... |
Task1_train_44854 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | TGAGTTTGGTCGGGACACAATGAACAGTGTGTCAAGGGTTGAGGCAACATCAGGGCAGATAATTACAGTGTATTGTGAGAAGTGGTAAATACGTGTATGTATGAAGTACTATGAAGTCACAGAAGAGGTGGTTACTCTGTGTTCGCTTAATTGTTTGGGGTCAAAACTAGTGAGAATGGTAACTAAACCCGCAAGTTCTGCTGTTTATGCTAGCTGCTGAGAGGCTTGCTAATGATGTTTAAATATCATTGATAGCTATTAGGTTGAACCATTATTGGCAGTTTTTAATGGTTTAACCCTAGTAGTATCTTGGTGTGACG... | TGAGTTTGGTCGGGACACAATGAACAGTGTGTCAAGGGTTGAGGCAACATCAGGGCAGATAATTACAGTGTATTGTGAGAAGTGGTAAATACGTGTATGTATGAAGTACTATGAAGTCACAGAAGAGGTGGTTACTCTGTGTTCGCTTAATTGTTTGGGGTCAAAACTAGTGAGAATGGTAACTAAACCCGCAAGTTCTGCTGTTTATGCTAGCTGCTGAGAGGCTTGCTAATGATGTTTAAATATCATTGATAGCTATTAGGTTGAACCATTATTGGCAGTTTTTAATGGTTTAACCCTAGTAGTATCTTGGTGTGACG... |
Task1_train_44855 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | ACTTAACAGTTTCTCTTTGTCATATCCAAAGTGCCAGCCTCACTCATGGGCCTTGTACTTTGGGGCCGTTATTAGTATGATAAGGATGAGGGTGGCTTGAACACAGGCGGTGAGATACTGCAACAGTCCCTCCGATCACTGAGATGGCTGATAAGTGACTGATGGGTAGGGAGCGTGTAGGGCGTGGGTATGCTGGACAAAGGGAAAATTCATGTCCCGGGTGGATAGAGTGGGATGGTGGAAGATTTCATCATGCTATTCAGGACGGCACAAAATTGAAAACTTATGAATTATTTCTGGAATTTTCCATGTAATATTTT... | ACTTAACAGTTTCTCTTTGTCATATCCAAAGTGCCAGCCTCACTCATGGGCCTTGTACTTTGGGGCCGTTATTAGTATGATAAGGATGAGGGTGGCTTGAACACAGGCGGTGAGATACTGCAACAGTCCCTCCGATCACTGAGATGGCTGATAAGTGACTGATGGGTAGGGAGCGTGTAGGGCGTGGGTATGCTGGACAAAGGGAAAATTCATGTCCCGGGTGGATAGAGTGGGATGGTGGAAGATTTCATCATGCTATTCAGGACGGCACAAAATTGAAAACTTATGAATTATTTCTGGAATTTTCCATGTAATATTTT... |
Task1_train_44856 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | CAACAAATACTGTCAGTTTTTCTTACAGCGACAGGCTCACTTCATTTATTTTGTGGCAACGCCTGCCAAATACCAATTCTGAATAACTATAGTTTATCAGTAATTCTAACAAATAAAAATAATGTTCCATGAAATGGCTGGTTGAGCCCAAATTCAATCATTCAAGTACTTCCTCACAAGACAATCATTGTACTCTGAGATGCAGAAGTGCTCTCTGGTACTAGCCATTATATTATACAAAATATTAAAAAGACATACATGAAAAGATGTGATTTAATAAAAATTTATTGCTTTATCAAGGACAACATTTGTTTAGAATT... | CAACAAATACTGTCAGTTTTTCTTACAGCGACAGGCTCACTTCATTTATTTTGTGGCAACGCCTGCCAAATACCAATTCTGAATAACTATAGTTTATCAGTAATTCTAACAAATAAAAATAATGTTCCATGAAATGGCTGGTTGAGCCCAAATTCAATCATTCAAGTACTTCCTCACAAGACAATCATTGTACTCTGAGATGCAGAAGTGCTCTCTGGTACTAGCCATTATATTATACAAAATATTAAAAAGACATACATGAAAAGATGTGATTTAATAAAAATTTATTGCTTTATCAAGGACAACATTTGTTTAGAATT... |
Task1_train_44857 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGTTTATCAGTAATTCTAACAAATAAAAATAATGTTCCATGAAATGGCTGGTTGAGCCCAAATTCAATCATTCAAGTACTTCCTCACAAGACAATCATTGTACTCTGAGATGCAGAAGTGCTCTCTGGTACTAGCCATTATATTATACAAAATATTAAAAAGACATACATGAAAAGATGTGATTTAATAAAAATTTATTGCTTTATCAAGGACAACATTTGTTTAGAATTTTGTCTTTCTCTGCATCTATTGACATGTTGATTTTTTCTTTTTATTTGTCAATATAATAAACACTTATGGATTAAAAAGTATCAAATTAT... | AGTTTATCAGTAATTCTAACAAATAAAAATAATGTTCCATGAAATGGCTGGTTGAGCCCAAATTCAATCATTCAAGTACTTCCTCACAAGACAATCATTGTACTCTGAGATGCAGAAGTGCTCTCTGGTACTAGCCATTATATTATACAAAATATTAAAAAGACATACATGAAAAGATGTGATTTAATAAAAATTTATTGCTTTATCAAGGACAACATTTGTTTAGAATTTTGTCTTTCTCTGCATCTATTGACATGTTGATTTTTTCTTTTTATTTGTCAATATAATAAACACTTATGGATTAAAAAGTATCAAATTAT... |
Task1_train_44858 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TCTGCTGCTGAAGCTCTTTTGAGTTTTTTAAAGTTTAGTCATTGTATTATTTAGCTCCAGAATTACTGTTTCTTTTTTGTGGTTTCTGTTTGTTGAAATTTACATTTTATTTATGTATTGATTTCCTGATTTTGTTTAGTAGTTTACCTGTGTTTTTGTGTGGGTCACCATGTTTCTTCAAATGATCACTTGAATTCTTTGTCAGGCAGTTCATATTTCTCCATTTCTTTGATGGTTTCTGAAGCTTTATTTTGTTCCTTTGGCTTTGCTAAGTTTCCTTGATTCCTTGTGTTTCCTGTAGCTTCACATTTGTGTTTGCA... | TCTGCTGCTGAAGCTCTTTTGAGTTTTTTAAAGTTTAGTCATTGTATTATTTAGCTCCAGAATTACTGTTTCTTTTTTGTGGTTTCTGTTTGTTGAAATTTACATTTTATTTATGTATTGATTTCCTGATTTTGTTTAGTAGTTTACCTGTGTTTTTGTGTGGGTCACCATGTTTCTTCAAATGATCACTTGAATTCTTTGTCAGGCAGTTCATATTTCTCCATTTCTTTGATGGTTTCTGAAGCTTTATTTTGTTCCTTTGGCTTTGCTAAGTTTCCTTGATTCCTTGTGTTTCCTGTAGCTTCACATTTGTGTTTGCA... |
Task1_train_44859 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CTCAGTATTCTTGGTGAGGCATGACAGAAGTGGTCCTCTTGGTTAGCATCCTGAAAGTCAGGGGAAGTTGTACATATGTTTTATTTTCTTTTTTACTTATGGAAGAACTCATGAGATGAGGGGATCTCTCTTTGTGCTACTCTGTGCTGGCTTGGGTGAGGGGTGATTCAGGTAATGTGACAGAGTTTTTTCTACAATGTTCAATATGGTGTTTTTTCTACTTCTGTGTACTACCAGGGTGCTATAAACTTTCACTTGGATTCTGGAGCTCTCACAAAGGTATTTTCATCTGTGGATGGTTGATAAATTAGTCTGTATGT... | CTCAGTATTCTTGGTGAGGCATGACAGAAGTGGTCCTCTTGGTTAGCATCCTGAAAGTCAGGGGAAGTTGTACATATGTTTTATTTTCTTTTTTACTTATGGAAGAACTCATGAGATGAGGGGATCTCTCTTTGTGCTACTCTGTGCTGGCTTGGGTGAGGGGTGATTCAGGTAATGTGACAGAGTTTTTTCTACAATGTTCAATATGGTGTTTTTTCTACTTCTGTGTACTACCAGGGTGCTATAAACTTTCACTTGGATTCTGGAGCTCTCACAAAGGTATTTTCATCTGTGGATGGTTGATAAATTAGTCTGTATGT... |
Task1_train_44860 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | TGCTCTACTACCTTTTATTATCAGACGATCGTGTCTGGGCTTCAGATAAGGTGAATAGGGAGCTGGTGAGCTAGAATTGCTATTATCTACAGCAATTACCATCTATGGCACAGCAGCCTGCAGTCAGATACCTGAAGGTAAACAGACAACAAGAATGAAAAACAGCACCCAGTTGTGACATTTTATTTTCCTATAGAAACGTATTGGTTGTGGCTGTAACGTACTGTACAGAGTCTTGCCACAACGTCTACTGACAAAGCTTTCCAAGTCGTTTTTGGCAACCATGCACAATAATCAATGTATTCTGAAACCGTTGGCCT... | TGCTCTACTACCTTTTATTATCAGACGATCGTGTCTGGGCTTCAGATAAGGTGAATAGGGAGCTGGTGAGCTAGAATTGCTATTATCTACAGCAATTACCATCTATGGCACAGCAGCCTGCAGTCAGATACCTGAAGGTAAACAGACAACAAGAATGAAAAACAGCACCCAGTTGTGACATTTTATTTTCCTATAGAAACGTATTGGTTGTGGCTGTAACGTACTGTACAGAGTCTTGCCACAACGTCTACTGACAAAGCTTTCCAAGTCGTTTTTGGCAACCATGCACAATAATCAATGTATTCTGAAACCGTTGGCCT... |
Task1_train_44861 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ATATTTCTTGGAGGCTTTGCTCATTTCTTTTTATTCTTTTTTCTCTAAACTTCCCTTCTCACTTCATTTCATTCATTTCATCTTCCATCGCTGATACCCTTTCTTCCAGTTAATCGCATCGGCTCCTGAGGCTTCTGCATTCTTCACGTAGTTCTCCAGCCTTGGTTTTCAGCTCCATCAGCTCCTTTAAGCACTTCTCTGTATTGGTTATTCTAGTTATACATTCTTCTAAATTTTTTCCAAAGTTTTCAACTTCTTTGCCTTTGGTTTGAATGTCCTCCCGTAGCTCAGAGTAATTTGATCGTCTGAAGCCTTCTTCT... | ATATTTCTTGGAGGCTTTGCTCATTTCTTTTTATTCTTTTTTCTCTAAACTTCCCTTCTCACTTCATTTCATTCATTTCATCTTCCATCGCTGATACCCTTTCTTCCAGTTAATCGCATCGGCTCCTGAGGCTTCTGCATTCTTCACGTAGTTCTCCAGCCTTGGTTTTCAGCTCCATCAGCTCCTTTAAGCACTTCTCTGTATTGGTTATTCTAGTTATACATTCTTCTAAATTTTTTCCAAAGTTTTCAACTTCTTTGCCTTTGGTTTGAATGTCCTCCCGTAGCTCAGAGTAATTTGATCGTCTGAAGCCTTCTTCT... |
Task1_train_44862 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ATACATTCTTCTAAATTTTTTCCAAAGTTTTCAACTTCTTTGCCTTTGGTTTGAATGTCCTCCCGTAGCTCAGAGTAATTTGATCGTCTGAAGCCTTCTTCTCTCAGCTCGTCACAGTCATTCCCCATCCAGCTTTGTTCCGTTGCTGGTGAGGAACTGCATTCCTTTGGAGGAGGAGAGGCCCTCTGCTTTCTAGAGTTTCCAGTTTTTCCCCCATCTTTGTGGTTTTATCTACTTTTGGTCTTTGATGATGGTGATGTACAGATGGGTTTTTGGTGTGGATGTCCTTTCTGTTTGTTAGTTTTCCTTCTAACAGACAG... | ATACATTCTTCTAAATTTTTTCCAAAGTTTTCAACTTCTTTGCCTTTGGTTTGAATGTCCTCCCGTAGCTCAGAGTAATTTGATCGTCTGAAGCCTTCTTCTCTCAGCTCGTCACAGTCATTCCCCATCCAGCTTTGTTCCGTTGCTGGTGAGGAACTGCATTCCTTTGGAGGAGGAGAGGCCCTCTGCTTTCTAGAGTTTCCAGTTTTTCCCCCATCTTTGTGGTTTTATCTACTTTTGGTCTTTGATGATGGTGATGTACAGATGGGTTTTTGGTGTGGATGTCCTTTCTGTTTGTTAGTTTTCCTTCTAACAGACAG... |
Task1_train_44863 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ACCAAAACTCATGTTGAAATGTGATCCCCAGTGTGGGAGGTGTTGGGAGGTAAAGCCTAGTGGGAAGCGTTTGAGTCAAGGGGGTGGATCCCTCATGAGTGGTCTGGTGCTGTTCTCATGGTAGTAAGTGTGTTCTCATTCTCTCAAGACTGGATTAATCTTAAGGGAATGTTCCTACAGGAGTGGGTTGTGATAAAACCAGTATACTTCTCGGGTTTTCTCTCTTCCCCTGTATCCACTTCCCTGTTGACCTTCTCTGACAGGTTATGATGCAGCAAGAAAGCCCTTGCCAGAAGCCAGGGCCACGCTCTTGAATGTCC... | ACCAAAACTCATGTTGAAATGTGATCCCCAGTGTGGGAGGTGTTGGGAGGTAAAGCCTAGTGGGAAGCGTTTGAGTCAAGGGGGTGGATCCCTCATGAGTGGTCTGGTGCTGTTCTCATGGTAGTAAGTGTGTTCTCATTCTCTCAAGACTGGATTAATCTTAAGGGAATGTTCCTACAGGAGTGGGTTGTGATAAAACCAGTATACTTCTCGGGTTTTCTCTCTTCCCCTGTATCCACTTCCCTGTTGACCTTCTCTGACAGGTTATGATGCAGCAAGAAAGCCCTTGCCAGAAGCCAGGGCCACGCTCTTGAATGTCC... |
Task1_train_44864 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GTCTGGTGCTGTTCTCATGGTAGTAAGTGTGTTCTCATTCTCTCAAGACTGGATTAATCTTAAGGGAATGTTCCTACAGGAGTGGGTTGTGATAAAACCAGTATACTTCTCGGGTTTTCTCTCTTCCCCTGTATCCACTTCCCTGTTGACCTTCTCTGACAGGTTATGATGCAGCAAGAAAGCCCTTGCCAGAAGCCAGGGCCACGCTCTTGAATGTCCCAGCCTACAGATCCATGAGACAATTCAACCTCTTTTCTTATAAATTCCCCAGTCTCAAGTATTCTGTTATAGCAACACAAAATGAACCAAGACAAAGGCCA... | GTCTGGTGCTGTTCTCATGGTAGTAAGTGTGTTCTCATTCTCTCAAGACTGGATTAATCTTAAGGGAATGTTCCTACAGGAGTGGGTTGTGATAAAACCAGTATACTTCTCGGGTTTTCTCTCTTCCCCTGTATCCACTTCCCTGTTGACCTTCTCTGACAGGTTATGATGCAGCAAGAAAGCCCTTGCCAGAAGCCAGGGCCACGCTCTTGAATGTCCCAGCCTACAGATCCATGAGACAATTCAACCTCTTTTCTTATAAATTCCCCAGTCTCAAGTATTCTGTTATAGCAACACAAAATGAACCAAGACAAAGGCCA... |
Task1_train_44865 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CGGGCGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAATGTGATGAAACCTCCATCTCTACTAAAAATACAAACAATAACAACAACAACAACAAAAAACTAGCCAGGCGTAGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCGGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCAAGATGCAGTGAGACTCCATCTCAAAAAAAAAAGAAAAAAAAAAAAAAAGAAAATATTCCATAATAGTCTATCTGAAGGAGGTAAAA... | CGGGCGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAATGTGATGAAACCTCCATCTCTACTAAAAATACAAACAATAACAACAACAACAACAAAAAACTAGCCAGGCGTAGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCGGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCAAGATGCAGTGAGACTCCATCTCAAAAAAAAAAGAAAAAAAAAAAAAAAGAAAATATTCCATAATAGTCTATCTGAAGGAGGTAAAA... |
Task1_train_44866 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCGGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCAAGATGCAGTGAGACTCCATCTCAAAAAAAAAAGAAAAAAAAAAAAAAAGAAAATATTCCATAATAGTCTATCTGAAGGAGGTAAAAATAAACAAGATATGGTTTTCCTTCCCCTAAAATCTTGCCCTCATCTTAGGTTGGATGTGCAGTTTGGTCACGTTGGCAGTATGAGTGAAGTGGAAATACGGAGGGAAAAGTTCACACCTACAGATGTAAACCTCACAGTTTACTAAGCAATGGTTG... | AGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCGGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCAAGATGCAGTGAGACTCCATCTCAAAAAAAAAAGAAAAAAAAAAAAAAAGAAAATATTCCATAATAGTCTATCTGAAGGAGGTAAAAATAAACAAGATATGGTTTTCCTTCCCCTAAAATCTTGCCCTCATCTTAGGTTGGATGTGCAGTTTGGTCACGTTGGCAGTATGAGTGAAGTGGAAATACGGAGGGAAAAGTTCACACCTACAGATGTAAACCTCACAGTTTACTAAGCAATGGTTG... |
Task1_train_44867 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ATGTGGTGTTTTAAGGAAGAGATTAAATGGGGGACAAAATGAGTACATTGTTTCTGAGATAACTGAAGTCACTTGGTTAACTGAGAAATTTAAAAGTGTTTTCTCCAGTTGATTTTGTGCACTGAGGACAGAGCAAGGACAAGCCTTTCCCAGTGTCATGTGCGGATGTTTTACTCTCTTCACTCCATGCCTCCTCTGCCAACAACTCCACACAATCTCTTCATGCAGTCTGCAATGCCCTCCCTGTCCCACACAACATCATGTCTGTTTGGTGAACCTGATTCATTCACCAAGACCCAGTTCAAGTCTCTCCTCTTCTT... | ATGTGGTGTTTTAAGGAAGAGATTAAATGGGGGACAAAATGAGTACATTGTTTCTGAGATAACTGAAGTCACTTGGTTAACTGAGAAATTTAAAAGTGTTTTCTCCAGTTGATTTTGTGCACTGAGGACAGAGCAAGGACAAGCCTTTCCCAGTGTCATGTGCGGATGTTTTACTCTCTTCACTCCATGCCTCCTCTGCCAACAACTCCACACAATCTCTTCATGCAGTCTGCAATGCCCTCCCTGTCCCACACAACATCATGTCTGTTTGGTGAACCTGATTCATTCACCAAGACCCAGTTCAAGTCTCTCCTCTTCTT... |
Task1_train_44868 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | GAAGACATAGCCTTAGAGTCATTGGTCAATCTACCATGCCTGAATGAAGGACAAGTAGAAGACCAGTGTCTGTGCAATGTAGAACCCTAACTGCACCTGGCAGCAACCAACCCACAGGACATGATTACAACTTTGGTTTTAGAGGGGAGTAGCTGACAATGTACACAGAAAAAATAATTTTAAATTAACTTGTTAGTCAAAGTCCAGTGTAAGGATTTAAGTAACAATAATAACACTAGCAATTAATTGAACAAGGAGTGTTGAATTGACACTTCATAGTGTGGTCCCTCTCTTTGAAGAAATGTGCTGGGCTGGTCTTT... | GAAGACATAGCCTTAGAGTCATTGGTCAATCTACCATGCCTGAATGAAGGACAAGTAGAAGACCAGTGTCTGTGCAATGTAGAACCCTAACTGCACCTGGCAGCAACCAACCCACAGGACATGATTACAACTTTGGTTTTAGAGGGGAGTAGCTGACAATGTACACAGAAAAAATAATTTTAAATTAACTTGTTAGTCAAAGTCCAGTGTAAGGATTTAAGTAACAATAATAACACTAGCAATTAATTGAACAAGGAGTGTTGAATTGACACTTCATAGTGTGGTCCCTCTCTTTGAAGAAATGTGCTGGGCTGGTCTTT... |
Task1_train_44869 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AGTTTATTTCACTTAGCATAATGTCATCCAGTTTGTATAAAAGGATATATTTTAACATTCTCACCACAAAAATGAGTTGTTGAAGGGATGGCTATGTTAATTACCTTGATTTAATCATTTTACAAAGCATATGCCAATCAATATCACACTGTACCCCATAAATATACACAATTATTATTCATCAATTAAAAATAAATTATTAAAATGTAATCTGCTTATTAGTTTGGGTTGATCCCTCAGAGAAAAATGGGAAAATTCTATCTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTG... | AGTTTATTTCACTTAGCATAATGTCATCCAGTTTGTATAAAAGGATATATTTTAACATTCTCACCACAAAAATGAGTTGTTGAAGGGATGGCTATGTTAATTACCTTGATTTAATCATTTTACAAAGCATATGCCAATCAATATCACACTGTACCCCATAAATATACACAATTATTATTCATCAATTAAAAATAAATTATTAAAATGTAATCTGCTTATTAGTTTGGGTTGATCCCTCAGAGAAAAATGGGAAAATTCTATCTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTG... |
Task1_train_44870 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGAAAGTTCATTTTAGGTTTGGGTCAGGTAAAAAGACATGCAGACATAAAAATTAAGAAAAGTTCAACCATTGTGGAAGTCAGTGTGGCGATTCCTCAGGGATCTAGAACTAGAAATACCACTTGACCCAGCCATCCCATTACTGGGTATATACCCAAAGGACTATAAATCATGCTGCTGTAAAGACACATGCACATGTATGTTTATTGCAGCACTATTCATGATAGCAAAGACTTGGAACCAACCCAAATGTCCAACAATGATTGACTGGATTAAGAAAATGTGGCACATATACACCATGGAATACTTTGCAGCTGTAA... | AGAAAGTTCATTTTAGGTTTGGGTCAGGTAAAAAGACATGCAGACATAAAAATTAAGAAAAGTTCAACCATTGTGGAAGTCAGTGTGGCGATTCCTCAGGGATCTAGAACTAGAAATACCACTTGACCCAGCCATCCCATTACTGGGTATATACCCAAAGGACTATAAATCATGCTGCTGTAAAGACACATGCACATGTATGTTTATTGCAGCACTATTCATGATAGCAAAGACTTGGAACCAACCCAAATGTCCAACAATGATTGACTGGATTAAGAAAATGTGGCACATATACACCATGGAATACTTTGCAGCTGTAA... |
Task1_train_44871 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | GGAGCCAGACACATTCATTCATTCATTCGTTTCAAAAGTGTTTACTGAGCACCTACTACATGCCAAACATAGCTATTTAGGAAAAATTCATGGACAAAACAGTCAAGATATCTGTCCTCGAAGATTTTATTGTCTAGTGGAGGATTTAAAAAATAAGTAAACATATAACAGAATGTCAGGAAATGTACTTTTTTTTTAGGAAAAAAACACACAAGGTAAATGGAAAGAGAGAGAGATGGGGGTTATTATTTTAAGTGGGTTGTTGAATGAGGACAGTGGGAACAGCAAGTATAAAAGCCCTGAGATGGAAATGTTCTTAG... | GGAGCCAGACACATTCATTCATTCATTCGTTTCAAAAGTGTTTACTGAGCACCTACTACATGCCAAACATAGCTATTTAGGAAAAATTCATGGACAAAACAGTCAAGATATCTGTCCTCGAAGATTTTATTGTCTAGTGGAGGATTTAAAAAATAAGTAAACATATAACAGAATGTCAGGAAATGTACTTTTTTTTTAGGAAAAAAACACACAAGGTAAATGGAAAGAGAGAGAGATGGGGGTTATTATTTTAAGTGGGTTGTTGAATGAGGACAGTGGGAACAGCAAGTATAAAAGCCCTGAGATGGAAATGTTCTTAG... |
Task1_train_44872 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CATTCATTCATTCGTTTCAAAAGTGTTTACTGAGCACCTACTACATGCCAAACATAGCTATTTAGGAAAAATTCATGGACAAAACAGTCAAGATATCTGTCCTCGAAGATTTTATTGTCTAGTGGAGGATTTAAAAAATAAGTAAACATATAACAGAATGTCAGGAAATGTACTTTTTTTTTAGGAAAAAAACACACAAGGTAAATGGAAAGAGAGAGAGATGGGGGTTATTATTTTAAGTGGGTTGTTGAATGAGGACAGTGGGAACAGCAAGTATAAAAGCCCTGAGATGGAAATGTTCTTAGCATTTTTGAAGATCA... | CATTCATTCATTCGTTTCAAAAGTGTTTACTGAGCACCTACTACATGCCAAACATAGCTATTTAGGAAAAATTCATGGACAAAACAGTCAAGATATCTGTCCTCGAAGATTTTATTGTCTAGTGGAGGATTTAAAAAATAAGTAAACATATAACAGAATGTCAGGAAATGTACTTTTTTTTTAGGAAAAAAACACACAAGGTAAATGGAAAGAGAGAGAGATGGGGGTTATTATTTTAAGTGGGTTGTTGAATGAGGACAGTGGGAACAGCAAGTATAAAAGCCCTGAGATGGAAATGTTCTTAGCATTTTTGAAGATCA... |
Task1_train_44873 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GTGTTTACTGAGCACCTACTACATGCCAAACATAGCTATTTAGGAAAAATTCATGGACAAAACAGTCAAGATATCTGTCCTCGAAGATTTTATTGTCTAGTGGAGGATTTAAAAAATAAGTAAACATATAACAGAATGTCAGGAAATGTACTTTTTTTTTAGGAAAAAAACACACAAGGTAAATGGAAAGAGAGAGAGATGGGGGTTATTATTTTAAGTGGGTTGTTGAATGAGGACAGTGGGAACAGCAAGTATAAAAGCCCTGAGATGGAAATGTTCTTAGCATTTTTGAAGATCAACTAAGAATACAGTGTGTTAAA... | GTGTTTACTGAGCACCTACTACATGCCAAACATAGCTATTTAGGAAAAATTCATGGACAAAACAGTCAAGATATCTGTCCTCGAAGATTTTATTGTCTAGTGGAGGATTTAAAAAATAAGTAAACATATAACAGAATGTCAGGAAATGTACTTTTTTTTTAGGAAAAAAACACACAAGGTAAATGGAAAGAGAGAGAGATGGGGGTTATTATTTTAAGTGGGTTGTTGAATGAGGACAGTGGGAACAGCAAGTATAAAAGCCCTGAGATGGAAATGTTCTTAGCATTTTTGAAGATCAACTAAGAATACAGTGTGTTAAA... |
Task1_train_44874 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AAAATTATAAAATAGCTAACCAAAGTCACAACACAGGCACGATTGTAAGAAAAACCATCTAATTCATCAACTGCATTTTAGACTGAAATGAAGAATGTCTCCCTCCACACTAACAAAACAAATAAGAAGCAGAAGAGGCCGGCGCAGGAGCTCACACCTGGAATCCCAGCACTCTGCAAGGCTGAGGTGGGCAGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGCGAAACCCTGTCTCTACTAAAAATACAAAAAGGAGCCAGGTGTGATGGTGCACGTCTGTAATCCCAGCTACTCAGGAGGCTGA... | AAAATTATAAAATAGCTAACCAAAGTCACAACACAGGCACGATTGTAAGAAAAACCATCTAATTCATCAACTGCATTTTAGACTGAAATGAAGAATGTCTCCCTCCACACTAACAAAACAAATAAGAAGCAGAAGAGGCCGGCGCAGGAGCTCACACCTGGAATCCCAGCACTCTGCAAGGCTGAGGTGGGCAGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGCGAAACCCTGTCTCTACTAAAAATACAAAAAGGAGCCAGGTGTGATGGTGCACGTCTGTAATCCCAGCTACTCAGGAGGCTGA... |
Task1_train_44875 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | TCCAAAACTCAAATAAAGACACATCTTACTGATTTTCCCCTGTGGATTTCCTGGGAGGGAGCCACTCTCCCAAATTTGCTCTCCCAGCATCCTCTCTGGCCCACTTACAAAGAAATCCACAAAACTGAGACCCAAATGGGGACAGTTAATGATGATGATGATGATGACAACAGTCGACTTTTGGTGGCCCCTGCCCGGCTCTCTTGCCTCACTTCCAGCCTTCTTTTCATTGCTCAACCATGCCAAGCTCAATCCCATCTTGGGGCTTTCGCCCTGATCCTTCTCATCATGTCGGCCTCAGGCCAAAGATGACCACTCTG... | TCCAAAACTCAAATAAAGACACATCTTACTGATTTTCCCCTGTGGATTTCCTGGGAGGGAGCCACTCTCCCAAATTTGCTCTCCCAGCATCCTCTCTGGCCCACTTACAAAGAAATCCACAAAACTGAGACCCAAATGGGGACAGTTAATGATGATGATGATGATGACAACAGTCGACTTTTGGTGGCCCCTGCCCGGCTCTCTTGCCTCACTTCCAGCCTTCTTTTCATTGCTCAACCATGCCAAGCTCAATCCCATCTTGGGGCTTTCGCCCTGATCCTTCTCATCATGTCGGCCTCAGGCCAAAGATGACCACTCTG... |
Task1_train_44876 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AACAAATACATAGAAATGGGGAATGGTTAGCTCTTCTCTATAACAGAATGCCAGGTAATAAATGCAGAAGCAATGATGGAGTTAGAAGATCATCTTCTCTGGGTGTGGTGGCTCATGCCTGTAATCCCAGCACTTCGGGAGGCCAAGGCAGGCGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGAGTAACATGGTAAAACCCCATCTGTACTAAAAATATAAAAATTAGCCGGGCGTGATGATGGGCAGCTGTGATCCCAGCTACCTGGAAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCCGAGGTTGCA... | AACAAATACATAGAAATGGGGAATGGTTAGCTCTTCTCTATAACAGAATGCCAGGTAATAAATGCAGAAGCAATGATGGAGTTAGAAGATCATCTTCTCTGGGTGTGGTGGCTCATGCCTGTAATCCCAGCACTTCGGGAGGCCAAGGCAGGCGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGAGTAACATGGTAAAACCCCATCTGTACTAAAAATATAAAAATTAGCCGGGCGTGATGATGGGCAGCTGTGATCCCAGCTACCTGGAAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCCGAGGTTGCA... |
Task1_train_44877 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | CCAGGAGTTCTGCAGCAGGAACTTCACGATGCCCAGCTGGTTGGTGCACGCGGCCAGGGACAGGGGCAGTTCACCTGCATGAACACAGGGCCCAGGTGGGCCTCAGGAGTGAGATCCAGCTGGCCCCTGAACCACCGGCCTCCAAACTCCCTCTGTCTCTGCCCAAACCTCCCCTTAGCAAAAGCCAAAAAGATCAGGGTCTGCCACACTGTCTCCCTACCGAAGTAGAATCCAGGCCGCCCTTTGGTTTTCTTAAAGAAGTCCCCATGGGCCGCAGCCTGGACGTCTGCTCCGTTCTCCACCAGGAGGGTCACCAGGGC... | CCAGGAGTTCTGCAGCAGGAACTTCACGATGCCCAGCTGGTTGGTGCACGCGGCCAGGGACAGGGGCAGTTCACCTGCATGAACACAGGGCCCAGGTGGGCCTCAGGAGTGAGATCCAGCTGGCCCCTGAACCACCGGCCTCCAAACTCCCTCTGTCTCTGCCCAAACCTCCCCTTAGCAAAAGCCAAAAAGATCAGGGTCTGCCACACTGTCTCCCTACCGAAGTAGAATCCAGGCCGCCCTTTGGTTTTCTTAAAGAAGTCCCCATGGGCCGCAGCCTGGACGTCTGCTCCGTTCTCCACCAGGAGGGTCACCAGGGC... |
Task1_train_44878 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CTGGCCTGAAAGCAAAGCTTTGGTTCCGAGGCCCCTAGCAGGCCTGCCATTCCGCTCCCAGCTCCTTCTGTCTCTGCACACCCTCCCCCTGCAAATCTTACAAGTCATCTCTTACCACAACTGTCCAGGCCCCTGGAGTGGCCTCCCACTGCCTTTCAGATTAACTCCAGGCCTCTAAACCCAGGGCCAGGGCCCAGAAGACGGCTTCCAGCCAGCACATCTGCCTTCTCCCGTCAGATGCCTCTCCCAGCTTTCCAAGTCCGGACTGCTCCCTCCTCATTCCCTGCCTGAGCCCTCTCCTCCTTCAGTCAAATGCTGGC... | CTGGCCTGAAAGCAAAGCTTTGGTTCCGAGGCCCCTAGCAGGCCTGCCATTCCGCTCCCAGCTCCTTCTGTCTCTGCACACCCTCCCCCTGCAAATCTTACAAGTCATCTCTTACCACAACTGTCCAGGCCCCTGGAGTGGCCTCCCACTGCCTTTCAGATTAACTCCAGGCCTCTAAACCCAGGGCCAGGGCCCAGAAGACGGCTTCCAGCCAGCACATCTGCCTTCTCCCGTCAGATGCCTCTCCCAGCTTTCCAAGTCCGGACTGCTCCCTCCTCATTCCCTGCCTGAGCCCTCTCCTCCTTCAGTCAAATGCTGGC... |
Task1_train_44879 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | CCTCACCCCTGGCCCTGCCATGCCCTTCCACCCCCGCCAGCCCTCACCCCCTGCCCTGCCCCTCCACCCCTCGCCAGTCCTCGCCCCTGGCCCTGCCATGCCCTTCCACCCCCGCCAGCCCTCACCCCCTGCCATGCCCCTCCACCCCCGCCAGTCCTTACCCACTGCCCTGCCCCTCCACCCCCCACCAGTCCTCACCCCCTGGGGTCCTCACCCCTGCCCTGCCCCTCCACCCCTGCCAGTCCTCACCCCCTGCCCTGCCCCACCACCCCTCGCCAGTCCTTACCCCCCACCCTGCCCTGCCCCTCCACCCCCGCCAG... | CCTCACCCCTGGCCCTGCCATGCCCTTCCACCCCCGCCAGCCCTCACCCCCTGCCCTGCCCCTCCACCCCTCGCCAGTCCTCGCCCCTGGCCCTGCCATGCCCTTCCACCCCCGCCAGCCCTCACCCCCTGCCATGCCCCTCCACCCCCGCCAGTCCTTACCCACTGCCCTGCCCCTCCACCCCCCACCAGTCCTCACCCCCTGGGGTCCTCACCCCTGCCCTGCCCCTCCACCCCTGCCAGTCCTCACCCCCTGCCCTGCCCCACCACCCCTCGCCAGTCCTTACCCCCCACCCTGCCCTGCCCCTCCACCCCCGCCAG... |
Task1_train_44880 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTGCCCCACAGCCTGGGACAGGGTCAGGGCTGAAGTTGCTGCACCCGGGGACCTAGGGCCTCATTTAACTCACCCCATTCCCAAAGGGAGAAGCCTTGTTCCAGTGCCCCCAGCCCTGGGAGCCTCGTGTTCTGTGAGCTCAGGAGGGCCAGCGTTCTGACTGGGAGGCAGGACTGGACTCTTAGGCTGAGCAGGACTAAGTTCTGTGGCCAAGGAGCCCGGGCGTTCCGGGCCAGGCCAGCCTGCACAGAGGCTGGGGCGGGACACGGGGCGGCAGTGAGGGGATGTGGCTGGTTGAACAGTGTTGAGCATGTTGAAGC... | TTGCCCCACAGCCTGGGACAGGGTCAGGGCTGAAGTTGCTGCACCCGGGGACCTAGGGCCTCATTTAACTCACCCCATTCCCAAAGGGAGAAGCCTTGTTCCAGTGCCCCCAGCCCTGGGAGCCTCGTGTTCTGTGAGCTCAGGAGGGCCAGCGTTCTGACTGGGAGGCAGGACTGGACTCTTAGGCTGAGCAGGACTAAGTTCTGTGGCCAAGGAGCCCGGGCGTTCCGGGCCAGGCCAGCCTGCACAGAGGCTGGGGCGGGACACGGGGCGGCAGTGAGGGGATGTGGCTGGTTGAACAGTGTTGAGCATGTTGAAGC... |
Task1_train_44881 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ATCGTGCCATTGCACAACAAGAGCGAAACTCCGTCTTGAAAGAAAGAAAAGAAAAGAAAAGAACACCTAGGTCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCCTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTCGCCGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGTAGAGATCGTGCCACTGCACTCC... | ATCGTGCCATTGCACAACAAGAGCGAAACTCCGTCTTGAAAGAAAGAAAAGAAAAGAAAAGAACACCTAGGTCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCCTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTCGCCGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGTAGAGATCGTGCCACTGCACTCC... |
Task1_train_44882 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | AAGAAAAGAACACCTGAGCTAAATTTAAGAAGAAACCACCTACGTCAGGACCTAGAGGAAGAGCAGTGTCAAGCAAAGGAACAGCAAGTACAAAGTCTTGTGGCCAGAATAATGCTGTACTGGCGAGCTAGAAGAATAGGACAGAATAACCCGATTATAAAAGGGGCAGTGGGAGAGAAAGGCGAGTACTAGGAGATGAAGTTGAAGAATTAAGCAGAGACCAGATCAAGTACTGCCTTGCTCTGGCCATGAAAAAAGTATGGATTTTAGTCTAAGTGTGCTCAAGCATCAGTTTTGTTTGTTTGTTATTTTTAATAAGC... | AAGAAAAGAACACCTGAGCTAAATTTAAGAAGAAACCACCTACGTCAGGACCTAGAGGAAGAGCAGTGTCAAGCAAAGGAACAGCAAGTACAAAGTCTTGTGGCCAGAATAATGCTGTACTGGCGAGCTAGAAGAATAGGACAGAATAACCCGATTATAAAAGGGGCAGTGGGAGAGAAAGGCGAGTACTAGGAGATGAAGTTGAAGAATTAAGCAGAGACCAGATCAAGTACTGCCTTGCTCTGGCCATGAAAAAAGTATGGATTTTAGTCTAAGTGTGCTCAAGCATCAGTTTTGTTTGTTTGTTATTTTTAATAAGC... |
Task1_train_44883 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGGGAATTATTTGTAAAGAATGTGGGAAAAGCAGAGGCAAGAAAGGCAGGCCGAAGGTTATTGCAACAGCCCTGGCAAGAAAGGGTAGCTTGAATTACAACGGCAGTGGAAATGGAGAGAAGTGAATGGGTTTAGGATATATTTTGGCCCTGAAATGGCAGGGCTTGCTGCTGGAATAGACGTGGGGATGTAGGAAAGAGGAGTCACAGGTAATCCCTCGAGTTCCTTGTACTGTAACTGGAGTATATCTCCCTCCTGAGGGTAGCTAAGGAACGGGTTGGGACAGAGGGTTGGTTTTTTGCACCAAAAGATCTATTTTG... | TGGGAATTATTTGTAAAGAATGTGGGAAAAGCAGAGGCAAGAAAGGCAGGCCGAAGGTTATTGCAACAGCCCTGGCAAGAAAGGGTAGCTTGAATTACAACGGCAGTGGAAATGGAGAGAAGTGAATGGGTTTAGGATATATTTTGGCCCTGAAATGGCAGGGCTTGCTGCTGGAATAGACGTGGGGATGTAGGAAAGAGGAGTCACAGGTAATCCCTCGAGTTCCTTGTACTGTAACTGGAGTATATCTCCCTCCTGAGGGTAGCTAAGGAACGGGTTGGGACAGAGGGTTGGTTTTTTGCACCAAAAGATCTATTTTG... |
Task1_train_44884 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TGCTCTTAAAGAAAACCAGCCTCAAAAAACTCCACTACACCCTCAATGGGAAGAGCAGCACTATCCCCAGCTGTGGGTTGCAAGTGAGCATCATTGACTACACCCTGTCGCGCTTGGAACGGGATGGGATTGTGGTTTTCTGTGACGTTTCCATGGATGAGGACCTGTTTACCGGTGACGGTGACTACCAGTTTGACATCTACAGGCTCATGAAGAAGGAGAATAACAACCGCTGGGGTGAATATCACCCTTATAGTAATGTGCTCTGGTTACATTACCTGACAGACAAGATGCTGAAACAAATGACCTTCAAGACTAAA... | TGCTCTTAAAGAAAACCAGCCTCAAAAAACTCCACTACACCCTCAATGGGAAGAGCAGCACTATCCCCAGCTGTGGGTTGCAAGTGAGCATCATTGACTACACCCTGTCGCGCTTGGAACGGGATGGGATTGTGGTTTTCTGTGACGTTTCCATGGATGAGGACCTGTTTACCGGTGACGGTGACTACCAGTTTGACATCTACAGGCTCATGAAGAAGGAGAATAACAACCGCTGGGGTGAATATCACCCTTATAGTAATGTGCTCTGGTTACATTACCTGACAGACAAGATGCTGAAACAAATGACCTTCAAGACTAAA... |
Task1_train_44885 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | TTGGCCAAGATGGTGAAACCCCATCTCTACTAAAACTACAAAAATTAGCTGGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGAGAACTGCTTGAACCTGGAGGCAGAGGTTGCAGTGAGCCGAGATCACGCCACAGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTCAAAAAATAAATAAATAAATAAAAGGCTTTCAGAGATAAGCAATTGGAGTTCAGAATTGTCTCTAGAAGACCACACTTAGAAGAATACTGATTTTAAAAGGGCTTCTCAGCCTCCACACTATTGACGTTT... | TTGGCCAAGATGGTGAAACCCCATCTCTACTAAAACTACAAAAATTAGCTGGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGAGAACTGCTTGAACCTGGAGGCAGAGGTTGCAGTGAGCCGAGATCACGCCACAGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTCAAAAAATAAATAAATAAATAAAAGGCTTTCAGAGATAAGCAATTGGAGTTCAGAATTGTCTCTAGAAGACCACACTTAGAAGAATACTGATTTTAAAAGGGCTTCTCAGCCTCCACACTATTGACGTTT... |
Task1_train_44886 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | AATTAGCTGGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGAGAACTGCTTGAACCTGGAGGCAGAGGTTGCAGTGAGCCGAGATCACGCCACAGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTCAAAAAATAAATAAATAAATAAAAGGCTTTCAGAGATAAGCAATTGGAGTTCAGAATTGTCTCTAGAAGACCACACTTAGAAGAATACTGATTTTAAAAGGGCTTCTCAGCCTCCACACTATTGACGTTTTGGGCCAGTTAGTTCTTGGTTGTGGGGGCTGTCCTGTACTGC... | AATTAGCTGGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGAGAACTGCTTGAACCTGGAGGCAGAGGTTGCAGTGAGCCGAGATCACGCCACAGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTCAAAAAATAAATAAATAAATAAAAGGCTTTCAGAGATAAGCAATTGGAGTTCAGAATTGTCTCTAGAAGACCACACTTAGAAGAATACTGATTTTAAAAGGGCTTCTCAGCCTCCACACTATTGACGTTTTGGGCCAGTTAGTTCTTGGTTGTGGGGGCTGTCCTGTACTGC... |
Task1_train_44887 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGGCATTGGTGAACCCGGGGTGCCCACTCAGTATGCGTGCCAAGGAGAAAGAACCATCCTGTAAAGCAAACAAACAGCTCAGCCCTCAAGAAGGGGTGCTAGGTGCCCACTCCATTGCCACCCCGATGCACGCTCACTGGGCCGGTGGGTGCCCACTCCATTGCCACCCAGGATGCACGCTCGCTGGGCCGGTGGGTTCCCACTCCATTGCCACCCAGGATGCACGCTCACTGGGCCGGTGGGTGCCCACTCCGTTGCCACCCAGGATGCACGCTCGCTGGGCTGGTGGGTGCCCACTCCGTTGCCACCCAGGATGCACG... | GGGCATTGGTGAACCCGGGGTGCCCACTCAGTATGCGTGCCAAGGAGAAAGAACCATCCTGTAAAGCAAACAAACAGCTCAGCCCTCAAGAAGGGGTGCTAGGTGCCCACTCCATTGCCACCCCGATGCACGCTCACTGGGCCGGTGGGTGCCCACTCCATTGCCACCCAGGATGCACGCTCGCTGGGCCGGTGGGTTCCCACTCCATTGCCACCCAGGATGCACGCTCACTGGGCCGGTGGGTGCCCACTCCGTTGCCACCCAGGATGCACGCTCGCTGGGCTGGTGGGTGCCCACTCCGTTGCCACCCAGGATGCACG... |
Task1_train_44888 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGGGTGCCCACTCAGTATGCGTGCCAAGGAGAAAGAACCATCCTGTAAAGCAAACAAACAGCTCAGCCCTCAAGAAGGGGTGCTAGGTGCCCACTCCATTGCCACCCCGATGCACGCTCACTGGGCCGGTGGGTGCCCACTCCATTGCCACCCAGGATGCACGCTCGCTGGGCCGGTGGGTTCCCACTCCATTGCCACCCAGGATGCACGCTCACTGGGCCGGTGGGTGCCCACTCCGTTGCCACCCAGGATGCACGCTCGCTGGGCTGGTGGGTGCCCACTCCGTTGCCACCCAGGATGCACGCTCACTGGCCAGGGAC... | GGGGTGCCCACTCAGTATGCGTGCCAAGGAGAAAGAACCATCCTGTAAAGCAAACAAACAGCTCAGCCCTCAAGAAGGGGTGCTAGGTGCCCACTCCATTGCCACCCCGATGCACGCTCACTGGGCCGGTGGGTGCCCACTCCATTGCCACCCAGGATGCACGCTCGCTGGGCCGGTGGGTTCCCACTCCATTGCCACCCAGGATGCACGCTCACTGGGCCGGTGGGTGCCCACTCCGTTGCCACCCAGGATGCACGCTCGCTGGGCTGGTGGGTGCCCACTCCGTTGCCACCCAGGATGCACGCTCACTGGCCAGGGAC... |
Task1_train_44889 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CAGGTGCCCGCCACCGTGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGATCTCGATCTCCTGATCTCATGATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCGGCCAAACCCCAGGTTTCTTTGCCACCAGTGGTCTTGGGGAGCCCATCCTTCCAAGACTAGGGAGCAGAAAGCCACTCTCAGGACTGTTGACTTCGGTTCCCCCTGTTGTCTTAGATGCTTCATCCCTTTTAAAATTCCTGGGCTGAGGGGAAAGACACCCCTCA... | CAGGTGCCCGCCACCGTGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGATCTCGATCTCCTGATCTCATGATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCGGCCAAACCCCAGGTTTCTTTGCCACCAGTGGTCTTGGGGAGCCCATCCTTCCAAGACTAGGGAGCAGAAAGCCACTCTCAGGACTGTTGACTTCGGTTCCCCCTGTTGTCTTAGATGCTTCATCCCTTTTAAAATTCCTGGGCTGAGGGGAAAGACACCCCTCA... |
Task1_train_44890 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | CTGGATCTGAGAGGGTCAGCTCAGCTCAGCCTTCTGGTCTCAGGCCCACTCACTGCCTGCACTTGCCCAGGATCTCCTGGAGGAGCATGACTGGCGGAGACCATGGCCTCGGTTTTCCTCCTGAGTCTGTGTTCTTGGCTTCTCAGCCTCCCTGCTCAGCCTCAGTAACTCTGTCCATCTCTGAGTCTCGGGACCTCCCACCCTTCGTCTGAGTTGTGCTCTGGCGTTTGTCCCTCTGTCCAGGTCTGTCTCTGTGTCCACCCATCCCCCACCCAGGCTTTGCCCTGTGTCTGGGACACGGGGGCCTGGCTCTTCTCTCA... | CTGGATCTGAGAGGGTCAGCTCAGCTCAGCCTTCTGGTCTCAGGCCCACTCACTGCCTGCACTTGCCCAGGATCTCCTGGAGGAGCATGACTGGCGGAGACCATGGCCTCGGTTTTCCTCCTGAGTCTGTGTTCTTGGCTTCTCAGCCTCCCTGCTCAGCCTCAGTAACTCTGTCCATCTCTGAGTCTCGGGACCTCCCACCCTTCGTCTGAGTTGTGCTCTGGCGTTTGTCCCTCTGTCCAGGTCTGTCTCTGTGTCCACCCATCCCCCACCCAGGCTTTGCCCTGTGTCTGGGACACGGGGGCCTGGCTCTTCTCTCA... |
Task1_train_44891 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GGCCCACTCACTGCCTGCACTTGCCCAGGATCTCCTGGAGGAGCATGACTGGCGGAGACCATGGCCTCGGTTTTCCTCCTGAGTCTGTGTTCTTGGCTTCTCAGCCTCCCTGCTCAGCCTCAGTAACTCTGTCCATCTCTGAGTCTCGGGACCTCCCACCCTTCGTCTGAGTTGTGCTCTGGCGTTTGTCCCTCTGTCCAGGTCTGTCTCTGTGTCCACCCATCCCCCACCCAGGCTTTGCCCTGTGTCTGGGACACGGGGGCCTGGCTCTTCTCTCATGCTCCTTTCCATCCCCTGGCAGTGCCCACAGGATCAGACAT... | GGCCCACTCACTGCCTGCACTTGCCCAGGATCTCCTGGAGGAGCATGACTGGCGGAGACCATGGCCTCGGTTTTCCTCCTGAGTCTGTGTTCTTGGCTTCTCAGCCTCCCTGCTCAGCCTCAGTAACTCTGTCCATCTCTGAGTCTCGGGACCTCCCACCCTTCGTCTGAGTTGTGCTCTGGCGTTTGTCCCTCTGTCCAGGTCTGTCTCTGTGTCCACCCATCCCCCACCCAGGCTTTGCCCTGTGTCTGGGACACGGGGGCCTGGCTCTTCTCTCATGCTCCTTTCCATCCCCTGGCAGTGCCCACAGGATCAGACAT... |
Task1_train_44892 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | AGGGGTCAGAGGCTGAGGCCCAGAAGAGCACACAGTGCCCTGGCCATGTAGGGGGTGGCAGGTGAAGACAGTGAGGCAGTGTGGCCCAAGAGGTGCTCCCGTTGCTGGCCCAGTGAGCCCAGGTCCCCTGCAGTGCAAGACCCTGCGGACACCTTGGGACCCAGCCACCAGAGCCCCTTCACACCCTCCACTTGGTGATCCGAGAACGCCTCCCCGATGTGCAGACAGAGAGGCTCTGCGCTCCACACCCACAGCGTCCACTGCAGCCCAGGAGCAGAGGCGGGCGGGGAGGCAGGCTGGAGGCGGGACGGGGCCTCCCA... | AGGGGTCAGAGGCTGAGGCCCAGAAGAGCACACAGTGCCCTGGCCATGTAGGGGGTGGCAGGTGAAGACAGTGAGGCAGTGTGGCCCAAGAGGTGCTCCCGTTGCTGGCCCAGTGAGCCCAGGTCCCCTGCAGTGCAAGACCCTGCGGACACCTTGGGACCCAGCCACCAGAGCCCCTTCACACCCTCCACTTGGTGATCCGAGAACGCCTCCCCGATGTGCAGACAGAGAGGCTCTGCGCTCCACACCCACAGCGTCCACTGCAGCCCAGGAGCAGAGGCGGGCGGGGAGGCAGGCTGGAGGCGGGACGGGGCCTCCCA... |
Task1_train_44893 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | CTGGATTGCAGATATGTAAAGTTCTACGCAAATTAAAAAGTTGGGCCCAAAAACTAGCTCTGAACTTCCTGGCCAAGAGAAAGGGAATGTTCTTAATTTTAAAAATATCTTGAGCAGAAGTTCCTGCTCTGTGCTGTCTGCTCCCTGGGATTACACATGAGAGACATCTTGGTGCCTGCCCAATTTCTGTGTCTGTAAAATGAGTTTCCTCTCAGAGGCCGACTACAAACATAAGTTTTAAAGAGGAACCACAGTGCACTTTGAAGATGATCCAGGTAACGTAGCACAGGCCACCTCCCACCTCGCCTTACAAAGGACTA... | CTGGATTGCAGATATGTAAAGTTCTACGCAAATTAAAAAGTTGGGCCCAAAAACTAGCTCTGAACTTCCTGGCCAAGAGAAAGGGAATGTTCTTAATTTTAAAAATATCTTGAGCAGAAGTTCCTGCTCTGTGCTGTCTGCTCCCTGGGATTACACATGAGAGACATCTTGGTGCCTGCCCAATTTCTGTGTCTGTAAAATGAGTTTCCTCTCAGAGGCCGACTACAAACATAAGTTTTAAAGAGGAACCACAGTGCACTTTGAAGATGATCCAGGTAACGTAGCACAGGCCACCTCCCACCTCGCCTTACAAAGGACTA... |
Task1_train_44894 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | TGTATTTCTGAGAAACTATGAGGAAGGAACTATCGTATAGAGTTCATGGACGAGCCTTAGGGCTTTAGTAAGCCCTTGAAATTCGTGCAAAATTTTACATACATGTTTGAATGTGTATTTTATGGGGAGAGAGGACCTAAAGCTTTTGAGTTTATAACCCAAAATATTAAGAACTATTGTTGTGGGGCTTTTCTGTTCTTCTGGATCAATTCTGCACAACATAAGACTGAGTCTTTAGGAAGTGAATTCTCAGGACAGCAGACAGAAGCATTTTCATGTTTAGGCTAAAACATGGCCCGGGCCAAAGAGAAGCCATCCCT... | TGTATTTCTGAGAAACTATGAGGAAGGAACTATCGTATAGAGTTCATGGACGAGCCTTAGGGCTTTAGTAAGCCCTTGAAATTCGTGCAAAATTTTACATACATGTTTGAATGTGTATTTTATGGGGAGAGAGGACCTAAAGCTTTTGAGTTTATAACCCAAAATATTAAGAACTATTGTTGTGGGGCTTTTCTGTTCTTCTGGATCAATTCTGCACAACATAAGACTGAGTCTTTAGGAAGTGAATTCTCAGGACAGCAGACAGAAGCATTTTCATGTTTAGGCTAAAACATGGCCCGGGCCAAAGAGAAGCCATCCCT... |
Task1_train_44895 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | AAAATAAAAAGGTAGAAAAAAATCATTATAAGCATTATATATAAATATATTGTTTTATACACACACACACATATATATTTACAAAATATAGGAAGGGTCAGAAGAAAATAATTATAACTTCTAATCCTACCCTTAAGGCTACAGAGATGATTGTCATCATTTGTTTCAGTATGTGGCTTTCCAAAACCTTCTTCTATGCATACCACCACCCCCACTTTTAAAAATAAATTGCCCTTACCGACTTTAAGGGAGGTAACATGGCTGCTAGTAATCCCAAAATCCTCTTCTGGGAACACTCAGCAAACACTTGCTCAGGGCTT... | AAAATAAAAAGGTAGAAAAAAATCATTATAAGCATTATATATAAATATATTGTTTTATACACACACACACATATATATTTACAAAATATAGGAAGGGTCAGAAGAAAATAATTATAACTTCTAATCCTACCCTTAAGGCTACAGAGATGATTGTCATCATTTGTTTCAGTATGTGGCTTTCCAAAACCTTCTTCTATGCATACCACCACCCCCACTTTTAAAAATAAATTGCCCTTACCGACTTTAAGGGAGGTAACATGGCTGCTAGTAATCCCAAAATCCTCTTCTGGGAACACTCAGCAAACACTTGCTCAGGGCTT... |
Task1_train_44896 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GTGAAACCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGTTACTTGAGAGGCTGAGGTAGGAGGATCATTGGAGCCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATCATACCACTGCACTCCAGCCTGGGCAACAGAGTGAGACCCTGTCTCAAAAAAAATAAGAAAAGTAATAGATTTTTATCCATTGAATTAAAAAAAACCCATAAAAAAACCCTATTAAGTCCATTCTGACATAAATAAAAGGATAAACGGGGAAGCACAGTGCTTATGGGTGGAAGGTTAGTTTTAA... | GTGAAACCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGTTACTTGAGAGGCTGAGGTAGGAGGATCATTGGAGCCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATCATACCACTGCACTCCAGCCTGGGCAACAGAGTGAGACCCTGTCTCAAAAAAAATAAGAAAAGTAATAGATTTTTATCCATTGAATTAAAAAAAACCCATAAAAAAACCCTATTAAGTCCATTCTGACATAAATAAAAGGATAAACGGGGAAGCACAGTGCTTATGGGTGGAAGGTTAGTTTTAA... |
Task1_train_44897 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | GATTAAACGTTATGTATGTATAATTAAGTAAGGGAGAAATTTCTTCTAAAGACAAAATGTAATTTGCCTTTCAACATACATTTTCTCTTCTAGACTTCAATTTTGTCACTCACTTACATGGTTTTTATATAACTTCATCAACTATAAAATGATGAGATTCATCTCTACAGCTTTTTCTGCGTCTCCTTTCTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTGGCCCAGGCGGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG... | GATTAAACGTTATGTATGTATAATTAAGTAAGGGAGAAATTTCTTCTAAAGACAAAATGTAATTTGCCTTTCAACATACATTTTCTCTTCTAGACTTCAATTTTGTCACTCACTTACATGGTTTTTATATAACTTCATCAACTATAAAATGATGAGATTCATCTCTACAGCTTTTTCTGCGTCTCCTTTCTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTGGCCCAGGCGGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG... |
Task1_train_44898 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAATCTGCAAAGTGCCATCTCCTTCAACAGTTCTGCATGGTTCTTCCCACTACTACTTCATATTCTCATAATACGCGTAGATACTAGAAAGAAGGTACTATGTGTATTCCTGGGGGGAAAAAAAAAGGAGATCTTTCACTAACTAATATGACTTTTTTTTTTTTTTTTGAGACAGAGTATCGCTCTGAGGCCCAGGCTGGAATGCAGTGGCGTGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGGTTGTCCCACCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCCGCCACCATGCCCAGCTAATTT... | AAATCTGCAAAGTGCCATCTCCTTCAACAGTTCTGCATGGTTCTTCCCACTACTACTTCATATTCTCATAATACGCGTAGATACTAGAAAGAAGGTACTATGTGTATTCCTGGGGGGAAAAAAAAAGGAGATCTTTCACTAACTAATATGACTTTTTTTTTTTTTTTTGAGACAGAGTATCGCTCTGAGGCCCAGGCTGGAATGCAGTGGCGTGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGGTTGTCCCACCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCCGCCACCATGCCCAGCTAATTT... |
Task1_train_44899 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GTCTACTTCCCCAGGTGGTAAACTGAGGCCCAAAGGAGTCAGAACAGGGGCTGGACCTGGGTAGGAGAGGTCAAACCAGGAGGGCTGGGATTTGAGTCCCAATGCTACCCCTCCCTCACCATGTGAGTCTACCTCTCCTAGCCTCAGTTTCCTCATCTGTAAACGGGGGCAGTGACACCAGCTGATGGGCTTGGGGAGGAATAGAGGTGATGAGGATGTGCCGTATAGATTCACACACTCGGCAGTGTGGCCCACCCAGGGAAGGGCCGGCTATGGGAGGTAAGGTGAGGAAGCGTGTTAGGGCCAGGCCCTGCACCCCA... | GTCTACTTCCCCAGGTGGTAAACTGAGGCCCAAAGGAGTCAGAACAGGGGCTGGACCTGGGTAGGAGAGGTCAAACCAGGAGGGCTGGGATTTGAGTCCCAATGCTACCCCTCCCTCACCATGTGAGTCTACCTCTCCTAGCCTCAGTTTCCTCATCTGTAAACGGGGGCAGTGACACCAGCTGATGGGCTTGGGGAGGAATAGAGGTGATGAGGATGTGCCGTATAGATTCACACACTCGGCAGTGTGGCCCACCCAGGGAAGGGCCGGCTATGGGAGGTAAGGTGAGGAAGCGTGTTAGGGCCAGGCCCTGCACCCCA... |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.