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_42600 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | AAGCTTTGAATGCACTACATTTGGAAAACTATGTCTTCTTAGTACAAAGTATCTTTCAAGACAAAAACCTCATAAATGTGGCACGCATGGAAAGAGTTTGAAATATATAGATTTCACTAGTGATTATGCTAGAAATAATCCTAATGGGTTTCAGGTACATGGAAAATCATTCTTCCATTCTAAACATGAGCAAACTGTTATTGGAATAAAATACTGTGAAAGTATTGAATCTGGAAAAACCGTCAATAAGAAATCGCAACTTATGTGCCAACAAATGTATATGGGCGAAAAACCCTTTGGATGCAGCTGTTGTGAGAAAG... | AAGCTTTGAATGCACTACATTTGGAAAACTATGTCTTCTTAGTACAAAGTATCTTTCAAGACAAAAACCTCATAAATGTGGCACGCATGGAAAGAGTTTGAAATATATAGATTTCACTAGTGATTATGCTAGAAATAATCCTAATGGGTTTCAGGTACATGGAAAATCATTCTTCCATTCTAAACATGAGCAAACTGTTATTGGAATAAAATACTGTGAAAGTATTGAATCTGGAAAAACCGTCAATAAGAAATCGCAACTTATGTGCCAACAAATGTATATGGGCGAAAAACCCTTTGGATGCAGCTGTTGTGAGAAAG... |
Task1_train_42601 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | CTTGATCTCTTGACCTCATGATCCGCCTGCCTCAGCCGCCCAAAGTGCTGGGATTACAGGCGTGAGTCACTGCACCCGGCCAGGAGACCTTATTCTTTAAGATTAAAGTCTTAACAGCAAGATGAAGTAAAAAGACCCACAACCTCGGACCCTCAGCGTGAAATTTCAGAACTTTAAGACCCACCCCCCCAAAAAATAAGAAAAAAAGAATCTAAGAGCTCCAAAAAATTATGAGGGGGGGAAAAGCATTTCAACTCAGAATTCTGTCCTTGCAAAATTGTTAACCAAACTTGAAGACAGATTAAAGACATTTTTAGAAC... | CTTGATCTCTTGACCTCATGATCCGCCTGCCTCAGCCGCCCAAAGTGCTGGGATTACAGGCGTGAGTCACTGCACCCGGCCAGGAGACCTTATTCTTTAAGATTAAAGTCTTAACAGCAAGATGAAGTAAAAAGACCCACAACCTCGGACCCTCAGCGTGAAATTTCAGAACTTTAAGACCCACCCCCCCAAAAAATAAGAAAAAAAGAATCTAAGAGCTCCAAAAAATTATGAGGGGGGGAAAAGCATTTCAACTCAGAATTCTGTCCTTGCAAAATTGTTAACCAAACTTGAAGACAGATTAAAGACATTTTTAGAAC... |
Task1_train_42602 | This variant lies on Chromosome 13. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGTTGATTGGCAAGCTTTAATGAAATAATGAGTATATTTGTTTACTTATTTTAGAGACAGCGTCTCGCTCTGTCACCCAGGCTCTAGTGCAGTAGCATGTTCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTTAAGCAATTCTCATGCCTCAGCCTCCCAAGCAGCTGGGATTACAGGCATGTGCCACCACGCCCTGCTAATTTTTGTACTTTAATAGAGATGGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAATCCCTGACCTCAAGTGATCCACCCCACTCGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGC... | AGTTGATTGGCAAGCTTTAATGAAATAATGAGTATATTTGTTTACTTATTTTAGAGACAGCGTCTCGCTCTGTCACCCAGGCTCTAGTGCAGTAGCATGTTCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTTAAGCAATTCTCATGCCTCAGCCTCCCAAGCAGCTGGGATTACAGGCATGTGCCACCACGCCCTGCTAATTTTTGTACTTTAATAGAGATGGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAATCCCTGACCTCAAGTGATCCACCCCACTCGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGC... |
Task1_train_42603 | A variant found on Chromosome 13 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CACCCAGGCTCTAGTGCAGTAGCATGTTCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTTAAGCAATTCTCATGCCTCAGCCTCCCAAGCAGCTGGGATTACAGGCATGTGCCACCACGCCCTGCTAATTTTTGTACTTTAATAGAGATGGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAATCCCTGACCTCAAGTGATCCACCCCACTCGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACTGTGCCCAGCCTGAAATAATAAGTACGCTGATAATTTGCAAACAAATTTCAAAACTTGTTCTACAGTCTC... | CACCCAGGCTCTAGTGCAGTAGCATGTTCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTTAAGCAATTCTCATGCCTCAGCCTCCCAAGCAGCTGGGATTACAGGCATGTGCCACCACGCCCTGCTAATTTTTGTACTTTAATAGAGATGGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAATCCCTGACCTCAAGTGATCCACCCCACTCGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACTGTGCCCAGCCTGAAATAATAAGTACGCTGATAATTTGCAAACAAATTTCAAAACTTGTTCTACAGTCTC... |
Task1_train_42604 | A mutation on Chromosome 13 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TCTCTTCTGCTGACCTCCAATCACCAGGATGTTGTTTCCAGTACTCTTACTAGGCATGTACTCTCCACAGTGTTCACAGCAGTTCATTATTAGACCATTGGCCAATCTGTACTTATTAAAGCAATGGTTACTGCACAGTTTATGTGTTACATTATTTACGCTGACTTCATGGCGAATCTAAAAGAAAAACCAGAATTCATTAACTAAGATATATGAACCAGATTAGCATAGCAAGCAATGAGATAACTAGTTTCTGCAATAGAAGCAAAGAATCCCTAATCATATCTCAGAGGAAGATATACCCAGGGAAAAGATTTTTT... | TCTCTTCTGCTGACCTCCAATCACCAGGATGTTGTTTCCAGTACTCTTACTAGGCATGTACTCTCCACAGTGTTCACAGCAGTTCATTATTAGACCATTGGCCAATCTGTACTTATTAAAGCAATGGTTACTGCACAGTTTATGTGTTACATTATTTACGCTGACTTCATGGCGAATCTAAAAGAAAAACCAGAATTCATTAACTAAGATATATGAACCAGATTAGCATAGCAAGCAATGAGATAACTAGTTTCTGCAATAGAAGCAAAGAATCCCTAATCATATCTCAGAGGAAGATATACCCAGGGAAAAGATTTTTT... |
Task1_train_42605 | This is a variant located on Chromosome 13. Is this mutation a likely cause of disease or not? | Benign | ACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCCATCTCTACTAAGAATACAAAAAATTAGCTAGGCGTGATGGCACACGCCTGCAATCCCAGCTACTCGGAAGGCTGAGGCCCGGGGATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCATTCCAGCCTGGGTGACAGAGACTCTGTCTCAAAAAAAAAAAAGGGAAAAAGCACTATTTTCCTGAAGGCAACAACATGATTAGGTTCTCAGGTTCTCGTTACTTTTCAGTACTTTCCTAAAATTCAACAGGCT... | ACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCCATCTCTACTAAGAATACAAAAAATTAGCTAGGCGTGATGGCACACGCCTGCAATCCCAGCTACTCGGAAGGCTGAGGCCCGGGGATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCATTCCAGCCTGGGTGACAGAGACTCTGTCTCAAAAAAAAAAAAGGGAAAAAGCACTATTTTCCTGAAGGCAACAACATGATTAGGTTCTCAGGTTCTCGTTACTTTTCAGTACTTTCCTAAAATTCAACAGGCT... |
Task1_train_42606 | This mutation occurs on Chromosome 13. Does this change lead to a known medical condition, or is it benign? | Benign | GCCACCAGGCCCGGCTAATTTTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGTATTTTTTTTTTTGTAGTGACAGGGTTTCTCCATGTTGGTCAGGCTGGTCTTGAACTCTCGACCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAAGTACTGAGATTCCAGGTGTGAGTCACCATGCCCAGCCCATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGACCAGGCTAGTCTCGAACTTCTGACCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCAT... | GCCACCAGGCCCGGCTAATTTTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGTATTTTTTTTTTTGTAGTGACAGGGTTTCTCCATGTTGGTCAGGCTGGTCTTGAACTCTCGACCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAAGTACTGAGATTCCAGGTGTGAGTCACCATGCCCAGCCCATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGACCAGGCTAGTCTCGAACTTCTGACCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCAT... |
Task1_train_42607 | A variant has been detected on Chromosome 13. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AATGAAGTACTGATACGTGCTGTTAGGTTGGTGCAAAAGTAATTGCGATTTTTCCCATTGAATGCAATTGCTTTTGCACCAACCAATACAATACAGATGAACCTTGAAAACATGATAAATGAAAGAAGCCAGTCACAAAAGACCACGTTTTATGATTCTGTTTATATGAAAGGTATAAATTAGGCAAATCTATAAAGATTTGCCAGGGAGTGTCTGCTAATGGATATTATGTTTCTTTTTGGGATGATGAAAATGTTTCAAAAGTGATTGTGGTGCTTGTTGCACAAATCTGTGACTATACCTAAACCATTGCATTGTAG... | AATGAAGTACTGATACGTGCTGTTAGGTTGGTGCAAAAGTAATTGCGATTTTTCCCATTGAATGCAATTGCTTTTGCACCAACCAATACAATACAGATGAACCTTGAAAACATGATAAATGAAAGAAGCCAGTCACAAAAGACCACGTTTTATGATTCTGTTTATATGAAAGGTATAAATTAGGCAAATCTATAAAGATTTGCCAGGGAGTGTCTGCTAATGGATATTATGTTTCTTTTTGGGATGATGAAAATGTTTCAAAAGTGATTGTGGTGCTTGTTGCACAAATCTGTGACTATACCTAAACCATTGCATTGTAG... |
Task1_train_42608 | Located on Chromosome 13, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAAAAAAAATTGTTGTTATTGCTTGTTAGCATTCTTTTTGTATTGTTTTATGGATGTTGTAAACATTAGAGAATAGCTTTCTTTTCCTGTACACTTTGGAGAGTTTAATGGTTGTATGAGTTACACCTATTCAAGTGCCTTATATTTTAAAGTAATACACCATTTATTATGACACAGTCTAAAAGTGAAGATTAGACTATCTCAATTCTTATTTAAAGTGAAATGCAGCTTATAAAACCTAGAGATTCAAAACAGTGGTGGCTTTTATATTAATAGCTATGGAGGTTGTATAAAGCATCAATGAGGTAGTTTCTATAGGA... | AAAAAAAAATTGTTGTTATTGCTTGTTAGCATTCTTTTTGTATTGTTTTATGGATGTTGTAAACATTAGAGAATAGCTTTCTTTTCCTGTACACTTTGGAGAGTTTAATGGTTGTATGAGTTACACCTATTCAAGTGCCTTATATTTTAAAGTAATACACCATTTATTATGACACAGTCTAAAAGTGAAGATTAGACTATCTCAATTCTTATTTAAAGTGAAATGCAGCTTATAAAACCTAGAGATTCAAAACAGTGGTGGCTTTTATATTAATAGCTATGGAGGTTGTATAAAGCATCAATGAGGTAGTTTCTATAGGA... |
Task1_train_42609 | A genomic variant on Chromosome 13 is under review. What is the biological outcome — benign or pathogenic? | Benign | TTTGGGTATGTACCTAGGAGGGGATTACTGGGTCATATGTTAACTTTGTTTAATTTTTGAGGAACCACCAAACTTTTTCACAGCAGCTGCACTATTTTATATTCCCCAAAAGATGTATAATTTTAAACTATTTAAGCCCTGTACACTAGAGCTAATCCCTTGAAGATTGGGACCTTACTTGTCTTATTTGGAGGTGCTTGTTAAATTTATGTAGTAGTATGATACCTGTACTTAAGCATCACTCAAGGGTAAGTGTTCTAGGAAGGTTGATTTAGCTTATATGGAAGAACTGTTGAATAATGGCTTGATGAAAATCTCTT... | TTTGGGTATGTACCTAGGAGGGGATTACTGGGTCATATGTTAACTTTGTTTAATTTTTGAGGAACCACCAAACTTTTTCACAGCAGCTGCACTATTTTATATTCCCCAAAAGATGTATAATTTTAAACTATTTAAGCCCTGTACACTAGAGCTAATCCCTTGAAGATTGGGACCTTACTTGTCTTATTTGGAGGTGCTTGTTAAATTTATGTAGTAGTATGATACCTGTACTTAAGCATCACTCAAGGGTAAGTGTTCTAGGAAGGTTGATTTAGCTTATATGGAAGAACTGTTGAATAATGGCTTGATGAAAATCTCTT... |
Task1_train_42610 | A genetic alteration is present on Chromosome 13. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ACGTCGTGGGAGGGATGCAGTGGGAGGTAACCGAATCACGGGGGCGGGTCTTTCCTATGCTGTTCTCATAATAGTGAATAAGTCTCACGAGATCTGATGGTTTTATAAAGGGGAGTTTCCCTGCACATACCCTCTTGCCTGCCACCATGTAAGACGTGTCTTTCTTCCCCCTCTGCCTTCTGCCATGATTGTGAGGCCTCCCCAGCCATGTGGAACTGTGAGTCCATTAAACCTCTTTCCTTTATAAATTACCCAGTCTTGGGTATGTCTTTATTAGCAGCGTGAGAACAGACTAATACACTCATCTTTAAAAAACCTCT... | ACGTCGTGGGAGGGATGCAGTGGGAGGTAACCGAATCACGGGGGCGGGTCTTTCCTATGCTGTTCTCATAATAGTGAATAAGTCTCACGAGATCTGATGGTTTTATAAAGGGGAGTTTCCCTGCACATACCCTCTTGCCTGCCACCATGTAAGACGTGTCTTTCTTCCCCCTCTGCCTTCTGCCATGATTGTGAGGCCTCCCCAGCCATGTGGAACTGTGAGTCCATTAAACCTCTTTCCTTTATAAATTACCCAGTCTTGGGTATGTCTTTATTAGCAGCGTGAGAACAGACTAATACACTCATCTTTAAAAAACCTCT... |
Task1_train_42611 | This sequence variant lies on Chromosome 13. Is it clinically significant, and what condition might it cause if any? | Benign | GTCTTCTAAACAGACTCTTTGAGCCTGCAAGCAGTAGTGTATTTGAGTCTTTAGGAGAAAGACTGTGGCTTTCAATTTTATGGAAAGTTACCAAAGCTATGCTGTTCTTTGTAGATGGAATTTTCAAACCAGGAGTACAGAATGTAGGTACCAAAGGAGAGTTGGTATATTCGGCATCTAAAAGACACATAAAATGGTCATTAAAAAACTATAACTATAGTATGCTTAACTGGACAGGAAGAAAATCTCATATTTACATATGTAATTATCATTAGCACTACTAAAATTCAGCAAGGATGCAAGAGTAATACACAATAACA... | GTCTTCTAAACAGACTCTTTGAGCCTGCAAGCAGTAGTGTATTTGAGTCTTTAGGAGAAAGACTGTGGCTTTCAATTTTATGGAAAGTTACCAAAGCTATGCTGTTCTTTGTAGATGGAATTTTCAAACCAGGAGTACAGAATGTAGGTACCAAAGGAGAGTTGGTATATTCGGCATCTAAAAGACACATAAAATGGTCATTAAAAAACTATAACTATAGTATGCTTAACTGGACAGGAAGAAAATCTCATATTTACATATGTAATTATCATTAGCACTACTAAAATTCAGCAAGGATGCAAGAGTAATACACAATAACA... |
Task1_train_42612 | A mutation has occurred on Chromosome 13. What is the medical relevance of this mutation? | Benign | AAATGTGAGTATCTAGCCCTGAAAGGTAAACACGAGCTTTGTGCCAAAATCCTACATGCCGTGGTCTTTTCTTTCGCTGAATTCAACATATTTTGATATTGATCGCTTTTTAAAAACACATTTTGCACAAGCTCAGAATAAAGTATTTCAAACCTCAGTTAGTGCTTTCAGGAATATATGCACATAAAGCCCTAAATGCTAAAAGAAAGATATGGCACAAAAATAATTTATTATTTGCCGTGATCTTTCACTGAATTCAACATGTATTAACTAAGGGCAGTTTTCAAAGACACATCCTGTCAAACCTCAGAAAACACAAT... | AAATGTGAGTATCTAGCCCTGAAAGGTAAACACGAGCTTTGTGCCAAAATCCTACATGCCGTGGTCTTTTCTTTCGCTGAATTCAACATATTTTGATATTGATCGCTTTTTAAAAACACATTTTGCACAAGCTCAGAATAAAGTATTTCAAACCTCAGTTAGTGCTTTCAGGAATATATGCACATAAAGCCCTAAATGCTAAAAGAAAGATATGGCACAAAAATAATTTATTATTTGCCGTGATCTTTCACTGAATTCAACATGTATTAACTAAGGGCAGTTTTCAAAGACACATCCTGTCAAACCTCAGAAAACACAAT... |
Task1_train_42613 | Given this context: Chromosome 13 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTCCGGCGAGCCCAGATGGCGCCACTGCACTCCAGCCTGGGCGGCGGAACTAGACTCCGTCTCAAAAAGAAAAAAAAAAAGGCCGGGTTCGGTGGCTGATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGAGGGCGGATCACGAGGTCAGGAAATCGAGACCATCTTGGCTAACACGGTGAAACCCCGTCTCTACTAAAACTACCAAAAATTAGGGGGCGTGGTGGCGGGCACCTGTAGTCCCACCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGTGCC... | TTCCGGCGAGCCCAGATGGCGCCACTGCACTCCAGCCTGGGCGGCGGAACTAGACTCCGTCTCAAAAAGAAAAAAAAAAAGGCCGGGTTCGGTGGCTGATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGAGGGCGGATCACGAGGTCAGGAAATCGAGACCATCTTGGCTAACACGGTGAAACCCCGTCTCTACTAAAACTACCAAAAATTAGGGGGCGTGGTGGCGGGCACCTGTAGTCCCACCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGTGCC... |
Task1_train_42614 | An alteration has been detected on Chromosome 13. Is it pathogenic, and if so, what disease is involved? | Benign | TTTCAAAGCAGGATACTTTCAATCCTTCTCTTAGGGCTTTGCAAAGTCTTATGGCTTTTTCTTCATTGGCCAGAAAAGCATTATCATTTTCATGCTTCATAATTCTAATCAGTCCTGTAATGAACTGTTCAGAAGACAAGAGTAACTGCAATCTTCCTTGAAGAGAACACAACGCTCCAAACTGACAAACTTTGGGAGTCTCTTCATCTAATTGTTCTTCAAGTATACTGCTCAATAATCGAGGTCTAAGTTTTTGAGGAAAGAGCATTATCAACTTAGTGTGAAATCCATGGTCTTTCCCTAAGTAGCACTGGCTGAGA... | TTTCAAAGCAGGATACTTTCAATCCTTCTCTTAGGGCTTTGCAAAGTCTTATGGCTTTTTCTTCATTGGCCAGAAAAGCATTATCATTTTCATGCTTCATAATTCTAATCAGTCCTGTAATGAACTGTTCAGAAGACAAGAGTAACTGCAATCTTCCTTGAAGAGAACACAACGCTCCAAACTGACAAACTTTGGGAGTCTCTTCATCTAATTGTTCTTCAAGTATACTGCTCAATAATCGAGGTCTAAGTTTTTGAGGAAAGAGCATTATCAACTTAGTGTGAAATCCATGGTCTTTCCCTAAGTAGCACTGGCTGAGA... |
Task1_train_42615 | Chromosome 13 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AAAAGGGACCTGAAAAGGGAAAGGAACAGCAATCATCATAATCTTCCCACAATTCCAAGATTTTAAAAAAACAATCACATATTTTCAAGTCAGTTAAGCCGACTATTTTATTTTACATAAATTATAATGCACACATCAAATCAAATTACAATATTTTTGATCAAATATTATCTAGACTTTGCTTTAAAACGTGAAGGCATCATGTACTTTACTCAAATTCAGAAATATTCTCAACATCTTACAGTAAAATTAATTTTATTTCCTGAAATGTCAGTACACTCTCGTTTATAAAGAATTACTTAATATACTATTTTTCATGA... | AAAAGGGACCTGAAAAGGGAAAGGAACAGCAATCATCATAATCTTCCCACAATTCCAAGATTTTAAAAAAACAATCACATATTTTCAAGTCAGTTAAGCCGACTATTTTATTTTACATAAATTATAATGCACACATCAAATCAAATTACAATATTTTTGATCAAATATTATCTAGACTTTGCTTTAAAACGTGAAGGCATCATGTACTTTACTCAAATTCAGAAATATTCTCAACATCTTACAGTAAAATTAATTTTATTTCCTGAAATGTCAGTACACTCTCGTTTATAAAGAATTACTTAATATACTATTTTTCATGA... |
Task1_train_42616 | This alteration on Chromosome 13 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGATGCACACCTGTAATCCTAGCTACTTGAGAGGATGAGGTAGGAGAATCGCTTGAACATGGGAGGCGGAGGTTTCAGTGAGCTGAGATCACGCCACTGCACTCTAGCCTGGGCAACAGAGTGAGACTTTGTCTCAGAAATAAATAAATAGATACAAATAAAAAAAATAAAAAAATAAAGACAAAGTGGGATTCAGGTGAATGTAGGAGAGCTTCCCTGCTGTAATTGGAGGCTGTTAAACATTGAATAATGGTCTAAGAGGAAGGTTGTGTAATTTCTTTCTCTTTACGGTCTCTCTGTGGTGGAAGGGAAGCTCCTAC... | TGATGCACACCTGTAATCCTAGCTACTTGAGAGGATGAGGTAGGAGAATCGCTTGAACATGGGAGGCGGAGGTTTCAGTGAGCTGAGATCACGCCACTGCACTCTAGCCTGGGCAACAGAGTGAGACTTTGTCTCAGAAATAAATAAATAGATACAAATAAAAAAAATAAAAAAATAAAGACAAAGTGGGATTCAGGTGAATGTAGGAGAGCTTCCCTGCTGTAATTGGAGGCTGTTAAACATTGAATAATGGTCTAAGAGGAAGGTTGTGTAATTTCTTTCTCTTTACGGTCTCTCTGTGGTGGAAGGGAAGCTCCTAC... |
Task1_train_42617 | Given this context: Chromosome 13 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | ATATGTAAATGTATAATTTCTCCAAGTCTTCCTTTGTGTATGTGTGTGTCTTTGTGTGTGTGTGTGTGTGCTTTAGTGTGTTTGTGGTTCTATAAATCAGAGTGATATATATATATATATATATGTATGTATAGACAGAGTGAGAAATCAAGAAGGCTGTTCAAAAAGCTGAGTGTTTATTTTCAGCTTATAGGATTGAGAAGATTTATTTTTAAATTTCTTATCTAATCTCTATATTTTAGATTTTTAAGCTTATATTATCTTTGTAGCACAAAATACATCCAGCTTCAGTGATATATTCAGCTTGTAAAGCTGTGTGC... | ATATGTAAATGTATAATTTCTCCAAGTCTTCCTTTGTGTATGTGTGTGTCTTTGTGTGTGTGTGTGTGTGCTTTAGTGTGTTTGTGGTTCTATAAATCAGAGTGATATATATATATATATATATGTATGTATAGACAGAGTGAGAAATCAAGAAGGCTGTTCAAAAAGCTGAGTGTTTATTTTCAGCTTATAGGATTGAGAAGATTTATTTTTAAATTTCTTATCTAATCTCTATATTTTAGATTTTTAAGCTTATATTATCTTTGTAGCACAAAATACATCCAGCTTCAGTGATATATTCAGCTTGTAAAGCTGTGTGC... |
Task1_train_42618 | This alteration occurs on Chromosome 13. Is it associated with a disease or is it a benign variant? | Benign | AGAAAGGCATTCCTGTAGGTGGTGTTTGTAAATGACTGGAAGCTGCTCACCATGCCATATTTATGTGGCCGGCACGTAAATATTAATTCAAATTAAAGAATCAAAGAAAGCAAAGCAAGGAAAGAAAGCAAAACTAAGTGAATAGAGATCACATGAGCATCACACAGGTATTAGGAGAGAGCAAAGAACACAGCCTCGGCTTGGAGGGGCAGCAGAAGATGAAGCTAGAGAAGGAGGCAAGGGCCAAATCATGAGGGCTTGGCGGGAGCAGCAGGGTAGTAGGAAGGGAAACTGGAGAATAACCAGGAGCTACTGAATAA... | AGAAAGGCATTCCTGTAGGTGGTGTTTGTAAATGACTGGAAGCTGCTCACCATGCCATATTTATGTGGCCGGCACGTAAATATTAATTCAAATTAAAGAATCAAAGAAAGCAAAGCAAGGAAAGAAAGCAAAACTAAGTGAATAGAGATCACATGAGCATCACACAGGTATTAGGAGAGAGCAAAGAACACAGCCTCGGCTTGGAGGGGCAGCAGAAGATGAAGCTAGAGAAGGAGGCAAGGGCCAAATCATGAGGGCTTGGCGGGAGCAGCAGGGTAGTAGGAAGGGAAACTGGAGAATAACCAGGAGCTACTGAATAA... |
Task1_train_42619 | A mutation located on Chromosome 13 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CACAGGTGTGTGGGGAAGGCATGGACACAGGTGTGTGGGAAAGTATGTATACAGGTGTGTGCAGTAAAGATATGGATACAGGTATTGGGGGAAGGTGTGGAAGTGGATGTGTGGGATGGGCATGGGTGCAGTAGTGTGTGGTTGTCAGGGCACGTGGGAAGAGGAAAAAGATGCCGAATTTGTTTAATTTGAATTCTTACCTCTGAATTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCACTCTGTCGCCCAGTTTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACTTCTGTCTCCCAGGTTCAAGCGATT... | CACAGGTGTGTGGGGAAGGCATGGACACAGGTGTGTGGGAAAGTATGTATACAGGTGTGTGCAGTAAAGATATGGATACAGGTATTGGGGGAAGGTGTGGAAGTGGATGTGTGGGATGGGCATGGGTGCAGTAGTGTGTGGTTGTCAGGGCACGTGGGAAGAGGAAAAAGATGCCGAATTTGTTTAATTTGAATTCTTACCTCTGAATTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCACTCTGTCGCCCAGTTTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACTTCTGTCTCCCAGGTTCAAGCGATT... |
Task1_train_42620 | Assess the clinical impact of this variant found on Chromosome 13. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GAGTATTCGGTATGTTGGATTCAACACAGGCTGCCATTTTAATGTCATGCTTTTGAAATCGTTGTGAGGTTTTCTTTTGGTATTTCCTAATTATTTTTTTTTCCATTTCAAATAAGAAGAAAAGATAGTGTTGAATGATACCTAGATATTTTCATTCCAGCGGTTTTTTTCCTAGTCTCACCTACACAGGTTCCAGTGAGCTCAGGAGTTTACCTTCATGTCCGTGGCACAGCCCATAATTACCCTTCTCTGTCCAGGGATGTATATTTGCATCTTTCCTTCAACTTATGAAGTGAATGGAGGGGAAATGTACAGTTTTA... | GAGTATTCGGTATGTTGGATTCAACACAGGCTGCCATTTTAATGTCATGCTTTTGAAATCGTTGTGAGGTTTTCTTTTGGTATTTCCTAATTATTTTTTTTTCCATTTCAAATAAGAAGAAAAGATAGTGTTGAATGATACCTAGATATTTTCATTCCAGCGGTTTTTTTCCTAGTCTCACCTACACAGGTTCCAGTGAGCTCAGGAGTTTACCTTCATGTCCGTGGCACAGCCCATAATTACCCTTCTCTGTCCAGGGATGTATATTTGCATCTTTCCTTCAACTTATGAAGTGAATGGAGGGGAAATGTACAGTTTTA... |
Task1_train_42621 | Here is a mutation located on Chromosome 13. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TCTGTCACCCGGGCTGGAGTGCAGTGGTGCAATTTCAGCCCACTGCAACTTCCACCTCCCGTGTTCAAGTGACTCTCCTGCCGCCTCAGCCCCCCAAGTAGCTGGGATTACAGGCACCTGTCACCACACCTGGCTAATTTTTTTGTATTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGCTGGTCTCAAACTCCTGATCTCAAGTGATCTGCCCATCTTGGCCTCCCAAAGTGCTGGGATTACGGACGTGAGCCACCCGCCCGGGCTCTGCATCCACTTCTTCATGGCACGTGGCCTCAGTGAGCATTCAGACCCTC... | TCTGTCACCCGGGCTGGAGTGCAGTGGTGCAATTTCAGCCCACTGCAACTTCCACCTCCCGTGTTCAAGTGACTCTCCTGCCGCCTCAGCCCCCCAAGTAGCTGGGATTACAGGCACCTGTCACCACACCTGGCTAATTTTTTTGTATTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGCTGGTCTCAAACTCCTGATCTCAAGTGATCTGCCCATCTTGGCCTCCCAAAGTGCTGGGATTACGGACGTGAGCCACCCGCCCGGGCTCTGCATCCACTTCTTCATGGCACGTGGCCTCAGTGAGCATTCAGACCCTC... |
Task1_train_42622 | This sequence change occurs on Chromosome 13. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CATAGTAAACCTTTCCCCTATTGTTACATAGTATGTAGTATGCACGTTTTCACCTGTTATAGATAATGCTGCAGGTAATGGCACACAATTGGCACACAGTTTTGGAACATTAGGAAGAATTTTAGGGATAGCAATACAGGGTGAAAGACATAGATGTCTTTTGCTCTTTAACTTTTCCAGAAAGATGTGCAGATTTACATGGCTATCAGCACTGTGAGAGGATCTGGGTTCTGACCAGTTGCACTATGCCCACGTTTTTGTTTTACTTCATTTTTTTAAATCCTAAAAGTCAGGTACAGGGTCTTTAGCCTGTAATACTA... | CATAGTAAACCTTTCCCCTATTGTTACATAGTATGTAGTATGCACGTTTTCACCTGTTATAGATAATGCTGCAGGTAATGGCACACAATTGGCACACAGTTTTGGAACATTAGGAAGAATTTTAGGGATAGCAATACAGGGTGAAAGACATAGATGTCTTTTGCTCTTTAACTTTTCCAGAAAGATGTGCAGATTTACATGGCTATCAGCACTGTGAGAGGATCTGGGTTCTGACCAGTTGCACTATGCCCACGTTTTTGTTTTACTTCATTTTTTTAAATCCTAAAAGTCAGGTACAGGGTCTTTAGCCTGTAATACTA... |
Task1_train_42623 | Consider a variant on Chromosome 13. Determine its clinical classification and disease relevance. | Benign | GGGAGGATCGCTTGAGCCTGGGAGGTTGGGGCTGCCATGAGCCATGATCTCGTCACTGCACTCCAGCCTGGGTAACAGAGTGGGTGACCCTGTCTCAAAGCAACAAAAAAACAAGCAGACAAACAAAACCCAGAAAAACAAAAAAACATGTAAACCATATTTGTTTAGCTTGCGGGAGGGAGGCTGAATTTGGCCTGTGGCTGTAGTTTGTTGAACCTTGAACCTTGCAGTGGATGAGCACTGAGGAGTGAGACTGAGTTTTTGACTTGGTGCATCTGGCAGCACTGCATGGAGGAGGTGGAACTAGAACTGGTCCCTGA... | GGGAGGATCGCTTGAGCCTGGGAGGTTGGGGCTGCCATGAGCCATGATCTCGTCACTGCACTCCAGCCTGGGTAACAGAGTGGGTGACCCTGTCTCAAAGCAACAAAAAAACAAGCAGACAAACAAAACCCAGAAAAACAAAAAAACATGTAAACCATATTTGTTTAGCTTGCGGGAGGGAGGCTGAATTTGGCCTGTGGCTGTAGTTTGTTGAACCTTGAACCTTGCAGTGGATGAGCACTGAGGAGTGAGACTGAGTTTTTGACTTGGTGCATCTGGCAGCACTGCATGGAGGAGGTGGAACTAGAACTGGTCCCTGA... |
Task1_train_42624 | A mutation on Chromosome 13 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GCAGACAAACAAAACCCAGAAAAACAAAAAAACATGTAAACCATATTTGTTTAGCTTGCGGGAGGGAGGCTGAATTTGGCCTGTGGCTGTAGTTTGTTGAACCTTGAACCTTGCAGTGGATGAGCACTGAGGAGTGAGACTGAGTTTTTGACTTGGTGCATCTGGCAGCACTGCATGGAGGAGGTGGAACTAGAACTGGTCCCTGATGGGTCGGGATGTAGTCGTAGTGGCAAACTTGTGTAATCTTCACTTTGTGCTTTTCATGTACTGACTCACTGAATGCAATATCCCCAGACGCTAGGTAGTTTTATTACCCTAGT... | GCAGACAAACAAAACCCAGAAAAACAAAAAAACATGTAAACCATATTTGTTTAGCTTGCGGGAGGGAGGCTGAATTTGGCCTGTGGCTGTAGTTTGTTGAACCTTGAACCTTGCAGTGGATGAGCACTGAGGAGTGAGACTGAGTTTTTGACTTGGTGCATCTGGCAGCACTGCATGGAGGAGGTGGAACTAGAACTGGTCCCTGATGGGTCGGGATGTAGTCGTAGTGGCAAACTTGTGTAATCTTCACTTTGTGCTTTTCATGTACTGACTCACTGAATGCAATATCCCCAGACGCTAGGTAGTTTTATTACCCTAGT... |
Task1_train_42625 | This alteration occurs on Chromosome 13. Is it associated with a disease or is it a benign variant? | Benign | GTCACCAACATTTAACGTATACAACTTGATGTGTTTGGAGTTAAATATACACCTGTGAAACCATCAAACCATCACTTATCAATGCCATGAACTTAGCCACCACTCCCAGAACTTTCCTTCCACCCCTTTTGCTTTGTTTTGTTCCCTTTTGTGGAAAGAGTACTTAACATAAGATAGACCTCTTAGCAAATGCTTCAGTATACCACATCGGATTGTCAATCATAGGCCCTGTATTGTACAGTAGATCTCCAGCATGATTCCTTTGGTTTAACATAAAAATGTACCCTGATGTAGTCTGAAACATGAAAATGACAGTTTTT... | GTCACCAACATTTAACGTATACAACTTGATGTGTTTGGAGTTAAATATACACCTGTGAAACCATCAAACCATCACTTATCAATGCCATGAACTTAGCCACCACTCCCAGAACTTTCCTTCCACCCCTTTTGCTTTGTTTTGTTCCCTTTTGTGGAAAGAGTACTTAACATAAGATAGACCTCTTAGCAAATGCTTCAGTATACCACATCGGATTGTCAATCATAGGCCCTGTATTGTACAGTAGATCTCCAGCATGATTCCTTTGGTTTAACATAAAAATGTACCCTGATGTAGTCTGAAACATGAAAATGACAGTTTTT... |
Task1_train_42626 | Given this context: Chromosome 13 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AAATATACACCTGTGAAACCATCAAACCATCACTTATCAATGCCATGAACTTAGCCACCACTCCCAGAACTTTCCTTCCACCCCTTTTGCTTTGTTTTGTTCCCTTTTGTGGAAAGAGTACTTAACATAAGATAGACCTCTTAGCAAATGCTTCAGTATACCACATCGGATTGTCAATCATAGGCCCTGTATTGTACAGTAGATCTCCAGCATGATTCCTTTGGTTTAACATAAAAATGTACCCTGATGTAGTCTGAAACATGAAAATGACAGTTTTTTCTAAGCATAAAATTGTTATATTAAACATGCACTTTAAAACT... | AAATATACACCTGTGAAACCATCAAACCATCACTTATCAATGCCATGAACTTAGCCACCACTCCCAGAACTTTCCTTCCACCCCTTTTGCTTTGTTTTGTTCCCTTTTGTGGAAAGAGTACTTAACATAAGATAGACCTCTTAGCAAATGCTTCAGTATACCACATCGGATTGTCAATCATAGGCCCTGTATTGTACAGTAGATCTCCAGCATGATTCCTTTGGTTTAACATAAAAATGTACCCTGATGTAGTCTGAAACATGAAAATGACAGTTTTTTCTAAGCATAAAATTGTTATATTAAACATGCACTTTAAAACT... |
Task1_train_42627 | Chromosome 13 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTTTTTCTAAGCATAAAATTGTTATATTAAACATGCACTTTAAAACTACCTTCCCTGCATCCCCCATCATCTGCCTGCCCCATCACATGCACAGGAGAATGTGCTAAGCCTGAGCTTGGGGATATTAACCTCAACGGAGACAGAATCAAGACCCTAGGGAAACCAACACAGGGAGTAGAAAGCAGGGTGTGGTCCTAGGCAGGTGCACAGGTTGAAGAATCTATGGCAATACCTTGAAAAATGACCGCAGTGATAATATGTACCAACCCATAGAGAAGTGGTACCAGGTGCTGTTCTTTGATATGTTTAGCCACTTCCTG... | TTTTTTCTAAGCATAAAATTGTTATATTAAACATGCACTTTAAAACTACCTTCCCTGCATCCCCCATCATCTGCCTGCCCCATCACATGCACAGGAGAATGTGCTAAGCCTGAGCTTGGGGATATTAACCTCAACGGAGACAGAATCAAGACCCTAGGGAAACCAACACAGGGAGTAGAAAGCAGGGTGTGGTCCTAGGCAGGTGCACAGGTTGAAGAATCTATGGCAATACCTTGAAAAATGACCGCAGTGATAATATGTACCAACCCATAGAGAAGTGGTACCAGGTGCTGTTCTTTGATATGTTTAGCCACTTCCTG... |
Task1_train_42628 | A mutation located on Chromosome 13 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AGGCAGGTGCACAGGTTGAAGAATCTATGGCAATACCTTGAAAAATGACCGCAGTGATAATATGTACCAACCCATAGAGAAGTGGTACCAGGTGCTGTTCTTTGATATGTTTAGCCACTTCCTGTGGAGTACTATTGTTGGGAAAAAGCTGAGTGTTGGGAGGGAAACTGAGGCAGGGCTTGCGTAACGTCCTCTGGAATGTGTCTAGACTTGCTGGCTCCTTGCTTCTAGCCTTCCTAGGCTCCTGTTCCCATTATCTCAAGTAGCAGAATATGTTCCATATAAATGCTAAACCATCGCAGCTGTAAATCATGTACTTA... | AGGCAGGTGCACAGGTTGAAGAATCTATGGCAATACCTTGAAAAATGACCGCAGTGATAATATGTACCAACCCATAGAGAAGTGGTACCAGGTGCTGTTCTTTGATATGTTTAGCCACTTCCTGTGGAGTACTATTGTTGGGAAAAAGCTGAGTGTTGGGAGGGAAACTGAGGCAGGGCTTGCGTAACGTCCTCTGGAATGTGTCTAGACTTGCTGGCTCCTTGCTTCTAGCCTTCCTAGGCTCCTGTTCCCATTATCTCAAGTAGCAGAATATGTTCCATATAAATGCTAAACCATCGCAGCTGTAAATCATGTACTTA... |
Task1_train_42629 | Here is a mutation located on Chromosome 13. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TCCTCTGGAATGTGTCTAGACTTGCTGGCTCCTTGCTTCTAGCCTTCCTAGGCTCCTGTTCCCATTATCTCAAGTAGCAGAATATGTTCCATATAAATGCTAAACCATCGCAGCTGTAAATCATGTACTTAATGCAACGTGTCCTTTTGACCTCCACATTCTCACCATCTGTTTCTTTGTTGGATTATCAATAAATACCGTGGGCTCCCAGAGCTCGGGGCCTTCGCAGCCTCCACCATAGTGATGGCATACTGGTGTCCCACCTTTCTCTCTCAAACTGTCTTTTTCTCAATCCTTTGACTCCACTGGACTTTGTCACC... | TCCTCTGGAATGTGTCTAGACTTGCTGGCTCCTTGCTTCTAGCCTTCCTAGGCTCCTGTTCCCATTATCTCAAGTAGCAGAATATGTTCCATATAAATGCTAAACCATCGCAGCTGTAAATCATGTACTTAATGCAACGTGTCCTTTTGACCTCCACATTCTCACCATCTGTTTCTTTGTTGGATTATCAATAAATACCGTGGGCTCCCAGAGCTCGGGGCCTTCGCAGCCTCCACCATAGTGATGGCATACTGGTGTCCCACCTTTCTCTCTCAAACTGTCTTTTTCTCAATCCTTTGACTCCACTGGACTTTGTCACC... |
Task1_train_42630 | Here is a genetic alteration on Chromosome 13. Based on the data, is it a benign variant or a cause of disease? | Benign | ATGTGTCTAGACTTGCTGGCTCCTTGCTTCTAGCCTTCCTAGGCTCCTGTTCCCATTATCTCAAGTAGCAGAATATGTTCCATATAAATGCTAAACCATCGCAGCTGTAAATCATGTACTTAATGCAACGTGTCCTTTTGACCTCCACATTCTCACCATCTGTTTCTTTGTTGGATTATCAATAAATACCGTGGGCTCCCAGAGCTCGGGGCCTTCGCAGCCTCCACCATAGTGATGGCATACTGGTGTCCCACCTTTCTCTCTCAAACTGTCTTTTTCTCAATCCTTTGACTCCACTGGACTTTGTCACCCCCATGACC... | ATGTGTCTAGACTTGCTGGCTCCTTGCTTCTAGCCTTCCTAGGCTCCTGTTCCCATTATCTCAAGTAGCAGAATATGTTCCATATAAATGCTAAACCATCGCAGCTGTAAATCATGTACTTAATGCAACGTGTCCTTTTGACCTCCACATTCTCACCATCTGTTTCTTTGTTGGATTATCAATAAATACCGTGGGCTCCCAGAGCTCGGGGCCTTCGCAGCCTCCACCATAGTGATGGCATACTGGTGTCCCACCTTTCTCTCTCAAACTGTCTTTTTCTCAATCCTTTGACTCCACTGGACTTTGTCACCCCCATGACC... |
Task1_train_42631 | This is a variant located on Chromosome 13. Is this mutation a likely cause of disease or not? | Benign | CCGTGGGCTCCCAGAGCTCGGGGCCTTCGCAGCCTCCACCATAGTGATGGCATACTGGTGTCCCACCTTTCTCTCTCAAACTGTCTTTTTCTCAATCCTTTGACTCCACTGGACTTTGTCACCCCCATGACCTGGTGTTGGGTCTGATCACCCCAACAACTATTATCACACCCACACTGGAGATGAGAACATGGAGGCACAGAAAGGTAAAGCAATTTGTCTAAAGTCTCACAGCTAACAAGCAGCAGAGCCAGGAGTGGCCGTGGGATCCACACTCTTGACCATCTGCAGTATGCTCCTGGCAGGCTTTTGGGTGCACT... | CCGTGGGCTCCCAGAGCTCGGGGCCTTCGCAGCCTCCACCATAGTGATGGCATACTGGTGTCCCACCTTTCTCTCTCAAACTGTCTTTTTCTCAATCCTTTGACTCCACTGGACTTTGTCACCCCCATGACCTGGTGTTGGGTCTGATCACCCCAACAACTATTATCACACCCACACTGGAGATGAGAACATGGAGGCACAGAAAGGTAAAGCAATTTGTCTAAAGTCTCACAGCTAACAAGCAGCAGAGCCAGGAGTGGCCGTGGGATCCACACTCTTGACCATCTGCAGTATGCTCCTGGCAGGCTTTTGGGTGCACT... |
Task1_train_42632 | The following genetic variant occurs on Chromosome 13. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGCTAAAATAGGCCACCCCAAAAGAGACTTCTTTGGCATATTTTGAGATGCTATTCAGAGGGACAGCAGACATAGGAGTAGCTCTGAAAAGCAGTCCTTTTGCAGGGAATATTTGCATCTGCAGAGGAATCGTATGTCAGTGAAGGAAACAGCAGATGCAAACAGGCTTTCTCTGAGACCCCCTTATCTGCCTTATCCAGATTTAGGAAAGATGAACTCCCAGGAAGAGGAGGCTAAAGTCTGATACTTTAAAGGGATGATAGAGAAACCGTTACCAGAGGTGCTTCTATTCTCTCAGGGCTGCTGCCTGCCAGACTTCA... | AGCTAAAATAGGCCACCCCAAAAGAGACTTCTTTGGCATATTTTGAGATGCTATTCAGAGGGACAGCAGACATAGGAGTAGCTCTGAAAAGCAGTCCTTTTGCAGGGAATATTTGCATCTGCAGAGGAATCGTATGTCAGTGAAGGAAACAGCAGATGCAAACAGGCTTTCTCTGAGACCCCCTTATCTGCCTTATCCAGATTTAGGAAAGATGAACTCCCAGGAAGAGGAGGCTAAAGTCTGATACTTTAAAGGGATGATAGAGAAACCGTTACCAGAGGTGCTTCTATTCTCTCAGGGCTGCTGCCTGCCAGACTTCA... |
Task1_train_42633 | Here’s a variant located on Chromosome 13. What is the predicted biological effect — harmless or disease-causing? | Benign | GGTATGAGTAGATTCCAGTACTTGAATAGATATTTCTCCAAAGAAGATACACAAAAGCCAGCAAGTGCATGCAAAGATGCTTGATGTCATTAGTCATTAGGGAAGTGCAAATCAGAACCACGGTGAGATCCCATTTCACACCCAGTGGGATGGCTGTTATTAAAAAACAAGTGGTGGCTGGGCAGAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATTGCTTGAGCTTGGGATTCGAGACCAGCCTAGGCCCATGGCGAAACACTGTCTCTACAGAAAATTAGCTGGGTGTGGTGGTGTGG... | GGTATGAGTAGATTCCAGTACTTGAATAGATATTTCTCCAAAGAAGATACACAAAAGCCAGCAAGTGCATGCAAAGATGCTTGATGTCATTAGTCATTAGGGAAGTGCAAATCAGAACCACGGTGAGATCCCATTTCACACCCAGTGGGATGGCTGTTATTAAAAAACAAGTGGTGGCTGGGCAGAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATTGCTTGAGCTTGGGATTCGAGACCAGCCTAGGCCCATGGCGAAACACTGTCTCTACAGAAAATTAGCTGGGTGTGGTGGTGTGG... |
Task1_train_42634 | A variant was discovered on Chromosome 13. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AGGTCAAGGCTCAGGGGCAAGGACAGCAAAGAGGCCCCCATTCTGCCCCATGAAGAAGCTGAGGATCTGCTCCATGCACTGCCACCAGATAGCTGGTGACCACTTGCTGAGGTGGTGGCCACAGGTAGGAGTCCAGGGGCCACAGAGGCAGGCAGGATGGGCAAGTCCTATGCAGACACCAAGTGGCCCCCTCTGTTCGATGTTTTCCTTACACATACACCGCATACCTTAGTGCCATCCAAAAGAACTAACTTTTAATGGGGAAGGGGCAATTCCAACAATGTAGGGGTGTTAGCCTCTCATGGAAAGCTTCTATGCAC... | AGGTCAAGGCTCAGGGGCAAGGACAGCAAAGAGGCCCCCATTCTGCCCCATGAAGAAGCTGAGGATCTGCTCCATGCACTGCCACCAGATAGCTGGTGACCACTTGCTGAGGTGGTGGCCACAGGTAGGAGTCCAGGGGCCACAGAGGCAGGCAGGATGGGCAAGTCCTATGCAGACACCAAGTGGCCCCCTCTGTTCGATGTTTTCCTTACACATACACCGCATACCTTAGTGCCATCCAAAAGAACTAACTTTTAATGGGGAAGGGGCAATTCCAACAATGTAGGGGTGTTAGCCTCTCATGGAAAGCTTCTATGCAC... |
Task1_train_42635 | A variant on Chromosome 13 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GGTCAAGGCTCAGGGGCAAGGACAGCAAAGAGGCCCCCATTCTGCCCCATGAAGAAGCTGAGGATCTGCTCCATGCACTGCCACCAGATAGCTGGTGACCACTTGCTGAGGTGGTGGCCACAGGTAGGAGTCCAGGGGCCACAGAGGCAGGCAGGATGGGCAAGTCCTATGCAGACACCAAGTGGCCCCCTCTGTTCGATGTTTTCCTTACACATACACCGCATACCTTAGTGCCATCCAAAAGAACTAACTTTTAATGGGGAAGGGGCAATTCCAACAATGTAGGGGTGTTAGCCTCTCATGGAAAGCTTCTATGCACA... | GGTCAAGGCTCAGGGGCAAGGACAGCAAAGAGGCCCCCATTCTGCCCCATGAAGAAGCTGAGGATCTGCTCCATGCACTGCCACCAGATAGCTGGTGACCACTTGCTGAGGTGGTGGCCACAGGTAGGAGTCCAGGGGCCACAGAGGCAGGCAGGATGGGCAAGTCCTATGCAGACACCAAGTGGCCCCCTCTGTTCGATGTTTTCCTTACACATACACCGCATACCTTAGTGCCATCCAAAAGAACTAACTTTTAATGGGGAAGGGGCAATTCCAACAATGTAGGGGTGTTAGCCTCTCATGGAAAGCTTCTATGCACA... |
Task1_train_42636 | Here is a genetic alteration on Chromosome 13. Based on the data, is it a benign variant or a cause of disease? | Benign | TCAAGCGATTCTCCTGCCTCAGCCTTCCAAGTGGCTGGGATTACAGGTGTCCGTCACTACGCCTGGCTAATTTTTTGTATTTTAAGTAGAGATGGGGTTTCACCATGTTGGCCAGGTTGGTCTCGAATTCCTGACCTCAGGTGATCCACCCGCCCTGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGACACCACACCCAGCATTTCTTTTTTCTTTCTTTCTTTTTTTTTTTTAAACCTCAACCCTTTTAGATAAAGCTGGCTGCATTTTAAGAGAAAAAAAACAAAGGACAGAAGAAAACTTCTCAAAGCTGTTAAT... | TCAAGCGATTCTCCTGCCTCAGCCTTCCAAGTGGCTGGGATTACAGGTGTCCGTCACTACGCCTGGCTAATTTTTTGTATTTTAAGTAGAGATGGGGTTTCACCATGTTGGCCAGGTTGGTCTCGAATTCCTGACCTCAGGTGATCCACCCGCCCTGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGACACCACACCCAGCATTTCTTTTTTCTTTCTTTCTTTTTTTTTTTTAAACCTCAACCCTTTTAGATAAAGCTGGCTGCATTTTAAGAGAAAAAAAACAAAGGACAGAAGAAAACTTCTCAAAGCTGTTAAT... |
Task1_train_42637 | A variant on Chromosome 13 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TATTTTAAGTAGAGATGGGGTTTCACCATGTTGGCCAGGTTGGTCTCGAATTCCTGACCTCAGGTGATCCACCCGCCCTGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGACACCACACCCAGCATTTCTTTTTTCTTTCTTTCTTTTTTTTTTTTAAACCTCAACCCTTTTAGATAAAGCTGGCTGCATTTTAAGAGAAAAAAAACAAAGGACAGAAGAAAACTTCTCAAAGCTGTTAATGCTAGTTGCATTAGGGTGTTGGGACATGGGTGATTTTTTTTTTCTATTCTTTTTAATTTCCAATTTTTCCTTAATGA... | TATTTTAAGTAGAGATGGGGTTTCACCATGTTGGCCAGGTTGGTCTCGAATTCCTGACCTCAGGTGATCCACCCGCCCTGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGACACCACACCCAGCATTTCTTTTTTCTTTCTTTCTTTTTTTTTTTTAAACCTCAACCCTTTTAGATAAAGCTGGCTGCATTTTAAGAGAAAAAAAACAAAGGACAGAAGAAAACTTCTCAAAGCTGTTAATGCTAGTTGCATTAGGGTGTTGGGACATGGGTGATTTTTTTTTTCTATTCTTTTTAATTTCCAATTTTTCCTTAATGA... |
Task1_train_42638 | This sequence variant lies on Chromosome 13. Is it clinically significant, and what condition might it cause if any? | Benign | CAATGAAATCTCAATACAGAAATTAAGGAGCATGCACAAAACTATATAAATAATTGTTAGACATGTCAAGACTATCCATTTTCTACTGGAGAGCCTTCACAAAGCAAATGCTGATCTTTATTGGAGACGTATCTCAGTTGTGGCAAAGATGCCATGAGGATTGTTGCAAAACTAGGCTCAGTTTTACTAGAAGAAAGAACCAGAGTCTTATATTTCTATACATATGTGGACACATCTACATACCTATACACAGAGAGAGAAACACTAATGCAACTGTGATAGACTTGCTTTTCACATGAGAAATTTAGAAAGCTGTCAGA... | CAATGAAATCTCAATACAGAAATTAAGGAGCATGCACAAAACTATATAAATAATTGTTAGACATGTCAAGACTATCCATTTTCTACTGGAGAGCCTTCACAAAGCAAATGCTGATCTTTATTGGAGACGTATCTCAGTTGTGGCAAAGATGCCATGAGGATTGTTGCAAAACTAGGCTCAGTTTTACTAGAAGAAAGAACCAGAGTCTTATATTTCTATACATATGTGGACACATCTACATACCTATACACAGAGAGAGAAACACTAATGCAACTGTGATAGACTTGCTTTTCACATGAGAAATTTAGAAAGCTGTCAGA... |
Task1_train_42639 | Here’s a variant located on Chromosome 13. What is the predicted biological effect — harmless or disease-causing? | Benign | TTATAATTATAAAATATGTTCATTTAGAGATATAATTTAGAAAATATAGAAAAGTATCAAGAAGAAAATTAAAATCTCCTAAAATCCCGAGAGCAATACGATCACTATTAATATTTTGGTATGTTTCCCTCCTGTATTTTTACCATCCCATAAATAGATCTGTGTGTTTATACCATACCACTTTTCATGTTTTCCTTATCAAAGAGGGAAATGTTATTTTCAAGTTACATTTTATTAACATATCTCAAAATACAAATGGAACATCACTTTGAAGGCTAGTGTCGATTTATATCTATATATATATTTTAGAGACAGGTCTT... | TTATAATTATAAAATATGTTCATTTAGAGATATAATTTAGAAAATATAGAAAAGTATCAAGAAGAAAATTAAAATCTCCTAAAATCCCGAGAGCAATACGATCACTATTAATATTTTGGTATGTTTCCCTCCTGTATTTTTACCATCCCATAAATAGATCTGTGTGTTTATACCATACCACTTTTCATGTTTTCCTTATCAAAGAGGGAAATGTTATTTTCAAGTTACATTTTATTAACATATCTCAAAATACAAATGGAACATCACTTTGAAGGCTAGTGTCGATTTATATCTATATATATATTTTAGAGACAGGTCTT... |
Task1_train_42640 | A variant has been detected on Chromosome 13. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCTCACTGCAACCTCGACCTCCCTCCCAGCAATCCTTTCACCCGGCCTACTTAGTAGCTGGGACCACAGGCCTGCACCACCATGCCCAGCTAATTTTGGTAGAGACAGGGTTCTTACTATGTTGCCAAGGCTGGTCACAAACTCCTGGGCTCAAGCCATCCTCCTGCCTCAGCCTCCCAGAGTGCTGGGGTTACAGGTGTGAGCTGCCACGCCCGGCCCAGAGTAAAAACATTTTAAACATAAATCTGCGGTCTGTTCTTAGCACCTGCGGCTGCGTGGGAGGTATGGAAAGGCGCACTTTGGGTTTCGTGAAATCTCAA... | GCTCACTGCAACCTCGACCTCCCTCCCAGCAATCCTTTCACCCGGCCTACTTAGTAGCTGGGACCACAGGCCTGCACCACCATGCCCAGCTAATTTTGGTAGAGACAGGGTTCTTACTATGTTGCCAAGGCTGGTCACAAACTCCTGGGCTCAAGCCATCCTCCTGCCTCAGCCTCCCAGAGTGCTGGGGTTACAGGTGTGAGCTGCCACGCCCGGCCCAGAGTAAAAACATTTTAAACATAAATCTGCGGTCTGTTCTTAGCACCTGCGGCTGCGTGGGAGGTATGGAAAGGCGCACTTTGGGTTTCGTGAAATCTCAA... |
Task1_train_42641 | A mutation is present on Chromosome 13. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AAGCATGAAAGTAAAAATTATTAGATTACATTTTTTAGGGATAATTTTGATGGCCATTTGGGGGATTATTTGGCGTAAGAGGATGACAGTGAAGGCTGAAGGATCACTTAGGCCATCATATCAGTAGACTCAGCAACTCATGAGAACTAAAACTTAACTAATAGCACTGGATAGGGACTGAGAATAGATATGACAAATGCAAAATAGGGAAAATTAATAAAACTCAGTAATGCTTGAACGTGAGGCATGAGGAAAAGGGAAGCATCATCAATGGTTTGTTACGCTTTGGTGACTAAGTCGATGGATTGTGGTATTCATCA... | AAGCATGAAAGTAAAAATTATTAGATTACATTTTTTAGGGATAATTTTGATGGCCATTTGGGGGATTATTTGGCGTAAGAGGATGACAGTGAAGGCTGAAGGATCACTTAGGCCATCATATCAGTAGACTCAGCAACTCATGAGAACTAAAACTTAACTAATAGCACTGGATAGGGACTGAGAATAGATATGACAAATGCAAAATAGGGAAAATTAATAAAACTCAGTAATGCTTGAACGTGAGGCATGAGGAAAAGGGAAGCATCATCAATGGTTTGTTACGCTTTGGTGACTAAGTCGATGGATTGTGGTATTCATCA... |
Task1_train_42642 | This genomic variant is located on Chromosome 13. Can you determine its pathogenicity and name any linked disease? | Benign | CGTCTGTGGTTGGTACAAACCTAAATCCAGAACATTGTAACATTAGCGATACTTACAATTAATTACTATGGAATTTTACTTTCTTGCACAGAATGAAGGCTGGGAAGAGGAAGCTAAAGTGGAATTTTTGAAAATGGTAAATAACAAGGCTGTTTCAATGAAAGTTTTTAGAGAAGAAGATGGTGTGCTTATTGTAGATCTGCAAAAACCACCACCGAATAAAATAAGCAGTGATATGCCTGTGTCTCTTAGAGATGCGCTAGTTTTTATGGAACTAGCAAAGTAAGTAACTTATTAAAACTTAAATATTCTTTGAGATT... | CGTCTGTGGTTGGTACAAACCTAAATCCAGAACATTGTAACATTAGCGATACTTACAATTAATTACTATGGAATTTTACTTTCTTGCACAGAATGAAGGCTGGGAAGAGGAAGCTAAAGTGGAATTTTTGAAAATGGTAAATAACAAGGCTGTTTCAATGAAAGTTTTTAGAGAAGAAGATGGTGTGCTTATTGTAGATCTGCAAAAACCACCACCGAATAAAATAAGCAGTGATATGCCTGTGTCTCTTAGAGATGCGCTAGTTTTTATGGAACTAGCAAAGTAAGTAACTTATTAAAACTTAAATATTCTTTGAGATT... |
Task1_train_42643 | This alteration occurs on Chromosome 13. Is it associated with a disease or is it a benign variant? | Benign | CTCCTTTGACATTTACACTGTAAACCAAAGAAAAAGAGAACAATGTAGTGGATACCAGATCTGAGCCCTTTGGTATCCTTTACTTAGACATAAATGTTTAGGCTTTATTTTAGAAATTCTGGTAGGTATATACCTACTAGATGTATTTATATGAAATGTAAATGTATTTATATGAAACAGGATGAGTAGCAAATAAATAATTGAACAGTATTTACGTTTAAAGATCCTTTCGGGTTCTATGTTTGGAGTTTAAGCACCTTTGGTCCAGGGACAGGATCAGGATATGGTTGTGGCTCTAGCTTAATCTTTTCTCTCTCTCT... | CTCCTTTGACATTTACACTGTAAACCAAAGAAAAAGAGAACAATGTAGTGGATACCAGATCTGAGCCCTTTGGTATCCTTTACTTAGACATAAATGTTTAGGCTTTATTTTAGAAATTCTGGTAGGTATATACCTACTAGATGTATTTATATGAAATGTAAATGTATTTATATGAAACAGGATGAGTAGCAAATAAATAATTGAACAGTATTTACGTTTAAAGATCCTTTCGGGTTCTATGTTTGGAGTTTAAGCACCTTTGGTCCAGGGACAGGATCAGGATATGGTTGTGGCTCTAGCTTAATCTTTTCTCTCTCTCT... |
Task1_train_42644 | A genetic alteration is present on Chromosome 13. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AAGGTAACATTTGAGTCAACACCTTAAAATGGTTAGAGGACAGACCACACGGGTGCAGGGAGATGAGTGCTGAGGCAGGAGCAGGGCTAGGAGGGAGGGGACTGCATTGGCAGAAGAGGGAATGGTAAGAAGAGATAGGACAAGATCTGCTGGGAGGCAGCAACAGTAATTCAGTGAGGAGCAGTAAAACAGTGAGGAGCAGTGAGTTTGGACAAAGGTGGGATCAGTGGAAATGAAGAGAATTGCTGTAGGTCAGCTTATCAGTTAGGGACACATTCAGCACCCAATAACTGTAAGTGAACTTTATTCAGAGTTTTAAA... | AAGGTAACATTTGAGTCAACACCTTAAAATGGTTAGAGGACAGACCACACGGGTGCAGGGAGATGAGTGCTGAGGCAGGAGCAGGGCTAGGAGGGAGGGGACTGCATTGGCAGAAGAGGGAATGGTAAGAAGAGATAGGACAAGATCTGCTGGGAGGCAGCAACAGTAATTCAGTGAGGAGCAGTAAAACAGTGAGGAGCAGTGAGTTTGGACAAAGGTGGGATCAGTGGAAATGAAGAGAATTGCTGTAGGTCAGCTTATCAGTTAGGGACACATTCAGCACCCAATAACTGTAAGTGAACTTTATTCAGAGTTTTAAA... |
Task1_train_42645 | A mutation on Chromosome 13 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TATAAAAAGATCATGCAGCCTCTTACCTTGCATTGGAAGATAATTTTTCTTGTATTTTTCTACCTGGGTTCCTGAAGAAATCTGACTGTTTTGAAATCGAACAGATGTGTTCTATAGTATAAGAGATAATTTTTTATTTAAAATGAGTGTTAGTCTATTAATACACTAAGTGAAACTAATAAAACTCAGCTAGTGCTAAGAATGCTGTGGGTTTTGTTTATTCATATTGTTTTCATTTATACAACAGGCCAAAGCAAACAAGCTGTTATCTAGGAATCACTGCGCGTGTGCACACACACGCACGCGCGCCCCTTTTGACA... | TATAAAAAGATCATGCAGCCTCTTACCTTGCATTGGAAGATAATTTTTCTTGTATTTTTCTACCTGGGTTCCTGAAGAAATCTGACTGTTTTGAAATCGAACAGATGTGTTCTATAGTATAAGAGATAATTTTTTATTTAAAATGAGTGTTAGTCTATTAATACACTAAGTGAAACTAATAAAACTCAGCTAGTGCTAAGAATGCTGTGGGTTTTGTTTATTCATATTGTTTTCATTTATACAACAGGCCAAAGCAAACAAGCTGTTATCTAGGAATCACTGCGCGTGTGCACACACACGCACGCGCGCCCCTTTTGACA... |
Task1_train_42646 | Located on Chromosome 13, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAAAGAGGCACCAAGACAAACACACACAGAGGAGAATGCCATGTGAAGACACACACAGAGGGAAGATGGCCATGTGACCACAGAGGCAGAGACTGGAGTGATGTAGCTGCAATCCAAGAAATACCAACGTGTGCCTGAAACCACCAGAAGCTGGAGGAGCCAGCATGGCCCGCCTTGCTGATGCCCGGACTTTGGACTTACAGCCTCCAGAATCACAAGAAAATACATTTCTATTGTTTAAAGCCACCCAGTTGCTGGTACTTTGTTACAGCAGCCCAGAGAAACCAATACACTAACTAGCCAAAGTACCACTTGAAGGT... | AAAAGAGGCACCAAGACAAACACACACAGAGGAGAATGCCATGTGAAGACACACACAGAGGGAAGATGGCCATGTGACCACAGAGGCAGAGACTGGAGTGATGTAGCTGCAATCCAAGAAATACCAACGTGTGCCTGAAACCACCAGAAGCTGGAGGAGCCAGCATGGCCCGCCTTGCTGATGCCCGGACTTTGGACTTACAGCCTCCAGAATCACAAGAAAATACATTTCTATTGTTTAAAGCCACCCAGTTGCTGGTACTTTGTTACAGCAGCCCAGAGAAACCAATACACTAACTAGCCAAAGTACCACTTGAAGGT... |
Task1_train_42647 | Located on Chromosome 13, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CTGTCATAGTGCGGTTCTACCTTTAAAAGTATCACAGCTGTTATTTAAGTGATCTTGATTATTCTTTGTATGTATTCCATAAAGAAACCCTAAGCCATTCAACTATTTTAAGGCACACAAATGTTTTCTATATTCTCTAAGATAAACATCCAAATTCCCTAAACCATTGTTTATGTGCTACAATTTCTCATGACCACACCCCACCTGACCCCTGCACCCAGCCTCACTCACTTGCCAAGTCTTTTTTTCCTTGTATTCTCAATGCCCAGCATAATCTCTGAGCAGAACAGGTGCTTTCCTGGGTCAGTAAAGTATATTTC... | CTGTCATAGTGCGGTTCTACCTTTAAAAGTATCACAGCTGTTATTTAAGTGATCTTGATTATTCTTTGTATGTATTCCATAAAGAAACCCTAAGCCATTCAACTATTTTAAGGCACACAAATGTTTTCTATATTCTCTAAGATAAACATCCAAATTCCCTAAACCATTGTTTATGTGCTACAATTTCTCATGACCACACCCCACCTGACCCCTGCACCCAGCCTCACTCACTTGCCAAGTCTTTTTTTCCTTGTATTCTCAATGCCCAGCATAATCTCTGAGCAGAACAGGTGCTTTCCTGGGTCAGTAAAGTATATTTC... |
Task1_train_42648 | Consider a variant on Chromosome 13. Determine its clinical classification and disease relevance. | Benign | TTAGCAGAGACAGGGTTTCACCATATTGGCCAGGCTGGTCTCGAATTCCTGACCTCATGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCAGCCACTGACTCTACTCTCTAAACATCCCTGGAACCCATCACCTCCCCCTTCACTTGTGTGTTACTATTTTAGTTTGGTAAAATTAAAAACTTTTGTCTCATAAGTTATCATAATAGTGTCTACACTCGCCTCCTAGCCTCCATTCCCACTCCCTTTGGCCTTCAAGATACCAAGCCACCTTTTTAAAAAGCACATCTAATCAA... | TTAGCAGAGACAGGGTTTCACCATATTGGCCAGGCTGGTCTCGAATTCCTGACCTCATGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCAGCCACTGACTCTACTCTCTAAACATCCCTGGAACCCATCACCTCCCCCTTCACTTGTGTGTTACTATTTTAGTTTGGTAAAATTAAAAACTTTTGTCTCATAAGTTATCATAATAGTGTCTACACTCGCCTCCTAGCCTCCATTCCCACTCCCTTTGGCCTTCAAGATACCAAGCCACCTTTTTAAAAAGCACATCTAATCAA... |
Task1_train_42649 | A mutation on Chromosome 13 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ATCTCTACTGAAAAATACAGAAATTAACCGGGCGTGGTGGCGTGCGCCTGTGATCCCAGTTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTCAGGAGACGGAGGTTGCAGTGAGCCGAGATGGCACCACTGTATTCCAGCCTGGGCAACAGAGCGAGACTCTGTCTCAAAATAAAGTAAAATATAAATTAAATTTAAAAAACAAAATAAAATGTACGTTTCTTTTTAATTATACAAACACAGAGGTGGTGTATTAGTCTGCTTGGCTGATACAACAAAATACCATAGACTGAGGTGGCTATAACAACAGACATTT... | ATCTCTACTGAAAAATACAGAAATTAACCGGGCGTGGTGGCGTGCGCCTGTGATCCCAGTTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTCAGGAGACGGAGGTTGCAGTGAGCCGAGATGGCACCACTGTATTCCAGCCTGGGCAACAGAGCGAGACTCTGTCTCAAAATAAAGTAAAATATAAATTAAATTTAAAAAACAAAATAAAATGTACGTTTCTTTTTAATTATACAAACACAGAGGTGGTGTATTAGTCTGCTTGGCTGATACAACAAAATACCATAGACTGAGGTGGCTATAACAACAGACATTT... |
Task1_train_42650 | A mutation located on Chromosome 13 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ACCAGGTGGAATTATGGAGAAATAATGCCCTGTAAGTAAAACAATACTTTATAGGTATTTAACCAAAGGCTGACTGTGGAATATTTCCTGGAGTTTCAATGCTGAACAGAGCAATTTCTATATATAGCGCCCCTTTAGCAGGTAGAAACATTTGCTACAGTGTCTGCAGCACAGCTGGCGCCCAGCAGTAGAACTGTCCTAATTACACTATCACTTCAGGCTAACTACGGATCACTGGAGAAGTGGATGCAGGCTTTTTCCTTGGCGTGTTATAAATATTTCATTCTCTAAATTAAGACACCAGCCCTAAATATGTTATC... | ACCAGGTGGAATTATGGAGAAATAATGCCCTGTAAGTAAAACAATACTTTATAGGTATTTAACCAAAGGCTGACTGTGGAATATTTCCTGGAGTTTCAATGCTGAACAGAGCAATTTCTATATATAGCGCCCCTTTAGCAGGTAGAAACATTTGCTACAGTGTCTGCAGCACAGCTGGCGCCCAGCAGTAGAACTGTCCTAATTACACTATCACTTCAGGCTAACTACGGATCACTGGAGAAGTGGATGCAGGCTTTTTCCTTGGCGTGTTATAAATATTTCATTCTCTAAATTAAGACACCAGCCCTAAATATGTTATC... |
Task1_train_42651 | Chromosome 13 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGGAAAACAGTAAGGGGAGCGAAGGGGATTATTGAAAATGCAGAGTTAGAGTGTTTGCTGAGGAGAGTGCATTAGGGAGTTGATAGGAGATGACTGCAAGATTTCTGAACTCTATCTTATAATCTGTGGTATAAATTATGAGTGCTGCATGGTTCCTTCTTTTCTAGATTTTAGTAGTCTGTATAGAAAAGGATAAATCCAACAATGAAGGTAATGAATGGGAAAACTGGGTATAAAATAATACCAATGAGATGATAATTTCAACATGGATGAAGGTGACCCTTGAACAGTCATTCAAGAAGTCCAAGCAGGAAGAGGCT... | GGGAAAACAGTAAGGGGAGCGAAGGGGATTATTGAAAATGCAGAGTTAGAGTGTTTGCTGAGGAGAGTGCATTAGGGAGTTGATAGGAGATGACTGCAAGATTTCTGAACTCTATCTTATAATCTGTGGTATAAATTATGAGTGCTGCATGGTTCCTTCTTTTCTAGATTTTAGTAGTCTGTATAGAAAAGGATAAATCCAACAATGAAGGTAATGAATGGGAAAACTGGGTATAAAATAATACCAATGAGATGATAATTTCAACATGGATGAAGGTGACCCTTGAACAGTCATTCAAGAAGTCCAAGCAGGAAGAGGCT... |
Task1_train_42652 | Consider this mutation on Chromosome 13. Is this a benign change or a disease-causing variant? | Benign | CTCCGGAGCTGAGGCGCAGGGCAGTTCCCTCAGCCGAACACCCCGGGAGGGAGACTCGCCTGGAAGTGTCTCGGAGCGACCCTTGCTCGGGTGCTGCCCCTTCAGTGTCCCGGACGTGCCGGGCAACGCGATGACCAGACCCTGAGCGCTCTTCGACCCATGCCCCAAGGGCCTTGGAGGCGCCCCACACCCCCTGGGAACCTAGGAGCGGGGCTATGGAGGGGAGGGATGAGAGGGACTTGTCAGAATTCATTATTGACTGCGAAAGTCACCACCCTCTTTCCGGGCCCTAAAAGAGACAATGGCAGGGCTGGGAAGGT... | CTCCGGAGCTGAGGCGCAGGGCAGTTCCCTCAGCCGAACACCCCGGGAGGGAGACTCGCCTGGAAGTGTCTCGGAGCGACCCTTGCTCGGGTGCTGCCCCTTCAGTGTCCCGGACGTGCCGGGCAACGCGATGACCAGACCCTGAGCGCTCTTCGACCCATGCCCCAAGGGCCTTGGAGGCGCCCCACACCCCCTGGGAACCTAGGAGCGGGGCTATGGAGGGGAGGGATGAGAGGGACTTGTCAGAATTCATTATTGACTGCGAAAGTCACCACCCTCTTTCCGGGCCCTAAAAGAGACAATGGCAGGGCTGGGAAGGT... |
Task1_train_42653 | Consider a variant on Chromosome 13. Determine its clinical classification and disease relevance. | Benign | TATGTAATTGGAGACACCGGGGTCGTGTCTGGGAGATTCTGAGCTCATCTACACTCTTGCTAAACTGCGGGGAACCCAGCCCTGGTGGGATCTGTGCATCTCACATGAGCTTTTTTACATAAAGAGCACAGACGCTGCATTTGGGGCCTGGTTTATCTAAGCGTGGGGTTTACCCCCAGGCTTGGGACTGGGTGCCCCGAACACAGTGGATTATTCTGAGTCTTAGGCCCAGCCTTGGTATTTGGGTCCTGGGTCAGAAAATCCTCTTTACCAAGCAGCAAGTTATTGTGTGTGTCAGGAAATCCCCCAGGTTACCCTGG... | TATGTAATTGGAGACACCGGGGTCGTGTCTGGGAGATTCTGAGCTCATCTACACTCTTGCTAAACTGCGGGGAACCCAGCCCTGGTGGGATCTGTGCATCTCACATGAGCTTTTTTACATAAAGAGCACAGACGCTGCATTTGGGGCCTGGTTTATCTAAGCGTGGGGTTTACCCCCAGGCTTGGGACTGGGTGCCCCGAACACAGTGGATTATTCTGAGTCTTAGGCCCAGCCTTGGTATTTGGGTCCTGGGTCAGAAAATCCTCTTTACCAAGCAGCAAGTTATTGTGTGTGTCAGGAAATCCCCCAGGTTACCCTGG... |
Task1_train_42654 | A mutation is present on Chromosome 13. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TTCTTTATTCAAGAAAATCCATAATACAAAGTATTGGCAAAGATGTGAGGAACTGGAACTGCCATACACTGCTAGTGGGAGTGGAAATTGGTGTAACCACTGTGGAAAACCGTTTGACGGTATCTACCAAACCTGAACATATCCCTTCCCTATGATCCAGGAATTCTACTTGTGGGCATAATCCTTTATACTGGTGTTTATGTCCACCATATATAAAACAATGTTCACAGCAGTGCTATGCATAATTACACAAAATTGGAACAACTTCCATGTGCTTCGTGAACATAATGGATAAAATAAATTATAAGATCTATTCATAC... | TTCTTTATTCAAGAAAATCCATAATACAAAGTATTGGCAAAGATGTGAGGAACTGGAACTGCCATACACTGCTAGTGGGAGTGGAAATTGGTGTAACCACTGTGGAAAACCGTTTGACGGTATCTACCAAACCTGAACATATCCCTTCCCTATGATCCAGGAATTCTACTTGTGGGCATAATCCTTTATACTGGTGTTTATGTCCACCATATATAAAACAATGTTCACAGCAGTGCTATGCATAATTACACAAAATTGGAACAACTTCCATGTGCTTCGTGAACATAATGGATAAAATAAATTATAAGATCTATTCATAC... |
Task1_train_42655 | This is a variant located on Chromosome 13. Is this mutation a likely cause of disease or not? | Benign | TTTAAGATCTCACATGCATTTATAATCCATTTCTAACATTAAACATTTTGATGTTTAATTTTTGTATTTGGCCAGGAGGAGCCCTGATCAGAAAGGTTTTTTGAGAAAACTATTGATTGAATGAAATAATAATATAGAAATGACAAATAAATCTGTGTTTACCACTTTTTTCTCCTGAGAAGTTCTATTTGTCAATCTAATGTGAATATATTTTTATTTCTCTCTAGGTCTCATGGACTGATTGGCTCTCATTCAGCAGGAACCTAACAGATAAGTCTTCCTGCTGTATATCAAGACAATGCTTGGTTTTCAAGCTGTTC... | TTTAAGATCTCACATGCATTTATAATCCATTTCTAACATTAAACATTTTGATGTTTAATTTTTGTATTTGGCCAGGAGGAGCCCTGATCAGAAAGGTTTTTTGAGAAAACTATTGATTGAATGAAATAATAATATAGAAATGACAAATAAATCTGTGTTTACCACTTTTTTCTCCTGAGAAGTTCTATTTGTCAATCTAATGTGAATATATTTTTATTTCTCTCTAGGTCTCATGGACTGATTGGCTCTCATTCAGCAGGAACCTAACAGATAAGTCTTCCTGCTGTATATCAAGACAATGCTTGGTTTTCAAGCTGTTC... |
Task1_train_42656 | This variant is found on Chromosome 13. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TTGTATAAGGAAAAGAGAAACTGAGCGCACTTTCAATATTTAAGTAAGTGTCTCTAACATGTTTTGCAACATAAAATGATGACCACTGTGTTGGTCATTACTTCTCTACTGCTAAAACAATGTTTTCTAAAATAATATACTCCTTAGAAAAAAATATAGTGCTTTGGGTGTGCACTGTTGTAATCCAAGGAATAGGAAATGTTTTGTAGTAAGTGCGATGGTGTTTGACATCGTGATTTATTAATTTATCACATTTGGTTTCATAGAAATAGAGTAAGCTACGTATTTGCTGTGCCGCAATTACCATGACATTACACTTG... | TTGTATAAGGAAAAGAGAAACTGAGCGCACTTTCAATATTTAAGTAAGTGTCTCTAACATGTTTTGCAACATAAAATGATGACCACTGTGTTGGTCATTACTTCTCTACTGCTAAAACAATGTTTTCTAAAATAATATACTCCTTAGAAAAAAATATAGTGCTTTGGGTGTGCACTGTTGTAATCCAAGGAATAGGAAATGTTTTGTAGTAAGTGCGATGGTGTTTGACATCGTGATTTATTAATTTATCACATTTGGTTTCATAGAAATAGAGTAAGCTACGTATTTGCTGTGCCGCAATTACCATGACATTACACTTG... |
Task1_train_42657 | A variant affecting Chromosome 13 has been observed. Determine if it's benign or associated with disease. | Benign | TTTTTTTTTAAAGGAATGGTTTAAACAGGTTACCTTCTTACTCCTCATTCATGCTTTAGTTGACTACATAAGGACCCCTCTCCCTATTGGCACCATTGAAATTGTTCAGGCAAAAATAACTGCCAGCGACACACTGCTTTAAGTAATGGACTTTTCCCAAGTTTTGTATTAATATTTCAGTATTTGGTAGTGCATCCTACTGCTAGTTTTTAAACTCTTCCCTTGTCATCTATCATCTCATTCTCTCTTGACAAATGTGAAAATGGAAGCTCAGAAATAAAACAAGAATTAAAACGAATAGTGATCCTTCAGGTAACAAG... | TTTTTTTTTAAAGGAATGGTTTAAACAGGTTACCTTCTTACTCCTCATTCATGCTTTAGTTGACTACATAAGGACCCCTCTCCCTATTGGCACCATTGAAATTGTTCAGGCAAAAATAACTGCCAGCGACACACTGCTTTAAGTAATGGACTTTTCCCAAGTTTTGTATTAATATTTCAGTATTTGGTAGTGCATCCTACTGCTAGTTTTTAAACTCTTCCCTTGTCATCTATCATCTCATTCTCTCTTGACAAATGTGAAAATGGAAGCTCAGAAATAAAACAAGAATTAAAACGAATAGTGATCCTTCAGGTAACAAG... |
Task1_train_42658 | This mutation is located on Chromosome 13. Is it associated with a disease or is it a benign polymorphism? | Benign | TTAAAAATTTCCCCCCTCCCCCAGATGGAACCATAGCATCTCTCTTTGCATAGAATGGTACAGAATCTTCTCTCCCATCTCCTTATTGCTGCTGCTCCTTCCCCTGGGAGCCTCCCCTGTGTATTGGAAGTCTAGCCATGTGTCACCTCCTTTGAGCACCCTTCTTGGGGCAGAACCACTTATTTCTCATAGTGCTTAGTCCATACATCTATGGTAGCACTTATTGGATCCTTGTGTGTGTGTGTGTGTGACCTCAGAGCTTAAGATGGTCCCTGGTGCATAGTGATGACTCTGTCAATGTTTGGGACAAGAGTGAAGTT... | TTAAAAATTTCCCCCCTCCCCCAGATGGAACCATAGCATCTCTCTTTGCATAGAATGGTACAGAATCTTCTCTCCCATCTCCTTATTGCTGCTGCTCCTTCCCCTGGGAGCCTCCCCTGTGTATTGGAAGTCTAGCCATGTGTCACCTCCTTTGAGCACCCTTCTTGGGGCAGAACCACTTATTTCTCATAGTGCTTAGTCCATACATCTATGGTAGCACTTATTGGATCCTTGTGTGTGTGTGTGTGTGACCTCAGAGCTTAAGATGGTCCCTGGTGCATAGTGATGACTCTGTCAATGTTTGGGACAAGAGTGAAGTT... |
Task1_train_42659 | A mutation found on Chromosome 13 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GTTTGAAATTGGAACTTATTAAAAGGGAAGCAGAGCATAAAGGTTTGGAAAATTTGCAGCCTGACTGTGAGGTGAAAAAGAAAACCCCATTTTCTGGGGAGAAATTCAAGCCAGCTGCAGAAATTTGTGTAAGTAACAAGGAGCTGAATGTTCATACCAAGACAATAGGGAAAATGTCTCCAGGGCATGTCAGAGATCTTCACAGCTGCCCCTTTCATCACAGGCCCAGAGGCCTAGGAGTAAAAGTGGTTTCGTGGGCCTGGCCCAGGGCCCCACTGCTCTATGCAGCCTCAGGACTTGGTGCCCTGTGTCCCAGATGC... | GTTTGAAATTGGAACTTATTAAAAGGGAAGCAGAGCATAAAGGTTTGGAAAATTTGCAGCCTGACTGTGAGGTGAAAAAGAAAACCCCATTTTCTGGGGAGAAATTCAAGCCAGCTGCAGAAATTTGTGTAAGTAACAAGGAGCTGAATGTTCATACCAAGACAATAGGGAAAATGTCTCCAGGGCATGTCAGAGATCTTCACAGCTGCCCCTTTCATCACAGGCCCAGAGGCCTAGGAGTAAAAGTGGTTTCGTGGGCCTGGCCCAGGGCCCCACTGCTCTATGCAGCCTCAGGACTTGGTGCCCTGTGTCCCAGATGC... |
Task1_train_42660 | Chromosome 13 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GTCTTGCCCTGTCTCCCAGGCTGGAGTGCAGTAGCGCCATCTCGGCTCCCTGCAACCTCCGCCTCCCAGGTTCAAGTGATTATTTCGCCTCAGACTCCCAAGTAGCTGGGATTACAGGTGCCCACCACCATGCCCCGCTAATTTTTATATTTTTAGTAGAGTCCAGGTTTCACCACGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGCGATCCGCCCACCTCGGTTTCCCAAAGTGCTGGGATTACAGGTGTGAGTGACCACACCCAGCCTAGAACATACACTTTTGATCCTTTCTGTAAGTCTGCTATCAGAATT... | GTCTTGCCCTGTCTCCCAGGCTGGAGTGCAGTAGCGCCATCTCGGCTCCCTGCAACCTCCGCCTCCCAGGTTCAAGTGATTATTTCGCCTCAGACTCCCAAGTAGCTGGGATTACAGGTGCCCACCACCATGCCCCGCTAATTTTTATATTTTTAGTAGAGTCCAGGTTTCACCACGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGCGATCCGCCCACCTCGGTTTCCCAAAGTGCTGGGATTACAGGTGTGAGTGACCACACCCAGCCTAGAACATACACTTTTGATCCTTTCTGTAAGTCTGCTATCAGAATT... |
Task1_train_42661 | A mutation is present on Chromosome 13. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ATATTTGTCCTTCTGTGCTTGATTTATTTCACTTAACACAATGACCTCTGGTTTTATCCAGCCAGGTTGCTGCAAATAACAGGATTTCATTCTTTTTATGGCTGAATGATATTCCATTGTGTATATATACATTGTCTGTATCCATTAATCTGTTGATGGATATCTATTGATTCCATATCTCAGCTGTCGTGAATAGTGAAACAATAAACATGGGAACACACATTTCAAAATACTGATTTCCTTTTTGTATATCCAGCAGTGGGATTGCTGGATCATGTGACAGTTCTGCTTTTTAGCTTTTTGAGGAGCCTCCCTACTGT... | ATATTTGTCCTTCTGTGCTTGATTTATTTCACTTAACACAATGACCTCTGGTTTTATCCAGCCAGGTTGCTGCAAATAACAGGATTTCATTCTTTTTATGGCTGAATGATATTCCATTGTGTATATATACATTGTCTGTATCCATTAATCTGTTGATGGATATCTATTGATTCCATATCTCAGCTGTCGTGAATAGTGAAACAATAAACATGGGAACACACATTTCAAAATACTGATTTCCTTTTTGTATATCCAGCAGTGGGATTGCTGGATCATGTGACAGTTCTGCTTTTTAGCTTTTTGAGGAGCCTCCCTACTGT... |
Task1_train_42662 | A variant on Chromosome 13 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AAGATCAGGCTGGCCAACACGGTGAAACCCCTTCTCCACTAAAAATACGAAAATTAGCTAGGCGTGGTAGCACACGCCTATAATCCGAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTAACCCAAATCGTGCCATTGTACTCAAGCCTGGGCAACGGAAGTGAGACTCCATCTCAGAAAAAAAGAAATGTTCCTGCATCTGAGGAAGCCTGCACACCTACAGACACTACCTGCTTCCTTCTTTCAGCCATCAGAGGTGCTGTTTAAAACACCACGGAGGCAGCTCTTCCTGT... | AAGATCAGGCTGGCCAACACGGTGAAACCCCTTCTCCACTAAAAATACGAAAATTAGCTAGGCGTGGTAGCACACGCCTATAATCCGAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTAACCCAAATCGTGCCATTGTACTCAAGCCTGGGCAACGGAAGTGAGACTCCATCTCAGAAAAAAAGAAATGTTCCTGCATCTGAGGAAGCCTGCACACCTACAGACACTACCTGCTTCCTTCTTTCAGCCATCAGAGGTGCTGTTTAAAACACCACGGAGGCAGCTCTTCCTGT... |
Task1_train_42663 | Here is a genetic alteration on Chromosome 13. Based on the data, is it a benign variant or a cause of disease? | Benign | GGTTACCCATCAATACCACCTGCTTTCTAGGCTTTGTGCAATTTCCTGTGCACATTTTCTCTCTGCCTTGCTTGGTGAACTCTTCCTCCTATTTATTGTTTCAAATCCTGCTTGGACATCAAGCTGTCTTCCCTCAGACAGAGCTAATACCCTCCTTCCTGTGCTATCTCTGCACTGCTTCCATATGAAGAAGGATGCTACTGCACGTATTGCCAAATTACATTTTGTTTCCATCACTCGTATCAAAATAAATTCCTTGAGAACAAGTCCTGTGTTTTGTTCTTTGTATCCTAGTGCCTTGGAATGTTTGAATTAAACTC... | GGTTACCCATCAATACCACCTGCTTTCTAGGCTTTGTGCAATTTCCTGTGCACATTTTCTCTCTGCCTTGCTTGGTGAACTCTTCCTCCTATTTATTGTTTCAAATCCTGCTTGGACATCAAGCTGTCTTCCCTCAGACAGAGCTAATACCCTCCTTCCTGTGCTATCTCTGCACTGCTTCCATATGAAGAAGGATGCTACTGCACGTATTGCCAAATTACATTTTGTTTCCATCACTCGTATCAAAATAAATTCCTTGAGAACAAGTCCTGTGTTTTGTTCTTTGTATCCTAGTGCCTTGGAATGTTTGAATTAAACTC... |
Task1_train_42664 | A mutation on Chromosome 13 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TGATAACCAAGACAACTACTAAGTGACTAATAGGTGGGTACCATATACAGCCTGGATACGCTGGACAAAGGGATGATTCATGTCCCAAGTGGGATGGAGCAAGATGGTGCAAGTTTTTTTTTCTCCATTTCCATTTTCCTTTCCTAAGATTTCCACATCCTAGTGGTGCAAGATTTCATCACACTACTCAGGATGACACACAATTTAAAACTTACTAATTGCTTACTTCTGGAATTTTCCATTAAAAATTTTTGGACCTAGGTTGATTGCAGATAACTGAAATCACCAAAAGTGAAACCATGGATAAGGGGGGACTACTA... | TGATAACCAAGACAACTACTAAGTGACTAATAGGTGGGTACCATATACAGCCTGGATACGCTGGACAAAGGGATGATTCATGTCCCAAGTGGGATGGAGCAAGATGGTGCAAGTTTTTTTTTCTCCATTTCCATTTTCCTTTCCTAAGATTTCCACATCCTAGTGGTGCAAGATTTCATCACACTACTCAGGATGACACACAATTTAAAACTTACTAATTGCTTACTTCTGGAATTTTCCATTAAAAATTTTTGGACCTAGGTTGATTGCAGATAACTGAAATCACCAAAAGTGAAACCATGGATAAGGGGGGACTACTA... |
Task1_train_42665 | Given this variant on Chromosome 13, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AATTTTTTTTTTGAAAGAGTCTTACTCTATCACCCAGGCTGGAGTGCAGTGGCGCGATCTCAGTTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTATCCTGCCTCAGCCTCCTAACTAGGTTTACAGGCATGTGCCACAATTCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTCACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGGCCGGCCCAAAAAGAAATTTAGTTGGAATATTAAAAAAT... | AATTTTTTTTTTGAAAGAGTCTTACTCTATCACCCAGGCTGGAGTGCAGTGGCGCGATCTCAGTTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTATCCTGCCTCAGCCTCCTAACTAGGTTTACAGGCATGTGCCACAATTCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTCACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGGCCGGCCCAAAAAGAAATTTAGTTGGAATATTAAAAAAT... |
Task1_train_42666 | This mutation occurs on Chromosome 13. Does this change lead to a known medical condition, or is it benign? | Benign | TTTTTTTTTTGACAGGGAGTCTCGCTCAGTCACCCAGGCTGGGAGTGCAGTGGTGTGATCTCGGCTCACTGCGACCTCTGCCTCCCAGGCAGGTTCAAGTGGTTCTCCTGCCTCAGCCTCCTAAGTAGCTAGGATTACAGGCACACGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGGCATGTTTTCGTCATGTTAGCCAGGCTGGTCTCAAACTCCTGACCTCAAGCAATCATCCCACCTCAGCATCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCACATCCAGCCCCAAAATAACAACCTTAAGAGCC... | TTTTTTTTTTGACAGGGAGTCTCGCTCAGTCACCCAGGCTGGGAGTGCAGTGGTGTGATCTCGGCTCACTGCGACCTCTGCCTCCCAGGCAGGTTCAAGTGGTTCTCCTGCCTCAGCCTCCTAAGTAGCTAGGATTACAGGCACACGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGGCATGTTTTCGTCATGTTAGCCAGGCTGGTCTCAAACTCCTGACCTCAAGCAATCATCCCACCTCAGCATCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCACATCCAGCCCCAAAATAACAACCTTAAGAGCC... |
Task1_train_42667 | This mutation occurs on Chromosome 13. Does this change lead to a known medical condition, or is it benign? | Benign | TCATAATACGAATGGTACTTGTTGGTACTACATACAACTTTCATTCTTATATATCTATTTTTCAAATAAATATACATATTATATCTAATCACCTCTACCATCTCCCACTACAATGTCTCCTTTAAATTCTATCGAATTTCCACTACTTTATTCACCTTTAATTTCAACATACTCCAATATGTTGTCTCAAATCTAACTTTTCTTCCTTAGGTTTCTTCTATACCCACTCTTAGTCAAGTGGTCCTAACTAGCAGACTCTTTTATCCAGTTTCCAAATTTCAGTTATTTATTGTCTCTGATGGTATATCCCAAATCTAGAA... | TCATAATACGAATGGTACTTGTTGGTACTACATACAACTTTCATTCTTATATATCTATTTTTCAAATAAATATACATATTATATCTAATCACCTCTACCATCTCCCACTACAATGTCTCCTTTAAATTCTATCGAATTTCCACTACTTTATTCACCTTTAATTTCAACATACTCCAATATGTTGTCTCAAATCTAACTTTTCTTCCTTAGGTTTCTTCTATACCCACTCTTAGTCAAGTGGTCCTAACTAGCAGACTCTTTTATCCAGTTTCCAAATTTCAGTTATTTATTGTCTCTGATGGTATATCCCAAATCTAGAA... |
Task1_train_42668 | Here is a genetic alteration on Chromosome 13. Based on the data, is it a benign variant or a cause of disease? | Benign | GGTCAGTGGTGTGAACATGGCTCACCGAAGCCTCCATCTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTTCCTAGTAGCTGGGACTACAGGCACACAGCACCATGACTGGTTAAGTTTTGGATTTTTTGGTAGAAATGGGGTCTCACTCTTTGCGCAGGCTAGTTGTGAACTCCTGGTATCAAGGGATTCTCCCAATGTGCTGGGATTTCGGCCTCCCAAAGTGCTGGGACTGCAGGCATGAGCCATCATGCCCAGCCTCTGTTTAACTGTTAACATCATGAGGTTTCCTTTCAATGAGGAAGGGAGGCCTGGGGAGG... | GGTCAGTGGTGTGAACATGGCTCACCGAAGCCTCCATCTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTTCCTAGTAGCTGGGACTACAGGCACACAGCACCATGACTGGTTAAGTTTTGGATTTTTTGGTAGAAATGGGGTCTCACTCTTTGCGCAGGCTAGTTGTGAACTCCTGGTATCAAGGGATTCTCCCAATGTGCTGGGATTTCGGCCTCCCAAAGTGCTGGGACTGCAGGCATGAGCCATCATGCCCAGCCTCTGTTTAACTGTTAACATCATGAGGTTTCCTTTCAATGAGGAAGGGAGGCCTGGGGAGG... |
Task1_train_42669 | Given this context: Chromosome 13 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TATGTGAGAGAGAGAGAGAGAGAAACAGAGGGAGAGAGAGAAACGGAAAGAGAGGAAAGAGACGGAGACAGGGAGATATAGACAGAAGCAGAGAGAGCAGAGAGATAGAAAAGAGAGAGACAGATGTAGATGGAGAGATGGAGAGATGAGACAAAAAGAGATACAGAGGCAGAGGATGGAGAGACAGACAGAGACAGAAAGATAGAGACAGAGCAAGAGACAGAGAGAGGGAAGACAGAGATAGAGCAATATAGACAGAGGACAGACAGAGGTAGAGCGATAAAGACAAAGAGAGAAAGAGAGAGAGATACAGACAGGGA... | TATGTGAGAGAGAGAGAGAGAGAAACAGAGGGAGAGAGAGAAACGGAAAGAGAGGAAAGAGACGGAGACAGGGAGATATAGACAGAAGCAGAGAGAGCAGAGAGATAGAAAAGAGAGAGACAGATGTAGATGGAGAGATGGAGAGATGAGACAAAAAGAGATACAGAGGCAGAGGATGGAGAGACAGACAGAGACAGAAAGATAGAGACAGAGCAAGAGACAGAGAGAGGGAAGACAGAGATAGAGCAATATAGACAGAGGACAGACAGAGGTAGAGCGATAAAGACAAAGAGAGAAAGAGAGAGAGATACAGACAGGGA... |
Task1_train_42670 | This variant is present on Chromosome 13. Is the change likely to result in a pathogenic outcome? | Benign | GTATTCATATACAGTTATACACCACGCAACGTTTCAGTCAATGATGAACTGGACTGCATATATGACAGTGGTCCCATAAGCTTACAATGCCGTGTTTTTAGCATACCCTTTCTATTTCTTTTTTTGAGACAGAGTCTCGCTCTATTACCTAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGTAACCTCTGCCTCCTGGGTTCAAATGATTCTCATGCCTCAGCCTCCCATGTAGCTTGGATTACACATGTGTGCCACCACACCTGGCTAATTTTTTTGTTTGTTTGTTTGTTTTAGTAGAGATGGGGTTTCACTAT... | GTATTCATATACAGTTATACACCACGCAACGTTTCAGTCAATGATGAACTGGACTGCATATATGACAGTGGTCCCATAAGCTTACAATGCCGTGTTTTTAGCATACCCTTTCTATTTCTTTTTTTGAGACAGAGTCTCGCTCTATTACCTAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGTAACCTCTGCCTCCTGGGTTCAAATGATTCTCATGCCTCAGCCTCCCATGTAGCTTGGATTACACATGTGTGCCACCACACCTGGCTAATTTTTTTGTTTGTTTGTTTGTTTTAGTAGAGATGGGGTTTCACTAT... |
Task1_train_42671 | A genomic variant on Chromosome 13 is under review. What is the biological outcome — benign or pathogenic? | Benign | AAAAAACCCAAACTTATGGACTGCTTTGTATCTGCATGGAAATTGGAATTAGGCTTCTATAATTCTCCTTTGATTTACATGTTCAGAAAAATTGTTCTCAGATATACTTCACCAATATTTCCTTCTCCCAGAGTGCTTTCCATAAATATTTATGTGAAAATCGATTTGACTGTCTTCTAGATTTTCTGGCCTGCTTGCTTATTTGATTTTTTCCCCTGCCAAATGAAGCCCTGAATGACAGAGTGGTTAAACAGCGAAATATTCAGGCTGTAGTAGACCGAACTCTCATGCACGATACCTGAAGACCCACAGGTAAGCTC... | AAAAAACCCAAACTTATGGACTGCTTTGTATCTGCATGGAAATTGGAATTAGGCTTCTATAATTCTCCTTTGATTTACATGTTCAGAAAAATTGTTCTCAGATATACTTCACCAATATTTCCTTCTCCCAGAGTGCTTTCCATAAATATTTATGTGAAAATCGATTTGACTGTCTTCTAGATTTTCTGGCCTGCTTGCTTATTTGATTTTTTCCCCTGCCAAATGAAGCCCTGAATGACAGAGTGGTTAAACAGCGAAATATTCAGGCTGTAGTAGACCGAACTCTCATGCACGATACCTGAAGACCCACAGGTAAGCTC... |
Task1_train_42672 | Mutation context: Chromosome 13. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CAATGGGCTAGTCACACAGTGACACAGGTAGATTTTTAAAATAATACTAAGTGAGAAAAGTAAGGAACAAAATGAAATTTTTAACCCTATATATTTTTATAGTTCAAAAGTATATCCACAAAAGAATGAGTAATATTTTATAAGGGCACATGCAAACAAAAGGAGAAACATTAAATACATTATAGTTATTGCCCATGGTGGTGGAAGGAAATGAAAATAGGAGATGGAGATAAAAGAGAAAAAACACATTTTAAAAGCTCAAATTATTGAAAAGTCATCATTCCCACTACCACTCATGATTCCATTAGGTATTTTATTCA... | CAATGGGCTAGTCACACAGTGACACAGGTAGATTTTTAAAATAATACTAAGTGAGAAAAGTAAGGAACAAAATGAAATTTTTAACCCTATATATTTTTATAGTTCAAAAGTATATCCACAAAAGAATGAGTAATATTTTATAAGGGCACATGCAAACAAAAGGAGAAACATTAAATACATTATAGTTATTGCCCATGGTGGTGGAAGGAAATGAAAATAGGAGATGGAGATAAAAGAGAAAAAACACATTTTAAAAGCTCAAATTATTGAAAAGTCATCATTCCCACTACCACTCATGATTCCATTAGGTATTTTATTCA... |
Task1_train_42673 | A genetic alteration is present on Chromosome 13. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CATAAATTGTGGAATATTTTTTGAGAAAAGAGAGTGTAGGTCACTGAGGCCATTTGTTCTTGTAGCTCTCTGGCTGGCGGGGATCCAAGTGTGTATGAAGATGAGTGACAGTGTGTGGCCAGCTTTTTCGCTGCTGGTCTTTCTATCTGCAGAAGCTTTGAGTGCATTTATCAGAAGCCAAACCATGCCAACTCTTTTGATATTAGGTCTTTGGGTGGAGCTTTCAAAATCATTCTTTGTTCCACTTTTCCTAGATTGTCAAACTGCGCCCAGTAGGTGGTTGAGAGTGTGAATTTCAAACATGTGCTTTTAATACGCCC... | CATAAATTGTGGAATATTTTTTGAGAAAAGAGAGTGTAGGTCACTGAGGCCATTTGTTCTTGTAGCTCTCTGGCTGGCGGGGATCCAAGTGTGTATGAAGATGAGTGACAGTGTGTGGCCAGCTTTTTCGCTGCTGGTCTTTCTATCTGCAGAAGCTTTGAGTGCATTTATCAGAAGCCAAACCATGCCAACTCTTTTGATATTAGGTCTTTGGGTGGAGCTTTCAAAATCATTCTTTGTTCCACTTTTCCTAGATTGTCAAACTGCGCCCAGTAGGTGGTTGAGAGTGTGAATTTCAAACATGTGCTTTTAATACGCCC... |
Task1_train_42674 | Chromosome 13 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TCAAATTCAGATTTGCAATGCCATTACAGTCTGGTCTTTTCATCATGTCATGGCCCCATAAAGAGGTAGTGTTTGTGCTAGACCTTGAAGGATGTGGAATTGGCATGTATGAGAAGGAGCACATTCCAAGCACATAGTCTGAGGAAAGGCATAAAGATGCCTGTGATCTAGGAGGAACCAGTGCCTTCAGCCCAGTATCAAGGAACATGAAGTTTGAGCTAATCATCCATTTACAGACAAGAGAATGCAAGAACTTATCCTATCTTGTCTCAATTTCTTACTTACCTTAGTCAACACTACAACACATACTTCCCTTTACC... | TCAAATTCAGATTTGCAATGCCATTACAGTCTGGTCTTTTCATCATGTCATGGCCCCATAAAGAGGTAGTGTTTGTGCTAGACCTTGAAGGATGTGGAATTGGCATGTATGAGAAGGAGCACATTCCAAGCACATAGTCTGAGGAAAGGCATAAAGATGCCTGTGATCTAGGAGGAACCAGTGCCTTCAGCCCAGTATCAAGGAACATGAAGTTTGAGCTAATCATCCATTTACAGACAAGAGAATGCAAGAACTTATCCTATCTTGTCTCAATTTCTTACTTACCTTAGTCAACACTACAACACATACTTCCCTTTACC... |
Task1_train_42675 | A variant found on Chromosome 13 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TTATAATAGACTGGTTAAAGTAGATTCCTGGCTCTCTCACTCTGTGCTGAAGTTTCCTTATCTATAATAAAATAGGGATAATAGTACTTACTTTGTAAGAGTATTGATTAGGTGAATACAATGAAAATATGAAAATGCTTAAAACAGTACCTGGCAGATATAAATTTAAAAAAAAATCATTGACTTCTTAAACTTAAAAAAAAATTATGCAATAAGCACTAGGTAGGAATGTCAGATGTTGTGAAAAGCAATGTATATCCTCTATATTTACCTTAGTGGCTGTAAGGTGCTTTTTAAAAAGAAATGTTCTGGGCAAGTTA... | TTATAATAGACTGGTTAAAGTAGATTCCTGGCTCTCTCACTCTGTGCTGAAGTTTCCTTATCTATAATAAAATAGGGATAATAGTACTTACTTTGTAAGAGTATTGATTAGGTGAATACAATGAAAATATGAAAATGCTTAAAACAGTACCTGGCAGATATAAATTTAAAAAAAAATCATTGACTTCTTAAACTTAAAAAAAAATTATGCAATAAGCACTAGGTAGGAATGTCAGATGTTGTGAAAAGCAATGTATATCCTCTATATTTACCTTAGTGGCTGTAAGGTGCTTTTTAAAAAGAAATGTTCTGGGCAAGTTA... |
Task1_train_42676 | This mutation on Chromosome 13 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GACCAAACGTGGCAATTTACAATTTCAAGGTTATTTTACAAAATGCCTACATTTACACAATAGGCTCCTGGCAGCATTTTCAGACAAATGTTCTTTTAATTTATCCTGACATGCTATAAGTGAATAAATTACACGATTTAAAGAATTAAAAGGAAAATGAGTTTTCCTTTATCTTGCATCAGAGAAAAAGAAAAGAACGTGCAAAAAGATTGAGAGGAAGAGCACGCACACACAGATAATTCAGAGAAGCAGACGGGGGTTAGGGAGGGTCAATGATCACAGAACCTCACAGTGTGCTCTCCAAGGGTAAAAGTCAACTG... | GACCAAACGTGGCAATTTACAATTTCAAGGTTATTTTACAAAATGCCTACATTTACACAATAGGCTCCTGGCAGCATTTTCAGACAAATGTTCTTTTAATTTATCCTGACATGCTATAAGTGAATAAATTACACGATTTAAAGAATTAAAAGGAAAATGAGTTTTCCTTTATCTTGCATCAGAGAAAAAGAAAAGAACGTGCAAAAAGATTGAGAGGAAGAGCACGCACACACAGATAATTCAGAGAAGCAGACGGGGGTTAGGGAGGGTCAATGATCACAGAACCTCACAGTGTGCTCTCCAAGGGTAAAAGTCAACTG... |
Task1_train_42677 | Chromosome 13 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ATTCTTATTTGAAATCAGCCCAGCTATTAGTCAGTGGAAGAAGTAACAATACCAAGTTTTGGCAGGTGCAGTACTAGATATTTTACCACAAGTCATTAGAAAAAGAAAAATGAAAGAATACATTTCCCCTTCATACAAAACGATTATTTTAGAATAAAAACATTGAAAAAAGTTATATAATGAAATAAAATTTACTTGCAAGGGAATATCATGTAACAAATGGCTCGAAGTTGACTATCAAAAAATTGGGGAGATTTTTATTTCCTAGTGAATCAGCAAGGCATTTTTTGGTTGTTGTTTAAAAAAGTATTATTTCCTTA... | ATTCTTATTTGAAATCAGCCCAGCTATTAGTCAGTGGAAGAAGTAACAATACCAAGTTTTGGCAGGTGCAGTACTAGATATTTTACCACAAGTCATTAGAAAAAGAAAAATGAAAGAATACATTTCCCCTTCATACAAAACGATTATTTTAGAATAAAAACATTGAAAAAAGTTATATAATGAAATAAAATTTACTTGCAAGGGAATATCATGTAACAAATGGCTCGAAGTTGACTATCAAAAAATTGGGGAGATTTTTATTTCCTAGTGAATCAGCAAGGCATTTTTTGGTTGTTGTTTAAAAAAGTATTATTTCCTTA... |
Task1_train_42678 | A variant found on Chromosome 13 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ATAACAAACCTGCACGTCCTGCACATGCCTGCACACCCCTGAGCTTAAAAGTTAAAAAGAGAAAAACTCAAGAAACACTAATTTCATTCAATTTCCTTTAATGAGTACTTGTTACAGTAAAAGAGGTATAAAGTCCTGTTCCCAAGTCCAAACCACTTTTTAACTTAAATCTTGAGTTTTTCTGAATTACTCAATTTGAAGTAATTCTCTTTATATCTGAAAAATGGTTTTATTGAAACGTTTGAGATTAAAAAATATGCATTGCAAGAAGCATATGACAAACATTCTGAGAGTACAAAATTAGTTGTAAAAAATAACAT... | ATAACAAACCTGCACGTCCTGCACATGCCTGCACACCCCTGAGCTTAAAAGTTAAAAAGAGAAAAACTCAAGAAACACTAATTTCATTCAATTTCCTTTAATGAGTACTTGTTACAGTAAAAGAGGTATAAAGTCCTGTTCCCAAGTCCAAACCACTTTTTAACTTAAATCTTGAGTTTTTCTGAATTACTCAATTTGAAGTAATTCTCTTTATATCTGAAAAATGGTTTTATTGAAACGTTTGAGATTAAAAAATATGCATTGCAAGAAGCATATGACAAACATTCTGAGAGTACAAAATTAGTTGTAAAAAATAACAT... |
Task1_train_42679 | This alteration on Chromosome 13 may affect genome function. Does it lead to a disease or is it benign? | Benign | ACTGGTAAGCCGCGTCCCGGCACAGCCCGCTGCCTTCGGCAGGGCGTTGCTGTCCCCTGGTCTCGCGGGGGCTGCAGGGGTCCCTGCTGAGGAGGCCATAGTGCTGGCGAACCGCGGACTCCGGGTGCCTTTCGGCCGTGAAGTCTGGCTGGATCCCCTGCATGACCTGGTGTTGCAGGTGCAGCCCGGGGACCGCTGCGCGGTTTCGGTACTAGACAACGACGCACTGGCCCAGCGACCGGGCCGCCTGAGTCCCAAGCGCTTCCCGTGCGACTTTGGCCCTGGCGAGGTGCGCTACTCTCACCTGGGCGCGCGCAGCC... | ACTGGTAAGCCGCGTCCCGGCACAGCCCGCTGCCTTCGGCAGGGCGTTGCTGTCCCCTGGTCTCGCGGGGGCTGCAGGGGTCCCTGCTGAGGAGGCCATAGTGCTGGCGAACCGCGGACTCCGGGTGCCTTTCGGCCGTGAAGTCTGGCTGGATCCCCTGCATGACCTGGTGTTGCAGGTGCAGCCCGGGGACCGCTGCGCGGTTTCGGTACTAGACAACGACGCACTGGCCCAGCGACCGGGCCGCCTGAGTCCCAAGCGCTTCCCGTGCGACTTTGGCCCTGGCGAGGTGCGCTACTCTCACCTGGGCGCGCGCAGCC... |
Task1_train_42680 | This mutation occurs on Chromosome 13. Does this change lead to a known medical condition, or is it benign? | Benign | ACTTGCCTCTGGTCGTGGAAGAGCTGCTGGGGACCAGCAATGCCCTGGACGCGCGGAGCCTGGAGTTCGCCTTCCAGCCCGAGACAGAGGAGTGCCGCGTGGGCATCCTGTCCGGCTTGGGCGCGCTGCCTCGCTATGGAGAACTCCTCCACTACCCGCAGGTCCCTGGAGGAGCCAGAGAGGGAGGCGCCCCGGAGACTCTCCTGATGGACTGCAAAGCTTTCCAGGAACTAGGCGTGCGCTATCGCCACACAGCCGCCAGTCGCTCACCAAACAGGGACTGGATACCCATGGTGGTGGAGCTGCGTTCACGAGGGGCT... | ACTTGCCTCTGGTCGTGGAAGAGCTGCTGGGGACCAGCAATGCCCTGGACGCGCGGAGCCTGGAGTTCGCCTTCCAGCCCGAGACAGAGGAGTGCCGCGTGGGCATCCTGTCCGGCTTGGGCGCGCTGCCTCGCTATGGAGAACTCCTCCACTACCCGCAGGTCCCTGGAGGAGCCAGAGAGGGAGGCGCCCCGGAGACTCTCCTGATGGACTGCAAAGCTTTCCAGGAACTAGGCGTGCGCTATCGCCACACAGCCGCCAGTCGCTCACCAAACAGGGACTGGATACCCATGGTGGTGGAGCTGCGTTCACGAGGGGCT... |
Task1_train_42681 | A sequence alteration has been identified on Chromosome 13. Is it disease-inducing or harmless? | Benign | TCTGCGGCTCCTGAAGATTGCCTACCAGCCCCCTTCTGAAGACTCTGACCAGGAGCGCCTCTTTGAACTGGAATTGGAGGTAGTGGATCTAGAAGGAGCAGCTTCAGACCCTTTTGCCTTCATGGTAGTGGTGAAGCCCATGAACACAATGGCTCCGGTGGTCACCCGGAATACCGGTCTTATTCTCTATGAGGGTCAGTCTCGGCCCCTCACAGGCCCTGCAGGCAGTGGTCCGCAAAACTTGGTCATCAGCGATGAGGATGACCTAGAAGCAGTGCGGCTAGAGGTGGTGGCTGGGCTCCGGCATGGTCACCTTGTCA... | TCTGCGGCTCCTGAAGATTGCCTACCAGCCCCCTTCTGAAGACTCTGACCAGGAGCGCCTCTTTGAACTGGAATTGGAGGTAGTGGATCTAGAAGGAGCAGCTTCAGACCCTTTTGCCTTCATGGTAGTGGTGAAGCCCATGAACACAATGGCTCCGGTGGTCACCCGGAATACCGGTCTTATTCTCTATGAGGGTCAGTCTCGGCCCCTCACAGGCCCTGCAGGCAGTGGTCCGCAAAACTTGGTCATCAGCGATGAGGATGACCTAGAAGCAGTGCGGCTAGAGGTGGTGGCTGGGCTCCGGCATGGTCACCTTGTCA... |
Task1_train_42682 | A mutation has occurred on Chromosome 13. What is the medical relevance of this mutation? | Benign | GAACCTCAGAGAGAATGATTCCTTTCATCAGCATCTTGGCAGTGAATTGTAGTGGATCCAAGAGGTGCTGACAACCAACTCTGTGTGCACAAGGAACCAGAGAGCTGTCAGGAAGTCTACAGCATTCAACAAGATATGCAGCCCTGCAATTCCTGGTTCTGTGCCCTTTTTTCTCTTGCCATTAAATGAATCATGTTTTACCTGCTACTGTAAAAGAAAAATATGATGCAATATTTATGTTAGTTATTGTTCTGAGATCTGTAAGACAGAAATATTTTTAATAAAATCTTTTTCATCTTCACTTTAAGATTAAAATAACA... | GAACCTCAGAGAGAATGATTCCTTTCATCAGCATCTTGGCAGTGAATTGTAGTGGATCCAAGAGGTGCTGACAACCAACTCTGTGTGCACAAGGAACCAGAGAGCTGTCAGGAAGTCTACAGCATTCAACAAGATATGCAGCCCTGCAATTCCTGGTTCTGTGCCCTTTTTTCTCTTGCCATTAAATGAATCATGTTTTACCTGCTACTGTAAAAGAAAAATATGATGCAATATTTATGTTAGTTATTGTTCTGAGATCTGTAAGACAGAAATATTTTTAATAAAATCTTTTTCATCTTCACTTTAAGATTAAAATAACA... |
Task1_train_42683 | A genomic variant on Chromosome 13 is under review. What is the biological outcome — benign or pathogenic? | Benign | TAACAAAATTTTAAATGTCTCTATTTCATATGTAATTTATAAGGATCACATATTTGATTGATATGCTGATTTTTCTAAGCCTGATTTTTATTACCTTTATTAGAGAATTTTCAAACTAAAGTTAGAGGAACTATAGCACAGAAAGCTAAAATAATGAATCCAAAGTCTAACCATGAAACATGGATAAAGTTCAGCAGCTGGTCTTTGATCTATCACCACAGTAGTTATCCAGATACTAATCTTTTGCCTTTTATTAAATGTACTTTTCTGTAGAGTTATGCTGGTCTCTATTTTTTAAAAGAAGAATTATAAACACAATT... | TAACAAAATTTTAAATGTCTCTATTTCATATGTAATTTATAAGGATCACATATTTGATTGATATGCTGATTTTTCTAAGCCTGATTTTTATTACCTTTATTAGAGAATTTTCAAACTAAAGTTAGAGGAACTATAGCACAGAAAGCTAAAATAATGAATCCAAAGTCTAACCATGAAACATGGATAAAGTTCAGCAGCTGGTCTTTGATCTATCACCACAGTAGTTATCCAGATACTAATCTTTTGCCTTTTATTAAATGTACTTTTCTGTAGAGTTATGCTGGTCTCTATTTTTTAAAAGAAGAATTATAAACACAATT... |
Task1_train_42684 | This variant is located on Chromosome 13. Evaluate its biological effect and specify any disease association. | Benign | TGGAAAGAAGAGCGTGTGGTTTAGCAGAGTGCCAAGTTCATTCAAGCCTGCGCTTGCTTCTACCCATGCCACACAGAGATATTCAGAATAGGAAAGAAAGACAAGACAAAACTCTGAGGCACAATAAAGTCTGCTCAGTCACTTAAAATTTTTAAGAAAATGTTCAAATTTCTTCAGGTGAAGGAGATGCATAGAACTGTCATTAAAATATTTAATATTCTCTCAAAAGTCAATAGGTTTTCTACAGATAATGTGCTTTAACGGTCAATCATTAAGCTTGAATTACAGAAGACAAGTTAACATTTAACTGTCATGAATAG... | TGGAAAGAAGAGCGTGTGGTTTAGCAGAGTGCCAAGTTCATTCAAGCCTGCGCTTGCTTCTACCCATGCCACACAGAGATATTCAGAATAGGAAAGAAAGACAAGACAAAACTCTGAGGCACAATAAAGTCTGCTCAGTCACTTAAAATTTTTAAGAAAATGTTCAAATTTCTTCAGGTGAAGGAGATGCATAGAACTGTCATTAAAATATTTAATATTCTCTCAAAAGTCAATAGGTTTTCTACAGATAATGTGCTTTAACGGTCAATCATTAAGCTTGAATTACAGAAGACAAGTTAACATTTAACTGTCATGAATAG... |
Task1_train_42685 | Assess the clinical impact of this variant found on Chromosome 13. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CTAATTCTCTCTATGAGCTTCATAACTCGATTTTTGTCAAACCAGCTCAAAGCTTTTTCATGTCTTTATCTTCCGTAAATATTTCCAAATTAACTCTGACAGCTATTTACTTAAAGAAACGCCCGATTTTTATTTGACAGGCCAATGAATTCATTCTATATATTATATACTCACATTAAAAGTAATGTAGCACTTTCACTGGGCAATAAACAATTAAAATAAAATGAACCATGCCATGATTTCCATTTTTTGGCTTGCAAGTTCATGCTCATAGTTTGTTGCAACTTTTCTATGTCCCTTTAAGGGTGCATTAACTCTCT... | CTAATTCTCTCTATGAGCTTCATAACTCGATTTTTGTCAAACCAGCTCAAAGCTTTTTCATGTCTTTATCTTCCGTAAATATTTCCAAATTAACTCTGACAGCTATTTACTTAAAGAAACGCCCGATTTTTATTTGACAGGCCAATGAATTCATTCTATATATTATATACTCACATTAAAAGTAATGTAGCACTTTCACTGGGCAATAAACAATTAAAATAAAATGAACCATGCCATGATTTCCATTTTTTGGCTTGCAAGTTCATGCTCATAGTTTGTTGCAACTTTTCTATGTCCCTTTAAGGGTGCATTAACTCTCT... |
Task1_train_42686 | A variant on Chromosome 13 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TTCAGGATTATCTGTCTTTTGACAGTTTGATTATGATGTGTGTTACTGTAGGTCTCTTGAGTTTATCTTTCTTGGGGGTCAGTTAGCTTCTTGGATGTTGATTAATGTTTTTTAAAGTCAAAATTGGTAATCTTTCTGTCATTGTTTCTTCACTGCCTTTTTTTCTTTGTTCTTTCCTTCTGGGCTTCCCCTTTATACTTATATTGTTAAATGGTGTCTTATCTCTGATGTTCTGTTCATTTTTTCAATTCTTTTTCTTTCTATTTCTCAGACTCAATAATCTTTAAGTTCCTGTCTTTAAGTTCGCTGATTATTTATTC... | TTCAGGATTATCTGTCTTTTGACAGTTTGATTATGATGTGTGTTACTGTAGGTCTCTTGAGTTTATCTTTCTTGGGGGTCAGTTAGCTTCTTGGATGTTGATTAATGTTTTTTAAAGTCAAAATTGGTAATCTTTCTGTCATTGTTTCTTCACTGCCTTTTTTTCTTTGTTCTTTCCTTCTGGGCTTCCCCTTTATACTTATATTGTTAAATGGTGTCTTATCTCTGATGTTCTGTTCATTTTTTCAATTCTTTTTCTTTCTATTTCTCAGACTCAATAATCTTTAAGTTCCTGTCTTTAAGTTCGCTGATTATTTATTC... |
Task1_train_42687 | A variant on Chromosome 13 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AACTCTACTAGAGGGCTAGGTTTTGCCCTGCCTTTTTACAGGCCTACTGAAAACAAGGTCAGTAGACTGAAAGGGCCAGCAGAAAACACAATGACTCAAGGGTTACAGTTATCCATCTTCCATTTATCAGCTGTCATGCCATAGAGACCTTGGATCTCCCCAACAAAATCCAGGCTTCCCCACCTCTCCTACAGGGTTCTAGAAAGCTCAAATGGACAGAGCACAGCAGGCAGACAGTATATCACAGACACAGCTACGAAGATAAAGTGCCATGTATGATGGCAAAAATGTTACAGGGTCTCCATGAAATTATCAGGATG... | AACTCTACTAGAGGGCTAGGTTTTGCCCTGCCTTTTTACAGGCCTACTGAAAACAAGGTCAGTAGACTGAAAGGGCCAGCAGAAAACACAATGACTCAAGGGTTACAGTTATCCATCTTCCATTTATCAGCTGTCATGCCATAGAGACCTTGGATCTCCCCAACAAAATCCAGGCTTCCCCACCTCTCCTACAGGGTTCTAGAAAGCTCAAATGGACAGAGCACAGCAGGCAGACAGTATATCACAGACACAGCTACGAAGATAAAGTGCCATGTATGATGGCAAAAATGTTACAGGGTCTCCATGAAATTATCAGGATG... |
Task1_train_42688 | A mutation is present on Chromosome 13. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GGATTACAGGCATGAGCCACTGTGCCCGGCCTAATACTGGGTTTTTAAATCAGGTTTTTAACCATGAGGATTTGGAACACCCAAGTTTCTTCAAATAATGAAATCCAAACATGTTTTCAGAGTAAACCAAATCTTTCCTTAATATCAGATATTATTTTACAGAGAGGATACTGATACCCAGGAGCTTAAATAATTTCCTCAAAGGCAAATGGCTAAAATGGACAGGGCTGCTACTCAGGTTTGTACGACTAAAAAGGCGTTGGTCTTTTTACGTTACCCTGATACCTTCCAGAACACAGAAACCATACTTTAAGCAATAT... | GGATTACAGGCATGAGCCACTGTGCCCGGCCTAATACTGGGTTTTTAAATCAGGTTTTTAACCATGAGGATTTGGAACACCCAAGTTTCTTCAAATAATGAAATCCAAACATGTTTTCAGAGTAAACCAAATCTTTCCTTAATATCAGATATTATTTTACAGAGAGGATACTGATACCCAGGAGCTTAAATAATTTCCTCAAAGGCAAATGGCTAAAATGGACAGGGCTGCTACTCAGGTTTGTACGACTAAAAAGGCGTTGGTCTTTTTACGTTACCCTGATACCTTCCAGAACACAGAAACCATACTTTAAGCAATAT... |
Task1_train_42689 | A genetic alteration is present on Chromosome 13. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TAGCAGTGCTGCAGGAAGGGCTGGCTGATGGGGAATACCTGACAGTGTCTTCTGAAGCTCTCAGAAGGAAAATAGTTTTTAAATGTCTGTGGCCTTTATTACCTTGGGACTTGATCCTTCATCTGTCCAAGCCAAGTCTCCTTCTTGCTGAGAACAAAGTGAGGAGAGAGGGATTCACTAAGTTGCACTGAGTATGTGATTTCTTGGCCTGTTCTTAGCAGGGATAAACCTGCCCTGGTTGCCCTCAATCATGAAGGGGAGTCAGACAAAGAGTGTCCTGTGTTCTGGCTGCTACAGGAGCAGGGCTGCTTAGAAGAAAT... | TAGCAGTGCTGCAGGAAGGGCTGGCTGATGGGGAATACCTGACAGTGTCTTCTGAAGCTCTCAGAAGGAAAATAGTTTTTAAATGTCTGTGGCCTTTATTACCTTGGGACTTGATCCTTCATCTGTCCAAGCCAAGTCTCCTTCTTGCTGAGAACAAAGTGAGGAGAGAGGGATTCACTAAGTTGCACTGAGTATGTGATTTCTTGGCCTGTTCTTAGCAGGGATAAACCTGCCCTGGTTGCCCTCAATCATGAAGGGGAGTCAGACAAAGAGTGTCCTGTGTTCTGGCTGCTACAGGAGCAGGGCTGCTTAGAAGAAAT... |
Task1_train_42690 | Consider this mutation on Chromosome 13. Is this a benign change or a disease-causing variant? | Benign | CCTCAAACAATCTTCCTGCCTCGGCCTCCTAAAGTGCTGGGATTACAGGCATGAATCTCCGTGCCTGGCCAAGAAATAACTCATAATTTCCATTTTGTGCCTTCAATGTTTTTCTTACATAAGTTTTAACTGCAGCAGGAAAGAACTATGTAGAATAAAAGTGATATCTAGATTTCACACCAAGACTTGACTATGCGCCCTAAACAAAGTAACCCACCTACCTTTTTTCCTCTTAGGCTGTTCTGGTGATGAGGCTCCCGGTGAGTCTGCATATTTTTCTTGCACCTGCTGTGTTTCCATCACTTCAGGAATCCCATCTA... | CCTCAAACAATCTTCCTGCCTCGGCCTCCTAAAGTGCTGGGATTACAGGCATGAATCTCCGTGCCTGGCCAAGAAATAACTCATAATTTCCATTTTGTGCCTTCAATGTTTTTCTTACATAAGTTTTAACTGCAGCAGGAAAGAACTATGTAGAATAAAAGTGATATCTAGATTTCACACCAAGACTTGACTATGCGCCCTAAACAAAGTAACCCACCTACCTTTTTTCCTCTTAGGCTGTTCTGGTGATGAGGCTCCCGGTGAGTCTGCATATTTTTCTTGCACCTGCTGTGTTTCCATCACTTCAGGAATCCCATCTA... |
Task1_train_42691 | This mutation is located on Chromosome 13. Is it associated with a disease or is it a benign polymorphism? | Benign | TTGTAGTAGAAACAGGATTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGGGCCACTGTGCCCAGCCTATTACATGTTTTAAGGTCATAAAACTGCTACTTCTGGAATATTTCTTAAACTTGCTTGATTTGTGTAAGGTCTGGCTGCTGGGCTCCCTGAAACCTTGCACATATCTTACTGTATGACTGTATTTCGTTTTGAGTCTCTGGATTCTGGGGTTTGGACAGATGACCATAGTGAGGCCTGCAGAAATATGCATGTCC... | TTGTAGTAGAAACAGGATTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGGGCCACTGTGCCCAGCCTATTACATGTTTTAAGGTCATAAAACTGCTACTTCTGGAATATTTCTTAAACTTGCTTGATTTGTGTAAGGTCTGGCTGCTGGGCTCCCTGAAACCTTGCACATATCTTACTGTATGACTGTATTTCGTTTTGAGTCTCTGGATTCTGGGGTTTGGACAGATGACCATAGTGAGGCCTGCAGAAATATGCATGTCC... |
Task1_train_42692 | A variant on Chromosome 13 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATTTTTGCAAATCATATATCTGATCATGGACTTTTACCTAGAAGATAAAGACCACTCACAACTCAATAATGAAAAGACAATTAAATTTAAAAACTGGCAAAGGATCTGAACAGTGATTTCTCCCAAGATGATACACAAATGGCCAAATAAGCACCAGAAAAGATGCTCAACATCATTAATCTTCAGGAAAATGCAAATCAAAACCACAATAACACACCACTTCACATTCATAGGATGGCAATAATTGAAAGGGCGGATAATAAGTGTTGGCAAGTACGTGGAGAAATATGAACCCTCATACACTGTGTGTAGAGCTGTAA... | ATTTTTGCAAATCATATATCTGATCATGGACTTTTACCTAGAAGATAAAGACCACTCACAACTCAATAATGAAAAGACAATTAAATTTAAAAACTGGCAAAGGATCTGAACAGTGATTTCTCCCAAGATGATACACAAATGGCCAAATAAGCACCAGAAAAGATGCTCAACATCATTAATCTTCAGGAAAATGCAAATCAAAACCACAATAACACACCACTTCACATTCATAGGATGGCAATAATTGAAAGGGCGGATAATAAGTGTTGGCAAGTACGTGGAGAAATATGAACCCTCATACACTGTGTGTAGAGCTGTAA... |
Task1_train_42693 | Here’s a variant located on Chromosome 13. What is the predicted biological effect — harmless or disease-causing? | Benign | TAGAGTTTATGTTTACAGCAGTCTTGGAGTTGGGAGTGAACAGTTATGAGTTTATATGTTAAGAGTGTGATACTTCAATGTGTAGTTAAATGTTGATTTTAATATTTGAAGTTATCTATATAAATATAAAACTGCTTTTCTTAAGTTGATCTCATAGAGGTAGAAAGAATGATAGATATCAGAGCTGGCAAGGGGAGTGTGGGGGAGAGATGAAGAGAGGTTGGTTAATGGGTACAAACATACAGTTAGATAGAAGGAATAAGTTTCAGTGTTTGCAGAGTAAGGGGACTGTAGTTAACAACAATATACTGTATATTTCA... | TAGAGTTTATGTTTACAGCAGTCTTGGAGTTGGGAGTGAACAGTTATGAGTTTATATGTTAAGAGTGTGATACTTCAATGTGTAGTTAAATGTTGATTTTAATATTTGAAGTTATCTATATAAATATAAAACTGCTTTTCTTAAGTTGATCTCATAGAGGTAGAAAGAATGATAGATATCAGAGCTGGCAAGGGGAGTGTGGGGGAGAGATGAAGAGAGGTTGGTTAATGGGTACAAACATACAGTTAGATAGAAGGAATAAGTTTCAGTGTTTGCAGAGTAAGGGGACTGTAGTTAACAACAATATACTGTATATTTCA... |
Task1_train_42694 | Here is a genetic alteration on Chromosome 13. Based on the data, is it a benign variant or a cause of disease? | Benign | CTCAAAACAAAACAAAACAAAACAAAACATAGGTTTCACCCTAGAGATGCATAAACGTCCGCCCTTTTAAAAGCCACCTCTGGTTGCAGTTTTAGCAACTACCAGTAGATGGCGCAAGTTCCTGAAAAAAAATTATTTGCCTTTATAAGTTTAACAACTTGAGTACTAAATTTCTAAGTTTGTAAAAAAGGTTTTTAAGTTACAGATATTCTAGGTGAGATTGGTGGAGAGGTTATGGTGGATTAAAAATGTCTGTTAACTTTAATTTTGCTTAAAAAAAAGTCTTTGCAATTTTTTTTTTTATCAGTGGTTCTCAAACT... | CTCAAAACAAAACAAAACAAAACAAAACATAGGTTTCACCCTAGAGATGCATAAACGTCCGCCCTTTTAAAAGCCACCTCTGGTTGCAGTTTTAGCAACTACCAGTAGATGGCGCAAGTTCCTGAAAAAAAATTATTTGCCTTTATAAGTTTAACAACTTGAGTACTAAATTTCTAAGTTTGTAAAAAAGGTTTTTAAGTTACAGATATTCTAGGTGAGATTGGTGGAGAGGTTATGGTGGATTAAAAATGTCTGTTAACTTTAATTTTGCTTAAAAAAAAGTCTTTGCAATTTTTTTTTTTATCAGTGGTTCTCAAACT... |
Task1_train_42695 | A genomic variant on Chromosome 13 is under review. What is the biological outcome — benign or pathogenic? | Benign | AACTCACAGAAAATGTCAAAAATAGACTACAAATATCCATATATCATTCACCTAGATATTGCTAACTGTTAAGATTTTACCACATTTGTGTTCTCACTCTGAGAAAGAGAGAGAAAATGTCTGTTTATACACACACACATACATGTCTTTTTTTCTGAAATATTTGGAAGTTGTAGACTTTTTTTTACTTTATCCCTTAAGTATCTCAACATGCATCTCATAAGAATAGGAATATTCTCCTTCATAACCACAATATCATTATCATACTTAAGGAAATTAGTAATTCAATAATATCATATAACATAGTCCATATTTAAACT... | AACTCACAGAAAATGTCAAAAATAGACTACAAATATCCATATATCATTCACCTAGATATTGCTAACTGTTAAGATTTTACCACATTTGTGTTCTCACTCTGAGAAAGAGAGAGAAAATGTCTGTTTATACACACACACATACATGTCTTTTTTTCTGAAATATTTGGAAGTTGTAGACTTTTTTTTACTTTATCCCTTAAGTATCTCAACATGCATCTCATAAGAATAGGAATATTCTCCTTCATAACCACAATATCATTATCATACTTAAGGAAATTAGTAATTCAATAATATCATATAACATAGTCCATATTTAAACT... |
Task1_train_42696 | Located on Chromosome 13, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TATATATATATATATGTGTGTGTGTGTGCGCGTGTGTGTGTGTATATGTGTGTGTGTGTGTGTAAAACATGCATGTTTTTCTCAAAATATCAGTAACTTAAAGTATATAACTGCCACTTAAAAGCCTCCAACTAATAGCTTGCTCAATTTAATTCTTTACTGTTTTTGATATTTCAATAGAGCAGCAACTATTTTTTCATTTAATAGATCTGATGATCATTATTACAAATCTTCCAAATCAATTATTTCCCTAAAATTAAAGTCCCACATTATCAGATGTATTCATAAAAATCATGTCATCTTAATGCTATTTATAACTT... | TATATATATATATATGTGTGTGTGTGTGCGCGTGTGTGTGTGTATATGTGTGTGTGTGTGTGTAAAACATGCATGTTTTTCTCAAAATATCAGTAACTTAAAGTATATAACTGCCACTTAAAAGCCTCCAACTAATAGCTTGCTCAATTTAATTCTTTACTGTTTTTGATATTTCAATAGAGCAGCAACTATTTTTTCATTTAATAGATCTGATGATCATTATTACAAATCTTCCAAATCAATTATTTCCCTAAAATTAAAGTCCCACATTATCAGATGTATTCATAAAAATCATGTCATCTTAATGCTATTTATAACTT... |
Task1_train_42697 | This mutation is located on Chromosome 13. Is it associated with a disease or is it a benign polymorphism? | Benign | AACATTTTATTACACACCTGTATTGCCTAAAGTTTCTATAACAAACATCTTACATTGGAACGATTTTCTTGTTTTTATTTTCTACAAAAAAAAAAGCGGGGGGACATTAAAATTAAGCATAGAAATGGTGGAACTTTGGGATTTCCTGTCCAGTCACCTGCGAGTCAGGTTTTATTCCAATTGATTCAACGTGGCAGATTAAATGTGAAAAGTAAAATGGTGGGCTCCTTTAGGCAGCAAGTCTTGCTTCTCTCCTGGTTACCTCTGCCTACATAGATATTTGGTTAAGCAAGATGTTTATACCCCCACACATATTCTAG... | AACATTTTATTACACACCTGTATTGCCTAAAGTTTCTATAACAAACATCTTACATTGGAACGATTTTCTTGTTTTTATTTTCTACAAAAAAAAAAGCGGGGGGACATTAAAATTAAGCATAGAAATGGTGGAACTTTGGGATTTCCTGTCCAGTCACCTGCGAGTCAGGTTTTATTCCAATTGATTCAACGTGGCAGATTAAATGTGAAAAGTAAAATGGTGGGCTCCTTTAGGCAGCAAGTCTTGCTTCTCTCCTGGTTACCTCTGCCTACATAGATATTTGGTTAAGCAAGATGTTTATACCCCCACACATATTCTAG... |
Task1_train_42698 | Here is a genetic alteration on Chromosome 13. Based on the data, is it a benign variant or a cause of disease? | Benign | GCTGATTGGTCAGGTCAAAGATGAAATCACAGGGAGTCCAAGTTGTCTTGCGTTATCAGTTCCTGGGTGGGGGCCACGAGATCAGATGAGCCAGTTTATCGATCTGGGTGATGCCAGCTGATTCATCAAGTGCGGGGTCTGCAAAATATCTCAAGCACTGGTGGTAGTTTTTACAATAGTGATGTTAGCTCCAGCAGCAATTTGGGGAGGGTCAGAATCTTGTAGCCTCCAGCTGCATGACTCCTAAGTCATAATTTCTGATCTTGTGGCTAATTTGTTAGTCCTACAAAGGCAGTCTAGTCCCCAGGCAAGAAGGAGGT... | GCTGATTGGTCAGGTCAAAGATGAAATCACAGGGAGTCCAAGTTGTCTTGCGTTATCAGTTCCTGGGTGGGGGCCACGAGATCAGATGAGCCAGTTTATCGATCTGGGTGATGCCAGCTGATTCATCAAGTGCGGGGTCTGCAAAATATCTCAAGCACTGGTGGTAGTTTTTACAATAGTGATGTTAGCTCCAGCAGCAATTTGGGGAGGGTCAGAATCTTGTAGCCTCCAGCTGCATGACTCCTAAGTCATAATTTCTGATCTTGTGGCTAATTTGTTAGTCCTACAAAGGCAGTCTAGTCCCCAGGCAAGAAGGAGGT... |
Task1_train_42699 | A mutation on Chromosome 13 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AAGCCACCCCAAATAAATAAATTTGCTTTACAAAAATTTGATGATGAGACAAATAATCTAGCCCTCCTTTGCAATGAGATTTATGACACTGAAAATCTTCTATTTAGAAATTCTGAAATTTCAAATCATTGGCACCTTCATAGAAGAGTAAAATTTAAAACAATCAATCTTACTTCTTGGTTAAACAGTATTTTCTGTGAGCTATATGCTATTAGATATAACAAAGCCAGATGAGACACAATATACCTTTTGAAGAGCAACAATCTCATAGGGAGTGTAAAACAAACACAAAGCAGAATGCCATAAGAACATATGGAGGT... | AAGCCACCCCAAATAAATAAATTTGCTTTACAAAAATTTGATGATGAGACAAATAATCTAGCCCTCCTTTGCAATGAGATTTATGACACTGAAAATCTTCTATTTAGAAATTCTGAAATTTCAAATCATTGGCACCTTCATAGAAGAGTAAAATTTAAAACAATCAATCTTACTTCTTGGTTAAACAGTATTTTCTGTGAGCTATATGCTATTAGATATAACAAAGCCAGATGAGACACAATATACCTTTTGAAGAGCAACAATCTCATAGGGAGTGTAAAACAAACACAAAGCAGAATGCCATAAGAACATATGGAGGT... |
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