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_32400 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | CTTAAATAATGGCGTTTTCATATCCCTGCCACATTGGGTGTCCAGCCCTTGCTTGGGTGGATAGTGATCTGACTTGGGCTGGTAATTAGCCCATATTTTTAGTTCATGGGCAATTCTCAATGGTAACTGGGTCTATTAAACTTGATTCAGATATGACAGCTTAAATTGTAAACAGCTGCGAAGAGTTTCATACTTAATTACCATATTTAAGTTTTGCCATAAAGTGCCTGTACTTCCATCAAAAATGTAAATGTTGGAGACATTCAAATGAGGTTTTATACTTTCGTGAAGTGTAATTGGCACGGATCAGTCAGTTTGTT... | CTTAAATAATGGCGTTTTCATATCCCTGCCACATTGGGTGTCCAGCCCTTGCTTGGGTGGATAGTGATCTGACTTGGGCTGGTAATTAGCCCATATTTTTAGTTCATGGGCAATTCTCAATGGTAACTGGGTCTATTAAACTTGATTCAGATATGACAGCTTAAATTGTAAACAGCTGCGAAGAGTTTCATACTTAATTACCATATTTAAGTTTTGCCATAAAGTGCCTGTACTTCCATCAAAAATGTAAATGTTGGAGACATTCAAATGAGGTTTTATACTTTCGTGAAGTGTAATTGGCACGGATCAGTCAGTTTGTT... |
Task1_train_32401 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | CAGATGGGCAGATAAACAGGTCGTCCCCTTGTGGCCTTGCCTGTACTTCTTGTTTTGCATACACTTCTGCGCATTTGCACAGCTACCTCTTTGTCCTTTTTTGTGGCCAGAGTGAGAGTTCTCTCATAATGACATGTTAGCAAAGCTTGAGGTGCACTTTTAATTTTTTGCACAGAAATCTTTTTCTCCATCAGGGTAAAAGAATTCCCCCATTACCTCTAGGCTGTGAATGCAAAAATGGACCAAGTATTGAGAAATCAAAGGGCAGGGGGAATCAAATCCAAGCAGGAAATAGAGCCAACTAGTTCTATTTGGTAGAG... | CAGATGGGCAGATAAACAGGTCGTCCCCTTGTGGCCTTGCCTGTACTTCTTGTTTTGCATACACTTCTGCGCATTTGCACAGCTACCTCTTTGTCCTTTTTTGTGGCCAGAGTGAGAGTTCTCTCATAATGACATGTTAGCAAAGCTTGAGGTGCACTTTTAATTTTTTGCACAGAAATCTTTTTCTCCATCAGGGTAAAAGAATTCCCCCATTACCTCTAGGCTGTGAATGCAAAAATGGACCAAGTATTGAGAAATCAAAGGGCAGGGGGAATCAAATCCAAGCAGGAAATAGAGCCAACTAGTTCTATTTGGTAGAG... |
Task1_train_32402 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CGCTGCCATTCAGAACTTGGAGGAAGAGGCCAGGTGCAATGGCTCATGCCTATAATCCAAAACTTTGGGAGGCTGAGGCAGAGAATCACTTGTGGCCAGGAGTTCAAGAGCAATCTGGGCAACATAGCGAGACCCCATATCTACAAAAGAATTTTTTTAATTACCTGGGGGTGGTGGTAGCACGCACCTGTAGTACCAAAGCTTTGGGGAGGCTGAGGCAGGAGGACTGTTTGAGCCCAGGAGTTCAAGGCTGCAATGAGCTATGATTGCGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCCATCTCAAAATAA... | CGCTGCCATTCAGAACTTGGAGGAAGAGGCCAGGTGCAATGGCTCATGCCTATAATCCAAAACTTTGGGAGGCTGAGGCAGAGAATCACTTGTGGCCAGGAGTTCAAGAGCAATCTGGGCAACATAGCGAGACCCCATATCTACAAAAGAATTTTTTTAATTACCTGGGGGTGGTGGTAGCACGCACCTGTAGTACCAAAGCTTTGGGGAGGCTGAGGCAGGAGGACTGTTTGAGCCCAGGAGTTCAAGGCTGCAATGAGCTATGATTGCGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCCATCTCAAAATAA... |
Task1_train_32403 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TGTGTGGTGGAGTGTGCACGCCCCTGCCCCCTCCACTAAAAACAAAACAAAAAAACCCTCCTTAATTGAAGGAAAAACCAAACAAAAAAAGTCTTTGTCAGATCATAAAGTGGGATTATCATATTTTAAACACATTATTTTAACTACTTATAAAACTTTAGTAATAAAACTGCCGCCCACTCCCTTGCCAAACAAATTTTGTATATATAGATATGGTATATAAGGCCCCAACCCCATCCCCCAGCAAAGATAAAACAAGAACTGCTCCCTGCACCCTGTGTCCACTCCCAGGGGCCCCAGCTTCCTCCGGAAAACCTCCA... | TGTGTGGTGGAGTGTGCACGCCCCTGCCCCCTCCACTAAAAACAAAACAAAAAAACCCTCCTTAATTGAAGGAAAAACCAAACAAAAAAAGTCTTTGTCAGATCATAAAGTGGGATTATCATATTTTAAACACATTATTTTAACTACTTATAAAACTTTAGTAATAAAACTGCCGCCCACTCCCTTGCCAAACAAATTTTGTATATATAGATATGGTATATAAGGCCCCAACCCCATCCCCCAGCAAAGATAAAACAAGAACTGCTCCCTGCACCCTGTGTCCACTCCCAGGGGCCCCAGCTTCCTCCGGAAAACCTCCA... |
Task1_train_32404 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | CACTCCTGACTCCCCTCACAGGGCACTGACCGGGGAAATCCCTCCATGGGGCCTGGACTATGGAAGAGTCAAGTGCAGGAAGAACTTTCCATAAGGACTGGAGCAAAAGGCTGGGAATTGGAGGAGATTGGGGGTGGGGCTGCTGAAGGAGGAGAGACCAATCCTGGGGACAGTTGGGGGCACCTTACCCAATTCCTCCACCCCCGCCCCTTAACTCCTCACTTGTCTCACCTGTTGACCTTCTCATGTGCCGATTCAGAGATTCCTCACACTCAGGCTCTGACCTCCACTGACTCTGATGGCCCACAGCAGGTGCAGGG... | CACTCCTGACTCCCCTCACAGGGCACTGACCGGGGAAATCCCTCCATGGGGCCTGGACTATGGAAGAGTCAAGTGCAGGAAGAACTTTCCATAAGGACTGGAGCAAAAGGCTGGGAATTGGAGGAGATTGGGGGTGGGGCTGCTGAAGGAGGAGAGACCAATCCTGGGGACAGTTGGGGGCACCTTACCCAATTCCTCCACCCCCGCCCCTTAACTCCTCACTTGTCTCACCTGTTGACCTTCTCATGTGCCGATTCAGAGATTCCTCACACTCAGGCTCTGACCTCCACTGACTCTGATGGCCCACAGCAGGTGCAGGG... |
Task1_train_32405 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTCTGCCACAGTGTTTGGGGAACCCCCCCCCCTTCCTTGAAGATGGTCCTGGGATGAATCTGAGACTTGGCTGTGAGATTTGGGGCAAGTTTCTTCTCCAATCTTGGCCTCAGTTTCCCCATCTTTAGAGAAGACCGCTGTGGCAAATAGATGTCAAAGCATGCACCAATGCCAGTTGACCGCCGATGGCTGCCTGGGATGCTATGTTGGGAGGGATTCTGAGTCCTGAAAGAATGTCATGACCCATTAGTGACATCTGTCATGAGTGAGGAAGGAAGGGGAAGCAGTGACCCTGCCACCATCTCCCACCTCTGGAGCAA... | CTCTGCCACAGTGTTTGGGGAACCCCCCCCCCTTCCTTGAAGATGGTCCTGGGATGAATCTGAGACTTGGCTGTGAGATTTGGGGCAAGTTTCTTCTCCAATCTTGGCCTCAGTTTCCCCATCTTTAGAGAAGACCGCTGTGGCAAATAGATGTCAAAGCATGCACCAATGCCAGTTGACCGCCGATGGCTGCCTGGGATGCTATGTTGGGAGGGATTCTGAGTCCTGAAAGAATGTCATGACCCATTAGTGACATCTGTCATGAGTGAGGAAGGAAGGGGAAGCAGTGACCCTGCCACCATCTCCCACCTCTGGAGCAA... |
Task1_train_32406 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CTGATTTTTTGCAACAGCACCATGAGTTGGTCATTATTAGAGGGCTCACTTCTAACCTGACTTTTTAAATTAGAAAATAAAACTCAGGCAGAAGGGGGCTTGCCAAAGGTCACACAGATAAACAAATGACAGAACCAGGATTTAAACTCAGGACTGTCTGATTCCAGAGGGCATATTATTTCTACTGCCCCAAGAGGCCTCCCTGCCATGGATCCATATGTAATTTATGAAGCAGGAATTCTGCACCAGGCACTGTGCTAGGCTCTGGGCTCATCTAGAAATCGACTATATGAATTTTTTTTTTTTTTTTTTTGAGATGG... | CTGATTTTTTGCAACAGCACCATGAGTTGGTCATTATTAGAGGGCTCACTTCTAACCTGACTTTTTAAATTAGAAAATAAAACTCAGGCAGAAGGGGGCTTGCCAAAGGTCACACAGATAAACAAATGACAGAACCAGGATTTAAACTCAGGACTGTCTGATTCCAGAGGGCATATTATTTCTACTGCCCCAAGAGGCCTCCCTGCCATGGATCCATATGTAATTTATGAAGCAGGAATTCTGCACCAGGCACTGTGCTAGGCTCTGGGCTCATCTAGAAATCGACTATATGAATTTTTTTTTTTTTTTTTTTGAGATGG... |
Task1_train_32407 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | CCTGTGGAGACCCGGTCTGGGGAGTCACGATTGGGGTGGGAGATGAGCAAACCTGCTGAATAAAGTTAAAACGTTATTTAAATGGGGAGCTGAGGAAGGAGCAAACGGGTTTTCGCGGTTAAACCCGTGGGTTTTGGAATGTGTGTTCCCGGCTGTGTGATCCTGGGCAAGAACTTGACCTCCCTGGACGCAGCGGCACCCCTCGGTTATTAAGGAGGGAGGAGTAGGGGATAGAAGTATTTCAAAATAGTTGTAATGCGCATGGCAAAGTGCCCAGCATATAGAAAGTGCTCAATAAACGATAACTGCTGTGACTTCTA... | CCTGTGGAGACCCGGTCTGGGGAGTCACGATTGGGGTGGGAGATGAGCAAACCTGCTGAATAAAGTTAAAACGTTATTTAAATGGGGAGCTGAGGAAGGAGCAAACGGGTTTTCGCGGTTAAACCCGTGGGTTTTGGAATGTGTGTTCCCGGCTGTGTGATCCTGGGCAAGAACTTGACCTCCCTGGACGCAGCGGCACCCCTCGGTTATTAAGGAGGGAGGAGTAGGGGATAGAAGTATTTCAAAATAGTTGTAATGCGCATGGCAAAGTGCCCAGCATATAGAAAGTGCTCAATAAACGATAACTGCTGTGACTTCTA... |
Task1_train_32408 | Consider a variant on Chromosome 1. Determine its clinical classification and disease relevance. | Benign | GGGCTGGGGTGGGCACATCCTCATCCTGCTCTTCCCTCCCACAGACAGCAGTGAAGAGGCACTGGAAGGAATGGTACGGGGGCTGAGGCAGGGTGGCGTGTCCCTCCTAGGCCAGCCACAGCCCCTGACCCAGGAACAGTGGCGGAGCTCTTTCATGCGGCGCAACCGAGACCCTCAGCTCAATGAGCGAGTGCACCGTGTGCGGGCGCTACAGAGCACACTCAAGGTCAGCTGGGGGGCTCTGGGCACAGCAAGGGACTAGGCTCTGGGCTTCAGGCTTTGGTTTGCGGCTGTCACCTCCACCCTGGGCACCAGACTCC... | GGGCTGGGGTGGGCACATCCTCATCCTGCTCTTCCCTCCCACAGACAGCAGTGAAGAGGCACTGGAAGGAATGGTACGGGGGCTGAGGCAGGGTGGCGTGTCCCTCCTAGGCCAGCCACAGCCCCTGACCCAGGAACAGTGGCGGAGCTCTTTCATGCGGCGCAACCGAGACCCTCAGCTCAATGAGCGAGTGCACCGTGTGCGGGCGCTACAGAGCACACTCAAGGTCAGCTGGGGGGCTCTGGGCACAGCAAGGGACTAGGCTCTGGGCTTCAGGCTTTGGTTTGCGGCTGTCACCTCCACCCTGGGCACCAGACTCC... |
Task1_train_32409 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCTTAGCCCCTCCTCTCCACACAGGCAAAGCTGCAGGAGCTGCAGGTCCTAGAAGAAGTGCTGGGTGACCCTGAGCTGACAGGAGAGAAGTTCCGCCAGTGGAAGGAGCAGAACCGGGAGCTGTACTCAGAGGGCCTGGGGGCCTGGGGAGTGGCACAGGCTGAAGGCAGCTCCCACATCTTGACCTCTGACTCCACAGAACAGTCCCCCCACTCCCTGCCCTCTGACCCTGAAGAGCACTCCCATCTCTGCCCCCTGACCTCAGAGAGCAGCCTCCGACCTCCTGACCTCTGACCCTGGCCAGCACTCTAGCTCCTGAC... | CCTTAGCCCCTCCTCTCCACACAGGCAAAGCTGCAGGAGCTGCAGGTCCTAGAAGAAGTGCTGGGTGACCCTGAGCTGACAGGAGAGAAGTTCCGCCAGTGGAAGGAGCAGAACCGGGAGCTGTACTCAGAGGGCCTGGGGGCCTGGGGAGTGGCACAGGCTGAAGGCAGCTCCCACATCTTGACCTCTGACTCCACAGAACAGTCCCCCCACTCCCTGCCCTCTGACCCTGAAGAGCACTCCCATCTCTGCCCCCTGACCTCAGAGAGCAGCCTCCGACCTCCTGACCTCTGACCCTGGCCAGCACTCTAGCTCCTGAC... |
Task1_train_32410 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GTGCCAGGCACTGACTGTGCAGACTGCCAGGGTCCCAGGGATAATAAGCACAACTGGGTCCTGTCTCAGACACACAGAAACTGTCATTACAAGTGCTCAAGTAGCACCCAGAGTACATGGAGGCTCAACGAAGGCACTCGAACCTAATCTCAGGGGTCAGAGCTGGCTTCCTGGAGAAAGTGACACTGGAGCTGAGAGTAAAGAAGTAGGATGTGATCTCAGTCACCACAACAAAGAAACAGAAAAAAAGAGCACGTAGGAGTTGGCCAGGCAAAGAGAGGTGGGGGAGACTTTTTGGGGAAAAGAAACAGCATGTGAGA... | GTGCCAGGCACTGACTGTGCAGACTGCCAGGGTCCCAGGGATAATAAGCACAACTGGGTCCTGTCTCAGACACACAGAAACTGTCATTACAAGTGCTCAAGTAGCACCCAGAGTACATGGAGGCTCAACGAAGGCACTCGAACCTAATCTCAGGGGTCAGAGCTGGCTTCCTGGAGAAAGTGACACTGGAGCTGAGAGTAAAGAAGTAGGATGTGATCTCAGTCACCACAACAAAGAAACAGAAAAAAAGAGCACGTAGGAGTTGGCCAGGCAAAGAGAGGTGGGGGAGACTTTTTGGGGAAAAGAAACAGCATGTGAGA... |
Task1_train_32411 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TCCTGTGTAAGTGTCTTATTGGACAAAGGGCTTGCAAAATGTACCAGTCTCCCTTTCTTTCTTTTCTTTCTTTTTTTTTTTTTTTTGAGATTATCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAACTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACGTGCCACCATGCCCAGATAATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACATCGTGATCCACCTGCCTCAGACTC... | TCCTGTGTAAGTGTCTTATTGGACAAAGGGCTTGCAAAATGTACCAGTCTCCCTTTCTTTCTTTTCTTTCTTTTTTTTTTTTTTTTGAGATTATCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAACTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACGTGCCACCATGCCCAGATAATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACATCGTGATCCACCTGCCTCAGACTC... |
Task1_train_32412 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGAGGAGGGAAGGGGCTGGGAAGGGCCTAGGGGCACCCCTGACAGGCTCTGCCACAGGGCGCTTCGTCTGGTGCATGTGTGCATGGCGGTGGAGCCCCTCGCCCGGATCATCCGCGTCATCCTGCAGTCGGTGCCTGACATGGCCAATATCATGGTCCTCATCCTCTTCTTCATGCTGGTCAGTGCCTGCCCCCGCCCCCAGCTGTTTCCCTTCCCTGAACAGGGCCCTTGGGTCATTGCAAATAGAGGGGTGTCTGGAAAAGCAGAGAGGCCTGTGGGCCTGAATCCCTGTGATTTCCTCAGCAGCGTTCATTTACATG... | TGAGGAGGGAAGGGGCTGGGAAGGGCCTAGGGGCACCCCTGACAGGCTCTGCCACAGGGCGCTTCGTCTGGTGCATGTGTGCATGGCGGTGGAGCCCCTCGCCCGGATCATCCGCGTCATCCTGCAGTCGGTGCCTGACATGGCCAATATCATGGTCCTCATCCTCTTCTTCATGCTGGTCAGTGCCTGCCCCCGCCCCCAGCTGTTTCCCTTCCCTGAACAGGGCCCTTGGGTCATTGCAAATAGAGGGGTGTCTGGAAAAGCAGAGAGGCCTGTGGGCCTGAATCCCTGTGATTTCCTCAGCAGCGTTCATTTACATG... |
Task1_train_32413 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GCTAATATTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTTTCGATCTCCTGACCTCATGATCCCCCCTCCTCAGCCTCCCAAAGTGCTGGGGATTACAGGCATGAGCCACTGCGCCCGGCCTCATCTTTTTCATCATAGCCATTCTGACAGGTGTGAGGTGGCTTGCCCATATTTTTAAAGAGTTGCTTAAGGCCGGGCATGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCTGAGGCAGGTGGATCACTTGAGCCCATGAGTTCGAGACCAGTCTGGGCAACATGGCGAAACCCCA... | GCTAATATTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTTTCGATCTCCTGACCTCATGATCCCCCCTCCTCAGCCTCCCAAAGTGCTGGGGATTACAGGCATGAGCCACTGCGCCCGGCCTCATCTTTTTCATCATAGCCATTCTGACAGGTGTGAGGTGGCTTGCCCATATTTTTAAAGAGTTGCTTAAGGCCGGGCATGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCTGAGGCAGGTGGATCACTTGAGCCCATGAGTTCGAGACCAGTCTGGGCAACATGGCGAAACCCCA... |
Task1_train_32414 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | GCAACAAGAGCGAAACTGTCTCAAAAAAAGGGGGGTGGGATACAATTCAGGACCAGCCAAATGACATAGGGTGAGGTCCAGGAGCATCCTGAGAGCAGAGCTTCCATGCCCTCTCCTTGTGGAATAAGAGCATGTAAACACAGCACATTTATGTGTTTACCTACCAGGAAGCTCCAGTGAGCTGCTGTGTCCAGAGTTTTTAGTTGGAGTTTTATCTATGTAGGCATGATTGAACTCAATCACCCGTCCCTCTGCCTTCCCCATAGTAGATTAGGCTTAAAGCAGTTGATTTTTCTGGTGATCTGCATCCATTCTGAGTC... | GCAACAAGAGCGAAACTGTCTCAAAAAAAGGGGGGTGGGATACAATTCAGGACCAGCCAAATGACATAGGGTGAGGTCCAGGAGCATCCTGAGAGCAGAGCTTCCATGCCCTCTCCTTGTGGAATAAGAGCATGTAAACACAGCACATTTATGTGTTTACCTACCAGGAAGCTCCAGTGAGCTGCTGTGTCCAGAGTTTTTAGTTGGAGTTTTATCTATGTAGGCATGATTGAACTCAATCACCCGTCCCTCTGCCTTCCCCATAGTAGATTAGGCTTAAAGCAGTTGATTTTTCTGGTGATCTGCATCCATTCTGAGTC... |
Task1_train_32415 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GATGGACTCCAACAGGAAAACTGGGGACACAGCGGGCCTGGCCGCCCAGCCTTCCAGCTCTTCTGGCTGGGGCTGCACTGCTTGCGGGCTGCCCTGAGAGAAACCTGTATCCACAGCTGGGGAGCACTTACAGGGTGCTAGGCGCGTTGGGGCACCCAAGGGGTGTTGTGGAATAATAGAGAACTAAGAGACTTGGGAAGACAACCCTGAGTGAGGAAGGCATCGGCCCACAGGGAGTCTGGGGAGATGGTCCTTTGGGGAGAGGCCAGGAGATGTCCAAGTGGAGCCTGCTGTGGTTATGGAGGTGACAGGGGACACTC... | GATGGACTCCAACAGGAAAACTGGGGACACAGCGGGCCTGGCCGCCCAGCCTTCCAGCTCTTCTGGCTGGGGCTGCACTGCTTGCGGGCTGCCCTGAGAGAAACCTGTATCCACAGCTGGGGAGCACTTACAGGGTGCTAGGCGCGTTGGGGCACCCAAGGGGTGTTGTGGAATAATAGAGAACTAAGAGACTTGGGAAGACAACCCTGAGTGAGGAAGGCATCGGCCCACAGGGAGTCTGGGGAGATGGTCCTTTGGGGAGAGGCCAGGAGATGTCCAAGTGGAGCCTGCTGTGGTTATGGAGGTGACAGGGGACACTC... |
Task1_train_32416 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GACTCCAACAGGAAAACTGGGGACACAGCGGGCCTGGCCGCCCAGCCTTCCAGCTCTTCTGGCTGGGGCTGCACTGCTTGCGGGCTGCCCTGAGAGAAACCTGTATCCACAGCTGGGGAGCACTTACAGGGTGCTAGGCGCGTTGGGGCACCCAAGGGGTGTTGTGGAATAATAGAGAACTAAGAGACTTGGGAAGACAACCCTGAGTGAGGAAGGCATCGGCCCACAGGGAGTCTGGGGAGATGGTCCTTTGGGGAGAGGCCAGGAGATGTCCAAGTGGAGCCTGCTGTGGTTATGGAGGTGACAGGGGACACTCTAAC... | GACTCCAACAGGAAAACTGGGGACACAGCGGGCCTGGCCGCCCAGCCTTCCAGCTCTTCTGGCTGGGGCTGCACTGCTTGCGGGCTGCCCTGAGAGAAACCTGTATCCACAGCTGGGGAGCACTTACAGGGTGCTAGGCGCGTTGGGGCACCCAAGGGGTGTTGTGGAATAATAGAGAACTAAGAGACTTGGGAAGACAACCCTGAGTGAGGAAGGCATCGGCCCACAGGGAGTCTGGGGAGATGGTCCTTTGGGGAGAGGCCAGGAGATGTCCAAGTGGAGCCTGCTGTGGTTATGGAGGTGACAGGGGACACTCTAAC... |
Task1_train_32417 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | TGAAGCAGGAGAATTGCTTGAACCGGGAGGCAGAGGCTGCAGTGAGCTGAGACAGTGCCACTGCACTCCAGTCTGGGCGACAGAGCGAGACTCCATCTCAAAAAAACAAACAAACAAAACAAACAAACAAACAAACAAAAAACAGGAAACTCCCAACAGCATTCAGTGGTTTTTACTATTAGTTGTAATAAGGGCATTATAACTTTGAAACACCTAGCATGCAGATTTTGGTCTCTACCATTTGCCACTAAAAAGAACCAGGGTTCCTTGGCAAATAGCCAATTCTAGATTTGGAGCAAAAAAAAAAAAAAATGTACAAA... | TGAAGCAGGAGAATTGCTTGAACCGGGAGGCAGAGGCTGCAGTGAGCTGAGACAGTGCCACTGCACTCCAGTCTGGGCGACAGAGCGAGACTCCATCTCAAAAAAACAAACAAACAAAACAAACAAACAAACAAACAAAAAACAGGAAACTCCCAACAGCATTCAGTGGTTTTTACTATTAGTTGTAATAAGGGCATTATAACTTTGAAACACCTAGCATGCAGATTTTGGTCTCTACCATTTGCCACTAAAAAGAACCAGGGTTCCTTGGCAAATAGCCAATTCTAGATTTGGAGCAAAAAAAAAAAAAAATGTACAAA... |
Task1_train_32418 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | CATGAGTGAGCATCTGTGAGCAAATGAATGAGCAAACATGCCTGGCACCTCGGGTCTGACTGGGGGCCTGCATGCTGGCTCCTGGGGGGCAGGTAACCCCCACGTTCCCTCCCATCTTGTCTCTGCTGCTCTGTCCCCTTCCTGCTTGAGCATCCACTCAAACTTCCCCAGGCTGCTTTCCCAAGCTGAGCTTGGCCTCTGCCTGGGCCCTGACTCCTCAAGCCAGGCTGCCCATTCCCCAGAATCTCTTTCTTCCCCAGTCAGCTCCACGGTCAAGAATCTATGGACCAGTCCACATTAAGCCCCTCTGCCCACTACCC... | CATGAGTGAGCATCTGTGAGCAAATGAATGAGCAAACATGCCTGGCACCTCGGGTCTGACTGGGGGCCTGCATGCTGGCTCCTGGGGGGCAGGTAACCCCCACGTTCCCTCCCATCTTGTCTCTGCTGCTCTGTCCCCTTCCTGCTTGAGCATCCACTCAAACTTCCCCAGGCTGCTTTCCCAAGCTGAGCTTGGCCTCTGCCTGGGCCCTGACTCCTCAAGCCAGGCTGCCCATTCCCCAGAATCTCTTTCTTCCCCAGTCAGCTCCACGGTCAAGAATCTATGGACCAGTCCACATTAAGCCCCTCTGCCCACTACCC... |
Task1_train_32419 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | GCATGCCAGCACACTCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACATGTTGGCCAGGCTGGTCTCCAACTCCTGTCCTCAGCCGATCCACCTGCCTTGGCTTCCCAAAGTGCTGGCATTACAGGCGTGAGTCACTGCTCCTGGCCTCGGGGATTTCAACTCTAGGCACTCGAGGCCGTCTCCCACCTCCAACTCACTCACCCAGACAACCCTCCTTAGGGAGCCGATGCCTTGGGGACTCCACTTTGTCCCTGGGGTTCTGAGTTCCATGTCTCCTTCAGGCAGGACCAGCTTCTGACCCCGGAACTCTGG... | GCATGCCAGCACACTCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACATGTTGGCCAGGCTGGTCTCCAACTCCTGTCCTCAGCCGATCCACCTGCCTTGGCTTCCCAAAGTGCTGGCATTACAGGCGTGAGTCACTGCTCCTGGCCTCGGGGATTTCAACTCTAGGCACTCGAGGCCGTCTCCCACCTCCAACTCACTCACCCAGACAACCCTCCTTAGGGAGCCGATGCCTTGGGGACTCCACTTTGTCCCTGGGGTTCTGAGTTCCATGTCTCCTTCAGGCAGGACCAGCTTCTGACCCCGGAACTCTGG... |
Task1_train_32420 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CAACTCTAGGCACTCGAGGCCGTCTCCCACCTCCAACTCACTCACCCAGACAACCCTCCTTAGGGAGCCGATGCCTTGGGGACTCCACTTTGTCCCTGGGGTTCTGAGTTCCATGTCTCCTTCAGGCAGGACCAGCTTCTGACCCCGGAACTCTGGCTCTTCGTACAGCACCCAGCTGTGGGCACAGAGATTCCAGGATCACAGATGGGGAGGAGGATGTGCCCAGGGCTGCTGGGTAGCTGATGGGGTTTCTCCCAGGCTGGACTGGTCACTCCTCACTCCCCTCTGCATCCCCCCAGGTTCACAGCCAAGTGCCTTGC... | CAACTCTAGGCACTCGAGGCCGTCTCCCACCTCCAACTCACTCACCCAGACAACCCTCCTTAGGGAGCCGATGCCTTGGGGACTCCACTTTGTCCCTGGGGTTCTGAGTTCCATGTCTCCTTCAGGCAGGACCAGCTTCTGACCCCGGAACTCTGGCTCTTCGTACAGCACCCAGCTGTGGGCACAGAGATTCCAGGATCACAGATGGGGAGGAGGATGTGCCCAGGGCTGCTGGGTAGCTGATGGGGTTTCTCCCAGGCTGGACTGGTCACTCCTCACTCCCCTCTGCATCCCCCCAGGTTCACAGCCAAGTGCCTTGC... |
Task1_train_32421 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGCAGGGAGAGCATCAGGGTCCTGCACAACCTCTTTCTGGGTGAGAGATGAGATGGGGCTCCCTTCAGAGTCCTGGACCCCCTTATCCTGTTTGGGGAGTGAGGTGGCAGGAGCAATTGGGCCTTGAACAGTCTCTTCCTTGGTGAGGGGCGGGGCAAGGCTGCCTGCAATACCCTGGACAGCCTCTTTTTGGATGCTACTGCTGCCTTTTGGGCCCTGGACAACCTCAGTTGACTTGGGGGACAAGGCAGCAGGAGCACCAGACCCCTGCACCACCTCCTTCTGGGTGGGAGATGAGGCAGCAGGAGCACAGGGGCCCT... | GGCAGGGAGAGCATCAGGGTCCTGCACAACCTCTTTCTGGGTGAGAGATGAGATGGGGCTCCCTTCAGAGTCCTGGACCCCCTTATCCTGTTTGGGGAGTGAGGTGGCAGGAGCAATTGGGCCTTGAACAGTCTCTTCCTTGGTGAGGGGCGGGGCAAGGCTGCCTGCAATACCCTGGACAGCCTCTTTTTGGATGCTACTGCTGCCTTTTGGGCCCTGGACAACCTCAGTTGACTTGGGGGACAAGGCAGCAGGAGCACCAGACCCCTGCACCACCTCCTTCTGGGTGGGAGATGAGGCAGCAGGAGCACAGGGGCCCT... |
Task1_train_32422 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CTTTCTGGGTGAGAGATGAGATGGGGCTCCCTTCAGAGTCCTGGACCCCCTTATCCTGTTTGGGGAGTGAGGTGGCAGGAGCAATTGGGCCTTGAACAGTCTCTTCCTTGGTGAGGGGCGGGGCAAGGCTGCCTGCAATACCCTGGACAGCCTCTTTTTGGATGCTACTGCTGCCTTTTGGGCCCTGGACAACCTCAGTTGACTTGGGGGACAAGGCAGCAGGAGCACCAGACCCCTGCACCACCTCCTTCTGGGTGGGAGATGAGGCAGCAGGAGCACAGGGGCCCTTCACAACCTCTTTCTGGGTGGGCGATGAGGCA... | CTTTCTGGGTGAGAGATGAGATGGGGCTCCCTTCAGAGTCCTGGACCCCCTTATCCTGTTTGGGGAGTGAGGTGGCAGGAGCAATTGGGCCTTGAACAGTCTCTTCCTTGGTGAGGGGCGGGGCAAGGCTGCCTGCAATACCCTGGACAGCCTCTTTTTGGATGCTACTGCTGCCTTTTGGGCCCTGGACAACCTCAGTTGACTTGGGGGACAAGGCAGCAGGAGCACCAGACCCCTGCACCACCTCCTTCTGGGTGGGAGATGAGGCAGCAGGAGCACAGGGGCCCTTCACAACCTCTTTCTGGGTGGGCGATGAGGCA... |
Task1_train_32423 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CCCCCAAACTAGGCCAAACCAGTCCACAGGCCCACATGCAGGCAAACACATGCTGTGTCACACAGACGCAGGCACAGACACACAGACAGATACCGACACAGACCCACAATCACACAGGCACAAAGATACACCTAGAAGCCTATAAAAACATACACAACCAGGGACACACACACAAATATACACTCACCCAAGAAATACAAACACGCACAGGCACTCAGAGCCACAACAGACACACAAATCACATACAGACAGAAACACAGGCACAGTGACACACACGTGCACACATTCACAATACACACACAGTCAATTCACAGCCCCAA... | CCCCCAAACTAGGCCAAACCAGTCCACAGGCCCACATGCAGGCAAACACATGCTGTGTCACACAGACGCAGGCACAGACACACAGACAGATACCGACACAGACCCACAATCACACAGGCACAAAGATACACCTAGAAGCCTATAAAAACATACACAACCAGGGACACACACACAAATATACACTCACCCAAGAAATACAAACACGCACAGGCACTCAGAGCCACAACAGACACACAAATCACATACAGACAGAAACACAGGCACAGTGACACACACGTGCACACATTCACAATACACACACAGTCAATTCACAGCCCCAA... |
Task1_train_32424 | This variant is located on Chromosome 1. Evaluate its biological effect and specify any disease association. | Benign | ACCAGGGACACACACACAAATATACACTCACCCAAGAAATACAAACACGCACAGGCACTCAGAGCCACAACAGACACACAAATCACATACAGACAGAAACACAGGCACAGTGACACACACGTGCACACATTCACAATACACACACAGTCAATTCACAGCCCCAAGCTCTCTTCCCCTTGAAATTCACCTACCCCTGAACGTGGACACACACGCTTGGATGCACACGTATCTTACACATTCCCACTGGCAGTCCCAGCTATGTCTCACTTCTTCTCGACTCCCATATTTGCCAATCTTGGCCCAGAGAACCTTCTCCCAGG... | ACCAGGGACACACACACAAATATACACTCACCCAAGAAATACAAACACGCACAGGCACTCAGAGCCACAACAGACACACAAATCACATACAGACAGAAACACAGGCACAGTGACACACACGTGCACACATTCACAATACACACACAGTCAATTCACAGCCCCAAGCTCTCTTCCCCTTGAAATTCACCTACCCCTGAACGTGGACACACACGCTTGGATGCACACGTATCTTACACATTCCCACTGGCAGTCCCAGCTATGTCTCACTTCTTCTCGACTCCCATATTTGCCAATCTTGGCCCAGAGAACCTTCTCCCAGG... |
Task1_train_32425 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CCCCCCAGCTAACCCTACTTCTCTTTCCCGTCCCCCTCTCCAAGGTAGCCTCCTCCACCCCCCTTCCCTCTCTCTGCAGCCCTTGTCCCCCAGCCCCTGACTTCTGGGGCATCCAAGCAGGTCTCAGAGCCAGCCTGGGTCCTACATCTCCCTCTTCCTTGGCACGGAAGCAGTCACATTGACCCCTGCTTGGAGGACCCCAGCATTCCTGATTCTGCCTCTGCTACTACAATGCTGCCCAATCCACCGCCATAGGAGCCTAGAAAACCCTGGAGCCCACACAGCAACCTCACTCAACCCTCCACTCTCTGCACAGGGCC... | CCCCCCAGCTAACCCTACTTCTCTTTCCCGTCCCCCTCTCCAAGGTAGCCTCCTCCACCCCCCTTCCCTCTCTCTGCAGCCCTTGTCCCCCAGCCCCTGACTTCTGGGGCATCCAAGCAGGTCTCAGAGCCAGCCTGGGTCCTACATCTCCCTCTTCCTTGGCACGGAAGCAGTCACATTGACCCCTGCTTGGAGGACCCCAGCATTCCTGATTCTGCCTCTGCTACTACAATGCTGCCCAATCCACCGCCATAGGAGCCTAGAAAACCCTGGAGCCCACACAGCAACCTCACTCAACCCTCCACTCTCTGCACAGGGCC... |
Task1_train_32426 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CTGCACCCCAGCCTGGGCAACAGAGTGAGACTCCCATCTCAAAAATGAAACAAAACAAAACAAAGCAAAACAAAAAAAGAGCACAAGGGACTGGGTCTGGTAGCTCAAACCCATAATCCCAGCACGATGGGAGGCCAAGCCAAATCAGTAGAGCTCAGGAGTTTGAGACCAGGCTGAGCAACATAGCCAAATTCCAACTCTACAAAAAATAAAAAGATTGGGTGGACATGTTGGCATGTTCCTAGCTACTTGGGAGGCTGAGGCAGGAGGAGTTTGAGGATGCAGTGTCCTATGATAGTGACACTGCATTCCAGCCTGGG... | CTGCACCCCAGCCTGGGCAACAGAGTGAGACTCCCATCTCAAAAATGAAACAAAACAAAACAAAGCAAAACAAAAAAAGAGCACAAGGGACTGGGTCTGGTAGCTCAAACCCATAATCCCAGCACGATGGGAGGCCAAGCCAAATCAGTAGAGCTCAGGAGTTTGAGACCAGGCTGAGCAACATAGCCAAATTCCAACTCTACAAAAAATAAAAAGATTGGGTGGACATGTTGGCATGTTCCTAGCTACTTGGGAGGCTGAGGCAGGAGGAGTTTGAGGATGCAGTGTCCTATGATAGTGACACTGCATTCCAGCCTGGG... |
Task1_train_32427 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TGCTATTCTAGATAAAGAGTACTAAAATAAAAAACCTGTTAAAAAATAAACTGTCAGCCAGGTGCAGTGGCTCATGCCTATAATCCCAGTGCTTTGGGAGGCTGAGGCAGGAGGATTGCTTAAGCCTAGGAATTTGAGACCAGCCTGGGCAACAAAGCAAAATCCCATCTCTACAAAACAATAAGAAAATTAAGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGAAGATCACCTGAGGTTGGGAGTTCAAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAAGG... | TGCTATTCTAGATAAAGAGTACTAAAATAAAAAACCTGTTAAAAAATAAACTGTCAGCCAGGTGCAGTGGCTCATGCCTATAATCCCAGTGCTTTGGGAGGCTGAGGCAGGAGGATTGCTTAAGCCTAGGAATTTGAGACCAGCCTGGGCAACAAAGCAAAATCCCATCTCTACAAAACAATAAGAAAATTAAGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGAAGATCACCTGAGGTTGGGAGTTCAAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAAGG... |
Task1_train_32428 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | TCTGTCGCTGGCTTTGCGAATCCAACTATAGTGAAAACTTCATTGTGCCGCTTTTCAAGGAATGGGACTTCTGTCTTGCATCCCTGAGCGTAAGCTCTTGCCTTGGTAACCTGCCAGGGACCCTAGCCCCTCTGGGTTGGAAGCTTGCCTTGCAGTTACTAGTCCCTCCCCTTCAGGATAAAGGGCCATACCTATGCAAGCATGGTAAACAATATGCAAACACTCAAGTCTCTATCCCCTGTTAACTTGGTCCCTGGAGAGCACATAACTAGGGGAAGTCCTTGTTCTGGGAGAGACTCCATTTGGAAGCAGCTCACATG... | TCTGTCGCTGGCTTTGCGAATCCAACTATAGTGAAAACTTCATTGTGCCGCTTTTCAAGGAATGGGACTTCTGTCTTGCATCCCTGAGCGTAAGCTCTTGCCTTGGTAACCTGCCAGGGACCCTAGCCCCTCTGGGTTGGAAGCTTGCCTTGCAGTTACTAGTCCCTCCCCTTCAGGATAAAGGGCCATACCTATGCAAGCATGGTAAACAATATGCAAACACTCAAGTCTCTATCCCCTGTTAACTTGGTCCCTGGAGAGCACATAACTAGGGGAAGTCCTTGTTCTGGGAGAGACTCCATTTGGAAGCAGCTCACATG... |
Task1_train_32429 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GAACTGCCCAATAACTTGTATTATTTAAAAAAATAAATAAATAATATGAAGGGTGCCCACCCAGACCCATAGATCGGGATTTTAGGCCCAGGGATCCAGCTCACCAGGTAGCCGTTCTTACCAGCCCCGAGACCAGAATTTGGGAATTTTTATGCCAGATGGAAAGCAGAGCTGGTGAAGGCATGCCAGGGGGAGGTGCAGAGGCAAAGTCTGAGGATCTGACAAAGCAGAGAACCCTGGGGGAGCAGGTTGCTCAGACTGGCTGATTAACAGGTCTTGATGGGGTCTGGTGGGAAAAGGGACCAGAGAGATGGGCAGGG... | GAACTGCCCAATAACTTGTATTATTTAAAAAAATAAATAAATAATATGAAGGGTGCCCACCCAGACCCATAGATCGGGATTTTAGGCCCAGGGATCCAGCTCACCAGGTAGCCGTTCTTACCAGCCCCGAGACCAGAATTTGGGAATTTTTATGCCAGATGGAAAGCAGAGCTGGTGAAGGCATGCCAGGGGGAGGTGCAGAGGCAAAGTCTGAGGATCTGACAAAGCAGAGAACCCTGGGGGAGCAGGTTGCTCAGACTGGCTGATTAACAGGTCTTGATGGGGTCTGGTGGGAAAAGGGACCAGAGAGATGGGCAGGG... |
Task1_train_32430 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | CGCTGCTCCTGGTGGTCTGGTTGGCAGAGGCAAGAGGGACGGGCATAATTCTTGCTCCAGGCTGACTTGGATGTATCAGCAAGAATCCTGGGACTGGGGCAGAGGGGTCTGACTGGGAGGAGGCGGGAGGTGTGTCGGAGACAGGGATCAGAGCCTGAATAGATCCTTGTCCTCTGCAGTTTGAGATGCTGACGGGCTCCCTGCCCTTCCAGGGGAAGGACCGGAAGGAGACCATGACACTGATTCTGAAGTAAGCCCCAGCCCTGCCCTGATAACAATGGACTCCTCCAAGCCCCAGCCCCAGTTTGGGGGTCAGAATA... | CGCTGCTCCTGGTGGTCTGGTTGGCAGAGGCAAGAGGGACGGGCATAATTCTTGCTCCAGGCTGACTTGGATGTATCAGCAAGAATCCTGGGACTGGGGCAGAGGGGTCTGACTGGGAGGAGGCGGGAGGTGTGTCGGAGACAGGGATCAGAGCCTGAATAGATCCTTGTCCTCTGCAGTTTGAGATGCTGACGGGCTCCCTGCCCTTCCAGGGGAAGGACCGGAAGGAGACCATGACACTGATTCTGAAGTAAGCCCCAGCCCTGCCCTGATAACAATGGACTCCTCCAAGCCCCAGCCCCAGTTTGGGGGTCAGAATA... |
Task1_train_32431 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | ATTTCTCCAAGCGGATGTTCCACAAATCCCTGTTGCTGTATTTCTCCAAGCGGAAGATTCCCAGGCAGACCACCACCACCTCCGTACCTTGTTGGGGTAACCTGGTGATCATTCATTGGCCCTTCTCATTCTGGACCCTGTGGGGCACTGAGGGCTGCATCATCACAGTCCCGGCTTTGTGGAAACGTAGTGTAGTGAGGGATACAGGTTTGCACACAAGGGGCAGAGATGCCTGGAGGCACAGATAGGCGGACGCTCTTGGCCAGGGGTGTGGACCGTGGAGACACAGAGCAGAGCAACTGGCCATGCCAAGCAGAGCC... | ATTTCTCCAAGCGGATGTTCCACAAATCCCTGTTGCTGTATTTCTCCAAGCGGAAGATTCCCAGGCAGACCACCACCACCTCCGTACCTTGTTGGGGTAACCTGGTGATCATTCATTGGCCCTTCTCATTCTGGACCCTGTGGGGCACTGAGGGCTGCATCATCACAGTCCCGGCTTTGTGGAAACGTAGTGTAGTGAGGGATACAGGTTTGCACACAAGGGGCAGAGATGCCTGGAGGCACAGATAGGCGGACGCTCTTGGCCAGGGGTGTGGACCGTGGAGACACAGAGCAGAGCAACTGGCCATGCCAAGCAGAGCC... |
Task1_train_32432 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ACTCCAACTGGGGCAACAAGATTGACGGTCCGTCTCAAAAAAAAAAAAAAAAAAGGGCCAGGTGTGGTGGAGCATGCCTGTAATCCCAGCTACTTAGGAGGCTGAGGGAGGAGAATCACTTGAACCCTGGAGTTGGAGATTGCATTCCAGCCTGGGCAACAACAGCAAAAGAAAGTCCATCTTAAATTTAAAAAAAAAATTGCTCCTCCCCTCTTTTGCTGAGCACATGCAGTCCAATTGGCCTACATTAACTGCAGGTGTGACGCAGCTCCTTAGTACCTTCATCAGGGACTGCACACTCTACTGCCATCATTTATAAG... | ACTCCAACTGGGGCAACAAGATTGACGGTCCGTCTCAAAAAAAAAAAAAAAAAAGGGCCAGGTGTGGTGGAGCATGCCTGTAATCCCAGCTACTTAGGAGGCTGAGGGAGGAGAATCACTTGAACCCTGGAGTTGGAGATTGCATTCCAGCCTGGGCAACAACAGCAAAAGAAAGTCCATCTTAAATTTAAAAAAAAAATTGCTCCTCCCCTCTTTTGCTGAGCACATGCAGTCCAATTGGCCTACATTAACTGCAGGTGTGACGCAGCTCCTTAGTACCTTCATCAGGGACTGCACACTCTACTGCCATCATTTATAAG... |
Task1_train_32433 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGCAACCCTGTGGATTTTTTCCCTTGGGCTACCTCTGATAGCAGCAGGGTGGGCCCTGGAGGTGAGACAGTCCCTTCCATATGCACAAATGACAGTATCAGGCTCCAAGTGTTTCATACCTTTTATTACAAAAATCAATAACTTAATTCAGTTCTGTATAAAGTCGATAGGACTTCTGGTCCAATAAGCAGCCTAAGCTTTCATTCTCATCCCAAGAAGGGACAGGAGTCTTGGCCCAGAGGCTGTGGGGACCACCAAAAGCCTCCCAGGCAGCTGGAACACTGTGTCCAAACCAAGGAAGTCCAATGTGGGGTGTGGCT... | AGCAACCCTGTGGATTTTTTCCCTTGGGCTACCTCTGATAGCAGCAGGGTGGGCCCTGGAGGTGAGACAGTCCCTTCCATATGCACAAATGACAGTATCAGGCTCCAAGTGTTTCATACCTTTTATTACAAAAATCAATAACTTAATTCAGTTCTGTATAAAGTCGATAGGACTTCTGGTCCAATAAGCAGCCTAAGCTTTCATTCTCATCCCAAGAAGGGACAGGAGTCTTGGCCCAGAGGCTGTGGGGACCACCAAAAGCCTCCCAGGCAGCTGGAACACTGTGTCCAAACCAAGGAAGTCCAATGTGGGGTGTGGCT... |
Task1_train_32434 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTCTCCCACAGGGGTTCCTGGTCCCCCTCTTCATTCTGTAGGCCATGCTTCTCCCAGAAAGGGTGTGGCAGCTGGGCCTGGCAGGGGTTAGCAGTACACCTGGAGCAAGGGTGCCCCCGACGAGTCTGTGTCGGTGCCCTGGAAGGATGAGTCATGGCTTGCTGGGTACCCTGGTAGGAAGGAGAGGAGAGGAGGAAACAGGCTCAGGGGAAGGAGCTCATCCAGATCCCATGACCAGGGAGAAGCCTGCTGAGAAGGAGCAGAGTGGGACTTGAGCCTGGGTCAGTCTGATCCTGGCTGGATGACCCACTCAGTTTATT... | CTCTCCCACAGGGGTTCCTGGTCCCCCTCTTCATTCTGTAGGCCATGCTTCTCCCAGAAAGGGTGTGGCAGCTGGGCCTGGCAGGGGTTAGCAGTACACCTGGAGCAAGGGTGCCCCCGACGAGTCTGTGTCGGTGCCCTGGAAGGATGAGTCATGGCTTGCTGGGTACCCTGGTAGGAAGGAGAGGAGAGGAGGAAACAGGCTCAGGGGAAGGAGCTCATCCAGATCCCATGACCAGGGAGAAGCCTGCTGAGAAGGAGCAGAGTGGGACTTGAGCCTGGGTCAGTCTGATCCTGGCTGGATGACCCACTCAGTTTATT... |
Task1_train_32435 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ATTCTGTAGGCCATGCTTCTCCCAGAAAGGGTGTGGCAGCTGGGCCTGGCAGGGGTTAGCAGTACACCTGGAGCAAGGGTGCCCCCGACGAGTCTGTGTCGGTGCCCTGGAAGGATGAGTCATGGCTTGCTGGGTACCCTGGTAGGAAGGAGAGGAGAGGAGGAAACAGGCTCAGGGGAAGGAGCTCATCCAGATCCCATGACCAGGGAGAAGCCTGCTGAGAAGGAGCAGAGTGGGACTTGAGCCTGGGTCAGTCTGATCCTGGCTGGATGACCCACTCAGTTTATTGACCTCTCTGAGCCCTAGCCTCCCTTTCTGTA... | ATTCTGTAGGCCATGCTTCTCCCAGAAAGGGTGTGGCAGCTGGGCCTGGCAGGGGTTAGCAGTACACCTGGAGCAAGGGTGCCCCCGACGAGTCTGTGTCGGTGCCCTGGAAGGATGAGTCATGGCTTGCTGGGTACCCTGGTAGGAAGGAGAGGAGAGGAGGAAACAGGCTCAGGGGAAGGAGCTCATCCAGATCCCATGACCAGGGAGAAGCCTGCTGAGAAGGAGCAGAGTGGGACTTGAGCCTGGGTCAGTCTGATCCTGGCTGGATGACCCACTCAGTTTATTGACCTCTCTGAGCCCTAGCCTCCCTTTCTGTA... |
Task1_train_32436 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | CCCAGAAAGGGTGTGGCAGCTGGGCCTGGCAGGGGTTAGCAGTACACCTGGAGCAAGGGTGCCCCCGACGAGTCTGTGTCGGTGCCCTGGAAGGATGAGTCATGGCTTGCTGGGTACCCTGGTAGGAAGGAGAGGAGAGGAGGAAACAGGCTCAGGGGAAGGAGCTCATCCAGATCCCATGACCAGGGAGAAGCCTGCTGAGAAGGAGCAGAGTGGGACTTGAGCCTGGGTCAGTCTGATCCTGGCTGGATGACCCACTCAGTTTATTGACCTCTCTGAGCCCTAGCCTCCCTTTCTGTAAAAGGATAATGATTCCACTC... | CCCAGAAAGGGTGTGGCAGCTGGGCCTGGCAGGGGTTAGCAGTACACCTGGAGCAAGGGTGCCCCCGACGAGTCTGTGTCGGTGCCCTGGAAGGATGAGTCATGGCTTGCTGGGTACCCTGGTAGGAAGGAGAGGAGAGGAGGAAACAGGCTCAGGGGAAGGAGCTCATCCAGATCCCATGACCAGGGAGAAGCCTGCTGAGAAGGAGCAGAGTGGGACTTGAGCCTGGGTCAGTCTGATCCTGGCTGGATGACCCACTCAGTTTATTGACCTCTCTGAGCCCTAGCCTCCCTTTCTGTAAAAGGATAATGATTCCACTC... |
Task1_train_32437 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CAGCCCAAAAAGGTAAGTCTGTTGTGTTTACACTGTGAGCCTCTCATGCCAAGGCTGAAATAGCCAACTCAGGAGGTGAGACAAACTTAGTCCTTCCCATGACCATAGTTGGGTGGTCACAGCTGGGATGGGGGTGGGAGCTGGTTTTAGTCACCAAGCAAAGAAAGCCTTTCTGTTCACTTTCCAGCCATTTTGAGCCCAGCAGCACAAGGGACTCAGAGCAGGTGAGGTGGCTGGACTCACCCTGGTGACCTGGGGCCTCCTCTGCAGCATTGTTTTTTCCACCCTGGCCAGAACCATCAAAGTCACCACTTCAGAGG... | CAGCCCAAAAAGGTAAGTCTGTTGTGTTTACACTGTGAGCCTCTCATGCCAAGGCTGAAATAGCCAACTCAGGAGGTGAGACAAACTTAGTCCTTCCCATGACCATAGTTGGGTGGTCACAGCTGGGATGGGGGTGGGAGCTGGTTTTAGTCACCAAGCAAAGAAAGCCTTTCTGTTCACTTTCCAGCCATTTTGAGCCCAGCAGCACAAGGGACTCAGAGCAGGTGAGGTGGCTGGACTCACCCTGGTGACCTGGGGCCTCCTCTGCAGCATTGTTTTTTCCACCCTGGCCAGAACCATCAAAGTCACCACTTCAGAGG... |
Task1_train_32438 | A mutation is present on Chromosome 1. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GGGAAGTAAGAGGGGCCAGATTAAGGAACTTCAGACTCTGCCACAAAGACTTCAGAGAAACCAGGCACAGTGGTTCACGCCTGTAATCCCAATGCTTTGGGAGGCTGAGGCAGAAGGATTGCTTTAGCCCAAGAGTTCAAGACCAGTCTGAGCAACATAATGAGACCCCATCTCGACAAAATTTTAAAAATTAGCTGCAGGTGGTGGTGTCACATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGCAGATTGCTTGTGCCCAGGAGTTCAAGGCTGCAGTGAGCTATGCCACAAAGCGAGATGCTATTTCTACA... | GGGAAGTAAGAGGGGCCAGATTAAGGAACTTCAGACTCTGCCACAAAGACTTCAGAGAAACCAGGCACAGTGGTTCACGCCTGTAATCCCAATGCTTTGGGAGGCTGAGGCAGAAGGATTGCTTTAGCCCAAGAGTTCAAGACCAGTCTGAGCAACATAATGAGACCCCATCTCGACAAAATTTTAAAAATTAGCTGCAGGTGGTGGTGTCACATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGCAGATTGCTTGTGCCCAGGAGTTCAAGGCTGCAGTGAGCTATGCCACAAAGCGAGATGCTATTTCTACA... |
Task1_train_32439 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGGGGAATGCCGTCATCCTCAGGCCGACTGCACCCATACTGAACCTATCATCCAAAATATACCTCAACACCTATCCTGGTCATCAAACATCTATCCTGAGTTCCATCACCACCCTGGGCTCCATCGCCTGCCAAGGCTTCCGTCATTCATCCTGGGCTCCACCACATTCACAGACTCCATCACCCACAGTAGTGCTCCAGCACACATCCTGGATTGCCTCGTCCCCCTGAACTCCATCACCTGCTTTTTCCTCCAACTCCCACCTTGGCCTGCATCAACACTCCTCAAGTGCTAAAGTCAATTTCATCACTTCTCCAAGC... | AGGGGAATGCCGTCATCCTCAGGCCGACTGCACCCATACTGAACCTATCATCCAAAATATACCTCAACACCTATCCTGGTCATCAAACATCTATCCTGAGTTCCATCACCACCCTGGGCTCCATCGCCTGCCAAGGCTTCCGTCATTCATCCTGGGCTCCACCACATTCACAGACTCCATCACCCACAGTAGTGCTCCAGCACACATCCTGGATTGCCTCGTCCCCCTGAACTCCATCACCTGCTTTTTCCTCCAACTCCCACCTTGGCCTGCATCAACACTCCTCAAGTGCTAAAGTCAATTTCATCACTTCTCCAAGC... |
Task1_train_32440 | Consider a variant on Chromosome 1. Determine its clinical classification and disease relevance. | Benign | ATCACCCAGCGCCACTCCTCAGCTAATTCTAGGCTACACCACCCACACGCACTAGGGTGCATTTCCCCCTAGGGCTCTCTACCCCTGCCTGCCTCGGTCCCATGCTTCACACCTCGGTTTCATTCCCATCCCACACAGGGCAGGTACCTCCAGGCACTTCCTCCATGAAGATCTTAAGGTAGCCGCCCTGGCTAGCTGAGCCCAGATAGCGCACTATGTTCTTGTGGCGCAGGCGTCTGTGAAGAGCGATCTCTTCATGCAGGGGCTGAGAGAACCTGAGGGGAGGTAAGGGAGAGAGGAAAGGGACCGAGGTGGGCAGA... | ATCACCCAGCGCCACTCCTCAGCTAATTCTAGGCTACACCACCCACACGCACTAGGGTGCATTTCCCCCTAGGGCTCTCTACCCCTGCCTGCCTCGGTCCCATGCTTCACACCTCGGTTTCATTCCCATCCCACACAGGGCAGGTACCTCCAGGCACTTCCTCCATGAAGATCTTAAGGTAGCCGCCCTGGCTAGCTGAGCCCAGATAGCGCACTATGTTCTTGTGGCGCAGGCGTCTGTGAAGAGCGATCTCTTCATGCAGGGGCTGAGAGAACCTGAGGGGAGGTAAGGGAGAGAGGAAAGGGACCGAGGTGGGCAGA... |
Task1_train_32441 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AATTGGTGGCTTGGACCAGTGACTGGGCTCCCACCCTCCCTGGGCCTCACCAGCCCAATAGGGTGAAGACAGAGCCAGAACTCAGACCCTCCCCTGCTCACAATTCCTTTCAGCCTTGGACCTCAGGGTTCAGAGCCAAGATGCAGACGATATAGTCCCTTTTCAGGACTCCTAAGCCCTAAGACCTCAGTGTCACCCAATGTCAGAGCCCTCAGAGAGGGAAGGAGCAGGGGGAGAAGTGGAGGCCCCAACTGTCACCCTGCTAAGTGGGTAAGCGAGGACTGGACAGTGTGTGTCAGGGGGAACATGGCTGAGGGACA... | AATTGGTGGCTTGGACCAGTGACTGGGCTCCCACCCTCCCTGGGCCTCACCAGCCCAATAGGGTGAAGACAGAGCCAGAACTCAGACCCTCCCCTGCTCACAATTCCTTTCAGCCTTGGACCTCAGGGTTCAGAGCCAAGATGCAGACGATATAGTCCCTTTTCAGGACTCCTAAGCCCTAAGACCTCAGTGTCACCCAATGTCAGAGCCCTCAGAGAGGGAAGGAGCAGGGGGAGAAGTGGAGGCCCCAACTGTCACCCTGCTAAGTGGGTAAGCGAGGACTGGACAGTGTGTGTCAGGGGGAACATGGCTGAGGGACA... |
Task1_train_32442 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | CTTGCTCTGTCACCCAGGCTGGAGTACAATGGTTGATCTCAGCTCACTGCAACCTCCATCTCCCAGGTTCAAGCGATTCTCTTGCCTCAGCCTCCCTAGTAGTTGGGATTATAGGCGCCCGCCACCATGCCCAGATAATTTTTTTGTATATTTAGTAGAGACAGGGTTTCGCCATATCGGCCAGGCTGGTCTGGAACTCCTGACCTCAGGTGATCTGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGAGCACAGCCTAAAAATAATAATTTTAAAATTTATTTTTCTTTTTTCTTAATACTTG... | CTTGCTCTGTCACCCAGGCTGGAGTACAATGGTTGATCTCAGCTCACTGCAACCTCCATCTCCCAGGTTCAAGCGATTCTCTTGCCTCAGCCTCCCTAGTAGTTGGGATTATAGGCGCCCGCCACCATGCCCAGATAATTTTTTTGTATATTTAGTAGAGACAGGGTTTCGCCATATCGGCCAGGCTGGTCTGGAACTCCTGACCTCAGGTGATCTGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGAGCACAGCCTAAAAATAATAATTTTAAAATTTATTTTTCTTTTTTCTTAATACTTG... |
Task1_train_32443 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CAACTGCCACGTGTGTTGCAGAATGTTGCAAACACTCACTAGAGTGATACCCTCAGGAACACCCCCAGCTGTGACAACCAAAAATGTCTCAGACATTGCCCAGTGTTCTCTTGGGCCAGAAGCACCTGGTTGAGAATGACTGGTTCAGAAACACAGCCAGCCCAAGGTGACTTTGACCCTACTCTTCCCTTTCCTCGGTCTCCTGCTGTTGGGACTCCCCAGTGGTTAAAGCCGACCAGAAGCCTGTGCCACAGAAGCCTGTTGATTTAGTCCACATAGATCAGCTCTTGGAAAAGACAGCTGAGCAGTGAAGGGTCGAC... | CAACTGCCACGTGTGTTGCAGAATGTTGCAAACACTCACTAGAGTGATACCCTCAGGAACACCCCCAGCTGTGACAACCAAAAATGTCTCAGACATTGCCCAGTGTTCTCTTGGGCCAGAAGCACCTGGTTGAGAATGACTGGTTCAGAAACACAGCCAGCCCAAGGTGACTTTGACCCTACTCTTCCCTTTCCTCGGTCTCCTGCTGTTGGGACTCCCCAGTGGTTAAAGCCGACCAGAAGCCTGTGCCACAGAAGCCTGTTGATTTAGTCCACATAGATCAGCTCTTGGAAAAGACAGCTGAGCAGTGAAGGGTCGAC... |
Task1_train_32444 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | ACATCAGCATCCTGGACACAGCTCCCAAACCCCGAATTCCCCCATTTTATTGATGCTAGCAGGCCAGGGAAGGGAAAACTTCCTTTGGGCTTTGAATAATAACGACTTTAGAATTGAAATCGTGGGCTGGAGGTGGACGCCACGCCTCATTCTGATGGGTCCAAGAGCCGAAATTTCGGCTTCTGGCACTCTCCTCACTCAGCTCTCTAAACTCCTCCATCATTCCTCTTTCCAGTCCTTTGGCCCTAAGCCCTTGCTAGCGGTTGGCTAAGAAGAAACCCGTCTCTTGCTCGGGATTCGCTGTGAGCTCCGGGAAGCCC... | ACATCAGCATCCTGGACACAGCTCCCAAACCCCGAATTCCCCCATTTTATTGATGCTAGCAGGCCAGGGAAGGGAAAACTTCCTTTGGGCTTTGAATAATAACGACTTTAGAATTGAAATCGTGGGCTGGAGGTGGACGCCACGCCTCATTCTGATGGGTCCAAGAGCCGAAATTTCGGCTTCTGGCACTCTCCTCACTCAGCTCTCTAAACTCCTCCATCATTCCTCTTTCCAGTCCTTTGGCCCTAAGCCCTTGCTAGCGGTTGGCTAAGAAGAAACCCGTCTCTTGCTCGGGATTCGCTGTGAGCTCCGGGAAGCCC... |
Task1_train_32445 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGGTTGCCCTGCCATCAAGGAGCCCATGATATAGTGGAGAGTGAACATGGGAAGCTGAGGTGCAAAGGGAACATAAGAGGTGTGCATACCAATAAAAATTAGAGACAGTAGGCCGGGCGCGGTGGCTCACGACTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATTGAGACCATCCTGGCTAACATGATGAAACCCCGTCTTTACTAAAAATACACAAAAAATTAGCCGGGAGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGCGAATGGTGTGAACCCGG... | AGGTTGCCCTGCCATCAAGGAGCCCATGATATAGTGGAGAGTGAACATGGGAAGCTGAGGTGCAAAGGGAACATAAGAGGTGTGCATACCAATAAAAATTAGAGACAGTAGGCCGGGCGCGGTGGCTCACGACTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATTGAGACCATCCTGGCTAACATGATGAAACCCCGTCTTTACTAAAAATACACAAAAAATTAGCCGGGAGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGCGAATGGTGTGAACCCGG... |
Task1_train_32446 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | GATTATCTAGTAATAGTCAACAGTGTATTGAGTACTTTGCTCCAGACTGAAATCCTAACATTTTTCTTTTTCAGGACTTGGAAGGAGTAGATATCATCCTAGGTGTCTGCTCTAGTGGCCTTCTGGTTTACAAAGATAAGCTGAGAATTAACCGCTTCCCTTGGCCCAAAGTGCTGAAGATTTCTTATAAACGTAGTAGCTTTTTCATCAAGATTCGGCCTGGAGAGGTACAGAATTTATATTTCCTTCCTCCCAAACCAGACACAGTCTGTATCTGAAATATCTACATTTCCATTTTCCTTATTAAGTCATCTGAGAAG... | GATTATCTAGTAATAGTCAACAGTGTATTGAGTACTTTGCTCCAGACTGAAATCCTAACATTTTTCTTTTTCAGGACTTGGAAGGAGTAGATATCATCCTAGGTGTCTGCTCTAGTGGCCTTCTGGTTTACAAAGATAAGCTGAGAATTAACCGCTTCCCTTGGCCCAAAGTGCTGAAGATTTCTTATAAACGTAGTAGCTTTTTCATCAAGATTCGGCCTGGAGAGGTACAGAATTTATATTTCCTTCCTCCCAAACCAGACACAGTCTGTATCTGAAATATCTACATTTCCATTTTCCTTATTAAGTCATCTGAGAAG... |
Task1_train_32447 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | CCAACACTTTGGGAGGCTGAGGTGGGCAGATCACCTCAGGTCAGGAGTTCGAGACCAGCCTGACCAATATGATGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGAAGTGGTGGCATGTACCTATGATCCCAACTACTTGGGAGGCTGACAGGAGAATCACTTGAACCTGGTTGGTGGAGACTGTAGTGAGCTGAGACTGCACCACTGCACTCCAGCCTGGGCAACAAGAGCAAAACTGTCTCAGGAAAAAAAAAAAAAAAAAAGTCCAGTATAGTTTTTTCCCCCTGGTTTTTGATTAGTTCAGATCTTAATG... | CCAACACTTTGGGAGGCTGAGGTGGGCAGATCACCTCAGGTCAGGAGTTCGAGACCAGCCTGACCAATATGATGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGAAGTGGTGGCATGTACCTATGATCCCAACTACTTGGGAGGCTGACAGGAGAATCACTTGAACCTGGTTGGTGGAGACTGTAGTGAGCTGAGACTGCACCACTGCACTCCAGCCTGGGCAACAAGAGCAAAACTGTCTCAGGAAAAAAAAAAAAAAAAAAGTCCAGTATAGTTTTTTCCCCCTGGTTTTTGATTAGTTCAGATCTTAATG... |
Task1_train_32448 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | TTTGAGATGGAGTCTTACTCTGTCGCCCAGGTTGGAGTGCAGTGGCACAATCTCGGCTCACTGTAACCTCCGCCTCCTGGGATCAAGTGATTCTCCTGCCTCAACTTCCCGAGTAGCTGGGACTACAGGTGCACGCCACCATGCCTGGCTAATTTTTTATTTTTAGAAGAGACGGGGTTTTACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCTGCCTGCCATGGCCTCCCGAAGTTCTGGGATTACAGGCATGAGCCACTGCGCCTGGCCTTATTTTTTTTTTTTTTTGGAGATGGAGTCTCACTC... | TTTGAGATGGAGTCTTACTCTGTCGCCCAGGTTGGAGTGCAGTGGCACAATCTCGGCTCACTGTAACCTCCGCCTCCTGGGATCAAGTGATTCTCCTGCCTCAACTTCCCGAGTAGCTGGGACTACAGGTGCACGCCACCATGCCTGGCTAATTTTTTATTTTTAGAAGAGACGGGGTTTTACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCTGCCTGCCATGGCCTCCCGAAGTTCTGGGATTACAGGCATGAGCCACTGCGCCTGGCCTTATTTTTTTTTTTTTTTGGAGATGGAGTCTCACTC... |
Task1_train_32449 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | CTGCCTGCGCAGGAGAAAGGCGCCTATTCGGGTGCCTGGTGTTAATCTGCAGAGGGGTTGGCAGCAGCTGCTAATTTCTGATTTGCCTGTCTTTGAATGGGGGTAATTGCTGGGAGTTGCCAGTGTTCCAGGTTGTTCTCTGGAAGAGGGGGAGGAAGAAGCAGCTGTCATGGGCTCTGCGGAGTGCTGCCTTCTGCAGGTAGCATGGTGAAGCCTCGCTGGATAGAGTGAGGGGATAATGAAATCTAGCCAGGCAGGGCCGCAAGGGCCCTCGGAGGCCACCTGATCTGACCGGCTCATTCTACAGGTGGAACCGAGAT... | CTGCCTGCGCAGGAGAAAGGCGCCTATTCGGGTGCCTGGTGTTAATCTGCAGAGGGGTTGGCAGCAGCTGCTAATTTCTGATTTGCCTGTCTTTGAATGGGGGTAATTGCTGGGAGTTGCCAGTGTTCCAGGTTGTTCTCTGGAAGAGGGGGAGGAAGAAGCAGCTGTCATGGGCTCTGCGGAGTGCTGCCTTCTGCAGGTAGCATGGTGAAGCCTCGCTGGATAGAGTGAGGGGATAATGAAATCTAGCCAGGCAGGGCCGCAAGGGCCCTCGGAGGCCACCTGATCTGACCGGCTCATTCTACAGGTGGAACCGAGAT... |
Task1_train_32450 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TCAGAGGTCCTACATTCGCCAGAGTTGGCATCCAGTTGATGGGTTCATTTGAATTAAATGGTTTGGAGGCTAACGTGATTTTTTAAATTGAATTTCATCACTATTCTGTGTATTCTATTTATCACTATTCTAAATGACTCATGGTTGGCTAATTGATTATCATGTAAGCAAGCTATTTGAAGAAATTGATTACATATATTTATATATAGGGGGTAACTAATTAATGATTACTTGATTAAATTGCTATGTGAACTGACAACTATTTATAAATCAATGCAATAGACTGTTGTTTGACCAAATTATTTTACTGAACTGACAAG... | TCAGAGGTCCTACATTCGCCAGAGTTGGCATCCAGTTGATGGGTTCATTTGAATTAAATGGTTTGGAGGCTAACGTGATTTTTTAAATTGAATTTCATCACTATTCTGTGTATTCTATTTATCACTATTCTAAATGACTCATGGTTGGCTAATTGATTATCATGTAAGCAAGCTATTTGAAGAAATTGATTACATATATTTATATATAGGGGGTAACTAATTAATGATTACTTGATTAAATTGCTATGTGAACTGACAACTATTTATAAATCAATGCAATAGACTGTTGTTTGACCAAATTATTTTACTGAACTGACAAG... |
Task1_train_32451 | A mutation is present on Chromosome 1. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TGTGCAGAGTCCCCTCATAGGAGGGACATCAGAGCAGCCCCTCCTCACCAGTGGCTGCCCCAGCACCCTCAGGAAGCTGTTTCTTGGGGGAAGATGCAGAAAGAAATGAAGTCTGGGTACATGTGTACTTGGCAGGCAAGAGGAGAGATTCAACAACCCCAGAGAGACCAGGACAAAACAGGCTGGTGACAAGGGACACCCTCTCACCCAGCTAGAGAGAGGCCCTGGGATACGAGCAAGAGGTTGCAGTGTCTAGATGATTTCAAGGGCTGTGTTTACCAAATGTTTGTCCTGGAAACCAGCCTGAGTGCCTCTCTGCC... | TGTGCAGAGTCCCCTCATAGGAGGGACATCAGAGCAGCCCCTCCTCACCAGTGGCTGCCCCAGCACCCTCAGGAAGCTGTTTCTTGGGGGAAGATGCAGAAAGAAATGAAGTCTGGGTACATGTGTACTTGGCAGGCAAGAGGAGAGATTCAACAACCCCAGAGAGACCAGGACAAAACAGGCTGGTGACAAGGGACACCCTCTCACCCAGCTAGAGAGAGGCCCTGGGATACGAGCAAGAGGTTGCAGTGTCTAGATGATTTCAAGGGCTGTGTTTACCAAATGTTTGTCCTGGAAACCAGCCTGAGTGCCTCTCTGCC... |
Task1_train_32452 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | GAGCAGGAAGTCAGCTCAGAGCATAAATGACCTGCCCAAGGACACACAGCTAGTAAGTGGGGGACAGAACTAAAATTCAGATCTATCTGTCTCCACAGTCTGTGTTTCTAACCACTAACACACTGCCTCTGTTCTTGCTCTGGACATCCTGTCCCCCTCATGTCCCCTCCAGCTGCCTTAGTAACAATCCTTGGGGGATTCCTGCCGAGAAGCTGTTTGGGAACTGCTGGGTGCAGATGCTATGGATGTGGGCCTGGTCCCAGTCCATGCCTAAGGCAGGGGAGCATTCTGTAGCCTGGAGGCCAGTCCAAGAGCACAAC... | GAGCAGGAAGTCAGCTCAGAGCATAAATGACCTGCCCAAGGACACACAGCTAGTAAGTGGGGGACAGAACTAAAATTCAGATCTATCTGTCTCCACAGTCTGTGTTTCTAACCACTAACACACTGCCTCTGTTCTTGCTCTGGACATCCTGTCCCCCTCATGTCCCCTCCAGCTGCCTTAGTAACAATCCTTGGGGGATTCCTGCCGAGAAGCTGTTTGGGAACTGCTGGGTGCAGATGCTATGGATGTGGGCCTGGTCCCAGTCCATGCCTAAGGCAGGGGAGCATTCTGTAGCCTGGAGGCCAGTCCAAGAGCACAAC... |
Task1_train_32453 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | TCAGCACACCGGCAGCTTCAGGGGGCTTAGGTAGTCTTCAGGGGTCTTTAGCAGAAAGGCTGGGAACCTCCCTTCTGGTCAGAGCCTCATATCCCAGTAAGAAAAGCTGAAGCCCAGAGAAGGCGATGTCTGTGTCCCAGGTCACACAGCAATCAGTATTTATCCAGCAAATACCTCTTGAGCACTTCCTGTGTACCAGGCCCTCTTCTAGATGTTGGGGATATGGCTGTGAGGAAGGGGAGGAAGAATAATGATGATAGCCAGTAGTTAGTGGCCTCGGACATGTTATTTGATCCTCACACCATCCTCATCCTCACTTT... | TCAGCACACCGGCAGCTTCAGGGGGCTTAGGTAGTCTTCAGGGGTCTTTAGCAGAAAGGCTGGGAACCTCCCTTCTGGTCAGAGCCTCATATCCCAGTAAGAAAAGCTGAAGCCCAGAGAAGGCGATGTCTGTGTCCCAGGTCACACAGCAATCAGTATTTATCCAGCAAATACCTCTTGAGCACTTCCTGTGTACCAGGCCCTCTTCTAGATGTTGGGGATATGGCTGTGAGGAAGGGGAGGAAGAATAATGATGATAGCCAGTAGTTAGTGGCCTCGGACATGTTATTTGATCCTCACACCATCCTCATCCTCACTTT... |
Task1_train_32454 | 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 | GTGGACAGAAGTGGGCAGTAGGAACTCTTGCACTTTACAGCTCAGGTTCTGTGAGCAGCACTCCCCCAGTACATGCATACGCAGCTACCCCATTTCTGACGCTCCTCCACCCTGGGCCTAGGGTGTTCGGGATGTTCCGCCAAGCCAGTGACCGCGAAGCTGTCTACGCCTGCTTCACCTTCTCCCACTGGCTGGTGTACGCCAACAGCGCTGCCAACCCCATCATCTACAACTTCCTCAGTGGTGAGCAGGCTGGGGATGCAAAATGACTGAGGGTGGCCAACAGTCCACATGACAAGTCTCCCCATCCCCAAGCCAGG... | GTGGACAGAAGTGGGCAGTAGGAACTCTTGCACTTTACAGCTCAGGTTCTGTGAGCAGCACTCCCCCAGTACATGCATACGCAGCTACCCCATTTCTGACGCTCCTCCACCCTGGGCCTAGGGTGTTCGGGATGTTCCGCCAAGCCAGTGACCGCGAAGCTGTCTACGCCTGCTTCACCTTCTCCCACTGGCTGGTGTACGCCAACAGCGCTGCCAACCCCATCATCTACAACTTCCTCAGTGGTGAGCAGGCTGGGGATGCAAAATGACTGAGGGTGGCCAACAGTCCACATGACAAGTCTCCCCATCCCCAAGCCAGG... |
Task1_train_32455 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | ATCATGTGAAGAAGGGAGGAGCCAGACGCACAAGGATGGTCACCCCTGCACTACTTACAGCAGGACGAAATTGCTTATGTCACTAACAGGTAACCTATTTGAGTATTTTTCTTGCACCAAGCACTGTGTTAAATGCCAAACATGTGTCATCTCATTTCATCCTCACCACCTCCCTAGGAGGTAAGCACTCTTCATACCCACATTTTGCAGATGAGAGAATTACACTTGAAAAGGTGAAGCCACTCACCTCGGTTGTTCAGATAGTGGCAAAGTCAAGATTGAATGTTAGCCTATTGGCCTCCAGGGCTCATGCTCCTCAC... | ATCATGTGAAGAAGGGAGGAGCCAGACGCACAAGGATGGTCACCCCTGCACTACTTACAGCAGGACGAAATTGCTTATGTCACTAACAGGTAACCTATTTGAGTATTTTTCTTGCACCAAGCACTGTGTTAAATGCCAAACATGTGTCATCTCATTTCATCCTCACCACCTCCCTAGGAGGTAAGCACTCTTCATACCCACATTTTGCAGATGAGAGAATTACACTTGAAAAGGTGAAGCCACTCACCTCGGTTGTTCAGATAGTGGCAAAGTCAAGATTGAATGTTAGCCTATTGGCCTCCAGGGCTCATGCTCCTCAC... |
Task1_train_32456 | Consider a variant on Chromosome 1. Determine its clinical classification and disease relevance. | Benign | AAAACAAGTAGAGTCTTCTTCTGCCTTTGGTGTATAAATGTTAGCTATGATTATTAATAAAATGATGATGATTATAAGTAAAAGAACAAAGGAAAGGGAAGTGGTGATATAGGGAACATGGCTGGTCACTGACTCCCCAGCTATGTGAGCCTGGAGAATATTATTAACCCTCCGAGCCTCAGTTTCCCCATCTGGTTATATGGGGCTAACGCCTATCTTACAGGGTAACTGTGAACACTAAAGGAAAAGCAAATTTAACACGAATTAAGCAATTTACCTTGTGCCTTGTGCTGTGCTAGGCACCTTTTTTTTGTTTGTTT... | AAAACAAGTAGAGTCTTCTTCTGCCTTTGGTGTATAAATGTTAGCTATGATTATTAATAAAATGATGATGATTATAAGTAAAAGAACAAAGGAAAGGGAAGTGGTGATATAGGGAACATGGCTGGTCACTGACTCCCCAGCTATGTGAGCCTGGAGAATATTATTAACCCTCCGAGCCTCAGTTTCCCCATCTGGTTATATGGGGCTAACGCCTATCTTACAGGGTAACTGTGAACACTAAAGGAAAAGCAAATTTAACACGAATTAAGCAATTTACCTTGTGCCTTGTGCTGTGCTAGGCACCTTTTTTTTGTTTGTTT... |
Task1_train_32457 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GTGGCCAACATCATGAAACCCCATCTCTACAAAAATACAGAAATTAGCTGGGCATGATGGCGGGTGCCTGTAATCCCAGCTGCTCGGGAGACTGAGGTGGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTAAGATCGCGGCACTGCACTCCAGCCTGAGCAACAGAGTGAGACTCTGTCTCAAAAAAAAAGAAAAGAAATGTAGCATTGTGATCAGCCCTAACTCCTGGGGGCAGCCCAGGAACCCTTGTGGGGGTGTGTAATTCTGAGGACCTGGGGAAATTGAGAGGCCCCAAGCTGAAAAAGGGAA... | GTGGCCAACATCATGAAACCCCATCTCTACAAAAATACAGAAATTAGCTGGGCATGATGGCGGGTGCCTGTAATCCCAGCTGCTCGGGAGACTGAGGTGGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTAAGATCGCGGCACTGCACTCCAGCCTGAGCAACAGAGTGAGACTCTGTCTCAAAAAAAAAGAAAAGAAATGTAGCATTGTGATCAGCCCTAACTCCTGGGGGCAGCCCAGGAACCCTTGTGGGGGTGTGTAATTCTGAGGACCTGGGGAAATTGAGAGGCCCCAAGCTGAAAAAGGGAA... |
Task1_train_32458 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CAGGCCCACACTGCCCCTCTCATTCTCTTCAAACTGTGACTTTTTACAGACTCGGGCGGGTGTTCTGCGGCCCCCCAGGTGCTATGGGGGAGGGGGGCGTTGAATGGAATTAAACCAGAAAGAAAGCAAGCGGCTCCGTGTCCTGCTTCCCCTCCTTGCGCCTTTCCTCCCGGTCTCCGCGGAGACAGCCCTCGGTTATGGAGGTACCGCCTGCGGGATTGGAGTGCCCCTTGCGGCTGTGGGAGGGGCAGTCGGGGGCTGGGGGGACGCAGGTACGCCTGTCGCCAGGACGCCTCTACCCTGGACGGTAGGAGGTTGCC... | CAGGCCCACACTGCCCCTCTCATTCTCTTCAAACTGTGACTTTTTACAGACTCGGGCGGGTGTTCTGCGGCCCCCCAGGTGCTATGGGGGAGGGGGGCGTTGAATGGAATTAAACCAGAAAGAAAGCAAGCGGCTCCGTGTCCTGCTTCCCCTCCTTGCGCCTTTCCTCCCGGTCTCCGCGGAGACAGCCCTCGGTTATGGAGGTACCGCCTGCGGGATTGGAGTGCCCCTTGCGGCTGTGGGAGGGGCAGTCGGGGGCTGGGGGGACGCAGGTACGCCTGTCGCCAGGACGCCTCTACCCTGGACGGTAGGAGGTTGCC... |
Task1_train_32459 | This variant is located on Chromosome 1. Evaluate its biological effect and specify any disease association. | Benign | CTCTTCAAACTGTGACTTTTTACAGACTCGGGCGGGTGTTCTGCGGCCCCCCAGGTGCTATGGGGGAGGGGGGCGTTGAATGGAATTAAACCAGAAAGAAAGCAAGCGGCTCCGTGTCCTGCTTCCCCTCCTTGCGCCTTTCCTCCCGGTCTCCGCGGAGACAGCCCTCGGTTATGGAGGTACCGCCTGCGGGATTGGAGTGCCCCTTGCGGCTGTGGGAGGGGCAGTCGGGGGCTGGGGGGACGCAGGTACGCCTGTCGCCAGGACGCCTCTACCCTGGACGGTAGGAGGTTGCCGTGGGAACGGCTGGGGCAAAGCCC... | CTCTTCAAACTGTGACTTTTTACAGACTCGGGCGGGTGTTCTGCGGCCCCCCAGGTGCTATGGGGGAGGGGGGCGTTGAATGGAATTAAACCAGAAAGAAAGCAAGCGGCTCCGTGTCCTGCTTCCCCTCCTTGCGCCTTTCCTCCCGGTCTCCGCGGAGACAGCCCTCGGTTATGGAGGTACCGCCTGCGGGATTGGAGTGCCCCTTGCGGCTGTGGGAGGGGCAGTCGGGGGCTGGGGGGACGCAGGTACGCCTGTCGCCAGGACGCCTCTACCCTGGACGGTAGGAGGTTGCCGTGGGAACGGCTGGGGCAAAGCCC... |
Task1_train_32460 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | AAACCTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGCCTTACTCCATCGCCCAGGCTGGAGTACAGTGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTCCTGTCTCAACCTGCTGAGCATCTGGGACTACAGGCGCCTGCCACCACGCCCGGCCAATCAATTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCTTATTGGTCAGACTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTCGGCTTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACCGCGCCTGGC... | AAACCTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGCCTTACTCCATCGCCCAGGCTGGAGTACAGTGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTCCTGTCTCAACCTGCTGAGCATCTGGGACTACAGGCGCCTGCCACCACGCCCGGCCAATCAATTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCTTATTGGTCAGACTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTCGGCTTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACCGCGCCTGGC... |
Task1_train_32461 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | TGTGCCACCATGCCCCCCTAATTTTTGTCTTTTTAGTAGAGACGGGGTTTCACCATATTGGCTATACTTGTCTCAAACTACTGACCTTGTGATCCACCCACCTCAGCCTCCCAACCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCTCCCAGACAGAGTGTTTTCATAATACAAACTACAGAAAGCTTGACAAAATCTTCAGTGAAGTGAATGCAGCCATTTCAACAGGGAAACTTGTTCCCTTAAGGGCATATCACAATCTCTGGGAAGACATAGATTTCTAAGTTTATCCAAAGGAATCAGTGTTTCAAAAGATTA... | TGTGCCACCATGCCCCCCTAATTTTTGTCTTTTTAGTAGAGACGGGGTTTCACCATATTGGCTATACTTGTCTCAAACTACTGACCTTGTGATCCACCCACCTCAGCCTCCCAACCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCTCCCAGACAGAGTGTTTTCATAATACAAACTACAGAAAGCTTGACAAAATCTTCAGTGAAGTGAATGCAGCCATTTCAACAGGGAAACTTGTTCCCTTAAGGGCATATCACAATCTCTGGGAAGACATAGATTTCTAAGTTTATCCAAAGGAATCAGTGTTTCAAAAGATTA... |
Task1_train_32462 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCACCACACTACAGTCTTCTCATTAGTGCCCAGCAGCACATGTGCTCTGAGCCTTGAGTAGCAGAGAGTAATACAACAATAAGTAAAATGTATTCCCTACCTTCTGAAAGTTCACAGTCTAGGAGGGACTACGTAATTGTTTATTCACTTAGTATTTATATCCCACTCTGTTCTAAAAAGGGATTAGAACTGGCTCACACTTAATCAGAAATAACTTGAATGCAAGAGAGATGGGGACAAATGCACATAAAAGGAAAGTGAAGATGAGAGGATTCTATTAAGGTTGGTGCAAAATTAATTGCAGCTTTTGCCATTAAAAG... | GCACCACACTACAGTCTTCTCATTAGTGCCCAGCAGCACATGTGCTCTGAGCCTTGAGTAGCAGAGAGTAATACAACAATAAGTAAAATGTATTCCCTACCTTCTGAAAGTTCACAGTCTAGGAGGGACTACGTAATTGTTTATTCACTTAGTATTTATATCCCACTCTGTTCTAAAAAGGGATTAGAACTGGCTCACACTTAATCAGAAATAACTTGAATGCAAGAGAGATGGGGACAAATGCACATAAAAGGAAAGTGAAGATGAGAGGATTCTATTAAGGTTGGTGCAAAATTAATTGCAGCTTTTGCCATTAAAAG... |
Task1_train_32463 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCGGCTAATTTTTTTGTACTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCTGGCTGATTTTATTTTTTAAAGATGCCTGTCACTCAGGCGGGAGTGCAGTGGCTCAAACATGGCTCACGGCAGCCCCAACCTCCCAGGCTCAAGCAATCCTCCTGTCTTAGCCTCCCAATATCTGGGACCCCAGCTGTGAGTCACCACGCCTGGGTAATTTTCAAAGTTTTTTGTAGAGATA... | CCGGCTAATTTTTTTGTACTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCTGGCTGATTTTATTTTTTAAAGATGCCTGTCACTCAGGCGGGAGTGCAGTGGCTCAAACATGGCTCACGGCAGCCCCAACCTCCCAGGCTCAAGCAATCCTCCTGTCTTAGCCTCCCAATATCTGGGACCCCAGCTGTGAGTCACCACGCCTGGGTAATTTTCAAAGTTTTTTGTAGAGATA... |
Task1_train_32464 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CAGAGAGGGCTCAGTAAATATTAACTATTAATCATTACTGTTTTCTTGCTAGGCTGGAACTATGGGCTGAATTTACAAGGTAACACTTAACAGATGTAAGCAATTATATTTTGGTTCAAACTATAAATTATACAAGTTTGAGACTAGGGAGAGCTGGCATGACAGCAGTTCCAGGTAAGACGAAACCTCAGAAACAAAAATGAAACCCAGCTCTCTGGAATTCAGGTGACAGTGCTCTGTGAACAACAGTGTCATTCCTATAGGGTGGGAGAGTTCACGGGGGCCATTCGTGCACCATCCTGATGAAGGAAGGTGAGCGA... | CAGAGAGGGCTCAGTAAATATTAACTATTAATCATTACTGTTTTCTTGCTAGGCTGGAACTATGGGCTGAATTTACAAGGTAACACTTAACAGATGTAAGCAATTATATTTTGGTTCAAACTATAAATTATACAAGTTTGAGACTAGGGAGAGCTGGCATGACAGCAGTTCCAGGTAAGACGAAACCTCAGAAACAAAAATGAAACCCAGCTCTCTGGAATTCAGGTGACAGTGCTCTGTGAACAACAGTGTCATTCCTATAGGGTGGGAGAGTTCACGGGGGCCATTCGTGCACCATCCTGATGAAGGAAGGTGAGCGA... |
Task1_train_32465 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AAGCCAGAATTCCAGTCCAAGTTGGTCTGCCTCCAGAGTCTGTGACCTCTCTGCTTCAGTCCTTTAAAGGGAAGGGGTTCATGTGCTGTGTTTCTGGAAGGGCAAGGAAAAGGTAAAGTTGGGAGATGATGTCCCGCGAGGCAGCCAGTTCTGAAAAAAGGGAACTCTGTAAGCTGAAGAGGGTGGTAACTAGAGAGGAAAGGGACCAGGCCTCTAGCTAGGAAAGTGAGAACACAAAAATTGGTATGGAAGTCACCCAACAGAGGCTCAAGAAGGAATCTGAAATCCCAGGAGTAGCCAGAGTGACTGTCACCATAAGG... | AAGCCAGAATTCCAGTCCAAGTTGGTCTGCCTCCAGAGTCTGTGACCTCTCTGCTTCAGTCCTTTAAAGGGAAGGGGTTCATGTGCTGTGTTTCTGGAAGGGCAAGGAAAAGGTAAAGTTGGGAGATGATGTCCCGCGAGGCAGCCAGTTCTGAAAAAAGGGAACTCTGTAAGCTGAAGAGGGTGGTAACTAGAGAGGAAAGGGACCAGGCCTCTAGCTAGGAAAGTGAGAACACAAAAATTGGTATGGAAGTCACCCAACAGAGGCTCAAGAAGGAATCTGAAATCCCAGGAGTAGCCAGAGTGACTGTCACCATAAGG... |
Task1_train_32466 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | CAAGGAAAAGGTAAAGTTGGGAGATGATGTCCCGCGAGGCAGCCAGTTCTGAAAAAAGGGAACTCTGTAAGCTGAAGAGGGTGGTAACTAGAGAGGAAAGGGACCAGGCCTCTAGCTAGGAAAGTGAGAACACAAAAATTGGTATGGAAGTCACCCAACAGAGGCTCAAGAAGGAATCTGAAATCCCAGGAGTAGCCAGAGTGACTGTCACCATAAGGCAACTCATACATGTGCAGACACACACACACACACACACACACACACACACACACACACACATGCACAGAGGGGAGGACTGTTCTTTGACACGGGCCACCCCA... | CAAGGAAAAGGTAAAGTTGGGAGATGATGTCCCGCGAGGCAGCCAGTTCTGAAAAAAGGGAACTCTGTAAGCTGAAGAGGGTGGTAACTAGAGAGGAAAGGGACCAGGCCTCTAGCTAGGAAAGTGAGAACACAAAAATTGGTATGGAAGTCACCCAACAGAGGCTCAAGAAGGAATCTGAAATCCCAGGAGTAGCCAGAGTGACTGTCACCATAAGGCAACTCATACATGTGCAGACACACACACACACACACACACACACACACACACACACACACATGCACAGAGGGGAGGACTGTTCTTTGACACGGGCCACCCCA... |
Task1_train_32467 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGCTAAGACCCAGAGGCAAGAAAACATGGCACATTGGAAAACAAAGTATTTCAGCTTAGGCTGGAACATAAAATCTGCAAGACTGGAGAATATGGGAGGTCAGCAGGGACTAGGCCCTAACCTAAGGGTCATGTGTGCTATATTAAGGGGCTTAAAATTTGCCATTAGGGACATGGGAGAAAGCAAGAGAGTATGGTGTCAGAGAAGCCAAGGGAAGAAGGCTTCTGAGGAGGAAGAACAGCTTCTGGCTCAAGCTAGCAGACTGAGAAAGCGCTGCTCTTTTCTCTCTCCTGTGATGCCACAAAAAGACAAACAAGGTG... | TGCTAAGACCCAGAGGCAAGAAAACATGGCACATTGGAAAACAAAGTATTTCAGCTTAGGCTGGAACATAAAATCTGCAAGACTGGAGAATATGGGAGGTCAGCAGGGACTAGGCCCTAACCTAAGGGTCATGTGTGCTATATTAAGGGGCTTAAAATTTGCCATTAGGGACATGGGAGAAAGCAAGAGAGTATGGTGTCAGAGAAGCCAAGGGAAGAAGGCTTCTGAGGAGGAAGAACAGCTTCTGGCTCAAGCTAGCAGACTGAGAAAGCGCTGCTCTTTTCTCTCTCCTGTGATGCCACAAAAAGACAAACAAGGTG... |
Task1_train_32468 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTGGGGATGTCATCCTGCTCTATCCCAGAATTGTCTAGAAGAAGAAATGCCATGTCAGCTCCCCAGAGTACCTGCTTAGCTTTCATCCATAAGCCTCAGACCCCTCATCCTTGTTTCAAACCACAGGGAGCACTGACACATACTTGTTGGGACAGACCTATCTTCTTTCCTTCTCAGCTGTTTGCAAGCAGTGCCCAGCTCACTGGAGGCTGCCGGCCCTGCTTGTGGACACCAAGGGCCTGCTGGGCAGCACTTCAAGGTCTTCTGCCCTTGGTGAAGGTTTTACAGGGATGTTATAAACCTGCTCCTAAGAGCCAAAG... | CTGGGGATGTCATCCTGCTCTATCCCAGAATTGTCTAGAAGAAGAAATGCCATGTCAGCTCCCCAGAGTACCTGCTTAGCTTTCATCCATAAGCCTCAGACCCCTCATCCTTGTTTCAAACCACAGGGAGCACTGACACATACTTGTTGGGACAGACCTATCTTCTTTCCTTCTCAGCTGTTTGCAAGCAGTGCCCAGCTCACTGGAGGCTGCCGGCCCTGCTTGTGGACACCAAGGGCCTGCTGGGCAGCACTTCAAGGTCTTCTGCCCTTGGTGAAGGTTTTACAGGGATGTTATAAACCTGCTCCTAAGAGCCAAAG... |
Task1_train_32469 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | CTAAGCCTACTAACATACTCCAGTTCCAATATTTTAAACACATGCCCCAAAGTAACCCCAAACTTTCTCTCTATCTTATGTTCCTTGCCGGCTACTGCCCATCCTGGCCTCCACAGCCTCACCTCCCATCCATTTGCTTCCCACCCTACTGCTGTCTGTTGCTGCCCCTAGAGCTTCACTGCAAAGTCTTCTTCCAAGGCCAAAGCCAATGGTCTCCTTCTAGCACTTTTCCAGCAAGACATTTGTCATCGTTGCCATGATCAGACATGCCCTAGTTGGAAACTCTTCCTGTGTTTGCATCACGATTCTCCTCCCGCCTC... | CTAAGCCTACTAACATACTCCAGTTCCAATATTTTAAACACATGCCCCAAAGTAACCCCAAACTTTCTCTCTATCTTATGTTCCTTGCCGGCTACTGCCCATCCTGGCCTCCACAGCCTCACCTCCCATCCATTTGCTTCCCACCCTACTGCTGTCTGTTGCTGCCCCTAGAGCTTCACTGCAAAGTCTTCTTCCAAGGCCAAAGCCAATGGTCTCCTTCTAGCACTTTTCCAGCAAGACATTTGTCATCGTTGCCATGATCAGACATGCCCTAGTTGGAAACTCTTCCTGTGTTTGCATCACGATTCTCCTCCCGCCTC... |
Task1_train_32470 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGAATATGTGGACTTTCATTAAAGTTCTTCCTCATGTCCCATCTTTTGATCTCAGAAAGGAGCTGTGTCCCATTCATCTAGGCAGCCCTGCTCATGTCCAAAAAATGTGTGAGTCAACCTCTGGCCCCTTGGGAGAAAGAGCCAGGGGGAAAAAGGCTACCTAGGCTGAGAAGTGTCCCCAGAGTAATCCGTTCCTTTGCGAGACCCCCTACTAGCCCAGACTTCCTTGATGGCACCTGATATCTTATAGGCCCCCAAATCCTGCCACACAACTACAGCTTGTCCCCTGGAGGGGCTTCCCTGGCCAGTCCAGAATGCTC... | TGAATATGTGGACTTTCATTAAAGTTCTTCCTCATGTCCCATCTTTTGATCTCAGAAAGGAGCTGTGTCCCATTCATCTAGGCAGCCCTGCTCATGTCCAAAAAATGTGTGAGTCAACCTCTGGCCCCTTGGGAGAAAGAGCCAGGGGGAAAAAGGCTACCTAGGCTGAGAAGTGTCCCCAGAGTAATCCGTTCCTTTGCGAGACCCCCTACTAGCCCAGACTTCCTTGATGGCACCTGATATCTTATAGGCCCCCAAATCCTGCCACACAACTACAGCTTGTCCCCTGGAGGGGCTTCCCTGGCCAGTCCAGAATGCTC... |
Task1_train_32471 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCAGGAAAGGGAACTCTAGTTCCCTTGTGGTCCACCAAGAAGGCTCAACATGGCCAAGGCCCATTCTATTGGTTGAGGAGAGGTAAACAAAGGTGAAGTCAAGTGGCAACTCAGATTGATTGGCTGTGGCTTGCCTATTGGGAGGGAATTCACAGCTGTGTCTGGACCCAAGCAGAAAGGGTGCAATGAACAATTAATTATGTCTGCCATGGGATTGGGAAGAAGGGGAATAGGTATACATGCCATGTAATTTTTATCCTTGGTGTCAATAACAAAAAGTGTGTGCATGTGGCAGGAAGAAGGAGTTGCTTATCCCTGGA... | GCAGGAAAGGGAACTCTAGTTCCCTTGTGGTCCACCAAGAAGGCTCAACATGGCCAAGGCCCATTCTATTGGTTGAGGAGAGGTAAACAAAGGTGAAGTCAAGTGGCAACTCAGATTGATTGGCTGTGGCTTGCCTATTGGGAGGGAATTCACAGCTGTGTCTGGACCCAAGCAGAAAGGGTGCAATGAACAATTAATTATGTCTGCCATGGGATTGGGAAGAAGGGGAATAGGTATACATGCCATGTAATTTTTATCCTTGGTGTCAATAACAAAAAGTGTGTGCATGTGGCAGGAAGAAGGAGTTGCTTATCCCTGGA... |
Task1_train_32472 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACATAGCTCTTCCCCAGGGTCCCCAAGCACCCTGGGCTACCAAGTCTTTGCCTCAGGACTCATCAGGACCCAGCAACTAAAGGTTTCCTGTCTGGCACAATAGGAAGCCTCTAAGACTGTAGACTGTGTCCATTCTGATTGACTGTTAAATGCAGTGACTACTCCCCTGGGTCTGTGTATGGTGACATGTGAATTGTGTGCCTGCCTGTTTCTGTTCGTGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTTTGTACACAATAAGCATTACCAGGAAGGCATGGACCCTGCTGGAAGCATTCCATGGTCACCGTTT... | ACATAGCTCTTCCCCAGGGTCCCCAAGCACCCTGGGCTACCAAGTCTTTGCCTCAGGACTCATCAGGACCCAGCAACTAAAGGTTTCCTGTCTGGCACAATAGGAAGCCTCTAAGACTGTAGACTGTGTCCATTCTGATTGACTGTTAAATGCAGTGACTACTCCCCTGGGTCTGTGTATGGTGACATGTGAATTGTGTGCCTGCCTGTTTCTGTTCGTGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTTTGTACACAATAAGCATTACCAGGAAGGCATGGACCCTGCTGGAAGCATTCCATGGTCACCGTTT... |
Task1_train_32473 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GCCTGTTTCTGTTCGTGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTTTGTACACAATAAGCATTACCAGGAAGGCATGGACCCTGCTGGAAGCATTCCATGGTCACCGTTTTGGAGACTCATCATGCCCTCTGAGAGGCTGGCCAGAGCTGGAACCTGTGCTGGACCTCCAGACTGCAAAGCCTAAGCCACAGCAGCTGAGCTCCCCTATGGGACTCCTTGATTTTTTCCCTTGGGTCTTCATCATCTTCTCCTTCAGCGCTCCCATGATAGAAGGCTGAGTAGTTTCCAGAATGCTTGGTGTGGGCCACCTCA... | GCCTGTTTCTGTTCGTGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTTTGTACACAATAAGCATTACCAGGAAGGCATGGACCCTGCTGGAAGCATTCCATGGTCACCGTTTTGGAGACTCATCATGCCCTCTGAGAGGCTGGCCAGAGCTGGAACCTGTGCTGGACCTCCAGACTGCAAAGCCTAAGCCACAGCAGCTGAGCTCCCCTATGGGACTCCTTGATTTTTTCCCTTGGGTCTTCATCATCTTCTCCTTCAGCGCTCCCATGATAGAAGGCTGAGTAGTTTCCAGAATGCTTGGTGTGGGCCACCTCA... |
Task1_train_32474 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TCCTCCACTTCAATCCCCTCCCAGGTCCAGGCACTTCCTCCCCCATGAGGACAGGGGTACTTTCTGCCATGCTGACCCATAGGGTCATGACTCCCATCTGACCTGCGAGGTGCTCTTGGCATGTTCTGACCTTTAGCTCATCACCTTGGGATTTGGTGCCTGCGCCCAGCATCACCAGGCCCCACATCTCCACTGGAGAACATTGGGGAAGACCGGGAGGGAGGACTCAGGTTTCCAAAGAGGACACAGCATAGAGAGGCTAGTGAGAACCAAGGTATAGGCTCCGGGCTTACCCTGCTGGGGTTCTGACCACAACTCAG... | TCCTCCACTTCAATCCCCTCCCAGGTCCAGGCACTTCCTCCCCCATGAGGACAGGGGTACTTTCTGCCATGCTGACCCATAGGGTCATGACTCCCATCTGACCTGCGAGGTGCTCTTGGCATGTTCTGACCTTTAGCTCATCACCTTGGGATTTGGTGCCTGCGCCCAGCATCACCAGGCCCCACATCTCCACTGGAGAACATTGGGGAAGACCGGGAGGGAGGACTCAGGTTTCCAAAGAGGACACAGCATAGAGAGGCTAGTGAGAACCAAGGTATAGGCTCCGGGCTTACCCTGCTGGGGTTCTGACCACAACTCAG... |
Task1_train_32475 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCAGGAAGCAAGCAACCAGCTGAGCTGAGGATATCCAAGGGACCTCAGGCTGTGGGCTGGGCTTCAGGGAGGGAGCCAGAGGGTCAGTGTCCCTAGAGGATCCCCAGGGAAGTGCCAAGGAGGAGAAGGAATGTCCTGGCTGACCTAAGGGACGACAGAAGATTGGGGAAGAGGGGGTATCAGGAAGAAATGGGTTTCAGTTCAGTTTAACAAACATCTATTGTGTGTTCACTGGGCCAGGCCAGTGCTAGGTGCTAGGGAGACAGAGGTGAAGAGCCTGCCCTCTAGCAGCTGACAGCCTGGCAAAAAAATAAGACAGG... | CCAGGAAGCAAGCAACCAGCTGAGCTGAGGATATCCAAGGGACCTCAGGCTGTGGGCTGGGCTTCAGGGAGGGAGCCAGAGGGTCAGTGTCCCTAGAGGATCCCCAGGGAAGTGCCAAGGAGGAGAAGGAATGTCCTGGCTGACCTAAGGGACGACAGAAGATTGGGGAAGAGGGGGTATCAGGAAGAAATGGGTTTCAGTTCAGTTTAACAAACATCTATTGTGTGTTCACTGGGCCAGGCCAGTGCTAGGTGCTAGGGAGACAGAGGTGAAGAGCCTGCCCTCTAGCAGCTGACAGCCTGGCAAAAAAATAAGACAGG... |
Task1_train_32476 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CGGGAGGAGTCTTGGGTCCTCCGATGCCGGGACGGGGGTTGCTGCGGAACGCCCGCCGCGACAGAGCCGCGCTCACCCAGGTGGCCTTGGCCAGGCTCCCACCCTCTTTCCATGGAATCCTTGTAACAACCCGAGGCGGGAGGAATACTATTGTTTCCACTCTATCGTGGAGGAGACTGAGGGGCCCAGAGGTTGTTCCTTATCCAAGGGGCCGCAGTTACTAAAAGGCAAGATTTGAACCCAGGGCCGCTTCCAGAGCCTGGCTCTAAACAGCTTTGCACTTGGGAAGAGGCACCTCCCCCTTGGGAACTTTGTGGCCT... | CGGGAGGAGTCTTGGGTCCTCCGATGCCGGGACGGGGGTTGCTGCGGAACGCCCGCCGCGACAGAGCCGCGCTCACCCAGGTGGCCTTGGCCAGGCTCCCACCCTCTTTCCATGGAATCCTTGTAACAACCCGAGGCGGGAGGAATACTATTGTTTCCACTCTATCGTGGAGGAGACTGAGGGGCCCAGAGGTTGTTCCTTATCCAAGGGGCCGCAGTTACTAAAAGGCAAGATTTGAACCCAGGGCCGCTTCCAGAGCCTGGCTCTAAACAGCTTTGCACTTGGGAAGAGGCACCTCCCCCTTGGGAACTTTGTGGCCT... |
Task1_train_32477 | 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 | GCCGAAAACCCGCCCCTGCCGCCGGCTCATTTCCTCCCTCCCCGGGGCAGCCGGAAGACTCTCGCCTGAGCTACCGTCCCCCACCCTCCAGGGGGTCGCGAGGCTGCAGTACTGGGGCAGGGCGCCCCCATCTTACAGGTGGGGACACTTGAGGACCACTGGCTGGTAACTGACTAAACAGGCACCTTTGGATTCAGGGAGTGTTTCCCAGCCAATACGGAGTGCTGGCAGACACGGGTGGGTGTCTGGGTGCGGTTCAGCTACCATCAAAAGACCCCGGGCTTCGTTCCTGCCTGTGCCACACTAGCTGTGGGATCTGA... | GCCGAAAACCCGCCCCTGCCGCCGGCTCATTTCCTCCCTCCCCGGGGCAGCCGGAAGACTCTCGCCTGAGCTACCGTCCCCCACCCTCCAGGGGGTCGCGAGGCTGCAGTACTGGGGCAGGGCGCCCCCATCTTACAGGTGGGGACACTTGAGGACCACTGGCTGGTAACTGACTAAACAGGCACCTTTGGATTCAGGGAGTGTTTCCCAGCCAATACGGAGTGCTGGCAGACACGGGTGGGTGTCTGGGTGCGGTTCAGCTACCATCAAAAGACCCCGGGCTTCGTTCCTGCCTGTGCCACACTAGCTGTGGGATCTGA... |
Task1_train_32478 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGGCAACATCTCCACTAAAAATTAAAAAATTAGCCGGGCATGGAGGCATGTGCCTGTAGTCTCAGCTACTTGGGAGGCTGAGGCAGAAGAATCACTTGAACCCAGAAGTAGGTTATAGTGAGACGAGATCGCGTCACTGTACTCCAGCCTGGGTGACAGAGTGAGATCTTGTCTCAAAAAAAAAAGAAAAAAAAAAAAAAACAAGTAGGGAAAATAGTTGTAATTCAATATGTCTGCTCCCTATTGATAGTGAATGGAGGGATTTTGTTGACAAAGATTTTGATGTCACACCTGGATACCATAGAAAATAATGTATTGGG... | GGGCAACATCTCCACTAAAAATTAAAAAATTAGCCGGGCATGGAGGCATGTGCCTGTAGTCTCAGCTACTTGGGAGGCTGAGGCAGAAGAATCACTTGAACCCAGAAGTAGGTTATAGTGAGACGAGATCGCGTCACTGTACTCCAGCCTGGGTGACAGAGTGAGATCTTGTCTCAAAAAAAAAAGAAAAAAAAAAAAAAACAAGTAGGGAAAATAGTTGTAATTCAATATGTCTGCTCCCTATTGATAGTGAATGGAGGGATTTTGTTGACAAAGATTTTGATGTCACACCTGGATACCATAGAAAATAATGTATTGGG... |
Task1_train_32479 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | GGTAGTTCAGGGAAAATGGAGAATGATGGCAATTCTCTTCAATAATATTTTTATTAAATTCCATGGTGGCCTTCTCTCAAAATTAGTAATGAAATGCTGAAATGTCCATTGATTAGTGAGGGCAATGTATGTAAGCCAGAAGAATGCAATAAATAAGGGTTATGTTTCTTCTTGTCAGACCCAGAAGGGAGATCTTTGAACAACAGTGCTTCAAATTGAGAATTCAGTCCCAGGAAGGGTCTCTCTGCCCCACAGACTGTGGTGGACAAACACTGGGTGTAACACTTTATCTTCATCCCCAAGCCCCAGAAAATTAGAGG... | GGTAGTTCAGGGAAAATGGAGAATGATGGCAATTCTCTTCAATAATATTTTTATTAAATTCCATGGTGGCCTTCTCTCAAAATTAGTAATGAAATGCTGAAATGTCCATTGATTAGTGAGGGCAATGTATGTAAGCCAGAAGAATGCAATAAATAAGGGTTATGTTTCTTCTTGTCAGACCCAGAAGGGAGATCTTTGAACAACAGTGCTTCAAATTGAGAATTCAGTCCCAGGAAGGGTCTCTCTGCCCCACAGACTGTGGTGGACAAACACTGGGTGTAACACTTTATCTTCATCCCCAAGCCCCAGAAAATTAGAGG... |
Task1_train_32480 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CTCCTAAAGTGCTAGAATTACAGGCATAAGCCACTGACTATGCTTGGTTTAATGAAAGAGTCTTGGCTGAGTGTAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAGATCACCTAAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCGGGTACCTGTAATCCCAGCTACTTGAGAGCCTGAGGCAGAAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCAGCATTGCACTCCAGCC... | CTCCTAAAGTGCTAGAATTACAGGCATAAGCCACTGACTATGCTTGGTTTAATGAAAGAGTCTTGGCTGAGTGTAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAGATCACCTAAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCGGGTACCTGTAATCCCAGCTACTTGAGAGCCTGAGGCAGAAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCAGCATTGCACTCCAGCC... |
Task1_train_32481 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | CAGAACCCTGGAGAACACCGGTAATTAAGAGGGAGGGAGGGAGGGAAGGGGATTAGGGAAGGAAACAGTTTGATAGGAGGAGAAGCAGGAGTGGCTATCAACGAAACCTAGGAAAAGAATTTCAAAATGAAGACACTGATCACTGGTGGTGTGCTCCAGAGAAGTGAAGTAGGAGGAGATCTGGATCCAGAAACTATCATTTTCAATCTGGGTATGGTGGCGCACACCTATAATCCCAGCTACTCCAGAGACTGAGGTGGAAGGATCATCGCTTAAGTCCAGGAGTTCGAGACTAGCCTGGGCAACATGGCAAGATCCTG... | CAGAACCCTGGAGAACACCGGTAATTAAGAGGGAGGGAGGGAGGGAAGGGGATTAGGGAAGGAAACAGTTTGATAGGAGGAGAAGCAGGAGTGGCTATCAACGAAACCTAGGAAAAGAATTTCAAAATGAAGACACTGATCACTGGTGGTGTGCTCCAGAGAAGTGAAGTAGGAGGAGATCTGGATCCAGAAACTATCATTTTCAATCTGGGTATGGTGGCGCACACCTATAATCCCAGCTACTCCAGAGACTGAGGTGGAAGGATCATCGCTTAAGTCCAGGAGTTCGAGACTAGCCTGGGCAACATGGCAAGATCCTG... |
Task1_train_32482 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TTAAACCCTCCTTAGTGCTGGTGGTGGATCACCTCCCTCAAGCATAGCCCTTTAATCGGGTTGTATTCACTTTCATAATCTGCATCTGCCTCTCCCTTCTTTTCTTATATTGTTACTGTTTTCAAATGAAAAGTGTGGAAGGTAAGTTTTTTTTTAATTGTACTTAATTACAATAACAACCAGCAGTAAGATATATCTTTGCCAGTTGCTCTTATTCATGGTGTAGATAAAAAAATCTGAGTACAGTGGGCAATAAATAGTGGAAAACCAATCCCACTTTATCTTTAGATTAAATTGAATGTACTTTCTTCTTAAAAATA... | TTAAACCCTCCTTAGTGCTGGTGGTGGATCACCTCCCTCAAGCATAGCCCTTTAATCGGGTTGTATTCACTTTCATAATCTGCATCTGCCTCTCCCTTCTTTTCTTATATTGTTACTGTTTTCAAATGAAAAGTGTGGAAGGTAAGTTTTTTTTTAATTGTACTTAATTACAATAACAACCAGCAGTAAGATATATCTTTGCCAGTTGCTCTTATTCATGGTGTAGATAAAAAAATCTGAGTACAGTGGGCAATAAATAGTGGAAAACCAATCCCACTTTATCTTTAGATTAAATTGAATGTACTTTCTTCTTAAAAATA... |
Task1_train_32483 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | AAATAGTGGAAAACCAATCCCACTTTATCTTTAGATTAAATTGAATGTACTTTCTTCTTAAAAATACTGTTTTGTTTAGTTGTTAAATCCTGAAAAGAAACTAGTATATTTGCTAACTGGAGTTATTTGGAAAAAACAAAAATGCATCTGTTCCCAGTCAGATATGAGAAAGCCTGCTGATTAACTGAAGAGTTTTTATTCTATATGTAAAGAAAATATTATTTGAAAGAGTTTTCTAGTAAATTTTACTTATTTGTAGCCAGCTGCTTAGGAGTAGTGGTTAATGTCAATGATCTATATCATAGTAGATAGGAAAAGTG... | AAATAGTGGAAAACCAATCCCACTTTATCTTTAGATTAAATTGAATGTACTTTCTTCTTAAAAATACTGTTTTGTTTAGTTGTTAAATCCTGAAAAGAAACTAGTATATTTGCTAACTGGAGTTATTTGGAAAAAACAAAAATGCATCTGTTCCCAGTCAGATATGAGAAAGCCTGCTGATTAACTGAAGAGTTTTTATTCTATATGTAAAGAAAATATTATTTGAAAGAGTTTTCTAGTAAATTTTACTTATTTGTAGCCAGCTGCTTAGGAGTAGTGGTTAATGTCAATGATCTATATCATAGTAGATAGGAAAAGTG... |
Task1_train_32484 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | AAGGGCCCAGTCTGTCTGACAGGGCTTTGCAGACCCGGCGGCTATTGCTTTGAAAAGGAGGAGAAAGACCACGCACGGGCAGCAGCCTGGAGGGACCCGGTGGGCTGCTGAGAGGGGGCTCCGCTGCGACGGGCCCTGGCCCAGCTTCAGGCCCTCACAGGAGGACAGTCAAGGGCTGGGAGCCCTAGGCCGGACTGCATTTCCGCTCCCGCAGGAGACTTTCTATGAAATAAATATAGAAAAGAGGGCATCCCCCAGCCCCACAGCACAAGACCCTGGCCCTCAGCGCTGGACAGCTGAGACAGACGCAGGCTCGCTGC... | AAGGGCCCAGTCTGTCTGACAGGGCTTTGCAGACCCGGCGGCTATTGCTTTGAAAAGGAGGAGAAAGACCACGCACGGGCAGCAGCCTGGAGGGACCCGGTGGGCTGCTGAGAGGGGGCTCCGCTGCGACGGGCCCTGGCCCAGCTTCAGGCCCTCACAGGAGGACAGTCAAGGGCTGGGAGCCCTAGGCCGGACTGCATTTCCGCTCCCGCAGGAGACTTTCTATGAAATAAATATAGAAAAGAGGGCATCCCCCAGCCCCACAGCACAAGACCCTGGCCCTCAGCGCTGGACAGCTGAGACAGACGCAGGCTCGCTGC... |
Task1_train_32485 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | CCCTGGCTGCTACAGAATAGCAGATGGGTATAGTTAAGAAACAACTTTAATTTGAGCAGGGGGAATGACAATACAGCACTTAACAGCTATATTGTAGTCTGAATCCTGCTTGAAAAAGAGGGTCTCTGAAGTTCAACGTTATATAAGATGAGGAAAGGAGGAAGGGAGGCTGGGTACGGTGGCTCACCTTTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCACTTGAGGTCAGGAGTTTAAGACCAGCCTGGCCAACTTGGTGAAATCCCACCTCTACTAAAAATACAAAAAAAAAAAAAAAATTAGCTGGG... | CCCTGGCTGCTACAGAATAGCAGATGGGTATAGTTAAGAAACAACTTTAATTTGAGCAGGGGGAATGACAATACAGCACTTAACAGCTATATTGTAGTCTGAATCCTGCTTGAAAAAGAGGGTCTCTGAAGTTCAACGTTATATAAGATGAGGAAAGGAGGAAGGGAGGCTGGGTACGGTGGCTCACCTTTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCACTTGAGGTCAGGAGTTTAAGACCAGCCTGGCCAACTTGGTGAAATCCCACCTCTACTAAAAATACAAAAAAAAAAAAAAAATTAGCTGGG... |
Task1_train_32486 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | CTTTGCAAACCAGAGATTTTCATACTTTCCGCAAGAGTGGAAGCCCCAGGGATCCACGTTTCTCCTCTCACTACCTTCCTCCTTGAAGAAGTGTATGGCTTCCTTTCCTGTCAATCGGTTTCCCTCAGCATTTACAAGTCGCCTCAGTCCAGTCTCCTTCCAGAGGCGCTGCCACACTGCCCTCAGGTGGTGACGGCCGGGAACACACCCTCGAGTCCATTCCCTCCTCTCACAGTCCTCATCCTGCCTCATCCTGTACCCCTCTTCCTTGTAGCCTGGCCTCCCCTGTTCTGCCTCTCCCCTCACTCCACCACCAGTTA... | CTTTGCAAACCAGAGATTTTCATACTTTCCGCAAGAGTGGAAGCCCCAGGGATCCACGTTTCTCCTCTCACTACCTTCCTCCTTGAAGAAGTGTATGGCTTCCTTTCCTGTCAATCGGTTTCCCTCAGCATTTACAAGTCGCCTCAGTCCAGTCTCCTTCCAGAGGCGCTGCCACACTGCCCTCAGGTGGTGACGGCCGGGAACACACCCTCGAGTCCATTCCCTCCTCTCACAGTCCTCATCCTGCCTCATCCTGTACCCCTCTTCCTTGTAGCCTGGCCTCCCCTGTTCTGCCTCTCCCCTCACTCCACCACCAGTTA... |
Task1_train_32487 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | TTGCTTGCTCAGCCCCTCTGCTGGCCTTTTCTTCTCCCTCCACCCTTTCCTTTCCGAGGTGATCTCGTCTCCTCCCATACTCCAGGGCTCACCTCTGAGCTCATGGCTCCCAGATCTCAAGGTCCCACTCCAGCTCCTTCCCTGGCACTGACCCATCCATCCCATTGCCTGTCACACATTTCCATCTATGGGTCCCCTAGGATGTACCTCAAATTCCCCCTGCTCAGAACAGGGCCCATCTTTGTCTCTTCCTCAACCCTTCAGTTGCCAAGCCTTTCCTCTCCACCCCAACTATTGCTCCCTATGCAGGCCTTCACTGT... | TTGCTTGCTCAGCCCCTCTGCTGGCCTTTTCTTCTCCCTCCACCCTTTCCTTTCCGAGGTGATCTCGTCTCCTCCCATACTCCAGGGCTCACCTCTGAGCTCATGGCTCCCAGATCTCAAGGTCCCACTCCAGCTCCTTCCCTGGCACTGACCCATCCATCCCATTGCCTGTCACACATTTCCATCTATGGGTCCCCTAGGATGTACCTCAAATTCCCCCTGCTCAGAACAGGGCCCATCTTTGTCTCTTCCTCAACCCTTCAGTTGCCAAGCCTTTCCTCTCCACCCCAACTATTGCTCCCTATGCAGGCCTTCACTGT... |
Task1_train_32488 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GGAAGCATAGCCCACAAGAGTATGAGGGCCTGAGCCAGGATGGTGGCAACAGGGATGGAGAGGAAGGCGTGCCAGGGCATGGTGGCTCACACCTATAATCCTAGCACTTTGAGAGGCTGAGGGAGGAGGATCATTTGAGCCCAAAAGTTAGAGACCAGCCTGGGAAACATAGTAAGACACTGCCTCAAAAAAAAAGGAAAAGAGGGTGTAGATATTGACAAGGCCGACTCTATTTTTGTTTGTTTGTTTGTTTTTGAGACGGAGTCTCCCTCTGTCGCCCAAGCTGGAGTGCAGTGGTGCGATCCCGGCTCACTGTAACC... | GGAAGCATAGCCCACAAGAGTATGAGGGCCTGAGCCAGGATGGTGGCAACAGGGATGGAGAGGAAGGCGTGCCAGGGCATGGTGGCTCACACCTATAATCCTAGCACTTTGAGAGGCTGAGGGAGGAGGATCATTTGAGCCCAAAAGTTAGAGACCAGCCTGGGAAACATAGTAAGACACTGCCTCAAAAAAAAAGGAAAAGAGGGTGTAGATATTGACAAGGCCGACTCTATTTTTGTTTGTTTGTTTGTTTTTGAGACGGAGTCTCCCTCTGTCGCCCAAGCTGGAGTGCAGTGGTGCGATCCCGGCTCACTGTAACC... |
Task1_train_32489 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTTCAGAAGGTGTCCCTTCACTGAGCCTGGGCCGACATCCCCATCTCATTTCCCTCTCCCTCCTGGATTCTCACCTCCTCCATGATTGTGGGCACCCAGGAGCCCAGGCTGCTGTGAGCTGGGTCTGGGACACTTGGCCAGAGGGGATTCTTCCTGCTGGAGAAGGGGGCAGGTGGAGGCTGAGTCAGACACACCCTCCGATCTTTCCATTTTTTGTCCCACCCACCCCACCTGAAGAGGTGCAGCTGCCCTTAGTGCAGAGAGAAGAAGCTGGGGGCTGGGACTCTCAGACATGGGCCCCAAAGTTTGGGAAGGCTGGA... | CTTCAGAAGGTGTCCCTTCACTGAGCCTGGGCCGACATCCCCATCTCATTTCCCTCTCCCTCCTGGATTCTCACCTCCTCCATGATTGTGGGCACCCAGGAGCCCAGGCTGCTGTGAGCTGGGTCTGGGACACTTGGCCAGAGGGGATTCTTCCTGCTGGAGAAGGGGGCAGGTGGAGGCTGAGTCAGACACACCCTCCGATCTTTCCATTTTTTGTCCCACCCACCCCACCTGAAGAGGTGCAGCTGCCCTTAGTGCAGAGAGAAGAAGCTGGGGGCTGGGACTCTCAGACATGGGCCCCAAAGTTTGGGAAGGCTGGA... |
Task1_train_32490 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CCTCCTTCTCCCACCCTCACAAACCTGTTTTACCAGGAGGGTATATAAGCTTCTGAACCCTTTTCGGGGTGGGTAATCATACTGTGATTCTCCCCGTGTATACATTTTAAATACATTTGTATGCCTTTTCTCCAATTAATCTGCCTTTTGTGAATTGATTTTTGAGCGAATCTTCAGGGGGCAAAGGGGAGGTTTCCCATTGGCTCCTACTTTGTCATTTCTCCATTTAATTAGAAAAATACTTCAGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGACCACGAGGTCAGGA... | CCTCCTTCTCCCACCCTCACAAACCTGTTTTACCAGGAGGGTATATAAGCTTCTGAACCCTTTTCGGGGTGGGTAATCATACTGTGATTCTCCCCGTGTATACATTTTAAATACATTTGTATGCCTTTTCTCCAATTAATCTGCCTTTTGTGAATTGATTTTTGAGCGAATCTTCAGGGGGCAAAGGGGAGGTTTCCCATTGGCTCCTACTTTGTCATTTCTCCATTTAATTAGAAAAATACTTCAGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGACCACGAGGTCAGGA... |
Task1_train_32491 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGAGGAGGTTGCAGTGAGCCGAGATCGCGCCATTGCACTCTAGCCTGGGCAACAAGAGCAAAACTCTGTCTCACAAAAAAAAAAAAGTACCCAGAAAATAGAGGAAAATGTCATATATGTACCAAAAGAAAAAATATATAGGCCAGGTGCAGTGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCTGAGGCGGGCGGATCACGAGGTCAAGAGATCAAGACCATCCTGGCTAACATGGTGAAAACCCGTCTCTAC... | GGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGAGGAGGTTGCAGTGAGCCGAGATCGCGCCATTGCACTCTAGCCTGGGCAACAAGAGCAAAACTCTGTCTCACAAAAAAAAAAAAGTACCCAGAAAATAGAGGAAAATGTCATATATGTACCAAAAGAAAAAATATATAGGCCAGGTGCAGTGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCTGAGGCGGGCGGATCACGAGGTCAAGAGATCAAGACCATCCTGGCTAACATGGTGAAAACCCGTCTCTAC... |
Task1_train_32492 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTGAACTATTATTTGCCAGTTGTGGAGGGTAAAGGCAACAAGCACAATGCCTGGCACACAGCTAGCTTTCGTCAAGTGTTGGCTTCCATCCTGCCTCAAACATGGCCTTTGTTTAGATTATCCCCTGTGCATGGAATGCCCCGCACCCCTCTCCTAGCCCCAGGTAAAATTCCCTTCAAGGCCTACCTCAAATGTCACTGTCATCAAGAAGGAGTTCCACAGGCAATTAGTTATCATCTCTATTCTCCCACAGCACCTGTTTTTACCTTAACTATAACACTTTTATTATTGTATTACAACTTAAGTCTCTGCAATCCAAA... | CTGAACTATTATTTGCCAGTTGTGGAGGGTAAAGGCAACAAGCACAATGCCTGGCACACAGCTAGCTTTCGTCAAGTGTTGGCTTCCATCCTGCCTCAAACATGGCCTTTGTTTAGATTATCCCCTGTGCATGGAATGCCCCGCACCCCTCTCCTAGCCCCAGGTAAAATTCCCTTCAAGGCCTACCTCAAATGTCACTGTCATCAAGAAGGAGTTCCACAGGCAATTAGTTATCATCTCTATTCTCCCACAGCACCTGTTTTTACCTTAACTATAACACTTTTATTATTGTATTACAACTTAAGTCTCTGCAATCCAAA... |
Task1_train_32493 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CAATCCAAAGTCTGGTCCTTGGACCATTAGCTGAGACTTCGTTTGAAATGCAGAATCTGGGCCCCATCCCAGACCTACAGAATCAGAATCCAAATTTTAACAAGATATCAGTGACTTATTTGCACATTAATCTTTCCCTGGTGGAACTGTGAGCCTTTCTAGGGCTCTCTTTTATTTCTGTCCCCAGAGCCCAACATAAGACTTGACACTTAAATGCTTTTTAAGTTTTATTTGCAATACTTATATGATAGATGTTTTTTAATTCCTGGAAAAATAAATACACATTATTAATAATAGTTATCTGGTAGATGGATAACGGT... | CAATCCAAAGTCTGGTCCTTGGACCATTAGCTGAGACTTCGTTTGAAATGCAGAATCTGGGCCCCATCCCAGACCTACAGAATCAGAATCCAAATTTTAACAAGATATCAGTGACTTATTTGCACATTAATCTTTCCCTGGTGGAACTGTGAGCCTTTCTAGGGCTCTCTTTTATTTCTGTCCCCAGAGCCCAACATAAGACTTGACACTTAAATGCTTTTTAAGTTTTATTTGCAATACTTATATGATAGATGTTTTTTAATTCCTGGAAAAATAAATACACATTATTAATAATAGTTATCTGGTAGATGGATAACGGT... |
Task1_train_32494 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CAGCCCCCAGTGGGTACAAATGGCAGTAGGGCATGAGCCAGGGCAATCTCAACCCACTGTCTTCCCTCCCATCCCTGCCCCAGCTTTTCTCTGAGACCCCGAATTTCCTCCTGCTGTTATCTCAGGGGTCCTCCCTAGGGATTTGAACCTCTTTTCAGGGGCACTGAGTTAGCCAAGGCGTTCAGACTCGTGAAAATGGGAGGGGCAGGCAGTGAAAGCGGGGAAGCTGTGGCCCCACCAGATCTGGGCCCAAGCAGAGGAAGAGAGCGCTCCCTCCCACACTGCTGGAGCGCAGCTTGCCACGGTCCTTGGGCAGGGCT... | CAGCCCCCAGTGGGTACAAATGGCAGTAGGGCATGAGCCAGGGCAATCTCAACCCACTGTCTTCCCTCCCATCCCTGCCCCAGCTTTTCTCTGAGACCCCGAATTTCCTCCTGCTGTTATCTCAGGGGTCCTCCCTAGGGATTTGAACCTCTTTTCAGGGGCACTGAGTTAGCCAAGGCGTTCAGACTCGTGAAAATGGGAGGGGCAGGCAGTGAAAGCGGGGAAGCTGTGGCCCCACCAGATCTGGGCCCAAGCAGAGGAAGAGAGCGCTCCCTCCCACACTGCTGGAGCGCAGCTTGCCACGGTCCTTGGGCAGGGCT... |
Task1_train_32495 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CACAGACACACACACACACACCCAAGGAAGCCTGGGGCAGTGGCCAGGCAGAACCAGAAGCAAGCAGACAGAGAAGAGGGGCCTGAGGCAGGAAGATTGAGGGCCAACGGGCAGAGGTCAGGAAGCTGGGGCCTGAGCTGAGAGGGTCAGAAGGCATGCAGCTGGAGCCACGGGTTACTCACGTCTTGGCCAGACATGTCCCAGTAAGGCCGCTCCCCAAAGGCCATCACCTCCCACATGATGATGCCGAAGCTCCACACGTCACTGGCAGAGCTGAAGTGGCCAAACTGAAGTGTCTCGGGAGCGGCCCATAGCGCTGG... | CACAGACACACACACACACACCCAAGGAAGCCTGGGGCAGTGGCCAGGCAGAACCAGAAGCAAGCAGACAGAGAAGAGGGGCCTGAGGCAGGAAGATTGAGGGCCAACGGGCAGAGGTCAGGAAGCTGGGGCCTGAGCTGAGAGGGTCAGAAGGCATGCAGCTGGAGCCACGGGTTACTCACGTCTTGGCCAGACATGTCCCAGTAAGGCCGCTCCCCAAAGGCCATCACCTCCCACATGATGATGCCGAAGCTCCACACGTCACTGGCAGAGCTGAAGTGGCCAAACTGAAGTGTCTCGGGAGCGGCCCATAGCGCTGG... |
Task1_train_32496 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CACACACACACACACCCAAGGAAGCCTGGGGCAGTGGCCAGGCAGAACCAGAAGCAAGCAGACAGAGAAGAGGGGCCTGAGGCAGGAAGATTGAGGGCCAACGGGCAGAGGTCAGGAAGCTGGGGCCTGAGCTGAGAGGGTCAGAAGGCATGCAGCTGGAGCCACGGGTTACTCACGTCTTGGCCAGACATGTCCCAGTAAGGCCGCTCCCCAAAGGCCATCACCTCCCACATGATGATGCCGAAGCTCCACACGTCACTGGCAGAGCTGAAGTGGCCAAACTGAAGTGTCTCGGGAGCGGCCCATAGCGCTGGGCTCCG... | CACACACACACACACCCAAGGAAGCCTGGGGCAGTGGCCAGGCAGAACCAGAAGCAAGCAGACAGAGAAGAGGGGCCTGAGGCAGGAAGATTGAGGGCCAACGGGCAGAGGTCAGGAAGCTGGGGCCTGAGCTGAGAGGGTCAGAAGGCATGCAGCTGGAGCCACGGGTTACTCACGTCTTGGCCAGACATGTCCCAGTAAGGCCGCTCCCCAAAGGCCATCACCTCCCACATGATGATGCCGAAGCTCCACACGTCACTGGCAGAGCTGAAGTGGCCAAACTGAAGTGTCTCGGGAGCGGCCCATAGCGCTGGGCTCCG... |
Task1_train_32497 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | AGACATCTGTAGGTGAACAAAGTCCAAGGTCATGAGCTGCAACAAGCTTGCTAAGAAAGATCACTCTTTCTAGGAGTGATATTCTAGGGGACCTATCACAGGTCAGAAAGGTCATCCTGGCCAGGCGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACGAGGTCAGGAGATCAAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAAAAAAAAAAAACAAAAAAATTAGCCGGGCCTGGTGGCAGGCACCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGA... | AGACATCTGTAGGTGAACAAAGTCCAAGGTCATGAGCTGCAACAAGCTTGCTAAGAAAGATCACTCTTTCTAGGAGTGATATTCTAGGGGACCTATCACAGGTCAGAAAGGTCATCCTGGCCAGGCGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACGAGGTCAGGAGATCAAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAAAAAAAAAAAACAAAAAAATTAGCCGGGCCTGGTGGCAGGCACCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGA... |
Task1_train_32498 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TTGCTAAGAAAGATCACTCTTTCTAGGAGTGATATTCTAGGGGACCTATCACAGGTCAGAAAGGTCATCCTGGCCAGGCGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACGAGGTCAGGAGATCAAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAAAAAAAAAAAACAAAAAAATTAGCCGGGCCTGGTGGCAGGCACCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGGCATGATCCCAGGAGGCAGAGCTTGCAGTGAGCCGAGATCTCAC... | TTGCTAAGAAAGATCACTCTTTCTAGGAGTGATATTCTAGGGGACCTATCACAGGTCAGAAAGGTCATCCTGGCCAGGCGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACGAGGTCAGGAGATCAAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAAAAAAAAAAAACAAAAAAATTAGCCGGGCCTGGTGGCAGGCACCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGGCATGATCCCAGGAGGCAGAGCTTGCAGTGAGCCGAGATCTCAC... |
Task1_train_32499 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTCCATCCTTCTGCATGCAATTCCTAAGCTTAGAATGCTCTAAGCTGCCTGGGAAAAAAAAACCTTCTCACCTTCTCTGGGAAGCCTTCTCCATGCTTAGAATTAGGTTCTCCCTTCCATGCTTCCTTAGCTCTCTGTTTATGTTTCACACCCTATAGTAACCACTTTTTCACCCAATGCATTTTCACTGAACACCTACCGTATGCCTTATCCTGTTATGAATGCTGGGGCTGCTGACACTAGTAACACCCAGTGCCTGAGCTCAAGAAGTTCCTAATCTAGGGTGTGGTCCCTATAGTCCCACCTACTCAGGAGGCTGA... | CTCCATCCTTCTGCATGCAATTCCTAAGCTTAGAATGCTCTAAGCTGCCTGGGAAAAAAAAACCTTCTCACCTTCTCTGGGAAGCCTTCTCCATGCTTAGAATTAGGTTCTCCCTTCCATGCTTCCTTAGCTCTCTGTTTATGTTTCACACCCTATAGTAACCACTTTTTCACCCAATGCATTTTCACTGAACACCTACCGTATGCCTTATCCTGTTATGAATGCTGGGGCTGCTGACACTAGTAACACCCAGTGCCTGAGCTCAAGAAGTTCCTAATCTAGGGTGTGGTCCCTATAGTCCCACCTACTCAGGAGGCTGA... |
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