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_33100 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TTCTTTATTTTATGAGCCTTTCCCCCACAAAAATATATTAAGATCATTGAAAAGATTAGTCCAAAAAAGCCAAGTAAAACGAGTTTGGAAAGAGGAAACAGGCTGTTATGAAGAAGACTGAATTTCAGCTTACCAGCAGGCGGGGTAAAGAAGGAAGTCATCTTGGTGAAGAGTTTTTCCATAGACTCTGGTTACAACTACTATTAGATTATTGCTAGTGTTAGACACACAAAAATAATGCCTTAAACAGGACAGATGTTTACTTCTCTCTTATGTTAAAAACAAAACAAAAATCCATCCGGGGTAGCTTGGAAGCCTTT... | TTCTTTATTTTATGAGCCTTTCCCCCACAAAAATATATTAAGATCATTGAAAAGATTAGTCCAAAAAAGCCAAGTAAAACGAGTTTGGAAAGAGGAAACAGGCTGTTATGAAGAAGACTGAATTTCAGCTTACCAGCAGGCGGGGTAAAGAAGGAAGTCATCTTGGTGAAGAGTTTTTCCATAGACTCTGGTTACAACTACTATTAGATTATTGCTAGTGTTAGACACACAAAAATAATGCCTTAAACAGGACAGATGTTTACTTCTCTCTTATGTTAAAAACAAAACAAAAATCCATCCGGGGTAGCTTGGAAGCCTTT... |
Task1_train_33101 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GATTAGTCCAAAAAAGCCAAGTAAAACGAGTTTGGAAAGAGGAAACAGGCTGTTATGAAGAAGACTGAATTTCAGCTTACCAGCAGGCGGGGTAAAGAAGGAAGTCATCTTGGTGAAGAGTTTTTCCATAGACTCTGGTTACAACTACTATTAGATTATTGCTAGTGTTAGACACACAAAAATAATGCCTTAAACAGGACAGATGTTTACTTCTCTCTTATGTTAAAAACAAAACAAAAATCCATCCGGGGTAGCTTGGAAGCCTTTGGTTGTGTGGCACTGAATACACTATTTTGAAGTGGCTATTAGATAGTCAAGTG... | GATTAGTCCAAAAAAGCCAAGTAAAACGAGTTTGGAAAGAGGAAACAGGCTGTTATGAAGAAGACTGAATTTCAGCTTACCAGCAGGCGGGGTAAAGAAGGAAGTCATCTTGGTGAAGAGTTTTTCCATAGACTCTGGTTACAACTACTATTAGATTATTGCTAGTGTTAGACACACAAAAATAATGCCTTAAACAGGACAGATGTTTACTTCTCTCTTATGTTAAAAACAAAACAAAAATCCATCCGGGGTAGCTTGGAAGCCTTTGGTTGTGTGGCACTGAATACACTATTTTGAAGTGGCTATTAGATAGTCAAGTG... |
Task1_train_33102 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CAGGAGTTTGGAAGAAGTTGACTCCAACCCTCATGGATGACTTGGAGGGGCTCAAGACTTCAGTGGAGGAAGTAACTGCAGATGTGGTAGAAATAGCAAGAGAACTAGAATTAGAAGTGGAGCCTGAAGATGAAACTGAATTGCTGCAATTCATGATAAAAGTTGAATGGATGAGGAGTTGCTTATGGATGAGCAAAGAAAGCAGTTTCATGAGATGGAATCTACTCTTGGTGAAGACGCTGTAAGCATTGTTGAAATGACAAGAAATGATTTAGAATATTCCATAAACTTGGTTGATAAAGCAGTGGCAGGATTTGAAG... | CAGGAGTTTGGAAGAAGTTGACTCCAACCCTCATGGATGACTTGGAGGGGCTCAAGACTTCAGTGGAGGAAGTAACTGCAGATGTGGTAGAAATAGCAAGAGAACTAGAATTAGAAGTGGAGCCTGAAGATGAAACTGAATTGCTGCAATTCATGATAAAAGTTGAATGGATGAGGAGTTGCTTATGGATGAGCAAAGAAAGCAGTTTCATGAGATGGAATCTACTCTTGGTGAAGACGCTGTAAGCATTGTTGAAATGACAAGAAATGATTTAGAATATTCCATAAACTTGGTTGATAAAGCAGTGGCAGGATTTGAAG... |
Task1_train_33103 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | AAGATGAGAAGTCCAGGGAGGGAGGGAGTAGCTTGGCAGCAAGCTGTGGAGGGCAGGCTCTGGAGCCAGGTGGGATGGGGAGCCAGAAGACCTTCCCACTCACAGGGACAGGAACACTCAGGCCTGGCTCCCGCTTTAGGCTCGATCCTGGAACTGGGTTGTTAACTAAGGAGATACAAGTGAAACCCCTCTTCCCTAAGCAGCTCCTTCCATAACTGCCTCCAGCACTTCAGGAACAGGAACAAAAAAGGTCAAAGTTATTTACAATAGCAAAGATGCACATACGATACATACATATTTATAGGAAACCAAAGTGACAA... | AAGATGAGAAGTCCAGGGAGGGAGGGAGTAGCTTGGCAGCAAGCTGTGGAGGGCAGGCTCTGGAGCCAGGTGGGATGGGGAGCCAGAAGACCTTCCCACTCACAGGGACAGGAACACTCAGGCCTGGCTCCCGCTTTAGGCTCGATCCTGGAACTGGGTTGTTAACTAAGGAGATACAAGTGAAACCCCTCTTCCCTAAGCAGCTCCTTCCATAACTGCCTCCAGCACTTCAGGAACAGGAACAAAAAAGGTCAAAGTTATTTACAATAGCAAAGATGCACATACGATACATACATATTTATAGGAAACCAAAGTGACAA... |
Task1_train_33104 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGCAGCAAGCTGTGGAGGGCAGGCTCTGGAGCCAGGTGGGATGGGGAGCCAGAAGACCTTCCCACTCACAGGGACAGGAACACTCAGGCCTGGCTCCCGCTTTAGGCTCGATCCTGGAACTGGGTTGTTAACTAAGGAGATACAAGTGAAACCCCTCTTCCCTAAGCAGCTCCTTCCATAACTGCCTCCAGCACTTCAGGAACAGGAACAAAAAAGGTCAAAGTTATTTACAATAGCAAAGATGCACATACGATACATACATATTTATAGGAAACCAAAGTGACAAAGAGGGGAGGGGAGGCACCCACCTCTGCCTGGGG... | GGCAGCAAGCTGTGGAGGGCAGGCTCTGGAGCCAGGTGGGATGGGGAGCCAGAAGACCTTCCCACTCACAGGGACAGGAACACTCAGGCCTGGCTCCCGCTTTAGGCTCGATCCTGGAACTGGGTTGTTAACTAAGGAGATACAAGTGAAACCCCTCTTCCCTAAGCAGCTCCTTCCATAACTGCCTCCAGCACTTCAGGAACAGGAACAAAAAAGGTCAAAGTTATTTACAATAGCAAAGATGCACATACGATACATACATATTTATAGGAAACCAAAGTGACAAAGAGGGGAGGGGAGGCACCCACCTCTGCCTGGGG... |
Task1_train_33105 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACAGGGCCCAAACCCCATGACAAAACCATCCAGTTCCTTATGCTGGAGCAGACAACACTAGCTCTTTGTCTCCCAAAACTGGGCAGGGTGATGGGAAAGCCCCTGGGAGCTCGTCCTTCCTGCAGGGCCAGGGATGGGCCTGTGGCTTTGGGGGCAAGTGAGAAGCAGTTTTCATTGTAGCGCTGGGAACTCTCAGGAGAGAAACTCTGTGGTCCCCACTTTCTTGGCATCTGACATGAAGGAGGGAGACTGAGATGAAGAACTCTCATAGATCCTTTCTCCTGGCCTAGATCCAGCTTGGAAACCCAGGACCTGTGTGC... | ACAGGGCCCAAACCCCATGACAAAACCATCCAGTTCCTTATGCTGGAGCAGACAACACTAGCTCTTTGTCTCCCAAAACTGGGCAGGGTGATGGGAAAGCCCCTGGGAGCTCGTCCTTCCTGCAGGGCCAGGGATGGGCCTGTGGCTTTGGGGGCAAGTGAGAAGCAGTTTTCATTGTAGCGCTGGGAACTCTCAGGAGAGAAACTCTGTGGTCCCCACTTTCTTGGCATCTGACATGAAGGAGGGAGACTGAGATGAAGAACTCTCATAGATCCTTTCTCCTGGCCTAGATCCAGCTTGGAAACCCAGGACCTGTGTGC... |
Task1_train_33106 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TGAGATCCTGCCACTGTGTTCCAGCCTGGGCAACACTGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAGAATAAATAAATGCTATTCCCTCTGCTTAGGCATCTTTTCCCACCTCCTTCACCTGCCCCAGTGTTGTGTCCTCTGGGAAGCCCCAGTTCCTTCTCTGGGCCTGAATGCACAGCACCTAGTGCTTACCTGAATGCCAGCAGCAGTCGCTGGCAGTAATCCCATCTCTGCTCCCCACTAGGTTCTGAGCCTCTTGAGCCTTTCATCTCTGAACCCCCGCACTTAGTAAATAGCTGGTGTTCAATAAATGTT... | TGAGATCCTGCCACTGTGTTCCAGCCTGGGCAACACTGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAGAATAAATAAATGCTATTCCCTCTGCTTAGGCATCTTTTCCCACCTCCTTCACCTGCCCCAGTGTTGTGTCCTCTGGGAAGCCCCAGTTCCTTCTCTGGGCCTGAATGCACAGCACCTAGTGCTTACCTGAATGCCAGCAGCAGTCGCTGGCAGTAATCCCATCTCTGCTCCCCACTAGGTTCTGAGCCTCTTGAGCCTTTCATCTCTGAACCCCCGCACTTAGTAAATAGCTGGTGTTCAATAAATGTT... |
Task1_train_33107 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CCCCCTTACTTGAGGAAGAATAAGCCCTTTTGTTACATTCAGGCCTTCAACAGACTGGACGGGGTCCACCCACATTAGGGTGGAGTTTGTTCTGCCACTGTGCAGTTATCATTCTGGGATGGGGGTACCTTACTCTCCCAATGAGAAATTCTAAATTTCCTCTTTTGAGCCTGGTGCCTCCACCTTCTCAGAACTGCATAGGGCGTGAGCTTTGTTGGTGATGTGACCTCCAGAACAGACTGTGAGCAGATTTTTTTCTTTAATCCTGAGCCTATGCTTGCTGCTGTCCTTCTTGACTTTCAACTAGGCCTAAAAAAGCG... | CCCCCTTACTTGAGGAAGAATAAGCCCTTTTGTTACATTCAGGCCTTCAACAGACTGGACGGGGTCCACCCACATTAGGGTGGAGTTTGTTCTGCCACTGTGCAGTTATCATTCTGGGATGGGGGTACCTTACTCTCCCAATGAGAAATTCTAAATTTCCTCTTTTGAGCCTGGTGCCTCCACCTTCTCAGAACTGCATAGGGCGTGAGCTTTGTTGGTGATGTGACCTCCAGAACAGACTGTGAGCAGATTTTTTTCTTTAATCCTGAGCCTATGCTTGCTGCTGTCCTTCTTGACTTTCAACTAGGCCTAAAAAAGCG... |
Task1_train_33108 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TTTCTATTCTGTGACCATAATTCTCACAGTTGATTAGCCTTTGTTTCTATATCTAAATCAGTGGTTTCCAATCTTGTCTACACAATATTCTCACTTGAGGTTGTGTCAAAAAATACTGATTCTGTGGCCCCATCTGTGAGATTCTGAATTGAATTAGTCTGGAGAGGGGCTTTGACGAGTCAATGTGTGACCTTTTACAAAGGTCTTTGACGAGTCTAATATGCAGCCAGGGTTGAGAGCCAGTCATAATGCGGTTTCCTCATTATGAGTCCTTTATATTCATTTACATCTTGTTGGGCTAGATTTTGTCATTAGGTGTT... | TTTCTATTCTGTGACCATAATTCTCACAGTTGATTAGCCTTTGTTTCTATATCTAAATCAGTGGTTTCCAATCTTGTCTACACAATATTCTCACTTGAGGTTGTGTCAAAAAATACTGATTCTGTGGCCCCATCTGTGAGATTCTGAATTGAATTAGTCTGGAGAGGGGCTTTGACGAGTCAATGTGTGACCTTTTACAAAGGTCTTTGACGAGTCTAATATGCAGCCAGGGTTGAGAGCCAGTCATAATGCGGTTTCCTCATTATGAGTCCTTTATATTCATTTACATCTTGTTGGGCTAGATTTTGTCATTAGGTGTT... |
Task1_train_33109 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCTGTGATAATTGTGTTAACTGCACAAATTGTTTAAACAATATGAAATCTGGGCACCTTGAAAAAAGAACAGGATAACAGCAATGTTCAGGGAACAAGGGAGATAACCTTAAACTCTGGCTGCCTGTGAGCTGGGTGGAACAGAGTCATATTTTTCTTCTTTCTAAATCAAATAGGAGAGATATCACTGAATTCTTTTTCTCAGCAAGGAACATCCCTGAGAAAGAGAATATGTCCCTAAGGGGAGGCCTCTGAAATGGCCGCTTTGGGGATGGCTGTCTTTTATGATCGTTGCTGAGGGATGAAATAAGCTCTGGTCTC... | CCTGTGATAATTGTGTTAACTGCACAAATTGTTTAAACAATATGAAATCTGGGCACCTTGAAAAAAGAACAGGATAACAGCAATGTTCAGGGAACAAGGGAGATAACCTTAAACTCTGGCTGCCTGTGAGCTGGGTGGAACAGAGTCATATTTTTCTTCTTTCTAAATCAAATAGGAGAGATATCACTGAATTCTTTTTCTCAGCAAGGAACATCCCTGAGAAAGAGAATATGTCCCTAAGGGGAGGCCTCTGAAATGGCCGCTTTGGGGATGGCTGTCTTTTATGATCGTTGCTGAGGGATGAAATAAGCTCTGGTCTC... |
Task1_train_33110 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCAGCTACCTGAATAGCTCTGAGGGCATTAAGCCAAGCAAGTAGAGGTGAAGCTATCTCCTGGCCTGCCCCCAGCCCACCATTGCCCGTGCCTTTCTTACCTACTGCCCATCAACTCTAAAAAAGGCTTGAGCAAGAAGGACATGCTGGGTTAACTATGATCCAGCGACTTGTCTTTGTGTCTTACATGTCTTTGCCTTTGGTTTATTGATTAATGTCTGATATTAACAGAACAGGAGATACCTCTGTGCTCCTGGAAATTGAGTCTGTGTCTACTGAGAATAATATAGTGAATGAAAATCAGTCATCTGGGGAGCCACA... | GCAGCTACCTGAATAGCTCTGAGGGCATTAAGCCAAGCAAGTAGAGGTGAAGCTATCTCCTGGCCTGCCCCCAGCCCACCATTGCCCGTGCCTTTCTTACCTACTGCCCATCAACTCTAAAAAAGGCTTGAGCAAGAAGGACATGCTGGGTTAACTATGATCCAGCGACTTGTCTTTGTGTCTTACATGTCTTTGCCTTTGGTTTATTGATTAATGTCTGATATTAACAGAACAGGAGATACCTCTGTGCTCCTGGAAATTGAGTCTGTGTCTACTGAGAATAATATAGTGAATGAAAATCAGTCATCTGGGGAGCCACA... |
Task1_train_33111 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACCTGAATAGCTCTGAGGGCATTAAGCCAAGCAAGTAGAGGTGAAGCTATCTCCTGGCCTGCCCCCAGCCCACCATTGCCCGTGCCTTTCTTACCTACTGCCCATCAACTCTAAAAAAGGCTTGAGCAAGAAGGACATGCTGGGTTAACTATGATCCAGCGACTTGTCTTTGTGTCTTACATGTCTTTGCCTTTGGTTTATTGATTAATGTCTGATATTAACAGAACAGGAGATACCTCTGTGCTCCTGGAAATTGAGTCTGTGTCTACTGAGAATAATATAGTGAATGAAAATCAGTCATCTGGGGAGCCACAGGACAA... | ACCTGAATAGCTCTGAGGGCATTAAGCCAAGCAAGTAGAGGTGAAGCTATCTCCTGGCCTGCCCCCAGCCCACCATTGCCCGTGCCTTTCTTACCTACTGCCCATCAACTCTAAAAAAGGCTTGAGCAAGAAGGACATGCTGGGTTAACTATGATCCAGCGACTTGTCTTTGTGTCTTACATGTCTTTGCCTTTGGTTTATTGATTAATGTCTGATATTAACAGAACAGGAGATACCTCTGTGCTCCTGGAAATTGAGTCTGTGTCTACTGAGAATAATATAGTGAATGAAAATCAGTCATCTGGGGAGCCACAGGACAA... |
Task1_train_33112 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | TGGATCTGTAGCGAGGGACTGTGCTTGTGGATGTTACCCCTCACTGTTTCAGCACCACACCAATAGGATCCTGAGTTTTCTCTCCAGACGGTTGGGAGCTGGAGTTCCGGGTACGTGCTCCAGTCTGACAGGATGACCTCGCCATCTCTGAAGAAGTTGAAGTGAAGTGGGGTGTCTGACCGCTCTGGAGGAAGCTGTGTTTCACAGCTCAGGTTTACAGAATTCCCCTCTGTAGGCTGAGAGTCTGTAGCTTTCAGCTCTGGATGTGGAAATAGTTCTAGAGAGAAGAGGTAAGTCAAGTTCTGAGCACGAGAGTATTT... | TGGATCTGTAGCGAGGGACTGTGCTTGTGGATGTTACCCCTCACTGTTTCAGCACCACACCAATAGGATCCTGAGTTTTCTCTCCAGACGGTTGGGAGCTGGAGTTCCGGGTACGTGCTCCAGTCTGACAGGATGACCTCGCCATCTCTGAAGAAGTTGAAGTGAAGTGGGGTGTCTGACCGCTCTGGAGGAAGCTGTGTTTCACAGCTCAGGTTTACAGAATTCCCCTCTGTAGGCTGAGAGTCTGTAGCTTTCAGCTCTGGATGTGGAAATAGTTCTAGAGAGAAGAGGTAAGTCAAGTTCTGAGCACGAGAGTATTT... |
Task1_train_33113 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | CACAGGGCTAAGTGTTACAAAGACATGGAAAATCTTGAACTTTGTTCTTTCTTGGGTTCAGAATCTAGAAAATGGATAAACAATGATAAGAGATGACAGGTCCCTTAGAGAAAGTTCACTATAAGGCACAAAGGGGCTTGGCAAGGTAATTCCAAATCAGCAGCAGGGTTAGAAAGGAGGAGAGCCTCCATATACAGCCTGGTGGTTGGTACCCAAAACCGGTTTACATATTTTCACCATAGAGAAAAAAACAGCAGAATGTATCACATAGAAGACAGAGACATTTGCCTCCTCCCTCTTCAAGGGACCTTAAAATTTTA... | CACAGGGCTAAGTGTTACAAAGACATGGAAAATCTTGAACTTTGTTCTTTCTTGGGTTCAGAATCTAGAAAATGGATAAACAATGATAAGAGATGACAGGTCCCTTAGAGAAAGTTCACTATAAGGCACAAAGGGGCTTGGCAAGGTAATTCCAAATCAGCAGCAGGGTTAGAAAGGAGGAGAGCCTCCATATACAGCCTGGTGGTTGGTACCCAAAACCGGTTTACATATTTTCACCATAGAGAAAAAAACAGCAGAATGTATCACATAGAAGACAGAGACATTTGCCTCCTCCCTCTTCAAGGGACCTTAAAATTTTA... |
Task1_train_33114 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TCTCCATAAATCCAATGTTTTCTGGTCACATTTTATATGCATTTATCTCTAAGGAATCTTTGATGCATCAATAAACCACAAAATAAAAGAGAACACTGGAGATCCTCTGTTTTGAAGATCAAAATAGAATCCAAACCCTTCTCCTATTCTTCAAGACTTCTCCAGATTTACATCCATGTCTCCATGTCTTTCTCTGACTATTACAGTTCATATTCATCTTCCCCTTTTCGGACTATTTTGTTGTGAGTTCAGGTTACCAAATGGAAGCACCACAGGGGCCTCTTAAAACTGCATGTGTTCAGTTGTGCTTCTAGTTGTCT... | TCTCCATAAATCCAATGTTTTCTGGTCACATTTTATATGCATTTATCTCTAAGGAATCTTTGATGCATCAATAAACCACAAAATAAAAGAGAACACTGGAGATCCTCTGTTTTGAAGATCAAAATAGAATCCAAACCCTTCTCCTATTCTTCAAGACTTCTCCAGATTTACATCCATGTCTCCATGTCTTTCTCTGACTATTACAGTTCATATTCATCTTCCCCTTTTCGGACTATTTTGTTGTGAGTTCAGGTTACCAAATGGAAGCACCACAGGGGCCTCTTAAAACTGCATGTGTTCAGTTGTGCTTCTAGTTGTCT... |
Task1_train_33115 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | TCCAGCACCTCTCCAGCACAGAAAGAGTATTGAAAATAAATGTAGATATTCTACTCAGGAAACAAGGAAACTTTTTATCTTTCTTTTAACTTAGAATTTAGAAATGATAATAAGATGAAACTAGGTTTGGACCTTTTTCAATAATTCTGACCACCGTTCAGTAAATTTACTGTATAAGAAAAGTAGAGGTTTGGGGTTGAATTTTGTTTTATTTTTTCCCAAAGATGTCTATCTCTGATATCTTAGGGCCTGGCAATTGTTTTTGGTCATAGGTGGGCTCTGAATAAATGTCAGTTGAACAAATATATAAAAACCAAACA... | TCCAGCACCTCTCCAGCACAGAAAGAGTATTGAAAATAAATGTAGATATTCTACTCAGGAAACAAGGAAACTTTTTATCTTTCTTTTAACTTAGAATTTAGAAATGATAATAAGATGAAACTAGGTTTGGACCTTTTTCAATAATTCTGACCACCGTTCAGTAAATTTACTGTATAAGAAAAGTAGAGGTTTGGGGTTGAATTTTGTTTTATTTTTTCCCAAAGATGTCTATCTCTGATATCTTAGGGCCTGGCAATTGTTTTTGGTCATAGGTGGGCTCTGAATAAATGTCAGTTGAACAAATATATAAAAACCAAACA... |
Task1_train_33116 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | AAGTAGAATAAATAGAATAATAAATACAACTGTTAGAAGTGGTTTTGAGCACAACCCCCAACCCCCACCCCAACTTGTAGGGGCAGAAATATGCAGGCACAATGGAAAGTAATCTGTTAAACATTAAGTGTTCATTGTGCCATGAAAATCAGTCAGGGTGCTTTACAGAGGGAAGAGAGCATGCTGTTTAGTTTGTTATATAAAAATATTTTGGCCAGGGGCGGTGGCTCACTCCTGTAATTCCAGCGCTTGGAGAGGGTGAGGCAGGCAGATCTCTTGAGGACAGGAGTTTGAAACCAGCCTAGCCAACATGGTGAAAC... | AAGTAGAATAAATAGAATAATAAATACAACTGTTAGAAGTGGTTTTGAGCACAACCCCCAACCCCCACCCCAACTTGTAGGGGCAGAAATATGCAGGCACAATGGAAAGTAATCTGTTAAACATTAAGTGTTCATTGTGCCATGAAAATCAGTCAGGGTGCTTTACAGAGGGAAGAGAGCATGCTGTTTAGTTTGTTATATAAAAATATTTTGGCCAGGGGCGGTGGCTCACTCCTGTAATTCCAGCGCTTGGAGAGGGTGAGGCAGGCAGATCTCTTGAGGACAGGAGTTTGAAACCAGCCTAGCCAACATGGTGAAAC... |
Task1_train_33117 | An alteration has been detected on Chromosome 1. Is it pathogenic, and if so, what disease is involved? | Benign | GGTGGAGGCTGCAGTGAGCCAAGATGGAGCCACTGCACTCCAGCCTGGGTGACGGGAGTGAAACCCTGTCTCAAAAGAAATTTACATGTAATTTTTACAGTCATACAAATAATGATATTTCAGCTTTTCATTTGTGAGATGTAACATAATTTTAACAAATCAGCACATTTTAATTCTAGTATGGATTAGTCTCTGGGCAGAACAAGGATCTCATTAACAGTAATTGACTTCCTCAACTAGAATCCAAGCACTGTGAGAATGAGATAGTTCACATATTTACTCAAAAAGAAATCTTAGTTGTCCAGATGAAAAAATTCAAG... | GGTGGAGGCTGCAGTGAGCCAAGATGGAGCCACTGCACTCCAGCCTGGGTGACGGGAGTGAAACCCTGTCTCAAAAGAAATTTACATGTAATTTTTACAGTCATACAAATAATGATATTTCAGCTTTTCATTTGTGAGATGTAACATAATTTTAACAAATCAGCACATTTTAATTCTAGTATGGATTAGTCTCTGGGCAGAACAAGGATCTCATTAACAGTAATTGACTTCCTCAACTAGAATCCAAGCACTGTGAGAATGAGATAGTTCACATATTTACTCAAAAAGAAATCTTAGTTGTCCAGATGAAAAAATTCAAG... |
Task1_train_33118 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCAGTGAGCCAAGATGGAGCCACTGCACTCCAGCCTGGGTGACGGGAGTGAAACCCTGTCTCAAAAGAAATTTACATGTAATTTTTACAGTCATACAAATAATGATATTTCAGCTTTTCATTTGTGAGATGTAACATAATTTTAACAAATCAGCACATTTTAATTCTAGTATGGATTAGTCTCTGGGCAGAACAAGGATCTCATTAACAGTAATTGACTTCCTCAACTAGAATCCAAGCACTGTGAGAATGAGATAGTTCACATATTTACTCAAAAAGAAATCTTAGTTGTCCAGATGAAAAAATTCAAGGCTTATCGGT... | GCAGTGAGCCAAGATGGAGCCACTGCACTCCAGCCTGGGTGACGGGAGTGAAACCCTGTCTCAAAAGAAATTTACATGTAATTTTTACAGTCATACAAATAATGATATTTCAGCTTTTCATTTGTGAGATGTAACATAATTTTAACAAATCAGCACATTTTAATTCTAGTATGGATTAGTCTCTGGGCAGAACAAGGATCTCATTAACAGTAATTGACTTCCTCAACTAGAATCCAAGCACTGTGAGAATGAGATAGTTCACATATTTACTCAAAAAGAAATCTTAGTTGTCCAGATGAAAAAATTCAAGGCTTATCGGT... |
Task1_train_33119 | A mutation is present on Chromosome 1. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ACAGCAACAAAATTCTGGTAGCAGATGCCAATAATTTCCCAAGACAAAATGATGTAGTAACTTCAGAAGTATATAAATGAAGACTGGATACCAGCAAGACATACTGGATGATTTTGTATCCAGATAGTGCTTTTTTTACTTATTAGGTTGGGTTATTGAAAAATGTTCCAGTGAAAAAAATTAGGCCTAAGATGATTTTAGAAATAATTTGTAATGGCAGTTTGCAAAATATTTTTAGTGGCAGAATGTTCAAAAGAAATCTTATTAACATAACAACATACAAAAGATACAAAGCCTATGGTTTACAGCAGGAGAGGGGA... | ACAGCAACAAAATTCTGGTAGCAGATGCCAATAATTTCCCAAGACAAAATGATGTAGTAACTTCAGAAGTATATAAATGAAGACTGGATACCAGCAAGACATACTGGATGATTTTGTATCCAGATAGTGCTTTTTTTACTTATTAGGTTGGGTTATTGAAAAATGTTCCAGTGAAAAAAATTAGGCCTAAGATGATTTTAGAAATAATTTGTAATGGCAGTTTGCAAAATATTTTTAGTGGCAGAATGTTCAAAAGAAATCTTATTAACATAACAACATACAAAAGATACAAAGCCTATGGTTTACAGCAGGAGAGGGGA... |
Task1_train_33120 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | CTTGTCTTCTCTTATACTAAGATTTAATTAACTGTTACTAGAAAATCAAAGGTATACTACATTGCTTTGACTATTTACTGCAGAAAAAAACTATTGTAAGTTTCAAACCCCAATTTTCATTTTTTCATAAACCATACACAAAGTTTTTCCTAAAAGCAGTTTATGTATCAGAATTCAATGACTCTACAATGGACCATGTTTTATTTAAGGCATGCTGGACTCCATGTGTGTCTATAGATGAAGATGATGGGTAAGGAAAGAAGGAAGGTGATAAGGATAATTCTAGTCACTTCAGAAAATACTTATTCTGCATATAAATA... | CTTGTCTTCTCTTATACTAAGATTTAATTAACTGTTACTAGAAAATCAAAGGTATACTACATTGCTTTGACTATTTACTGCAGAAAAAAACTATTGTAAGTTTCAAACCCCAATTTTCATTTTTTCATAAACCATACACAAAGTTTTTCCTAAAAGCAGTTTATGTATCAGAATTCAATGACTCTACAATGGACCATGTTTTATTTAAGGCATGCTGGACTCCATGTGTGTCTATAGATGAAGATGATGGGTAAGGAAAGAAGGAAGGTGATAAGGATAATTCTAGTCACTTCAGAAAATACTTATTCTGCATATAAATA... |
Task1_train_33121 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GACTATTTACTGCAGAAAAAAACTATTGTAAGTTTCAAACCCCAATTTTCATTTTTTCATAAACCATACACAAAGTTTTTCCTAAAAGCAGTTTATGTATCAGAATTCAATGACTCTACAATGGACCATGTTTTATTTAAGGCATGCTGGACTCCATGTGTGTCTATAGATGAAGATGATGGGTAAGGAAAGAAGGAAGGTGATAAGGATAATTCTAGTCACTTCAGAAAATACTTATTCTGCATATAAATACAGATAATTAGTCATAATCTGTTTGCTCATTTTTCTTGAATGTCTACATTATTGCTGTTCAAAGTGGG... | GACTATTTACTGCAGAAAAAAACTATTGTAAGTTTCAAACCCCAATTTTCATTTTTTCATAAACCATACACAAAGTTTTTCCTAAAAGCAGTTTATGTATCAGAATTCAATGACTCTACAATGGACCATGTTTTATTTAAGGCATGCTGGACTCCATGTGTGTCTATAGATGAAGATGATGGGTAAGGAAAGAAGGAAGGTGATAAGGATAATTCTAGTCACTTCAGAAAATACTTATTCTGCATATAAATACAGATAATTAGTCATAATCTGTTTGCTCATTTTTCTTGAATGTCTACATTATTGCTGTTCAAAGTGGG... |
Task1_train_33122 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TTGTCATAAAGCAAGTGCCCATATGGGTATGAGTCTTTGGGTATTTTCAGCTTCCATTTACTCACTTATTTCTGGCAACTAGCAATCCCCGCCACAGTCACTATATCAGGCACAAGCAGGCTAATTGGTCCAAATTTAGGTTCAGGATCTTGAGTCTAGACTTGACGTAACATCCTCTGCATCCATAATAAGGGAGTAAATAGTATTTATTTTTGAGACTTTTAGCTTCCCTAGATTGAATAACCAATTGTCGGGAGTGGAACCAAAGCAAAAGAAAATGCTTGCCACTAAGGAATGGCTGCAGATTGAAGGTAGCAGAG... | TTGTCATAAAGCAAGTGCCCATATGGGTATGAGTCTTTGGGTATTTTCAGCTTCCATTTACTCACTTATTTCTGGCAACTAGCAATCCCCGCCACAGTCACTATATCAGGCACAAGCAGGCTAATTGGTCCAAATTTAGGTTCAGGATCTTGAGTCTAGACTTGACGTAACATCCTCTGCATCCATAATAAGGGAGTAAATAGTATTTATTTTTGAGACTTTTAGCTTCCCTAGATTGAATAACCAATTGTCGGGAGTGGAACCAAAGCAAAAGAAAATGCTTGCCACTAAGGAATGGCTGCAGATTGAAGGTAGCAGAG... |
Task1_train_33123 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | TAAACCTTGTTCAGGCCTCATTTTATGCCTGAAGCTTTTCAAACCACTGCTTAAACTTATCTTCTACCCTCTAACCTGTATCCTTAGCACAAATATATGTATCATTGTATTACTGTCTGGCATTATCCAAGTGCTCTGAATAGCTCTGAATTTTCTGTATTACTGAATGACAGAAAAAGCATGAATTTTTTCAAACAGCAAGTGATCAAATATACTTTTATACTTAAAATACATTACAGATTTTGGGTCAGCAGATAGTACTTCTAAAGAGGTTTGTCTTGAGCAAACATAAAAATGAATTTTTCATTCCCAAATACAAG... | TAAACCTTGTTCAGGCCTCATTTTATGCCTGAAGCTTTTCAAACCACTGCTTAAACTTATCTTCTACCCTCTAACCTGTATCCTTAGCACAAATATATGTATCATTGTATTACTGTCTGGCATTATCCAAGTGCTCTGAATAGCTCTGAATTTTCTGTATTACTGAATGACAGAAAAAGCATGAATTTTTTCAAACAGCAAGTGATCAAATATACTTTTATACTTAAAATACATTACAGATTTTGGGTCAGCAGATAGTACTTCTAAAGAGGTTTGTCTTGAGCAAACATAAAAATGAATTTTTCATTCCCAAATACAAG... |
Task1_train_33124 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ACTTATCTTCTACCCTCTAACCTGTATCCTTAGCACAAATATATGTATCATTGTATTACTGTCTGGCATTATCCAAGTGCTCTGAATAGCTCTGAATTTTCTGTATTACTGAATGACAGAAAAAGCATGAATTTTTTCAAACAGCAAGTGATCAAATATACTTTTATACTTAAAATACATTACAGATTTTGGGTCAGCAGATAGTACTTCTAAAGAGGTTTGTCTTGAGCAAACATAAAAATGAATTTTTCATTCCCAAATACAAGAATTAAAAAGAAGAAAACTGGCCCAAATGGAGGGAGGATTTCAAAGGTATTAAA... | ACTTATCTTCTACCCTCTAACCTGTATCCTTAGCACAAATATATGTATCATTGTATTACTGTCTGGCATTATCCAAGTGCTCTGAATAGCTCTGAATTTTCTGTATTACTGAATGACAGAAAAAGCATGAATTTTTTCAAACAGCAAGTGATCAAATATACTTTTATACTTAAAATACATTACAGATTTTGGGTCAGCAGATAGTACTTCTAAAGAGGTTTGTCTTGAGCAAACATAAAAATGAATTTTTCATTCCCAAATACAAGAATTAAAAAGAAGAAAACTGGCCCAAATGGAGGGAGGATTTCAAAGGTATTAAA... |
Task1_train_33125 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | CAAAAAAAATTAACTGAATGATAAAAGAAATGACAAAATTTGCAAAATGCAGCTAAAGCTTTGCTTTGGGAAAAATTATATATTTAAAATCGATATGTTAGAAAAGATGAAAGGCTAAAATTTTGATAATCTAATTGTACATCTCAAGAAATTAAAAGAAAACATTAAAGTAATTCCAAATAAAGTAAAAAAAGATAATAATATATAAAGCTTTTAATGGAATAGAATACACAAAAACCCAGAGAAAAATTAAAAAGCTGAATGTTGGTTGTCTAAAAAAAAATTGATGAAAACCCAGTAGCAAGATTCATGAGAGAGAG... | CAAAAAAAATTAACTGAATGATAAAAGAAATGACAAAATTTGCAAAATGCAGCTAAAGCTTTGCTTTGGGAAAAATTATATATTTAAAATCGATATGTTAGAAAAGATGAAAGGCTAAAATTTTGATAATCTAATTGTACATCTCAAGAAATTAAAAGAAAACATTAAAGTAATTCCAAATAAAGTAAAAAAAGATAATAATATATAAAGCTTTTAATGGAATAGAATACACAAAAACCCAGAGAAAAATTAAAAAGCTGAATGTTGGTTGTCTAAAAAAAAATTGATGAAAACCCAGTAGCAAGATTCATGAGAGAGAG... |
Task1_train_33126 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | AAAATGTAAAACATCATTATCCATTAAGGAAATGCACATATGAGCTACAATGAGGTATCACTATATATCTATGTGAATGACTAAAATAAAAGTAGTGACAACACAGAATGCTAGCAGGGATATAGGGAAACTGCAAACTGCATCATTTATGCATTGTTGTTAAGAGTGCAAAATGATATAGCCATACAAACAGGAAAGGAATTTGGCTTTTTTTTTTTTTTTGGTCCAAAACTAAATAGGCAGTTACTATATGGTTCAGTGATTGGGGTCCTGTACATTTATCCCAGAGAAATAGACTTATGTTTGCATTAAAATCTGTG... | AAAATGTAAAACATCATTATCCATTAAGGAAATGCACATATGAGCTACAATGAGGTATCACTATATATCTATGTGAATGACTAAAATAAAAGTAGTGACAACACAGAATGCTAGCAGGGATATAGGGAAACTGCAAACTGCATCATTTATGCATTGTTGTTAAGAGTGCAAAATGATATAGCCATACAAACAGGAAAGGAATTTGGCTTTTTTTTTTTTTTTGGTCCAAAACTAAATAGGCAGTTACTATATGGTTCAGTGATTGGGGTCCTGTACATTTATCCCAGAGAAATAGACTTATGTTTGCATTAAAATCTGTG... |
Task1_train_33127 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CCTGAGCAAAGTATCTAGCCCATCCTACCCTCCAGATTATTTATAAACTCCACGGGACTTTGTGAGGGTCCTGAAAGTCCAGGGAGAATGATGAAAGCTGCAAGAAGATTTGCTATGCTAAACTTTCCCAAGTATTTGCAAATATATCAGTACTTGCACTAGTCTACTCTCCCTAATCTGCTTTTTCGTCTATTCATGGTCACAGAGTGACCCTGCTGCCAAGTCAGACCCAGAGTTGCCTTCTTCCCAGATGGCTCAAGTACAGTTTTCCCAGATGTCCCAACCTGCATCCCAATTGTCAATCATTCCCCAGGAGTGTT... | CCTGAGCAAAGTATCTAGCCCATCCTACCCTCCAGATTATTTATAAACTCCACGGGACTTTGTGAGGGTCCTGAAAGTCCAGGGAGAATGATGAAAGCTGCAAGAAGATTTGCTATGCTAAACTTTCCCAAGTATTTGCAAATATATCAGTACTTGCACTAGTCTACTCTCCCTAATCTGCTTTTTCGTCTATTCATGGTCACAGAGTGACCCTGCTGCCAAGTCAGACCCAGAGTTGCCTTCTTCCCAGATGGCTCAAGTACAGTTTTCCCAGATGTCCCAACCTGCATCCCAATTGTCAATCATTCCCCAGGAGTGTT... |
Task1_train_33128 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TCAGAGGGAAGACTGTTTTTCTGTGATATGGTCACAGAACATATTTTATATTTCTACTCATGGAACATTAAAGTCTCAGGATACAAAATCAATGTGTAAAAATCACAAGCATTCTTATACACCAATAACAGACAAACAGAGAGCCAAATCATGAGTGAACTCCCATTCACAATTGCTTCAAAGAGAATAAAATACCTAGGAATCCACCTTACAAGGGATGTGAAGGACCTCTTCAAGGAGAACTACAAACCACTGCTCAATGAAATAAAAGAGGATACAAACAAATGGAAGAATATTCCATGCTCATGGGTAGGAAGAAT... | TCAGAGGGAAGACTGTTTTTCTGTGATATGGTCACAGAACATATTTTATATTTCTACTCATGGAACATTAAAGTCTCAGGATACAAAATCAATGTGTAAAAATCACAAGCATTCTTATACACCAATAACAGACAAACAGAGAGCCAAATCATGAGTGAACTCCCATTCACAATTGCTTCAAAGAGAATAAAATACCTAGGAATCCACCTTACAAGGGATGTGAAGGACCTCTTCAAGGAGAACTACAAACCACTGCTCAATGAAATAAAAGAGGATACAAACAAATGGAAGAATATTCCATGCTCATGGGTAGGAAGAAT... |
Task1_train_33129 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | TAATATTATTTGAAATTAGACTATGATAGATTAAAAAAATCTATATTTTAATTCCTGGAATAGTGGCTTTCAAATTTGTGCTTTTGGGATCCCTTTACAATTTTAAAAATTATTAAGAATGCAAAATATCTTTTGCTTATATAGTTAGACTGATTAATAGTTCCCATATAAGAAATCAAAACAAGAAGCTTTGAAAGAAAAGAATGTACAAGCATATACTCCATTAGACAGAACAGTGACATCATCACCCATCTCTAGGCTCTGGGAAACTCCATTCTATGCTTATAAAAGAATAAGTCTGTAAAAGAAAATAATAGTCT... | TAATATTATTTGAAATTAGACTATGATAGATTAAAAAAATCTATATTTTAATTCCTGGAATAGTGGCTTTCAAATTTGTGCTTTTGGGATCCCTTTACAATTTTAAAAATTATTAAGAATGCAAAATATCTTTTGCTTATATAGTTAGACTGATTAATAGTTCCCATATAAGAAATCAAAACAAGAAGCTTTGAAAGAAAAGAATGTACAAGCATATACTCCATTAGACAGAACAGTGACATCATCACCCATCTCTAGGCTCTGGGAAACTCCATTCTATGCTTATAAAAGAATAAGTCTGTAAAAGAAAATAATAGTCT... |
Task1_train_33130 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | TTGGCATCAACTGATTCTTCAATCAACAGAGGGAAAATCCCAGTGTAATCTGCACTGCTTATACCATACCTGGCTTATGATGTTCAAAACTGAACATCATACTTAAGCATCAGGAATTTCTGAATTGGATGAAAAGAATGAACAGAGGTATTGAAACTATATGAAGTGAGAAGCTAAAGAAATGGAACAGTTTACTATAAAAATAGTTCAACACTGCATAACTAAGATCTGCCTTCACAGATCTGGAAGCTCCCATATGGAAAAGAGACCTGATTTAATTCATAGGGCTTTGTAAATTAGATTCTGAATTCTGGAACTTC... | TTGGCATCAACTGATTCTTCAATCAACAGAGGGAAAATCCCAGTGTAATCTGCACTGCTTATACCATACCTGGCTTATGATGTTCAAAACTGAACATCATACTTAAGCATCAGGAATTTCTGAATTGGATGAAAAGAATGAACAGAGGTATTGAAACTATATGAAGTGAGAAGCTAAAGAAATGGAACAGTTTACTATAAAAATAGTTCAACACTGCATAACTAAGATCTGCCTTCACAGATCTGGAAGCTCCCATATGGAAAAGAGACCTGATTTAATTCATAGGGCTTTGTAAATTAGATTCTGAATTCTGGAACTTC... |
Task1_train_33131 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GATGAAGCTGGAAGCCATCATTCTCAGCAGACTAACACAGGAATGAAAAGCCAAACACCGCATGTTCTCACTCATAAGTAGGAGTTGAACAATGACAACACATGGACACAGGGAGGGGAACATCACACACCGGGGCCTGTCGAGGACTTAAATACCTAATGCATGCAGGGCTTAAAATCTAGATGACAGGTTGATAGGTGCAGCAAACCACCATGGTACATGTATACTTATGTAACAAACCTGCAGTTTTTGCACATGTATCCCAGAACTTAAAGTAAAATAAATTAAAACCAAAAATCAGATAACTTATAAGGAAATAA... | GATGAAGCTGGAAGCCATCATTCTCAGCAGACTAACACAGGAATGAAAAGCCAAACACCGCATGTTCTCACTCATAAGTAGGAGTTGAACAATGACAACACATGGACACAGGGAGGGGAACATCACACACCGGGGCCTGTCGAGGACTTAAATACCTAATGCATGCAGGGCTTAAAATCTAGATGACAGGTTGATAGGTGCAGCAAACCACCATGGTACATGTATACTTATGTAACAAACCTGCAGTTTTTGCACATGTATCCCAGAACTTAAAGTAAAATAAATTAAAACCAAAAATCAGATAACTTATAAGGAAATAA... |
Task1_train_33132 | Here is a variant on Chromosome 1. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGCATTTTTTTCTCTGTTGGCTATGGGAACCTAAACCAGAACTATTGAAGTTAGGGTAGCCCAGCTTTACATAGCATGTGATCCACCAGGTGAAGACCAGGGAACAAATATTTAGGTAAGCAACTTTCTCACCTAACATGCTAGAAATATTTCAGATATTCATAAATTTCACCTCCCCATCCCTACCTTTCAATTGTTCTCAGTTTGGAATTTCCAACACCTACTGAAAAGATTACTTCAAATTTTCTACTAAATAGGCCCTTCCCTTGCCTCTATTGTATTCCTTTGAATTTTATTTTATCTGCACTATGTCTTCAGGA... | TGCATTTTTTTCTCTGTTGGCTATGGGAACCTAAACCAGAACTATTGAAGTTAGGGTAGCCCAGCTTTACATAGCATGTGATCCACCAGGTGAAGACCAGGGAACAAATATTTAGGTAAGCAACTTTCTCACCTAACATGCTAGAAATATTTCAGATATTCATAAATTTCACCTCCCCATCCCTACCTTTCAATTGTTCTCAGTTTGGAATTTCCAACACCTACTGAAAAGATTACTTCAAATTTTCTACTAAATAGGCCCTTCCCTTGCCTCTATTGTATTCCTTTGAATTTTATTTTATCTGCACTATGTCTTCAGGA... |
Task1_train_33133 | A variant on Chromosome 1 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | ATTATAGAAAATGAAATTAAGGCAATGTTAGTAAATATGGAAAGAAGAGGAAAGTTTTTAAATTTATTAGTCAAAAAGCTAAATGAATCATCTGTGTTTTTGACACTACCATTTAGTGAATACACCAAATATTTTTTACTGTAAATAAAGAAAGTGAAGATGTTTAACCTTGGAAAAGGCAAACAATAACTAAAATTGATATTTGTGGAAACCAAAGTATATTACTGTAAATAGTATCTTATCTTGTAGTTTTCTTTTAAACATGTGTGGCAGTACTAATAATCTAATCTTACTAAACATGTAATTATTCTAATGAATAG... | ATTATAGAAAATGAAATTAAGGCAATGTTAGTAAATATGGAAAGAAGAGGAAAGTTTTTAAATTTATTAGTCAAAAAGCTAAATGAATCATCTGTGTTTTTGACACTACCATTTAGTGAATACACCAAATATTTTTTACTGTAAATAAAGAAAGTGAAGATGTTTAACCTTGGAAAAGGCAAACAATAACTAAAATTGATATTTGTGGAAACCAAAGTATATTACTGTAAATAGTATCTTATCTTGTAGTTTTCTTTTAAACATGTGTGGCAGTACTAATAATCTAATCTTACTAAACATGTAATTATTCTAATGAATAG... |
Task1_train_33134 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AATAAGACTTGCATTTAAAAACTTCTAAAAATATGATGATGTTGATTATATCAACAGAGGGAATAGAAATCATAGTGAAAATGAATAAAAGTGGAGAGGAAAGAGTGTTTACTGATTGAGTATTCCAGAGAATCATGATCCTGGATGAAGTTTATTCTGACTGCCACAGCTGTGCCCCAGTGCCCAGCTTTATACTCTATTCCTCTATGAGAGATAAGGTTTTATAGCCCCAGGACAACTTTTGAAACCTGACCCTGGGGAATGTCTAATTACTATGTAGCATTGTTCTTCTAATTTGTCCCTTAGAGGGGAGAGAAAGA... | AATAAGACTTGCATTTAAAAACTTCTAAAAATATGATGATGTTGATTATATCAACAGAGGGAATAGAAATCATAGTGAAAATGAATAAAAGTGGAGAGGAAAGAGTGTTTACTGATTGAGTATTCCAGAGAATCATGATCCTGGATGAAGTTTATTCTGACTGCCACAGCTGTGCCCCAGTGCCCAGCTTTATACTCTATTCCTCTATGAGAGATAAGGTTTTATAGCCCCAGGACAACTTTTGAAACCTGACCCTGGGGAATGTCTAATTACTATGTAGCATTGTTCTTCTAATTTGTCCCTTAGAGGGGAGAGAAAGA... |
Task1_train_33135 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | AGAGGAAAGAGTGTTTACTGATTGAGTATTCCAGAGAATCATGATCCTGGATGAAGTTTATTCTGACTGCCACAGCTGTGCCCCAGTGCCCAGCTTTATACTCTATTCCTCTATGAGAGATAAGGTTTTATAGCCCCAGGACAACTTTTGAAACCTGACCCTGGGGAATGTCTAATTACTATGTAGCATTGTTCTTCTAATTTGTCCCTTAGAGGGGAGAGAAAGATACATAATTTTCCTTTAGACATTGCATCATCCAAAGAGAAACTCCCAGGAAAGACCATCTTTCCATTCTAGTTATTCCTGGAAGAGGCTTCAGA... | AGAGGAAAGAGTGTTTACTGATTGAGTATTCCAGAGAATCATGATCCTGGATGAAGTTTATTCTGACTGCCACAGCTGTGCCCCAGTGCCCAGCTTTATACTCTATTCCTCTATGAGAGATAAGGTTTTATAGCCCCAGGACAACTTTTGAAACCTGACCCTGGGGAATGTCTAATTACTATGTAGCATTGTTCTTCTAATTTGTCCCTTAGAGGGGAGAGAAAGATACATAATTTTCCTTTAGACATTGCATCATCCAAAGAGAAACTCCCAGGAAAGACCATCTTTCCATTCTAGTTATTCCTGGAAGAGGCTTCAGA... |
Task1_train_33136 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | CTTTTGAAACCTGACCCTGGGGAATGTCTAATTACTATGTAGCATTGTTCTTCTAATTTGTCCCTTAGAGGGGAGAGAAAGATACATAATTTTCCTTTAGACATTGCATCATCCAAAGAGAAACTCCCAGGAAAGACCATCTTTCCATTCTAGTTATTCCTGGAAGAGGCTTCAGAGACATTTGTACCCTTATTGACAGGCTAGGAGAAGAGGTGGCTGCAGAGATTTTGAGGAGCATTCTCATGGTGTCAGGCAGGGTAAGTACTAAAGACTGCATTGAAAGGGCATCATCCAACCTCCTTTTACTTCTACTTTGCCGC... | CTTTTGAAACCTGACCCTGGGGAATGTCTAATTACTATGTAGCATTGTTCTTCTAATTTGTCCCTTAGAGGGGAGAGAAAGATACATAATTTTCCTTTAGACATTGCATCATCCAAAGAGAAACTCCCAGGAAAGACCATCTTTCCATTCTAGTTATTCCTGGAAGAGGCTTCAGAGACATTTGTACCCTTATTGACAGGCTAGGAGAAGAGGTGGCTGCAGAGATTTTGAGGAGCATTCTCATGGTGTCAGGCAGGGTAAGTACTAAAGACTGCATTGAAAGGGCATCATCCAACCTCCTTTTACTTCTACTTTGCCGC... |
Task1_train_33137 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GGGGAATGTCTAATTACTATGTAGCATTGTTCTTCTAATTTGTCCCTTAGAGGGGAGAGAAAGATACATAATTTTCCTTTAGACATTGCATCATCCAAAGAGAAACTCCCAGGAAAGACCATCTTTCCATTCTAGTTATTCCTGGAAGAGGCTTCAGAGACATTTGTACCCTTATTGACAGGCTAGGAGAAGAGGTGGCTGCAGAGATTTTGAGGAGCATTCTCATGGTGTCAGGCAGGGTAAGTACTAAAGACTGCATTGAAAGGGCATCATCCAACCTCCTTTTACTTCTACTTTGCCGCCCAATAGCTTCCTTACAT... | GGGGAATGTCTAATTACTATGTAGCATTGTTCTTCTAATTTGTCCCTTAGAGGGGAGAGAAAGATACATAATTTTCCTTTAGACATTGCATCATCCAAAGAGAAACTCCCAGGAAAGACCATCTTTCCATTCTAGTTATTCCTGGAAGAGGCTTCAGAGACATTTGTACCCTTATTGACAGGCTAGGAGAAGAGGTGGCTGCAGAGATTTTGAGGAGCATTCTCATGGTGTCAGGCAGGGTAAGTACTAAAGACTGCATTGAAAGGGCATCATCCAACCTCCTTTTACTTCTACTTTGCCGCCCAATAGCTTCCTTACAT... |
Task1_train_33138 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TCCTTTAGACATTGCATCATCCAAAGAGAAACTCCCAGGAAAGACCATCTTTCCATTCTAGTTATTCCTGGAAGAGGCTTCAGAGACATTTGTACCCTTATTGACAGGCTAGGAGAAGAGGTGGCTGCAGAGATTTTGAGGAGCATTCTCATGGTGTCAGGCAGGGTAAGTACTAAAGACTGCATTGAAAGGGCATCATCCAACCTCCTTTTACTTCTACTTTGCCGCCCAATAGCTTCCTTACATCCTCAACTCTTCAGAACCCAACTGTTGCCCTGCTGTTTCACGGCAAACTGTCATATTTTAAGAACTTTGTTACA... | TCCTTTAGACATTGCATCATCCAAAGAGAAACTCCCAGGAAAGACCATCTTTCCATTCTAGTTATTCCTGGAAGAGGCTTCAGAGACATTTGTACCCTTATTGACAGGCTAGGAGAAGAGGTGGCTGCAGAGATTTTGAGGAGCATTCTCATGGTGTCAGGCAGGGTAAGTACTAAAGACTGCATTGAAAGGGCATCATCCAACCTCCTTTTACTTCTACTTTGCCGCCCAATAGCTTCCTTACATCCTCAACTCTTCAGAACCCAACTGTTGCCCTGCTGTTTCACGGCAAACTGTCATATTTTAAGAACTTTGTTACA... |
Task1_train_33139 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | GAAGAGGTGGCTGCAGAGATTTTGAGGAGCATTCTCATGGTGTCAGGCAGGGTAAGTACTAAAGACTGCATTGAAAGGGCATCATCCAACCTCCTTTTACTTCTACTTTGCCGCCCAATAGCTTCCTTACATCCTCAACTCTTCAGAACCCAACTGTTGCCCTGCTGTTTCACGGCAAACTGTCATATTTTAAGAACTTTGTTACATGAGTGAAATATTATACTAAGGGTAAATGAAATCGGGAAGGGATAACAGAAAGAATATGGTTCAGCTAACAGTTTGAAGATACTGATAATGTCTAAGGTCTTTTAAACATTAAA... | GAAGAGGTGGCTGCAGAGATTTTGAGGAGCATTCTCATGGTGTCAGGCAGGGTAAGTACTAAAGACTGCATTGAAAGGGCATCATCCAACCTCCTTTTACTTCTACTTTGCCGCCCAATAGCTTCCTTACATCCTCAACTCTTCAGAACCCAACTGTTGCCCTGCTGTTTCACGGCAAACTGTCATATTTTAAGAACTTTGTTACATGAGTGAAATATTATACTAAGGGTAAATGAAATCGGGAAGGGATAACAGAAAGAATATGGTTCAGCTAACAGTTTGAAGATACTGATAATGTCTAAGGTCTTTTAAACATTAAA... |
Task1_train_33140 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | CAGGCAGGGTAAGTACTAAAGACTGCATTGAAAGGGCATCATCCAACCTCCTTTTACTTCTACTTTGCCGCCCAATAGCTTCCTTACATCCTCAACTCTTCAGAACCCAACTGTTGCCCTGCTGTTTCACGGCAAACTGTCATATTTTAAGAACTTTGTTACATGAGTGAAATATTATACTAAGGGTAAATGAAATCGGGAAGGGATAACAGAAAGAATATGGTTCAGCTAACAGTTTGAAGATACTGATAATGTCTAAGGTCTTTTAAACATTAAATCTTGTTGAAACCCTAATAATTGTGGATTCTTGAAGAGTCACA... | CAGGCAGGGTAAGTACTAAAGACTGCATTGAAAGGGCATCATCCAACCTCCTTTTACTTCTACTTTGCCGCCCAATAGCTTCCTTACATCCTCAACTCTTCAGAACCCAACTGTTGCCCTGCTGTTTCACGGCAAACTGTCATATTTTAAGAACTTTGTTACATGAGTGAAATATTATACTAAGGGTAAATGAAATCGGGAAGGGATAACAGAAAGAATATGGTTCAGCTAACAGTTTGAAGATACTGATAATGTCTAAGGTCTTTTAAACATTAAATCTTGTTGAAACCCTAATAATTGTGGATTCTTGAAGAGTCACA... |
Task1_train_33141 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AACTGTTGCCCTGCTGTTTCACGGCAAACTGTCATATTTTAAGAACTTTGTTACATGAGTGAAATATTATACTAAGGGTAAATGAAATCGGGAAGGGATAACAGAAAGAATATGGTTCAGCTAACAGTTTGAAGATACTGATAATGTCTAAGGTCTTTTAAACATTAAATCTTGTTGAAACCCTAATAATTGTGGATTCTTGAAGAGTCACAGAGAAAGTTACTGCTTTTCTTCAAAGTCAAGTCTAATCTAATTCAAGTGTCTTTACGTCATACAAGAAATATTTTTAGATTGAACTCCTTGGACACTACTAAATATCT... | AACTGTTGCCCTGCTGTTTCACGGCAAACTGTCATATTTTAAGAACTTTGTTACATGAGTGAAATATTATACTAAGGGTAAATGAAATCGGGAAGGGATAACAGAAAGAATATGGTTCAGCTAACAGTTTGAAGATACTGATAATGTCTAAGGTCTTTTAAACATTAAATCTTGTTGAAACCCTAATAATTGTGGATTCTTGAAGAGTCACAGAGAAAGTTACTGCTTTTCTTCAAAGTCAAGTCTAATCTAATTCAAGTGTCTTTACGTCATACAAGAAATATTTTTAGATTGAACTCCTTGGACACTACTAAATATCT... |
Task1_train_33142 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTACTGCTTTTCTTCAAAGTCAAGTCTAATCTAATTCAAGTGTCTTTACGTCATACAAGAAATATTTTTAGATTGAACTCCTTGGACACTACTAAATATCTTTAACAGTAGGATTTTATTGATGGTTCTTTATGTATTTCAGGAACAAGAATAATATTTATTTACCTTTATATAGCCCTTGAACCTATGGCATCATCGACACATAGCAGAAGATCAATCGATATATGAGTGTTAGTTGAATAAATGTACCGATGATGAATAATGATGCAGCTTTACTACTGAGAAGGGCCCCGTGCGTACAGCAACAAAGTAGTCACTCT... | TTACTGCTTTTCTTCAAAGTCAAGTCTAATCTAATTCAAGTGTCTTTACGTCATACAAGAAATATTTTTAGATTGAACTCCTTGGACACTACTAAATATCTTTAACAGTAGGATTTTATTGATGGTTCTTTATGTATTTCAGGAACAAGAATAATATTTATTTACCTTTATATAGCCCTTGAACCTATGGCATCATCGACACATAGCAGAAGATCAATCGATATATGAGTGTTAGTTGAATAAATGTACCGATGATGAATAATGATGCAGCTTTACTACTGAGAAGGGCCCCGTGCGTACAGCAACAAAGTAGTCACTCT... |
Task1_train_33143 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGAATGCTTCCAGTTTTTGCCCATTCAGTATGATATTGAGAAGGGGAACATCACACACTGGGGACTGTTGTGGGGTTGGGGGATGGGGGAGGGATAGCATTAGGAGATACTCCTAATGCTAAATGATGAGTTAATGGGTGCAGCACACCAACATGGCACATGTATACATATGTAAAAAACTTGCACGTTGTGCACATGTACCCTAAATAAAATAATAATGAAATAAAATAAAATAAAATAAAAAAGAAAATAATAGGGGCAAATTTACCTAGCATAGATTTAGTGATACTTAGTCATCAAAAATGTCCAGGACAAAAAAT... | GGAATGCTTCCAGTTTTTGCCCATTCAGTATGATATTGAGAAGGGGAACATCACACACTGGGGACTGTTGTGGGGTTGGGGGATGGGGGAGGGATAGCATTAGGAGATACTCCTAATGCTAAATGATGAGTTAATGGGTGCAGCACACCAACATGGCACATGTATACATATGTAAAAAACTTGCACGTTGTGCACATGTACCCTAAATAAAATAATAATGAAATAAAATAAAATAAAATAAAAAAGAAAATAATAGGGGCAAATTTACCTAGCATAGATTTAGTGATACTTAGTCATCAAAAATGTCCAGGACAAAAAAT... |
Task1_train_33144 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GCATTAGGAGATACTCCTAATGCTAAATGATGAGTTAATGGGTGCAGCACACCAACATGGCACATGTATACATATGTAAAAAACTTGCACGTTGTGCACATGTACCCTAAATAAAATAATAATGAAATAAAATAAAATAAAATAAAAAAGAAAATAATAGGGGCAAATTTACCTAGCATAGATTTAGTGATACTTAGTCATCAAAAATGTCCAGGACAAAAAATTTTACCAAAAGTCAAACACAACTTGTTTTTAATAATTTTATTTCTTGTCATTTTTATTCTAGATGAAACACTAAATGAAATATATTTATAAATAGA... | GCATTAGGAGATACTCCTAATGCTAAATGATGAGTTAATGGGTGCAGCACACCAACATGGCACATGTATACATATGTAAAAAACTTGCACGTTGTGCACATGTACCCTAAATAAAATAATAATGAAATAAAATAAAATAAAATAAAAAAGAAAATAATAGGGGCAAATTTACCTAGCATAGATTTAGTGATACTTAGTCATCAAAAATGTCCAGGACAAAAAATTTTACCAAAAGTCAAACACAACTTGTTTTTAATAATTTTATTTCTTGTCATTTTTATTCTAGATGAAACACTAAATGAAATATATTTATAAATAGA... |
Task1_train_33145 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CAAAAATGTCCAGGACAAAAAATTTTACCAAAAGTCAAACACAACTTGTTTTTAATAATTTTATTTCTTGTCATTTTTATTCTAGATGAAACACTAAATGAAATATATTTATAAATAGAATGCTACATATATAAATAGAACAATTCAAGTTCCCATTTGATAGAGTATAATATTTTGAATTCCTGGTGATTATTTAATGTAAAAACATTTATCTGCTTAAAATTCTCAATAAACTTCAAAGACAAGTGAAAAAAAAGGAGAATGCATGTTTATCTTAATACTACTTCCCACAATTATAATTAATTATAACTAATTATAAA... | CAAAAATGTCCAGGACAAAAAATTTTACCAAAAGTCAAACACAACTTGTTTTTAATAATTTTATTTCTTGTCATTTTTATTCTAGATGAAACACTAAATGAAATATATTTATAAATAGAATGCTACATATATAAATAGAACAATTCAAGTTCCCATTTGATAGAGTATAATATTTTGAATTCCTGGTGATTATTTAATGTAAAAACATTTATCTGCTTAAAATTCTCAATAAACTTCAAAGACAAGTGAAAAAAAAGGAGAATGCATGTTTATCTTAATACTACTTCCCACAATTATAATTAATTATAACTAATTATAAA... |
Task1_train_33146 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTCTTGTAGTTAATATTTGATCCTCCATTCATGGAAGGATACATAAAGAATACATAATATTAGCTATTAATTGAATCCCCAGATCTCTCATATGCTACATTTTAGAATTATTTTTCACACGTTTCAGGAAATAATTAGCTTACAATTCAATAAAGAAATGGTTCGATGTAAAAAGTAATCCTATTTCTTTCCACTGACTCAACTCCTATACTTTCATACATTATACTGGCCATAGATATTAGGACCACTAAGACAGGTACATGAAACTTGTCAGAACAGAACTGTGACAAACTATACTTTTCAAGTATAGTATACTTGTA... | TTCTTGTAGTTAATATTTGATCCTCCATTCATGGAAGGATACATAAAGAATACATAATATTAGCTATTAATTGAATCCCCAGATCTCTCATATGCTACATTTTAGAATTATTTTTCACACGTTTCAGGAAATAATTAGCTTACAATTCAATAAAGAAATGGTTCGATGTAAAAAGTAATCCTATTTCTTTCCACTGACTCAACTCCTATACTTTCATACATTATACTGGCCATAGATATTAGGACCACTAAGACAGGTACATGAAACTTGTCAGAACAGAACTGTGACAAACTATACTTTTCAAGTATAGTATACTTGTA... |
Task1_train_33147 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TATATACCATTTTCTCTTGTAGGCTCACTTATGTCTGTAAAGATGGGAAAAAAATACAAGAACATTGTTCTACTAAAAGGATTAGAGGTCATCAATGATTATCATTTTAGAATGGTTAAGTCCTTACTGAGCAACGATTTAAAACTTAATTTAAAAATGAGAGAAGAGTATGACAAAATTCAGATTGCTGACTTGATGGAAGAAAAGTTCCGAGGTGATGCTGGTTTGGGCAAACTAATAAAAATTTTCGAAGATATACCAACGCTTGAAGACCTGGCTGAAACTCTTAAAAAAGAAAAGTTAAAAGGTAATTGGGAAGA... | TATATACCATTTTCTCTTGTAGGCTCACTTATGTCTGTAAAGATGGGAAAAAAATACAAGAACATTGTTCTACTAAAAGGATTAGAGGTCATCAATGATTATCATTTTAGAATGGTTAAGTCCTTACTGAGCAACGATTTAAAACTTAATTTAAAAATGAGAGAAGAGTATGACAAAATTCAGATTGCTGACTTGATGGAAGAAAAGTTCCGAGGTGATGCTGGTTTGGGCAAACTAATAAAAATTTTCGAAGATATACCAACGCTTGAAGACCTGGCTGAAACTCTTAAAAAAGAAAAGTTAAAAGGTAATTGGGAAGA... |
Task1_train_33148 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | ATATTATGCTTAGCTGATTTAACTTCTTGTTTGAAGTACTGTTTCATACTCCATTATACATGTCTTCTAGGGTGGCTTACTTTTAATTGTGCTGTTTTCTCTACACTCAGTTTAAATGACTGTACATATATATGTGGTTGTAGAGTTAATGAATAATGAGCTACAAACCAGAACAATGTGACTAGATAGATAGGATGATCTAGATTTGAGATCTGGGCAGATTGGGAAAGAGTGACTATATGGAGAAGAAAGAAGTAGTTACATATTGAAATAACAGTCTACTTAATGAGGACGTGCAACATTCTTTCTCAAACTTACAA... | ATATTATGCTTAGCTGATTTAACTTCTTGTTTGAAGTACTGTTTCATACTCCATTATACATGTCTTCTAGGGTGGCTTACTTTTAATTGTGCTGTTTTCTCTACACTCAGTTTAAATGACTGTACATATATATGTGGTTGTAGAGTTAATGAATAATGAGCTACAAACCAGAACAATGTGACTAGATAGATAGGATGATCTAGATTTGAGATCTGGGCAGATTGGGAAAGAGTGACTATATGGAGAAGAAAGAAGTAGTTACATATTGAAATAACAGTCTACTTAATGAGGACGTGCAACATTCTTTCTCAAACTTACAA... |
Task1_train_33149 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGAAACTTGAGCTAGTGTCTTGGGAGAAAAGGGGGAAATCTCTACGAGGTACCCATCCTTCTGCACCTTAGGTCTGAGGTGCTTGGCCCCCTAGGAAGCCCTACATGAATGGGACAGAAGGTCCTTAACAACACTGGAGATGAAGCAGCCGATGCTGTTTTGGACAAATGAAACAGCGTCCCCTAACCAGCCCTTTCTATCTCATTGTTCTGACTTGGACACGCCATGGCTCACCGCTCCCAAAGTCCCCACTATGTCTCCCTAGCTGAGGAAATAAAAGCAGAGAGGGGTGATGAAACAGTGACGATCCTGGGGAAACA... | TGAAACTTGAGCTAGTGTCTTGGGAGAAAAGGGGGAAATCTCTACGAGGTACCCATCCTTCTGCACCTTAGGTCTGAGGTGCTTGGCCCCCTAGGAAGCCCTACATGAATGGGACAGAAGGTCCTTAACAACACTGGAGATGAAGCAGCCGATGCTGTTTTGGACAAATGAAACAGCGTCCCCTAACCAGCCCTTTCTATCTCATTGTTCTGACTTGGACACGCCATGGCTCACCGCTCCCAAAGTCCCCACTATGTCTCCCTAGCTGAGGAAATAAAAGCAGAGAGGGGTGATGAAACAGTGACGATCCTGGGGAAACA... |
Task1_train_33150 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | CAGCGTCCCCTAACCAGCCCTTTCTATCTCATTGTTCTGACTTGGACACGCCATGGCTCACCGCTCCCAAAGTCCCCACTATGTCTCCCTAGCTGAGGAAATAAAAGCAGAGAGGGGTGATGAAACAGTGACGATCCTGGGGAAACAGCTGAGGAGGGGAGGGAGGGGGAAGAAGCCACTAAAAAAGTGAAATGTGCTTGGGAGAATCGGCCTGCCTGCAGGGTAGATGCCCTTTCTCTCTGCTGGCCAGCTCTGCCCCTCAGTGAGAAACTTTACATATTGCTAAGATGCCTGGCCAATGAAACAGTTCCAGAGACTTT... | CAGCGTCCCCTAACCAGCCCTTTCTATCTCATTGTTCTGACTTGGACACGCCATGGCTCACCGCTCCCAAAGTCCCCACTATGTCTCCCTAGCTGAGGAAATAAAAGCAGAGAGGGGTGATGAAACAGTGACGATCCTGGGGAAACAGCTGAGGAGGGGAGGGAGGGGGAAGAAGCCACTAAAAAAGTGAAATGTGCTTGGGAGAATCGGCCTGCCTGCAGGGTAGATGCCCTTTCTCTCTGCTGGCCAGCTCTGCCCCTCAGTGAGAAACTTTACATATTGCTAAGATGCCTGGCCAATGAAACAGTTCCAGAGACTTT... |
Task1_train_33151 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CAATATTGGGCAAAAACAAATAAGTTGAAATGTGAGGTAGTCAAGCTCCTTCTGGAGCTGGGAGAGCCCTTCCTACTTATCTTAAGGTGAAGCAATACCCTAAATAGTCAAACCACTGGAGGTAGTATATCCCTGGGAAGGGAGCATGATCTTGGAAGAAGCAACTATTTAACAAGAACAATTCTTGAAGAGGAACTCAACTGAGAGCCATTAGCCCAAGGCACTCCCAGCAGCTGGAGGAATGCTTGTGTGGGTCCTGAAGGAATGCAATCCAGGTGATGTGCTGCAGCATTCACCAAATACAACTTCAGATAGAAGAC... | CAATATTGGGCAAAAACAAATAAGTTGAAATGTGAGGTAGTCAAGCTCCTTCTGGAGCTGGGAGAGCCCTTCCTACTTATCTTAAGGTGAAGCAATACCCTAAATAGTCAAACCACTGGAGGTAGTATATCCCTGGGAAGGGAGCATGATCTTGGAAGAAGCAACTATTTAACAAGAACAATTCTTGAAGAGGAACTCAACTGAGAGCCATTAGCCCAAGGCACTCCCAGCAGCTGGAGGAATGCTTGTGTGGGTCCTGAAGGAATGCAATCCAGGTGATGTGCTGCAGCATTCACCAAATACAACTTCAGATAGAAGAC... |
Task1_train_33152 | A variant on Chromosome 1 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GGTCCTGAAGGAATGCAATCCAGGTGATGTGCTGCAGCATTCACCAAATACAACTTCAGATAGAAGACAGTGTGACATTGGCCAGCAGAACTTTACCTGATGGCTTCTAATTAGATTAAGCAGAACTACTAAGCAAAATCTAATTGTCTCTTGACCAACCTCACAGAAACAAACTATATCATTTCTAGAAATCTGGACACTAAAACAAAGATCTCTTTTATCTCCAGTCAGACTTCACATGACAATTTTTGTCAAAGAAAGACAGGTTAACTTGACTTAAATAATTTATTTCCAATGAATTGTCCCATTTTCAACATCCA... | GGTCCTGAAGGAATGCAATCCAGGTGATGTGCTGCAGCATTCACCAAATACAACTTCAGATAGAAGACAGTGTGACATTGGCCAGCAGAACTTTACCTGATGGCTTCTAATTAGATTAAGCAGAACTACTAAGCAAAATCTAATTGTCTCTTGACCAACCTCACAGAAACAAACTATATCATTTCTAGAAATCTGGACACTAAAACAAAGATCTCTTTTATCTCCAGTCAGACTTCACATGACAATTTTTGTCAAAGAAAGACAGGTTAACTTGACTTAAATAATTTATTTCCAATGAATTGTCCCATTTTCAACATCCA... |
Task1_train_33153 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | TGTGCCTCAGTGCTAAGCAGAGTCATGTGAGTGGTCTTTAGAAGAAGGACTGAAATGGGGCTCATTACATATGAGCTGACTTTAATTTATTGTAGTATTTCAGGTCCTATCACAGCTGGACAGGTCTTCATAAGCTATATTTGCTCTTCCTTCCATTTCCTTTGAAGAATTATAGACTTCCAAGAGTGGGGAGGATGCTAACCAAATCATAATAGCCATTCTTCTACCTCAAGACAGACAAGTTTCAGCCAGATAAGATGATATTTTAGCCGTGTGTTTCTCAATGGGAACTTTATTGGTATTTGGAAGAAGGGAATTCT... | TGTGCCTCAGTGCTAAGCAGAGTCATGTGAGTGGTCTTTAGAAGAAGGACTGAAATGGGGCTCATTACATATGAGCTGACTTTAATTTATTGTAGTATTTCAGGTCCTATCACAGCTGGACAGGTCTTCATAAGCTATATTTGCTCTTCCTTCCATTTCCTTTGAAGAATTATAGACTTCCAAGAGTGGGGAGGATGCTAACCAAATCATAATAGCCATTCTTCTACCTCAAGACAGACAAGTTTCAGCCAGATAAGATGATATTTTAGCCGTGTGTTTCTCAATGGGAACTTTATTGGTATTTGGAAGAAGGGAATTCT... |
Task1_train_33154 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TGAGTGGTCTTTAGAAGAAGGACTGAAATGGGGCTCATTACATATGAGCTGACTTTAATTTATTGTAGTATTTCAGGTCCTATCACAGCTGGACAGGTCTTCATAAGCTATATTTGCTCTTCCTTCCATTTCCTTTGAAGAATTATAGACTTCCAAGAGTGGGGAGGATGCTAACCAAATCATAATAGCCATTCTTCTACCTCAAGACAGACAAGTTTCAGCCAGATAAGATGATATTTTAGCCGTGTGTTTCTCAATGGGAACTTTATTGGTATTTGGAAGAAGGGAATTCTTCCTTGGGCAGAATCACCACAAGTTTT... | TGAGTGGTCTTTAGAAGAAGGACTGAAATGGGGCTCATTACATATGAGCTGACTTTAATTTATTGTAGTATTTCAGGTCCTATCACAGCTGGACAGGTCTTCATAAGCTATATTTGCTCTTCCTTCCATTTCCTTTGAAGAATTATAGACTTCCAAGAGTGGGGAGGATGCTAACCAAATCATAATAGCCATTCTTCTACCTCAAGACAGACAAGTTTCAGCCAGATAAGATGATATTTTAGCCGTGTGTTTCTCAATGGGAACTTTATTGGTATTTGGAAGAAGGGAATTCTTCCTTGGGCAGAATCACCACAAGTTTT... |
Task1_train_33155 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | TCTGTTTTTTCATCCATAAAATGGGATTCACTAGATCACCTATCTTATAAGATTACTGTGGCAATTAAATGAGTCAGTATGTGCTAAGTGCTTAGAAGACTATCTAGCACATAATAAATGCTCAATAAGTCCTGAGGAGCAACTGGATTGACAGGAGAAGTTGGTGCTGGTTATTATTATTACTATAATTATTACCCTGGGTAAGTTTTTAATAGTTCCAGCAATGAAAAAATGAGAATAGCCTCCTTGCAGCAGTAATTCCCTCTTACTGGAACAGTTCAAAAAGTCGCTGATAACGACCAGTCAATCATTAGAGAGGA... | TCTGTTTTTTCATCCATAAAATGGGATTCACTAGATCACCTATCTTATAAGATTACTGTGGCAATTAAATGAGTCAGTATGTGCTAAGTGCTTAGAAGACTATCTAGCACATAATAAATGCTCAATAAGTCCTGAGGAGCAACTGGATTGACAGGAGAAGTTGGTGCTGGTTATTATTATTACTATAATTATTACCCTGGGTAAGTTTTTAATAGTTCCAGCAATGAAAAAATGAGAATAGCCTCCTTGCAGCAGTAATTCCCTCTTACTGGAACAGTTCAAAAAGTCGCTGATAACGACCAGTCAATCATTAGAGAGGA... |
Task1_train_33156 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GTCAAACAGGAAAAAATTCTGATCTATGAAATCTTGACCTCCAAGGACATATTCTGTGATTCCAGGGGGAGATAATTCAAACCAATACTTAGTGCTGTTAGAAAAAGCAGTAGTGGAAGCAAGACCTGCTGTTCGGTAATGCGGTGAGCATCGTTACTTCCAGGGTGAGGAGAGTGGGTCCTAAGGATCCAGAAGATCCAGGCAAGAGCAGGATGTGCTGGGGCTCCCTAACTGTTACTCCTCATTAGTCTCAGGCCATCAGGCCTGCTCAGAAGGCTGTCTGGGAATGGGGGTGTCTGGCTTATCAAAGAGATGATACA... | GTCAAACAGGAAAAAATTCTGATCTATGAAATCTTGACCTCCAAGGACATATTCTGTGATTCCAGGGGGAGATAATTCAAACCAATACTTAGTGCTGTTAGAAAAAGCAGTAGTGGAAGCAAGACCTGCTGTTCGGTAATGCGGTGAGCATCGTTACTTCCAGGGTGAGGAGAGTGGGTCCTAAGGATCCAGAAGATCCAGGCAAGAGCAGGATGTGCTGGGGCTCCCTAACTGTTACTCCTCATTAGTCTCAGGCCATCAGGCCTGCTCAGAAGGCTGTCTGGGAATGGGGGTGTCTGGCTTATCAAAGAGATGATACA... |
Task1_train_33157 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | ATGTGGGCCAAAAAGAGCTTCTTAAGGGAAGTAAGAAGGGAGCTCTCCAGAGCCCTGTATCTCAGGAATTGGAGTGATCTGGGGAAGGAAAACAAACAGCTTCTAGAAAGGGCATGAAGAGGGAGTGCTGTGGAGCTGGTGGTGGGAGAAGGGGGTGGGAAGGGAGCCAGGGCTGCAGGAGACGGGGCAGGGAAGGTTTGGACCAAGGGTTGGCAAACTTGTGGCCCATGGGCCAAACCCAGCACACTGCCTGTTTTTGTAGATAAAGTTTTACTGTAACACACACATGCTCATTGGTTTATTTTGTTTGAGAGCTTTCA... | ATGTGGGCCAAAAAGAGCTTCTTAAGGGAAGTAAGAAGGGAGCTCTCCAGAGCCCTGTATCTCAGGAATTGGAGTGATCTGGGGAAGGAAAACAAACAGCTTCTAGAAAGGGCATGAAGAGGGAGTGCTGTGGAGCTGGTGGTGGGAGAAGGGGGTGGGAAGGGAGCCAGGGCTGCAGGAGACGGGGCAGGGAAGGTTTGGACCAAGGGTTGGCAAACTTGTGGCCCATGGGCCAAACCCAGCACACTGCCTGTTTTTGTAGATAAAGTTTTACTGTAACACACACATGCTCATTGGTTTATTTTGTTTGAGAGCTTTCA... |
Task1_train_33158 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GATCCGCCCTCCTCAGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACCACACCCAGCCCAAAAATAATTTTTCAAATGGCCCTTAATGATCAAAGATCTGTGTGACTGACCTGGTACAGACCCCTTATTTTTCAGTGGTACTGAAGCCTGGGGCAGGGTGATGTGTGGAAGGGCACACAGCTGATCTGTGGCAGCACCAGGAGGAGCAGGTAGGAGCAGCTAGGTCTTGGCTGACATCCAGTGCAATTCTCTTTGTGTGTTACATTCCTGCTCTGCATTAACACTGAAGTCATCTCCAGTGTGAGAGGAGGTTGTT... | GATCCGCCCTCCTCAGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACCACACCCAGCCCAAAAATAATTTTTCAAATGGCCCTTAATGATCAAAGATCTGTGTGACTGACCTGGTACAGACCCCTTATTTTTCAGTGGTACTGAAGCCTGGGGCAGGGTGATGTGTGGAAGGGCACACAGCTGATCTGTGGCAGCACCAGGAGGAGCAGGTAGGAGCAGCTAGGTCTTGGCTGACATCCAGTGCAATTCTCTTTGTGTGTTACATTCCTGCTCTGCATTAACACTGAAGTCATCTCCAGTGTGAGAGGAGGTTGTT... |
Task1_train_33159 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | TTACTTTTTGGATTGTTGTTTTTGTTGGCTCATTTCAATTCCAAGACACCAAAGGACTTTCCCTGTTTCTTTTGAAGCCCTTCCAAAGCAACCCCAGATAAATTCCCTTCACTCTTTCCCCCTTTGTTAGCAAGGTGGGAAACGCTGCCCTTCGTACCACCATGAGATGATACAGTAGGTCTAAAGCTGGGAAGGCACAGGTTTCCTTGCTAAAGTTGCCCAATAATACTTCCTGGAGACTCAGGGAGTGCCTGTTAGAAGGACATTAAAAGGATAATGACACAACATCAACATAATGGTGCTGACTCATGGACTCCTAG... | TTACTTTTTGGATTGTTGTTTTTGTTGGCTCATTTCAATTCCAAGACACCAAAGGACTTTCCCTGTTTCTTTTGAAGCCCTTCCAAAGCAACCCCAGATAAATTCCCTTCACTCTTTCCCCCTTTGTTAGCAAGGTGGGAAACGCTGCCCTTCGTACCACCATGAGATGATACAGTAGGTCTAAAGCTGGGAAGGCACAGGTTTCCTTGCTAAAGTTGCCCAATAATACTTCCTGGAGACTCAGGGAGTGCCTGTTAGAAGGACATTAAAAGGATAATGACACAACATCAACATAATGGTGCTGACTCATGGACTCCTAG... |
Task1_train_33160 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCTCAGCCTCCACCGAGAGCCCGTAGACTTGTGCCCCAGTAGGAAACTTTCTGCCTAGAAAGTTAGCTAAACACTGTGGGCGTGTTTATGTAGGAAGAAGCCTCCTAGTTTAGAGGCTGGCAAGGTAAAAGGAGGCACAGGAAGGCCTTCCCCCGACCCCAACTGACTAGTGTGTGACAGGACTGGGACTTGCAGGCCGGGACAGCACCCCCACGTGATCTTGCTCACCTCTTACTTCAAGCCTGGGCAGGGACTAACAGTGAGGTCACTCTGCCCAGGGCCCTAGGGGTGTTTTCGGTGTTGGGACCCAGGGCTCAGAC... | CCTCAGCCTCCACCGAGAGCCCGTAGACTTGTGCCCCAGTAGGAAACTTTCTGCCTAGAAAGTTAGCTAAACACTGTGGGCGTGTTTATGTAGGAAGAAGCCTCCTAGTTTAGAGGCTGGCAAGGTAAAAGGAGGCACAGGAAGGCCTTCCCCCGACCCCAACTGACTAGTGTGTGACAGGACTGGGACTTGCAGGCCGGGACAGCACCCCCACGTGATCTTGCTCACCTCTTACTTCAAGCCTGGGCAGGGACTAACAGTGAGGTCACTCTGCCCAGGGCCCTAGGGGTGTTTTCGGTGTTGGGACCCAGGGCTCAGAC... |
Task1_train_33161 | Here is a variant on Chromosome 1. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGCTTTCACTCCATGGCATCGTTGATAAATCCAGTCTCCTCTACTAGATGCTTCTAGAGTCCTCAAAGATGGGAAGCCTTCCCTTCTGTGTGGTCCCTAATCCAACAGTCTCTCTCAGGGTTCCGCACACATTCTAGGCCACCAGCCCCACAACAGTCCCCGACCCATCTCCCCTTCACTGCCCAGAGGGCTTATGACAGAAGAGCATTGTCCTTAGCAACCTCTACCTCCTGTTGCTTAGCAACTGCAGTTCCGAGTCCCCTACACAAAGGCTGAGAGGCCCCTTCCACACTGTGAGGCAGTAAAAGGGTTAATGGGCT... | TGCTTTCACTCCATGGCATCGTTGATAAATCCAGTCTCCTCTACTAGATGCTTCTAGAGTCCTCAAAGATGGGAAGCCTTCCCTTCTGTGTGGTCCCTAATCCAACAGTCTCTCTCAGGGTTCCGCACACATTCTAGGCCACCAGCCCCACAACAGTCCCCGACCCATCTCCCCTTCACTGCCCAGAGGGCTTATGACAGAAGAGCATTGTCCTTAGCAACCTCTACCTCCTGTTGCTTAGCAACTGCAGTTCCGAGTCCCCTACACAAAGGCTGAGAGGCCCCTTCCACACTGTGAGGCAGTAAAAGGGTTAATGGGCT... |
Task1_train_33162 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AGCAAGCATGTTGGTGGAAAACGGGATAGGTGGTGAGTGACAGCATACCAAAACTTCCCTGTGAGGGGGCCCTTTAGACCCACTCTTCTCCCCAAAGGAGGGCCTGAAAAAGCACGTGGACTTGGGGGAAGGCACTGGGAGTTGGGGCAAAGACAGCAGAGTGGGTTTTGCCAGAGCCACCCAGTGAGGACGGAAGGACCCAACACAGCTCCTGCAGAGTTGTGGTCACTTAATTTGACTTTATTGCCAGCCAGTCTTCCCTCAGAAGTATGGCTCTCTGGATACCCACCCCTGAGCACCTCCTTCCCCTGGAAAGAAGA... | AGCAAGCATGTTGGTGGAAAACGGGATAGGTGGTGAGTGACAGCATACCAAAACTTCCCTGTGAGGGGGCCCTTTAGACCCACTCTTCTCCCCAAAGGAGGGCCTGAAAAAGCACGTGGACTTGGGGGAAGGCACTGGGAGTTGGGGCAAAGACAGCAGAGTGGGTTTTGCCAGAGCCACCCAGTGAGGACGGAAGGACCCAACACAGCTCCTGCAGAGTTGTGGTCACTTAATTTGACTTTATTGCCAGCCAGTCTTCCCTCAGAAGTATGGCTCTCTGGATACCCACCCCTGAGCACCTCCTTCCCCTGGAAAGAAGA... |
Task1_train_33163 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AAAGGATTTTAGGCCTGAACTGACATGAAATATAATACTGTGGAACTTTTTTTGTCTTTTTGTGAGTGTTTTCTGACTGCAAAAGAACAGTTCATCAAATTACTTATCTTTTAAAAAACACAATCACAAAATCATATTCATATACTGCTACTGTAGTATTAGGGAATCCCAAGCCTAGACAGGCTGTTTAATTAAAAAAAAAAATGTAAGGATGCTTGTTTAAACAACTCAGAAAGCATTTTTCCCCCAGAAATATTACAGTGATAAGGGAAACGATCTGACCACCTAAGCCTCAGTTCCACAATCTCCCTCTAAATTCT... | AAAGGATTTTAGGCCTGAACTGACATGAAATATAATACTGTGGAACTTTTTTTGTCTTTTTGTGAGTGTTTTCTGACTGCAAAAGAACAGTTCATCAAATTACTTATCTTTTAAAAAACACAATCACAAAATCATATTCATATACTGCTACTGTAGTATTAGGGAATCCCAAGCCTAGACAGGCTGTTTAATTAAAAAAAAAAATGTAAGGATGCTTGTTTAAACAACTCAGAAAGCATTTTTCCCCCAGAAATATTACAGTGATAAGGGAAACGATCTGACCACCTAAGCCTCAGTTCCACAATCTCCCTCTAAATTCT... |
Task1_train_33164 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AATTGCAGGGAGCTTACAAAATGGAGCAGTCTCAGTTTGGACTAACATTCTCCAGTCTGTTTCTCCCCCTCTCCCTGGAAATGACCTGGGCCACCCCCTGTCCCTCAATGCCTCTACTGTCCCCTCAGGATGATCACAAATTAACCTTGGAAGAGCTGAGCACCAAGTACTCCGTGGACCTGACAAAGGTGAGTAAGAAGCTCCCTGAGGAGGCAGAGAGTCTCCAACTCTGACTGTGAGGCTGCCAGGACAAAAGCTGAACTAGGAATCCAGCCCCCTAACTTCAAGTCCAACGTTCCCACCCCTCACCCTCTGCCTGG... | AATTGCAGGGAGCTTACAAAATGGAGCAGTCTCAGTTTGGACTAACATTCTCCAGTCTGTTTCTCCCCCTCTCCCTGGAAATGACCTGGGCCACCCCCTGTCCCTCAATGCCTCTACTGTCCCCTCAGGATGATCACAAATTAACCTTGGAAGAGCTGAGCACCAAGTACTCCGTGGACCTGACAAAGGTGAGTAAGAAGCTCCCTGAGGAGGCAGAGAGTCTCCAACTCTGACTGTGAGGCTGCCAGGACAAAAGCTGAACTAGGAATCCAGCCCCCTAACTTCAAGTCCAACGTTCCCACCCCTCACCCTCTGCCTGG... |
Task1_train_33165 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GATGGGTTTGGTAAGTGTCCCAAAGGATCAGGAGAGCCTACTGTCACCTAAGGCTCACTGTTGCTTCGGTCTTACGTCTTTGTGAGGGATGTATATGTGTTTGTGTCTGTGTGTAGTGTCAGTAACTGACTCCCAAACAGGGGGTAGTGTTTATTTGTCTTTGCTGCTCATCCCTTCCCTCTCCTGCTTCCCCTTCCTTTGCCTTACCTGGCATTATCTCTTTTTGTCACGTGTTCACATCCCTAATCTTACAGCCTAAGACTCCCTGATACCATTGTCTTTCTATTTTAGTGTGGATGGTAATAGACTTCATGCCTACT... | GATGGGTTTGGTAAGTGTCCCAAAGGATCAGGAGAGCCTACTGTCACCTAAGGCTCACTGTTGCTTCGGTCTTACGTCTTTGTGAGGGATGTATATGTGTTTGTGTCTGTGTGTAGTGTCAGTAACTGACTCCCAAACAGGGGGTAGTGTTTATTTGTCTTTGCTGCTCATCCCTTCCCTCTCCTGCTTCCCCTTCCTTTGCCTTACCTGGCATTATCTCTTTTTGTCACGTGTTCACATCCCTAATCTTACAGCCTAAGACTCCCTGATACCATTGTCTTTCTATTTTAGTGTGGATGGTAATAGACTTCATGCCTACT... |
Task1_train_33166 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCAATCTGAGTTGTAGTAAAGGAATGGGTGCTCATAAGCCCGGGTTTACAAATCTTCATTAGTAGCTCCACAGTTTTGAGAGTAGACAGTGAATGAGGGTAAGGTTATACAAGGGTGGCGTAGTGGATAATTGTGAGGCTTTTTTGTCTGCCTACCACCTGAATCCCACTTCTATTATTTGTAGAATTCCTTAATTCATAAGAAGTGAAAGTGGAAAATGCCAGATATTCAATTCCCAGCCCCCCTTGGAGATAGGACATGGACATGTGACCTAGGATTGGCCACTCAATCCCAGACTTTGAATTATAAGCTAGAGATGA... | GCAATCTGAGTTGTAGTAAAGGAATGGGTGCTCATAAGCCCGGGTTTACAAATCTTCATTAGTAGCTCCACAGTTTTGAGAGTAGACAGTGAATGAGGGTAAGGTTATACAAGGGTGGCGTAGTGGATAATTGTGAGGCTTTTTTGTCTGCCTACCACCTGAATCCCACTTCTATTATTTGTAGAATTCCTTAATTCATAAGAAGTGAAAGTGGAAAATGCCAGATATTCAATTCCCAGCCCCCCTTGGAGATAGGACATGGACATGTGACCTAGGATTGGCCACTCAATCCCAGACTTTGAATTATAAGCTAGAGATGA... |
Task1_train_33167 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TGGTGGGCACCGTGACCACTAGCCAACTTGCAATCCATTCTACTCCAAAGGACCGGGCTGAAAGAGCAAGAAAACCCTATATGCTTAGGTATCTTTATCTTGACTAATGTATTGAGAAGGGGCAAGTGTACTGGACACTGGTGTGGGAGCTCACAGAGCAGGGAAATTAATTTCTTCCCTGAATCCCATCCTATTTGGCTGGGACATTCTTTTCCTCAATCTCCCCAAACATAAAGTATAAAAAATGCAGAAATTCCTTAAATATCACTGGCTTACCTGGGCCCTGTGCTCAAAGGTTACCTCGACATATCTGTGGCCTG... | TGGTGGGCACCGTGACCACTAGCCAACTTGCAATCCATTCTACTCCAAAGGACCGGGCTGAAAGAGCAAGAAAACCCTATATGCTTAGGTATCTTTATCTTGACTAATGTATTGAGAAGGGGCAAGTGTACTGGACACTGGTGTGGGAGCTCACAGAGCAGGGAAATTAATTTCTTCCCTGAATCCCATCCTATTTGGCTGGGACATTCTTTTCCTCAATCTCCCCAAACATAAAGTATAAAAAATGCAGAAATTCCTTAAATATCACTGGCTTACCTGGGCCCTGTGCTCAAAGGTTACCTCGACATATCTGTGGCCTG... |
Task1_train_33168 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | ACTTGCAATCCATTCTACTCCAAAGGACCGGGCTGAAAGAGCAAGAAAACCCTATATGCTTAGGTATCTTTATCTTGACTAATGTATTGAGAAGGGGCAAGTGTACTGGACACTGGTGTGGGAGCTCACAGAGCAGGGAAATTAATTTCTTCCCTGAATCCCATCCTATTTGGCTGGGACATTCTTTTCCTCAATCTCCCCAAACATAAAGTATAAAAAATGCAGAAATTCCTTAAATATCACTGGCTTACCTGGGCCCTGTGCTCAAAGGTTACCTCGACATATCTGTGGCCTGGGAAAGCATTGCTCCCCTACTCTGG... | ACTTGCAATCCATTCTACTCCAAAGGACCGGGCTGAAAGAGCAAGAAAACCCTATATGCTTAGGTATCTTTATCTTGACTAATGTATTGAGAAGGGGCAAGTGTACTGGACACTGGTGTGGGAGCTCACAGAGCAGGGAAATTAATTTCTTCCCTGAATCCCATCCTATTTGGCTGGGACATTCTTTTCCTCAATCTCCCCAAACATAAAGTATAAAAAATGCAGAAATTCCTTAAATATCACTGGCTTACCTGGGCCCTGTGCTCAAAGGTTACCTCGACATATCTGTGGCCTGGGAAAGCATTGCTCCCCTACTCTGG... |
Task1_train_33169 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AAATCCCATAAGATTAAAAATTGGCAGAGAATTGACCAGATCAGAGCTTGCCTCTTGGTTGTATGTGTGGAGAGGCTCTAGAAGCTCTACCAATCTGGTCTCTAGAACTCTAGTTTTGTCTCCTCTGTGAAGCTGATCTCAGATCGCTAAAAGATTGCTCAGACTACAGAGGTGATAAAAGTTTCCTGGACTTCCCCTATATGTTTTAATTGAGCAATTTTTATCCTGGTTTTCACCATTTCCTGTGTTCTAGCCTCATATCTTACACTCCTTCTGCATTTCCCATGGTGATCAGCACAGCACTGGGCACTTTGCTGATG... | AAATCCCATAAGATTAAAAATTGGCAGAGAATTGACCAGATCAGAGCTTGCCTCTTGGTTGTATGTGTGGAGAGGCTCTAGAAGCTCTACCAATCTGGTCTCTAGAACTCTAGTTTTGTCTCCTCTGTGAAGCTGATCTCAGATCGCTAAAAGATTGCTCAGACTACAGAGGTGATAAAAGTTTCCTGGACTTCCCCTATATGTTTTAATTGAGCAATTTTTATCCTGGTTTTCACCATTTCCTGTGTTCTAGCCTCATATCTTACACTCCTTCTGCATTTCCCATGGTGATCAGCACAGCACTGGGCACTTTGCTGATG... |
Task1_train_33170 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | AACTCAGTCACCTCTACGCTGTCACATACGATGTCCACCCCCATTGCAGTCTCCCTGATGCCTTTGTCCATATTAAAAGTCCTTCATTGCATGTGACAGAAAGCTAGCACAAACTGCCTTGAGCAAAATAGAAAATGTATTGGGTCACTGTATTAGTTATCTGTTGCTGTGTAACAAATTGCCCCAAACTTCACAGCTAAAAACAATAAGCATTTTTGATGAAAAATAAAAAATTGAAAAAAAATTTAAAAACCAAACATTTATTATCTCACAGTTTCTCTTGATAAGGAATCTGGGCATGGCTTAGCTGGGTGCCTCTG... | AACTCAGTCACCTCTACGCTGTCACATACGATGTCCACCCCCATTGCAGTCTCCCTGATGCCTTTGTCCATATTAAAAGTCCTTCATTGCATGTGACAGAAAGCTAGCACAAACTGCCTTGAGCAAAATAGAAAATGTATTGGGTCACTGTATTAGTTATCTGTTGCTGTGTAACAAATTGCCCCAAACTTCACAGCTAAAAACAATAAGCATTTTTGATGAAAAATAAAAAATTGAAAAAAAATTTAAAAACCAAACATTTATTATCTCACAGTTTCTCTTGATAAGGAATCTGGGCATGGCTTAGCTGGGTGCCTCTG... |
Task1_train_33171 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | TGTATTGGGTCACTGTATTAGTTATCTGTTGCTGTGTAACAAATTGCCCCAAACTTCACAGCTAAAAACAATAAGCATTTTTGATGAAAAATAAAAAATTGAAAAAAAATTTAAAAACCAAACATTTATTATCTCACAGTTTCTCTTGATAAGGAATCTGGGCATGGCTTAGCTGGGTGCCTCTGGCTTAAGGTACTCACACAACTAACATCACGGTGTCAGCCAGGGCTGCAGTCATTTCAAGGACCTCCTGGGGAGGATCCACTTCCAGTCTCACTCATGTGATTCTTGGCTAGCCTCAGTCCTCATGGACAGTTGGC... | TGTATTGGGTCACTGTATTAGTTATCTGTTGCTGTGTAACAAATTGCCCCAAACTTCACAGCTAAAAACAATAAGCATTTTTGATGAAAAATAAAAAATTGAAAAAAAATTTAAAAACCAAACATTTATTATCTCACAGTTTCTCTTGATAAGGAATCTGGGCATGGCTTAGCTGGGTGCCTCTGGCTTAAGGTACTCACACAACTAACATCACGGTGTCAGCCAGGGCTGCAGTCATTTCAAGGACCTCCTGGGGAGGATCCACTTCCAGTCTCACTCATGTGATTCTTGGCTAGCCTCAGTCCTCATGGACAGTTGGC... |
Task1_train_33172 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | CTCTCCTCCTTATGAATCCCTAAGCCTCAGTTTCCTTACCTTCCAAAATGAAGGTATCTATTTTCACTCAGTATTGAGCGAAAGAGAAAGAGGGGCCAGCCGGGAGGGGGCAGGATTGAGCAGCGGTTAAGAGCATCAGGGACAAGACTAGCTGTAGTCAAATCCTGGCCCTACCACTTACTCGGGAAAATACTTAATCTTTACGTGCCCGAGTTTCCTCATCTACAAAAAATAAATACGGATAGTTATTGTCTATGCTTCATGGGGTTTTAGGCAGACTAAATAAACTTATTCATGAAAAGCATTTAGAACTGTGCCTC... | CTCTCCTCCTTATGAATCCCTAAGCCTCAGTTTCCTTACCTTCCAAAATGAAGGTATCTATTTTCACTCAGTATTGAGCGAAAGAGAAAGAGGGGCCAGCCGGGAGGGGGCAGGATTGAGCAGCGGTTAAGAGCATCAGGGACAAGACTAGCTGTAGTCAAATCCTGGCCCTACCACTTACTCGGGAAAATACTTAATCTTTACGTGCCCGAGTTTCCTCATCTACAAAAAATAAATACGGATAGTTATTGTCTATGCTTCATGGGGTTTTAGGCAGACTAAATAAACTTATTCATGAAAAGCATTTAGAACTGTGCCTC... |
Task1_train_33173 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GGTTGTTAGGAGTAAAGAGTCTGGAGTCTGGAGCCTGGCCGGGCGTGGTGGCTCACACCTGTAATCCCAACACTTTGGGAGCCGAAGGGGGCGGATCGCCAAAGGTCAGGAGTTGGAGACCAGCCTGGCCAACATGGTGAAATCACATCTCTACTAAAAATACAAAAATCAGCTGGGCGTGGTGGTGGGCACCTGTAATCCCAGCTACTTGGTAGGCTGAGACAGGAGAATCATTTGAACCTGGGAGGCACAAGTTGCAGTGAGCTGAGACTGCGCCATTGCACTCCAGCCTGGGCAACAACAGCAAAACTCCATCTCAA... | GGTTGTTAGGAGTAAAGAGTCTGGAGTCTGGAGCCTGGCCGGGCGTGGTGGCTCACACCTGTAATCCCAACACTTTGGGAGCCGAAGGGGGCGGATCGCCAAAGGTCAGGAGTTGGAGACCAGCCTGGCCAACATGGTGAAATCACATCTCTACTAAAAATACAAAAATCAGCTGGGCGTGGTGGTGGGCACCTGTAATCCCAGCTACTTGGTAGGCTGAGACAGGAGAATCATTTGAACCTGGGAGGCACAAGTTGCAGTGAGCTGAGACTGCGCCATTGCACTCCAGCCTGGGCAACAACAGCAAAACTCCATCTCAA... |
Task1_train_33174 | Consider a variant on Chromosome 1. Determine its clinical classification and disease relevance. | Benign | TGCTGTGCTTTTGACGTGCACATACATAAACATCTCGGTGCATTAAAAAGCAGTATTGCCGCCAGCATGTCTCACCTCCAGCCCTAAGGTGGTTTTCTCCTATCTCAGTAAATAGAACATACAATCGGGTTTTACACCAAAACATTCCATTGCCCAGGGATAAGCAGAAGACAGATGCCTTCCTCTTATCTCAACTGCAAAGAGGCCTTCCTCTTTTACTAATCCTCCTCAGCACAGACCCTTTGTGGGTGTCGGGCTGGGGGACAGTCAGGTCTTTCCCTTCCCACGAGGCCATATCTCAGGCTATCACATGGGGAGAA... | TGCTGTGCTTTTGACGTGCACATACATAAACATCTCGGTGCATTAAAAAGCAGTATTGCCGCCAGCATGTCTCACCTCCAGCCCTAAGGTGGTTTTCTCCTATCTCAGTAAATAGAACATACAATCGGGTTTTACACCAAAACATTCCATTGCCCAGGGATAAGCAGAAGACAGATGCCTTCCTCTTATCTCAACTGCAAAGAGGCCTTCCTCTTTTACTAATCCTCCTCAGCACAGACCCTTTGTGGGTGTCGGGCTGGGGGACAGTCAGGTCTTTCCCTTCCCACGAGGCCATATCTCAGGCTATCACATGGGGAGAA... |
Task1_train_33175 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AGAGCTCTTCCTGGACGTTTCTCTTAATCTGGATTTAAAAGGGACAGGAGGTATCTTAGGGTCCAAGAACATAACAGGAATGGGCAACTCTAGAAGTGTTTGTGTGTGGAAGGCCCTAACCTGGCCCTGTCCTCCCTGTCTCTACCTTTGGCTTTCATGAAGAGAGATTCACAGCTCAGAGGAAGGGAGGAATTTCTCCAGTCTTCACTTTAACAAACTCTTTTAAGTTTTCTGCCTACCTTATGTTCCCTTTGGCCAATGACCCACTCCCTGGGAACAAGATCTTGTTGACTTTCTTGGGAATCTCCTAAGAGATAAGT... | AGAGCTCTTCCTGGACGTTTCTCTTAATCTGGATTTAAAAGGGACAGGAGGTATCTTAGGGTCCAAGAACATAACAGGAATGGGCAACTCTAGAAGTGTTTGTGTGTGGAAGGCCCTAACCTGGCCCTGTCCTCCCTGTCTCTACCTTTGGCTTTCATGAAGAGAGATTCACAGCTCAGAGGAAGGGAGGAATTTCTCCAGTCTTCACTTTAACAAACTCTTTTAAGTTTTCTGCCTACCTTATGTTCCCTTTGGCCAATGACCCACTCCCTGGGAACAAGATCTTGTTGACTTTCTTGGGAATCTCCTAAGAGATAAGT... |
Task1_train_33176 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | CAGGAGGCTGCCAGGGTCAGGCCCTGGCCCTCTTCTAGTGCTGGACCAGGATTCAGTGAGGGCAGGGGAGGCACTGCAAATGGGGAAAGGCAGGGGTCACAGGTCTACACAATCCCTGTCAGGAGGCCCCCACTCATCGCATTTCAGTCTTGCACAAGTACAAACTTTCAGGCCCCCTTTCCTTCTCTTATTTCATGGAGACGCAGATGAATGGTAGAAATTCAGGTGACTTTGTATCCTTCTCTACTGTGCGAATTTTTTACAATGAACGTAGGTTATTTTAAAAAATAAAATAATGAAGTAATTAAAAAACTAACCAG... | CAGGAGGCTGCCAGGGTCAGGCCCTGGCCCTCTTCTAGTGCTGGACCAGGATTCAGTGAGGGCAGGGGAGGCACTGCAAATGGGGAAAGGCAGGGGTCACAGGTCTACACAATCCCTGTCAGGAGGCCCCCACTCATCGCATTTCAGTCTTGCACAAGTACAAACTTTCAGGCCCCCTTTCCTTCTCTTATTTCATGGAGACGCAGATGAATGGTAGAAATTCAGGTGACTTTGTATCCTTCTCTACTGTGCGAATTTTTTACAATGAACGTAGGTTATTTTAAAAAATAAAATAATGAAGTAATTAAAAAACTAACCAG... |
Task1_train_33177 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | ATTGTTGAATCTTGGCTTTAAGGTACAGGTGGGGAACAGGTCCTGGTAATCTTCCAATCTCTGTAACTGTGCCTTTCCTGCCCATGCCATCCCCATGCTGTGTTCTCTGAGGACCAAGAGTTGGGAAGAGGAGGGGAAAGCCCTGCTGTGCTATCAGACCCTGCATTACATGCCCATCCTCACTGCAGCCCTGGCCACTGTCTCCTTTCTTCCTTTCTTTATTTCTTTTCTTTTTTTCTTTCTTTCTTTCGCCAGGGTCTCACTATGTTACCCAGGCTGGTCTTGAACTCCTGAACTCCTGGCCTCAAGTGATTCTCCTG... | ATTGTTGAATCTTGGCTTTAAGGTACAGGTGGGGAACAGGTCCTGGTAATCTTCCAATCTCTGTAACTGTGCCTTTCCTGCCCATGCCATCCCCATGCTGTGTTCTCTGAGGACCAAGAGTTGGGAAGAGGAGGGGAAAGCCCTGCTGTGCTATCAGACCCTGCATTACATGCCCATCCTCACTGCAGCCCTGGCCACTGTCTCCTTTCTTCCTTTCTTTATTTCTTTTCTTTTTTTCTTTCTTTCTTTCGCCAGGGTCTCACTATGTTACCCAGGCTGGTCTTGAACTCCTGAACTCCTGGCCTCAAGTGATTCTCCTG... |
Task1_train_33178 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | TGTTCTTGTTATCCTGCACCTTCATGTTCTTGTCAATTGTATTTGTAGCCACGTGCTTACTATGTTTCCTTCCTGTGATTGGGAACTTCCAGAGGTGAGGGATGGAATTTTCCTTTCTCTGTTGGTCCCTCAGAACCCAGGATAGGGGTCTGCCAACCAAAGGAACGGACCCTGAGGATAAAGGCAGGCACCATGGTTGTGGATCTTTGCCACCTTCAAGTGCATATGGAGAGTGGATGTGGACAGAAATTTGATAACAGTAAGTAACAGCAGCTGCTATTTGTTGAGCACTTACTAGATGCTGAGTGTTATGCTAGTTC... | TGTTCTTGTTATCCTGCACCTTCATGTTCTTGTCAATTGTATTTGTAGCCACGTGCTTACTATGTTTCCTTCCTGTGATTGGGAACTTCCAGAGGTGAGGGATGGAATTTTCCTTTCTCTGTTGGTCCCTCAGAACCCAGGATAGGGGTCTGCCAACCAAAGGAACGGACCCTGAGGATAAAGGCAGGCACCATGGTTGTGGATCTTTGCCACCTTCAAGTGCATATGGAGAGTGGATGTGGACAGAAATTTGATAACAGTAAGTAACAGCAGCTGCTATTTGTTGAGCACTTACTAGATGCTGAGTGTTATGCTAGTTC... |
Task1_train_33179 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGCCAGTCCTGGGGAGTGGGGCGTGGCGTTGAAGGGGTCGGCCGGGGCACGAAGAAGCTGTATCGGAGGCGTGTGTCCTGGGGGTTGCCAGCCACTAGGACTTGCAGTGTCAAAGGCTGGGCCAGTGGCCCATGGCCTGACAGTGTCTCTGAGGCTGCAGTGGCCCCGCTGTAGCGCAAGCTGACTGCCCCAGGCAGTACCACATCTGTGGGGGAGGGCATCAGCGTGTATTCACCATTGAGGGCATAGGAGCCATCTGGCAGCTTCAGGGCCAAGTAGATGCTCCGGTGGCCAGGGTTTCCCTGCTGCCGGACAAGAAT... | AGCCAGTCCTGGGGAGTGGGGCGTGGCGTTGAAGGGGTCGGCCGGGGCACGAAGAAGCTGTATCGGAGGCGTGTGTCCTGGGGGTTGCCAGCCACTAGGACTTGCAGTGTCAAAGGCTGGGCCAGTGGCCCATGGCCTGACAGTGTCTCTGAGGCTGCAGTGGCCCCGCTGTAGCGCAAGCTGACTGCCCCAGGCAGTACCACATCTGTGGGGGAGGGCATCAGCGTGTATTCACCATTGAGGGCATAGGAGCCATCTGGCAGCTTCAGGGCCAAGTAGATGCTCCGGTGGCCAGGGTTTCCCTGCTGCCGGACAAGAAT... |
Task1_train_33180 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GCACTTAACTATGGTTTTAGGTGAGGGGAATACAACTTCTCTCCGTAGGAGTGGGGGTGGGAGTGGGGGAGTTCCAGCCTAATATCTTGTCTTTGAAGACTTGTTGGCATCCTCCTAGTCATACCCTGAATGTGAAGGATCAACAAGGGAGGCTAAGGAAGAAGGAGCCTCCTTACTTAGTTTGTGGAGAGTGGCCCTTATTCCCATTATGCTCTCCACAGTGGAGTGATGCTTCGGGGCTCAGGCATCCAGTGGGACCTGCGGAAGACCCAGCCCTATGATGTTTACGACCAGGTTGAGTTTGATGTTCCTGTTGGTTC... | GCACTTAACTATGGTTTTAGGTGAGGGGAATACAACTTCTCTCCGTAGGAGTGGGGGTGGGAGTGGGGGAGTTCCAGCCTAATATCTTGTCTTTGAAGACTTGTTGGCATCCTCCTAGTCATACCCTGAATGTGAAGGATCAACAAGGGAGGCTAAGGAAGAAGGAGCCTCCTTACTTAGTTTGTGGAGAGTGGCCCTTATTCCCATTATGCTCTCCACAGTGGAGTGATGCTTCGGGGCTCAGGCATCCAGTGGGACCTGCGGAAGACCCAGCCCTATGATGTTTACGACCAGGTTGAGTTTGATGTTCCTGTTGGTTC... |
Task1_train_33181 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CCCACCTTACCTAGCCAAGCCACAAGTAAAATATTCAGCAGGTGACAGGGAAGAATCAAGCATAGAGTGATAAAGAATATGTGAGAGACTTGGATGTAGTATGTCGGGTGTATATGTGTGCTTGTAGCCATGTGGGCAAACAGGTATCCATGTCCCAGAGTGTCCATGTGAGTGCCCTCTAGCCCAAGGTGGCTGGCTGCCCACCCCCCATGCCTCCCTGGGTGGGGCAGATGCTGAGGGGCCCTGGAGAAAGTGTGGGTCTTTAATGTTTTGCTTCTTTTGTCTCTGCAGAAATCAGATGGTGTTTACACGGTAAGTGT... | CCCACCTTACCTAGCCAAGCCACAAGTAAAATATTCAGCAGGTGACAGGGAAGAATCAAGCATAGAGTGATAAAGAATATGTGAGAGACTTGGATGTAGTATGTCGGGTGTATATGTGTGCTTGTAGCCATGTGGGCAAACAGGTATCCATGTCCCAGAGTGTCCATGTGAGTGCCCTCTAGCCCAAGGTGGCTGGCTGCCCACCCCCCATGCCTCCCTGGGTGGGGCAGATGCTGAGGGGCCCTGGAGAAAGTGTGGGTCTTTAATGTTTTGCTTCTTTTGTCTCTGCAGAAATCAGATGGTGTTTACACGGTAAGTGT... |
Task1_train_33182 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGAAACCCTGTTTCTACTAAAAATACAAAATTAGCCGGGCATGGTGGCGCTTGCCTGTAATCCCAGCTACTCGGGAGACTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCGGTGAGCCAAGATCACACCACTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAATTGAGATCTGAAGCATTGTTAGAGAGAAACTACCTAGTCCCACCTATCCATTGTACAAAGAAATGCAACTGATTAGACCCAAGAGCTCAGCAGTTAATGGCACAGCCAAAATCG... | AGAAACCCTGTTTCTACTAAAAATACAAAATTAGCCGGGCATGGTGGCGCTTGCCTGTAATCCCAGCTACTCGGGAGACTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCGGTGAGCCAAGATCACACCACTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAATTGAGATCTGAAGCATTGTTAGAGAGAAACTACCTAGTCCCACCTATCCATTGTACAAAGAAATGCAACTGATTAGACCCAAGAGCTCAGCAGTTAATGGCACAGCCAAAATCG... |
Task1_train_33183 | A mutation is present on Chromosome 1. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GTAGGCAAAAAGGAAAAAGTGATTTTAAATTTAAAATTTTTCTTGAATGCCCCTTTTATTCAGAGTCACAAATGAATACTGAATTCACCTGTGTGAATTCAAGTCATGCCTTTTTATTTCTTATGTGGATGGAAGATTTTATGCAGGGTACAGTATGGTCTGAATGTTTCTGTGCCCCCAAAATTCATATGATATGAATTAATCAAATAGCAACCCCCAGGGTGATGGTATTAGGAGGTGAGGTCTTTGGGTAGGTGATTAGGTCATGAGGGCAGAGCCCTTATAAAAGAGGGCCGAGGGAGCTCAAAGGCCTCTTCCGC... | GTAGGCAAAAAGGAAAAAGTGATTTTAAATTTAAAATTTTTCTTGAATGCCCCTTTTATTCAGAGTCACAAATGAATACTGAATTCACCTGTGTGAATTCAAGTCATGCCTTTTTATTTCTTATGTGGATGGAAGATTTTATGCAGGGTACAGTATGGTCTGAATGTTTCTGTGCCCCCAAAATTCATATGATATGAATTAATCAAATAGCAACCCCCAGGGTGATGGTATTAGGAGGTGAGGTCTTTGGGTAGGTGATTAGGTCATGAGGGCAGAGCCCTTATAAAAGAGGGCCGAGGGAGCTCAAAGGCCTCTTCCGC... |
Task1_train_33184 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | TTCCCCGACGGGGAGGTCACGGGAAATTGTGTGAGGATTTTGTCAACCTTCAGAAGTCTCAGAAATGTCTCCTTGTTTTGGCTTTCAGCGGAAATCCGAACGCCAGCAGATCTGAATGGAATGTTCTGGATTGAAGAAAGTGGGAAATGGCCTCAATTCACAAAGTCACAACCTGATAAAAACCAGTGTGACTTTACTGCCCAGTGAACCCATCTCGTCCTCCAGCCTTTAGGAGGTAGGTTGGACTGGAGCCTGCAGTAGTTTACTCTCCACCTGAGTCCTGGTCTCCAGCTGGGAACCCACTTAGGCCATAAAGAAAA... | TTCCCCGACGGGGAGGTCACGGGAAATTGTGTGAGGATTTTGTCAACCTTCAGAAGTCTCAGAAATGTCTCCTTGTTTTGGCTTTCAGCGGAAATCCGAACGCCAGCAGATCTGAATGGAATGTTCTGGATTGAAGAAAGTGGGAAATGGCCTCAATTCACAAAGTCACAACCTGATAAAAACCAGTGTGACTTTACTGCCCAGTGAACCCATCTCGTCCTCCAGCCTTTAGGAGGTAGGTTGGACTGGAGCCTGCAGTAGTTTACTCTCCACCTGAGTCCTGGTCTCCAGCTGGGAACCCACTTAGGCCATAAAGAAAA... |
Task1_train_33185 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GCTCATGCCCCGATCTGCCCGAACCTTCTCCCGGGGTCAGCGCCGCGCCGCGCCACCCGGCTGAGTCAGCCCGGGCGGGCGAGAGGCTCTCAACTGGGCGGGAAGGTGCGGGAAGGTGCGGAAAGGTTCGCGAAAGTTCGCGGCGGCGGGGGTCGGGTGAGGCGCAAAAGGATAAAAAGCCGGTGGAAGCGGAGCTGAGCAGATCCGAGCCGGGCTGGCTGCAGAGAAACCGCAGGGAGAGCCTCACTGCTGAGCGCCCCTCGACGGCGGAGCGGCAGCAGCCTCCGTGGCCTCCAGCATCCGACAAGAAGCTTCAGCCA... | GCTCATGCCCCGATCTGCCCGAACCTTCTCCCGGGGTCAGCGCCGCGCCGCGCCACCCGGCTGAGTCAGCCCGGGCGGGCGAGAGGCTCTCAACTGGGCGGGAAGGTGCGGGAAGGTGCGGAAAGGTTCGCGAAAGTTCGCGGCGGCGGGGGTCGGGTGAGGCGCAAAAGGATAAAAAGCCGGTGGAAGCGGAGCTGAGCAGATCCGAGCCGGGCTGGCTGCAGAGAAACCGCAGGGAGAGCCTCACTGCTGAGCGCCCCTCGACGGCGGAGCGGCAGCAGCCTCCGTGGCCTCCAGCATCCGACAAGAAGCTTCAGCCA... |
Task1_train_33186 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TACCATCCCTAGCCTGTATTGTTGCTTTGCTGTGAGGGAACGGTTGGGACAGAAAAAGTGTTTGTGTAGCTCTGAAACTTCAATTTCTAGGAATGCAGCTACTCACTGGGGCTTCCCTGCTTGAAGATCATGGGCTTTTCCCTTCCACTGGAGACCAAGGAAAAGTCGAGAGTTGGATAAGGGATCTGGCTCTGAGTTCTATGTTTCCTGCTGCTTGTAGAGAGGCCTGAGGATGATGGGGTTGCAAATCCAGAGAAATGTTCAGAGATGCTGCTGCTACTGCTCTTATTACCCCCATGGGATGGGGGTCATTTGTCTTG... | TACCATCCCTAGCCTGTATTGTTGCTTTGCTGTGAGGGAACGGTTGGGACAGAAAAAGTGTTTGTGTAGCTCTGAAACTTCAATTTCTAGGAATGCAGCTACTCACTGGGGCTTCCCTGCTTGAAGATCATGGGCTTTTCCCTTCCACTGGAGACCAAGGAAAAGTCGAGAGTTGGATAAGGGATCTGGCTCTGAGTTCTATGTTTCCTGCTGCTTGTAGAGAGGCCTGAGGATGATGGGGTTGCAAATCCAGAGAAATGTTCAGAGATGCTGCTGCTACTGCTCTTATTACCCCCATGGGATGGGGGTCATTTGTCTTG... |
Task1_train_33187 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TCCAGCCTGGTGACAGAGTGAGACCCTGTCCCCCCACAAAATGAAATAAAATAAAATAAAATGACAACATAGAAACAGATTCATCTTCTAGAACTTGCATTGCTCAGTGAAAAATCAGGTTAAAGAACAGTTTTTAGAGTATATCCTCATTTACACTTATGTATGTCTGTATGTGAACAGCGTGTGTCTGTGTGTGATCACAGAAAGAAATCCAACAGGATGTATGCCAAGGTGATAATATTTTGCTCCTGCGTATTTTCTATTTTTCTGTAGTGATCATGGATTACCTGTGCAATTTCTACCCCCTCCCAACAAAAGAA... | TCCAGCCTGGTGACAGAGTGAGACCCTGTCCCCCCACAAAATGAAATAAAATAAAATAAAATGACAACATAGAAACAGATTCATCTTCTAGAACTTGCATTGCTCAGTGAAAAATCAGGTTAAAGAACAGTTTTTAGAGTATATCCTCATTTACACTTATGTATGTCTGTATGTGAACAGCGTGTGTCTGTGTGTGATCACAGAAAGAAATCCAACAGGATGTATGCCAAGGTGATAATATTTTGCTCCTGCGTATTTTCTATTTTTCTGTAGTGATCATGGATTACCTGTGCAATTTCTACCCCCTCCCAACAAAAGAA... |
Task1_train_33188 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GGATCAACGTGCTCCAGGAGGACTCTGTGACTCTGACATGCCGGGGGACTCACAGCCCTGAGAGCGACTCCATTCAGTGGTTCCACAATGGGAATCTCATTCCCACCCACACGCAGCCCAGCTACAGGTTCAAGGCCAACAACAATGACAGCGGGGAGTACACGTGCCAGACTGGCCAGACCAGCCTCAGCGACCCTGTGCATCTGACTGTGCTTTCTGGTCAGTGGAGGAAGGCCCCAGGGTGGACCTGGGAGGGCCAGGACGGATGAAATCTGCTTTCAGGCAGAGGTTTGCAGGAAAGGGGGGTGGCCTGCTTACTG... | GGATCAACGTGCTCCAGGAGGACTCTGTGACTCTGACATGCCGGGGGACTCACAGCCCTGAGAGCGACTCCATTCAGTGGTTCCACAATGGGAATCTCATTCCCACCCACACGCAGCCCAGCTACAGGTTCAAGGCCAACAACAATGACAGCGGGGAGTACACGTGCCAGACTGGCCAGACCAGCCTCAGCGACCCTGTGCATCTGACTGTGCTTTCTGGTCAGTGGAGGAAGGCCCCAGGGTGGACCTGGGAGGGCCAGGACGGATGAAATCTGCTTTCAGGCAGAGGTTTGCAGGAAAGGGGGGTGGCCTGCTTACTG... |
Task1_train_33189 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCACTGCCAGGGAAAATTCAAGTGGCAGAGGACATTAAAGTAAAGATGGCTGAAAAGTGAAGACCTGCAAGGGGGAGGAAGAAAGGAGGAGAGACACTGCTGGGTACTGAAAGCTCTTTGTTAGATAACATATTCAAGGCTGAGGAGCCAAGTGAAGTTTGGGAAAATCAGAATATGAAAGAAAGTCCCCGAGGAAGGTCTGAGGACTGAAGTAGACCATATTTGCACAGTGAAGTAAAAAGAACATTGATTTTGGACTCAGACACACCTGCCTTTCCCGATCCATTGCTTAGTCTCTTTTTAAGCTTTGGGTATGTTAA... | CCACTGCCAGGGAAAATTCAAGTGGCAGAGGACATTAAAGTAAAGATGGCTGAAAAGTGAAGACCTGCAAGGGGGAGGAAGAAAGGAGGAGAGACACTGCTGGGTACTGAAAGCTCTTTGTTAGATAACATATTCAAGGCTGAGGAGCCAAGTGAAGTTTGGGAAAATCAGAATATGAAAGAAAGTCCCCGAGGAAGGTCTGAGGACTGAAGTAGACCATATTTGCACAGTGAAGTAAAAAGAACATTGATTTTGGACTCAGACACACCTGCCTTTCCCGATCCATTGCTTAGTCTCTTTTTAAGCTTTGGGTATGTTAA... |
Task1_train_33190 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | CTCAGGTGACCTTCTACCGAGATGGCTCAGCTCTGGGTCCCCCCGGGCCTAACAGGGAATTCTCCATCACCGTGGTACAAAAGGCAGACAGCGGGCACTACCACTGCAGTGGCATCTTCCAGAGCCCTGGTCCTGGGATCCCAGAAACAGCATCTGTTGTGGCTATCACAGTCCAAGGTGAGAGCTAGAAGCAGCATTGTCATGGCAGGGGAGGGTAAGGAGAGACAGGGAGCCCAAATTGTCTTTCTTTAGCCTGGAGGTAGCAAGATCATCAACAGACTATGGAGCAGGTTGCTGGCAAATGCCCAAGTTGGGCTTCG... | CTCAGGTGACCTTCTACCGAGATGGCTCAGCTCTGGGTCCCCCCGGGCCTAACAGGGAATTCTCCATCACCGTGGTACAAAAGGCAGACAGCGGGCACTACCACTGCAGTGGCATCTTCCAGAGCCCTGGTCCTGGGATCCCAGAAACAGCATCTGTTGTGGCTATCACAGTCCAAGGTGAGAGCTAGAAGCAGCATTGTCATGGCAGGGGAGGGTAAGGAGAGACAGGGAGCCCAAATTGTCTTTCTTTAGCCTGGAGGTAGCAAGATCATCAACAGACTATGGAGCAGGTTGCTGGCAAATGCCCAAGTTGGGCTTCG... |
Task1_train_33191 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | AAAATGCAAAAATTAGCTGGGTGTGATGGCGCCCACCGGTAATCCCAGCTACTCGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCAAGAGGTGGAGGTTGCAGTGAACCGAGTTTGTGCCACTGCACTGCAGCTTGGGCGACAAGAGCAAGACCATGTCTCAAAAAAAGAAAAAGAACAAGAAAAAAAGAAAGAAAAAGAAAAGAAAAGAAAGCGGTGGGAGATGGCGGGGAAGGGAGGGAGAGGAGTTAAGAGGAGAAAGCTGGAAGGCTGTGAGAGTGGGAGATCTCCAGGGCTGGACTTTCTGTGGAGTCAAGCGT... | AAAATGCAAAAATTAGCTGGGTGTGATGGCGCCCACCGGTAATCCCAGCTACTCGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCAAGAGGTGGAGGTTGCAGTGAACCGAGTTTGTGCCACTGCACTGCAGCTTGGGCGACAAGAGCAAGACCATGTCTCAAAAAAAGAAAAAGAACAAGAAAAAAAGAAAGAAAAAGAAAAGAAAAGAAAGCGGTGGGAGATGGCGGGGAAGGGAGGGAGAGGAGTTAAGAGGAGAAAGCTGGAAGGCTGTGAGAGTGGGAGATCTCCAGGGCTGGACTTTCTGTGGAGTCAAGCGT... |
Task1_train_33192 | This alteration occurs on Chromosome 1. Is it associated with a disease or is it a benign variant? | Benign | AAATATTTATTTTTTATTATGTTTTCTAAGTGTATATTAATACAATATTTTCAAGTCAAATTTTTTTTTCAGTGGATTGTTACATGTGCTTCAAGTATATAGCATATTACCTTGCTAAAAGGCACGCTGTCTCTTTTGTTTTAATGTTTTTTAAATTTCTTCTTTTAGTGTAATTATACTAGAATTACAGAAAAAGCAGGTATCTATTTTTTATCCTGACTTTAATTGTAATGCATTCAGCATTGGACTTGGCTGTATAATTACTGATAGCTTTTTAATGTTAAGAAAGTATTCCTCGGATCCTTGTTTTCTAGGATTTT... | AAATATTTATTTTTTATTATGTTTTCTAAGTGTATATTAATACAATATTTTCAAGTCAAATTTTTTTTTCAGTGGATTGTTACATGTGCTTCAAGTATATAGCATATTACCTTGCTAAAAGGCACGCTGTCTCTTTTGTTTTAATGTTTTTTAAATTTCTTCTTTTAGTGTAATTATACTAGAATTACAGAAAAAGCAGGTATCTATTTTTTATCCTGACTTTAATTGTAATGCATTCAGCATTGGACTTGGCTGTATAATTACTGATAGCTTTTTAATGTTAAGAAAGTATTCCTCGGATCCTTGTTTTCTAGGATTTT... |
Task1_train_33193 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | TTAATACAATATTTTCAAGTCAAATTTTTTTTTCAGTGGATTGTTACATGTGCTTCAAGTATATAGCATATTACCTTGCTAAAAGGCACGCTGTCTCTTTTGTTTTAATGTTTTTTAAATTTCTTCTTTTAGTGTAATTATACTAGAATTACAGAAAAAGCAGGTATCTATTTTTTATCCTGACTTTAATTGTAATGCATTCAGCATTGGACTTGGCTGTATAATTACTGATAGCTTTTTAATGTTAAGAAAGTATTCCTCGGATCCTTGTTTTCTAGGATTTTATTGAGGAATACTTGTCGAATATTATCAAATACCTT... | TTAATACAATATTTTCAAGTCAAATTTTTTTTTCAGTGGATTGTTACATGTGCTTCAAGTATATAGCATATTACCTTGCTAAAAGGCACGCTGTCTCTTTTGTTTTAATGTTTTTTAAATTTCTTCTTTTAGTGTAATTATACTAGAATTACAGAAAAAGCAGGTATCTATTTTTTATCCTGACTTTAATTGTAATGCATTCAGCATTGGACTTGGCTGTATAATTACTGATAGCTTTTTAATGTTAAGAAAGTATTCCTCGGATCCTTGTTTTCTAGGATTTTATTGAGGAATACTTGTCGAATATTATCAAATACCTT... |
Task1_train_33194 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | GCTGAAATGGTAGAAGTATGGGGGCCCAGGGAAGTTCACTTCCATGGCAAAGGGAGAGATGGAGTGTTGGGCTCAGGGCCTGTTCTCAAGAGCACAAAGGCCAGGCTGCCCAGAGCTGGTGCACAAGTGGTAGCCTCTTCTCTGACCCCAAGGCAGTCTGCAGAAACACAGCAGGACCCCTGCTTCAGAAACTTAAACATTCTCTCCTGCTCCCACCCTCACCTCTAAGGCCCAAGAACTGCCTTCTCGCTTAGCTTCCTCCAGGCCAGCGTTCATGAGATTTTGCCCTGGGGTCCATTTCTATGGGCTATTTCACTGCT... | GCTGAAATGGTAGAAGTATGGGGGCCCAGGGAAGTTCACTTCCATGGCAAAGGGAGAGATGGAGTGTTGGGCTCAGGGCCTGTTCTCAAGAGCACAAAGGCCAGGCTGCCCAGAGCTGGTGCACAAGTGGTAGCCTCTTCTCTGACCCCAAGGCAGTCTGCAGAAACACAGCAGGACCCCTGCTTCAGAAACTTAAACATTCTCTCCTGCTCCCACCCTCACCTCTAAGGCCCAAGAACTGCCTTCTCGCTTAGCTTCCTCCAGGCCAGCGTTCATGAGATTTTGCCCTGGGGTCCATTTCTATGGGCTATTTCACTGCT... |
Task1_train_33195 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CAGGCAGGAAAACACGCGACAGTAGGCTTTCTGGAGCCCCAACTCTGGGCGCTTGCTGGGAAAAGGCTCTTCTCTCCCAATCCTCTCCAAAAGGCCCTACATCCCCAAAGCCAGGGCTCCCTTCCTAGGCAGGCAGAAGGGTTCCCTTCATTTGATTAATGATTTCAGTGGGCAAGCATTGAGCTTGTTTGAGTAGAAATGTTCCTTGGGATGCTGTCTGGGGGAAGAAGACTTGTAATGTTTTCCTTGCAAAGATTGGGTTTCTTCTAATACTAATATTTGCTTTAGGGCTGTTGTCAAACACAGAATGGATCAGTGGA... | CAGGCAGGAAAACACGCGACAGTAGGCTTTCTGGAGCCCCAACTCTGGGCGCTTGCTGGGAAAAGGCTCTTCTCTCCCAATCCTCTCCAAAAGGCCCTACATCCCCAAAGCCAGGGCTCCCTTCCTAGGCAGGCAGAAGGGTTCCCTTCATTTGATTAATGATTTCAGTGGGCAAGCATTGAGCTTGTTTGAGTAGAAATGTTCCTTGGGATGCTGTCTGGGGGAAGAAGACTTGTAATGTTTTCCTTGCAAAGATTGGGTTTCTTCTAATACTAATATTTGCTTTAGGGCTGTTGTCAAACACAGAATGGATCAGTGGA... |
Task1_train_33196 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GTGACCTTGTCCTGGATCCCAGCCCAGCTGGAGCCTGGCAGTCAATTGGACTTTGGGATGCAGGCTGGGTGGGGTTGGGGACAGAATGGGGTGAGAAGCATGGCTCGAGGGCACAGGGCCGCAGTGGTCTCACAGCACATGATGCGATGGGGATCGAGCCCAGCCTCCCTCCCACTCTGTGGGGAACGACCACAAATGAGGTTTTAGCAGCACACTGATAAGCAGAGCAGCTCTGCTAAGCCACAGATAAGACTCTGGAGGAAAAGCCTTTGGGAGGTGAGGGAGGACCCTCCACACCACCTGCTGGCCAAGCCCTGAGG... | GTGACCTTGTCCTGGATCCCAGCCCAGCTGGAGCCTGGCAGTCAATTGGACTTTGGGATGCAGGCTGGGTGGGGTTGGGGACAGAATGGGGTGAGAAGCATGGCTCGAGGGCACAGGGCCGCAGTGGTCTCACAGCACATGATGCGATGGGGATCGAGCCCAGCCTCCCTCCCACTCTGTGGGGAACGACCACAAATGAGGTTTTAGCAGCACACTGATAAGCAGAGCAGCTCTGCTAAGCCACAGATAAGACTCTGGAGGAAAAGCCTTTGGGAGGTGAGGGAGGACCCTCCACACCACCTGCTGGCCAAGCCCTGAGG... |
Task1_train_33197 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGATGGACCAGGAGGTTCACTCAGAAATGGAGGCAGAGTCAGGGCTGCCCACTGGACACATTACTTGGTAACAGGAAGCAATAGGTTCCCATGTTTACCTGCCTATTTTCACCTGGCTCAAAGCAGCCAAGAAAAGACGTCTCCTGGGTCAAAACTGATTCTATTCTGCCCCAGCACTGGATGGCTGTTCTAAGTGAATGATGGTAGTGCCTGAGAGCTCAGTCCCGGGTGAGCTCAGCCCCATCTGCCTCTTACCTGCCTTATACTCAGAGGCATATTTTCCTCCACATTCCCCCCTCAGAAGATCTACCGTCAAAGAA... | AGATGGACCAGGAGGTTCACTCAGAAATGGAGGCAGAGTCAGGGCTGCCCACTGGACACATTACTTGGTAACAGGAAGCAATAGGTTCCCATGTTTACCTGCCTATTTTCACCTGGCTCAAAGCAGCCAAGAAAAGACGTCTCCTGGGTCAAAACTGATTCTATTCTGCCCCAGCACTGGATGGCTGTTCTAAGTGAATGATGGTAGTGCCTGAGAGCTCAGTCCCGGGTGAGCTCAGCCCCATCTGCCTCTTACCTGCCTTATACTCAGAGGCATATTTTCCTCCACATTCCCCCCTCAGAAGATCTACCGTCAAAGAA... |
Task1_train_33198 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | CTGAGAGACAGTTTGTTATAATTTCTGTTCTTCCACATTTGCTGAGGAATGCTTTACTTCCAACTATGTGGTCAATTTTGGAATAAGTGCTGTGTGGTGCTGAGAAGAATGTATATTCTGTGGATTTGGGGTGGAGAGTTCTGTAGATGTCTATTAGGTCTGATTGGTGCAGAGCTGAGTTCAATTCCTGGATATCCTTGTTAACTTTCTGTCTTGTTGATCTGTCTAATGTGGACAGTGGGGTGTTAAAGTCTCCCATTATTATTGTATGGGAGTCTAAGCCTCTTTGTAGGTCTCTAAGGACTTGCTTTATGAATCTG... | CTGAGAGACAGTTTGTTATAATTTCTGTTCTTCCACATTTGCTGAGGAATGCTTTACTTCCAACTATGTGGTCAATTTTGGAATAAGTGCTGTGTGGTGCTGAGAAGAATGTATATTCTGTGGATTTGGGGTGGAGAGTTCTGTAGATGTCTATTAGGTCTGATTGGTGCAGAGCTGAGTTCAATTCCTGGATATCCTTGTTAACTTTCTGTCTTGTTGATCTGTCTAATGTGGACAGTGGGGTGTTAAAGTCTCCCATTATTATTGTATGGGAGTCTAAGCCTCTTTGTAGGTCTCTAAGGACTTGCTTTATGAATCTG... |
Task1_train_33199 | A variant on Chromosome 1 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TCTGAGCTAAATAATCTTGTTTCATCAAAATATCCCAGGCTGGGTTACATCAACTATTGATGCCAGAGATGAAATAGGCCCTCAAGTTTATTCTTCTGGAATTAAAGTTTGTTATTGGGCTGAAGATTTGAATTTACCCACCACAGAGGCATGATTTCTTTGAGACCCACGGGGCAAGATGGTTTTCCTGATAGAGTCAGTATAGATAAAAAGTGGTGATGATTTTATTCTACACTTCATTAGGTAGACAGTAAGTTTAAAACGCATTAACAAAAAGCTATTATTTTCTAATGACTTATGATACTACTTATTTTTAGAGT... | TCTGAGCTAAATAATCTTGTTTCATCAAAATATCCCAGGCTGGGTTACATCAACTATTGATGCCAGAGATGAAATAGGCCCTCAAGTTTATTCTTCTGGAATTAAAGTTTGTTATTGGGCTGAAGATTTGAATTTACCCACCACAGAGGCATGATTTCTTTGAGACCCACGGGGCAAGATGGTTTTCCTGATAGAGTCAGTATAGATAAAAAGTGGTGATGATTTTATTCTACACTTCATTAGGTAGACAGTAAGTTTAAAACGCATTAACAAAAAGCTATTATTTTCTAATGACTTATGATACTACTTATTTTTAGAGT... |
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