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 |
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Task1_train_46100 | Here is a variant on Chromosome 18. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GCTTGTTTAAAACAGACTTACTACCAAAAGGTGGATAAGAAGTTTTGCATGAAGCCATCACCTTATTTAGTGCAACCTAGGCCTCAAAAAATTTCAATCTCAAAAAAATTCAATCTGAAAATGATAATTTTTCCTGATCTTATTTCCTACTCAATGAGAATACTATTGTGTCCCTTTAGTAATATAGAAGGTAGAGCATTCTCTACCTGGGTAACTCCAGACTCACTGACTTAATCATAGTTAAGAAGGATAATTCTCAGCATTTAGGTTCATCTGGTACAAGTGCAGAGAAGGGAATTTATGAACTTCACAAGGAGAAT... | GCTTGTTTAAAACAGACTTACTACCAAAAGGTGGATAAGAAGTTTTGCATGAAGCCATCACCTTATTTAGTGCAACCTAGGCCTCAAAAAATTTCAATCTCAAAAAAATTCAATCTGAAAATGATAATTTTTCCTGATCTTATTTCCTACTCAATGAGAATACTATTGTGTCCCTTTAGTAATATAGAAGGTAGAGCATTCTCTACCTGGGTAACTCCAGACTCACTGACTTAATCATAGTTAAGAAGGATAATTCTCAGCATTTAGGTTCATCTGGTACAAGTGCAGAGAAGGGAATTTATGAACTTCACAAGGAGAAT... |
Task1_train_46101 | Chromosome 18 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TGCAGTGGTATTACCTATGCATCACAAGCATCATGAATTATAATTTACTCACTTGTACTCCTAAAATTAACAGTTTTCAATACTTTATTACTATAAATGATAACATATGAATATCTTAATCATCAAAGCATTTTTTAACATTCCATATTATTTAGTGTTCCCTGAAGAACAATGAATAGGTATACAGATACATTTTTTAAAGTAAAAAATTGATATGCACTTATACAATCACTAAAATGTCTATGACTAATTAAGAACTACATATGCGTATCAGAAGGCAACATTTTATGAACTGGAACTATAATGGAAAAGTGGGAACA... | TGCAGTGGTATTACCTATGCATCACAAGCATCATGAATTATAATTTACTCACTTGTACTCCTAAAATTAACAGTTTTCAATACTTTATTACTATAAATGATAACATATGAATATCTTAATCATCAAAGCATTTTTTAACATTCCATATTATTTAGTGTTCCCTGAAGAACAATGAATAGGTATACAGATACATTTTTTAAAGTAAAAAATTGATATGCACTTATACAATCACTAAAATGTCTATGACTAATTAAGAACTACATATGCGTATCAGAAGGCAACATTTTATGAACTGGAACTATAATGGAAAAGTGGGAACA... |
Task1_train_46102 | This sequence variant lies on Chromosome 18. Is it clinically significant, and what condition might it cause if any? | Benign | TTTTGTAGTCCATCTTGAAAGCAAGAGATGCGTGGGTAAAGCAGCAATTGCAAGGCCTTTAGCAGTGTTTGAGGTCTCTAGATAGATTAGCACAGTTACAGATGAAGGGGAGTTAGACAAAAACTTAAAATTTTCCCATCTCCCCTGACCCCATGATATAACTTCATCTACCACTCTGTAGCAGAAACTTTTTAGCAGACAAAATTTTCAGAAACAAAGGCAAGGGAGGTGATGACATAAAAATAAATCCTGCTAGGCCAAATATGGTGCCATTTTTTAAAACAATCTCTCTGTGCAAACAACACTGAACACATACACGC... | TTTTGTAGTCCATCTTGAAAGCAAGAGATGCGTGGGTAAAGCAGCAATTGCAAGGCCTTTAGCAGTGTTTGAGGTCTCTAGATAGATTAGCACAGTTACAGATGAAGGGGAGTTAGACAAAAACTTAAAATTTTCCCATCTCCCCTGACCCCATGATATAACTTCATCTACCACTCTGTAGCAGAAACTTTTTAGCAGACAAAATTTTCAGAAACAAAGGCAAGGGAGGTGATGACATAAAAATAAATCCTGCTAGGCCAAATATGGTGCCATTTTTTAAAACAATCTCTCTGTGCAAACAACACTGAACACATACACGC... |
Task1_train_46103 | Chromosome 18 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGGTATACCTTTACAAATTAATTTGTGTGTTGGTATTTGTATGGAAAGTTGATTTTAATTCCTTTACAAAGCTTTGCATTGGGCTAAGACTCTGTGTAGTGTTATCTATGCTGTAAAGTTTCCTCATTTCTAAGCGATAGTCATAACTTCTTCAGTACCCCTTAGATTACCTTGACCATACCTAAGAATCTAACACTGACTTGACACATATTACATAATAAATAAAGTTATTGAACAAATGCACATATTTGTTATAATGTGAATTATGTATCTTTAAAACTTAACTCTGCTTCTCTCACCCACCAGACTGTAAAATCTTT... | TGGTATACCTTTACAAATTAATTTGTGTGTTGGTATTTGTATGGAAAGTTGATTTTAATTCCTTTACAAAGCTTTGCATTGGGCTAAGACTCTGTGTAGTGTTATCTATGCTGTAAAGTTTCCTCATTTCTAAGCGATAGTCATAACTTCTTCAGTACCCCTTAGATTACCTTGACCATACCTAAGAATCTAACACTGACTTGACACATATTACATAATAAATAAAGTTATTGAACAAATGCACATATTTGTTATAATGTGAATTATGTATCTTTAAAACTTAACTCTGCTTCTCTCACCCACCAGACTGTAAAATCTTT... |
Task1_train_46104 | This mutation is located on Chromosome 18. Is it associated with a disease or is it a benign polymorphism? | Benign | GAGGAACATAAATATATGCTTCATTACACAAATGCAGTTAATTAAAATCTTTTATAAAAATATTTTATTAATTTAACATATGCCATTTGCTTTTTCAGTTTTTCAGTTACTGACAAGACATTCCCACATCCTACACAAGAAAATCTAAAAAATTAAAATTATAAATATGGTGATTCTTATCTTAAACATTCCAATGAAGTTACAAACTTAGTACAATTTTATTATAATTTTCAATGTAAATTCACAGGTCTAAGTCAATACTCAATATCTTTTAAATATTCTATTTTATCACCCAAAACTTAAAATGCACTCAAATGTTA... | GAGGAACATAAATATATGCTTCATTACACAAATGCAGTTAATTAAAATCTTTTATAAAAATATTTTATTAATTTAACATATGCCATTTGCTTTTTCAGTTTTTCAGTTACTGACAAGACATTCCCACATCCTACACAAGAAAATCTAAAAAATTAAAATTATAAATATGGTGATTCTTATCTTAAACATTCCAATGAAGTTACAAACTTAGTACAATTTTATTATAATTTTCAATGTAAATTCACAGGTCTAAGTCAATACTCAATATCTTTTAAATATTCTATTTTATCACCCAAAACTTAAAATGCACTCAAATGTTA... |
Task1_train_46105 | Given this variant on Chromosome 18, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TAGACATTCTGTTTCTTAATCTCAGCCTTGACTATTCCTGTTTTTCTTGTTTTGTTTTGCTTTTCTGCCACTCTTATGTTCTTCACATGCCCAGAGATCTTTGATTTTTCCACTCACAATGATGAATGATATGGATTTATTTGAGGTATTTGGTGTGGGTTTCCTTTGCTGCTGTTTATAAAAACTTGCTTTCCTGCCTCCTCTCTCTTTTGAGTGGTACAGTTCATTGAGAGTTCTGTTGACAATGGAAGGGTTTATTATTGGATTTAATTCCCTGTAGTTTAATGACAAGGTTTCAGAGGTTAAACGGGGGCATTCAG... | TAGACATTCTGTTTCTTAATCTCAGCCTTGACTATTCCTGTTTTTCTTGTTTTGTTTTGCTTTTCTGCCACTCTTATGTTCTTCACATGCCCAGAGATCTTTGATTTTTCCACTCACAATGATGAATGATATGGATTTATTTGAGGTATTTGGTGTGGGTTTCCTTTGCTGCTGTTTATAAAAACTTGCTTTCCTGCCTCCTCTCTCTTTTGAGTGGTACAGTTCATTGAGAGTTCTGTTGACAATGGAAGGGTTTATTATTGGATTTAATTCCCTGTAGTTTAATGACAAGGTTTCAGAGGTTAAACGGGGGCATTCAG... |
Task1_train_46106 | A variant on Chromosome 18 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTGAAGGGTTTAATGTTTTTTCTTAAATGTAATCAGGCCCATTTCAGGGACATTTAGTTTCCAATATTCACTGTAAATACCAGCAACAACAAAACAATGCTGAGACAAATATTCTCATAATCACAACATTTCACACAGCTATGAGTATATCTGTGAAATAAATTCCTGGAAATAGAATGGTTGTATCTGACTTTATGTGCATTTTTAATTAAAAAAATATTGCCAGTGTTTCTCCATGAATGAATCCTTATTTCTCCACATTTTACTGGCAGATTACCTTACCATACTTAGCCTTTGCCAGTCTGAAGACATCTTGATTT... | TTGAAGGGTTTAATGTTTTTTCTTAAATGTAATCAGGCCCATTTCAGGGACATTTAGTTTCCAATATTCACTGTAAATACCAGCAACAACAAAACAATGCTGAGACAAATATTCTCATAATCACAACATTTCACACAGCTATGAGTATATCTGTGAAATAAATTCCTGGAAATAGAATGGTTGTATCTGACTTTATGTGCATTTTTAATTAAAAAAATATTGCCAGTGTTTCTCCATGAATGAATCCTTATTTCTCCACATTTTACTGGCAGATTACCTTACCATACTTAGCCTTTGCCAGTCTGAAGACATCTTGATTT... |
Task1_train_46107 | A genetic alteration is present on Chromosome 18. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGATGCTAAGCTTGCTTCACCATGCAAACCAATAAATTCACTCACAGAATCTTTGATTGATCTGATAGTAGAGTGCTTTCTTGTAAACTGCCTTTCAAGTTTGTTACACTAATATATTTGTGGAAACATTTCATGAATCCAGGTATAAAAAGATCTTTAAGCAAACATAATAAAAATGAGAGTTTACCCTTCTTGCATATACTTAAGCACAACCAGGAAATGGTCGTTTTTATTTTTTCACTCCTGAAAAGGGTTAAAAGAAACTCACAAATTTTATAATTCACAGAAATGTGGGCACTTACCATTTCTGTAATTCACAA... | TGATGCTAAGCTTGCTTCACCATGCAAACCAATAAATTCACTCACAGAATCTTTGATTGATCTGATAGTAGAGTGCTTTCTTGTAAACTGCCTTTCAAGTTTGTTACACTAATATATTTGTGGAAACATTTCATGAATCCAGGTATAAAAAGATCTTTAAGCAAACATAATAAAAATGAGAGTTTACCCTTCTTGCATATACTTAAGCACAACCAGGAAATGGTCGTTTTTATTTTTTCACTCCTGAAAAGGGTTAAAAGAAACTCACAAATTTTATAATTCACAGAAATGTGGGCACTTACCATTTCTGTAATTCACAA... |
Task1_train_46108 | This mutation on Chromosome 18 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CTTTTAAAAAAGAGAATGAAGTAGTTCTAATGTCTTTTTTTGACAGTCCAACCTATTAACTCTTTAATAATCCTTCAAAATATTATTCTACAAAAACCTGAAAAAGTTGGATACCTAATATAGACCGTTGCAAAGCTCCCTTTCATTCCCCAAATTCACAACAATAAATGTGACTAGACTGGCATGAGTAGACAAAGGCTAAGGATGAAGAAGGGAATCCCAAAATTGTGTATGACAGAGCACCAATTTATTTCTTGCTGAAGTGGCTGATGAAATAAAGCAAGGTTTCTTGATTCTACAGTTGGCATCAAGAAGCAATC... | CTTTTAAAAAAGAGAATGAAGTAGTTCTAATGTCTTTTTTTGACAGTCCAACCTATTAACTCTTTAATAATCCTTCAAAATATTATTCTACAAAAACCTGAAAAAGTTGGATACCTAATATAGACCGTTGCAAAGCTCCCTTTCATTCCCCAAATTCACAACAATAAATGTGACTAGACTGGCATGAGTAGACAAAGGCTAAGGATGAAGAAGGGAATCCCAAAATTGTGTATGACAGAGCACCAATTTATTTCTTGCTGAAGTGGCTGATGAAATAAAGCAAGGTTTCTTGATTCTACAGTTGGCATCAAGAAGCAATC... |
Task1_train_46109 | Here is a mutation located on Chromosome 18. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGAATTCATAATCTGATATGTTTAAAATTATTTAGAAATATGGAGGCAAATATAAGAGACAGCTTTAAAAGCTGAATATTAATATCTCAGACATGTGTAAGTGACACTGGGACAGGGCTGTCCGCTGGCATCTTTCAGTTGTGTGTGGCATGCACACCTGTTTTCATGAGACTCTTCAAAGCACCAAGGCTTTATGAGCACTGCCTCCTCCGCCTCACCCTTCCCCATTGCTGCCCAGTAAACCTTCCTTCCAGGGTGAACTCAGATGTCACCTGAGATGTAAGGGACTCCCAGACTCATCGGTCAGAATTGCTCCCTGT... | AGAATTCATAATCTGATATGTTTAAAATTATTTAGAAATATGGAGGCAAATATAAGAGACAGCTTTAAAAGCTGAATATTAATATCTCAGACATGTGTAAGTGACACTGGGACAGGGCTGTCCGCTGGCATCTTTCAGTTGTGTGTGGCATGCACACCTGTTTTCATGAGACTCTTCAAAGCACCAAGGCTTTATGAGCACTGCCTCCTCCGCCTCACCCTTCCCCATTGCTGCCCAGTAAACCTTCCTTCCAGGGTGAACTCAGATGTCACCTGAGATGTAAGGGACTCCCAGACTCATCGGTCAGAATTGCTCCCTGT... |
Task1_train_46110 | A sequence alteration has been identified on Chromosome 18. Is it disease-inducing or harmless? | Benign | GAACAGCTCACGATATAATGAGAGGGATTTCATAAGGTACCATTATGCATGCTGATACTTCTGATGCACTGGCTCATTTTACTTCTTCACGCTGAAGATGCTTCTGGAAAGCAGATGAGCAAGACCTGGCAATGTAGATGGCAACTTAGCCTTGACGTTGGAGGTGCAGAAAGTGCTGCCCCCCACCCGCCAGACCAACCTGCCTGCCCGAGGTATCTGCTTGGGGGATGAGGGTGTCAACTGATAAGGTTTTGATGAACAGACTCTACTTCCCTAAGTTGTAAGGTCATGAAAAACACGAAGGGAGATTCTTGGTTACA... | GAACAGCTCACGATATAATGAGAGGGATTTCATAAGGTACCATTATGCATGCTGATACTTCTGATGCACTGGCTCATTTTACTTCTTCACGCTGAAGATGCTTCTGGAAAGCAGATGAGCAAGACCTGGCAATGTAGATGGCAACTTAGCCTTGACGTTGGAGGTGCAGAAAGTGCTGCCCCCCACCCGCCAGACCAACCTGCCTGCCCGAGGTATCTGCTTGGGGGATGAGGGTGTCAACTGATAAGGTTTTGATGAACAGACTCTACTTCCCTAAGTTGTAAGGTCATGAAAAACACGAAGGGAGATTCTTGGTTACA... |
Task1_train_46111 | Chromosome 18 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTTTAAAATGTTTATTTCAAGCTGTGAACCTGTGTTTTGATGGGGAAAGTGAGAAAAGAACTTGGTGTTCAGTGTTTCAGGTTATTGCTACCTATCACTCTTTTACAGACAACAGGACAAGATATGTACTTTAAAAGACAATACTTCCACCAAGAGATGAGTGGATAAAATATGCTATATAAGTACAGTGGAATAGTCAGTCATTAAAAGGAATAAATCCTGACTCATGTTGCAATATAAATGAACCCTGAAAACATTATGCTAAATGAAATAAGCCAGACACAAAAAGACAAATATTGTATGATTCCACTTACATGTGG... | TTTTAAAATGTTTATTTCAAGCTGTGAACCTGTGTTTTGATGGGGAAAGTGAGAAAAGAACTTGGTGTTCAGTGTTTCAGGTTATTGCTACCTATCACTCTTTTACAGACAACAGGACAAGATATGTACTTTAAAAGACAATACTTCCACCAAGAGATGAGTGGATAAAATATGCTATATAAGTACAGTGGAATAGTCAGTCATTAAAAGGAATAAATCCTGACTCATGTTGCAATATAAATGAACCCTGAAAACATTATGCTAAATGAAATAAGCCAGACACAAAAAGACAAATATTGTATGATTCCACTTACATGTGG... |
Task1_train_46112 | A mutation located on Chromosome 18 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GACCCACTCTGACCTCCCAGAGCGAAACCCCACTGTTTAAAGGGCACAGAGGGCAAAGCCCTGGTGGCTTCCCTCCTTCCCCCCCTCCATCTCACACCCGTCTTCCTGTAAACCTTTTTGCTTGTAGAGAACCTGCCTAGAAGGTGAGCATGGCCCAAAGTATGCCCCGACCACCACAGAAAGGCATTGCACCCAGCGCAGCTCTGGGGAAAATCGGAGCCTCCACCCAATAGCCCGAAGCCCGCCCTTTCCTTTGGAATCCACTAGTCCTAGGCCTGGCCGTTGAACTTTGGTTTTAATTTGCTCGTGCCACAGGGTGA... | GACCCACTCTGACCTCCCAGAGCGAAACCCCACTGTTTAAAGGGCACAGAGGGCAAAGCCCTGGTGGCTTCCCTCCTTCCCCCCCTCCATCTCACACCCGTCTTCCTGTAAACCTTTTTGCTTGTAGAGAACCTGCCTAGAAGGTGAGCATGGCCCAAAGTATGCCCCGACCACCACAGAAAGGCATTGCACCCAGCGCAGCTCTGGGGAAAATCGGAGCCTCCACCCAATAGCCCGAAGCCCGCCCTTTCCTTTGGAATCCACTAGTCCTAGGCCTGGCCGTTGAACTTTGGTTTTAATTTGCTCGTGCCACAGGGTGA... |
Task1_train_46113 | Assess the clinical impact of this variant found on Chromosome 18. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GTAAATGTTGTGTTTTGTATTTTCTTAACATTTATTCAGATTCATAGGAGAAACATGTTCACCAACTTCTTCAACACTGAGTACTGCAAATGCATTTTCATGTTTTCACTTGGACTGAAGCATCTGATTGCTCTAAAGTTCTCAACTACTTCTTTGCTCATTATTTATTCTTACCTTGAGCCTATTAAATTTTGGTAACAGTAGTGTGTTATGGCTTCTACTCTAAATCACTTCTTTTTGCTATATACATATGTGTGTGTGTGTGTGTGTGTGTTTTGTTTTTTTTTTTAACCAAACCCTCTTTTCAGCAATAATCTCAT... | GTAAATGTTGTGTTTTGTATTTTCTTAACATTTATTCAGATTCATAGGAGAAACATGTTCACCAACTTCTTCAACACTGAGTACTGCAAATGCATTTTCATGTTTTCACTTGGACTGAAGCATCTGATTGCTCTAAAGTTCTCAACTACTTCTTTGCTCATTATTTATTCTTACCTTGAGCCTATTAAATTTTGGTAACAGTAGTGTGTTATGGCTTCTACTCTAAATCACTTCTTTTTGCTATATACATATGTGTGTGTGTGTGTGTGTGTGTTTTGTTTTTTTTTTTAACCAAACCCTCTTTTCAGCAATAATCTCAT... |
Task1_train_46114 | This mutation on Chromosome 18 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TATAAAAGTCCCAATACCAGAATCAATTTTCCATTGTATTCATTGTGACTAACAAAAAGAGTCTGAGGATGTGTTTTCACCTCTATCTGTGAGTGGGGCGGAAGTTGCTGGGTGTCACACATGGAAGTGGGGTGAGAGCATGCGCGCTGGAGCCTGTGTGGCCTCTTGGTCAGGTGCTTGTGGAGGTTTAGCTGATGCCCTTTGGCTGTTTCTGGACTAAGATCATCAACTTTCTTAAACTGAATCTGGTTTTCCTTGGGCTCTGTCGTCTGTGTTGTGGGTTTGTGGTGGTGGACACAGGATGTGACATTCTTGCTGGG... | TATAAAAGTCCCAATACCAGAATCAATTTTCCATTGTATTCATTGTGACTAACAAAAAGAGTCTGAGGATGTGTTTTCACCTCTATCTGTGAGTGGGGCGGAAGTTGCTGGGTGTCACACATGGAAGTGGGGTGAGAGCATGCGCGCTGGAGCCTGTGTGGCCTCTTGGTCAGGTGCTTGTGGAGGTTTAGCTGATGCCCTTTGGCTGTTTCTGGACTAAGATCATCAACTTTCTTAAACTGAATCTGGTTTTCCTTGGGCTCTGTCGTCTGTGTTGTGGGTTTGTGGTGGTGGACACAGGATGTGACATTCTTGCTGGG... |
Task1_train_46115 | Consider this mutation on Chromosome 18. Is this a benign change or a disease-causing variant? | Benign | GCAGGCCAGCCTCTTTTCTTCCTGTTCCTTCTGGTGTAAAGGCCTTCTGCTTTCATTTCTGAATTTCCACATGTGCCTGCACGGGAGGCTTTGACCAGATGAGGAATCCTCCCACCCTCATGCTGGGCCCCTCTGGGCTAAGTTCCAGGCTCTTCTCATCGAAGCCCTTCCAACTGGATCATTGCATCTGTGTTCAAACCTTTCCTGGCCCAGTGTCAGTTGTGTTCATTACTGTGCAAAACTGAAACTGACTTTACTTAAAGCAACATTTTTTATGAGATGTAATTCCATGTCATTGTCCTTGTCACGGTGGAATTACT... | GCAGGCCAGCCTCTTTTCTTCCTGTTCCTTCTGGTGTAAAGGCCTTCTGCTTTCATTTCTGAATTTCCACATGTGCCTGCACGGGAGGCTTTGACCAGATGAGGAATCCTCCCACCCTCATGCTGGGCCCCTCTGGGCTAAGTTCCAGGCTCTTCTCATCGAAGCCCTTCCAACTGGATCATTGCATCTGTGTTCAAACCTTTCCTGGCCCAGTGTCAGTTGTGTTCATTACTGTGCAAAACTGAAACTGACTTTACTTAAAGCAACATTTTTTATGAGATGTAATTCCATGTCATTGTCCTTGTCACGGTGGAATTACT... |
Task1_train_46116 | A mutation on Chromosome 18 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGCTAGCATTATTGCCTAGTGAACGGAAAGTCTTAATGCTAAAGTGACCATACCGAAGATTGCTCTGGTGCCACATTGAAGATGAAGAGGAACAGAGAAAGACCAGCTGGGCAGGAAGGATGGGAGGGAATGAACTGAAGAATCAACTTCAAAAAAGCCCAACCTGTAGAAATTGGTAATTGATTGGATATGGCGTATATAGGAGAAATCATGCTGGTAGGAAGTAATTGCAGAAGAGATTGAGTTTGGGTCTAGATCTCCTGAGTTTTGGAAACTGGAAGCATGCTCAAGTGGAAGGCACCGTAAGCATTCCAGAGTTT... | AGCTAGCATTATTGCCTAGTGAACGGAAAGTCTTAATGCTAAAGTGACCATACCGAAGATTGCTCTGGTGCCACATTGAAGATGAAGAGGAACAGAGAAAGACCAGCTGGGCAGGAAGGATGGGAGGGAATGAACTGAAGAATCAACTTCAAAAAAGCCCAACCTGTAGAAATTGGTAATTGATTGGATATGGCGTATATAGGAGAAATCATGCTGGTAGGAAGTAATTGCAGAAGAGATTGAGTTTGGGTCTAGATCTCCTGAGTTTTGGAAACTGGAAGCATGCTCAAGTGGAAGGCACCGTAAGCATTCCAGAGTTT... |
Task1_train_46117 | A change on Chromosome 18 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GTGTTATGAGGGTTCCAGTTTTTCCACATTCTTGCCAACGCTTGTTATCTGATTTTTTGAGTATAGCTATCTTAGTGGGTTTGAAATGGTATCTCCTTGTGGGTTTGATTTGCATTTCTTTAGTGACTACTGATGTAGAGTATCTTTTCATATGTGTATTATGTATATTTTCTATGAAGAAATGTATTTCATATTCTGTGCTCATTTTAAATTGATTTATCTTACTATTGAGAATAAAAGTTTTAAAAATATATTTTAGATGCAAGTCCCTTATCAGATATCTGATTTGCAAAAATGTGTTCCCATTCTGTGGGCTCTGT... | GTGTTATGAGGGTTCCAGTTTTTCCACATTCTTGCCAACGCTTGTTATCTGATTTTTTGAGTATAGCTATCTTAGTGGGTTTGAAATGGTATCTCCTTGTGGGTTTGATTTGCATTTCTTTAGTGACTACTGATGTAGAGTATCTTTTCATATGTGTATTATGTATATTTTCTATGAAGAAATGTATTTCATATTCTGTGCTCATTTTAAATTGATTTATCTTACTATTGAGAATAAAAGTTTTAAAAATATATTTTAGATGCAAGTCCCTTATCAGATATCTGATTTGCAAAAATGTGTTCCCATTCTGTGGGCTCTGT... |
Task1_train_46118 | An alteration has been detected on Chromosome 18. Is it pathogenic, and if so, what disease is involved? | Benign | TAGGACTTGGGCTTCTGTTAGAGGTTAAGGAGGGGAAGGCCTCACTTCTAGACTTGCATCACAGCAGTTTTGTTTTAATATATTTTACAGAGTAGGAGCTCATTGAAATGTTTTTTGAAAGGAGAGCTTCTCTTTTTGTTTTTTTTTTAAAAGGGTAGTAAATTGAAGTATGCTGGTACAGAGAATTGAAATATGGGAGTTTTTCTGCAAGCTTGTTGAGAAATCACTTTTTCTACCAAAGATACCATAGTATTTCTTCTGGAGTCAACAATAGGGTGACATGGTGTTCCTAAAATCCTACTTCATACTTTTTGATAAAA... | TAGGACTTGGGCTTCTGTTAGAGGTTAAGGAGGGGAAGGCCTCACTTCTAGACTTGCATCACAGCAGTTTTGTTTTAATATATTTTACAGAGTAGGAGCTCATTGAAATGTTTTTTGAAAGGAGAGCTTCTCTTTTTGTTTTTTTTTTAAAAGGGTAGTAAATTGAAGTATGCTGGTACAGAGAATTGAAATATGGGAGTTTTTCTGCAAGCTTGTTGAGAAATCACTTTTTCTACCAAAGATACCATAGTATTTCTTCTGGAGTCAACAATAGGGTGACATGGTGTTCCTAAAATCCTACTTCATACTTTTTGATAAAA... |
Task1_train_46119 | This alteration occurs on Chromosome 18. Is it associated with a disease or is it a benign variant? | Benign | TCCTAAAAAATCACGTACAATGGCAACAAAAAATGTTCACTCAAAACCAAGAACTTCTAAATCAATAGCAAAGAATAGTGATTCAAAAGGATTACGAAATGTGGGAAGCACGTTTAAAGATTTCAGAGGAAGTATTTCTAAACAAAGTGGTAGTAGCAGTGAGCTTCTTGTTGAAATGATGCCTTCCAGAAATACTTTGTCACAGGAAGTAGAGATTGTTGAAGAACATGTTACTTCCCTTGGTCTAGCTCAGAATCCTGAAAACCAGAGTAGAAAGCTAGACACCTTAGTAACCTCAGAGGGTCTCTTAGAGAAATTGG... | TCCTAAAAAATCACGTACAATGGCAACAAAAAATGTTCACTCAAAACCAAGAACTTCTAAATCAATAGCAAAGAATAGTGATTCAAAAGGATTACGAAATGTGGGAAGCACGTTTAAAGATTTCAGAGGAAGTATTTCTAAACAAAGTGGTAGTAGCAGTGAGCTTCTTGTTGAAATGATGCCTTCCAGAAATACTTTGTCACAGGAAGTAGAGATTGTTGAAGAACATGTTACTTCCCTTGGTCTAGCTCAGAATCCTGAAAACCAGAGTAGAAAGCTAGACACCTTAGTAACCTCAGAGGGTCTCTTAGAGAAATTGG... |
Task1_train_46120 | A mutation on Chromosome 18 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AATATCTTTTTAAAGATCATCTAACTGCTGGGGAGGCTGTCTCTTTGAAGATGATTTACTTCTTCTAACTGGGTTTCATTTTTCTCTCCTAGCTTATGTTCCTGAGGAAGAATTGAAGGCAGCAGAAATAGATGAAGAGCACGTGGAGGATGACGGGCTGTCTTTGGACATTCAGGAAAGTGAGTACATGTGCAATGAAGAGACGGAGATCAAAGAGGCGCAGAGCTACCAGAACTCCCCAGTCAGCTCTGCGACTAACCAGGACGCCGGCTACGGGTCGCCCTTCAGTGAGAGCAGCGACCAGCTAGCCCATTTCAAAG... | AATATCTTTTTAAAGATCATCTAACTGCTGGGGAGGCTGTCTCTTTGAAGATGATTTACTTCTTCTAACTGGGTTTCATTTTTCTCTCCTAGCTTATGTTCCTGAGGAAGAATTGAAGGCAGCAGAAATAGATGAAGAGCACGTGGAGGATGACGGGCTGTCTTTGGACATTCAGGAAAGTGAGTACATGTGCAATGAAGAGACGGAGATCAAAGAGGCGCAGAGCTACCAGAACTCCCCAGTCAGCTCTGCGACTAACCAGGACGCCGGCTACGGGTCGCCCTTCAGTGAGAGCAGCGACCAGCTAGCCCATTTCAAAG... |
Task1_train_46121 | Consider a variant on Chromosome 18. Determine its clinical classification and disease relevance. | Benign | CAGATCCATACTGGGGACAGATTCCTGGGTGTGGGGGACCCTGGGCACAGGGACCCTGGGCAAGGGCACAAGGCCACCCGGGTGTGGAGTCCTGAGTCCCAGGGTTACCTGAGCATAGGCCTAGCTGAGTAAAGGGCCACCGGGTAAGGGGCTAATGAGCGAGCCTACTTGAGTATACGTTTACCTGGAAGCAGGAACCCCCTGAGCCTGGGATCCCAGGACCCAGGCCACCTGGGTACACTTGCTCACCTGGTGCAGGTTCAGGGGCGCCCTCCTCACCACTGTCTTCGGCAGCCTCGTCGGCCAGGCCAGAGCCCGGG... | CAGATCCATACTGGGGACAGATTCCTGGGTGTGGGGGACCCTGGGCACAGGGACCCTGGGCAAGGGCACAAGGCCACCCGGGTGTGGAGTCCTGAGTCCCAGGGTTACCTGAGCATAGGCCTAGCTGAGTAAAGGGCCACCGGGTAAGGGGCTAATGAGCGAGCCTACTTGAGTATACGTTTACCTGGAAGCAGGAACCCCCTGAGCCTGGGATCCCAGGACCCAGGCCACCTGGGTACACTTGCTCACCTGGTGCAGGTTCAGGGGCGCCCTCCTCACCACTGTCTTCGGCAGCCTCGTCGGCCAGGCCAGAGCCCGGG... |
Task1_train_46122 | This sequence change occurs on Chromosome 18. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GCACTTAGGTACCAAACACAGTACCAAACATAGTACTGCACACAGGTACCAAACAGTACTGCCCACTGGTACCGCATAAAGTACCAAACATAGTACTGCACACAGGTACCAAACAGTACTGCCCACTGGTACCTCATATAGTACCAAACACAGTACTGCACACAGGTACCACATACAGTACCAAACAGTACTGCACACAGGCATCATGCATGCTACCAAACACAGTAATAAACAGTACTGCACACAAGTAGTACATAGAGTACCAAACACAGTACTGCGCTCAGGTACTGCATACAGTACTAAACACAGTACTACACACA... | GCACTTAGGTACCAAACACAGTACCAAACATAGTACTGCACACAGGTACCAAACAGTACTGCCCACTGGTACCGCATAAAGTACCAAACATAGTACTGCACACAGGTACCAAACAGTACTGCCCACTGGTACCTCATATAGTACCAAACACAGTACTGCACACAGGTACCACATACAGTACCAAACAGTACTGCACACAGGCATCATGCATGCTACCAAACACAGTAATAAACAGTACTGCACACAAGTAGTACATAGAGTACCAAACACAGTACTGCGCTCAGGTACTGCATACAGTACTAAACACAGTACTACACACA... |
Task1_train_46123 | The following genetic variant occurs on Chromosome 18. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TCTTTTTCAGGAAGGTGTCTTTATTTCTTTTAATACATTAGTGAGAAATTTGAGGAACTGTTTTTAGGTACAGCTTTGCTTTTAAATGAGATGCAGTGGTTTTTAGATGCTGTTGGACAGCAAAAATTAACATTGAATTTTATATAATTCAGTAACCTTCCTCCTTTTAAAATTATATTTATATCTGAATTTTAATGTTGGAAATACAGAAGAGTTACAATATTTTAGGAAAGCTATTTGGTTGATCCAATTAACTTTCTCGAGTACACTTAATATAAGAAGTATTGTGCTAGGTCCTATCAAAACTACATAGTGCATGG... | TCTTTTTCAGGAAGGTGTCTTTATTTCTTTTAATACATTAGTGAGAAATTTGAGGAACTGTTTTTAGGTACAGCTTTGCTTTTAAATGAGATGCAGTGGTTTTTAGATGCTGTTGGACAGCAAAAATTAACATTGAATTTTATATAATTCAGTAACCTTCCTCCTTTTAAAATTATATTTATATCTGAATTTTAATGTTGGAAATACAGAAGAGTTACAATATTTTAGGAAAGCTATTTGGTTGATCCAATTAACTTTCTCGAGTACACTTAATATAAGAAGTATTGTGCTAGGTCCTATCAAAACTACATAGTGCATGG... |
Task1_train_46124 | A mutation on Chromosome 18 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TACAAAACAAAAATCTTTGGATTAATGAGGTTATTATAAATCGAGCAACTCTATTTAGCCTCTTTTTCTGTTCATCAGCAGAATCATTTTCCCAGTGTCAGCATCTGGGGTCACTGAGACGGGCCAGCCAGTCCCACTTCCACATGCGGGTTCCTGGGGCTTCTCGCACTGGTTGTGTTGGAGGAAGTTAAACATTTTCTCGGACGTGGTGTTGCTCCCTCCCTGGGAGGGAGACCAGTCACGTCGCCTGGGAACCCTCTGGGAGAAGAGGATCTGGCCTTGCAGGGCTGGGTCCCCGGCACAGAAGCAAGAGACCAGAC... | TACAAAACAAAAATCTTTGGATTAATGAGGTTATTATAAATCGAGCAACTCTATTTAGCCTCTTTTTCTGTTCATCAGCAGAATCATTTTCCCAGTGTCAGCATCTGGGGTCACTGAGACGGGCCAGCCAGTCCCACTTCCACATGCGGGTTCCTGGGGCTTCTCGCACTGGTTGTGTTGGAGGAAGTTAAACATTTTCTCGGACGTGGTGTTGCTCCCTCCCTGGGAGGGAGACCAGTCACGTCGCCTGGGAACCCTCTGGGAGAAGAGGATCTGGCCTTGCAGGGCTGGGTCCCCGGCACAGAAGCAAGAGACCAGAC... |
Task1_train_46125 | Assess the clinical impact of this variant found on Chromosome 18. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACATTCCAAGGTCTTACCTTTCCCTGCGACGGGGGTGGTGTGCGAGGCGTCACCTGGAAAGACACAGAGAACCGTGGGCTGCACTGGGAGCCCTGTGCCGCCGTCCATTTCCTAACGGGCTCCTGCCTGCTGAGGGTGGCTAGCATCCATCAGCTGCCAGAAGCACCCGGGTGCCCAGCCTCCCCACTTCTGTCCTAGTTGGTGAAGAAGTATAGACCTGAGATTGAAAATATTCTAGATGATGCAGATCTCCCAGAGCACTCAGGAAGTGTTTCAGAGGATGGAAAACACCTCCCAGAGGCTCCGTAGCTGGGGAATGG... | ACATTCCAAGGTCTTACCTTTCCCTGCGACGGGGGTGGTGTGCGAGGCGTCACCTGGAAAGACACAGAGAACCGTGGGCTGCACTGGGAGCCCTGTGCCGCCGTCCATTTCCTAACGGGCTCCTGCCTGCTGAGGGTGGCTAGCATCCATCAGCTGCCAGAAGCACCCGGGTGCCCAGCCTCCCCACTTCTGTCCTAGTTGGTGAAGAAGTATAGACCTGAGATTGAAAATATTCTAGATGATGCAGATCTCCCAGAGCACTCAGGAAGTGTTTCAGAGGATGGAAAACACCTCCCAGAGGCTCCGTAGCTGGGGAATGG... |
Task1_train_46126 | This alteration on Chromosome 18 may affect genome function. Does it lead to a disease or is it benign? | Benign | AGGAGGATTAAAAGTCAAACAAAATAACTTACAATTAACATTTACAAATTCAGGCAGAAATAGAAACATCACAAGAAAGTTTGGTCTCTTGTTTTTTTTTTTTCTTTTTTCCCCAGCGTTTCGTGGCTACCTTTAATCAGCGCACACAGCTAGGACCACCACTGACCAAACTCAAACCCGACGTTTTAAATCATGGAGGAGCCATGAGCTACCAGGTGTAAAACAAGCGACGTGTCTTACACTTTCTTATCTTTGGGCAGAACTGTGATACTTCTGGAGGATTTTCAAAGAGGATTTGAACAAAATAGCTTTGTTTAACC... | AGGAGGATTAAAAGTCAAACAAAATAACTTACAATTAACATTTACAAATTCAGGCAGAAATAGAAACATCACAAGAAAGTTTGGTCTCTTGTTTTTTTTTTTTCTTTTTTCCCCAGCGTTTCGTGGCTACCTTTAATCAGCGCACACAGCTAGGACCACCACTGACCAAACTCAAACCCGACGTTTTAAATCATGGAGGAGCCATGAGCTACCAGGTGTAAAACAAGCGACGTGTCTTACACTTTCTTATCTTTGGGCAGAACTGTGATACTTCTGGAGGATTTTCAAAGAGGATTTGAACAAAATAGCTTTGTTTAACC... |
Task1_train_46127 | A change on Chromosome 18 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AGGATTTGAACAAAATAGCTTTGTTTAACCCGGAGTTAGTAGAAGTGGTTGTTTCAGAACAGTTAACTCCCTGGGAGTTACTCCAGCATTTACAGCAATTTTTAACTGTGTTCTTTTCCCTCAGATTTCTGTTTTTCCCACAAAAAAAAAAAAAAAACAAAACCTCAAAAAACAAAACACACACACGCGCGCACGCACGCGCACACACACACACACACACACACACACACACACACCCCCTCTGCCGCGGTACCCTTCCCCTGGCCTTCCTCCACTGAAGGGCGGCTGGGTTCCAGGCTCTCAGCCGTGACCACAGCCCC... | AGGATTTGAACAAAATAGCTTTGTTTAACCCGGAGTTAGTAGAAGTGGTTGTTTCAGAACAGTTAACTCCCTGGGAGTTACTCCAGCATTTACAGCAATTTTTAACTGTGTTCTTTTCCCTCAGATTTCTGTTTTTCCCACAAAAAAAAAAAAAAAACAAAACCTCAAAAAACAAAACACACACACGCGCGCACGCACGCGCACACACACACACACACACACACACACACACACACCCCCTCTGCCGCGGTACCCTTCCCCTGGCCTTCCTCCACTGAAGGGCGGCTGGGTTCCAGGCTCTCAGCCGTGACCACAGCCCC... |
Task1_train_46128 | Chromosome 18 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AAACACACACACGCGCGCACGCACGCGCACACACACACACACACACACACACACACACACACCCCCTCTGCCGCGGTACCCTTCCCCTGGCCTTCCTCCACTGAAGGGCGGCTGGGTTCCAGGCTCTCAGCCGTGACCACAGCCCCGGCCCCAACCGCTAAGGAGGTGCTCATCACTGGAGGTGGCCGCCAGGGAGCTCAGTGCGGGACCTGCTCAATCCATACGGTCCCCTGACTTGAGGGTGACCGTCCTTAAACTGTCCCCCGGAGCTTCGCCAGATAAAATGTCCAAAACACACACTGGAGTTCCCTGACGTTTCC... | AAACACACACACGCGCGCACGCACGCGCACACACACACACACACACACACACACACACACACCCCCTCTGCCGCGGTACCCTTCCCCTGGCCTTCCTCCACTGAAGGGCGGCTGGGTTCCAGGCTCTCAGCCGTGACCACAGCCCCGGCCCCAACCGCTAAGGAGGTGCTCATCACTGGAGGTGGCCGCCAGGGAGCTCAGTGCGGGACCTGCTCAATCCATACGGTCCCCTGACTTGAGGGTGACCGTCCTTAAACTGTCCCCCGGAGCTTCGCCAGATAAAATGTCCAAAACACACACTGGAGTTCCCTGACGTTTCC... |
Task1_train_46129 | Here’s a variant located on Chromosome 18. What is the predicted biological effect — harmless or disease-causing? | Benign | TGCCCCCATGATTCAATTACCTCTCACTGGGTCCCTCCCATTATGTGTGGAGATTATGGGAATGACAATTCAAGATGAGAGCTGGGTGGGGTCACAGCCAAACCATATCAGTGGGATTGCTGCCAGCTCACGCTCTGATGCTTCCCCTCCCAATGTCCAAGCATGCTCTAAAATATTACAGCCTGGACTATGTCTGAGAGAAAGAAGTTACTTGAGTCCTAACCTTTGGCCAAGAGGCTGAAAGGTGCACCTCTTTGCGCTTAATGTTCCTTTTTTCCTATGAGAAGTAAACTTGCTGGTGAAGTGAACAGAAAGCTGAA... | TGCCCCCATGATTCAATTACCTCTCACTGGGTCCCTCCCATTATGTGTGGAGATTATGGGAATGACAATTCAAGATGAGAGCTGGGTGGGGTCACAGCCAAACCATATCAGTGGGATTGCTGCCAGCTCACGCTCTGATGCTTCCCCTCCCAATGTCCAAGCATGCTCTAAAATATTACAGCCTGGACTATGTCTGAGAGAAAGAAGTTACTTGAGTCCTAACCTTTGGCCAAGAGGCTGAAAGGTGCACCTCTTTGCGCTTAATGTTCCTTTTTTCCTATGAGAAGTAAACTTGCTGGTGAAGTGAACAGAAAGCTGAA... |
Task1_train_46130 | This sequence variant lies on Chromosome 18. Is it clinically significant, and what condition might it cause if any? | Benign | GTAAGTAACCTTACCTTAAATCTGGAATGTCTCCGCGCTGCGTAAAGATGAGAAATCCGCGTGGTGGGGACCACACCGGCCACAGCGCGGCCCCCTGTCAGGTGTTGATGTGAGTTTGAAAGGTTACAGATTAGTTTAGCAATGTTAAGTGAACTGGCAAAGGCATCTCTAATTTTGCTGGAAATGAGGAAGCCGGATGGTAAAGGGGAATCCTAATGAGCCCATCGAAAGCCGGCTTTGTACTCAACAGACAGGGTAGCCGCAGATTGTATGAAAATATTGGAAATCAATGGCTTCTATGGAATTTCATTAAGAAGCAG... | GTAAGTAACCTTACCTTAAATCTGGAATGTCTCCGCGCTGCGTAAAGATGAGAAATCCGCGTGGTGGGGACCACACCGGCCACAGCGCGGCCCCCTGTCAGGTGTTGATGTGAGTTTGAAAGGTTACAGATTAGTTTAGCAATGTTAAGTGAACTGGCAAAGGCATCTCTAATTTTGCTGGAAATGAGGAAGCCGGATGGTAAAGGGGAATCCTAATGAGCCCATCGAAAGCCGGCTTTGTACTCAACAGACAGGGTAGCCGCAGATTGTATGAAAATATTGGAAATCAATGGCTTCTATGGAATTTCATTAAGAAGCAG... |
Task1_train_46131 | Consider this mutation on Chromosome 18. Is this a benign change or a disease-causing variant? | Benign | GAAATGAGGAAGCCGGATGGTAAAGGGGAATCCTAATGAGCCCATCGAAAGCCGGCTTTGTACTCAACAGACAGGGTAGCCGCAGATTGTATGAAAATATTGGAAATCAATGGCTTCTATGGAATTTCATTAAGAAGCAGGATCCACAATTGATAGGGCCTCATAATTTGATGGATTGGGCTAAGAAAATGATTAGCTAGCTAGAAAGAGTCATAGAATACGCACGCTGGGACGTCAGAAATGTCGAAGTGGGGTAATTTGTACAAAATAAAAAATATTGATTTTACTCGTGCAAAATTTTGAGACGGAGGGCGGGCGCC... | GAAATGAGGAAGCCGGATGGTAAAGGGGAATCCTAATGAGCCCATCGAAAGCCGGCTTTGTACTCAACAGACAGGGTAGCCGCAGATTGTATGAAAATATTGGAAATCAATGGCTTCTATGGAATTTCATTAAGAAGCAGGATCCACAATTGATAGGGCCTCATAATTTGATGGATTGGGCTAAGAAAATGATTAGCTAGCTAGAAAGAGTCATAGAATACGCACGCTGGGACGTCAGAAATGTCGAAGTGGGGTAATTTGTACAAAATAAAAAATATTGATTTTACTCGTGCAAAATTTTGAGACGGAGGGCGGGCGCC... |
Task1_train_46132 | The following genetic variant occurs on Chromosome 18. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGTGAGGGTCAGGAGATGGTGTTGTTGCTGTCAGTTATTGAGTGAGGGTGAGAAGACGGTGTTGTCCCTGTCAGTAGTTGAGGGTCAGGAGAAGGTGTTGTCATTGTCAGTTGTTGAGTGAGGGTGAAGAAATGTTGTTGTCACTTTCAGTTGCTGAGTGAGGGTCAGAAGATGTTGTCACTGTCAGGTGTTGACTGAGGGTCAGATGGTGTTGTCACTGTCAGTAGTTGAGTGAGGGTGAGAAGATGCTGTTGTCACTGTCAGTAGTTGAGTGAGGGTGAGGAGACGGCGTTATCACTGTCAGGTACTGAGTGAGGGTG... | AGTGAGGGTCAGGAGATGGTGTTGTTGCTGTCAGTTATTGAGTGAGGGTGAGAAGACGGTGTTGTCCCTGTCAGTAGTTGAGGGTCAGGAGAAGGTGTTGTCATTGTCAGTTGTTGAGTGAGGGTGAAGAAATGTTGTTGTCACTTTCAGTTGCTGAGTGAGGGTCAGAAGATGTTGTCACTGTCAGGTGTTGACTGAGGGTCAGATGGTGTTGTCACTGTCAGTAGTTGAGTGAGGGTGAGAAGATGCTGTTGTCACTGTCAGTAGTTGAGTGAGGGTGAGGAGACGGCGTTATCACTGTCAGGTACTGAGTGAGGGTG... |
Task1_train_46133 | This variant is present on Chromosome 18. Is the change likely to result in a pathogenic outcome? | Benign | TCTTTCTCAGTGAGAACAGACTGAGTCTGCAGAAATTGAGCCATGGCCTGTTATCTTCCTCTCTACCCCAGCTCCATGTGCAGGAAGCTCTACTCTAAGCCCATGCAGCCAAAAAGTCAGGGGCTCTGTCTTCCTGCACTTCCTAGGCTATGGCTGCAGCCCCACCCAGGAGGGGCTGGCCATGGTTCTTATTTTCCCCAGACTCATGTTGCCGAAGCCCAATTCCTGACAGGCTTGGCCTAGGGCACTAACATAAAGTAACTTAAAGTGGACTATATTCTAGACTCTACCTGGGCTCCTGAGCATTGTATCCCAGTGAG... | TCTTTCTCAGTGAGAACAGACTGAGTCTGCAGAAATTGAGCCATGGCCTGTTATCTTCCTCTCTACCCCAGCTCCATGTGCAGGAAGCTCTACTCTAAGCCCATGCAGCCAAAAAGTCAGGGGCTCTGTCTTCCTGCACTTCCTAGGCTATGGCTGCAGCCCCACCCAGGAGGGGCTGGCCATGGTTCTTATTTTCCCCAGACTCATGTTGCCGAAGCCCAATTCCTGACAGGCTTGGCCTAGGGCACTAACATAAAGTAACTTAAAGTGGACTATATTCTAGACTCTACCTGGGCTCCTGAGCATTGTATCCCAGTGAG... |
Task1_train_46134 | This mutation on Chromosome 18 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TCTACCCCAGCTCCATGTGCAGGAAGCTCTACTCTAAGCCCATGCAGCCAAAAAGTCAGGGGCTCTGTCTTCCTGCACTTCCTAGGCTATGGCTGCAGCCCCACCCAGGAGGGGCTGGCCATGGTTCTTATTTTCCCCAGACTCATGTTGCCGAAGCCCAATTCCTGACAGGCTTGGCCTAGGGCACTAACATAAAGTAACTTAAAGTGGACTATATTCTAGACTCTACCTGGGCTCCTGAGCATTGTATCCCAGTGAGTTCCAGCCCCAGCAGCTTGTAAGGCAGAGGTGACAGTGCTGGAGGGGCTACACCACAACCC... | TCTACCCCAGCTCCATGTGCAGGAAGCTCTACTCTAAGCCCATGCAGCCAAAAAGTCAGGGGCTCTGTCTTCCTGCACTTCCTAGGCTATGGCTGCAGCCCCACCCAGGAGGGGCTGGCCATGGTTCTTATTTTCCCCAGACTCATGTTGCCGAAGCCCAATTCCTGACAGGCTTGGCCTAGGGCACTAACATAAAGTAACTTAAAGTGGACTATATTCTAGACTCTACCTGGGCTCCTGAGCATTGTATCCCAGTGAGTTCCAGCCCCAGCAGCTTGTAAGGCAGAGGTGACAGTGCTGGAGGGGCTACACCACAACCC... |
Task1_train_46135 | Here is a genetic alteration on Chromosome 18. Based on the data, is it a benign variant or a cause of disease? | Benign | TGTGTCACTGGTATGAGCAGTTTAACTTTGAGAGTGTTACCTCCACACAGGTTTGCTCCTGCACCACCCCTCAGCCTTGTCCCAGAGAGCCTGTTTCTTCACCCATCACCAGCTAAAACTGTTGCACTTTTACCTCTAATGGGAAAGTAGTGTTTTTTATTTTGACACCTTCCCTGACTGAACACGGTTAGCACCGTTTCATGAGCTCATTGCAGGCATTTCCATGTCTTGCTTTAACACGCACATCAGGCCCCGTGACTCCTGCAGGGCTCCCCCAACTCTGGAAGGCGAATGCAGGGTGAGGCTTGTGAGCTTTGGGA... | TGTGTCACTGGTATGAGCAGTTTAACTTTGAGAGTGTTACCTCCACACAGGTTTGCTCCTGCACCACCCCTCAGCCTTGTCCCAGAGAGCCTGTTTCTTCACCCATCACCAGCTAAAACTGTTGCACTTTTACCTCTAATGGGAAAGTAGTGTTTTTTATTTTGACACCTTCCCTGACTGAACACGGTTAGCACCGTTTCATGAGCTCATTGCAGGCATTTCCATGTCTTGCTTTAACACGCACATCAGGCCCCGTGACTCCTGCAGGGCTCCCCCAACTCTGGAAGGCGAATGCAGGGTGAGGCTTGTGAGCTTTGGGA... |
Task1_train_46136 | Mutation context: Chromosome 18. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGGTAACCAGTCGGGGAGAGGCACATTTGGAGCTGAATGCATTTCGAAGGAAGCATGATTGTGCACTAGTCATATCTGGGGACTCTCTGGAGGTAAGGCTGGACCCTGAGTGAGTACATGTCTGTCTGTGTCTCTGAGGCAAGGCTGGTCCCTGGCTGAGTGTCTGTTTGTCTCTCAGGCAAGGCTGGACCCTGAGTGAGTACATGTCTGTCTGTCTGTCTGTCTGTGTCTCTGAGGCAAGGCTGGACCCTGGCCCAGTGTGTGTCTGTCTGTCCATTCCAGTGCATCAAGGCCTTCTTGAGTCAAGTGCTTTTGCCCAT... | AGGTAACCAGTCGGGGAGAGGCACATTTGGAGCTGAATGCATTTCGAAGGAAGCATGATTGTGCACTAGTCATATCTGGGGACTCTCTGGAGGTAAGGCTGGACCCTGAGTGAGTACATGTCTGTCTGTGTCTCTGAGGCAAGGCTGGTCCCTGGCTGAGTGTCTGTTTGTCTCTCAGGCAAGGCTGGACCCTGAGTGAGTACATGTCTGTCTGTCTGTCTGTCTGTGTCTCTGAGGCAAGGCTGGACCCTGGCCCAGTGTGTGTCTGTCTGTCCATTCCAGTGCATCAAGGCCTTCTTGAGTCAAGTGCTTTTGCCCAT... |
Task1_train_46137 | Consider this mutation on Chromosome 18. Is this a benign change or a disease-causing variant? | Benign | TATCATACATACAATTAGAATTGTAAAAGATATTCTAACCATTTGTGGAACTTTTGTGAAGTGAGCTCACCAAATGTCAGAGAAGATCTCACTGTGTAATTTCTGTAGAAAGGCTCCCCCGGACAGCGTCACTGCACCTGCTGCAGAAATAGCATTCCAAAGCTGGGGAACCCATGGGCTGCATGTTTCCTGTGTATTTCCAAGTTTGTCAGTAGTTGTGGATTTCAGAATTATCCCTGAAAAGTGATAACATGTGTCTGTCCCTAGGGTCCATAGACTATTTTTGCAGTGATGTCACCAAGAAAAAAATCCACCCCAGA... | TATCATACATACAATTAGAATTGTAAAAGATATTCTAACCATTTGTGGAACTTTTGTGAAGTGAGCTCACCAAATGTCAGAGAAGATCTCACTGTGTAATTTCTGTAGAAAGGCTCCCCCGGACAGCGTCACTGCACCTGCTGCAGAAATAGCATTCCAAAGCTGGGGAACCCATGGGCTGCATGTTTCCTGTGTATTTCCAAGTTTGTCAGTAGTTGTGGATTTCAGAATTATCCCTGAAAAGTGATAACATGTGTCTGTCCCTAGGGTCCATAGACTATTTTTGCAGTGATGTCACCAAGAAAAAAATCCACCCCAGA... |
Task1_train_46138 | A variant on Chromosome 18 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AATTACTGATTTCCCTAATAATGATTTTAAAAAATATTTTATTGAGTGTAATTAACACATAATGATTCTTAGGACTAGCTGTGTACCAGAATCTTCTGTTTTGTTCTAAAAGATGGATTCGTAGGATATGAGCCAGTATCAGAATCTCCATGAGGGGGATTTCACAGTCTGTGTTTTCATCCAATCCTTGAGGAGTTTTCTTTGTAGCTGGTGATTAGGGCACCTTGACAGTGATAAGCCTGTTAAAATCTGTTTACATATGTAGGTCCTTAGATCTAAAACACATCCACCATCCATCATCATCCATCCATCATCAAACC... | AATTACTGATTTCCCTAATAATGATTTTAAAAAATATTTTATTGAGTGTAATTAACACATAATGATTCTTAGGACTAGCTGTGTACCAGAATCTTCTGTTTTGTTCTAAAAGATGGATTCGTAGGATATGAGCCAGTATCAGAATCTCCATGAGGGGGATTTCACAGTCTGTGTTTTCATCCAATCCTTGAGGAGTTTTCTTTGTAGCTGGTGATTAGGGCACCTTGACAGTGATAAGCCTGTTAAAATCTGTTTACATATGTAGGTCCTTAGATCTAAAACACATCCACCATCCATCATCATCCATCCATCATCAAACC... |
Task1_train_46139 | A variant was discovered on Chromosome 18. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GGGAGCCCGTGTGATGGGGAAGCTGTGTGTGGGGTGCCCCATCCAGGTGGAGCCCCGGGGGTGGGTGCAGAGGTCCTGGGGCTGCAGGAGTGGGGAGGAGTCCCGCACGGTGAGGGAGAGCGTGTAGGAGATGGCGGCGGGGGGCCACGTTGGGGATTTTAATAAGTGATTCAAAGCCTGTAAGTCAAAAAGGGAAAGCTTTCTCTCCACGTTGACTTTTCAAGCACTGGGAGGAATGTACGCACCTGGGAATTCATTCCAAATCCCTGAGTTTGCCTCGAGAGCTGTAATCCAAGTTTCCCGCAGACAGGGCACAGTCA... | GGGAGCCCGTGTGATGGGGAAGCTGTGTGTGGGGTGCCCCATCCAGGTGGAGCCCCGGGGGTGGGTGCAGAGGTCCTGGGGCTGCAGGAGTGGGGAGGAGTCCCGCACGGTGAGGGAGAGCGTGTAGGAGATGGCGGCGGGGGGCCACGTTGGGGATTTTAATAAGTGATTCAAAGCCTGTAAGTCAAAAAGGGAAAGCTTTCTCTCCACGTTGACTTTTCAAGCACTGGGAGGAATGTACGCACCTGGGAATTCATTCCAAATCCCTGAGTTTGCCTCGAGAGCTGTAATCCAAGTTTCCCGCAGACAGGGCACAGTCA... |
Task1_train_46140 | Here is a genetic alteration on Chromosome 18. Based on the data, is it a benign variant or a cause of disease? | Benign | GTCTGGCCCACAAGGTCCCGCCTCCGCCCAGCCAGCCTGGCCCACGGAATCTCCGCCTCTGCCCAGCCAGCCTGGCCCATGTGGTCCCCGCCTCCACCCATCCAGCCTGTCCCACAGGGTCCCCGCCTCCACCCCAGCCTGTCCCGTGGGGTCCCCGCCTCCCCACTCCTCGCTGCTGCCTGTGAGTGCCTCCCGGCCCGTTACTATTTCAGTCTCGGCTTCCATGAGACGTTTCCTTCTTGTCTCTTCCCTCAGCTGCTTCTGCTCTAAAGACCCACCTGGTGTAGCTGCTGACTCCATCGCAGCTGCCCTGAGCACTG... | GTCTGGCCCACAAGGTCCCGCCTCCGCCCAGCCAGCCTGGCCCACGGAATCTCCGCCTCTGCCCAGCCAGCCTGGCCCATGTGGTCCCCGCCTCCACCCATCCAGCCTGTCCCACAGGGTCCCCGCCTCCACCCCAGCCTGTCCCGTGGGGTCCCCGCCTCCCCACTCCTCGCTGCTGCCTGTGAGTGCCTCCCGGCCCGTTACTATTTCAGTCTCGGCTTCCATGAGACGTTTCCTTCTTGTCTCTTCCCTCAGCTGCTTCTGCTCTAAAGACCCACCTGGTGTAGCTGCTGACTCCATCGCAGCTGCCCTGAGCACTG... |
Task1_train_46141 | Assess the clinical impact of this variant found on Chromosome 18. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGGGACTGTCATCCTCTCTGCCTCGTCTCTGTTAGACAGCACAATTCGATGTCAGCCCGCCACCTGACGTTGTGTATCTGTCATCCTCTCTGCCTCATCTCTGTCAGACGGCACTGATTCGATGTCAGCCCGCCACCTGACGTTGTGTATCTGTTTGCTTAACCAACCCTGGCATATGTGATCATTCTAGTCCCTTGACCTCCAAATTTTCATTCCTATGCGAAGACCTGGCATCGAGATTTGTGGTTGGAGAGGCAGGAGGCAGGCGTGTGTCCCCACAGTAGCCAGCTGTGAAGGATTTGGCCCTTTTGCCTCTGAGT... | GGGGACTGTCATCCTCTCTGCCTCGTCTCTGTTAGACAGCACAATTCGATGTCAGCCCGCCACCTGACGTTGTGTATCTGTCATCCTCTCTGCCTCATCTCTGTCAGACGGCACTGATTCGATGTCAGCCCGCCACCTGACGTTGTGTATCTGTTTGCTTAACCAACCCTGGCATATGTGATCATTCTAGTCCCTTGACCTCCAAATTTTCATTCCTATGCGAAGACCTGGCATCGAGATTTGTGGTTGGAGAGGCAGGAGGCAGGCGTGTGTCCCCACAGTAGCCAGCTGTGAAGGATTTGGCCCTTTTGCCTCTGAGT... |
Task1_train_46142 | This is a variant located on Chromosome 18. Is this mutation a likely cause of disease or not? | Benign | AGTGATGAAAGATGGAATGCTTTCTCACTAAAATGAAGAATAAGATAGGTGCATCCACTCTCACCGCCTATAACCAGGATAAGCAATAAAAAGAAATAAAAGCAACTACATTGGTAAGGAAGAATTAAAACTATATTTGCAAATGACAGAATCATATATAGAGAATCTACTAAACAACTCTTAGAACAAACCAGTTCAGCAGAATTGCATGATACAAGATCAACATGCAATGATCAATTACATTTCTATAAAGTAGCAATGAAGCAGCAGAACTGAAATTAAGAAAACAATTCCATTTACAATAGCATCAAAAAGGATAA... | AGTGATGAAAGATGGAATGCTTTCTCACTAAAATGAAGAATAAGATAGGTGCATCCACTCTCACCGCCTATAACCAGGATAAGCAATAAAAAGAAATAAAAGCAACTACATTGGTAAGGAAGAATTAAAACTATATTTGCAAATGACAGAATCATATATAGAGAATCTACTAAACAACTCTTAGAACAAACCAGTTCAGCAGAATTGCATGATACAAGATCAACATGCAATGATCAATTACATTTCTATAAAGTAGCAATGAAGCAGCAGAACTGAAATTAAGAAAACAATTCCATTTACAATAGCATCAAAAAGGATAA... |
Task1_train_46143 | This mutation is located on Chromosome 18. Is it associated with a disease or is it a benign polymorphism? | Benign | GCACCCAGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCTAGTTTGCCAGGATGGTCTCGATCTCCTGACCTCCTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCTTATCCCATGATATTTAAAATGTCATACGTGGGCCAGGTGTGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGTCAAGGTGGGCAGATCACCTGAGGCCATGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACTCCGTCTCTACTGAAAGTATAAACATTAGCTGGGCCT... | GCACCCAGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCTAGTTTGCCAGGATGGTCTCGATCTCCTGACCTCCTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCTTATCCCATGATATTTAAAATGTCATACGTGGGCCAGGTGTGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGTCAAGGTGGGCAGATCACCTGAGGCCATGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACTCCGTCTCTACTGAAAGTATAAACATTAGCTGGGCCT... |
Task1_train_46144 | A variant affecting Chromosome 18 has been observed. Determine if it's benign or associated with disease. | Benign | ACCTTGTCTTGTTGGGAGGCTTTTGTCCCCCAAGGCACACAAATTCTGTGGCAAAACTGAAGCATTTTGCAAAACTACCTTAGAAACCAGTTAATGGTTAGTTAGTTAATTCAACTAACGCTTAACTGGTTTCTTCATAAATTTGACTAACAAGTCTAAAATGTAGTTTTTAAAAAGCCTCACTTCGTTATCAGAGAAAATGTGTTATGTTAAAGTAACAGTAAGGTATTTGAAAGCACAGGCTACTGAACAGGTCCTAGTATTTGGGAAGAGTCGGTGGAAGGAATTGTGCAAAGTCTGATCAAAAGCTCTGCAGTCAA... | ACCTTGTCTTGTTGGGAGGCTTTTGTCCCCCAAGGCACACAAATTCTGTGGCAAAACTGAAGCATTTTGCAAAACTACCTTAGAAACCAGTTAATGGTTAGTTAGTTAATTCAACTAACGCTTAACTGGTTTCTTCATAAATTTGACTAACAAGTCTAAAATGTAGTTTTTAAAAAGCCTCACTTCGTTATCAGAGAAAATGTGTTATGTTAAAGTAACAGTAAGGTATTTGAAAGCACAGGCTACTGAACAGGTCCTAGTATTTGGGAAGAGTCGGTGGAAGGAATTGTGCAAAGTCTGATCAAAAGCTCTGCAGTCAA... |
Task1_train_46145 | This sequence change occurs on Chromosome 18. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ATGGTTAGTTAGTTAATTCAACTAACGCTTAACTGGTTTCTTCATAAATTTGACTAACAAGTCTAAAATGTAGTTTTTAAAAAGCCTCACTTCGTTATCAGAGAAAATGTGTTATGTTAAAGTAACAGTAAGGTATTTGAAAGCACAGGCTACTGAACAGGTCCTAGTATTTGGGAAGAGTCGGTGGAAGGAATTGTGCAAAGTCTGATCAAAAGCTCTGCAGTCAACAATGCTGGTGTTACGTGGAGCCCGGCTGTAAGTATGGTGGTGGGGATGTGGCTAACGGGTTTACCCTCTGTGTTCCTCTGTAGCTTGATCAG... | ATGGTTAGTTAGTTAATTCAACTAACGCTTAACTGGTTTCTTCATAAATTTGACTAACAAGTCTAAAATGTAGTTTTTAAAAAGCCTCACTTCGTTATCAGAGAAAATGTGTTATGTTAAAGTAACAGTAAGGTATTTGAAAGCACAGGCTACTGAACAGGTCCTAGTATTTGGGAAGAGTCGGTGGAAGGAATTGTGCAAAGTCTGATCAAAAGCTCTGCAGTCAACAATGCTGGTGTTACGTGGAGCCCGGCTGTAAGTATGGTGGTGGGGATGTGGCTAACGGGTTTACCCTCTGTGTTCCTCTGTAGCTTGATCAG... |
Task1_train_46146 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | CACACCACGCTCTCAGCTCAAGTGCCTCTATTCAGAAGCCTCTACTAGGAACGTGGGGCAGGGGCCTCCCCGAGGGAGGCTGGGTCCTTCAACCTGCAGCAGCCTTTTGTTTAGGCCCCTCTCAGCAGTGAAATGACCCTCGTGTGTGCTGATCCACCTGACCCTTGACCCCAGCACTGTGCTGGGAGAAACGCAAGGGGCGGGTTGGCTTCTGGCTTCTACCATCACAGCAGGTGAGTTTGCTTGATAGCTGAGCTGCGCTGAGCCCAGCAGGGGAGCCCTCGGATGTGAGAAACACAGTCCCAGAACGGCCATAAGGA... | CACACCACGCTCTCAGCTCAAGTGCCTCTATTCAGAAGCCTCTACTAGGAACGTGGGGCAGGGGCCTCCCCGAGGGAGGCTGGGTCCTTCAACCTGCAGCAGCCTTTTGTTTAGGCCCCTCTCAGCAGTGAAATGACCCTCGTGTGTGCTGATCCACCTGACCCTTGACCCCAGCACTGTGCTGGGAGAAACGCAAGGGGCGGGTTGGCTTCTGGCTTCTACCATCACAGCAGGTGAGTTTGCTTGATAGCTGAGCTGCGCTGAGCCCAGCAGGGGAGCCCTCGGATGTGAGAAACACAGTCCCAGAACGGCCATAAGGA... |
Task1_train_46147 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTGAGTGCTGGGATTACAGGCGCCTGCTACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGCCTGATCTAGAACTCCTGACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGCGCCCAACAATTTTTGTATTTTTAGTACAGACAGGGTTTCACTACGTTGGCCAGGCTAGGCTCAAACTCCTGACCTCATGATCCGCCTACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCATCCGGCCAATTTACATGTC... | TTGAGTGCTGGGATTACAGGCGCCTGCTACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGCCTGATCTAGAACTCCTGACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGCGCCCAACAATTTTTGTATTTTTAGTACAGACAGGGTTTCACTACGTTGGCCAGGCTAGGCTCAAACTCCTGACCTCATGATCCGCCTACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCATCCGGCCAATTTACATGTC... |
Task1_train_46148 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | TCTCTTCCACTAGGCAGGCAGAACCCCACGTGGCACGTGGCTGGGCAAGGCCATCTGAATGGAAACTGCAGATACAGCACTGCCTTAGACCATCCTGCACGCACCCGCGCTCACCACACACACACGTCGTGAATATAAACATCCATATACTGGTACAGGTGTGAGTGCTTCTCTGGCCCCTGCTCTGCATGCTAATTGTCTCTTCTGCACCTTCCGGGTGGATGCGAGCTCTGCCCGGCAGATGCCCTTGTGCAGGGTAAGGGGGCCAAGCAGTGGGGCCCTGGTGACCCTAAGGGGGCTGGAAGAACCGTGCCCAGAGC... | TCTCTTCCACTAGGCAGGCAGAACCCCACGTGGCACGTGGCTGGGCAAGGCCATCTGAATGGAAACTGCAGATACAGCACTGCCTTAGACCATCCTGCACGCACCCGCGCTCACCACACACACACGTCGTGAATATAAACATCCATATACTGGTACAGGTGTGAGTGCTTCTCTGGCCCCTGCTCTGCATGCTAATTGTCTCTTCTGCACCTTCCGGGTGGATGCGAGCTCTGCCCGGCAGATGCCCTTGTGCAGGGTAAGGGGGCCAAGCAGTGGGGCCCTGGTGACCCTAAGGGGGCTGGAAGAACCGTGCCCAGAGC... |
Task1_train_46149 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GTGCTGGGATGACAGGCGTGAGCCACCGCGCCCGGCGTATTCACATCAGTTTTATCGTAACAGTCCTAAACTGGAAGCCACCCAAATACCCTTCAGTGGGTGCCTGGATCGGCAAATTCTGGAATTGAACCGGCGACGACAAGGAATAAACTACCGACGCACGCGAGAGTCTCAGATGCAGGGCGGGGGGCGGCAGAAGCCGGGTCAAGCCCGCAGGCTGCGGGGTTCAGACTTTCGGAAAAGCAAAAGGTACAGGGCGTAGAGCGAGGTCAGTGGTTGCCGGTGGCCAGGAGTCCGGCCTGAGCTGGGGCGAGAGATGA... | GTGCTGGGATGACAGGCGTGAGCCACCGCGCCCGGCGTATTCACATCAGTTTTATCGTAACAGTCCTAAACTGGAAGCCACCCAAATACCCTTCAGTGGGTGCCTGGATCGGCAAATTCTGGAATTGAACCGGCGACGACAAGGAATAAACTACCGACGCACGCGAGAGTCTCAGATGCAGGGCGGGGGGCGGCAGAAGCCGGGTCAAGCCCGCAGGCTGCGGGGTTCAGACTTTCGGAAAAGCAAAAGGTACAGGGCGTAGAGCGAGGTCAGTGGTTGCCGGTGGCCAGGAGTCCGGCCTGAGCTGGGGCGAGAGATGA... |
Task1_train_46150 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | GCTCATCTTACATGGGGAGATCCAGGCATACCCCTTACCACAGCGTCCCTTCCTGCGAGGAGACAGGGTCCGAGCCCCACTGCCTCTTGCCCTGGGTCTCCCGTTTGCTCCCAAACTCCTCACTCTCCTTTGGCCACCGCCCAGAGGGCCACCGTTCCCTAGCCACTCCCAGTGTCTGGCCACCTCCTTAACTGGCCAACCCCACCTACCCTAAGTTTGCTGGATGTGGTGGCAGCTGGGGGAGGGGAGCCGAGCAGTGGGGACAGGAGGAGCCCGGGAAGGGTGCAGAGAAAGCCGCCCACGCTGCCCCTACGAGGCCG... | GCTCATCTTACATGGGGAGATCCAGGCATACCCCTTACCACAGCGTCCCTTCCTGCGAGGAGACAGGGTCCGAGCCCCACTGCCTCTTGCCCTGGGTCTCCCGTTTGCTCCCAAACTCCTCACTCTCCTTTGGCCACCGCCCAGAGGGCCACCGTTCCCTAGCCACTCCCAGTGTCTGGCCACCTCCTTAACTGGCCAACCCCACCTACCCTAAGTTTGCTGGATGTGGTGGCAGCTGGGGGAGGGGAGCCGAGCAGTGGGGACAGGAGGAGCCCGGGAAGGGTGCAGAGAAAGCCGCCCACGCTGCCCCTACGAGGCCG... |
Task1_train_46151 | Chromosome 19 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGGGACGGGGTCCTGCCCTGAGGGGTGTGGGGGGGGCACGGGGTCCTGCCCTGAGGGGTGTGGGGGGGACGGGGTCCTGCCCTGAGGGGTGTGGGGGGGACGGGGTCCTGCCCTGAGGGGTGTGGGGGGGACGGGGTCCTGCCCTGAGGGGTCTGAGGGGGAGACGGGTCCTGCCCTGAGGGGTGTGGAGGGGGGATGGGGTCCTGCCCTGAGGGGTCTGAGGGGGGGACGGGTCCTGCCCCGAGGGGTGTGGAGGGGGGAACGGGGTCCTGCCCTGAGGGGTGTGGGGGGAACGGGGTCCTGCCCTGAGGGGTGTGGAG... | GGGGACGGGGTCCTGCCCTGAGGGGTGTGGGGGGGGCACGGGGTCCTGCCCTGAGGGGTGTGGGGGGGACGGGGTCCTGCCCTGAGGGGTGTGGGGGGGACGGGGTCCTGCCCTGAGGGGTGTGGGGGGGACGGGGTCCTGCCCTGAGGGGTCTGAGGGGGAGACGGGTCCTGCCCTGAGGGGTGTGGAGGGGGGATGGGGTCCTGCCCTGAGGGGTCTGAGGGGGGGACGGGTCCTGCCCCGAGGGGTGTGGAGGGGGGAACGGGGTCCTGCCCTGAGGGGTGTGGGGGGAACGGGGTCCTGCCCTGAGGGGTGTGGAG... |
Task1_train_46152 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGGCATATGCAGGGGATCCAGGCTGCTGGGTCCTGGGGTGTGTTCACCTAATGGGTAAAGGGTGGGACAGGTTTGGCGGCCCTAGGCTGAGGGCTGTGGGCTGAGGAGAGAGCAGCCCCACCACCCCCTCTCTGCGCCCTGCATGCCTCCCAGGCTGCATCCCTCAGGGAGGTCCCGGGGCAGTGTCGCACCCTCCCAAGCTCCGGGATTAGGGTCTTTCTGGATGGGAGGTTTGTAAGGTGGTCCAGGTGCCATCCCTCCCTGGCACACAGAGGGCTCAGTCACACGGCACCCCCGGTGTGTTTCCTTCCTGTCCCTTG... | AGGCATATGCAGGGGATCCAGGCTGCTGGGTCCTGGGGTGTGTTCACCTAATGGGTAAAGGGTGGGACAGGTTTGGCGGCCCTAGGCTGAGGGCTGTGGGCTGAGGAGAGAGCAGCCCCACCACCCCCTCTCTGCGCCCTGCATGCCTCCCAGGCTGCATCCCTCAGGGAGGTCCCGGGGCAGTGTCGCACCCTCCCAAGCTCCGGGATTAGGGTCTTTCTGGATGGGAGGTTTGTAAGGTGGTCCAGGTGCCATCCCTCCCTGGCACACAGAGGGCTCAGTCACACGGCACCCCCGGTGTGTTTCCTTCCTGTCCCTTG... |
Task1_train_46153 | This mutation on Chromosome 19 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CTTCTCCCACTAAAGAAAAAGGGATTTGTCCTCCCATGGGGCACCCTGATACCCATGTTAATGGACGTGAGGTCGTGAGTTTCAAGCAAAGGGCTCCCGGGGATAAAGCAGAAGCTGGGAGACCCGGGAGGTCTTTGTGGTGGGGGTGGGGCTGGGGTGGGCAGAGAGGAGGCTGGATTTGAGGGATATTTTACAGAACACGGGCCCTCACGGGCCTCAGTCTCCCCATCAGTCCCACAGGGGATGGAGCAGAAGGCCAGGGCAGAAAGCCCCCAAGCACCTTCTCTCTCCACGCCAGCCTCCTCCCAACTCTCCTCGTC... | CTTCTCCCACTAAAGAAAAAGGGATTTGTCCTCCCATGGGGCACCCTGATACCCATGTTAATGGACGTGAGGTCGTGAGTTTCAAGCAAAGGGCTCCCGGGGATAAAGCAGAAGCTGGGAGACCCGGGAGGTCTTTGTGGTGGGGGTGGGGCTGGGGTGGGCAGAGAGGAGGCTGGATTTGAGGGATATTTTACAGAACACGGGCCCTCACGGGCCTCAGTCTCCCCATCAGTCCCACAGGGGATGGAGCAGAAGGCCAGGGCAGAAAGCCCCCAAGCACCTTCTCTCTCCACGCCAGCCTCCTCCCAACTCTCCTCGTC... |
Task1_train_46154 | Assess the clinical impact of this variant found on Chromosome 19. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TGTGCCGAGGCCAGGGAGGGTCCCCGTGCACACTGACAGGCGCTGGCCTGGGTAAGCCTGTGGGCTGCAGAGCCGTCGCCAGGATCTGGTGACAAGGACCCCGAGCCACAGCCTCCCTTGTGACTTGCGGGTTCTGCCGGCGCCTGCAGGAGGCGTCTTTCTGCTTCTCCCACTGCCAGGCATGGGCGGTTCTCGTGCCGTGCGGGTCCCGCCTCCTCCCTGCTCCCAGCCGCGAGCCCTGGGGCTCTGGCGACCTGCCCGGCCTGACATCTTCCCAGGGTGAACATAAAAGAACCCCCTTCAGCTGGAGCACGCATCTG... | TGTGCCGAGGCCAGGGAGGGTCCCCGTGCACACTGACAGGCGCTGGCCTGGGTAAGCCTGTGGGCTGCAGAGCCGTCGCCAGGATCTGGTGACAAGGACCCCGAGCCACAGCCTCCCTTGTGACTTGCGGGTTCTGCCGGCGCCTGCAGGAGGCGTCTTTCTGCTTCTCCCACTGCCAGGCATGGGCGGTTCTCGTGCCGTGCGGGTCCCGCCTCCTCCCTGCTCCCAGCCGCGAGCCCTGGGGCTCTGGCGACCTGCCCGGCCTGACATCTTCCCAGGGTGAACATAAAAGAACCCCCTTCAGCTGGAGCACGCATCTG... |
Task1_train_46155 | This variant is found on Chromosome 19. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AAATCTCACACCCTCAAGTCGAGCCCCAGGCCCAGTGCACACTGCACGGCCTCGGGGGCCAGACCCAGCTGGCTCACCTGATGGACGGGGAGGTGGGAGACATAGGCGGCAGGGTCGGAGGCGCGCACAGCGTTCGCCACCTCCATACAGCAGGCCAGCGTCTGCCAGGGTTCCTCCGCGCCCATCCACCACTTTCGGCCCTGCGGGGACAGCGGATGGGGGGCAGTGAGGCCCGGGCCCGATCCCTGAGCCCGCTGGGAGGCTGTGTTGCGGGGAGGTGGGAAATGGGGAGGAGACGCACACCCGTGATAGTGAACACG... | AAATCTCACACCCTCAAGTCGAGCCCCAGGCCCAGTGCACACTGCACGGCCTCGGGGGCCAGACCCAGCTGGCTCACCTGATGGACGGGGAGGTGGGAGACATAGGCGGCAGGGTCGGAGGCGCGCACAGCGTTCGCCACCTCCATACAGCAGGCCAGCGTCTGCCAGGGTTCCTCCGCGCCCATCCACCACTTTCGGCCCTGCGGGGACAGCGGATGGGGGGCAGTGAGGCCCGGGCCCGATCCCTGAGCCCGCTGGGAGGCTGTGTTGCGGGGAGGTGGGAAATGGGGAGGAGACGCACACCCGTGATAGTGAACACG... |
Task1_train_46156 | This mutation on Chromosome 19 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TCTATTGCTGGCCGGGCATGGCGGCTCACGTCGGTCATCCCAGCACTTTGGGAGGCCGAGGCAGGAAGATCACCTAAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTATTAGAAATCCAAAAAATTAGCTGGGCGTGGTGGCATGTGTCTATAGTACCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAGCCTGGGAGGCAGAGGTTGCAGTGACTCAAGATAGCGCCATTGAACTCCAGCCTGGGCAACAGAACAATAATCCATCTAAAAAAAAAAGACTGTTGAAATAAGCCGG... | TCTATTGCTGGCCGGGCATGGCGGCTCACGTCGGTCATCCCAGCACTTTGGGAGGCCGAGGCAGGAAGATCACCTAAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTATTAGAAATCCAAAAAATTAGCTGGGCGTGGTGGCATGTGTCTATAGTACCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAGCCTGGGAGGCAGAGGTTGCAGTGACTCAAGATAGCGCCATTGAACTCCAGCCTGGGCAACAGAACAATAATCCATCTAAAAAAAAAAGACTGTTGAAATAAGCCGG... |
Task1_train_46157 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | ATGTGGTGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGATCAAGACCATCCTGGCTAACACGGTGAAACCCCGTCCCTACTAAAAATACGAAAAATTAACCGGGCGTGGTGGTGCGCGCCTGTAGTTCCAGCTACTCGGGAGGTTGAGGCAGGAGAATTGCTTGAACTCGGGAGGCGGAGGCTGCAGTGAGCCAAGATCGCACCATTGCACTCCAGCCTAGCAACAGATTGAGAATCCGTCTCAAGAAAAAAAAAATTGCTGAAATAAAAAGACAAGCGTGATGTCCGC... | ATGTGGTGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGATCAAGACCATCCTGGCTAACACGGTGAAACCCCGTCCCTACTAAAAATACGAAAAATTAACCGGGCGTGGTGGTGCGCGCCTGTAGTTCCAGCTACTCGGGAGGTTGAGGCAGGAGAATTGCTTGAACTCGGGAGGCGGAGGCTGCAGTGAGCCAAGATCGCACCATTGCACTCCAGCCTAGCAACAGATTGAGAATCCGTCTCAAGAAAAAAAAAATTGCTGAAATAAAAAGACAAGCGTGATGTCCGC... |
Task1_train_46158 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TATCCACCCCACTCACCAGGGGCCCAGGCTGGGGATGGGGACAGGCACCCCCTCCTACTCACCAGGGACCCTGGCTGGGGATGGGGACAGGCACCCCCACCCACTCACCAGGGGCCCAGGCTGGGGATGGGAACAGGCACCCCCTCCTACTCACCAGGGACCCTGGCTGGGGATGGGGACAGGCACCCCCACCCACTCACCAGGGGCCCAGGCTGGGGATGGGGACAGGCACCCCCACCCACTCACCAGGGGCCCAGGCTGGGGATGGGGACAGGCACCCCCTCCTACTCACCAGGGGCCCAGGCTGGGGATGGGGACAG... | TATCCACCCCACTCACCAGGGGCCCAGGCTGGGGATGGGGACAGGCACCCCCTCCTACTCACCAGGGACCCTGGCTGGGGATGGGGACAGGCACCCCCACCCACTCACCAGGGGCCCAGGCTGGGGATGGGAACAGGCACCCCCTCCTACTCACCAGGGACCCTGGCTGGGGATGGGGACAGGCACCCCCACCCACTCACCAGGGGCCCAGGCTGGGGATGGGGACAGGCACCCCCACCCACTCACCAGGGGCCCAGGCTGGGGATGGGGACAGGCACCCCCTCCTACTCACCAGGGGCCCAGGCTGGGGATGGGGACAG... |
Task1_train_46159 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GCAGGAGGATCACCTGAGGTCAGAGATTTGAGACCAGCCTGGCCAAGATGGCGAAACCCAGTCTCTACTAAAAATGCAAAAATTAGGTGGATTAGTGGCGGGCGCCTGTAATCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGGAGGTTTCAGTGAGCCGAGATCAAGCCACTGCACTCCAGCCTGGGGGACAGAGCGAGAATCTGTCTAAAAAAGGAAGGTATGGACAGGGTGGGGCAGTTCTGGTGGGTTTGGGGCCTTGGAATGAGCCGAGTGTTACCCACTCCCTGGGCCTCAGTT... | GCAGGAGGATCACCTGAGGTCAGAGATTTGAGACCAGCCTGGCCAAGATGGCGAAACCCAGTCTCTACTAAAAATGCAAAAATTAGGTGGATTAGTGGCGGGCGCCTGTAATCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGGAGGTTTCAGTGAGCCGAGATCAAGCCACTGCACTCCAGCCTGGGGGACAGAGCGAGAATCTGTCTAAAAAAGGAAGGTATGGACAGGGTGGGGCAGTTCTGGTGGGTTTGGGGCCTTGGAATGAGCCGAGTGTTACCCACTCCCTGGGCCTCAGTT... |
Task1_train_46160 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGCAGATCACCTGAGCTCAGGAGTTCGAGACCAACCTGGCCAACATGGTGAGACCTCGTCTCTACTAAAAATACAAAAAATTAGCCGGACTTGGGAGGTTAGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCACGAGAATTGCTTGAACCTGGAAGCAGAGGTTGCAGTGAGCTGACATTGTGCCACTGCACTCCAGGCTGGGCAACAGAGCGAGACTCCATCTCAAAAAAAAAAAAATCAAGGCTGAGCTGGACTCCACAGGGCAGGTGTGTGTGTCTGGGAGATAAGGTGGGCAGGGCACCCTGATTTTATTGG... | GGCAGATCACCTGAGCTCAGGAGTTCGAGACCAACCTGGCCAACATGGTGAGACCTCGTCTCTACTAAAAATACAAAAAATTAGCCGGACTTGGGAGGTTAGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCACGAGAATTGCTTGAACCTGGAAGCAGAGGTTGCAGTGAGCTGACATTGTGCCACTGCACTCCAGGCTGGGCAACAGAGCGAGACTCCATCTCAAAAAAAAAAAAATCAAGGCTGAGCTGGACTCCACAGGGCAGGTGTGTGTGTCTGGGAGATAAGGTGGGCAGGGCACCCTGATTTTATTGG... |
Task1_train_46161 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCTTCCTGCAGCCACACACCCACCCGGGGTGTCCTGGGGACCCAAGGGGTGGGGGGGTCACACCAGAGAGAGGCAGGGGGCCTGGCCGGCTCCTGCAGGATCATGCAGCTGGGGCGCGGCGGCCGCGGCTGCGACACCCCAACCCCAGCCCTCTAATCAAGTCACGTGATTCTCCCTTCACCCCGCCCCCAGGGCCTTCCCTTCTGCCCCCAGGCGGGCTCCCCGCTGCTCCAGCTGCGGAGCTGGTCGACATAATCTCTGTATTATATACTTTGCAGTTGCAGACGTCTGTGCCTAGCAATATTTCCAGTTGACCAAAT... | CCTTCCTGCAGCCACACACCCACCCGGGGTGTCCTGGGGACCCAAGGGGTGGGGGGGTCACACCAGAGAGAGGCAGGGGGCCTGGCCGGCTCCTGCAGGATCATGCAGCTGGGGCGCGGCGGCCGCGGCTGCGACACCCCAACCCCAGCCCTCTAATCAAGTCACGTGATTCTCCCTTCACCCCGCCCCCAGGGCCTTCCCTTCTGCCCCCAGGCGGGCTCCCCGCTGCTCCAGCTGCGGAGCTGGTCGACATAATCTCTGTATTATATACTTTGCAGTTGCAGACGTCTGTGCCTAGCAATATTTCCAGTTGACCAAAT... |
Task1_train_46162 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGGGAAGGGGGTCAGATGGGGGAGGCCCAGAGAAGGGAAGGGGCTCAGATGGAGGAGGTGCAGAGAAGGGAAGGGGCTCAGATGGAGGAGGTGCAGAGAAGAGAAGGGCCTCAGATGGAGGAGGTGCAGAGAAGGGAAGGGCCTCAGATGGAGGAGGTGCGGAGAAGGGAAGGGGGTCAGATGGAGGAGGTGCAGAGAAGGGAAGGGGGTCAGATGGGGGAGGCCCAGGGAAGGGAAGGGGCTCAGATGGAGGAGGGGCAGAGAAGGGAAGGGGGTCAGATGGGGGAGGCCCAGGGAAGGGAAGGGGCTCAGATGGGGGA... | AGGGAAGGGGGTCAGATGGGGGAGGCCCAGAGAAGGGAAGGGGCTCAGATGGAGGAGGTGCAGAGAAGGGAAGGGGCTCAGATGGAGGAGGTGCAGAGAAGAGAAGGGCCTCAGATGGAGGAGGTGCAGAGAAGGGAAGGGCCTCAGATGGAGGAGGTGCGGAGAAGGGAAGGGGGTCAGATGGAGGAGGTGCAGAGAAGGGAAGGGGGTCAGATGGGGGAGGCCCAGGGAAGGGAAGGGGCTCAGATGGAGGAGGGGCAGAGAAGGGAAGGGGGTCAGATGGGGGAGGCCCAGGGAAGGGAAGGGGCTCAGATGGGGGA... |
Task1_train_46163 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | CTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGGCCCTTTTTTTTTCTTTTTTGAAACGGAATCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGTTTACTGCAGCCTCAGCCTCCTGGGGTCAAATGATTCTCCTGCCTCCGCCTCTTGAGTAGCTGGGATTACAAGCACACACCACCACACCTGGCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTTGGTCAGGCTGGTCTCGAACTCCTGACCTGAGGGGGATTTTCAATGCCTCAGTTTGTTCATC... | CTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGGCCCTTTTTTTTTCTTTTTTGAAACGGAATCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGTTTACTGCAGCCTCAGCCTCCTGGGGTCAAATGATTCTCCTGCCTCCGCCTCTTGAGTAGCTGGGATTACAAGCACACACCACCACACCTGGCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTTGGTCAGGCTGGTCTCGAACTCCTGACCTGAGGGGGATTTTCAATGCCTCAGTTTGTTCATC... |
Task1_train_46164 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | CAACGTCCCTGGCTCTTAGGGAGATTTTGAGGACCCCTGGGGGAACCGCGAGGCGACGAGGACCTTGGGAAGCCGGGGGCGGGGACAGCAGAGCTTCAGGGCCACAGGCCGCCTCTCAGCACCCCCATGCCCTGCCTGCCTCGCCCACCCCACTGTACCTGAGTGAGGTAGAAGCTCATGACAGCCAGCTTGTGACAGTGGTCTGACAGACCCCCCCCCCACCTAGTGACGCAAAGCCCACCCCGGCTCAAGTGGTCAGGAACTGATGGGACCAGGGGGCATCCTGTCCCCACTCCACGCGTCCAGACCTCAGCCAGGTC... | CAACGTCCCTGGCTCTTAGGGAGATTTTGAGGACCCCTGGGGGAACCGCGAGGCGACGAGGACCTTGGGAAGCCGGGGGCGGGGACAGCAGAGCTTCAGGGCCACAGGCCGCCTCTCAGCACCCCCATGCCCTGCCTGCCTCGCCCACCCCACTGTACCTGAGTGAGGTAGAAGCTCATGACAGCCAGCTTGTGACAGTGGTCTGACAGACCCCCCCCCCACCTAGTGACGCAAAGCCCACCCCGGCTCAAGTGGTCAGGAACTGATGGGACCAGGGGGCATCCTGTCCCCACTCCACGCGTCCAGACCTCAGCCAGGTC... |
Task1_train_46165 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | GTGAGGTGGGAGGTGCGGGACCACCTGAGACAGGCCCAGTAAAGGGGGCGGGACCCCCCACACGGAGGAGGGTTGGTCTCCCAGGTGCCTGGGGAGCTTGAGGCTTAGAGACCCAGTAAAGGGGACGGGGCCCACACAGGGACGAGGGTCGGTCCGCCACGTGCCCGGGGAGCCTGAGGTGCAGGGAAGGTGCTTGTGACGCTCCCATTTGAGGCTGGACAGAAGCAGGTACATGGGGACTTCCACACCACCTCTGCCCAGACACCCGGCCTGGAGGTGCCGGGACCTCTGAACGACAAGATTCTGGTGGCAAAAGCTGC... | GTGAGGTGGGAGGTGCGGGACCACCTGAGACAGGCCCAGTAAAGGGGGCGGGACCCCCCACACGGAGGAGGGTTGGTCTCCCAGGTGCCTGGGGAGCTTGAGGCTTAGAGACCCAGTAAAGGGGACGGGGCCCACACAGGGACGAGGGTCGGTCCGCCACGTGCCCGGGGAGCCTGAGGTGCAGGGAAGGTGCTTGTGACGCTCCCATTTGAGGCTGGACAGAAGCAGGTACATGGGGACTTCCACACCACCTCTGCCCAGACACCCGGCCTGGAGGTGCCGGGACCTCTGAACGACAAGATTCTGGTGGCAAAAGCTGC... |
Task1_train_46166 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ACGGCCCTGCTGTACCCGCTGCCCGGCTGGGTGCTGGGCGACTTCATGTGCAAGTTCGTCAACTACATCCAGCAGGTGCGCTCCGGAGCAGGAGGGGAGAGGGCGCACTTGGGGACGGGCGGGGGTGCGCTCCGCAGTGGGAGGGGAGGGGACGCACTTGGGGACAGGCGGGAGTGCGCTCCGCAGTGGGAGGGGAGGGGATCGTACGTGGGGACGGGGAGGGGGGGTGCGCTGCGGAGCAGGAGGGGAGGGAGCGCACGTGGGGACGGAGGGAGATGCACTCAGAAGCTGGAGGGGAGGGGGCGCATGGTGGGGCGGGG... | ACGGCCCTGCTGTACCCGCTGCCCGGCTGGGTGCTGGGCGACTTCATGTGCAAGTTCGTCAACTACATCCAGCAGGTGCGCTCCGGAGCAGGAGGGGAGAGGGCGCACTTGGGGACGGGCGGGGGTGCGCTCCGCAGTGGGAGGGGAGGGGACGCACTTGGGGACAGGCGGGAGTGCGCTCCGCAGTGGGAGGGGAGGGGATCGTACGTGGGGACGGGGAGGGGGGGTGCGCTGCGGAGCAGGAGGGGAGGGAGCGCACGTGGGGACGGAGGGAGATGCACTCAGAAGCTGGAGGGGAGGGGGCGCATGGTGGGGCGGGG... |
Task1_train_46167 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGGAGAATCGCTTGAACCCGGGAGGCAGAGGTAGCAGTGAGCCGAGATCGCACCATTGCACTCCAACCTGGGCCACAGAGCAAGACTGTCGCAAAATAAAGAAAGAAAATAAAAATGAGGTTGGAGGAAACTCTGGAGGCACAGCAGGTCCTTGGATTGGACTCCCTCCCTCCCTCCCAGGATAAAATGAAATCCAGGCCTCGTTCACACGGCCCTGCACGGCCCGGCCCCGCTCCGTGGTCCTGCCCCAGGGCCTTCGCACGGGCCTGCCCCGCACACGGTTCTCTGGGGGTCGCTGGCTCCCCGCTCAAACGGCCCCT... | AGGAGAATCGCTTGAACCCGGGAGGCAGAGGTAGCAGTGAGCCGAGATCGCACCATTGCACTCCAACCTGGGCCACAGAGCAAGACTGTCGCAAAATAAAGAAAGAAAATAAAAATGAGGTTGGAGGAAACTCTGGAGGCACAGCAGGTCCTTGGATTGGACTCCCTCCCTCCCTCCCAGGATAAAATGAAATCCAGGCCTCGTTCACACGGCCCTGCACGGCCCGGCCCCGCTCCGTGGTCCTGCCCCAGGGCCTTCGCACGGGCCTGCCCCGCACACGGTTCTCTGGGGGTCGCTGGCTCCCCGCTCAAACGGCCCCT... |
Task1_train_46168 | Mutation context: Chromosome 19. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GAAATCCTCCTCCTGTTCTCTGTGTAGGCGACGGGTGTGTGAGCGGTGAGTCAGGAGTGGGCTGGAAACCTGAGAGCCAGGGCTGTGGGGCGGGAGCTGGTCCGCCCCTCCCACGCCACAGGGACAGGGACCTCCCGGGAGGCACTGATGTTCTGAAGCTGCCCGGTCTGTCCCGGCCCTGGGCAGTGGTGGTCACCAGAGCTGCCCTCTGTGGTTTGGGGCTGACCTGGATCCTGCTTCCTCTGGTGCCATTTAACCCTCCCCAGCCACCCTGGGTTTTGCATGCGAGGAAAGCGAGGCCCAGAGAGGGCATGGCTGTC... | GAAATCCTCCTCCTGTTCTCTGTGTAGGCGACGGGTGTGTGAGCGGTGAGTCAGGAGTGGGCTGGAAACCTGAGAGCCAGGGCTGTGGGGCGGGAGCTGGTCCGCCCCTCCCACGCCACAGGGACAGGGACCTCCCGGGAGGCACTGATGTTCTGAAGCTGCCCGGTCTGTCCCGGCCCTGGGCAGTGGTGGTCACCAGAGCTGCCCTCTGTGGTTTGGGGCTGACCTGGATCCTGCTTCCTCTGGTGCCATTTAACCCTCCCCAGCCACCCTGGGTTTTGCATGCGAGGAAAGCGAGGCCCAGAGAGGGCATGGCTGTC... |
Task1_train_46169 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | AACCCACAACCCCCCAGAGCATCTCAGCCCTCGAACCCACAAACCCCCCCAAGAGCATCTCAGTCCTCGAACCCACAACCCCCTCCAGAGCATCTCAGTCCTCGAACCCACAACCCCCCCCAGAGCATCTCAGCCCTCGAACCCACAACCCCCACCAGAGCATCTCAGCCCTCCCCAGGTGTCCTGGAAGGGGCTCCCTGTCCTCTTCCTCAGATGGAGCTGCCTGGCTTCCTGCCGGAGCTTAAGCTGCCACCACCCTGGGTCAGGCCACCACAGCCTGCCCAGAAGCGACTTCCTGTTGAATGGTGGGAGCCGCCTGC... | AACCCACAACCCCCCAGAGCATCTCAGCCCTCGAACCCACAAACCCCCCCAAGAGCATCTCAGTCCTCGAACCCACAACCCCCTCCAGAGCATCTCAGTCCTCGAACCCACAACCCCCCCCAGAGCATCTCAGCCCTCGAACCCACAACCCCCACCAGAGCATCTCAGCCCTCCCCAGGTGTCCTGGAAGGGGCTCCCTGTCCTCTTCCTCAGATGGAGCTGCCTGGCTTCCTGCCGGAGCTTAAGCTGCCACCACCCTGGGTCAGGCCACCACAGCCTGCCCAGAAGCGACTTCCTGTTGAATGGTGGGAGCCGCCTGC... |
Task1_train_46170 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGAACCGAGCCATCCCTCCCTCCGTCCCTCCCCAGTCGTCTCAAAATCCAATCCATTTTACTGGCTGGCACTTGGCATTTTATTCATTTCATGGAGGATTTTTTTCCTACCTCTCCAACGCTGGCTCCAAAAGGAGATGACGTTTGGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAAAATCGCCGGAGTGTAGATCCATTAATTAGAGCTGAATGTTCCCAACACAGCGGCTGTTCTGCTGCCCCGCGGGATCTGGGGAGACACCGTCGGGAGGACAGGATGAGGAATGCCTGGGCAGGGAGGAGG... | GGAACCGAGCCATCCCTCCCTCCGTCCCTCCCCAGTCGTCTCAAAATCCAATCCATTTTACTGGCTGGCACTTGGCATTTTATTCATTTCATGGAGGATTTTTTTCCTACCTCTCCAACGCTGGCTCCAAAAGGAGATGACGTTTGGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAAAATCGCCGGAGTGTAGATCCATTAATTAGAGCTGAATGTTCCCAACACAGCGGCTGTTCTGCTGCCCCGCGGGATCTGGGGAGACACCGTCGGGAGGACAGGATGAGGAATGCCTGGGCAGGGAGGAGG... |
Task1_train_46171 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GGCCTCTGCCCCTTCCTTGCCCAGGCCCCTTCCCTCCTTCCCCACAGACCCTTCCCTGGTCCCTGGGACCTCCTGGTCCCCACCCGGCTCTGGGTGGCTGGGCTGGAGGACAGGCGGTCTCCCTCCTCACTCTAGGGGTGCAGTTTCGGGGTCTGCAGGTCTGGATCTCCCTCCTTCCAGCATTCTCCCCGTCCCCTCCCAGAGGCCTCCAAGATCCCAGAGCAGCCTCCATCATTCCAACCCCGACTCCATTCCCACCCCCCAACCCCTGGCAGCCTTCAAGTTCCTCTCTTCTAACCCCACCCCAGGCCCAGATCCCG... | GGCCTCTGCCCCTTCCTTGCCCAGGCCCCTTCCCTCCTTCCCCACAGACCCTTCCCTGGTCCCTGGGACCTCCTGGTCCCCACCCGGCTCTGGGTGGCTGGGCTGGAGGACAGGCGGTCTCCCTCCTCACTCTAGGGGTGCAGTTTCGGGGTCTGCAGGTCTGGATCTCCCTCCTTCCAGCATTCTCCCCGTCCCCTCCCAGAGGCCTCCAAGATCCCAGAGCAGCCTCCATCATTCCAACCCCGACTCCATTCCCACCCCCCAACCCCTGGCAGCCTTCAAGTTCCTCTCTTCTAACCCCACCCCAGGCCCAGATCCCG... |
Task1_train_46172 | Located on Chromosome 19, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TCCCAACTCCGGACATGGGCCTGGCTGAGCTCTATGCCCCAGCTGCCCCTCCTTCCCAACCCACTCAGAGGCCCCTCCAGCCCCTCCCTCTCCTCAGGGAGGGAGACCCTGACGCTAGAGGGGGGGTCTCTTAGCCCAGCTCTCCAGGTGTCAAGGGGACCCCTGTCCCCCCACCGCCCTAGGGCTGGTGGGAGAGGCGGGGCCCAAACCCAGGCCTGGGGCGCCCTCTGCTGCCGTCTCCAGGAGCTGCACCGCCGCAAGCCGGGGCGTGGGACCGACCTAGCGTCTTAGGGACTGGCTTGGCCCCCTGGGGACTGAGC... | TCCCAACTCCGGACATGGGCCTGGCTGAGCTCTATGCCCCAGCTGCCCCTCCTTCCCAACCCACTCAGAGGCCCCTCCAGCCCCTCCCTCTCCTCAGGGAGGGAGACCCTGACGCTAGAGGGGGGGTCTCTTAGCCCAGCTCTCCAGGTGTCAAGGGGACCCCTGTCCCCCCACCGCCCTAGGGCTGGTGGGAGAGGCGGGGCCCAAACCCAGGCCTGGGGCGCCCTCTGCTGCCGTCTCCAGGAGCTGCACCGCCGCAAGCCGGGGCGTGGGACCGACCTAGCGTCTTAGGGACTGGCTTGGCCCCCTGGGGACTGAGC... |
Task1_train_46173 | A genomic variant on Chromosome 19 is under review. What is the biological outcome — benign or pathogenic? | Benign | GGACTGTAAAGGAATCAGGGAGGGACCTGAGGCTGGAGGCGTTCCAAGCTGGAGCCTGGGCTCTGCCTGGAGGATGGAGAAGTCTGAATAGAGGAGGAGCAATGTGCTTGGGTTTTGAAGGATGTGTAGGAGTTGGTGGGCATAGAGAGAGAAAGATATTCCATCCGGGGAATGGCACATGCAAAAAAAAAACAAAAAACACCAAGTGTGCCCATGACAAGGGTAGCTGGAGCCAAGAGAGGCTGGGAGACTGAGCTTTGTGGGGATGGTGATGGGGAACGATGGAAGGGTTTAGAGCAGGGCTGGGGCTGGGGGGAGGT... | GGACTGTAAAGGAATCAGGGAGGGACCTGAGGCTGGAGGCGTTCCAAGCTGGAGCCTGGGCTCTGCCTGGAGGATGGAGAAGTCTGAATAGAGGAGGAGCAATGTGCTTGGGTTTTGAAGGATGTGTAGGAGTTGGTGGGCATAGAGAGAGAAAGATATTCCATCCGGGGAATGGCACATGCAAAAAAAAAACAAAAAACACCAAGTGTGCCCATGACAAGGGTAGCTGGAGCCAAGAGAGGCTGGGAGACTGAGCTTTGTGGGGATGGTGATGGGGAACGATGGAAGGGTTTAGAGCAGGGCTGGGGCTGGGGGGAGGT... |
Task1_train_46174 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | TGTGCTGGTGGCGGTGCTGCAGGCGCACGCCTGGGAAGACGTCGGCCTGGCCCTGTGCCGCACTCAGGACCCCGGCGGCCTGGTGGCCCTCTGGACAAGCCGGGCTGGCCGGCCCCCACAGCTGGTCCTGGACCTAAGCCGGCGGGACACGGGAGATGCAGGACTGCGGGCACGCCTGGCCCCGATGGCGGCGCCAGTGGGGGGTGAAGCACCGGTACCCGCGGCGGTCCTCCTCGGCTGTGACATCGCCCGTGCCCGTCGGGTGCTGGAGGCCGTACCTCCCGGCCCCCACTGGCTGTTGGGGACACCACTGCCGCCCA... | TGTGCTGGTGGCGGTGCTGCAGGCGCACGCCTGGGAAGACGTCGGCCTGGCCCTGTGCCGCACTCAGGACCCCGGCGGCCTGGTGGCCCTCTGGACAAGCCGGGCTGGCCGGCCCCCACAGCTGGTCCTGGACCTAAGCCGGCGGGACACGGGAGATGCAGGACTGCGGGCACGCCTGGCCCCGATGGCGGCGCCAGTGGGGGGTGAAGCACCGGTACCCGCGGCGGTCCTCCTCGGCTGTGACATCGCCCGTGCCCGTCGGGTGCTGGAGGCCGTACCTCCCGGCCCCCACTGGCTGTTGGGGACACCACTGCCGCCCA... |
Task1_train_46175 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTCTGCCCCGTAGTGTCTCTGAACTTTTGGATCTGCCCAGTGGTGTCCCCTGGGGGTGCCTGGCCTGCTCCCCAGCCCCTGGTGTCCCCTGTGAAACGGTAGTAAAGCGTAGACGCCATGCTGTCAGGTGAGCCGACTGCTGCCGGCGGCTCTTCCAATGTAAACGCTGCACAGCTGAGCCGTCAAAGCCTTTTCATCATACGGAAACTTCCATCAGATGCTGCTGACCCACAGGCACGATGGGATTCAAGTTTGGGTTTTTGGTGGTGCTGGAATCCCGTGGGGAGGCCGTGGCTGGTGTGACCTCAGCAGCCAGACCC... | TTCTGCCCCGTAGTGTCTCTGAACTTTTGGATCTGCCCAGTGGTGTCCCCTGGGGGTGCCTGGCCTGCTCCCCAGCCCCTGGTGTCCCCTGTGAAACGGTAGTAAAGCGTAGACGCCATGCTGTCAGGTGAGCCGACTGCTGCCGGCGGCTCTTCCAATGTAAACGCTGCACAGCTGAGCCGTCAAAGCCTTTTCATCATACGGAAACTTCCATCAGATGCTGCTGACCCACAGGCACGATGGGATTCAAGTTTGGGTTTTTGGTGGTGCTGGAATCCCGTGGGGAGGCCGTGGCTGGTGTGACCTCAGCAGCCAGACCC... |
Task1_train_46176 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GGTGGTGGGATAGGCGTCCAGCCCAGGGCGAGGTCCAGGTGGAGATGGACTTGCCGGCGTTTAGAACAGAGGGTCTCCACCCGGGGTGATCCTGCCCCCCGCCCCAGGGGACCCTGGACAGTGTGTGTCTAGAGACAGCTGTGGTGGTCACGCCTGGGGTGTGCTCTGGGCATGGAGTGGGTGGAGGCCAGGAATGCAGCCTCGGCGCCCTGCAGTGCCCAGGACGGCCCCACCCCGGAGAACGGCGCGCCCCTCAATGGTCAGGGGTCCTGAGGGGCAGGCAGAGGCGCTGACGGGGTCCCCCGCGCAGCTGCACCACC... | GGTGGTGGGATAGGCGTCCAGCCCAGGGCGAGGTCCAGGTGGAGATGGACTTGCCGGCGTTTAGAACAGAGGGTCTCCACCCGGGGTGATCCTGCCCCCCGCCCCAGGGGACCCTGGACAGTGTGTGTCTAGAGACAGCTGTGGTGGTCACGCCTGGGGTGTGCTCTGGGCATGGAGTGGGTGGAGGCCAGGAATGCAGCCTCGGCGCCCTGCAGTGCCCAGGACGGCCCCACCCCGGAGAACGGCGCGCCCCTCAATGGTCAGGGGTCCTGAGGGGCAGGCAGAGGCGCTGACGGGGTCCCCCGCGCAGCTGCACCACC... |
Task1_train_46177 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | TGGTTGCACAACATTGCAGACGTACGAAATGCTGTGAAATGGTGCGGTTTCAGGTGGTTGAAGTGGTAAACGTCAGGTGTGATATAGCGGGGAGGTGAGAAGGCAGGGCGGGGAGGCAGATCCGGCCAGGTTTGTCCTGCACCGGGAGTGGATTAGAGCTGATGTTTATCAGTGAGTTCTAAGCCGGTTGTCGGCCTGCTTGGAGGGCGGTTTATCTGTGCCCGCCTGCAGTGGCTGGGGCGCCCCCAATGATGGGAAAAGGGAGCATCTGCGTGGGTGTGGTGAGGGGGGACCTCCAGGCCGCTCTATCTGCTGTTGCC... | TGGTTGCACAACATTGCAGACGTACGAAATGCTGTGAAATGGTGCGGTTTCAGGTGGTTGAAGTGGTAAACGTCAGGTGTGATATAGCGGGGAGGTGAGAAGGCAGGGCGGGGAGGCAGATCCGGCCAGGTTTGTCCTGCACCGGGAGTGGATTAGAGCTGATGTTTATCAGTGAGTTCTAAGCCGGTTGTCGGCCTGCTTGGAGGGCGGTTTATCTGTGCCCGCCTGCAGTGGCTGGGGCGCCCCCAATGATGGGAAAAGGGAGCATCTGCGTGGGTGTGGTGAGGGGGGACCTCCAGGCCGCTCTATCTGCTGTTGCC... |
Task1_train_46178 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGGACGGTGTCTGGTGTAGACCGGCAGCGTGGGTGGGACACGGTGTCTGGTGTAGACGGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGCAGCGTGGGTGGGACACGGTGTCTGGTGTAGACGGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACACATTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCATGGGTGGGACA... | GGGACGGTGTCTGGTGTAGACCGGCAGCGTGGGTGGGACACGGTGTCTGGTGTAGACGGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGCAGCGTGGGTGGGACACGGTGTCTGGTGTAGACGGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACACATTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCATGGGTGGGACA... |
Task1_train_46179 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CGGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGCAGCGTGGGTGGGACACGGTGTCTGGTGTAGACGGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACACATTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCATGGGTGGGACACGGTGTCTGGTGTAGACGGTAAGCGTGGGTGGGACACGGTGTCTGGTGTAGACCGG... | CGGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGCAGCGTGGGTGGGACACGGTGTCTGGTGTAGACGGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACACATTGTCTGGTGTAGACCGGGAGCGTGGGTGGGACGGTGTCTGGTGTAGACCGGGAGCATGGGTGGGACACGGTGTCTGGTGTAGACGGTAAGCGTGGGTGGGACACGGTGTCTGGTGTAGACCGG... |
Task1_train_46180 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CTCCAGCTGGGCAACTGCCTGTCTCTCTGGGTGCCTGGGTTTGCTTTCTTGGGCCTCGGTTTCCACTTCTGTAGAGTGGGGTGATAGTCCAGCACTTCCCCTGGGCGTGTGAAATGTCCAGCACTGCCAATATTCGTTGCTGTTATCTTCGGAGAACAGTGAGGGGAAAGGAATCCTTGCCTGGGCTGGGCCAGGCAGGAGGCTGGGGGTCAGGACCTGGAAGAGGCTTCCAGGTGAGGCTTGGGGTGGAGCCTGGTGACGAAAGCGTTAAGCCCAAACTCGGTCCCTGGAGGATTAGAGGATGATCTTTAAGTCCCCAG... | CTCCAGCTGGGCAACTGCCTGTCTCTCTGGGTGCCTGGGTTTGCTTTCTTGGGCCTCGGTTTCCACTTCTGTAGAGTGGGGTGATAGTCCAGCACTTCCCCTGGGCGTGTGAAATGTCCAGCACTGCCAATATTCGTTGCTGTTATCTTCGGAGAACAGTGAGGGGAAAGGAATCCTTGCCTGGGCTGGGCCAGGCAGGAGGCTGGGGGTCAGGACCTGGAAGAGGCTTCCAGGTGAGGCTTGGGGTGGAGCCTGGTGACGAAAGCGTTAAGCCCAAACTCGGTCCCTGGAGGATTAGAGGATGATCTTTAAGTCCCCAG... |
Task1_train_46181 | With a mutation on Chromosome 19, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CCAGGCCGCCAATACATGGCATGGGAGTGAGCTCTCCATCGCTGGAGGCATGCAAGCGGTGCCGGGCGACCCGATGGGGGTGGAGTCAGGCAGAGTCCACAGGGCCTCAGCACCAGGCGTCTCCCCGCAGGCCACTTCCCAAACAAGCCACTGCCATCGGCGGGCACCGTGCCCTGGCTCCAGGGTCTCATCTGTAATGTGAACAACACCTGCTTTCCGCAGCTGACACCGGGCGAGGAGCCCGGGCGCCTGAGCAACTTCAACGACTCCCTGTGAGCCAGAGGCAGTGGGTGCGGCCGGCCTGCAAACTCGGGGCTGCA... | CCAGGCCGCCAATACATGGCATGGGAGTGAGCTCTCCATCGCTGGAGGCATGCAAGCGGTGCCGGGCGACCCGATGGGGGTGGAGTCAGGCAGAGTCCACAGGGCCTCAGCACCAGGCGTCTCCCCGCAGGCCACTTCCCAAACAAGCCACTGCCATCGGCGGGCACCGTGCCCTGGCTCCAGGGTCTCATCTGTAATGTGAACAACACCTGCTTTCCGCAGCTGACACCGGGCGAGGAGCCCGGGCGCCTGAGCAACTTCAACGACTCCCTGTGAGCCAGAGGCAGTGGGTGCGGCCGGCCTGCAAACTCGGGGCTGCA... |
Task1_train_46182 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GTCTGCCTGGGAACTGGCCAGAGCGCTGGACCCCTAGTGAGTGTTCAAAATCATTGTCCCCCTTGTGGTCTTTCTCCCCAGGAATCCCTGGGGTTGGCACTGGGCCAAGCCCAGGAGCCCTTGCACAGCTTGTTGGAGGCCGCTGAGGACCTGGCCCAGGAGGTACGAGGCCCCACTCATCCTCAACCCCCATGGAGGCAACGTTGGCAGGCAGCCTGCGCCGGGAGGGTCTGGGGCAGCCCGGGCACTTCCCTTGGGTGGGTTTTCAGGAGGATTAGACAGCGAGAGGGAGAGGCTGCCCCTGGCCCAGTGCCCTGCCC... | GTCTGCCTGGGAACTGGCCAGAGCGCTGGACCCCTAGTGAGTGTTCAAAATCATTGTCCCCCTTGTGGTCTTTCTCCCCAGGAATCCCTGGGGTTGGCACTGGGCCAAGCCCAGGAGCCCTTGCACAGCTTGTTGGAGGCCGCTGAGGACCTGGCCCAGGAGGTACGAGGCCCCACTCATCCTCAACCCCCATGGAGGCAACGTTGGCAGGCAGCCTGCGCCGGGAGGGTCTGGGGCAGCCCGGGCACTTCCCTTGGGTGGGTTTTCAGGAGGATTAGACAGCGAGAGGGAGAGGCTGCCCCTGGCCCAGTGCCCTGCCC... |
Task1_train_46183 | Here is a mutation located on Chromosome 19. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TCAACCCTCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCGGCCGCACCTGGCCTACGTTCTTAACCCTGATCTCTGTCTGCCGGGACAGTCCCCTCACAGGTCACCAATGCCTCTTCCCCAGGGAGACTGGGGTGGGGCGTGAGCCGGGGCTCCCTGAAGCACCCCTTTGTCCACACAGGCACTCCTCAGCTGCTGGCCCTGGTACAGCACTGGGTGCCCGGGGCACGGCTGGTGGAGGAGCTGCCACACGAGCTGGTGCTGGTGCTGCCCTACACGGGTGCCCATGACGGCAGCTTCGCCACACTCTTCCGAG... | TCAACCCTCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCGGCCGCACCTGGCCTACGTTCTTAACCCTGATCTCTGTCTGCCGGGACAGTCCCCTCACAGGTCACCAATGCCTCTTCCCCAGGGAGACTGGGGTGGGGCGTGAGCCGGGGCTCCCTGAAGCACCCCTTTGTCCACACAGGCACTCCTCAGCTGCTGGCCCTGGTACAGCACTGGGTGCCCGGGGCACGGCTGGTGGAGGAGCTGCCACACGAGCTGGTGCTGGTGCTGCCCTACACGGGTGCCCATGACGGCAGCTTCGCCACACTCTTCCGAG... |
Task1_train_46184 | A variant on Chromosome 19 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CCAACCCAAAGCACATTTATTGAGGGCACTGGGGAGCCATGGGTGGTTGTAGAGCAGGAGCAGGGACAGGTGCAAGCAAGCCTGGAGGGTGGATGGAAGCAGCAGCTGATGGGCTGGTCCCCCAGATCGTGCTGCCTGCCCTCTTTGTGGGCCTGGCCCTCGTGTTCAGCCTCATCGTGCCTCCTTTCGGGCACTACCCGGCTCTGCGGCTCAGTCCCACCATGTACGGTGCTCAGGTGTCCTTCTTCAGGTGGGTGCAGAAGGAAGGGGCTGGTGGCAGGAAGACTAGGGACCTGGGGGTACAGCCCTGACCCTACATC... | CCAACCCAAAGCACATTTATTGAGGGCACTGGGGAGCCATGGGTGGTTGTAGAGCAGGAGCAGGGACAGGTGCAAGCAAGCCTGGAGGGTGGATGGAAGCAGCAGCTGATGGGCTGGTCCCCCAGATCGTGCTGCCTGCCCTCTTTGTGGGCCTGGCCCTCGTGTTCAGCCTCATCGTGCCTCCTTTCGGGCACTACCCGGCTCTGCGGCTCAGTCCCACCATGTACGGTGCTCAGGTGTCCTTCTTCAGGTGGGTGCAGAAGGAAGGGGCTGGTGGCAGGAAGACTAGGGACCTGGGGGTACAGCCCTGACCCTACATC... |
Task1_train_46185 | This variant is found on Chromosome 19. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTCCACCCACACCATGGCCCCGCCCCATACTCATGCTGGCTCCACCCACACCATGGCCCCACCCCATACTCATGCTGTCTCCACCCACACCATGGCCCTGCCCCATACTCATGCTGGCTCTACCCACACCATGGCCCCGCCGCATACTCATGCTGGCTCCACCAGTGTGGCCCCGCCCCATACTCATGCTGGCTCCACCCACACCATGGCCCCGCCCCATACTCATGCTGGCTCCACCAGTGTGGCCCCGCCCCATACTCATGCTGTCTCCACCCACACCATGGCCCCGCCCCATACTCATGCTGGCTCCACCCACACTA... | CTCCACCCACACCATGGCCCCGCCCCATACTCATGCTGGCTCCACCCACACCATGGCCCCACCCCATACTCATGCTGTCTCCACCCACACCATGGCCCTGCCCCATACTCATGCTGGCTCTACCCACACCATGGCCCCGCCGCATACTCATGCTGGCTCCACCAGTGTGGCCCCGCCCCATACTCATGCTGGCTCCACCCACACCATGGCCCCGCCCCATACTCATGCTGGCTCCACCAGTGTGGCCCCGCCCCATACTCATGCTGTCTCCACCCACACCATGGCCCCGCCCCATACTCATGCTGGCTCCACCCACACTA... |
Task1_train_46186 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GGTTCTGGGCCTCAGTTTCCCCACCTGTCCTCGACCTGACCCACTTCACGGGGCTGCAGGGCGGGTGATGGGGGGGACCCTACTCTGCCCGGCCCTGCTGGGGCCCGGCCACACCCTAGGGTCTGCAGGAGAGGCGGTGGAGCGGGCTTGCCTTCAGGGAAAAGGGGGCTGCAGGGGCGCAGCTTCGGCCTGTGCGTGTGTCTGGGGTCTGAGGGCGAGGCTCCAGGGGCTTGGTGGCGTCTGAGCGCGTGTGGAGGTCCGGGTCTCTGCGTGTCATCGTGCACGTGTCTGTGCACGCCCACTCGCGTCCGGGAGTGAGA... | GGTTCTGGGCCTCAGTTTCCCCACCTGTCCTCGACCTGACCCACTTCACGGGGCTGCAGGGCGGGTGATGGGGGGGACCCTACTCTGCCCGGCCCTGCTGGGGCCCGGCCACACCCTAGGGTCTGCAGGAGAGGCGGTGGAGCGGGCTTGCCTTCAGGGAAAAGGGGGCTGCAGGGGCGCAGCTTCGGCCTGTGCGTGTGTCTGGGGTCTGAGGGCGAGGCTCCAGGGGCTTGGTGGCGTCTGAGCGCGTGTGGAGGTCCGGGTCTCTGCGTGTCATCGTGCACGTGTCTGTGCACGCCCACTCGCGTCCGGGAGTGAGA... |
Task1_train_46187 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CGGAGGTGCTGGGACCCAGCGGCCTGCAGGCCGGCAGTTCCGTTTTCTCCTCCACGCGGCCGCTGACAGCCCTGCTTCCTGCCGAGTTATTTTCATCTGCTTCCTGTTTGTCCCTGGCAGCCCAGGCGGGCACCTCATGTGCTGCCTTCAGCCCCCGGCTCCTCCCAGAAACCACAGTGCCAGGGTCATGCCAGGCGCTCTGATCTGCTCCCAGCAGCCGCCCATTTTACAGATGACGAAACTAAGTCTCTAGTGAGGCCCTGACCCCTGGCTCACCCAGCCAGGGCAGGGCAGAGCCAGGACTGGACCTCAAGTGGTGG... | CGGAGGTGCTGGGACCCAGCGGCCTGCAGGCCGGCAGTTCCGTTTTCTCCTCCACGCGGCCGCTGACAGCCCTGCTTCCTGCCGAGTTATTTTCATCTGCTTCCTGTTTGTCCCTGGCAGCCCAGGCGGGCACCTCATGTGCTGCCTTCAGCCCCCGGCTCCTCCCAGAAACCACAGTGCCAGGGTCATGCCAGGCGCTCTGATCTGCTCCCAGCAGCCGCCCATTTTACAGATGACGAAACTAAGTCTCTAGTGAGGCCCTGACCCCTGGCTCACCCAGCCAGGGCAGGGCAGAGCCAGGACTGGACCTCAAGTGGTGG... |
Task1_train_46188 | This variant is found on Chromosome 19. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ACCTCATGCCCTGTTCTGCTCCTGATTTTTATCCTCACCTCCATATAGAGAGGCTCACCCGATATCAGTCAGCATGAAGCAGCCTGAACCCCTTTTTTCGGCTGTGCAGGGCTCAGCTGAGGAGATTGAGTAGGTTATTTCATGGACGTCTTGGGAGTGGCTGAGCTGTTGCTGTTACGAACACCATTGCTATGACAAGCTTGTGCCCCTGTCTCAAGGATGCCTGAGGGATCAGTGCCCAAAATAGAACTGCTGGGTCAAGGGGCGTGCGTGTATGAGCTACCCTCCCAGGCCACAGCCCTGCTTTTCCTCTTCTGTGA... | ACCTCATGCCCTGTTCTGCTCCTGATTTTTATCCTCACCTCCATATAGAGAGGCTCACCCGATATCAGTCAGCATGAAGCAGCCTGAACCCCTTTTTTCGGCTGTGCAGGGCTCAGCTGAGGAGATTGAGTAGGTTATTTCATGGACGTCTTGGGAGTGGCTGAGCTGTTGCTGTTACGAACACCATTGCTATGACAAGCTTGTGCCCCTGTCTCAAGGATGCCTGAGGGATCAGTGCCCAAAATAGAACTGCTGGGTCAAGGGGCGTGCGTGTATGAGCTACCCTCCCAGGCCACAGCCCTGCTTTTCCTCTTCTGTGA... |
Task1_train_46189 | A mutation on Chromosome 19 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGGACCACGACAAGGCTCGCTTCCTCGTGGCCAAGGCGGAGGAGGAGCAGGCTGGCAGCGCGCCGGGAGCAGGCAGCACGGCCACCAAGACCCTGGACAAGCGGCGGCGGCTGGAGGAGGAGGCCAAGAACAAGGTGAGGGCGGGTGGAGGCAGGGCTGGAGGTCCCTGGAGGAGGAGATCCAATGCTTGGTGTGACATTTACTACCTCCAGACCTTTGTTTTTGTTTTTTTGTTTTTTTGTTTGTTTTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACAGTCTCGGCTCACTGCAAGCTCCGC... | AGGACCACGACAAGGCTCGCTTCCTCGTGGCCAAGGCGGAGGAGGAGCAGGCTGGCAGCGCGCCGGGAGCAGGCAGCACGGCCACCAAGACCCTGGACAAGCGGCGGCGGCTGGAGGAGGAGGCCAAGAACAAGGTGAGGGCGGGTGGAGGCAGGGCTGGAGGTCCCTGGAGGAGGAGATCCAATGCTTGGTGTGACATTTACTACCTCCAGACCTTTGTTTTTGTTTTTTTGTTTTTTTGTTTGTTTTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACAGTCTCGGCTCACTGCAAGCTCCGC... |
Task1_train_46190 | A mutation on Chromosome 19 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GGCTGGAAATCCCGGATCACGCGCCCCCGGGCGCCGCCCCGCCCCCGCACCTTGGCCTAGCGCGGTGGCGTCACAGTCGCGCAGTCCTGACTACGGCCTCCGGGCCCTTTGTCCCCGCTAGCGGCGCTCGGGGTGGGGGAGCCAGGAGGGGCGGGAGACGGGCGGGTATGGGCCGCGCGGGCGCAGGCTCCCCCGGGCGCCGCAGGCAGCGGTGCCAGAGCCGGGGCAGGCGGCGGCCGCGAGCCCCTCGGCGGCGGAAGGCCCCAGCGTGCAGGCGCAGGAGGGCGCGGCGCCGGCGGAAGAAGCCCTGTCCCCGCAGC... | GGCTGGAAATCCCGGATCACGCGCCCCCGGGCGCCGCCCCGCCCCCGCACCTTGGCCTAGCGCGGTGGCGTCACAGTCGCGCAGTCCTGACTACGGCCTCCGGGCCCTTTGTCCCCGCTAGCGGCGCTCGGGGTGGGGGAGCCAGGAGGGGCGGGAGACGGGCGGGTATGGGCCGCGCGGGCGCAGGCTCCCCCGGGCGCCGCAGGCAGCGGTGCCAGAGCCGGGGCAGGCGGCGGCCGCGAGCCCCTCGGCGGCGGAAGGCCCCAGCGTGCAGGCGCAGGAGGGCGCGGCGCCGGCGGAAGAAGCCCTGTCCCCGCAGC... |
Task1_train_46191 | Mutation context: Chromosome 19. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GAGGCTGGCTTTCCCTGGACCCCTGCCTCCCCAGAACCCCACCCTCCCCTAGGCCCCTGGACCCTGCCCTCCCCTAGACTCCTAGACCCCACCTCCCCCAGCTCTCAGCCACCTCCTCCCCGGGGGTCCTAGACTGGGTCCTCCCCCAGACCCCTGGATGCCACCTCCCTGAGCCCCTAGAAGCCCCCTTCCCCCCTGGGGGTCCTAGACCCGGCCCTCCTCCAGACCACTGAGCCCCACGTTCTCCAGCCCCCATCTACCCCCTCCCCCAGGCTCTTAGATCCGGCCCTCCCTAGACCCCTGCCCCTGCCCCGCCCCCC... | GAGGCTGGCTTTCCCTGGACCCCTGCCTCCCCAGAACCCCACCCTCCCCTAGGCCCCTGGACCCTGCCCTCCCCTAGACTCCTAGACCCCACCTCCCCCAGCTCTCAGCCACCTCCTCCCCGGGGGTCCTAGACTGGGTCCTCCCCCAGACCCCTGGATGCCACCTCCCTGAGCCCCTAGAAGCCCCCTTCCCCCCTGGGGGTCCTAGACCCGGCCCTCCTCCAGACCACTGAGCCCCACGTTCTCCAGCCCCCATCTACCCCCTCCCCCAGGCTCTTAGATCCGGCCCTCCCTAGACCCCTGCCCCTGCCCCGCCCCCC... |
Task1_train_46192 | This variant is found on Chromosome 19. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GTCGCGCCCCCACGTCTCTCCCGCCGCCGAGGCCCCGTGCGGCGCCGGAGAAGCTGCCAGAGAGATGGGCCCAGGACGCGGGACTTAGGCCGGGCTGTGGTCGGGGGACGTGGGGGCGGCGGCGACCAACGCGGGAGTCGCCACGACGGGCTCGGCGAGGCGCGGCGGAAAGAGTCTCTCGTCGAGGCCAGCCGCCAGCTTGTCCAGCACCGACCCGGATGGTAGGACGCACAGGCCCGAGCCGGGGCACCCCCCGCCGCCCGGCTCCTCCTCGATGACGGGGATGGCGGGGTCGTCGCCGGCGCCGCCCAGGGTGCGAC... | GTCGCGCCCCCACGTCTCTCCCGCCGCCGAGGCCCCGTGCGGCGCCGGAGAAGCTGCCAGAGAGATGGGCCCAGGACGCGGGACTTAGGCCGGGCTGTGGTCGGGGGACGTGGGGGCGGCGGCGACCAACGCGGGAGTCGCCACGACGGGCTCGGCGAGGCGCGGCGGAAAGAGTCTCTCGTCGAGGCCAGCCGCCAGCTTGTCCAGCACCGACCCGGATGGTAGGACGCACAGGCCCGAGCCGGGGCACCCCCCGCCGCCCGGCTCCTCCTCGATGACGGGGATGGCGGGGTCGTCGCCGGCGCCGCCCAGGGTGCGAC... |
Task1_train_46193 | Mutation context: Chromosome 19. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GGAGGGCCCTGTGGGGAGGAAGCCTGGTCAGCTCCAGCTAGACCTACTTCTCCTGCAGGAGCCACTGCAGACAAGCTGGGTCTTCCCTGCAGGAGCAGGAGCCCACACAGGGGGCAGTGACTCATGGAGAGGTAGCAGAGCCGGAGGCAGCCTCCACCCGGCTTGGCTCTGCCCAGCGGGCCCCGGGGGCTCTCTCTGGACCTCCATCTCCCATCCCCATGGCGGGGGAGGAGGCCTGGCCCTCTGAGGGTGCGCCTGTACCCATCACAACTGCACACAGCCGGTGCGGCCTGTCCTGCAAGGTAGCGCCAGGCCCTGGA... | GGAGGGCCCTGTGGGGAGGAAGCCTGGTCAGCTCCAGCTAGACCTACTTCTCCTGCAGGAGCCACTGCAGACAAGCTGGGTCTTCCCTGCAGGAGCAGGAGCCCACACAGGGGGCAGTGACTCATGGAGAGGTAGCAGAGCCGGAGGCAGCCTCCACCCGGCTTGGCTCTGCCCAGCGGGCCCCGGGGGCTCTCTCTGGACCTCCATCTCCCATCCCCATGGCGGGGGAGGAGGCCTGGCCCTCTGAGGGTGCGCCTGTACCCATCACAACTGCACACAGCCGGTGCGGCCTGTCCTGCAAGGTAGCGCCAGGCCCTGGA... |
Task1_train_46194 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AAGGCTGTCTTGGGGCAGGGGGGTAGGGGGCCGGGCAGGCTGGGCCGCAGGGTGGGGGCTTCACCCTGCCCTCCTCCCTGCCTCCCTCCCCATGGGCCCCAAGCAGAGAAGGTTACGCCAGCTACTGCCAGTGGAGAGGAGAGCCGGGAGGGAGAGCTGGGAGGCGGTCGGTTCTGAGTCATCCCAGCCTATGTCACTTCTCAGAAACCTCCGCCACCCCCCCCCCCATCCCGGCCACTGGGGAGAGCAGGGCTCTGGCCCATACCCAGAGCAGGGGGCTTGGCGAGGACAGGGTGAGATTCAACCCACACCCACCCTGA... | AAGGCTGTCTTGGGGCAGGGGGGTAGGGGGCCGGGCAGGCTGGGCCGCAGGGTGGGGGCTTCACCCTGCCCTCCTCCCTGCCTCCCTCCCCATGGGCCCCAAGCAGAGAAGGTTACGCCAGCTACTGCCAGTGGAGAGGAGAGCCGGGAGGGAGAGCTGGGAGGCGGTCGGTTCTGAGTCATCCCAGCCTATGTCACTTCTCAGAAACCTCCGCCACCCCCCCCCCCATCCCGGCCACTGGGGAGAGCAGGGCTCTGGCCCATACCCAGAGCAGGGGGCTTGGCGAGGACAGGGTGAGATTCAACCCACACCCACCCTGA... |
Task1_train_46195 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | GCTCATGAATATAAGACGCAGGCGCGCCCTCTGATTGGCCCAGGATGTGTAGGGGGCGGGGCCCGGCGGAAGCGTATATAAGGCCGGGCTCGGGGACGCCCCCCCCTCACTCGCGCGTTAGGAGGCTCGGGTCGTTGTGGTGCGCTGTCTTCCCGCTTGCGTCAGGGACCTGCCCGACTCAGTGGTGAGGGCCCTGGCTGCACCGGCTCCGAGGAGCTCGGGGCGGCGGGCGGCCTGCGGCGGCCAGGCGAGGCGGGGCCGCAGCGGCACGCCCCTGGGAGGGGGCGGGCCCGGGGTGGAGTCCGCCCCGCCGGCGGCGA... | GCTCATGAATATAAGACGCAGGCGCGCCCTCTGATTGGCCCAGGATGTGTAGGGGGCGGGGCCCGGCGGAAGCGTATATAAGGCCGGGCTCGGGGACGCCCCCCCCTCACTCGCGCGTTAGGAGGCTCGGGTCGTTGTGGTGCGCTGTCTTCCCGCTTGCGTCAGGGACCTGCCCGACTCAGTGGTGAGGGCCCTGGCTGCACCGGCTCCGAGGAGCTCGGGGCGGCGGGCGGCCTGCGGCGGCCAGGCGAGGCGGGGCCGCAGCGGCACGCCCCTGGGAGGGGGCGGGCCCGGGGTGGAGTCCGCCCCGCCGGCGGCGA... |
Task1_train_46196 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GTCTAGTTCTCAGAGCCACTGGGTGGCGGCCATTCCCAGCCAGTGAATGCTTTGTCTGTGTCAGCACTGACCGCCCCCTTAAATAGCCAGTTCTCCTAAATGCCACTTCCCCTGCCTGGAAATCCTGCCTTATCACTTCCGGGGCCATCCCTTCCCGATTCCCGGCCTAGGTCCTGGCTATGGAAGTCAGTACCTGCCCTGAGGTGCCCCCCAGGACGGGGCGGCCTCCCTGACAGCCAGCCCCCCCCCCAGTCTCAGGAGGCATTTTACAGTGAGCAGAAGCACGTTCTGGTCCAGCAACAAGTAGATGTCAGTTGGTT... | GTCTAGTTCTCAGAGCCACTGGGTGGCGGCCATTCCCAGCCAGTGAATGCTTTGTCTGTGTCAGCACTGACCGCCCCCTTAAATAGCCAGTTCTCCTAAATGCCACTTCCCCTGCCTGGAAATCCTGCCTTATCACTTCCGGGGCCATCCCTTCCCGATTCCCGGCCTAGGTCCTGGCTATGGAAGTCAGTACCTGCCCTGAGGTGCCCCCCAGGACGGGGCGGCCTCCCTGACAGCCAGCCCCCCCCCCAGTCTCAGGAGGCATTTTACAGTGAGCAGAAGCACGTTCTGGTCCAGCAACAAGTAGATGTCAGTTGGTT... |
Task1_train_46197 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | TGAAGGCTCAGCTTTCTGGGTAAAAATTCACCCTGTTCACCATGTTTTTCTTCATACAAGGGAACGCGAATCCCCTGAGCTGAAGGAGAAGGAAAAATGGATCCGCTTTCTTAAACCTTTCCAGAATTTGCCCCTAGAACCACTCCTATTCTTGACGCCCAGAATGGTCAGTGGTGAGCATCAAGGTCATCTCGTACCCCCGTGGCCTCCAGTACACAAGACGAGGAAGGACTTTGCTGCCATAAGGGGGGAGGTCCTCCTTTTTCCTTTCCTCTTCCTATAGTAAGATTTGCTGTGGTACTGTCGCTGCCTGGCCAGTC... | TGAAGGCTCAGCTTTCTGGGTAAAAATTCACCCTGTTCACCATGTTTTTCTTCATACAAGGGAACGCGAATCCCCTGAGCTGAAGGAGAAGGAAAAATGGATCCGCTTTCTTAAACCTTTCCAGAATTTGCCCCTAGAACCACTCCTATTCTTGACGCCCAGAATGGTCAGTGGTGAGCATCAAGGTCATCTCGTACCCCCGTGGCCTCCAGTACACAAGACGAGGAAGGACTTTGCTGCCATAAGGGGGGAGGTCCTCCTTTTTCCTTTCCTCTTCCTATAGTAAGATTTGCTGTGGTACTGTCGCTGCCTGGCCAGTC... |
Task1_train_46198 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GTCTCCCTCATCACCGACTACAGGGTCCGGTTAGGTACGTGGGGTGCTGGGGAGGGGTGGAGCTGGGCAGCAGGCGTCCAGCCTCTGAAGACCCCTTGGACGGGCTGGGCCGGAGCTGCCTGGAGGCGGGGCATATTTCCGTGGGCCTGGGGCATTCCCTGTGGGTGGGCTGGGGTTCTGGCCTGGCCTGATTATTTCCTAAACAGAGACGCCGGGCCAGCCCCTGGAACACACTTCCTGGGACTCCTCTTAGGTCTACACAGTGCTCTCTCCCCTCCACCCCCTGCAGGCTGCGGGTCTTTTGCTGGCTCTTTCCTGGA... | GTCTCCCTCATCACCGACTACAGGGTCCGGTTAGGTACGTGGGGTGCTGGGGAGGGGTGGAGCTGGGCAGCAGGCGTCCAGCCTCTGAAGACCCCTTGGACGGGCTGGGCCGGAGCTGCCTGGAGGCGGGGCATATTTCCGTGGGCCTGGGGCATTCCCTGTGGGTGGGCTGGGGTTCTGGCCTGGCCTGATTATTTCCTAAACAGAGACGCCGGGCCAGCCCCTGGAACACACTTCCTGGGACTCCTCTTAGGTCTACACAGTGCTCTCTCCCCTCCACCCCCTGCAGGCTGCGGGTCTTTTGCTGGCTCTTTCCTGGA... |
Task1_train_46199 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TAATGACCCTTTATTTTATTTTTTGAGATGGAGTCTCCCTCTGTCACCCAAGCTGGAGTGCAGTGGCGCAGCCTCTGCTCACTGCAACCTCTACCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGATTACAGGTACCTGCTACTACACCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGCCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTCGGCCTCCTGAAGTGCTGGAATTACAGGCATGAGCCACCACGCCCAGGCATTAATGATCCCTT... | TAATGACCCTTTATTTTATTTTTTGAGATGGAGTCTCCCTCTGTCACCCAAGCTGGAGTGCAGTGGCGCAGCCTCTGCTCACTGCAACCTCTACCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGATTACAGGTACCTGCTACTACACCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGCCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTCGGCCTCCTGAAGTGCTGGAATTACAGGCATGAGCCACCACGCCCAGGCATTAATGATCCCTT... |
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