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_40100 | This variant lies on Chromosome 10. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACCCGCCGCCACGCCCAGCTCATTTTTTTTTTGTATTTTTAGTAAAGATGGGGTTTCACCGTGTTAGGCAGGATGGTCTCGATCTCCTGACCTCCTGATCTGCCTGCCTCAGCCTTCCAAAGTGCTGGGATTACAGGTGTGAACCACCGCGCCTGGCCTAATTATTTTTAAATTTTTGTCATTTTCTATTTTTGTTATTTTATTTTATTTATTTTATTTTATTATTATTTTTCTGAGATGGAGTCTCGCTGTGTCACCCAGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTCCGTCTCCTGGGTTCAAGAG... | ACCCGCCGCCACGCCCAGCTCATTTTTTTTTTGTATTTTTAGTAAAGATGGGGTTTCACCGTGTTAGGCAGGATGGTCTCGATCTCCTGACCTCCTGATCTGCCTGCCTCAGCCTTCCAAAGTGCTGGGATTACAGGTGTGAACCACCGCGCCTGGCCTAATTATTTTTAAATTTTTGTCATTTTCTATTTTTGTTATTTTATTTTATTTATTTTATTTTATTATTATTTTTCTGAGATGGAGTCTCGCTGTGTCACCCAGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTCCGTCTCCTGGGTTCAAGAG... |
Task1_train_40101 | A mutation on Chromosome 10 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TCCTGATCTGCCTGCCTCAGCCTTCCAAAGTGCTGGGATTACAGGTGTGAACCACCGCGCCTGGCCTAATTATTTTTAAATTTTTGTCATTTTCTATTTTTGTTATTTTATTTTATTTATTTTATTTTATTATTATTTTTCTGAGATGGAGTCTCGCTGTGTCACCCAGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTCCGTCTCCTGGGTTCAAGAGATTCTCCTGCCTTAGCCTCCTGAGTAGCTGGGATTACAGGCGCCTGCCACCACGTCTGGCTAATTTTTGTATTTTAGTAGAGACAGGGTTTT... | TCCTGATCTGCCTGCCTCAGCCTTCCAAAGTGCTGGGATTACAGGTGTGAACCACCGCGCCTGGCCTAATTATTTTTAAATTTTTGTCATTTTCTATTTTTGTTATTTTATTTTATTTATTTTATTTTATTATTATTTTTCTGAGATGGAGTCTCGCTGTGTCACCCAGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTCCGTCTCCTGGGTTCAAGAGATTCTCCTGCCTTAGCCTCCTGAGTAGCTGGGATTACAGGCGCCTGCCACCACGTCTGGCTAATTTTTGTATTTTAGTAGAGACAGGGTTTT... |
Task1_train_40102 | Given a variant located on Chromosome 10, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCTACAAGGAACACCCATTAACTTTACATTTTTCTCACCAACTTCCTTTCCTTCAATTGGAACTTTAATTTCTGTCTTCTTTTCTACTGAAATAGTTTTCTTTCTTTCCTTTTTTTTTTTTTTTTTTGTTTTTGTTTTGTTTTCTTAGAGACAGGGTCTCACCCTCACCTACGCAGGAGTGCAATGGTGCAGTCATAGCTCATTTCAGCCTCTAACTCCTGGGCTCAAGTAATCCTCGCACCTTAGCCCCCTAGCAGCTACGACAGGCACACCACCATCCTGGCTAATTTTTAAAATTTTTATCTTTGTAGAGATTGGAT... | TCTACAAGGAACACCCATTAACTTTACATTTTTCTCACCAACTTCCTTTCCTTCAATTGGAACTTTAATTTCTGTCTTCTTTTCTACTGAAATAGTTTTCTTTCTTTCCTTTTTTTTTTTTTTTTTTGTTTTTGTTTTGTTTTCTTAGAGACAGGGTCTCACCCTCACCTACGCAGGAGTGCAATGGTGCAGTCATAGCTCATTTCAGCCTCTAACTCCTGGGCTCAAGTAATCCTCGCACCTTAGCCCCCTAGCAGCTACGACAGGCACACCACCATCCTGGCTAATTTTTAAAATTTTTATCTTTGTAGAGATTGGAT... |
Task1_train_40103 | A variant was discovered on Chromosome 10. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CCCTGCTAATTTTTGTATTTCTAGTAGAGGAATGATTTCACCATGTTGCCCAGCCTGGTCTTGAACTCCTGAGTTAAAGCGATCTGCCTGTCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCTGGCCTATTCCTATTATTTAAGTTATAAATATTATTTATGCTTCTTTGGCTTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTGGTTTGTTGCCCAGGCTGGAGTACAGTGGCACAATCATAGCTCACTGCAGCCTTGAACTCCTGAGCTCAAATGATCCTTCCACACCTGGCTAATGTT... | CCCTGCTAATTTTTGTATTTCTAGTAGAGGAATGATTTCACCATGTTGCCCAGCCTGGTCTTGAACTCCTGAGTTAAAGCGATCTGCCTGTCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCTGGCCTATTCCTATTATTTAAGTTATAAATATTATTTATGCTTCTTTGGCTTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTGGTTTGTTGCCCAGGCTGGAGTACAGTGGCACAATCATAGCTCACTGCAGCCTTGAACTCCTGAGCTCAAATGATCCTTCCACACCTGGCTAATGTT... |
Task1_train_40104 | With a mutation on Chromosome 10, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTGTAATCCCAGCACTTTGGGAGACTGAGGCGGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCCCTACTAAAAATACAAAAATTAGCTGGATATGATTGTGGGCACCTGTCATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGTGCCACTGCATCCCAGCCAGGGCAACAGAGCGAGACTTCATCTCAAAAAAAAAAAAAAAAAAGTACTTTTCTTCATTTGGTTAGTATTCTCTTATGAGTTGATG... | CTGTAATCCCAGCACTTTGGGAGACTGAGGCGGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCCCTACTAAAAATACAAAAATTAGCTGGATATGATTGTGGGCACCTGTCATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGTGCCACTGCATCCCAGCCAGGGCAACAGAGCGAGACTTCATCTCAAAAAAAAAAAAAAAAAAGTACTTTTCTTCATTTGGTTAGTATTCTCTTATGAGTTGATG... |
Task1_train_40105 | Chromosome 10 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGAACATTTTTTTTCTGGAGACAAATTCTTGCTCTGTTGCCCGGGCTAGAGCGCAGTGGTGCGATCTTGGCTCACTGCAACCTCTGCCTTCTGGGTCCAGGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCATGCACCACCATGCCCGACTAATTTTTGTATTAAAGACGGGGCTTCACCATGTTGGCCAGGCTTGTCCCGAACTGCTGACCTCAAGTGATCTGCCTGCCTTGGTCTCTGAAAGTGCTGGGATTACAAGTGTGAGCCAGCGCGCCCAGCCAGATATGTTTTTTAAAGATCATTCAGA... | TGAACATTTTTTTTCTGGAGACAAATTCTTGCTCTGTTGCCCGGGCTAGAGCGCAGTGGTGCGATCTTGGCTCACTGCAACCTCTGCCTTCTGGGTCCAGGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCATGCACCACCATGCCCGACTAATTTTTGTATTAAAGACGGGGCTTCACCATGTTGGCCAGGCTTGTCCCGAACTGCTGACCTCAAGTGATCTGCCTGCCTTGGTCTCTGAAAGTGCTGGGATTACAAGTGTGAGCCAGCGCGCCCAGCCAGATATGTTTTTTAAAGATCATTCAGA... |
Task1_train_40106 | This alteration occurs on Chromosome 10. Is it associated with a disease or is it a benign variant? | Benign | AAGGCCACTGACTGTGAAGGGGAGGACGTGGTGGACATGCTCAGGGAAGCCATCAAGAGGAGAAACGTAGGATGTGGTGTTGAGGCTCATGCCTGCTCTTGCTGCCTTCCCCAGGCCCCTCTGCTCTGCCATCCTCTGCCCAGTTCCTATGACTCTGGCCTCTGTCTGCCTTGGGATAACATGCCCCTCCTAAACCTGTTTGGCTTGCACATTCAACTCATAGTAAAGCTGGGTTTTTTTTGTTTTTGTTTTTGTTTTTAGGAGTTTGACCTGGACATTGTTGCAGTCGTGAATGATACAGTGGGGACCATGATGACCTG... | AAGGCCACTGACTGTGAAGGGGAGGACGTGGTGGACATGCTCAGGGAAGCCATCAAGAGGAGAAACGTAGGATGTGGTGTTGAGGCTCATGCCTGCTCTTGCTGCCTTCCCCAGGCCCCTCTGCTCTGCCATCCTCTGCCCAGTTCCTATGACTCTGGCCTCTGTCTGCCTTGGGATAACATGCCCCTCCTAAACCTGTTTGGCTTGCACATTCAACTCATAGTAAAGCTGGGTTTTTTTTGTTTTTGTTTTTGTTTTTAGGAGTTTGACCTGGACATTGTTGCAGTCGTGAATGATACAGTGGGGACCATGATGACCTG... |
Task1_train_40107 | Chromosome 10 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCACTGACTGTGAAGGGGAGGACGTGGTGGACATGCTCAGGGAAGCCATCAAGAGGAGAAACGTAGGATGTGGTGTTGAGGCTCATGCCTGCTCTTGCTGCCTTCCCCAGGCCCCTCTGCTCTGCCATCCTCTGCCCAGTTCCTATGACTCTGGCCTCTGTCTGCCTTGGGATAACATGCCCCTCCTAAACCTGTTTGGCTTGCACATTCAACTCATAGTAAAGCTGGGTTTTTTTTGTTTTTGTTTTTGTTTTTAGGAGTTTGACCTGGACATTGTTGCAGTCGTGAATGATACAGTGGGGACCATGATGACCTGTGGC... | CCACTGACTGTGAAGGGGAGGACGTGGTGGACATGCTCAGGGAAGCCATCAAGAGGAGAAACGTAGGATGTGGTGTTGAGGCTCATGCCTGCTCTTGCTGCCTTCCCCAGGCCCCTCTGCTCTGCCATCCTCTGCCCAGTTCCTATGACTCTGGCCTCTGTCTGCCTTGGGATAACATGCCCCTCCTAAACCTGTTTGGCTTGCACATTCAACTCATAGTAAAGCTGGGTTTTTTTTGTTTTTGTTTTTGTTTTTAGGAGTTTGACCTGGACATTGTTGCAGTCGTGAATGATACAGTGGGGACCATGATGACCTGTGGC... |
Task1_train_40108 | Consider a variant on Chromosome 10. Determine its clinical classification and disease relevance. | Benign | GGCTACACCGCCATTTACCTGCTGAATCCCCTGTATGGTCATATAGGTTGTTTCTCAATTGTCTTTCTTGATAACACTCTTCTTCTCTAAGTATTACCTGAGACAGTCAAGGATACAACTTCACATTGCTTGGTGTGGGAGTCAGGGCTCCGTTTAAGTACCATTAGTTCACTGTGAGATGACCAGGGTCTAGACTTGAAGCCAGCCTGCCCCTATGATGGGTGTTTCTCTGCATGTGTTTACAGTCCTATCAGGTTCCCCTTCTCTAAGGTTCTGATTGTATTTTGTATATTCATTTATTCACTTGCTCATTGAATATA... | GGCTACACCGCCATTTACCTGCTGAATCCCCTGTATGGTCATATAGGTTGTTTCTCAATTGTCTTTCTTGATAACACTCTTCTTCTCTAAGTATTACCTGAGACAGTCAAGGATACAACTTCACATTGCTTGGTGTGGGAGTCAGGGCTCCGTTTAAGTACCATTAGTTCACTGTGAGATGACCAGGGTCTAGACTTGAAGCCAGCCTGCCCCTATGATGGGTGTTTCTCTGCATGTGTTTACAGTCCTATCAGGTTCCCCTTCTCTAAGGTTCTGATTGTATTTTGTATATTCATTTATTCACTTGCTCATTGAATATA... |
Task1_train_40109 | A mutation located on Chromosome 10 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TAATTCCTGATTAGTATCTGAAAGTGGACAATACAAGCTCAAGGAGTTGCTTCCACCTCGAGGCAAGAGGTGAGGGTCTTGGGCACGCCTGGGGTGGTTATCTTTCCCTCAGTCCTACAAGAGTAGCTTACAATGCCCTCTTCAGCTTCTTTGAGAAGGGCTTTGCAAAGTCCAGCTCAGGTGCATCCCTCCTGCCTCCCAGGGTTTTTCGTTTGTTTGTTTGTTGTTGTTGTTTTTGAAACAGAATTTCACTCTTATTGCCCAGGCTGGAATGCTATGGTGCAATCTTGGCTCACTACAACCTCTGCCTCCCAGGTTCA... | TAATTCCTGATTAGTATCTGAAAGTGGACAATACAAGCTCAAGGAGTTGCTTCCACCTCGAGGCAAGAGGTGAGGGTCTTGGGCACGCCTGGGGTGGTTATCTTTCCCTCAGTCCTACAAGAGTAGCTTACAATGCCCTCTTCAGCTTCTTTGAGAAGGGCTTTGCAAAGTCCAGCTCAGGTGCATCCCTCCTGCCTCCCAGGGTTTTTCGTTTGTTTGTTTGTTGTTGTTGTTTTTGAAACAGAATTTCACTCTTATTGCCCAGGCTGGAATGCTATGGTGCAATCTTGGCTCACTACAACCTCTGCCTCCCAGGTTCA... |
Task1_train_40110 | A change on Chromosome 10 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GGCTATTTAAATTCTGGCTTTACATATGATATTGTTAATGATGAACTAATCACTATGTGTACAGAGTGCCTTGAGAGAATTAGCTAATGACACTACTAGGCCACCAAATTTTAAAATAGTTCATCTTTATCTCTTTATTTATTTATTTTTTGGAAACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCATTGCAACCTCTCCCTCCTGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCCAAGTACCTGGGATTACAGGCGTGCGCCACCATGCCCGACCTATGTTTTTATTTTTTTTAAA... | GGCTATTTAAATTCTGGCTTTACATATGATATTGTTAATGATGAACTAATCACTATGTGTACAGAGTGCCTTGAGAGAATTAGCTAATGACACTACTAGGCCACCAAATTTTAAAATAGTTCATCTTTATCTCTTTATTTATTTATTTTTTGGAAACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCATTGCAACCTCTCCCTCCTGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCCAAGTACCTGGGATTACAGGCGTGCGCCACCATGCCCGACCTATGTTTTTATTTTTTTTAAA... |
Task1_train_40111 | A sequence alteration has been identified on Chromosome 10. Is it disease-inducing or harmless? | Benign | TGATTGCCCTTCTTTGAGCTGCTTTATTGTAAAGGGAAAAAGGTGGTAGGGCTAGTGGTTAGGAGTGGGGGCAAGGATCATCCTTGGGCGCAGAGAGTGTTGGCAGACATTTTGGGAGGCCTAGGTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCAGGGCGTGGTGGCGCACGCCTGTAATCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGATTCTGCCACTGC... | TGATTGCCCTTCTTTGAGCTGCTTTATTGTAAAGGGAAAAAGGTGGTAGGGCTAGTGGTTAGGAGTGGGGGCAAGGATCATCCTTGGGCGCAGAGAGTGTTGGCAGACATTTTGGGAGGCCTAGGTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCAGGGCGTGGTGGCGCACGCCTGTAATCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGATTCTGCCACTGC... |
Task1_train_40112 | A variant was discovered on Chromosome 10. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TTCCTGCGAGACCGATTGCCAGACCACCTGGTTTGGTGAGATCAGAGTCCCTTTATTAGGGGCATGGTGCTGGTGTCTACGGAGCAGTGATTTTTTGGAGAACACAGATAACATTACACCTTCCAGTGTGCATTGACAATGTTACATGGCTCTTCTGCAGGGGAACCAGGGCGTGGAGGCTGAGTTGGCAAGCAGGAGGTGTGCCCCTGGGATGGGCTGGGCCAGACCGGGAGCTTTCTGGGAGTTGGGACAGTTGCTGCTTTCTGCCCTCTAGCTTCTTGCTGCAGAAGTGGGAGTGGGAGCTGTGCTGCTGCTTTGTA... | TTCCTGCGAGACCGATTGCCAGACCACCTGGTTTGGTGAGATCAGAGTCCCTTTATTAGGGGCATGGTGCTGGTGTCTACGGAGCAGTGATTTTTTGGAGAACACAGATAACATTACACCTTCCAGTGTGCATTGACAATGTTACATGGCTCTTCTGCAGGGGAACCAGGGCGTGGAGGCTGAGTTGGCAAGCAGGAGGTGTGCCCCTGGGATGGGCTGGGCCAGACCGGGAGCTTTCTGGGAGTTGGGACAGTTGCTGCTTTCTGCCCTCTAGCTTCTTGCTGCAGAAGTGGGAGTGGGAGCTGTGCTGCTGCTTTGTA... |
Task1_train_40113 | A variant on Chromosome 10 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GAGATCAGAGTCCCTTTATTAGGGGCATGGTGCTGGTGTCTACGGAGCAGTGATTTTTTGGAGAACACAGATAACATTACACCTTCCAGTGTGCATTGACAATGTTACATGGCTCTTCTGCAGGGGAACCAGGGCGTGGAGGCTGAGTTGGCAAGCAGGAGGTGTGCCCCTGGGATGGGCTGGGCCAGACCGGGAGCTTTCTGGGAGTTGGGACAGTTGCTGCTTTCTGCCCTCTAGCTTCTTGCTGCAGAAGTGGGAGTGGGAGCTGTGCTGCTGCTTTGTAGGTGGCTTTTGTGTGAAATAGTTAAAAGTCATGGCTA... | GAGATCAGAGTCCCTTTATTAGGGGCATGGTGCTGGTGTCTACGGAGCAGTGATTTTTTGGAGAACACAGATAACATTACACCTTCCAGTGTGCATTGACAATGTTACATGGCTCTTCTGCAGGGGAACCAGGGCGTGGAGGCTGAGTTGGCAAGCAGGAGGTGTGCCCCTGGGATGGGCTGGGCCAGACCGGGAGCTTTCTGGGAGTTGGGACAGTTGCTGCTTTCTGCCCTCTAGCTTCTTGCTGCAGAAGTGGGAGTGGGAGCTGTGCTGCTGCTTTGTAGGTGGCTTTTGTGTGAAATAGTTAAAAGTCATGGCTA... |
Task1_train_40114 | Located on Chromosome 10, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CCCTGCCTCCAGCCTGTGATGCCCACCTCAGCAGCCTGAAAATGTCCCAGGCTCCATCATGGACTCGTTCTGCCTCAGTCTCCTGCCGCTTTGTGGCCTGAGCATATAGAGAGTCTCCCCCAGACACACGCCTACACATGTCCCTAACACGTGCCTGTGTGCAAACACATCTACAAATATGCCCACACACTTGCACGTGTACACACAGGCAGAAATGGGTGCCGCATGTTCACGTGACATGTACAGTCACATACACGTGTGCATGCATGCATATCCTTATCTAAGGATGCAAGGGTGCATATTTGAGTAGCAGAGTGGTG... | CCCTGCCTCCAGCCTGTGATGCCCACCTCAGCAGCCTGAAAATGTCCCAGGCTCCATCATGGACTCGTTCTGCCTCAGTCTCCTGCCGCTTTGTGGCCTGAGCATATAGAGAGTCTCCCCCAGACACACGCCTACACATGTCCCTAACACGTGCCTGTGTGCAAACACATCTACAAATATGCCCACACACTTGCACGTGTACACACAGGCAGAAATGGGTGCCGCATGTTCACGTGACATGTACAGTCACATACACGTGTGCATGCATGCATATCCTTATCTAAGGATGCAAGGGTGCATATTTGAGTAGCAGAGTGGTG... |
Task1_train_40115 | Assess the clinical impact of this variant found on Chromosome 10. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CCACAGCCACAGAGCAGCCTCTACTCTGCCACTTCCCCTCCTTCCTGCCCTGGGCTTCCCACCTTCATCCCACCCTGTTGGCAGCCCTGGGAGAGTCCAAACAGCACAGTGGCCAGTGGGGGTGCTGTAAGTGGGCCAGTGGGCCCGGGTAGGTGCAGAGGGACATGGTGGGCCAGGACTGTGTCTGTGGTGCCTTGAGAGTAGGGGGAAGCCACCCGGGAGGAACCTCCCCACGTGTGGCCTTAGGCAAGGCCCTGACCCTGGCGGCACCCCATGAGTACGTAGCTCAGCCAATCATGTCGTTCAGTGCTGTAAGCTCA... | CCACAGCCACAGAGCAGCCTCTACTCTGCCACTTCCCCTCCTTCCTGCCCTGGGCTTCCCACCTTCATCCCACCCTGTTGGCAGCCCTGGGAGAGTCCAAACAGCACAGTGGCCAGTGGGGGTGCTGTAAGTGGGCCAGTGGGCCCGGGTAGGTGCAGAGGGACATGGTGGGCCAGGACTGTGTCTGTGGTGCCTTGAGAGTAGGGGGAAGCCACCCGGGAGGAACCTCCCCACGTGTGGCCTTAGGCAAGGCCCTGACCCTGGCGGCACCCCATGAGTACGTAGCTCAGCCAATCATGTCGTTCAGTGCTGTAAGCTCA... |
Task1_train_40116 | A variant found on Chromosome 10 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TAACTGAGACAAGTCTCCTCTGAGCTAACTTTAGAGATTTGTGGTAGAGAAGAGGAAAATTTCCATTTGAATTGGGTAGGGCATAGGAGAGAAAGAGAGATGCAAGAGGCATTAACCCCTGAGAAGACACCACCTTTGCACTCTAATGTGCTGGAAAAGCAACCTCTCCACCAGTTCCTGGGGCCTGGCAGCACCGCGCCTGACCTGGGTTGGCCCACTTCTTCCCAGGACACCCCTGGCCAATTCAAGGAGGCCTCTGTAGTTCAACTAGCAGGTAGGGTGCCCGTCCTTCACTTTCCTATTCCCAAGCAGCAGGCGAA... | TAACTGAGACAAGTCTCCTCTGAGCTAACTTTAGAGATTTGTGGTAGAGAAGAGGAAAATTTCCATTTGAATTGGGTAGGGCATAGGAGAGAAAGAGAGATGCAAGAGGCATTAACCCCTGAGAAGACACCACCTTTGCACTCTAATGTGCTGGAAAAGCAACCTCTCCACCAGTTCCTGGGGCCTGGCAGCACCGCGCCTGACCTGGGTTGGCCCACTTCTTCCCAGGACACCCCTGGCCAATTCAAGGAGGCCTCTGTAGTTCAACTAGCAGGTAGGGTGCCCGTCCTTCACTTTCCTATTCCCAAGCAGCAGGCGAA... |
Task1_train_40117 | Given this variant on Chromosome 10, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCTAAAGTACAGGGTTCAGAGAGCTTCCAGGTTGGTGAACATGTCCACATGCCAGGACAGTGATGCACCCCAACTCCATGGGGACAGAAGCCCCTGTGCTCAGGACCCTTCTAGACCACGCCCTATGTGCCCCTTCATCTGAATGTTCATTTTTATCCTTTAAAACATCCTTCGTCATAAATCAGCAACAGCAAGTAAACTGTCTCCCTGGCTTCCATCAGCTGCTCTAGCAAATTATTTAACCCAAGGAGAGAGTCATGAGAATCTCTATCTTGTAGCCAAGTGGGACAGAAGCGTGGGTAAGCTGGGGACCTATGGAC... | CCTAAAGTACAGGGTTCAGAGAGCTTCCAGGTTGGTGAACATGTCCACATGCCAGGACAGTGATGCACCCCAACTCCATGGGGACAGAAGCCCCTGTGCTCAGGACCCTTCTAGACCACGCCCTATGTGCCCCTTCATCTGAATGTTCATTTTTATCCTTTAAAACATCCTTCGTCATAAATCAGCAACAGCAAGTAAACTGTCTCCCTGGCTTCCATCAGCTGCTCTAGCAAATTATTTAACCCAAGGAGAGAGTCATGAGAATCTCTATCTTGTAGCCAAGTGGGACAGAAGCGTGGGTAAGCTGGGGACCTATGGAC... |
Task1_train_40118 | This variant is found on Chromosome 10. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCCAACACCAAACAAAGTGGGAGGAGCCAAGGCAAACACAACACTTTCCTTCACTGCCTCGTTGATACCCACAACAATCCCGTCAGTTGGTGGGTCAGATATGACATGGTTTCACTCCTCTGGGTCCCTATTTACGTACACGCTAACACTTCTGTAGCACACGACGTGACAGGCTCCGTTCCACGACATTCAGCGTCAACTCCCGGGGAGGCAGCTTAGACAGGTTAAGTGACTTGCCCGGGATCAGACAGGGGCGTCCTACTACACACTCTGCAGGGGTAGCTTCCAACAGACCTGGCAGTCTCCTTAGGAGCAAGGGG... | CCCAACACCAAACAAAGTGGGAGGAGCCAAGGCAAACACAACACTTTCCTTCACTGCCTCGTTGATACCCACAACAATCCCGTCAGTTGGTGGGTCAGATATGACATGGTTTCACTCCTCTGGGTCCCTATTTACGTACACGCTAACACTTCTGTAGCACACGACGTGACAGGCTCCGTTCCACGACATTCAGCGTCAACTCCCGGGGAGGCAGCTTAGACAGGTTAAGTGACTTGCCCGGGATCAGACAGGGGCGTCCTACTACACACTCTGCAGGGGTAGCTTCCAACAGACCTGGCAGTCTCCTTAGGAGCAAGGGG... |
Task1_train_40119 | Given this variant on Chromosome 10, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GGCCTGTGAAAGGACCCTCCAAGGCAATCCCATGTGCTCCCGTCTCCTGGAAAGAAGCCACATTTCTTCAAGTTGATGCAGGGGTGTTGGGGGAAAGCCAGAGTAAACAGGGCTCTCCTGGTACCTCCTTAGAGTACACAAGTCATTTGTGCTGGGGAAGAGTTTAGTGTGTGTCCTTCAGGAGTCTCCAAATGGCACTCCGGCTGCAGCTTCAGTTGACCAACTTCTCCCTCCCAGGAAGCAGGGAGGAGAGAGACCTTGGGCAAGGCTTTGTACCTGCAGCCCCAGTGAGCAGATGTGTTTCCCAATGTGGAAAATGC... | GGCCTGTGAAAGGACCCTCCAAGGCAATCCCATGTGCTCCCGTCTCCTGGAAAGAAGCCACATTTCTTCAAGTTGATGCAGGGGTGTTGGGGGAAAGCCAGAGTAAACAGGGCTCTCCTGGTACCTCCTTAGAGTACACAAGTCATTTGTGCTGGGGAAGAGTTTAGTGTGTGTCCTTCAGGAGTCTCCAAATGGCACTCCGGCTGCAGCTTCAGTTGACCAACTTCTCCCTCCCAGGAAGCAGGGAGGAGAGAGACCTTGGGCAAGGCTTTGTACCTGCAGCCCCAGTGAGCAGATGTGTTTCCCAATGTGGAAAATGC... |
Task1_train_40120 | This variant is present on Chromosome 10. Is the change likely to result in a pathogenic outcome? | Benign | CCCGTGTCCAAGTGTTCTCATTGTTCAGTTCCCACCTATGAGTGAGAACATGCGGTGTTTGGTTTTTTGTCCTTGCGATGGTTTGCTGAGAATGATGGTTTCCACCTTCATCCATGTCCCTACAAAGGACGTGAATTCATCATTTTTTATGGCTACATAGTATTCCATGGTGTATATGAAGGCACTTCTTTTGTCAAGAGGACCTAACATCAGATCATTAACTCTGGGAGGCTCTGTCATATTCATTGTTATCATCAGCACTGGAGCTGTTGTGTCTTGAGGGCACAGTAAATCTTGTTTGAGTGTTTGGACTTTTACCT... | CCCGTGTCCAAGTGTTCTCATTGTTCAGTTCCCACCTATGAGTGAGAACATGCGGTGTTTGGTTTTTTGTCCTTGCGATGGTTTGCTGAGAATGATGGTTTCCACCTTCATCCATGTCCCTACAAAGGACGTGAATTCATCATTTTTTATGGCTACATAGTATTCCATGGTGTATATGAAGGCACTTCTTTTGTCAAGAGGACCTAACATCAGATCATTAACTCTGGGAGGCTCTGTCATATTCATTGTTATCATCAGCACTGGAGCTGTTGTGTCTTGAGGGCACAGTAAATCTTGTTTGAGTGTTTGGACTTTTACCT... |
Task1_train_40121 | Consider this mutation on Chromosome 10. Is this a benign change or a disease-causing variant? | Benign | TCAAAGCCCGGGGATTATACAACATGGGTTCACATTTATACTTTCGTAAGACCTCTCTGGCCACCAGGGAGAGGGAGGGCGGGGAGGAGGTGGAGACGCTGGTCAGAAGGGTACTGCTGTGGAGGCAAAGGGGGATGGGGGTCTGGATCAGGTGCCAGCTGTAGAGAGGTGCAGTGTAGACAGATTTGGAGGGGAACTCAGCACAGGGTGGCTGGGAGGGCCTGTGGGGGAAAAGCCATAGAGTAACCTAAACAGGCTTCAGTTTTCCCAGCAGTAAGGGGCAGATTATATCATTTTTTTTCTTTTTTCTTTTTCTTATT... | TCAAAGCCCGGGGATTATACAACATGGGTTCACATTTATACTTTCGTAAGACCTCTCTGGCCACCAGGGAGAGGGAGGGCGGGGAGGAGGTGGAGACGCTGGTCAGAAGGGTACTGCTGTGGAGGCAAAGGGGGATGGGGGTCTGGATCAGGTGCCAGCTGTAGAGAGGTGCAGTGTAGACAGATTTGGAGGGGAACTCAGCACAGGGTGGCTGGGAGGGCCTGTGGGGGAAAAGCCATAGAGTAACCTAAACAGGCTTCAGTTTTCCCAGCAGTAAGGGGCAGATTATATCATTTTTTTTCTTTTTTCTTTTTCTTATT... |
Task1_train_40122 | This alteration occurs on Chromosome 10. Is it associated with a disease or is it a benign variant? | Benign | CTGTACATGGCCTGCGGGGACCCCGTGACAGGCGGGAAGAGCCCCCATCCCCCTTTCTGCAGGAGGCTTCTGTTTGGCCAAGAGTTTGTCTAATCTGACTTTGGGTCCCGAGCAGTTTGTCTGTGCCTGGCAGGCAGTTGATGAGTTTGATGAATGAACAAATGAATGAGGAGGAGGGAGGGGACAGAGTGGTGAGGGACAGAGCAGGGCAGCCTCTGGGGGTGGGACCCTGTCACCACAGCCACCCTTGCGTGCATGACAGCTCTGGGCCCACCTGGGCACTTCATGCCCACAATTGTGGTCAGCCCTCACCTGTGCTC... | CTGTACATGGCCTGCGGGGACCCCGTGACAGGCGGGAAGAGCCCCCATCCCCCTTTCTGCAGGAGGCTTCTGTTTGGCCAAGAGTTTGTCTAATCTGACTTTGGGTCCCGAGCAGTTTGTCTGTGCCTGGCAGGCAGTTGATGAGTTTGATGAATGAACAAATGAATGAGGAGGAGGGAGGGGACAGAGTGGTGAGGGACAGAGCAGGGCAGCCTCTGGGGGTGGGACCCTGTCACCACAGCCACCCTTGCGTGCATGACAGCTCTGGGCCCACCTGGGCACTTCATGCCCACAATTGTGGTCAGCCCTCACCTGTGCTC... |
Task1_train_40123 | A variant on Chromosome 10 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TAGAGCCATATCCGGGCAGAGCTTCTACCCTAAAAGAGCTCACCCACTGTGGGGACAGACAGCTGTCCAGAGCCACCTTCTTACCAGCGAGATGGAGCTGATCAGGAAGGCGTCCCTCAGAAAGTGACGTGGGCAGGCGGGGGCATAGGCAGAGGGAGGTGGGATTGGCCCACAAGGCTCTCCACAGGTACTGCCCCTGAGGCCCCACCAGGGCAATGGGGGGCCTGGCTGGACTAGGCCCACGGCAGCCTGCCCACCCCATAGGGATCCAGTTCACCAAATACGGCTGCCGGCGCAGACGAGACCACCACATGGTGCAG... | TAGAGCCATATCCGGGCAGAGCTTCTACCCTAAAAGAGCTCACCCACTGTGGGGACAGACAGCTGTCCAGAGCCACCTTCTTACCAGCGAGATGGAGCTGATCAGGAAGGCGTCCCTCAGAAAGTGACGTGGGCAGGCGGGGGCATAGGCAGAGGGAGGTGGGATTGGCCCACAAGGCTCTCCACAGGTACTGCCCCTGAGGCCCCACCAGGGCAATGGGGGGCCTGGCTGGACTAGGCCCACGGCAGCCTGCCCACCCCATAGGGATCCAGTTCACCAAATACGGCTGCCGGCGCAGACGAGACCACCACATGGTGCAG... |
Task1_train_40124 | A mutation on Chromosome 10 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GTACTATACAACAAGAAAAATGAACAGGCCTGAACTGTACTTACCAAAATAGATAAACTTCTGTTATAGAGAATACATTTAGGTGAGAAAAAGTACTTCAGTATGAAGTAAAAAAGCACTTCCAATGGATGTCATTTCCTTAATGTTTAGAGGGACACAACACAATCTGAAAATATTCTGGGATGCTCATTTATTAAGGCTGGTGGTGGCATCTGGATAGGGTTTTGTGAATAACTCCATACTTTTCTGTATTTTGAAATATTGCATTATGAATATTTGTAAAGAACCAAAAATCCACACACAACTCATGCATTTTATAT... | GTACTATACAACAAGAAAAATGAACAGGCCTGAACTGTACTTACCAAAATAGATAAACTTCTGTTATAGAGAATACATTTAGGTGAGAAAAAGTACTTCAGTATGAAGTAAAAAAGCACTTCCAATGGATGTCATTTCCTTAATGTTTAGAGGGACACAACACAATCTGAAAATATTCTGGGATGCTCATTTATTAAGGCTGGTGGTGGCATCTGGATAGGGTTTTGTGAATAACTCCATACTTTTCTGTATTTTGAAATATTGCATTATGAATATTTGTAAAGAACCAAAAATCCACACACAACTCATGCATTTTATAT... |
Task1_train_40125 | A variant affecting Chromosome 10 has been observed. Determine if it's benign or associated with disease. | Benign | GGGATGCTCATTTATTAAGGCTGGTGGTGGCATCTGGATAGGGTTTTGTGAATAACTCCATACTTTTCTGTATTTTGAAATATTGCATTATGAATATTTGTAAAGAACCAAAAATCCACACACAACTCATGCATTTTATATGTCTCCATAATATATAGCTTCATTTGTTTTGATATAAAACAGATTGCTGGTCTTCAAAGGACCCCACAGATAAAAGTAACAGAGAGATGGCAGATAGTGGAAGATACTGGCCCTGTCGCAATAAGCAAAATATAGAGATGAATCTCTAAATTTAACTTTTATTAAGTAAGAATTGCAAT... | GGGATGCTCATTTATTAAGGCTGGTGGTGGCATCTGGATAGGGTTTTGTGAATAACTCCATACTTTTCTGTATTTTGAAATATTGCATTATGAATATTTGTAAAGAACCAAAAATCCACACACAACTCATGCATTTTATATGTCTCCATAATATATAGCTTCATTTGTTTTGATATAAAACAGATTGCTGGTCTTCAAAGGACCCCACAGATAAAAGTAACAGAGAGATGGCAGATAGTGGAAGATACTGGCCCTGTCGCAATAAGCAAAATATAGAGATGAATCTCTAAATTTAACTTTTATTAAGTAAGAATTGCAAT... |
Task1_train_40126 | Here is a mutation located on Chromosome 10. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTGGTCCATGAGCCGTTACCTGCAATTCCAAAATGTTTATTTCTAAGTTTGGTGCAAACTTACCTGGCAGCAAAATCTGACCTGAACTAATGAGATCATTTATTCTTTTGATATAGAAATTTAGCCATATTTAGTTACAAGGTGATATCTCAGGCTCCATTGAGGATGTTCTATAATATAAACACAGAATATAATGTTTCTGATCCCAAAAGTTCTGAATTCTGAACTATATCTGGTTCCAATATTTTCAGACAAGCAATTGTAGATATGAGCTGCCTTCATAGGGCTGGTGAGATAATTGGATGAGAGAATGCATGCAC... | CTGGTCCATGAGCCGTTACCTGCAATTCCAAAATGTTTATTTCTAAGTTTGGTGCAAACTTACCTGGCAGCAAAATCTGACCTGAACTAATGAGATCATTTATTCTTTTGATATAGAAATTTAGCCATATTTAGTTACAAGGTGATATCTCAGGCTCCATTGAGGATGTTCTATAATATAAACACAGAATATAATGTTTCTGATCCCAAAAGTTCTGAATTCTGAACTATATCTGGTTCCAATATTTTCAGACAAGCAATTGTAGATATGAGCTGCCTTCATAGGGCTGGTGAGATAATTGGATGAGAGAATGCATGCAC... |
Task1_train_40127 | Given a variant located on Chromosome 10, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCATGAGCCGTTACCTGCAATTCCAAAATGTTTATTTCTAAGTTTGGTGCAAACTTACCTGGCAGCAAAATCTGACCTGAACTAATGAGATCATTTATTCTTTTGATATAGAAATTTAGCCATATTTAGTTACAAGGTGATATCTCAGGCTCCATTGAGGATGTTCTATAATATAAACACAGAATATAATGTTTCTGATCCCAAAAGTTCTGAATTCTGAACTATATCTGGTTCCAATATTTTCAGACAAGCAATTGTAGATATGAGCTGCCTTCATAGGGCTGGTGAGATAATTGGATGAGAGAATGCATGCACTCCTG... | CCATGAGCCGTTACCTGCAATTCCAAAATGTTTATTTCTAAGTTTGGTGCAAACTTACCTGGCAGCAAAATCTGACCTGAACTAATGAGATCATTTATTCTTTTGATATAGAAATTTAGCCATATTTAGTTACAAGGTGATATCTCAGGCTCCATTGAGGATGTTCTATAATATAAACACAGAATATAATGTTTCTGATCCCAAAAGTTCTGAATTCTGAACTATATCTGGTTCCAATATTTTCAGACAAGCAATTGTAGATATGAGCTGCCTTCATAGGGCTGGTGAGATAATTGGATGAGAGAATGCATGCACTCCTG... |
Task1_train_40128 | This mutation occurs on Chromosome 10. Does this change lead to a known medical condition, or is it benign? | Benign | CAGGGGACAATGACCTTGTAAATCCTCAATGCCTCCTCCCATCCCAATTTTCCAGGGAATTTGCAGAAATGTCATGGAAGACATTGGACTTCCCAGAGAGTCTTCTCTAGATCTTATGATTTCAGAAATGTAACCACAGCTTTTGGCTAGGGTGGGTAAGGCAGTATAATACAGTTTTGTTTTGTTTTGTTTTGTTTTGAATTCTGAGACGGAGTCTCGCTCTGTTGCCCAAGCTAGAGTGCACTGGCATGATCTTGGCTCACTGCAACCTCTACCCCTCAGGTTGAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCT... | CAGGGGACAATGACCTTGTAAATCCTCAATGCCTCCTCCCATCCCAATTTTCCAGGGAATTTGCAGAAATGTCATGGAAGACATTGGACTTCCCAGAGAGTCTTCTCTAGATCTTATGATTTCAGAAATGTAACCACAGCTTTTGGCTAGGGTGGGTAAGGCAGTATAATACAGTTTTGTTTTGTTTTGTTTTGTTTTGAATTCTGAGACGGAGTCTCGCTCTGTTGCCCAAGCTAGAGTGCACTGGCATGATCTTGGCTCACTGCAACCTCTACCCCTCAGGTTGAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCT... |
Task1_train_40129 | A change on Chromosome 10 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AGGCCAGCACATTCCAGCCAGGAGTACAGGCAAGGAGTACAGGCAAATGTAGGTTTGGAGGGCACCAAGGAGACCCTTCCCCCAAAGTGGGCTCCCAGAGGCGCCTGCTGGGCTAAACGTGTTCCCACAAGGGTCTGTGCCTTTTCCTCCACATTGGGCTTTGCACTTAACGGAGGGCTTTGTCTCACAACAGTCCAGGAGGAAGATTCTTAATCTTCCTGCTGGACGGGTGGAGAATCCGAGGCCCTGAGAGGGGATGCTAGCAGGTAGTTGGTGGCAGGACACGACCTCAGCGAAAGGTTCTGTGGACCCCACATCCC... | AGGCCAGCACATTCCAGCCAGGAGTACAGGCAAGGAGTACAGGCAAATGTAGGTTTGGAGGGCACCAAGGAGACCCTTCCCCCAAAGTGGGCTCCCAGAGGCGCCTGCTGGGCTAAACGTGTTCCCACAAGGGTCTGTGCCTTTTCCTCCACATTGGGCTTTGCACTTAACGGAGGGCTTTGTCTCACAACAGTCCAGGAGGAAGATTCTTAATCTTCCTGCTGGACGGGTGGAGAATCCGAGGCCCTGAGAGGGGATGCTAGCAGGTAGTTGGTGGCAGGACACGACCTCAGCGAAAGGTTCTGTGGACCCCACATCCC... |
Task1_train_40130 | A variant found on Chromosome 10 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AAGAAAAGAGGGTTAATTGGCTCATGGTTCTGCATATTTGTACAAACATGGCTTCAACATCTGCTTCCGGTGAGACCTCAGGAAGCTTACAATCATGGCGGAAGGCAAAACTTGAGCAGGCACGTCACATGGCAAGAGTGAGAGCAAGAAAGAGAGTGGGGGGAGGTCCTAGGCTTATAAACAACCGGATCTCACCTGAACTAACTGAGCAAGAACTCATTCATGAAAGATGCACCCCCGTGATCCAGTCATCTCCCACCAGACCTCATCTCCAATGTCGGGAATCACATTTCAACATGAGATTTGGAGGATAGGCATCC... | AAGAAAAGAGGGTTAATTGGCTCATGGTTCTGCATATTTGTACAAACATGGCTTCAACATCTGCTTCCGGTGAGACCTCAGGAAGCTTACAATCATGGCGGAAGGCAAAACTTGAGCAGGCACGTCACATGGCAAGAGTGAGAGCAAGAAAGAGAGTGGGGGGAGGTCCTAGGCTTATAAACAACCGGATCTCACCTGAACTAACTGAGCAAGAACTCATTCATGAAAGATGCACCCCCGTGATCCAGTCATCTCCCACCAGACCTCATCTCCAATGTCGGGAATCACATTTCAACATGAGATTTGGAGGATAGGCATCC... |
Task1_train_40131 | This variant is located on Chromosome 10. Evaluate its biological effect and specify any disease association. | Benign | CTGGTCGTGCAGAGTCCGTTCATTCAGCAAACATTGACAAGGGTGCCTGCAGTGTGCCTGGGCCCCTCCCGACTCACTGGCTTCAAGGCTTGCAGGAAGGATGCCTGTACTTGGAACCAGCAGACACAGATTCCCATTCCCAGCCAGTCCTCCCCGGTGTGCTGAGGAGTCCAGCATGGGCCCCAGTCTGCTTGGCTGTGTAACTTCACTCTTGTCATCTACTAGTTATGTGACCCTGGGCAAGTTACTCAACCTTTCTGAGCCTCAGACCCCTCTGTGAAATGGGTCTTAGAGTAGTACCTAATATATTAGGCTGTTGT... | CTGGTCGTGCAGAGTCCGTTCATTCAGCAAACATTGACAAGGGTGCCTGCAGTGTGCCTGGGCCCCTCCCGACTCACTGGCTTCAAGGCTTGCAGGAAGGATGCCTGTACTTGGAACCAGCAGACACAGATTCCCATTCCCAGCCAGTCCTCCCCGGTGTGCTGAGGAGTCCAGCATGGGCCCCAGTCTGCTTGGCTGTGTAACTTCACTCTTGTCATCTACTAGTTATGTGACCCTGGGCAAGTTACTCAACCTTTCTGAGCCTCAGACCCCTCTGTGAAATGGGTCTTAGAGTAGTACCTAATATATTAGGCTGTTGT... |
Task1_train_40132 | A mutation found on Chromosome 10 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTCCCCAGGATGACTAGGCGAAGGAATGTTCTCCCAGGGAACATTGTGCTGGCAGACAAAGGCCCCACACCCCGCCCTCCTCCAGGACATGAGTCCACGCCTCTCCCCAGCATCACCTCTGTGCTCCTCTGCTCGCATCTTGACTACAGCCAGAGTCCATTTGCAGCTCCCTGAACATGCCTCACTCTCTCTCCCAAGACACATGCACTTATATCCTCCCATTCGTCGTTACCATCCAGCATAGACATTGCCTCCAAATGGCCTTCCACGATGCCCAGGGTGGGTTTTGTGCCCCTCAGATGTGCTGTGTGATGCCCTGG... | CTCCCCAGGATGACTAGGCGAAGGAATGTTCTCCCAGGGAACATTGTGCTGGCAGACAAAGGCCCCACACCCCGCCCTCCTCCAGGACATGAGTCCACGCCTCTCCCCAGCATCACCTCTGTGCTCCTCTGCTCGCATCTTGACTACAGCCAGAGTCCATTTGCAGCTCCCTGAACATGCCTCACTCTCTCTCCCAAGACACATGCACTTATATCCTCCCATTCGTCGTTACCATCCAGCATAGACATTGCCTCCAAATGGCCTTCCACGATGCCCAGGGTGGGTTTTGTGCCCCTCAGATGTGCTGTGTGATGCCCTGG... |
Task1_train_40133 | This mutation is located on Chromosome 10. Is it associated with a disease or is it a benign polymorphism? | Benign | GAATCAGAAAGGATTTGTTTGGTATTTGGCACTTCTCCGCACCAGGCAGGCTTCTGAGTGCTTCACGTGTAATAATCCTTTTAATCTTCATCACAGCCCTACGAGGTGGGTATTATTAACACCCCCATTGTATAGATGAGGATACAGAGGCACAGTGAGGTTAAGGGACTTGCTGAAGGTCACACAACTAGAAGAAGTAGAGCCAGGTTTGGACTCGGATGTTTTGATTCTGGAGTCTGAGTTCCTAATTACAGTGCTAATTTTTATACCTTTGCCCTCCCTCAAGTACTACCCAGGCTAATAGAACTTATGGTGGAGAG... | GAATCAGAAAGGATTTGTTTGGTATTTGGCACTTCTCCGCACCAGGCAGGCTTCTGAGTGCTTCACGTGTAATAATCCTTTTAATCTTCATCACAGCCCTACGAGGTGGGTATTATTAACACCCCCATTGTATAGATGAGGATACAGAGGCACAGTGAGGTTAAGGGACTTGCTGAAGGTCACACAACTAGAAGAAGTAGAGCCAGGTTTGGACTCGGATGTTTTGATTCTGGAGTCTGAGTTCCTAATTACAGTGCTAATTTTTATACCTTTGCCCTCCCTCAAGTACTACCCAGGCTAATAGAACTTATGGTGGAGAG... |
Task1_train_40134 | A genetic alteration is present on Chromosome 10. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTGCTCCAGGAACCTGTCTTCTTCTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAATCTTACTCTGTCACCTAGGCTGGAGTGCAGTGATGCGGTCTTGGCTCACTGCAATGTCCATCTCCCGAGTTTAGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGTTGCACACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGGTGGGGTTTCACCATTGGGTCAGGCTGGTCTTGAACTCCTAACCTCAAGTGACCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGGATGAC... | TTGCTCCAGGAACCTGTCTTCTTCTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAATCTTACTCTGTCACCTAGGCTGGAGTGCAGTGATGCGGTCTTGGCTCACTGCAATGTCCATCTCCCGAGTTTAGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGTTGCACACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGGTGGGGTTTCACCATTGGGTCAGGCTGGTCTTGAACTCCTAACCTCAAGTGACCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGGATGAC... |
Task1_train_40135 | This variant is found on Chromosome 10. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTGGGCCCACATTCCCTCTTGGCTGAAACACATCAGCAGCTGCCACTTTTCAACAGAGAGCATGTGGACTCCAACTGGCCATCATCCCCACCCACCCAGCAACACCCTCATCTAAATTCCCTGCTGGCCTTGTAAGCATTTCAGTTTGCAACCCCTGTGATAGGCTGTTAATATTCAGAAACTCAAGGCAGTGGAAACACAGGGATAGGATGTGTAGGGGGAAGAGTTGCCTCTTATTATTCAAATACATCTTAGAATCTTTTGTGTTTCGTCATGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAG... | CTGGGCCCACATTCCCTCTTGGCTGAAACACATCAGCAGCTGCCACTTTTCAACAGAGAGCATGTGGACTCCAACTGGCCATCATCCCCACCCACCCAGCAACACCCTCATCTAAATTCCCTGCTGGCCTTGTAAGCATTTCAGTTTGCAACCCCTGTGATAGGCTGTTAATATTCAGAAACTCAAGGCAGTGGAAACACAGGGATAGGATGTGTAGGGGGAAGAGTTGCCTCTTATTATTCAAATACATCTTAGAATCTTTTGTGTTTCGTCATGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAG... |
Task1_train_40136 | Assess the clinical impact of this variant found on Chromosome 10. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CCTTCCCTATTTTCTCTGCACCACCCCCTTCTTATTCATTTTTCAGGCATTTATGAAGCATCTACTGCATGCCAGGCACCGTCTGTGCTGTGCAGTGAGCCCCACAGGTGCCTGCCCTGCCCTCGTCCTTCCCCAAACCCTTTTCCTTTGACAAAGGCAAATGATGGGGGCCAAGGAGGTATGGTTTGGTCACACAGTGACCTGGAACTGAGGCCTCCACACCACAGTGACCCCTCGCCAAGGGGTTCAATGACATGGCAGTCAGATCTTCCCAAGACCAAGCTGCAGTTGTAACAGTCCAACAAGACCATGCATTGATG... | CCTTCCCTATTTTCTCTGCACCACCCCCTTCTTATTCATTTTTCAGGCATTTATGAAGCATCTACTGCATGCCAGGCACCGTCTGTGCTGTGCAGTGAGCCCCACAGGTGCCTGCCCTGCCCTCGTCCTTCCCCAAACCCTTTTCCTTTGACAAAGGCAAATGATGGGGGCCAAGGAGGTATGGTTTGGTCACACAGTGACCTGGAACTGAGGCCTCCACACCACAGTGACCCCTCGCCAAGGGGTTCAATGACATGGCAGTCAGATCTTCCCAAGACCAAGCTGCAGTTGTAACAGTCCAACAAGACCATGCATTGATG... |
Task1_train_40137 | This mutation occurs on Chromosome 10. Does this change lead to a known medical condition, or is it benign? | Benign | GAGCACCTGCCACGCGCCAGGTGCTGTGCAAGGTGGTGGTCACAGTGACCCACCAGACAGGCCTGGGGTCCTAGAGGGAGCTCACAGCAGGCCCAGGAAAGCAGTGACCACACAAGGCGGCCACAGTGGGCCAAGCCCTGGGCTTCCCAGCCTCCACCCCACCCTGACCTTGCACCCCTGGCCCGGCTCCCACAGGTGATTGTGTACGTGGAGGACATCAACGATGAGGCCCCCGTGTTCACACAGCAGCAGTACAGCCGTCTGGGGCTTCGAGAGACCGCAGGCATTGGAACGTCAGTCATCGTGGTCCAAGCCACAGA... | GAGCACCTGCCACGCGCCAGGTGCTGTGCAAGGTGGTGGTCACAGTGACCCACCAGACAGGCCTGGGGTCCTAGAGGGAGCTCACAGCAGGCCCAGGAAAGCAGTGACCACACAAGGCGGCCACAGTGGGCCAAGCCCTGGGCTTCCCAGCCTCCACCCCACCCTGACCTTGCACCCCTGGCCCGGCTCCCACAGGTGATTGTGTACGTGGAGGACATCAACGATGAGGCCCCCGTGTTCACACAGCAGCAGTACAGCCGTCTGGGGCTTCGAGAGACCGCAGGCATTGGAACGTCAGTCATCGTGGTCCAAGCCACAGA... |
Task1_train_40138 | A variant on Chromosome 10 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GCTGGATCACTACATCCTCCAGGTGGGGCCTGGCCTCCCTTGGACTGAGAGACCACTGGCTAAGTGCCTAGACCGGTCACTACTCTCCATCCAGGAGAGAGCCTGTCCATCAGCACACTCTGGTGGTCAGTGCCCCTGCTGTCACCAAGTAACATGGGGCCAGCTGCACCCATCGGGGCCAAGAGCACAGTGAGGCTGACCCAGGATAGGGAAACCTGGGAGGGACCTTAGATACCCAGGAGGAGGTAGTTGAGGTGTCTTCCCCTGCTGTAAGAGCCAGGAGGATGAGGGAGAGCCTGGTGGAGCTGGGAGAGCCCCAG... | GCTGGATCACTACATCCTCCAGGTGGGGCCTGGCCTCCCTTGGACTGAGAGACCACTGGCTAAGTGCCTAGACCGGTCACTACTCTCCATCCAGGAGAGAGCCTGTCCATCAGCACACTCTGGTGGTCAGTGCCCCTGCTGTCACCAAGTAACATGGGGCCAGCTGCACCCATCGGGGCCAAGAGCACAGTGAGGCTGACCCAGGATAGGGAAACCTGGGAGGGACCTTAGATACCCAGGAGGAGGTAGTTGAGGTGTCTTCCCCTGCTGTAAGAGCCAGGAGGATGAGGGAGAGCCTGGTGGAGCTGGGAGAGCCCCAG... |
Task1_train_40139 | A genomic change on Chromosome 10 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GACCAGCCTGGGCAACATAGCGAGAGTGCATCTCTACCAAAAGTGATTTTTTTGATTTTTTGGGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACTTCTGCCTCCCAGGTTCAAGCAGCTCTCATGTCTCAGCCTCCCGAGTAGCTGGGATTACAGATGCCTGCCACCATGCCAGGCAAATTTTGGGTTGTTTTTTTTTTGAGATGGAGTCTTGCTCTATCAGCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGTAACCTCTGACTCCCGGGTTCAAGCGATTCT... | GACCAGCCTGGGCAACATAGCGAGAGTGCATCTCTACCAAAAGTGATTTTTTTGATTTTTTGGGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACTTCTGCCTCCCAGGTTCAAGCAGCTCTCATGTCTCAGCCTCCCGAGTAGCTGGGATTACAGATGCCTGCCACCATGCCAGGCAAATTTTGGGTTGTTTTTTTTTTGAGATGGAGTCTTGCTCTATCAGCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGTAACCTCTGACTCCCGGGTTCAAGCGATTCT... |
Task1_train_40140 | A genomic variant on Chromosome 10 is under review. What is the biological outcome — benign or pathogenic? | Benign | CCCCGGCCACTCTATCTCACTTTCCCTGGCATAAAGGCTTTGACCTTGGGCAACATACCCAGGGCAACCCAGCACCTCGGCAGGCTGGTGATCAATCTTCTCAACTTACAGATCCTGCTGACCATGCCTGCAACCAGGCCTCCCATCTGCTATCTCCCTCAGTGCACACTGTCCTAGGGAGTTGGGTGAATATCTATTATAGTGTGTCCATGTCACAGTTCAGAATCCTGAGGTCCCAGAGCAATTCAAATGCTTCTGGCTCCTTTCAGTGGAAAGCTGCAGCCAGCCTAAATCATCTCCCTGTGCTGGGCCCAGGAAGA... | CCCCGGCCACTCTATCTCACTTTCCCTGGCATAAAGGCTTTGACCTTGGGCAACATACCCAGGGCAACCCAGCACCTCGGCAGGCTGGTGATCAATCTTCTCAACTTACAGATCCTGCTGACCATGCCTGCAACCAGGCCTCCCATCTGCTATCTCCCTCAGTGCACACTGTCCTAGGGAGTTGGGTGAATATCTATTATAGTGTGTCCATGTCACAGTTCAGAATCCTGAGGTCCCAGAGCAATTCAAATGCTTCTGGCTCCTTTCAGTGGAAAGCTGCAGCCAGCCTAAATCATCTCCCTGTGCTGGGCCCAGGAAGA... |
Task1_train_40141 | A variant has been detected on Chromosome 10. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | ATATTCGAATAAAGATGACTGTCAAGGAAAGCCACCATGTCCATCTTGTGGCTCTGCAGGGCCTGGAGGCAGCTGTGAGTACTCTCTACTGGTGAGGGGCCCAGCCTTGAGCCTTCCTGAGTCCCCTTACTTGCCGGCAAGAATACAAGAGCACCACATTGCAGGAAAGGGGCTGAATTCCAGCCTCCCTGTTGGGGAGGGGATGCTGACATTTCCCACATTCCCAAACTCACCTCCCAAACTCCCTGAGCTAGAAACAACTTTAGAAATCAAGCCAGGTCCTTTATTAAACAGACAGAAAAGGTCCAGAGAGGGGATGT... | ATATTCGAATAAAGATGACTGTCAAGGAAAGCCACCATGTCCATCTTGTGGCTCTGCAGGGCCTGGAGGCAGCTGTGAGTACTCTCTACTGGTGAGGGGCCCAGCCTTGAGCCTTCCTGAGTCCCCTTACTTGCCGGCAAGAATACAAGAGCACCACATTGCAGGAAAGGGGCTGAATTCCAGCCTCCCTGTTGGGGAGGGGATGCTGACATTTCCCACATTCCCAAACTCACCTCCCAAACTCCCTGAGCTAGAAACAACTTTAGAAATCAAGCCAGGTCCTTTATTAAACAGACAGAAAAGGTCCAGAGAGGGGATGT... |
Task1_train_40142 | Here is a mutation located on Chromosome 10. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ACCCTCCCTGAAAGCTCCCCGTTCCTTCAGAGGCCTGCCTGGGCTCCCTTTCGGGATCAGCACACACAAGGTGGGCCAGGGTTTGTCCAGCATCAGCACAACCCCAAGGTGGCATCTCTCTATTAGCCCATTTTTCAGATGAGAACATCAAGGCAAGGCTCCTTAACATGCCCAAGGGCACACAGGCATGAAGTCCAGATGCAGACCTAGATATGATTGGACGAAAGCCTAGGCTTTTAACCTCCTGTCTCCAGGAGTTGTGGAGGGATGGGGAAGTCTGGCCCCAGAGCAAGCTGCCAAGGAGAAGAATTTGCACAGGG... | ACCCTCCCTGAAAGCTCCCCGTTCCTTCAGAGGCCTGCCTGGGCTCCCTTTCGGGATCAGCACACACAAGGTGGGCCAGGGTTTGTCCAGCATCAGCACAACCCCAAGGTGGCATCTCTCTATTAGCCCATTTTTCAGATGAGAACATCAAGGCAAGGCTCCTTAACATGCCCAAGGGCACACAGGCATGAAGTCCAGATGCAGACCTAGATATGATTGGACGAAAGCCTAGGCTTTTAACCTCCTGTCTCCAGGAGTTGTGGAGGGATGGGGAAGTCTGGCCCCAGAGCAAGCTGCCAAGGAGAAGAATTTGCACAGGG... |
Task1_train_40143 | Given a variant located on Chromosome 10, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGTGCTGGGATTACAGGCGTGAGCCACCATGCCCAGCATGTTGTTTTTTGACTTTTTAATAATAGCCGTTCTGACTGGTGTGAGAGGGTACCTCACTGTGGCTTATTGCATTTCTCTGATGATTAGCAACACTAAGCATTTTTTCTTTTTTTCTTTTTTTTTGAGATGGAGTCTTGCTCTGTCATCTGGGCTGGAGTGCAGTGGCGTGATATCCGCTCGCTGCAAGCTCCGCCTCCTGGGTTCATGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCGTGCCACCACGCCCAGCTAATTTTTTGTG... | AGTGCTGGGATTACAGGCGTGAGCCACCATGCCCAGCATGTTGTTTTTTGACTTTTTAATAATAGCCGTTCTGACTGGTGTGAGAGGGTACCTCACTGTGGCTTATTGCATTTCTCTGATGATTAGCAACACTAAGCATTTTTTCTTTTTTTCTTTTTTTTTGAGATGGAGTCTTGCTCTGTCATCTGGGCTGGAGTGCAGTGGCGTGATATCCGCTCGCTGCAAGCTCCGCCTCCTGGGTTCATGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCGTGCCACCACGCCCAGCTAATTTTTTGTG... |
Task1_train_40144 | This sequence variant lies on Chromosome 10. Is it clinically significant, and what condition might it cause if any? | Benign | GGGGAAGGATGGGTGCAGCTCCGGGAGATGGTGGGCTGGGGCTCCCGGGCCTCCTATGAGCACAAAGAAGCCACAGGTCTGGTTGGAAGAGACAGTCGTGGTCATTGTTCCCCAGGGTGGTCTGAGAGCTGCCCCACCATCCCTCAAGAAGGGCATGTAAGGTGTGAGGACTACCCCGGAGGGGAGTGGGTCCACCCCTCACTGCTCCCTCCACCCCAGGAGTGCAGGGCATCCCAGGGCCTTCTGGAAGCCCTGGGGAGCATCTATAACTAGAAGTGGGAGGTCAGGGGGTCCTGGGTAGGCCAGTGTAGCCCTCTCCC... | GGGGAAGGATGGGTGCAGCTCCGGGAGATGGTGGGCTGGGGCTCCCGGGCCTCCTATGAGCACAAAGAAGCCACAGGTCTGGTTGGAAGAGACAGTCGTGGTCATTGTTCCCCAGGGTGGTCTGAGAGCTGCCCCACCATCCCTCAAGAAGGGCATGTAAGGTGTGAGGACTACCCCGGAGGGGAGTGGGTCCACCCCTCACTGCTCCCTCCACCCCAGGAGTGCAGGGCATCCCAGGGCCTTCTGGAAGCCCTGGGGAGCATCTATAACTAGAAGTGGGAGGTCAGGGGGTCCTGGGTAGGCCAGTGTAGCCCTCTCCC... |
Task1_train_40145 | A variant was discovered on Chromosome 10. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ACCTGGCCTGGTCTGGTCCACAGGATCTGTAATGGTGAAGTCCCCCATGAATCGGGAGCTGGTTGCCACCTATGAGGTCACTCTCTCAGTGATTGACAATGCCAGCGACCTACCAGAGCGCTCTGTCAGTGTGCCAAATGGTAAGGTTCCCTGCAGACATCTCTCATTGGTCACTCAGAGCCAATCAGGGCAGGGGGCAGGTGGGGAACAGGCACTGGTCTGTCCCCAGGGAGGGAGCAACAAGACCCAGTTGCTCTGGGGGCCAGGAGTCAGGCAACACAAGAGGCATGAAAGGTGGCAGCCACCGTGAGGCCCAGGGT... | ACCTGGCCTGGTCTGGTCCACAGGATCTGTAATGGTGAAGTCCCCCATGAATCGGGAGCTGGTTGCCACCTATGAGGTCACTCTCTCAGTGATTGACAATGCCAGCGACCTACCAGAGCGCTCTGTCAGTGTGCCAAATGGTAAGGTTCCCTGCAGACATCTCTCATTGGTCACTCAGAGCCAATCAGGGCAGGGGGCAGGTGGGGAACAGGCACTGGTCTGTCCCCAGGGAGGGAGCAACAAGACCCAGTTGCTCTGGGGGCCAGGAGTCAGGCAACACAAGAGGCATGAAAGGTGGCAGCCACCGTGAGGCCCAGGGT... |
Task1_train_40146 | A mutation on Chromosome 10 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CACCTATGAGGTCACTCTCTCAGTGATTGACAATGCCAGCGACCTACCAGAGCGCTCTGTCAGTGTGCCAAATGGTAAGGTTCCCTGCAGACATCTCTCATTGGTCACTCAGAGCCAATCAGGGCAGGGGGCAGGTGGGGAACAGGCACTGGTCTGTCCCCAGGGAGGGAGCAACAAGACCCAGTTGCTCTGGGGGCCAGGAGTCAGGCAACACAAGAGGCATGAAAGGTGGCAGCCACCGTGAGGCCCAGGGTGGTGATGGCTACATAGAGCTCAGCAGTGGAGGATCCAGAAGCTCAGAATTGTGTGTGATCTGAACC... | CACCTATGAGGTCACTCTCTCAGTGATTGACAATGCCAGCGACCTACCAGAGCGCTCTGTCAGTGTGCCAAATGGTAAGGTTCCCTGCAGACATCTCTCATTGGTCACTCAGAGCCAATCAGGGCAGGGGGCAGGTGGGGAACAGGCACTGGTCTGTCCCCAGGGAGGGAGCAACAAGACCCAGTTGCTCTGGGGGCCAGGAGTCAGGCAACACAAGAGGCATGAAAGGTGGCAGCCACCGTGAGGCCCAGGGTGGTGATGGCTACATAGAGCTCAGCAGTGGAGGATCCAGAAGCTCAGAATTGTGTGTGATCTGAACC... |
Task1_train_40147 | Mutation context: Chromosome 10. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGGGCTCTCTGTGGACCTGCAAATGCATTCCTTCAACGAGCCATCCCCAGGCCCCTTCTATGTCCCAGGCAGTGGCTCCTGCACACGTCCTCATGACTGCACAGGGGTGAGACTTGGGCTCTGGACTCAAACAGCCTGGGTTGGAGCCCCCCCATGTTGGCCCTCTACAGCTGTGAAAGGTTAGACAAGATACTTAACATTTCTGAGTCTTCGGTTCCTCTTTTGTAAAACATGGCTAATAATGGGACCAGCATTGTTGTAAAGATTAAATGAGAAAATGTAAAAGCATTTAGCCCACTGCCTGGCACATAGTTGGTGTC... | AGGGCTCTCTGTGGACCTGCAAATGCATTCCTTCAACGAGCCATCCCCAGGCCCCTTCTATGTCCCAGGCAGTGGCTCCTGCACACGTCCTCATGACTGCACAGGGGTGAGACTTGGGCTCTGGACTCAAACAGCCTGGGTTGGAGCCCCCCCATGTTGGCCCTCTACAGCTGTGAAAGGTTAGACAAGATACTTAACATTTCTGAGTCTTCGGTTCCTCTTTTGTAAAACATGGCTAATAATGGGACCAGCATTGTTGTAAAGATTAAATGAGAAAATGTAAAAGCATTTAGCCCACTGCCTGGCACATAGTTGGTGTC... |
Task1_train_40148 | Located on Chromosome 10, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GTCCAAAACTATTACTACAATAAGATACTGGATATGAGACAGAGAGACCACATTCACATCACTTTTATTACAATGTATTGTTATAATTGTTCTATTTTGTTAGTTATTGTTATTAATCTCTTACTGTGCCTGATTAATAAACTAAACTTTATCAAAGGTTTCTATATACAGTTGGCCCTCCATATCCAGGGATTCTCCATCTGTGGATTCAACCAACTGCAGATTGAAAATATTTGAAAAAAAAATCCAGCCTGGGCAACAAAGTAAAACCCCCTCATCTCTACAAAGATTAGCTGGGCATGATGGTACATGCCTGTAAG... | GTCCAAAACTATTACTACAATAAGATACTGGATATGAGACAGAGAGACCACATTCACATCACTTTTATTACAATGTATTGTTATAATTGTTCTATTTTGTTAGTTATTGTTATTAATCTCTTACTGTGCCTGATTAATAAACTAAACTTTATCAAAGGTTTCTATATACAGTTGGCCCTCCATATCCAGGGATTCTCCATCTGTGGATTCAACCAACTGCAGATTGAAAATATTTGAAAAAAAAATCCAGCCTGGGCAACAAAGTAAAACCCCCTCATCTCTACAAAGATTAGCTGGGCATGATGGTACATGCCTGTAAG... |
Task1_train_40149 | A genetic alteration is present on Chromosome 10. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ATAGCTTTTAGAAGACATAAGGGGACTGAATCCAACGTTGCGGAAATTGGTATTCCTTGCTTAAGGAACAATTTCATCTATACCAAGAAATTTTATTCTGTGACTTTATAAAAAAACATGGTGATGTTTGATGTGGAGAAAGTTGTCTATTACATGCAATAGAAACAGGAAATACAAAATATAATTTCTATCTTTGGTTTGCTGAAGGAAAAAAGGGGTAAGAGAAAATGGGAAAATAAAGAAGGCTACAAACCACTTGAAATAAATCATGCAAATAAAAGAGAGCAACTAAATGATTACATGAAAGAAATATTTAACAA... | ATAGCTTTTAGAAGACATAAGGGGACTGAATCCAACGTTGCGGAAATTGGTATTCCTTGCTTAAGGAACAATTTCATCTATACCAAGAAATTTTATTCTGTGACTTTATAAAAAAACATGGTGATGTTTGATGTGGAGAAAGTTGTCTATTACATGCAATAGAAACAGGAAATACAAAATATAATTTCTATCTTTGGTTTGCTGAAGGAAAAAAGGGGTAAGAGAAAATGGGAAAATAAAGAAGGCTACAAACCACTTGAAATAAATCATGCAAATAAAAGAGAGCAACTAAATGATTACATGAAAGAAATATTTAACAA... |
Task1_train_40150 | This mutation is located on Chromosome 10. Is it associated with a disease or is it a benign polymorphism? | Benign | GAAACAGGAAATACAAAATATAATTTCTATCTTTGGTTTGCTGAAGGAAAAAAGGGGTAAGAGAAAATGGGAAAATAAAGAAGGCTACAAACCACTTGAAATAAATCATGCAAATAAAAGAGAGCAACTAAATGATTACATGAAAGAAATATTTAACAATAATGTAAAATAAAGCCTCCACTTAGAAATAATTGCTTTGTTTTATATGCCAACTAGATGGTAAAATCATAAAAGATGATAAATGAAACAAAGAAAAAATATAGTTTTCATTAAATAAATAATCCAAATTCATGAAATGACTGTATTGACAAATTGTTAGC... | GAAACAGGAAATACAAAATATAATTTCTATCTTTGGTTTGCTGAAGGAAAAAAGGGGTAAGAGAAAATGGGAAAATAAAGAAGGCTACAAACCACTTGAAATAAATCATGCAAATAAAAGAGAGCAACTAAATGATTACATGAAAGAAATATTTAACAATAATGTAAAATAAAGCCTCCACTTAGAAATAATTGCTTTGTTTTATATGCCAACTAGATGGTAAAATCATAAAAGATGATAAATGAAACAAAGAAAAAATATAGTTTTCATTAAATAAATAATCCAAATTCATGAAATGACTGTATTGACAAATTGTTAGC... |
Task1_train_40151 | This genomic variant is located on Chromosome 10. Can you determine its pathogenicity and name any linked disease? | Benign | TTTTTGATTAATGTGTTTTTGGAAAAGAAAAGATGAGAGTGGCTAACAGCAGGAGCTGCAACATTGAACTTTGCTTCTCAGTAGTGAGTGGGAAAAGAGCTTTGCTGTAGAACCCCAAGGATATCTGAAAGCTGAGGCAGAAGAGAGCAGGCCTGGAATACTGAAAATGGCAGATAAATAAAAGAAACTTTGGTACAGGACCTACCTGACCTGAGAATATATACATGGGCAATAAATTATGAAGGTGCTAAGGATAAATAGAACCCATCTGGGTCCATGATGCAGAATAGAAAAACAGGTAAAATCTTGTGAGCCTGGCT... | TTTTTGATTAATGTGTTTTTGGAAAAGAAAAGATGAGAGTGGCTAACAGCAGGAGCTGCAACATTGAACTTTGCTTCTCAGTAGTGAGTGGGAAAAGAGCTTTGCTGTAGAACCCCAAGGATATCTGAAAGCTGAGGCAGAAGAGAGCAGGCCTGGAATACTGAAAATGGCAGATAAATAAAAGAAACTTTGGTACAGGACCTACCTGACCTGAGAATATATACATGGGCAATAAATTATGAAGGTGCTAAGGATAAATAGAACCCATCTGGGTCCATGATGCAGAATAGAAAAACAGGTAAAATCTTGTGAGCCTGGCT... |
Task1_train_40152 | A mutation has occurred on Chromosome 10. What is the medical relevance of this mutation? | Benign | AGGTTGCATGGTGGTTACAATAAAAAGATAACTAAGCCACAATGTAAATTTGCATTCCAAATTAAAAAGGAAACTTCTTATCCTTGGTGATATAAACTGAAAATGAAGTCTACAAGTTATATGGCCTAGCACACATAATAAAACTTGGTTCTAAAGGTTATAACACATTTCTCTCCAGGAAAGATTCCTGCAAATCGAATAAATTGCATGTCTATTTTGAAATAGCTCAAGGGCTAATAGAATTAAGAAGGTACATTTATAACTTGTCTAAGAGTCTTAAAAGAAACAAACATAAAAGTGAATATTAAATGAAATAATAA... | AGGTTGCATGGTGGTTACAATAAAAAGATAACTAAGCCACAATGTAAATTTGCATTCCAAATTAAAAAGGAAACTTCTTATCCTTGGTGATATAAACTGAAAATGAAGTCTACAAGTTATATGGCCTAGCACACATAATAAAACTTGGTTCTAAAGGTTATAACACATTTCTCTCCAGGAAAGATTCCTGCAAATCGAATAAATTGCATGTCTATTTTGAAATAGCTCAAGGGCTAATAGAATTAAGAAGGTACATTTATAACTTGTCTAAGAGTCTTAAAAGAAACAAACATAAAAGTGAATATTAAATGAAATAATAA... |
Task1_train_40153 | A variant on Chromosome 10 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCTCTGCAGTTCTGTACATATATACATATTATAATTATTTTTTGAGTTATCTTTTTATTACTGATTTGTAAGTACAGTAATTCCAAAAAAGAACAATATAATATGGGAGCCAAGGTAAAACCCTATTTAAACACACAGCATTCAGTCACTCTCAAATATTTAATGAGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGTAGGCTGAGATGGGCGGATCATGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCTGGGTGTGGTGGCAGG... | TCTCTGCAGTTCTGTACATATATACATATTATAATTATTTTTTGAGTTATCTTTTTATTACTGATTTGTAAGTACAGTAATTCCAAAAAAGAACAATATAATATGGGAGCCAAGGTAAAACCCTATTTAAACACACAGCATTCAGTCACTCTCAAATATTTAATGAGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGTAGGCTGAGATGGGCGGATCATGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCTGGGTGTGGTGGCAGG... |
Task1_train_40154 | Here is a genetic alteration on Chromosome 10. Based on the data, is it a benign variant or a cause of disease? | Benign | AAGTCATAGTTCTGCTCCTTCTCCTCCTTGGAAACAGACTCGGATTCTTTTTTGCCAACAGCTTCCTGCAGCAGCTGGTCCAGCTGATCTGGTGAGAGATCTAACCACTGGTCATCTGAAAAAGAAGAAAGCATAATACTGCCATTCTACATTCACATAAGTCCTCTTAGGAGAGGATCCTGTGAGACTGAGTAGAACATTTTAATTTTTTTTTTTTAACCCTTCCACTGTATCCTGGTCCATCACTTACCATCCTCTGGGGGAAGATTAGCTGCTTCTTTCTTAAGGTCTTCTATATCAAATGGTATTGTCTGTAATAA... | AAGTCATAGTTCTGCTCCTTCTCCTCCTTGGAAACAGACTCGGATTCTTTTTTGCCAACAGCTTCCTGCAGCAGCTGGTCCAGCTGATCTGGTGAGAGATCTAACCACTGGTCATCTGAAAAAGAAGAAAGCATAATACTGCCATTCTACATTCACATAAGTCCTCTTAGGAGAGGATCCTGTGAGACTGAGTAGAACATTTTAATTTTTTTTTTTTAACCCTTCCACTGTATCCTGGTCCATCACTTACCATCCTCTGGGGGAAGATTAGCTGCTTCTTTCTTAAGGTCTTCTATATCAAATGGTATTGTCTGTAATAA... |
Task1_train_40155 | A variant was discovered on Chromosome 10. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TGATGAGTATCAATGCAGAAATCCTTAACAAAATATCAGCAATCTGAATTCAACAACACATTAAATAGATTATTCACCACGACCAAGCGAGATTTATTCCTGGGATGCAAGGATGGTTCAACACACGAAAATCAATGTACAGTTAATATCCCACATTAACAGAATGAAGGTCAAACAAGTGCATTACAGAGTGTCTCAAGAGCTGCCATGGCAAACAATAGGTAGAAGAACAGCCCAACCAACTCTTCTTCTCCCCACCCCAGATCTCAAGTTTCTTCAACTAGAGAACTCCAATTAAAGTAACTATTTTTGTCTATATT... | TGATGAGTATCAATGCAGAAATCCTTAACAAAATATCAGCAATCTGAATTCAACAACACATTAAATAGATTATTCACCACGACCAAGCGAGATTTATTCCTGGGATGCAAGGATGGTTCAACACACGAAAATCAATGTACAGTTAATATCCCACATTAACAGAATGAAGGTCAAACAAGTGCATTACAGAGTGTCTCAAGAGCTGCCATGGCAAACAATAGGTAGAAGAACAGCCCAACCAACTCTTCTTCTCCCCACCCCAGATCTCAAGTTTCTTCAACTAGAGAACTCCAATTAAAGTAACTATTTTTGTCTATATT... |
Task1_train_40156 | A mutation is present on Chromosome 10. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AGATCTTAGAATTTTAGAAAAACTCAGAAGACAAACTTTCAAAGGACATAGCCCTGAAGGGACAATTTCTTGTCCTGTATCTCCAACATGAGATACATCTATAGCTGAGCCTCAGCAAACAGCCTAAGACCTGCTTGCCCGGGGTCTGCCTAAGTCAGCAGTGCTCTGAAGATGCAGCTTTCAATGACATCAGAAAGAAAACTTCTCCTTATATACTTCACTACAGTGGGATAGGGATTTCTCTCAAGCCTATGTGAGCTTTCCACTTAACATCATACAGCATCGTAATTTCTTGTTGCTGTTGCTGTTTTATATTAAAT... | AGATCTTAGAATTTTAGAAAAACTCAGAAGACAAACTTTCAAAGGACATAGCCCTGAAGGGACAATTTCTTGTCCTGTATCTCCAACATGAGATACATCTATAGCTGAGCCTCAGCAAACAGCCTAAGACCTGCTTGCCCGGGGTCTGCCTAAGTCAGCAGTGCTCTGAAGATGCAGCTTTCAATGACATCAGAAAGAAAACTTCTCCTTATATACTTCACTACAGTGGGATAGGGATTTCTCTCAAGCCTATGTGAGCTTTCCACTTAACATCATACAGCATCGTAATTTCTTGTTGCTGTTGCTGTTTTATATTAAAT... |
Task1_train_40157 | A mutation is present on Chromosome 10. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CTCTGGGTATTTCCCTACTCTTTCCCAGGCAGTCATGGCAAGCTGCAGAAGACACACTGAAGAACAGACTCAAGGAAAATCACACAGACACCAACCGTTCTTTCAACACTCAGCACACACCCTCACACCTCCCTTCCACCATCATTCCCTTCCATTCTAACATTCTTCTCCCTCAAATTTTTTTCCAATCCCCCTCTCACACACGGTTGGTTTCTTGTTACTCAACTTTACCTTCTCCCAATATGGCATTGTCCCTCGCCACACTTCTGTCTGTGGCTCAATCACTTACACTCATTTCTGCCATGCTTCTGATTTTGGCC... | CTCTGGGTATTTCCCTACTCTTTCCCAGGCAGTCATGGCAAGCTGCAGAAGACACACTGAAGAACAGACTCAAGGAAAATCACACAGACACCAACCGTTCTTTCAACACTCAGCACACACCCTCACACCTCCCTTCCACCATCATTCCCTTCCATTCTAACATTCTTCTCCCTCAAATTTTTTTCCAATCCCCCTCTCACACACGGTTGGTTTCTTGTTACTCAACTTTACCTTCTCCCAATATGGCATTGTCCCTCGCCACACTTCTGTCTGTGGCTCAATCACTTACACTCATTTCTGCCATGCTTCTGATTTTGGCC... |
Task1_train_40158 | A change on Chromosome 10 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GGAAGATGTAATGAGGAGGAAACAGGCCAGGGGTTGAAGTAGGCTCATCAGTCAAATACCCACTGACATCCCCATCCCTTAATTGCAGATACATTCAAGCCCTCTGGGAGGCAGACACAAACCATCTGCACTCCAGCAGAAACGCACGAGCAGAAATAGGTACCTGTTAGTTGCTAAAGCCAGGCCAGTGAGACATAGAGCTGAGACAGGCAATGGGAGCCCTGGATTAGGGGAAGAGAAGAGGAGAGAGGTCCATACCGCTGCACAGTGAGGACAAGCTGATTTCCTGAGGCATCGATGAGGCTCATGGCACTGGCATG... | GGAAGATGTAATGAGGAGGAAACAGGCCAGGGGTTGAAGTAGGCTCATCAGTCAAATACCCACTGACATCCCCATCCCTTAATTGCAGATACATTCAAGCCCTCTGGGAGGCAGACACAAACCATCTGCACTCCAGCAGAAACGCACGAGCAGAAATAGGTACCTGTTAGTTGCTAAAGCCAGGCCAGTGAGACATAGAGCTGAGACAGGCAATGGGAGCCCTGGATTAGGGGAAGAGAAGAGGAGAGAGGTCCATACCGCTGCACAGTGAGGACAAGCTGATTTCCTGAGGCATCGATGAGGCTCATGGCACTGGCATG... |
Task1_train_40159 | This variant is present on Chromosome 10. Is the change likely to result in a pathogenic outcome? | Benign | AATTTTTTGTATTTCTAGTAGAGACAGGGTTTCGCCATGTTGGCAAGGATAGTCTCGATTTCTTGACTTCGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTCAGCCACCGCACCCGGCCTCAAATACATTTTTTTAATGGCCTTGTCTTTCCTGGTTTTAGGCCCTTTTCCACAATTTCTGATGGAAATACAGAAACCTTGCCATCATTCTTACTGCTGGTTTGCATCTCATTTATGGTGTATCTGGGATTTCTTCTCATGAACAGAAAGATTCAGTGGCTGTTATATGCCTTGTCAATTTAATG... | AATTTTTTGTATTTCTAGTAGAGACAGGGTTTCGCCATGTTGGCAAGGATAGTCTCGATTTCTTGACTTCGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTCAGCCACCGCACCCGGCCTCAAATACATTTTTTTAATGGCCTTGTCTTTCCTGGTTTTAGGCCCTTTTCCACAATTTCTGATGGAAATACAGAAACCTTGCCATCATTCTTACTGCTGGTTTGCATCTCATTTATGGTGTATCTGGGATTTCTTCTCATGAACAGAAAGATTCAGTGGCTGTTATATGCCTTGTCAATTTAATG... |
Task1_train_40160 | An alteration has been detected on Chromosome 10. Is it pathogenic, and if so, what disease is involved? | Benign | AAGTGCTTTACTTATAGTATCTTACTTAATCCTCACAATGATTAAATGAGGTAGGCACCACTCTCTGCCTTTCTTTGACAGCTAAGGAAACAGTTTAGGGAGGGGAAGTAACCTGTCTGAGGTCATCCAATTTGGAGTCACGGAGCCAGACCCTAGTCTGTCTGATTTCCAAGCATAACTTATTGCAACCATTCTGCCAGGCTTTGCCAGTCCTCTGGGACGGCCCACACCTCCTCTCCCAGGACCACCTCCCAGCCTTCTCTTCTTCCTCTGACCCCACCTATCCCAGGCCCTTCCAGCCCCTCTCCCCCGTCAACCAG... | AAGTGCTTTACTTATAGTATCTTACTTAATCCTCACAATGATTAAATGAGGTAGGCACCACTCTCTGCCTTTCTTTGACAGCTAAGGAAACAGTTTAGGGAGGGGAAGTAACCTGTCTGAGGTCATCCAATTTGGAGTCACGGAGCCAGACCCTAGTCTGTCTGATTTCCAAGCATAACTTATTGCAACCATTCTGCCAGGCTTTGCCAGTCCTCTGGGACGGCCCACACCTCCTCTCCCAGGACCACCTCCCAGCCTTCTCTTCTTCCTCTGACCCCACCTATCCCAGGCCCTTCCAGCCCCTCTCCCCCGTCAACCAG... |
Task1_train_40161 | Chromosome 10 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGGGCTGCCCGGGCTCCCTGGGCTCCCCGGCGGCTGCACGGAGTCAAGGCGCCCCGTCCCGGGCGTCCCCCGCGGGTGCCGATCCAGGCTGCCCGGAGTCCGGAGCCCAGAGAGGAGAGAGACAGCTGGGGAGCCTGGTCACCGCGGGCATCTCCCCTGCGCTGCAGTCGCCCGCCTGGCCTGCCTTCCCGTTCCTCCGCCTCTTGCCCTGACTTCTCCTTCCTTTGCAGAGCCGCCGTCTAGCGCCCCGACCTCGCCACCATGAGAGCCCTGCTGGCGCGCCTGCTTCTCTGCGTCCTGGTCGTGAGCGACTCCAAAGT... | TGGGCTGCCCGGGCTCCCTGGGCTCCCCGGCGGCTGCACGGAGTCAAGGCGCCCCGTCCCGGGCGTCCCCCGCGGGTGCCGATCCAGGCTGCCCGGAGTCCGGAGCCCAGAGAGGAGAGAGACAGCTGGGGAGCCTGGTCACCGCGGGCATCTCCCCTGCGCTGCAGTCGCCCGCCTGGCCTGCCTTCCCGTTCCTCCGCCTCTTGCCCTGACTTCTCCTTCCTTTGCAGAGCCGCCGTCTAGCGCCCCGACCTCGCCACCATGAGAGCCCTGCTGGCGCGCCTGCTTCTCTGCGTCCTGGTCGTGAGCGACTCCAAAGT... |
Task1_train_40162 | A variant on Chromosome 10 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AAGATCCCATCTCTAAAATAAAATAAAAATTTAAAAAATTGTTTAAAATCCTGTAGAGAGTTCAGAGTGGTTGGAGCAGAGTAATGGAGAATAGTAGACAATGGAGTTAGAGAGGCAATGAGAGGTAAAGGGAAGTGGCTTGAACCTGTAGGGCCTCATAGACTATTGTAAAGATTTTTGCTTTTTAGTGAGTGTTGTTGGAAGCATTACAGGGTTTTGAACAAAGGAATGACATACTTTGGCTTGCATTTAAAAAGGACAGCTCTATGTGCGTGGAGTCAAGGATGGAAGCAGAGAGGTTAGGAAATCATCGCAACAGT... | AAGATCCCATCTCTAAAATAAAATAAAAATTTAAAAAATTGTTTAAAATCCTGTAGAGAGTTCAGAGTGGTTGGAGCAGAGTAATGGAGAATAGTAGACAATGGAGTTAGAGAGGCAATGAGAGGTAAAGGGAAGTGGCTTGAACCTGTAGGGCCTCATAGACTATTGTAAAGATTTTTGCTTTTTAGTGAGTGTTGTTGGAAGCATTACAGGGTTTTGAACAAAGGAATGACATACTTTGGCTTGCATTTAAAAAGGACAGCTCTATGTGCGTGGAGTCAAGGATGGAAGCAGAGAGGTTAGGAAATCATCGCAACAGT... |
Task1_train_40163 | A mutation found on Chromosome 10 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CCAGCCCCAGGTTGCAAGTTCCTGCAGCAGACTATTTGGTCAGTCACTGAGCCTTGTAATCACAACCTCTTGTGGCAAGAAAGGCTTTCAGTAACCAGATACCCTGAATTATGTGATGGCTCCACAAAGGGGTGTGTGACACATTGGGCTGAAGTCAGAGCACAGATTAGGGAGCTGAAGTCCCTCTGGCCTCTGTGGAATTCCACTGAAGTACACCCTGCAGCAATAACTGTATATTGTCTTACCCCCGATGCGTCCCTAAGCTGTGCCCTTCTCTCCAAAATAGCCTTGTAGCCTTTGCTGGATTAGGGTAGCCAACA... | CCAGCCCCAGGTTGCAAGTTCCTGCAGCAGACTATTTGGTCAGTCACTGAGCCTTGTAATCACAACCTCTTGTGGCAAGAAAGGCTTTCAGTAACCAGATACCCTGAATTATGTGATGGCTCCACAAAGGGGTGTGTGACACATTGGGCTGAAGTCAGAGCACAGATTAGGGAGCTGAAGTCCCTCTGGCCTCTGTGGAATTCCACTGAAGTACACCCTGCAGCAATAACTGTATATTGTCTTACCCCCGATGCGTCCCTAAGCTGTGCCCTTCTCTCCAAAATAGCCTTGTAGCCTTTGCTGGATTAGGGTAGCCAACA... |
Task1_train_40164 | Given a variant located on Chromosome 10, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TAATCCCAGCACTTCGGGAGGCTGAGGCAGGTGGATCACCTGAGTTCAGGAGTTGGAGACCAGCCTGGCCAACACAGTGAAATCCTGTCTCTACTAAAAATACAAAAATCAGTCAGGTATAGTGGCAGGTGTCTGTTACTCTTGCTACTCAGGAGGCTGAGACAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCGAGATTGCGCCATTGAGGGACATCTCAAAAAAAAAAAAAAATTAGCTGGGCGTGGTGGCGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAAGAGAATCGCTTGAACC... | TAATCCCAGCACTTCGGGAGGCTGAGGCAGGTGGATCACCTGAGTTCAGGAGTTGGAGACCAGCCTGGCCAACACAGTGAAATCCTGTCTCTACTAAAAATACAAAAATCAGTCAGGTATAGTGGCAGGTGTCTGTTACTCTTGCTACTCAGGAGGCTGAGACAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCGAGATTGCGCCATTGAGGGACATCTCAAAAAAAAAAAAAAATTAGCTGGGCGTGGTGGCGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAAGAGAATCGCTTGAACC... |
Task1_train_40165 | This alteration on Chromosome 10 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGCCTCCTCATGGCTTCCTTCAATCTCCCCCTGCAGCCTCAGATTCTGCACCCAATCCACAGAGACCCAAGAAGGTGACCTGCTGGAACCCAAGCCCCAGGCCCAGAGTGTGGCTCTGTCGCAGCCTCAGTGCATCCACCCCAGCCAACAGGGGCAGGCTGCCCATACTCAGATGGGGATGACTGGCTTCTGGAGCCACTATCTTGGGTCCCACTGATGGTGCATGAGCAAGAAACCGCAACAAGCATTGAGTTGTCAGGTGGAAGAGGGATCCAAGGGAATTGGGAATGGGCAGGTGGGGCTACTGAGCTGGAACTGGG... | TGCCTCCTCATGGCTTCCTTCAATCTCCCCCTGCAGCCTCAGATTCTGCACCCAATCCACAGAGACCCAAGAAGGTGACCTGCTGGAACCCAAGCCCCAGGCCCAGAGTGTGGCTCTGTCGCAGCCTCAGTGCATCCACCCCAGCCAACAGGGGCAGGCTGCCCATACTCAGATGGGGATGACTGGCTTCTGGAGCCACTATCTTGGGTCCCACTGATGGTGCATGAGCAAGAAACCGCAACAAGCATTGAGTTGTCAGGTGGAAGAGGGATCCAAGGGAATTGGGAATGGGCAGGTGGGGCTACTGAGCTGGAACTGGG... |
Task1_train_40166 | A mutation is present on Chromosome 10. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CTTTTTCCTTTTTTTTTTCTTTCTTTGAGACAGAGTTTCGCTCTTATTGTCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGCCTCCTGGATTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGTGATTGCAGGCGTCCACCACCACACCTGGCTAATTTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTTCTGACCTCAAGTGATCCACCTGTCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCCCTGTGCACTT... | CTTTTTCCTTTTTTTTTTCTTTCTTTGAGACAGAGTTTCGCTCTTATTGTCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGCCTCCTGGATTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGTGATTGCAGGCGTCCACCACCACACCTGGCTAATTTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTTCTGACCTCAAGTGATCCACCTGTCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCCCTGTGCACTT... |
Task1_train_40167 | This genomic variant is located on Chromosome 10. Can you determine its pathogenicity and name any linked disease? | Benign | AGGATGCTCTGGGGGTCTGACCCGAGAATGAGAGAGGAGTGTCTGGATATGCGGTCACTGCAGGGCAGAGGGCAGTGTAGTGTGGTGGAGTTGGGGAAGCCCCCAGGACCCAGAGGAGTCCAACAGCCACACTGGTCTGGAGCCATCAGGTGGGGCTGCACCACCCCAGGCAGGAGATGGGGCTTTGGGAAGTGGGACAGGCTCCGGGCTCAGGCCTGCGGAGCTTGGCATGGGGTGAGGCTGCCCCCTGGTGGCCAATGGGTGTGTCACAGCCCAGCCTTGCCAGGGAGCAGGCAGCCAGGCTCCACCCCCAGGAGGCT... | AGGATGCTCTGGGGGTCTGACCCGAGAATGAGAGAGGAGTGTCTGGATATGCGGTCACTGCAGGGCAGAGGGCAGTGTAGTGTGGTGGAGTTGGGGAAGCCCCCAGGACCCAGAGGAGTCCAACAGCCACACTGGTCTGGAGCCATCAGGTGGGGCTGCACCACCCCAGGCAGGAGATGGGGCTTTGGGAAGTGGGACAGGCTCCGGGCTCAGGCCTGCGGAGCTTGGCATGGGGTGAGGCTGCCCCCTGGTGGCCAATGGGTGTGTCACAGCCCAGCCTTGCCAGGGAGCAGGCAGCCAGGCTCCACCCCCAGGAGGCT... |
Task1_train_40168 | Here’s a variant located on Chromosome 10. What is the predicted biological effect — harmless or disease-causing? | Benign | TTTCTTTTCTTTTTTTTTTTTTTTTTTTTAGTAGAGACAAAGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGAACTTAAGTGATTCTCCCACCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGACACCGCTCCTGGCCTCCAAACCTTTTTAACACTTCAAGAGCTGGCCCCTGTCGCCTCATCTCAGATTGTCCCTCCCCCACCTTCAGCTCGAGAAACATGGAGGAACTTGCAGTTCCTTGAGGCTGCCATGGTTTCTGACCTCCAGCCTTACCACATGCTATTCCAAATACCTGCAAATTGTTTCC... | TTTCTTTTCTTTTTTTTTTTTTTTTTTTTAGTAGAGACAAAGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGAACTTAAGTGATTCTCCCACCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGACACCGCTCCTGGCCTCCAAACCTTTTTAACACTTCAAGAGCTGGCCCCTGTCGCCTCATCTCAGATTGTCCCTCCCCCACCTTCAGCTCGAGAAACATGGAGGAACTTGCAGTTCCTTGAGGCTGCCATGGTTTCTGACCTCCAGCCTTACCACATGCTATTCCAAATACCTGCAAATTGTTTCC... |
Task1_train_40169 | Consider a variant on Chromosome 10. Determine its clinical classification and disease relevance. | Benign | AACATGGTGAAACCCCGCCTCCACAAAAAAAAATACAAAAATTAGCCTGGTGTGGTGGCATGTGCCTGTAGTCCCAGCTACTCAGGAGGCTAACGTGGGAGGATCACTTGAGCCCAGGAGGTCGAGGATGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCAACAGAGAGGATCCTGTCTCAAAAATAATTACTAAATAAATAAATAAATAAATAAAAGTAAAATATTAAAGAAAAGAAATTTCTCCTCTCTTTAGAACAATGACTCTCAATCTTGGGTACACATTAAAATACCAATGCCCAGGTCAATTAC... | AACATGGTGAAACCCCGCCTCCACAAAAAAAAATACAAAAATTAGCCTGGTGTGGTGGCATGTGCCTGTAGTCCCAGCTACTCAGGAGGCTAACGTGGGAGGATCACTTGAGCCCAGGAGGTCGAGGATGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCAACAGAGAGGATCCTGTCTCAAAAATAATTACTAAATAAATAAATAAATAAATAAAAGTAAAATATTAAAGAAAAGAAATTTCTCCTCTCTTTAGAACAATGACTCTCAATCTTGGGTACACATTAAAATACCAATGCCCAGGTCAATTAC... |
Task1_train_40170 | A variant found on Chromosome 10 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AGATGATCAATTTAAGATGAGGTCTTGCTGCCGTAAGGCAGGCTCCTAGGCCAATCTGACCAGTGTCCTTATTAAAAGGGGAAATTTGGAGACAGACACACATGGACGGAGAACATCATGTGAACACAAAGGCAGAGATCAGTGTGATGTCGGCAAACCAAGGAGCACCAAGGATTACCAGCAAGCCACCAGAAGCGAGGAGAGAGGCCCGGGACAGATCTCTCCCTAGCGCCTTCAGCCTGCGTGGCCTCACTGACACTTTGATCTTGGGCTTCTGTCCTCCAGAACTGTGAGACAATCAATTTCTGCTGTGTAAGCCA... | AGATGATCAATTTAAGATGAGGTCTTGCTGCCGTAAGGCAGGCTCCTAGGCCAATCTGACCAGTGTCCTTATTAAAAGGGGAAATTTGGAGACAGACACACATGGACGGAGAACATCATGTGAACACAAAGGCAGAGATCAGTGTGATGTCGGCAAACCAAGGAGCACCAAGGATTACCAGCAAGCCACCAGAAGCGAGGAGAGAGGCCCGGGACAGATCTCTCCCTAGCGCCTTCAGCCTGCGTGGCCTCACTGACACTTTGATCTTGGGCTTCTGTCCTCCAGAACTGTGAGACAATCAATTTCTGCTGTGTAAGCCA... |
Task1_train_40171 | A variant found on Chromosome 10 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TTTGCACCAACCTAATATGTTTTAAGATAGTATATTATGAGCAAAGGAGAAAACGTTTAAAATCATGTTTATTTTGTAAACTCCAAAATGCATGTTACATGTGAAGTGACTCACTGGAGGAAGGTGAGTACTTTACCAAGTAGGCACTTGGGAAATGCTGTGTCCACATACTTAGGAAATGGCTTCAGTTAACACTGGGCTTGGGAAGGGCTCTCTTATCCAAGGAGCAGTCTTCTCTGGAGCCATGAAACCAGCCTGGCAGCACTGGTAATAAACTAGTCTGTGAAATCTGGCAAAGCCTCTGTCCTGTTTGGATATAC... | TTTGCACCAACCTAATATGTTTTAAGATAGTATATTATGAGCAAAGGAGAAAACGTTTAAAATCATGTTTATTTTGTAAACTCCAAAATGCATGTTACATGTGAAGTGACTCACTGGAGGAAGGTGAGTACTTTACCAAGTAGGCACTTGGGAAATGCTGTGTCCACATACTTAGGAAATGGCTTCAGTTAACACTGGGCTTGGGAAGGGCTCTCTTATCCAAGGAGCAGTCTTCTCTGGAGCCATGAAACCAGCCTGGCAGCACTGGTAATAAACTAGTCTGTGAAATCTGGCAAAGCCTCTGTCCTGTTTGGATATAC... |
Task1_train_40172 | This sequence change occurs on Chromosome 10. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GCCATCAAATTCTTAAGTGCTTATTCATGGCCAAACAAGAAAGAAGGGGGCAATCAAAACCAGCCACATCACACCATCTCCACAGCTGCCATTTTTAGCTCGGTTTTGCATAGCTTCACCAAAGCTCAGTTTATGTTAGGGCTTTGTTGCCCCAAGAACATTTTAAAAACAAAAAAAGAAGGAAAGGGGAGAATTGAAAGACCCATAAATCCCTGCACCATCAGTTCCAGATGGCCAAGATGCAAAGGATTTTTTCCTTTCCTCCTTCCTACTGAAAAAGTTTTAACACCCTCTAATATGCAGTTAGCTGCACAAGTTCC... | GCCATCAAATTCTTAAGTGCTTATTCATGGCCAAACAAGAAAGAAGGGGGCAATCAAAACCAGCCACATCACACCATCTCCACAGCTGCCATTTTTAGCTCGGTTTTGCATAGCTTCACCAAAGCTCAGTTTATGTTAGGGCTTTGTTGCCCCAAGAACATTTTAAAAACAAAAAAAGAAGGAAAGGGGAGAATTGAAAGACCCATAAATCCCTGCACCATCAGTTCCAGATGGCCAAGATGCAAAGGATTTTTTCCTTTCCTCCTTCCTACTGAAAAAGTTTTAACACCCTCTAATATGCAGTTAGCTGCACAAGTTCC... |
Task1_train_40173 | A mutation has occurred on Chromosome 10. What is the medical relevance of this mutation? | Benign | AGTACAGTATGATCAAAACTGTTGCTGTAATGCTTCCTCCTCTTTTACTTAATGCCTGCTGGGTTCTGAGTTGACAATTTCCTTACCCATTTTCAGTATGTCCCTAATTCATGCTTCATTGGGCATCTTTTATCATAAAGCTCTATTCTCCTGGAATTAATATCCTTGCCATATTTCACAGGGCAGAAACAGCTGAGCTTATAAATAGGCACAGTCCTTTTGAAGGATGGGTTGATCCTACAACAACACACTTTCCTAAGGATGATGACAACTCGCATCACCCCTAGAACGGCTGGTATGAACCGAGTTTCCACACAGTC... | AGTACAGTATGATCAAAACTGTTGCTGTAATGCTTCCTCCTCTTTTACTTAATGCCTGCTGGGTTCTGAGTTGACAATTTCCTTACCCATTTTCAGTATGTCCCTAATTCATGCTTCATTGGGCATCTTTTATCATAAAGCTCTATTCTCCTGGAATTAATATCCTTGCCATATTTCACAGGGCAGAAACAGCTGAGCTTATAAATAGGCACAGTCCTTTTGAAGGATGGGTTGATCCTACAACAACACACTTTCCTAAGGATGATGACAACTCGCATCACCCCTAGAACGGCTGGTATGAACCGAGTTTCCACACAGTC... |
Task1_train_40174 | This variant lies on Chromosome 10. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGATTAAAAATTATCATTCAGAAAAGAATCAGAAATTATTCCCCTCATTCTCATCTGATTTTGTGGGTCTTGATCCAGAGCTTGCCTCTGCCCAAGAAAAGCAGTAAATCCACGAGAGAGAGTGTTCGCAGGTGTGAGGGTGGGAGTAGTGGGAGCCTTTCTGGAGGTGGGACACATACGTGGCTGCCTCCTCAAGCAATTGGGGACATTGTCTCAATCCTGCACAGCCCTGGGGTATGGGGCAGTGGTCCCATTTCAAGCCGACATGAGACTAGGATGGCTCACTGAGGCCTGGAACTGAGCCCTGAGTGCCAACATCA... | AGATTAAAAATTATCATTCAGAAAAGAATCAGAAATTATTCCCCTCATTCTCATCTGATTTTGTGGGTCTTGATCCAGAGCTTGCCTCTGCCCAAGAAAAGCAGTAAATCCACGAGAGAGAGTGTTCGCAGGTGTGAGGGTGGGAGTAGTGGGAGCCTTTCTGGAGGTGGGACACATACGTGGCTGCCTCCTCAAGCAATTGGGGACATTGTCTCAATCCTGCACAGCCCTGGGGTATGGGGCAGTGGTCCCATTTCAAGCCGACATGAGACTAGGATGGCTCACTGAGGCCTGGAACTGAGCCCTGAGTGCCAACATCA... |
Task1_train_40175 | Here is a mutation located on Chromosome 10. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GGAGGATCCTTCTACCCCAAGGCCTCACTGCTGCCATCTGTAAGTGAAGGAACTGGACCAGATGGGGAATAAGGAGGCCTCCATCTCATGCCAAAGGCCAAGGCTAGGAGTGGCTGCCTGGGGTGCAGTGCTGGGATGGTTTGCAAGGGGAGTGTCAAGGCTGGTCAGTGATTATGGGGAAGAGTCAGGGCCCATCAGGGGAATGAAGTGGCTAAGGGTGCCTCCAGCTCTAATAGCCACAAGTGAATTCTGTTGAAAGGGAGTTCTAGCATCTCACAGACCAAGTGGATCCTGGGGATGGAAACTGAAGGCCAGACAGG... | GGAGGATCCTTCTACCCCAAGGCCTCACTGCTGCCATCTGTAAGTGAAGGAACTGGACCAGATGGGGAATAAGGAGGCCTCCATCTCATGCCAAAGGCCAAGGCTAGGAGTGGCTGCCTGGGGTGCAGTGCTGGGATGGTTTGCAAGGGGAGTGTCAAGGCTGGTCAGTGATTATGGGGAAGAGTCAGGGCCCATCAGGGGAATGAAGTGGCTAAGGGTGCCTCCAGCTCTAATAGCCACAAGTGAATTCTGTTGAAAGGGAGTTCTAGCATCTCACAGACCAAGTGGATCCTGGGGATGGAAACTGAAGGCCAGACAGG... |
Task1_train_40176 | Given this context: Chromosome 10 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GAGCTGCGCCCCACCTGCCCCCACCCTGCACTGGCCTGACTCCCCCATTCCACACCTGGCCCAGCACCCACCACATGGTGTGGCAGACAGCACTGGGGCAGCTGAAAGACTCCATGCTACAAATTGGCACTGCCCAGCTTCCTGCTTCTGGGAGTGGGGTCCATTGGCTGAGCTTCCGCTCCCTGGAAGAGCTCCAGACTCCTCAATGGTTTGGGATTTTTCAAACCAATTCCAAATAAGCCAGGGGAGATTTTCCTGTCTTGGTTCCCATCATTACCACCTCCACAGTTGGAGATTCCCTCCTAATCCAGATGCTCAAA... | GAGCTGCGCCCCACCTGCCCCCACCCTGCACTGGCCTGACTCCCCCATTCCACACCTGGCCCAGCACCCACCACATGGTGTGGCAGACAGCACTGGGGCAGCTGAAAGACTCCATGCTACAAATTGGCACTGCCCAGCTTCCTGCTTCTGGGAGTGGGGTCCATTGGCTGAGCTTCCGCTCCCTGGAAGAGCTCCAGACTCCTCAATGGTTTGGGATTTTTCAAACCAATTCCAAATAAGCCAGGGGAGATTTTCCTGTCTTGGTTCCCATCATTACCACCTCCACAGTTGGAGATTCCCTCCTAATCCAGATGCTCAAA... |
Task1_train_40177 | Consider this mutation on Chromosome 10. Is this a benign change or a disease-causing variant? | Benign | TAGGATGGTTTCTATCTCCTGACAGCATGATCCGCCTCCCAGGTTCACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGTCCACCACCGCGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTTCACCTGACAGGGGTTTCACCTGACAGCATGATCCGCCCGCCTCGGCCTCCCAAAGTTCTGGGATTACAGGCATGAGCCACCACGCCCAGCCTTGTTTGCCCCTTTTATGGGGCCATGGTTCATCCAGGTGTCACTGACATCTTTTGAACACAGGTGTCATTTAAAT... | TAGGATGGTTTCTATCTCCTGACAGCATGATCCGCCTCCCAGGTTCACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGTCCACCACCGCGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTTCACCTGACAGGGGTTTCACCTGACAGCATGATCCGCCCGCCTCGGCCTCCCAAAGTTCTGGGATTACAGGCATGAGCCACCACGCCCAGCCTTGTTTGCCCCTTTTATGGGGCCATGGTTCATCCAGGTGTCACTGACATCTTTTGAACACAGGTGTCATTTAAAT... |
Task1_train_40178 | This mutation on Chromosome 10 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TGTGTCCCTGGAGGCCTCTGACTCTTCAGGATTCCAGGGTTAGGGCAAAGTCTGCTTTAAAATACCTCCAGAGCTGCAGGTAGAGCCCAGCAGTGGCTGGAGCCCAGAAGCAGCCTGCCCCCTATTTGAACCAAGAGCACGTCTAAGGTGAGATATCTGATGGCCACATACCAAGGTCAGGCCCCCACCTGCCTTGTACCCCCAGAGCAGAACCCCAGTCCTAGTTCCCAGAACAGTATCTGGTTTCTGGGCTGCCTTGGGATGTGCAGCAGCATCACTGGGGACTCCCATACCTGGCCCCTCTGAGCTAAGAAATGCAG... | TGTGTCCCTGGAGGCCTCTGACTCTTCAGGATTCCAGGGTTAGGGCAAAGTCTGCTTTAAAATACCTCCAGAGCTGCAGGTAGAGCCCAGCAGTGGCTGGAGCCCAGAAGCAGCCTGCCCCCTATTTGAACCAAGAGCACGTCTAAGGTGAGATATCTGATGGCCACATACCAAGGTCAGGCCCCCACCTGCCTTGTACCCCCAGAGCAGAACCCCAGTCCTAGTTCCCAGAACAGTATCTGGTTTCTGGGCTGCCTTGGGATGTGCAGCAGCATCACTGGGGACTCCCATACCTGGCCCCTCTGAGCTAAGAAATGCAG... |
Task1_train_40179 | A mutation has occurred on Chromosome 10. What is the medical relevance of this mutation? | Benign | TGAGCGTGACCGGGGGCCAGAAAGAAGCTATGTGGTTGGAGCTGAGTAGGGGTGGCAGCACCAAATTCAGAGGAGCAGCAGGGGTACAGGGGTACAGGGTGGTCCTGCCGGGACTCATGGGCTGCTGTAAGGTGTGTGATTTGTCCAAGGGAGACGAGCATCCCTGGTGGGACTCCCCCACGGAATATTGCTGAGCAGGAATGCTGAAGGTGCTGAGGAATAAGGAATTGTTCCCCACAAAGGCAGGATCTGGGTCATATTTACCCTCCATGATACGTCGGGGATGTCACCAGAGTGACTCAAGCTTCACCCTCCACCCC... | TGAGCGTGACCGGGGGCCAGAAAGAAGCTATGTGGTTGGAGCTGAGTAGGGGTGGCAGCACCAAATTCAGAGGAGCAGCAGGGGTACAGGGGTACAGGGTGGTCCTGCCGGGACTCATGGGCTGCTGTAAGGTGTGTGATTTGTCCAAGGGAGACGAGCATCCCTGGTGGGACTCCCCCACGGAATATTGCTGAGCAGGAATGCTGAAGGTGCTGAGGAATAAGGAATTGTTCCCCACAAAGGCAGGATCTGGGTCATATTTACCCTCCATGATACGTCGGGGATGTCACCAGAGTGACTCAAGCTTCACCCTCCACCCC... |
Task1_train_40180 | Mutation context: Chromosome 10. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GGTATTGGTGAGGCTGGCCTCGAACTCCTAACGTCAAGTGATAAGGTGGTAAAATTTTGAAGGAAGGCGAAGCTATTTGGGTATACCAATAGATCCTGGAGATTGGAGATTTGTCTTGTCCACAGTGTTGTTTGTTGGTGTCAAATCTGACAACCTATGTCCTGATTTCCCCATATGTACAATGGAGGTGTTGAACTGAAAATTTTCAAAGGTGCATTTCTGTTCTACGATTTAGTGTCTGTGACTAGTTAGAATATAGTTGGAGGAAAGCTTTGGGGACTTCAAATTGGGATCTTGTGGAGCTGGCAGATGCTCCCCTT... | GGTATTGGTGAGGCTGGCCTCGAACTCCTAACGTCAAGTGATAAGGTGGTAAAATTTTGAAGGAAGGCGAAGCTATTTGGGTATACCAATAGATCCTGGAGATTGGAGATTTGTCTTGTCCACAGTGTTGTTTGTTGGTGTCAAATCTGACAACCTATGTCCTGATTTCCCCATATGTACAATGGAGGTGTTGAACTGAAAATTTTCAAAGGTGCATTTCTGTTCTACGATTTAGTGTCTGTGACTAGTTAGAATATAGTTGGAGGAAAGCTTTGGGGACTTCAAATTGGGATCTTGTGGAGCTGGCAGATGCTCCCCTT... |
Task1_train_40181 | The following genetic variant occurs on Chromosome 10. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGTTCACAGCCTAGTGGATATTCTGTATGGGACACCCATGGGGGCACTTCCATAAATACCTTCTGAGGGACAGACTTCATGCTGCCTTCTTCAGATCTGGGAGATGTTCTGTTCCCAGAAAGGGTTCTTTGACAACTTGTGAAGTAGAAATGCTTTCTTTCAGGAACAGGTCTACTGACCTTTATCCTGCAAATACTCACAGTGCAGTTCTTGGTAGGTGCCTGCTATGCATGTCTTGAGTGGCACTGGAGTAGAAAGAAACTAAGATTTTACTCTGAGAAGAGAAGGTGACTCACTAGGGCTGGGGCATTAGCCTGGTG... | AGTTCACAGCCTAGTGGATATTCTGTATGGGACACCCATGGGGGCACTTCCATAAATACCTTCTGAGGGACAGACTTCATGCTGCCTTCTTCAGATCTGGGAGATGTTCTGTTCCCAGAAAGGGTTCTTTGACAACTTGTGAAGTAGAAATGCTTTCTTTCAGGAACAGGTCTACTGACCTTTATCCTGCAAATACTCACAGTGCAGTTCTTGGTAGGTGCCTGCTATGCATGTCTTGAGTGGCACTGGAGTAGAAAGAAACTAAGATTTTACTCTGAGAAGAGAAGGTGACTCACTAGGGCTGGGGCATTAGCCTGGTG... |
Task1_train_40182 | This alteration on Chromosome 10 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGTAGGGCTGTAGGGGGTAAAGGAAAGCCCAGAGTGGCAGCGAGTGGGAAGACAGGGGCTGGAGGCCAACTCCACAGATGACAGCTGTAAGCCATGCAATGTAACCTCACCCTCTGTCCTTCCAACATCTTTTCTCAAATCTACAGTGTTCACTACTGTGTGTGTGCATGCATGTGCATGTGTGAATGTATTCAGTTTAGGGCGAGTAAAGAAATGCCCCACGGATTTATTCTGGGCTTATAAGGAGGTACGCTGAGCACAGTGTCAAAGTGAGGGTACAGGGCAAATATGGAGACCACATGAGAGGACAGCTGACATTG... | TGTAGGGCTGTAGGGGGTAAAGGAAAGCCCAGAGTGGCAGCGAGTGGGAAGACAGGGGCTGGAGGCCAACTCCACAGATGACAGCTGTAAGCCATGCAATGTAACCTCACCCTCTGTCCTTCCAACATCTTTTCTCAAATCTACAGTGTTCACTACTGTGTGTGTGCATGCATGTGCATGTGTGAATGTATTCAGTTTAGGGCGAGTAAAGAAATGCCCCACGGATTTATTCTGGGCTTATAAGGAGGTACGCTGAGCACAGTGTCAAAGTGAGGGTACAGGGCAAATATGGAGACCACATGAGAGGACAGCTGACATTG... |
Task1_train_40183 | Here is a variant on Chromosome 10. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GATTCTACCTGCTGGTATACCCTGATGATATTTGTGGGAAATGCTATCCTGGCTACATTTTTTGTCTCTGTTTCACTGGTGAACCTGACAGGCAGACTTTCTATATTTTCATACATACAAATCATGCTAACAAGATGGTGCTGAGAGCGAAACAAAAGCCTGAAATTTTTTCTTTACTTCTTGTTGAAATTGATTTATTGATTAGAACTTTTAGGCTCATATTTTTAGCTCATATATTTTAGGCTCATATTTCTCATATAACACTAATGAGAATGGAGTAATATTCCCCAAGAATTTCCAAATATGTAGCTGTGCAGTTT... | GATTCTACCTGCTGGTATACCCTGATGATATTTGTGGGAAATGCTATCCTGGCTACATTTTTTGTCTCTGTTTCACTGGTGAACCTGACAGGCAGACTTTCTATATTTTCATACATACAAATCATGCTAACAAGATGGTGCTGAGAGCGAAACAAAAGCCTGAAATTTTTTCTTTACTTCTTGTTGAAATTGATTTATTGATTAGAACTTTTAGGCTCATATTTTTAGCTCATATATTTTAGGCTCATATTTCTCATATAACACTAATGAGAATGGAGTAATATTCCCCAAGAATTTCCAAATATGTAGCTGTGCAGTTT... |
Task1_train_40184 | Given this variant on Chromosome 10, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTAAGAAGCCCACCTGCTCTCCACCACCACAGCCCAGGAACTCTCAACCCCATCGGATGCATTTACACAGGCCATGTGTGTGCGCTGGTGCAGTGCAGGGGCCCCGCCCTCAGTGCCTGGCATACTGCTGCTATCACCTTGAGGAGATCATAAAGTGTTTTTTAATATGCTGATCTTTGCCCTGATATCCCAGCCACCATGACTACTGCAAAATAACACATCATCAGACAGTCTTCTGCCTCCAGGATGAAACACAGTGTTTGGCACTAAGAGGCTGCTTAATGTTTATTGCATTAATGAATAAAAGAAGGAAGAGAGAG... | CTAAGAAGCCCACCTGCTCTCCACCACCACAGCCCAGGAACTCTCAACCCCATCGGATGCATTTACACAGGCCATGTGTGTGCGCTGGTGCAGTGCAGGGGCCCCGCCCTCAGTGCCTGGCATACTGCTGCTATCACCTTGAGGAGATCATAAAGTGTTTTTTAATATGCTGATCTTTGCCCTGATATCCCAGCCACCATGACTACTGCAAAATAACACATCATCAGACAGTCTTCTGCCTCCAGGATGAAACACAGTGTTTGGCACTAAGAGGCTGCTTAATGTTTATTGCATTAATGAATAAAAGAAGGAAGAGAGAG... |
Task1_train_40185 | This variant is found on Chromosome 10. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GACGGGCTCAGAGTGAGGGAGAGAGATGCCGGACTGCTCTGGATGGGGGCTGCAGGGTGGGCCAGCGTAGGCCCAGGCCATCCCACTGAGGAGCTAAGGGGAGGAGGTGGTGCTGAGGGACAGGGCTCAGGGTAGGCTCCAAGGGAAGAGGCAGCACCTGGGCTGGGTTAAGAAGTAGCCTGGAGTTGACCAGAGAGAAAGGCTTGTGTAGGGGGGCTTAAGAGGGGACAACAGGCAGAAGTCAAGCAAGACTTATATAGTTGGGGCAGCCCTACGCCCAAACCCTTCCAGCAGCACCAAAGGCCCACAGGATAAAATCT... | GACGGGCTCAGAGTGAGGGAGAGAGATGCCGGACTGCTCTGGATGGGGGCTGCAGGGTGGGCCAGCGTAGGCCCAGGCCATCCCACTGAGGAGCTAAGGGGAGGAGGTGGTGCTGAGGGACAGGGCTCAGGGTAGGCTCCAAGGGAAGAGGCAGCACCTGGGCTGGGTTAAGAAGTAGCCTGGAGTTGACCAGAGAGAAAGGCTTGTGTAGGGGGGCTTAAGAGGGGACAACAGGCAGAAGTCAAGCAAGACTTATATAGTTGGGGCAGCCCTACGCCCAAACCCTTCCAGCAGCACCAAAGGCCCACAGGATAAAATCT... |
Task1_train_40186 | Located on Chromosome 10, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TCTTCAAAAATTTATCATAGGAAATTCCACATTAATAAATTATCTACTACATTACATGTATGTGTGTGTTTTACACATGTGCATATCTAAATATATATATATGTCCATCTAATTTTAAAATATCTGCTCTTAGGAGTGGTAATAACATTGTGTTTATGTTTTTTAAAACTTCATCTGTTAGACCTCAAACTAAAACATTTACAGGTAAATTGGTGTGAAGCTTTGTATTTGTTTTAAAACACTCCAGTTAAAAAAAAATGTTGAGGGCAAGGACAAGATGAAATAAGCTTGGGAAATGTTAAAACTTGCTGAAGGTGACA... | TCTTCAAAAATTTATCATAGGAAATTCCACATTAATAAATTATCTACTACATTACATGTATGTGTGTGTTTTACACATGTGCATATCTAAATATATATATATGTCCATCTAATTTTAAAATATCTGCTCTTAGGAGTGGTAATAACATTGTGTTTATGTTTTTTAAAACTTCATCTGTTAGACCTCAAACTAAAACATTTACAGGTAAATTGGTGTGAAGCTTTGTATTTGTTTTAAAACACTCCAGTTAAAAAAAAATGTTGAGGGCAAGGACAAGATGAAATAAGCTTGGGAAATGTTAAAACTTGCTGAAGGTGACA... |
Task1_train_40187 | This genomic variant is located on Chromosome 10. Can you determine its pathogenicity and name any linked disease? | Benign | ATCTACTACATTACATGTATGTGTGTGTTTTACACATGTGCATATCTAAATATATATATATGTCCATCTAATTTTAAAATATCTGCTCTTAGGAGTGGTAATAACATTGTGTTTATGTTTTTTAAAACTTCATCTGTTAGACCTCAAACTAAAACATTTACAGGTAAATTGGTGTGAAGCTTTGTATTTGTTTTAAAACACTCCAGTTAAAAAAAAATGTTGAGGGCAAGGACAAGATGAAATAAGCTTGGGAAATGTTAAAACTTGCTGAAGGTGACAGAAGAGGAGGAATGAGATTCTCTCTACTTTTGGCGTGACTA... | ATCTACTACATTACATGTATGTGTGTGTTTTACACATGTGCATATCTAAATATATATATATGTCCATCTAATTTTAAAATATCTGCTCTTAGGAGTGGTAATAACATTGTGTTTATGTTTTTTAAAACTTCATCTGTTAGACCTCAAACTAAAACATTTACAGGTAAATTGGTGTGAAGCTTTGTATTTGTTTTAAAACACTCCAGTTAAAAAAAAATGTTGAGGGCAAGGACAAGATGAAATAAGCTTGGGAAATGTTAAAACTTGCTGAAGGTGACAGAAGAGGAGGAATGAGATTCTCTCTACTTTTGGCGTGACTA... |
Task1_train_40188 | This mutation is located on Chromosome 10. Is it associated with a disease or is it a benign polymorphism? | Benign | CATGTAGGGCCTGGGCAGGCTGGACATGGAGAGAGATTACAAGGTTGCTCTTGCCAATGGAGTTGGAGGCCATGCAGGTGTAATTACCACTGTCTACCAGGTGGGCAGCAGGTATGGCCAGCTCTGACAGAGCAGTGTCTTCTCCAGTAGAAGATGTCAACACTGGGTGGAAAGAAAAACAAAACAGCTGTGCATTTATCTGATAGACTGCTGGAAAGTGTCTAGCAATGCCAGTTTTGTTTTGTTTTGCTTTGTTTTTTGTTATTGTTGTTGTTAGAAGATGGTGGTAACCTCTTATGAACCTCGTACCTGGTGTCAGG... | CATGTAGGGCCTGGGCAGGCTGGACATGGAGAGAGATTACAAGGTTGCTCTTGCCAATGGAGTTGGAGGCCATGCAGGTGTAATTACCACTGTCTACCAGGTGGGCAGCAGGTATGGCCAGCTCTGACAGAGCAGTGTCTTCTCCAGTAGAAGATGTCAACACTGGGTGGAAAGAAAAACAAAACAGCTGTGCATTTATCTGATAGACTGCTGGAAAGTGTCTAGCAATGCCAGTTTTGTTTTGTTTTGCTTTGTTTTTTGTTATTGTTGTTGTTAGAAGATGGTGGTAACCTCTTATGAACCTCGTACCTGGTGTCAGG... |
Task1_train_40189 | Given this context: Chromosome 10 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GACTTGGCACAGGTACCCTGGATGCTCCTCATGCCAGAGATCGGCTTTATAAATAAGGAACAAATTGAGCCTTCTGCTGGGAACATTCACTTTCCCCAGTGCACAGAGACAACATCTCAGTGGTTTCCTAGCTCCAAGAAAAAGCAAACAGCAATTTTCCTTTGAAGTAACTTGATGAGCAACCAGGAAGGCTCCGAGACACCCTCAAGAACCCAGGTAGGTTTTGGTAAGAATCACAAAGGCTGCTGCATGGGACAGAGGTGAATGTGCCAGACAGCACAGAGTGTAATGAGGTCTCTTGGATCCCTCCAGCCTGACAT... | GACTTGGCACAGGTACCCTGGATGCTCCTCATGCCAGAGATCGGCTTTATAAATAAGGAACAAATTGAGCCTTCTGCTGGGAACATTCACTTTCCCCAGTGCACAGAGACAACATCTCAGTGGTTTCCTAGCTCCAAGAAAAAGCAAACAGCAATTTTCCTTTGAAGTAACTTGATGAGCAACCAGGAAGGCTCCGAGACACCCTCAAGAACCCAGGTAGGTTTTGGTAAGAATCACAAAGGCTGCTGCATGGGACAGAGGTGAATGTGCCAGACAGCACAGAGTGTAATGAGGTCTCTTGGATCCCTCCAGCCTGACAT... |
Task1_train_40190 | Consider this mutation on Chromosome 10. Is this a benign change or a disease-causing variant? | Benign | AGTTCCTTTTCCCACCTCCCCCTCACCCCATCTCACCAGTGGTTGCTGCCTTGTGTCATTGGTTAAACGCACTTAATGATACATCTGCAACCCAAGATTCATCAATGCCTGGCTCCAGTGGTGAGCTACCTGGCTTTCGTTTTATCACAATAGGGCCAGAAAGAATGAATGTAAAAGGCAAAGTTAAACAACAGTGAAACTTTCACTTGCCAGACTGACAAAAGTTAAACATTTTGGCCATTTTAATTGTTAGTTCCATGAGTGTATACGTTTTCACCTCTTTTGTTCTCTGCTGTATTCCCAGCACCTAGAATTGGAAG... | AGTTCCTTTTCCCACCTCCCCCTCACCCCATCTCACCAGTGGTTGCTGCCTTGTGTCATTGGTTAAACGCACTTAATGATACATCTGCAACCCAAGATTCATCAATGCCTGGCTCCAGTGGTGAGCTACCTGGCTTTCGTTTTATCACAATAGGGCCAGAAAGAATGAATGTAAAAGGCAAAGTTAAACAACAGTGAAACTTTCACTTGCCAGACTGACAAAAGTTAAACATTTTGGCCATTTTAATTGTTAGTTCCATGAGTGTATACGTTTTCACCTCTTTTGTTCTCTGCTGTATTCCCAGCACCTAGAATTGGAAG... |
Task1_train_40191 | This mutation occurs on Chromosome 10. Does this change lead to a known medical condition, or is it benign? | Benign | AGGTAGTACTAATTTACATTACCACCAGCAGTACCTAAATGTTCCCTTTTCATCACATCTATGCCAATATCTATTGTTTTTTGACTTTTTAATAATAGCCATTCTGGCTGGGATAAGGTGATATCTCATTGTGGTTTTAATTTGCACGTCCCTGATGATTAGTGATGTTGAGCATTTTTTTTTCATGTTTCTTGGTCATTGTATACCTTCTTTTGAAAAATGTTTGTTGATGTTATTTGCCCACTTTTTGATGGGATTATTTTTTTCCTTGCAGATTAGTTGGAGTTCCTTATAGATTCTGGATACTAATCTTTTGTTAG... | AGGTAGTACTAATTTACATTACCACCAGCAGTACCTAAATGTTCCCTTTTCATCACATCTATGCCAATATCTATTGTTTTTTGACTTTTTAATAATAGCCATTCTGGCTGGGATAAGGTGATATCTCATTGTGGTTTTAATTTGCACGTCCCTGATGATTAGTGATGTTGAGCATTTTTTTTTCATGTTTCTTGGTCATTGTATACCTTCTTTTGAAAAATGTTTGTTGATGTTATTTGCCCACTTTTTGATGGGATTATTTTTTTCCTTGCAGATTAGTTGGAGTTCCTTATAGATTCTGGATACTAATCTTTTGTTAG... |
Task1_train_40192 | This sequence change occurs on Chromosome 10. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CATCTTTTTATGCTTTTCACTGATAGCACATGTTTATACCTTTTTTCTTATTGGCAATAGACATATTACAATAAAGTCCATTTTTAAATTGTCACTGATATTTTCAGAAGTCTTAAATTGCTTTAAGAGTTTTAACTTGGAACTAGAATATCTTACCATGTTTGAGGGTGAAAAGGAAAAACAAATCCCCATTCAACCAACCAATTGATCGTGCCTCCTTCCTAATTACTTTTTATTCCCTTTGGTAGATTTTGGTTTGTTTAATATGGTCCTGCTCTATTTTTTCACTAATCTTTCAAGGTTTTTGATCACTTTGGCAC... | CATCTTTTTATGCTTTTCACTGATAGCACATGTTTATACCTTTTTTCTTATTGGCAATAGACATATTACAATAAAGTCCATTTTTAAATTGTCACTGATATTTTCAGAAGTCTTAAATTGCTTTAAGAGTTTTAACTTGGAACTAGAATATCTTACCATGTTTGAGGGTGAAAAGGAAAAACAAATCCCCATTCAACCAACCAATTGATCGTGCCTCCTTCCTAATTACTTTTTATTCCCTTTGGTAGATTTTGGTTTGTTTAATATGGTCCTGCTCTATTTTTTCACTAATCTTTCAAGGTTTTTGATCACTTTGGCAC... |
Task1_train_40193 | A mutation on Chromosome 10 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTCATCAGTACCCCTGGTGGGAACTAGGTTTCTGCTTCACCCTAAACGTAGGGTAGGTTCCTTGAAGGGTGTGCTACAGAGTAGGCACAGTGGATGATAGACTTCAAAGGAATGACAGCAATGGGCAGGGAGGTAACATAGAGTGTCAGAGACGAGGAGATACAAGAGCAGAAATGGATGTAGCAGGGGATTTGAAGACAAAAGAGCCTTTGTGTGGGGAGAATGGTAACTGTGGTCTGTTTAGCTGGTCCCAAGGTTTCCACTGTGCAATTGGTCAAGTTTAGATATTACCCCAGAGGAAGACTAGGGTGCCCCTCCCC... | CTCATCAGTACCCCTGGTGGGAACTAGGTTTCTGCTTCACCCTAAACGTAGGGTAGGTTCCTTGAAGGGTGTGCTACAGAGTAGGCACAGTGGATGATAGACTTCAAAGGAATGACAGCAATGGGCAGGGAGGTAACATAGAGTGTCAGAGACGAGGAGATACAAGAGCAGAAATGGATGTAGCAGGGGATTTGAAGACAAAAGAGCCTTTGTGTGGGGAGAATGGTAACTGTGGTCTGTTTAGCTGGTCCCAAGGTTTCCACTGTGCAATTGGTCAAGTTTAGATATTACCCCAGAGGAAGACTAGGGTGCCCCTCCCC... |
Task1_train_40194 | A mutation located on Chromosome 10 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GGAAGTACAGCTCCCGCTCCCAGTGAGGCTGCTCCCACTTCTCCTGCTCAAACCTGGGGCTCCAGGAGAACTGTTTGTAAAGACTGGGGGAACTTCTGGAAGAGGAGTGATATCTCTGTCCACTCCAGGGCTCCAACACTCCCAGCACTGTGCCAGGACATGGCCCCCACTTAGGATGACCGCTGCCCGGTCGGGCTCCCCTAAACGCAGCCTCTGTGGCAGGCCTAGCCCGAGCAGCCCTCCCTGGAAGCCGTGTGTTCAGCTTCCCTTCTCTCCAGCTCCTGCTGCCTCCTCTAAGACAGGGCAAGGGGCAGGCCCGG... | GGAAGTACAGCTCCCGCTCCCAGTGAGGCTGCTCCCACTTCTCCTGCTCAAACCTGGGGCTCCAGGAGAACTGTTTGTAAAGACTGGGGGAACTTCTGGAAGAGGAGTGATATCTCTGTCCACTCCAGGGCTCCAACACTCCCAGCACTGTGCCAGGACATGGCCCCCACTTAGGATGACCGCTGCCCGGTCGGGCTCCCCTAAACGCAGCCTCTGTGGCAGGCCTAGCCCGAGCAGCCCTCCCTGGAAGCCGTGTGTTCAGCTTCCCTTCTCTCCAGCTCCTGCTGCCTCCTCTAAGACAGGGCAAGGGGCAGGCCCGG... |
Task1_train_40195 | A mutation on Chromosome 10 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CCAGCCCCCTTTGGAACACACAGTTCCTCTTGAGGTCTCCTCCCTCTCTGCATGGGCTGTGGTTACATGACCAGAGGTGCTGCCCATCTCCAGGAATGGGTCCCTGAGAGCTGCCCTTCTAGCCCTTTGTGGCTAGAGTCTGGGGATTGTGACATCTGCAGCAGCACAGATGCATGCTCAACTTCAGAAGTGTTTTTGAGAAGTGAGGGCTATTAAACCCTGGAAGTGTTTAGATAGGAGACCTTCTTGTGGAGGAATGGCCTGGTCCCCCCAGGGCCCTACTGTGGGGTTTCTCTACAATAGCCAGGGCAAGAGAGGGC... | CCAGCCCCCTTTGGAACACACAGTTCCTCTTGAGGTCTCCTCCCTCTCTGCATGGGCTGTGGTTACATGACCAGAGGTGCTGCCCATCTCCAGGAATGGGTCCCTGAGAGCTGCCCTTCTAGCCCTTTGTGGCTAGAGTCTGGGGATTGTGACATCTGCAGCAGCACAGATGCATGCTCAACTTCAGAAGTGTTTTTGAGAAGTGAGGGCTATTAAACCCTGGAAGTGTTTAGATAGGAGACCTTCTTGTGGAGGAATGGCCTGGTCCCCCCAGGGCCCTACTGTGGGGTTTCTCTACAATAGCCAGGGCAAGAGAGGGC... |
Task1_train_40196 | This mutation occurs on Chromosome 10. Does this change lead to a known medical condition, or is it benign? | Benign | ATAACTTTGGAAAGCTAATTAAAGTGAAAATTCTTACTTAGATATTATAAAGTAGAAAGCTCAGGTTATTAATGTAGAAATCACACCAGGGTCATTGTGTCATAAATAAGCAAGATCTTTGTCATTCAGGAATAGTTCAAGCTGAAAGTCAATAAAATCAAACCACATGAAACAATGGGATGGGGGTAAAGTAGAATGATATATATCTTGATACTAATTAGCCTTTTCCCCCGTTATTTATTTAACAATTTTACTTTGAGGCATTTAAAAGTTCACTGTCTATATTAATAATCACCAAACCTTAATTGGAGAGATTATGT... | ATAACTTTGGAAAGCTAATTAAAGTGAAAATTCTTACTTAGATATTATAAAGTAGAAAGCTCAGGTTATTAATGTAGAAATCACACCAGGGTCATTGTGTCATAAATAAGCAAGATCTTTGTCATTCAGGAATAGTTCAAGCTGAAAGTCAATAAAATCAAACCACATGAAACAATGGGATGGGGGTAAAGTAGAATGATATATATCTTGATACTAATTAGCCTTTTCCCCCGTTATTTATTTAACAATTTTACTTTGAGGCATTTAAAAGTTCACTGTCTATATTAATAATCACCAAACCTTAATTGGAGAGATTATGT... |
Task1_train_40197 | A change on Chromosome 10 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AAGACAAAGTTCAAGAGAGGTTGTGATTTACCCCAGGTCAAACATGAGCAGTGTGGCCTGGCATACTGTTCCTTTTAACACCGATGTTTTAGCACATTGAGTGCACAAAACTTAGTGCTAAATAAATTCTGAGGAACAAGTGAAGTAATAACTCCTAGCAAACAATGAGAAGTGCTGATAACCTTGTTAACGCCAACAAGCAACTCACTACGAAGTCCAGTCTGATTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCTCCCAGGCTGGGGTGCAGTGTCACCATCTCAGCTCACTGCAACCTCCGCCTCC... | AAGACAAAGTTCAAGAGAGGTTGTGATTTACCCCAGGTCAAACATGAGCAGTGTGGCCTGGCATACTGTTCCTTTTAACACCGATGTTTTAGCACATTGAGTGCACAAAACTTAGTGCTAAATAAATTCTGAGGAACAAGTGAAGTAATAACTCCTAGCAAACAATGAGAAGTGCTGATAACCTTGTTAACGCCAACAAGCAACTCACTACGAAGTCCAGTCTGATTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCTCCCAGGCTGGGGTGCAGTGTCACCATCTCAGCTCACTGCAACCTCCGCCTCC... |
Task1_train_40198 | A variant was discovered on Chromosome 10. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CGTCCCCTAGTGGTAAGAAAGCAGTGCTGCTTCTGACCCTACCCTCTGCAGCTGCCTTTGTGTGTGTGTGCACGTGTGTTGAGTGAGCATGTGGGTGCATTTGTGAGAATGTGTGGGTGTACATGCGTGTGAATGTACACATGCGTGTGCGGCCCAATAGCAGACAGCACAGGAGCAGTGGGGCGCACCCCAGGGACGGGTGTTGGCTGGGTGAGCTGTCCCAGCACCTGTGACACAGCAAGCTCTGCTTTACGCATTGTACGCTTATTAGTTCATTTAATAGACACAAAATCCATGAGACGGTGTGGAAACTAAGGCCC... | CGTCCCCTAGTGGTAAGAAAGCAGTGCTGCTTCTGACCCTACCCTCTGCAGCTGCCTTTGTGTGTGTGTGCACGTGTGTTGAGTGAGCATGTGGGTGCATTTGTGAGAATGTGTGGGTGTACATGCGTGTGAATGTACACATGCGTGTGCGGCCCAATAGCAGACAGCACAGGAGCAGTGGGGCGCACCCCAGGGACGGGTGTTGGCTGGGTGAGCTGTCCCAGCACCTGTGACACAGCAAGCTCTGCTTTACGCATTGTACGCTTATTAGTTCATTTAATAGACACAAAATCCATGAGACGGTGTGGAAACTAAGGCCC... |
Task1_train_40199 | A variant on Chromosome 10 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TATTAGAGACATGTCAAGATTTAACAACATTAATTTTTACTGCTTCATCAAAGACATTCTTAAGAAATTCAGGCTATGTTTTTTACCTGTAGGGGACAGTGAAGAATAGAAAGACTACTAATGTAATTGGTACCACTGCCTTGATTTATGCTGAGAAACCAGCCATTGTACCCACTTTTGCTTTTATACAATCATGGCAAGTGTCAATAAAAAAGCAGGCAATGACTTTGTATTACTTTCACAAATTTTTAAAATTTTTCATCAGCTTTCTCAGGTTTAATTAGTATGATTCAGAACAGTGTTGGCCAGGCACAGTGGCT... | TATTAGAGACATGTCAAGATTTAACAACATTAATTTTTACTGCTTCATCAAAGACATTCTTAAGAAATTCAGGCTATGTTTTTTACCTGTAGGGGACAGTGAAGAATAGAAAGACTACTAATGTAATTGGTACCACTGCCTTGATTTATGCTGAGAAACCAGCCATTGTACCCACTTTTGCTTTTATACAATCATGGCAAGTGTCAATAAAAAAGCAGGCAATGACTTTGTATTACTTTCACAAATTTTTAAAATTTTTCATCAGCTTTCTCAGGTTTAATTAGTATGATTCAGAACAGTGTTGGCCAGGCACAGTGGCT... |
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