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_41000 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ATAAAATATCTGTCTCCTCCTTTATCTTGTAAGCAAACAAATAGAACTTTTCATCATGAGCTAATGAATGTGGCAAGTGACTGCCTACCATGAATACATTCCAGATTTCTGACAGAGGAGGAATTGTGTTGAGCTCTCTAAGTAAACTTGTGATCCTCTCAGTCACCTCTCAACTATTGAAGGGCCAATTATCCAGTTCCTAGATTTACACAGACCTTTTGCTTTTCTTCTTTCTCGCAATTTTTCTCTCTCCTTCCCTTCCAATTCAGATCTCATTATTACCTCAAAAGGAAAAATGGTGCTCTAAGAGACATATTGAC... | ATAAAATATCTGTCTCCTCCTTTATCTTGTAAGCAAACAAATAGAACTTTTCATCATGAGCTAATGAATGTGGCAAGTGACTGCCTACCATGAATACATTCCAGATTTCTGACAGAGGAGGAATTGTGTTGAGCTCTCTAAGTAAACTTGTGATCCTCTCAGTCACCTCTCAACTATTGAAGGGCCAATTATCCAGTTCCTAGATTTACACAGACCTTTTGCTTTTCTTCTTTCTCGCAATTTTTCTCTCTCCTTCCCTTCCAATTCAGATCTCATTATTACCTCAAAAGGAAAAATGGTGCTCTAAGAGACATATTGAC... |
Task1_train_41001 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | AGAGTAAGACCCTGTCTCTTAAAAAAAAAAGAAAAGAAAGAAAGAAGCTAGCTATTTTGAAATGTAATTTTCAAAATTTACATGCAGAACTAACTGGTCAGGTTTTTCAGTCTTAAGACATTTTGATGAGTTGAGGGTTATGTAAGTCATTACTATGAAAACATAAAGTAATTGTGCCATAATTACATAAAAATCTTTGTGCCTTTTCTTCATAGGCATGCATTCCTCAGCAGCAACTGAGCTGTTTGCTACTGGACCTTTGCCAAGCACTGGAACACTTCCACCATCTCTCTCTGCTTATCAGCATCCCACCACCTTCA... | AGAGTAAGACCCTGTCTCTTAAAAAAAAAAGAAAAGAAAGAAAGAAGCTAGCTATTTTGAAATGTAATTTTCAAAATTTACATGCAGAACTAACTGGTCAGGTTTTTCAGTCTTAAGACATTTTGATGAGTTGAGGGTTATGTAAGTCATTACTATGAAAACATAAAGTAATTGTGCCATAATTACATAAAAATCTTTGTGCCTTTTCTTCATAGGCATGCATTCCTCAGCAGCAACTGAGCTGTTTGCTACTGGACCTTTGCCAAGCACTGGAACACTTCCACCATCTCTCTCTGCTTATCAGCATCCCACCACCTTCA... |
Task1_train_41002 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ACGAAGGCACCGTTTAAAACGACATAATGACTGCTTTGTTGGTTCAGAAGCTGTGGATGTCATTTTTTCTCACCTAATTCAGAATAAGTATTTTGGTGATGTAGATATTCCTCGAGCCAAAGTGGTGAGAGTGTGTCAAGCGCTTATGGACTACAAAGTATTTGAAGCAGTTCCAACCAAAGTCTTTGGAAAAGACAAAAAACCTACATTTGAAGATAGTAGTTGCAGCCTTTATAGATTCACCACAATACCTAACCAAGACAGTCAGTTAGGCAAAGAGAACAAACTATATTCACCTGCCAGGTTGGTATATAATGTTA... | ACGAAGGCACCGTTTAAAACGACATAATGACTGCTTTGTTGGTTCAGAAGCTGTGGATGTCATTTTTTCTCACCTAATTCAGAATAAGTATTTTGGTGATGTAGATATTCCTCGAGCCAAAGTGGTGAGAGTGTGTCAAGCGCTTATGGACTACAAAGTATTTGAAGCAGTTCCAACCAAAGTCTTTGGAAAAGACAAAAAACCTACATTTGAAGATAGTAGTTGCAGCCTTTATAGATTCACCACAATACCTAACCAAGACAGTCAGTTAGGCAAAGAGAACAAACTATATTCACCTGCCAGGTTGGTATATAATGTTA... |
Task1_train_41003 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | GGCTCTAGCCCATGAAATTGTAGTAAATGGAGACTTTCAGATTAAACCAGTTGAATTACCAGAAAACAGGTAAGGTGGTTGCTAAATTATCTTGCTTAGTAGAACACTGTCATTTCCCAGTTTTGAAAATGTTTCCTTCAGTTGATACCAATATATTCAAACGTATTTTTCCTTTTGTACATTATTGCTAAAAAATATTCCTGAACAAGGAACAACCTAAAAATCAAATAAAAGCTCTAAAAATCTTTTGTGAAAGTCTGCCTACTCAGTAGGATCTAGCTGCCTCATCTTGTGTTTTCATTGCCTTGTTTCATTCACTT... | GGCTCTAGCCCATGAAATTGTAGTAAATGGAGACTTTCAGATTAAACCAGTTGAATTACCAGAAAACAGGTAAGGTGGTTGCTAAATTATCTTGCTTAGTAGAACACTGTCATTTCCCAGTTTTGAAAATGTTTCCTTCAGTTGATACCAATATATTCAAACGTATTTTTCCTTTTGTACATTATTGCTAAAAAATATTCCTGAACAAGGAACAACCTAAAAATCAAATAAAAGCTCTAAAAATCTTTTGTGAAAGTCTGCCTACTCAGTAGGATCTAGCTGCCTCATCTTGTGTTTTCATTGCCTTGTTTCATTCACTT... |
Task1_train_41004 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | TTTTGTATTTGTAGTAGAGACAGGGTTTCACCTTGTTGGTCAGGCTGGTCTCAAACTCCTGACCTTGTTATCTATCTGCCTCAGCCTCCCAAAGTGCTGGGACTACAGGTGTGAGCCACTGCGCCAGCCATTGTTGTTTTTTGAGACGGAATCTTGCTCAGTTGCCTAGGCTGGAGTGCAGTGGTGCAGTCTCAGCTCACTGCAGCCTCCATCTCCTAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGACTATAAAGCATGCACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATAGTATT... | TTTTGTATTTGTAGTAGAGACAGGGTTTCACCTTGTTGGTCAGGCTGGTCTCAAACTCCTGACCTTGTTATCTATCTGCCTCAGCCTCCCAAAGTGCTGGGACTACAGGTGTGAGCCACTGCGCCAGCCATTGTTGTTTTTTGAGACGGAATCTTGCTCAGTTGCCTAGGCTGGAGTGCAGTGGTGCAGTCTCAGCTCACTGCAGCCTCCATCTCCTAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGACTATAAAGCATGCACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATAGTATT... |
Task1_train_41005 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | CAAATGCCTCAGTCTACAAGGACTCTTTACTATTCATATATGTAGATGTTTAATATATGTCAGTCAGTACCCTTAAAAAGCAAAATGGACAGTCTGGAGGAATCTTCTCTGGATGATCAAAATCCAAACAAGCCAAGACGGGATAAATAGCAAAGGGGTGAGCTGTAGTTACTTACAAATTGAAGGGTTCTCAAAACCTATAAGAAATACTCTTTTAAGGCCAAGAAAAACTAGTTGTACCAAGGAGTTTATAAGGCATAGAGTTTATATTAGTCCCTAAAGACTTGCTTTGGAGGTCTCTAATGTGACTTAGTATCTTA... | CAAATGCCTCAGTCTACAAGGACTCTTTACTATTCATATATGTAGATGTTTAATATATGTCAGTCAGTACCCTTAAAAAGCAAAATGGACAGTCTGGAGGAATCTTCTCTGGATGATCAAAATCCAAACAAGCCAAGACGGGATAAATAGCAAAGGGGTGAGCTGTAGTTACTTACAAATTGAAGGGTTCTCAAAACCTATAAGAAATACTCTTTTAAGGCCAAGAAAAACTAGTTGTACCAAGGAGTTTATAAGGCATAGAGTTTATATTAGTCCCTAAAGACTTGCTTTGGAGGTCTCTAATGTGACTTAGTATCTTA... |
Task1_train_41006 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ATTCTTGTTTGGCTTATAGGGTTAGGTCTTCAGTCTTTTCTCCTAGGAGCCTGCCTTTACTTCTTTGAGTTCAGTTTGGGCCTCCTCTCAGCCAAAAGTACAGAACTCTTTCCCTCAATTATGACCACTGGAGATGGAAATCCCCTGGCCCTCCACTTCCTGCCCTGGAGCTGCTGTTCCCAGTGTTGATGCCACAAACCTGGAGGGTGAGGCACAACAAGCAGCTGTGACATCATCAACTGAGATTCAGGACTGACCTTAGCTCTGACCTAAGAGGAAGAAAATTAAGCAGCAGATGCTCTTCAATTCCCAGCATCTCC... | ATTCTTGTTTGGCTTATAGGGTTAGGTCTTCAGTCTTTTCTCCTAGGAGCCTGCCTTTACTTCTTTGAGTTCAGTTTGGGCCTCCTCTCAGCCAAAAGTACAGAACTCTTTCCCTCAATTATGACCACTGGAGATGGAAATCCCCTGGCCCTCCACTTCCTGCCCTGGAGCTGCTGTTCCCAGTGTTGATGCCACAAACCTGGAGGGTGAGGCACAACAAGCAGCTGTGACATCATCAACTGAGATTCAGGACTGACCTTAGCTCTGACCTAAGAGGAAGAAAATTAAGCAGCAGATGCTCTTCAATTCCCAGCATCTCC... |
Task1_train_41007 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ACATTTAAGACAAACCATGATAGGTCTGGAGATAAGATTTGAAAATTTGGCTGACAGTTAGCAGCCAAGGAGGGCATCTGCAGGTGGAGTTTGCAACTAGGAACTCTATAGACTCTAGCTAATTATTGTACAGATATAGAAAAGCCTCTTTTTTGGGAAAAGGGTGATGACAAATCCAAGGTATAGTGGATAAAACAGGCACAATTTCAAGTCCAGCTGAATAAACCTGGGCAAGCAGACACACACATGCATGTGTGCATGCTGTCAGTGCTACCACATACACTTCCATCCCTCATACAGAGAGTTCACCTAGCACCTAG... | ACATTTAAGACAAACCATGATAGGTCTGGAGATAAGATTTGAAAATTTGGCTGACAGTTAGCAGCCAAGGAGGGCATCTGCAGGTGGAGTTTGCAACTAGGAACTCTATAGACTCTAGCTAATTATTGTACAGATATAGAAAAGCCTCTTTTTTGGGAAAAGGGTGATGACAAATCCAAGGTATAGTGGATAAAACAGGCACAATTTCAAGTCCAGCTGAATAAACCTGGGCAAGCAGACACACACATGCATGTGTGCATGCTGTCAGTGCTACCACATACACTTCCATCCCTCATACAGAGAGTTCACCTAGCACCTAG... |
Task1_train_41008 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGGAGCATTAGGCTATACCATATACCCTGGGTGTGCAGTAGGCTATACCATTTAGGTTTGTGTATGCACTCTGCTGTTCACACAATGATGAAATCACCTAGTGACACATTTCGCAGAACATATCCCCATCCACAGTGACAAGTGACTGTATTTTAAAGCTGTTCTTTATATAAAAGATAAACTTAAAAAAATACAGTAGAGAATTTTAAACTCCATCCTTTCTTACCTCATCCAGCTTTCATTGCCTTTCTTTTGATTAGACTCAGGATTCTCTTCAAATTCAGATAAAATAACACTGCCTCCTGAGCTGTGTTAATGAC... | AGGAGCATTAGGCTATACCATATACCCTGGGTGTGCAGTAGGCTATACCATTTAGGTTTGTGTATGCACTCTGCTGTTCACACAATGATGAAATCACCTAGTGACACATTTCGCAGAACATATCCCCATCCACAGTGACAAGTGACTGTATTTTAAAGCTGTTCTTTATATAAAAGATAAACTTAAAAAAATACAGTAGAGAATTTTAAACTCCATCCTTTCTTACCTCATCCAGCTTTCATTGCCTTTCTTTTGATTAGACTCAGGATTCTCTTCAAATTCAGATAAAATAACACTGCCTCCTGAGCTGTGTTAATGAC... |
Task1_train_41009 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | AGCATTTCACATATATGATGAAAATTTCCTATGAGCTGATTTTAGTGCTATAAAAGCCCATTTAATTTTAAAAGATGCGCCAATGAGTGGTTTATGGTGGTCACATAAAATGGTAGTGCATGGATTAGTAAAATTCTACTAGAAAGAACATAGTCCTTTATGTCTTTTTGATCAAAAATATTTCATCTTGAGTCCTGCATTCACCTATTTTTAACTTTGCTAGTTTTTTTAAAGAGCCAGTTGGAAATGGTTATTTTAGCTCATTTGGTAGAAAGCTTTATTTTATACATACACAAACTATTTCTGAACATGCAAATAAA... | AGCATTTCACATATATGATGAAAATTTCCTATGAGCTGATTTTAGTGCTATAAAAGCCCATTTAATTTTAAAAGATGCGCCAATGAGTGGTTTATGGTGGTCACATAAAATGGTAGTGCATGGATTAGTAAAATTCTACTAGAAAGAACATAGTCCTTTATGTCTTTTTGATCAAAAATATTTCATCTTGAGTCCTGCATTCACCTATTTTTAACTTTGCTAGTTTTTTTAAAGAGCCAGTTGGAAATGGTTATTTTAGCTCATTTGGTAGAAAGCTTTATTTTATACATACACAAACTATTTCTGAACATGCAAATAAA... |
Task1_train_41010 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | ATTGTGATTTGAAATTGTGGATCTTCAGTCTTTAGCTATTTGACATATCTGCAGCTTTTGTACATTGCTTCCATTCAGTTACACAAATGTCCACTTGTCCATTTAGAAACTAAAGACCTTCAGTATCACATAAAACTGATCATCAGTTGTTCTTTGGATATAACACATTAGACTTGCTGTGGTCTACTCAAATGGAGAGTTCCCAGTAATAAAGGCTGCCAGAAACTTACCCATGCTTCAAGCTAATTCCTCCTCCAGTCCCAGTGACCCAGCCTAAATGGTAAAACTGTTTGCAAAGTTCTGGGATCAGGTATCTTGGA... | ATTGTGATTTGAAATTGTGGATCTTCAGTCTTTAGCTATTTGACATATCTGCAGCTTTTGTACATTGCTTCCATTCAGTTACACAAATGTCCACTTGTCCATTTAGAAACTAAAGACCTTCAGTATCACATAAAACTGATCATCAGTTGTTCTTTGGATATAACACATTAGACTTGCTGTGGTCTACTCAAATGGAGAGTTCCCAGTAATAAAGGCTGCCAGAAACTTACCCATGCTTCAAGCTAATTCCTCCTCCAGTCCCAGTGACCCAGCCTAAATGGTAAAACTGTTTGCAAAGTTCTGGGATCAGGTATCTTGGA... |
Task1_train_41011 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ATACCATCTTTGTCTCTTTGCTAATTTGTCTCTTCCACTGTACAGCATGTTCTAGGGGAGAAGGAACCAGATGCAGCTTGCACTTATAAATCCACAATGCCTGGCACATAGTAGGCGCTCACTAAATATTCGTTGAATTAATCACTTACAGTTGAACATTCCCCTTCCTTAAGGCCAAAGAGACTGTCTCTTTCCATTGCCCATGACCCCCTAAAACTACAATGAAATTTTATGACTTCTTAAAACTTTTCTTATTGCTGTTTTTATGTATTTGTACAAAACCAGACAAATACAAATATCTAGAGGGGCTCATGTATTTA... | ATACCATCTTTGTCTCTTTGCTAATTTGTCTCTTCCACTGTACAGCATGTTCTAGGGGAGAAGGAACCAGATGCAGCTTGCACTTATAAATCCACAATGCCTGGCACATAGTAGGCGCTCACTAAATATTCGTTGAATTAATCACTTACAGTTGAACATTCCCCTTCCTTAAGGCCAAAGAGACTGTCTCTTTCCATTGCCCATGACCCCCTAAAACTACAATGAAATTTTATGACTTCTTAAAACTTTTCTTATTGCTGTTTTTATGTATTTGTACAAAACCAGACAAATACAAATATCTAGAGGGGCTCATGTATTTA... |
Task1_train_41012 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCACTAAATATTCGTTGAATTAATCACTTACAGTTGAACATTCCCCTTCCTTAAGGCCAAAGAGACTGTCTCTTTCCATTGCCCATGACCCCCTAAAACTACAATGAAATTTTATGACTTCTTAAAACTTTTCTTATTGCTGTTTTTATGTATTTGTACAAAACCAGACAAATACAAATATCTAGAGGGGCTCATGTATTTAACTAGATATGCAAATCCAGTGTGAGTAGTGGAAGCTGTGGTAACCTGGCCAGCACCCTCTGTAAAGGTGGTGTTCACTAGTAACCGCAATCCAGATCCCATGAAAAAATAAGGGCCCA... | TCACTAAATATTCGTTGAATTAATCACTTACAGTTGAACATTCCCCTTCCTTAAGGCCAAAGAGACTGTCTCTTTCCATTGCCCATGACCCCCTAAAACTACAATGAAATTTTATGACTTCTTAAAACTTTTCTTATTGCTGTTTTTATGTATTTGTACAAAACCAGACAAATACAAATATCTAGAGGGGCTCATGTATTTAACTAGATATGCAAATCCAGTGTGAGTAGTGGAAGCTGTGGTAACCTGGCCAGCACCCTCTGTAAAGGTGGTGTTCACTAGTAACCGCAATCCAGATCCCATGAAAAAATAAGGGCCCA... |
Task1_train_41013 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TCTTTCCATTGCCCATGACCCCCTAAAACTACAATGAAATTTTATGACTTCTTAAAACTTTTCTTATTGCTGTTTTTATGTATTTGTACAAAACCAGACAAATACAAATATCTAGAGGGGCTCATGTATTTAACTAGATATGCAAATCCAGTGTGAGTAGTGGAAGCTGTGGTAACCTGGCCAGCACCCTCTGTAAAGGTGGTGTTCACTAGTAACCGCAATCCAGATCCCATGAAAAAATAAGGGCCCAATGTCACCATGTGTTCTGAGGTTTTAAAAGAAGCTGAAATGATTCTGGATTTTGAAATGTTGGCTTGGCA... | TCTTTCCATTGCCCATGACCCCCTAAAACTACAATGAAATTTTATGACTTCTTAAAACTTTTCTTATTGCTGTTTTTATGTATTTGTACAAAACCAGACAAATACAAATATCTAGAGGGGCTCATGTATTTAACTAGATATGCAAATCCAGTGTGAGTAGTGGAAGCTGTGGTAACCTGGCCAGCACCCTCTGTAAAGGTGGTGTTCACTAGTAACCGCAATCCAGATCCCATGAAAAAATAAGGGCCCAATGTCACCATGTGTTCTGAGGTTTTAAAAGAAGCTGAAATGATTCTGGATTTTGAAATGTTGGCTTGGCA... |
Task1_train_41014 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGGTTTTAAAAGAAGCTGAAATGATTCTGGATTTTGAAATGTTGGCTTGGCAGGGCGTGGTGGCTTACACCTGTAATCCCAGCACTTTGGGCAGCTTAGGGGGGTGGATCACCTGAGATAACGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCAGTCTCTACTAAAAATACAAAAATTAACTGGGTGTGGTGACATGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAAAATCGCTTGAACCAAGGAGGCAGAAGTTGCAGTGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGCAACAAGAGCAA... | AGGTTTTAAAAGAAGCTGAAATGATTCTGGATTTTGAAATGTTGGCTTGGCAGGGCGTGGTGGCTTACACCTGTAATCCCAGCACTTTGGGCAGCTTAGGGGGGTGGATCACCTGAGATAACGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCAGTCTCTACTAAAAATACAAAAATTAACTGGGTGTGGTGACATGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAAAATCGCTTGAACCAAGGAGGCAGAAGTTGCAGTGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGCAACAAGAGCAA... |
Task1_train_41015 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | TATTTTTCCTCAGTTTTTTGAAGATATTACTTCATTGTTTTCTGACCTCTGTTGCAGCTGCTGAGAAGTGTACTCTCAGTCTTTCCATTGAGGTAATCTGTTTTTTTTCCCCTTTGATAGATTTTTAAAAGATTATGTTTTTATCGTTGATAGAATGCGGTTTCTTTACATTGTATCTAATATGGATTCATGTTTATATAGTCTAATACTCTTTTTTCTGTTTAAGTTTTTATCAAGGTATAACTTGCATAAACTTTAGGCTCAATTAAATTTTGTATACATGTATACCCATGTTACCACCACCTAGATCAAGATTTAGA... | TATTTTTCCTCAGTTTTTTGAAGATATTACTTCATTGTTTTCTGACCTCTGTTGCAGCTGCTGAGAAGTGTACTCTCAGTCTTTCCATTGAGGTAATCTGTTTTTTTTCCCCTTTGATAGATTTTTAAAAGATTATGTTTTTATCGTTGATAGAATGCGGTTTCTTTACATTGTATCTAATATGGATTCATGTTTATATAGTCTAATACTCTTTTTTCTGTTTAAGTTTTTATCAAGGTATAACTTGCATAAACTTTAGGCTCAATTAAATTTTGTATACATGTATACCCATGTTACCACCACCTAGATCAAGATTTAGA... |
Task1_train_41016 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | AGCGGCCAATACTGATTGGTGCTGATGTGCGAGCTCGGAAAAGGGAGTGTCGGTTCAAAGTTGTTGGCTACAGCGGGTTCCTCTTTCCGCTGGAATCACATCCTCTGTGGCTCGGAGACATTCCCAGAGATTTACATAAAGCAGCGTGAATCACCCAGACAGAAACTGAGAAAGCAAAGGGACCCTGCCTGATCCTAGCCTGGCGGAGCTCGGAAAGAGGTGGAAATCTGTCTGAAGTTTGCAGGAGACCCGCGCTGCCTAGGCAAAGGGACCCGGCGACCAAGACACCCCCGCGAGGGCCCAGGGCGCGTCCCTCCCGC... | AGCGGCCAATACTGATTGGTGCTGATGTGCGAGCTCGGAAAAGGGAGTGTCGGTTCAAAGTTGTTGGCTACAGCGGGTTCCTCTTTCCGCTGGAATCACATCCTCTGTGGCTCGGAGACATTCCCAGAGATTTACATAAAGCAGCGTGAATCACCCAGACAGAAACTGAGAAAGCAAAGGGACCCTGCCTGATCCTAGCCTGGCGGAGCTCGGAAAGAGGTGGAAATCTGTCTGAAGTTTGCAGGAGACCCGCGCTGCCTAGGCAAAGGGACCCGGCGACCAAGACACCCCCGCGAGGGCCCAGGGCGCGTCCCTCCCGC... |
Task1_train_41017 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGTCAGACTGAGTGACCTTAGCTGCTAGGAAGCATCTTATTGTGCCTTCCCTCCCTCTCTGACTTTGGCCTTGACACTGATCTGAGCCTGCAGATAACAGAAAGGAGGAGCTTATCTAGACAGGAGTGGTGGAAGTAGCCAGTAACAAATCATTGAAGTGAGGAGAATGAAGGTAAAGAAATTGATCAGCTTTAAATAGGAGGTGACTCCGCATTCCTCTTGCTTGGAAATGATCCCCAGGATGGAATTGTGTCCAGGGTGTGAGGTTGTTTGTGAATCAGTCCTTTCCAGATAGAATATATGAGGCTTGAAACTACATA... | AGTCAGACTGAGTGACCTTAGCTGCTAGGAAGCATCTTATTGTGCCTTCCCTCCCTCTCTGACTTTGGCCTTGACACTGATCTGAGCCTGCAGATAACAGAAAGGAGGAGCTTATCTAGACAGGAGTGGTGGAAGTAGCCAGTAACAAATCATTGAAGTGAGGAGAATGAAGGTAAAGAAATTGATCAGCTTTAAATAGGAGGTGACTCCGCATTCCTCTTGCTTGGAAATGATCCCCAGGATGGAATTGTGTCCAGGGTGTGAGGTTGTTTGTGAATCAGTCCTTTCCAGATAGAATATATGAGGCTTGAAACTACATA... |
Task1_train_41018 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGCTTCTTTTGTTAATAAAGTTTAACAAAACTGTTGAACTCATTCTGAGCAGGGGGTGAAGGGGCAAAGACTGTACAGGAAAACAGGACATAAGTCTGCTTTCCTTAAAAGAAAAAAGTTAAGAGACAGGACAAGCCATTTCTTTTCTGCCTCTTCGTATTACAAGTTCCTTGTTGCTATGCCTGTTGCCTGCAGATAGCTGCTAACACCTCCCGTGCCCTCTCGATGGCTTGCCTCCATGCCCATCTGAGTGGCTTAACTCACTCTTCTGACCACAACAGCATGTTTGATTTGGAGGTGAGACTTCGGTTCCTCCTTCT... | TGCTTCTTTTGTTAATAAAGTTTAACAAAACTGTTGAACTCATTCTGAGCAGGGGGTGAAGGGGCAAAGACTGTACAGGAAAACAGGACATAAGTCTGCTTTCCTTAAAAGAAAAAAGTTAAGAGACAGGACAAGCCATTTCTTTTCTGCCTCTTCGTATTACAAGTTCCTTGTTGCTATGCCTGTTGCCTGCAGATAGCTGCTAACACCTCCCGTGCCCTCTCGATGGCTTGCCTCCATGCCCATCTGAGTGGCTTAACTCACTCTTCTGACCACAACAGCATGTTTGATTTGGAGGTGAGACTTCGGTTCCTCCTTCT... |
Task1_train_41019 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | CTCACTTTGACACTGATGTTAGCATTACCTTTTTTCACATGCGATCCCTATTTATTATGGAATATAATACCTGAGCCTTCTCCCTGGCTTTCCTCGCTGCTGGCCTCGCTGGCTCCAGCCCATTCTGCCACACTTCTGCCCAAGGAAGCTTCCTGAGCACAGTCCATCTTGCCCTATGACCTTCGATGTTAACTGCGTCCCCGCAGCTGTGCTGTGACCTGGTACCACAGGTGCTTCCATCTGCCTGCCGGGGCACCTCTCCTGGAGTCTGTTCCAGCCAGGCTGTGACCTGATGGTGCACCTGTCTCAGCAGCTTTCTC... | CTCACTTTGACACTGATGTTAGCATTACCTTTTTTCACATGCGATCCCTATTTATTATGGAATATAATACCTGAGCCTTCTCCCTGGCTTTCCTCGCTGCTGGCCTCGCTGGCTCCAGCCCATTCTGCCACACTTCTGCCCAAGGAAGCTTCCTGAGCACAGTCCATCTTGCCCTATGACCTTCGATGTTAACTGCGTCCCCGCAGCTGTGCTGTGACCTGGTACCACAGGTGCTTCCATCTGCCTGCCGGGGCACCTCTCCTGGAGTCTGTTCCAGCCAGGCTGTGACCTGATGGTGCACCTGTCTCAGCAGCTTTCTC... |
Task1_train_41020 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | CCTAGGCCTTTTACGAAAGAAGGAAAAGAGAGCTACTTCCTGGCCGGACCTCATTGCCAAGGTTTTCCGGATCGATGTGAAGGCAGATGTTGACTCGATCCACCCCACTGAGTTCTGCCATAACTGCTGGAGCATCATGCACAGGAAGTTTAGCAGTGCCCCATGTGAGGTTTACTTCCCGAGGAACGTGACCATGGAGTGGCACCCCCACACACCATCCTGTGACATCTGCAACACTGCCCGTCGGGGACTCAAGAGGAAGAGTCTTCAGCCAAACTTGCAGCTCAGCAAAAAACTCAAAACTGTGCTTGACCAAGCAA... | CCTAGGCCTTTTACGAAAGAAGGAAAAGAGAGCTACTTCCTGGCCGGACCTCATTGCCAAGGTTTTCCGGATCGATGTGAAGGCAGATGTTGACTCGATCCACCCCACTGAGTTCTGCCATAACTGCTGGAGCATCATGCACAGGAAGTTTAGCAGTGCCCCATGTGAGGTTTACTTCCCGAGGAACGTGACCATGGAGTGGCACCCCCACACACCATCCTGTGACATCTGCAACACTGCCCGTCGGGGACTCAAGAGGAAGAGTCTTCAGCCAAACTTGCAGCTCAGCAAAAAACTCAAAACTGTGCTTGACCAAGCAA... |
Task1_train_41021 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GTGTCAGTATGATAAATGTTGTGTTCTGTTACTTTCTGTATGTGGACATCTTTTTTGAGAAGCTTGTGTATGTTGACTAAGTTAACTAAGGGCATTTTCAGAATTCTTGTCTTCCTACATAGAGGATTCTGACTTCTTCAGCTCAGATTCCCCTTTCTCTTCAATGGTAGTTAGACTAAAATATTAGAAGAATCCATTCTGTTCTTACTTTCTTCTCAACAGAAACAATTAGTTGCTCAAAAAATTCACATAGAAGAGAATGAGGACAGAGACACAGGACTGGAACAGAGACATAATAAAGAAGACCCAGACTGCATCAA... | GTGTCAGTATGATAAATGTTGTGTTCTGTTACTTTCTGTATGTGGACATCTTTTTTGAGAAGCTTGTGTATGTTGACTAAGTTAACTAAGGGCATTTTCAGAATTCTTGTCTTCCTACATAGAGGATTCTGACTTCTTCAGCTCAGATTCCCCTTTCTCTTCAATGGTAGTTAGACTAAAATATTAGAAGAATCCATTCTGTTCTTACTTTCTTCTCAACAGAAACAATTAGTTGCTCAAAAAATTCACATAGAAGAGAATGAGGACAGAGACACAGGACTGGAACAGAGACATAATAAAGAAGACCCAGACTGCATCAA... |
Task1_train_41022 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGCCGAGGTGGGTGCATCACAAGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCAGGAGGCGGAACTTGTGGTGAGCAGAGATCGCGCCACTGCACTCCAGCTTGGGGACTCTCGCTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAACCAGAGACATGGGACCACTCCTTCTAGGTCTCAGCAGGACGGAAATCCATAGAAT... | GGCCGAGGTGGGTGCATCACAAGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCAGGAGGCGGAACTTGTGGTGAGCAGAGATCGCGCCACTGCACTCCAGCTTGGGGACTCTCGCTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAACCAGAGACATGGGACCACTCCTTCTAGGTCTCAGCAGGACGGAAATCCATAGAAT... |
Task1_train_41023 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | CAGAGGGTACACTGTGTAAGGGTGTCTCCTTTGTGGACTGATTCGAGTGGCTCCCTCCCAAACGAAGGCTCACCCTTGTCTGCTTTTTGGTATGGCTAATGGTTATGTTGAATGTAATGTGTTCAAAACCAACCTGAGACTTTCTCTCATTTGAAAAGTTCAGATCTTAGGAACAGTATGTGAAATGTGATCATTGAACATCACTTTCCATCAGTGCTGATACATTTCGGAATTCTCTTTCACTTGTGAGGTGGATTCCTGCTTCATGTTTCCAGGTGGAACTATAGTGTTTACCTATTCTCTTCCACTGATCTAGCACC... | CAGAGGGTACACTGTGTAAGGGTGTCTCCTTTGTGGACTGATTCGAGTGGCTCCCTCCCAAACGAAGGCTCACCCTTGTCTGCTTTTTGGTATGGCTAATGGTTATGTTGAATGTAATGTGTTCAAAACCAACCTGAGACTTTCTCTCATTTGAAAAGTTCAGATCTTAGGAACAGTATGTGAAATGTGATCATTGAACATCACTTTCCATCAGTGCTGATACATTTCGGAATTCTCTTTCACTTGTGAGGTGGATTCCTGCTTCATGTTTCCAGGTGGAACTATAGTGTTTACCTATTCTCTTCCACTGATCTAGCACC... |
Task1_train_41024 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTATTTTTTTTAATGGTGGCTTTGGTAAAGCTGAATGTTTCCATAGTGATGCATTCTGTTTATTTAAAACTTTACTTATACATGATTCCACCCACACGCTCTCCTCAGAGGGACCTGGTCTACAACTGCCCTCTTTCCCAACCCCATTTTCTGTTTGGAAGGAACACGCATGTGAGACCCTTGTCAGACTGGTGCTGCTTGAATCCATTCTTAGATGTGATTCCTGCATCTGGGTGTCAATAGGGAAATGACTTCAGTGTTTATTTACTACAGTGACTAATGGTGCCTTTTCCAGCTGGTCTAAAGCTGATGTGCCTCCA... | TTATTTTTTTTAATGGTGGCTTTGGTAAAGCTGAATGTTTCCATAGTGATGCATTCTGTTTATTTAAAACTTTACTTATACATGATTCCACCCACACGCTCTCCTCAGAGGGACCTGGTCTACAACTGCCCTCTTTCCCAACCCCATTTTCTGTTTGGAAGGAACACGCATGTGAGACCCTTGTCAGACTGGTGCTGCTTGAATCCATTCTTAGATGTGATTCCTGCATCTGGGTGTCAATAGGGAAATGACTTCAGTGTTTATTTACTACAGTGACTAATGGTGCCTTTTCCAGCTGGTCTAAAGCTGATGTGCCTCCA... |
Task1_train_41025 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GCCTTTTTCTGGGAGCCCCAGCGGGAGCTCACCACTGGCCAGGTAGTGGGAGGAGGCGGTGGGCGCCTGAGGGCCTTGTGACCGTGTTGTGAGGTGCTGCTCCCCGCAGGAAGGACGGGGGCAGGCGAGTGGGACAGGGACCTGGAGGCCGGAGGCCGGAGGCCGGGAACCCAGTGCTAGCCCCGCAGCCTCCAGGCTATGTGTGGCCAAACCCGTTCCTGCGGCACAAGAGGCGGAGCCAGAAGGGCCACCTCGCAGGAAGGCACCCAGGCCCCTCGCACCCTGGGAGGCCAGCTGGGTCATCGCTGCCTGAGTCTGAG... | GCCTTTTTCTGGGAGCCCCAGCGGGAGCTCACCACTGGCCAGGTAGTGGGAGGAGGCGGTGGGCGCCTGAGGGCCTTGTGACCGTGTTGTGAGGTGCTGCTCCCCGCAGGAAGGACGGGGGCAGGCGAGTGGGACAGGGACCTGGAGGCCGGAGGCCGGAGGCCGGGAACCCAGTGCTAGCCCCGCAGCCTCCAGGCTATGTGTGGCCAAACCCGTTCCTGCGGCACAAGAGGCGGAGCCAGAAGGGCCACCTCGCAGGAAGGCACCCAGGCCCCTCGCACCCTGGGAGGCCAGCTGGGTCATCGCTGCCTGAGTCTGAG... |
Task1_train_41026 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | TGAAATTATATCTTTTTTTTTTTTTTTGAGACGGAGTCTTGCTCCATTGCCCAGGCTGGTGTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCACCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGCACCCGCTGCCACGCCTAGCTAACTTTTTTTTTTTAATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGATCCGTCCGCCTAAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCTGAAATTC... | TGAAATTATATCTTTTTTTTTTTTTTTGAGACGGAGTCTTGCTCCATTGCCCAGGCTGGTGTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCACCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGCACCCGCTGCCACGCCTAGCTAACTTTTTTTTTTTAATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGATCCGTCCGCCTAAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCTGAAATTC... |
Task1_train_41027 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TTTTTGAGACGGAGTCTTGCTCCATTGCCCAGGCTGGTGTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCACCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGCACCCGCTGCCACGCCTAGCTAACTTTTTTTTTTTAATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGATCCGTCCGCCTAAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCTGAAATTCTAACTTTGTAACCTGCCACTAA... | TTTTTGAGACGGAGTCTTGCTCCATTGCCCAGGCTGGTGTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCACCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGCACCCGCTGCCACGCCTAGCTAACTTTTTTTTTTTAATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGATCCGTCCGCCTAAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCTGAAATTCTAACTTTGTAACCTGCCACTAA... |
Task1_train_41028 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | CCGCACCCGGCTGAAATTCTAACTTTGTAACCTGCCACTAAGGCCTCAAGTGATTGTCCCCCCTTCCCATCCCCCTCTCTCACTCTGCTTTAGCCAACAAGCCTCCTTGCTGTTTGTTCTTCGAATACACCAAGTGTATTCTTGCCTTAGCGTCTTTGCACTAAGACTCCCTCTGCCCAGACACTCTCTTCCCACCTTGTCACATGACTGGTTCCATCTTTGTCCATTGCAGGGCAAACCGCTGCAGTGTAGTGGCTCAGGAGCCACGCTGCTGGGGTTTGAATCTCAGCTCTTGCTACTTCCTGCTGTGGGACCTTGGG... | CCGCACCCGGCTGAAATTCTAACTTTGTAACCTGCCACTAAGGCCTCAAGTGATTGTCCCCCCTTCCCATCCCCCTCTCTCACTCTGCTTTAGCCAACAAGCCTCCTTGCTGTTTGTTCTTCGAATACACCAAGTGTATTCTTGCCTTAGCGTCTTTGCACTAAGACTCCCTCTGCCCAGACACTCTCTTCCCACCTTGTCACATGACTGGTTCCATCTTTGTCCATTGCAGGGCAAACCGCTGCAGTGTAGTGGCTCAGGAGCCACGCTGCTGGGGTTTGAATCTCAGCTCTTGCTACTTCCTGCTGTGGGACCTTGGG... |
Task1_train_41029 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | AGTTTTCTTAGCTTCTCTGTGCCTTGACTTTTCTACCTGTAAATGGCGATAAGAAATGTATGGTATTTGTTACCCAGGGTGGTTGGGAGGATTAAATAATATAGTGAACACATTGAGTTCACGCATCAAAAGTGTGCAGAGCATGGCCATACTAAGCACTTAGCATGTTATTATTGCCCTTCTGGTGGCAGCTTAAATATCCAGGCTCTGAGCAGCCTTTCCTGGTCCCGTGCTCTAAGCATCTCACCACCTGCATCCCCAGCTCATCGCCCTACTTTATTTCACCACAAAACATGTTCTTCTTCGTGTGTGTATCATCT... | AGTTTTCTTAGCTTCTCTGTGCCTTGACTTTTCTACCTGTAAATGGCGATAAGAAATGTATGGTATTTGTTACCCAGGGTGGTTGGGAGGATTAAATAATATAGTGAACACATTGAGTTCACGCATCAAAAGTGTGCAGAGCATGGCCATACTAAGCACTTAGCATGTTATTATTGCCCTTCTGGTGGCAGCTTAAATATCCAGGCTCTGAGCAGCCTTTCCTGGTCCCGTGCTCTAAGCATCTCACCACCTGCATCCCCAGCTCATCGCCCTACTTTATTTCACCACAAAACATGTTCTTCTTCGTGTGTGTATCATCT... |
Task1_train_41030 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CACTTGAGGCCAGGAGTTTGAGACCAGCCTGGCCAACAAGGTGAAACCCGGTCTCTACTAAAAATGCAAAATTAGCCAGGCATGCTGGCAAACGCCTGTAATCCCAGCTACTTCGGGGGCTGAGGCAGGAGAATCTCCTGAACCCAGGAGGCAGAGATTGCAGTGAGCCAAGACAGCGCCATTGACTCCAGTCTGGGTAGAAAAAGTGAAACTCTGTCTCAAAAAACAAAAACAAAAAACTACAGGATGAGCTTTAATTTCTGGATGTCTGGTAGCTTGTGTTCTACCCAGATGTGGGATGGCTAATCGTACTCTAAGTT... | CACTTGAGGCCAGGAGTTTGAGACCAGCCTGGCCAACAAGGTGAAACCCGGTCTCTACTAAAAATGCAAAATTAGCCAGGCATGCTGGCAAACGCCTGTAATCCCAGCTACTTCGGGGGCTGAGGCAGGAGAATCTCCTGAACCCAGGAGGCAGAGATTGCAGTGAGCCAAGACAGCGCCATTGACTCCAGTCTGGGTAGAAAAAGTGAAACTCTGTCTCAAAAAACAAAAACAAAAAACTACAGGATGAGCTTTAATTTCTGGATGTCTGGTAGCTTGTGTTCTACCCAGATGTGGGATGGCTAATCGTACTCTAAGTT... |
Task1_train_41031 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | CTAAGAACCTATGAGGGCTACAGAAAATCCCCTACAAATGAAAGGGGCAGAAATGACAAACTGCGATGAAAGGCCATAAGGATGCTCACACCCGAATCTAAAAAGCCCTTTGTGTGGGCCGCAGCCAAGCATACTTTGGCAAGAAATTTCTGTGGCTCTAACCTCCTTTGAAAACTGGAGAACCAAGGCCAGGAGGCAGAAGGAGGTGGCAGACCCGGCCCGGCGGCGGCCCAGCACGCGCAGGCCACCCAGAGTGGAGGTGGGAAACGGCATTACGCCCCTTTCCCTTTTCCTGGTCCCGCGGTGCTACCTCGTGTGCC... | CTAAGAACCTATGAGGGCTACAGAAAATCCCCTACAAATGAAAGGGGCAGAAATGACAAACTGCGATGAAAGGCCATAAGGATGCTCACACCCGAATCTAAAAAGCCCTTTGTGTGGGCCGCAGCCAAGCATACTTTGGCAAGAAATTTCTGTGGCTCTAACCTCCTTTGAAAACTGGAGAACCAAGGCCAGGAGGCAGAAGGAGGTGGCAGACCCGGCCCGGCGGCGGCCCAGCACGCGCAGGCCACCCAGAGTGGAGGTGGGAAACGGCATTACGCCCCTTTCCCTTTTCCTGGTCCCGCGGTGCTACCTCGTGTGCC... |
Task1_train_41032 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CAGGAATCATAGATACTTCTCCTATGAGAATAATTTAGGGTAATGTTTGAGAGTGCCAGCTCTGAGCCCCGACTGGGTCCATACCCTATTTGGCCACTTCCTGGCCATGTGGCACTTTGCTTCACCTCTTTATCTGTATGAGCCTCAGTTTCCTCATCTGTAAAACAGGGATCATAATGGTACCTGTCCTGTAACAGGTTAGTATGATTTGTAATTCAATTAGAATAGTGCCTGGCATATAATAGGCACTTGATTAATGTGAATTCATTATGACTAGCTGTGTGAGCACCTAAAAAACAGAGCAGGGTCGAGCATGGAGG... | CAGGAATCATAGATACTTCTCCTATGAGAATAATTTAGGGTAATGTTTGAGAGTGCCAGCTCTGAGCCCCGACTGGGTCCATACCCTATTTGGCCACTTCCTGGCCATGTGGCACTTTGCTTCACCTCTTTATCTGTATGAGCCTCAGTTTCCTCATCTGTAAAACAGGGATCATAATGGTACCTGTCCTGTAACAGGTTAGTATGATTTGTAATTCAATTAGAATAGTGCCTGGCATATAATAGGCACTTGATTAATGTGAATTCATTATGACTAGCTGTGTGAGCACCTAAAAAACAGAGCAGGGTCGAGCATGGAGG... |
Task1_train_41033 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | TGTCTGTGTGTGGAGCAGTGGGTGTCTGTGTGTGGAACTGTGTGTGCCTGCATGTGGAGCTGTGGGTGTCTGTGTGTGGAGCCTTGGGGGTCTGTGATCTGAATGCCTGATCTCATTCCAACTGGAGGTGAAGAGGAAGGTGGAGGAAGTGGGGAAGGGCCACTGAATCTTTCTAAATCTTCTCTCAGTTCTGTCCTATGGGTTTGGGAGTATGTGGCTCATTCGAGGCCACATGGGCATGTGTTCTTGGGGTATGACCACATCGGCTCCTAAAGAAGATGCTCTCTGCGTGTGTGTGTGTAGAGTGCAATTGTAGACAA... | TGTCTGTGTGTGGAGCAGTGGGTGTCTGTGTGTGGAACTGTGTGTGCCTGCATGTGGAGCTGTGGGTGTCTGTGTGTGGAGCCTTGGGGGTCTGTGATCTGAATGCCTGATCTCATTCCAACTGGAGGTGAAGAGGAAGGTGGAGGAAGTGGGGAAGGGCCACTGAATCTTTCTAAATCTTCTCTCAGTTCTGTCCTATGGGTTTGGGAGTATGTGGCTCATTCGAGGCCACATGGGCATGTGTTCTTGGGGTATGACCACATCGGCTCCTAAAGAAGATGCTCTCTGCGTGTGTGTGTGTAGAGTGCAATTGTAGACAA... |
Task1_train_41034 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | GAGATACATTGTTAAAGCCTGAAGCACTTAGGCAGCATTTATTATGTGGTATGTTGGTGGTGATGTTTTAGTCACCATGCACATCCATGGAGACACAGGCGGAGGTGGCGTGTGCTGCTGGGGACCAGGTACAGCCGGAGTCAGGCCAAGGGGTTGCTTGGAAGGAGGCTCTGTCGTAGACGGGCCAAGGAGACCTGCCTCATTTTGCTCTGGTGTAGGATGGCCTGTGGGTGCCCCCAGCCTTGCAGACCTGTGCACCCCTCAGAGGTGCCAGCCTTTTCTTGGAGAGAGGAGGCAGCCCGGCTGCTGGAACAAGCACC... | GAGATACATTGTTAAAGCCTGAAGCACTTAGGCAGCATTTATTATGTGGTATGTTGGTGGTGATGTTTTAGTCACCATGCACATCCATGGAGACACAGGCGGAGGTGGCGTGTGCTGCTGGGGACCAGGTACAGCCGGAGTCAGGCCAAGGGGTTGCTTGGAAGGAGGCTCTGTCGTAGACGGGCCAAGGAGACCTGCCTCATTTTGCTCTGGTGTAGGATGGCCTGTGGGTGCCCCCAGCCTTGCAGACCTGTGCACCCCTCAGAGGTGCCAGCCTTTTCTTGGAGAGAGGAGGCAGCCCGGCTGCTGGAACAAGCACC... |
Task1_train_41035 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTGAGGCTTCACCTGATCTGGAGAAATGAGGAACTGGTGGGCAAGGAAGGGCAGTGCCTTCCTGGCAGAGGTAACAGAGCCTGTGAGGTCCCCGAAATGAGAGGCACTGTGGTTCATTCAGGGAACATCAAATTCAGTGAGTGGAGCAGAAGACTGTGTTAGATACCAAACTCCTGGCCCATGGGTTTTGAGATTTGGTAGTCATACCACCTTCCCTCCAATCTTATTCCTTGGGTTTTGGCTGAAGGTCTATGTGACCTCCCCACTTCCCATGGGAACCAGAGGCAGTGGGGCAGGGAGAGGTGGCCCTGGGGCTGGCA... | CTGAGGCTTCACCTGATCTGGAGAAATGAGGAACTGGTGGGCAAGGAAGGGCAGTGCCTTCCTGGCAGAGGTAACAGAGCCTGTGAGGTCCCCGAAATGAGAGGCACTGTGGTTCATTCAGGGAACATCAAATTCAGTGAGTGGAGCAGAAGACTGTGTTAGATACCAAACTCCTGGCCCATGGGTTTTGAGATTTGGTAGTCATACCACCTTCCCTCCAATCTTATTCCTTGGGTTTTGGCTGAAGGTCTATGTGACCTCCCCACTTCCCATGGGAACCAGAGGCAGTGGGGCAGGGAGAGGTGGCCCTGGGGCTGGCA... |
Task1_train_41036 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | GCCAGCTGCGGCAGCACTCGGCCAGGGGCTTGGCAGAACGGGGACCTGGGAGGGAAGGAGCAGCATCACCTCGCCGGGTCTCACTCCTTCCAACACTGGCCATGCTAGACAGGTCTCTGGGATCTCAGGGGATGGCTGCTGTCCCACCAAACACTGCCAAGAGACACAGGACTCTTACCAAGCTGGCCCAAGTGAGCCCCCAGGACCCCTGGGAGGCATGAGGTAACTGTAAGATAAACCTGTCTGTCCTCCCCATCACCTTCCTGGGGGGTGGTTCTGAGTTGAGTCCGCAGATCCAGGCAGGGAGGGCTTGCCTGTCA... | GCCAGCTGCGGCAGCACTCGGCCAGGGGCTTGGCAGAACGGGGACCTGGGAGGGAAGGAGCAGCATCACCTCGCCGGGTCTCACTCCTTCCAACACTGGCCATGCTAGACAGGTCTCTGGGATCTCAGGGGATGGCTGCTGTCCCACCAAACACTGCCAAGAGACACAGGACTCTTACCAAGCTGGCCCAAGTGAGCCCCCAGGACCCCTGGGAGGCATGAGGTAACTGTAAGATAAACCTGTCTGTCCTCCCCATCACCTTCCTGGGGGGTGGTTCTGAGTTGAGTCCGCAGATCCAGGCAGGGAGGGCTTGCCTGTCA... |
Task1_train_41037 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CCCTGGGAGGCATGAGGTAACTGTAAGATAAACCTGTCTGTCCTCCCCATCACCTTCCTGGGGGGTGGTTCTGAGTTGAGTCCGCAGATCCAGGCAGGGAGGGCTTGCCTGTCAGTAGGGTCAGCCCATACATCATTTAATCCTGCCACAGGGATCAGCCCATACCCTTGGTCACCAGAAAGCAGGACCCACATGTGCAGAGGCTGGGCCCCCTCCCTGTGTCCGGCTGCAAGGAGCAGTCTGTCCGATGGCCCCTGTGGATGGGAGCACGATGTGACTGAACTGGAAGCCTGCCTTGGGGGACAGGGGGACAGCAGGGC... | CCCTGGGAGGCATGAGGTAACTGTAAGATAAACCTGTCTGTCCTCCCCATCACCTTCCTGGGGGGTGGTTCTGAGTTGAGTCCGCAGATCCAGGCAGGGAGGGCTTGCCTGTCAGTAGGGTCAGCCCATACATCATTTAATCCTGCCACAGGGATCAGCCCATACCCTTGGTCACCAGAAAGCAGGACCCACATGTGCAGAGGCTGGGCCCCCTCCCTGTGTCCGGCTGCAAGGAGCAGTCTGTCCGATGGCCCCTGTGGATGGGAGCACGATGTGACTGAACTGGAAGCCTGCCTTGGGGGACAGGGGGACAGCAGGGC... |
Task1_train_41038 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | AGCCTGTCAGCATGTGCTGCAGTGATTTAAAGATGCAGATTCCATATTAGTAGTCTTTTATCCCTCACCCCCTTCCCACTCTTCCCCCCAAGTCCGCAAAGTCCGTTGTATCAATCTTATGCCTTTGTGTCATATGGCACAGTGTATACTGCTTGGGTCATGGGTGCACCAAAATCTCACAAGTCACCACTGAAGAACTTCCTCATGTAACCAAACACCACCTGTACCCCAATAACTTATGGAAAAAAAAGTGTGCAGATTCCAGCAAGGCCACAGGATGGCCCCAAGCAATGCAGACGTGGCCTCAGAAAGTCTGGTGC... | AGCCTGTCAGCATGTGCTGCAGTGATTTAAAGATGCAGATTCCATATTAGTAGTCTTTTATCCCTCACCCCCTTCCCACTCTTCCCCCCAAGTCCGCAAAGTCCGTTGTATCAATCTTATGCCTTTGTGTCATATGGCACAGTGTATACTGCTTGGGTCATGGGTGCACCAAAATCTCACAAGTCACCACTGAAGAACTTCCTCATGTAACCAAACACCACCTGTACCCCAATAACTTATGGAAAAAAAAGTGTGCAGATTCCAGCAAGGCCACAGGATGGCCCCAAGCAATGCAGACGTGGCCTCAGAAAGTCTGGTGC... |
Task1_train_41039 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TCAGAAAATACCAATGTCAAAAAACAAAGGACACCTTCATGACCCCCATGTCCCCCAGGAGCTGGTCGTCCCAGGTGGGCATGACAGCATCTCTTCATTGGCAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCGGCAGGCTGGCTGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCCACCTCACTGGCTGACCAGGTCTGAGGAAGCCTTGCCGGGTGGGGTGTGGCAGGCTGGGGGCTGGGATGTGATGGGTGTCTCTGCTCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCG... | TCAGAAAATACCAATGTCAAAAAACAAAGGACACCTTCATGACCCCCATGTCCCCCAGGAGCTGGTCGTCCCAGGTGGGCATGACAGCATCTCTTCATTGGCAGGTGTGATCCTGCTGCGGCTGGACCGGCTCCGGCAGGCTGGCTGGGAGCAGATGTGGAGGCTGACAGCCAGGCGGGAGCTCCTTAGCCTGCCTGCCACCTCACTGGCTGACCAGGTCTGAGGAAGCCTTGCCGGGTGGGGTGTGGCAGGCTGGGGGCTGGGATGTGATGGGTGTCTCTGCTCAGGACATCTTCAACGCTGTGATCAAGGAGCACCCG... |
Task1_train_41040 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TCTAAACTGTATGTTGAAATGACATACACTTTGTGGTTGCCAACTAACTACATTCCTAATTTTCACTATTCCTTAGAAATATAATCAAGATCAAGAGGCTTTCCCCTAACTGTTGTTCTTTTGATGAAGCAGTGTGTGGACTGATATTCAGATGCACCCTCTTTTAAGCAAGTAACAGCACCCTTATTGGCCACTCACACCCAAATCATCTTTGCCAGTTTAGATCAAGCTCATAAAATAATTAAGTGAAAAAAAATGTCCTCTCTTGTGGAATAAATTTTTTTTTTTTTTTTTGAGGCGGAGTCTCACTCTGTCACCCA... | TCTAAACTGTATGTTGAAATGACATACACTTTGTGGTTGCCAACTAACTACATTCCTAATTTTCACTATTCCTTAGAAATATAATCAAGATCAAGAGGCTTTCCCCTAACTGTTGTTCTTTTGATGAAGCAGTGTGTGGACTGATATTCAGATGCACCCTCTTTTAAGCAAGTAACAGCACCCTTATTGGCCACTCACACCCAAATCATCTTTGCCAGTTTAGATCAAGCTCATAAAATAATTAAGTGAAAAAAAATGTCCTCTCTTGTGGAATAAATTTTTTTTTTTTTTTTTGAGGCGGAGTCTCACTCTGTCACCCA... |
Task1_train_41041 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GCACCCAGAAGATTCCACGCTGAGTGGGACCCGGTCCTCACCCTCAGGGAGGCCACAGTTAATAAAGGAGACTGATGTGGAGATATATAAATAAACGAAGTGCCGTGATAAAAGCAAACACAGCAATAAAGCAAAAATGGCTGGGCACGGTGGCCCATGCCTGTAATCCCAACACTTTGGGAGGCCGAAGCGGGTGGATCACCTGAGGTCAGGAGTTCCAGACAAGCCTGGCAAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGCATGGTGGCGCACGCCTGTAGTCTCAGCTAGTCAGGAGGCTAAGGCAGGA... | GCACCCAGAAGATTCCACGCTGAGTGGGACCCGGTCCTCACCCTCAGGGAGGCCACAGTTAATAAAGGAGACTGATGTGGAGATATATAAATAAACGAAGTGCCGTGATAAAAGCAAACACAGCAATAAAGCAAAAATGGCTGGGCACGGTGGCCCATGCCTGTAATCCCAACACTTTGGGAGGCCGAAGCGGGTGGATCACCTGAGGTCAGGAGTTCCAGACAAGCCTGGCAAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGCATGGTGGCGCACGCCTGTAGTCTCAGCTAGTCAGGAGGCTAAGGCAGGA... |
Task1_train_41042 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GGAATGCAGTGTGATGCAGTACCTATTCCTTGGGGTTGCAGTTTATGAAATGATCTAAGTGTTTGTCAGGGGCTTAGCACAGTGCCTGACACATAGGGGCTCAGTAAATGTCAGCCGTGACACTGGTGATTTTGGGGGAGACCCAGCGCTCTCCACCCATGCCTGCTGTCCTGCCCCTGCAGCTCCCTCCGGCCCAGGTGGTCTGCTTTGAGTGGGGCACTATTTGGGGTCATAAGAGCACTGCCCTGACCTCCCTGTCATCTGAGGCAGCTGGAAACTCCAATAGGCAGAGACCAAGAGCTGAGCTGTGCAGAACTCTG... | GGAATGCAGTGTGATGCAGTACCTATTCCTTGGGGTTGCAGTTTATGAAATGATCTAAGTGTTTGTCAGGGGCTTAGCACAGTGCCTGACACATAGGGGCTCAGTAAATGTCAGCCGTGACACTGGTGATTTTGGGGGAGACCCAGCGCTCTCCACCCATGCCTGCTGTCCTGCCCCTGCAGCTCCCTCCGGCCCAGGTGGTCTGCTTTGAGTGGGGCACTATTTGGGGTCATAAGAGCACTGCCCTGACCTCCCTGTCATCTGAGGCAGCTGGAAACTCCAATAGGCAGAGACCAAGAGCTGAGCTGTGCAGAACTCTG... |
Task1_train_41043 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGCTTTGATGATGTCACATTCCCCTTCTAGCTTTAGGTGTCACTGAACCAAACAGGAACCCAAACCCCCAGCTGCTCTGACACCAAGGACTTCCCTAAGCATGCCAAGGTGTTTCTAGCACCTGGCCTTGCATATGTTGTCAATTTCCTCTGGAGCGACCATCACATCTACTGAACACTTTCCTATCCTTCAAGGACTGCTTCAAATGTCACCACTTTTGCTGAGACTTCAGGGAGCACCCTCCCTCCTGCACTGTGTTCTGAAGGCACCTTTAGCACGACAAAAATGGAACTCTTTGTTTATTTATAAGAGACAGGGTC... | AGCTTTGATGATGTCACATTCCCCTTCTAGCTTTAGGTGTCACTGAACCAAACAGGAACCCAAACCCCCAGCTGCTCTGACACCAAGGACTTCCCTAAGCATGCCAAGGTGTTTCTAGCACCTGGCCTTGCATATGTTGTCAATTTCCTCTGGAGCGACCATCACATCTACTGAACACTTTCCTATCCTTCAAGGACTGCTTCAAATGTCACCACTTTTGCTGAGACTTCAGGGAGCACCCTCCCTCCTGCACTGTGTTCTGAAGGCACCTTTAGCACGACAAAAATGGAACTCTTTGTTTATTTATAAGAGACAGGGTC... |
Task1_train_41044 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TCTTGCTAGAAGACAAGTTTATCATTCCCCACATACCTTTGGGAAGAGACAAGGATTGCTAGGTGGTGATGATAAGAAACGCAGATTTGTCAAAACCAACCTGTGCATTTTTTAAAAGTTAAAAACAATTTTAAATACAAGTAGATATGAGGTTTCATTATGTTGCCTAGGCTGGTCTTGAACTCCTGGGCTCAAGCAATCTTCCCGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGCGAGCTACCACGCCAGACCCTAATTGTGCACTTTTGCAAAGGCCCTATGGGCAGGAGGGAACTCTACCTCAGAATGGGGA... | TCTTGCTAGAAGACAAGTTTATCATTCCCCACATACCTTTGGGAAGAGACAAGGATTGCTAGGTGGTGATGATAAGAAACGCAGATTTGTCAAAACCAACCTGTGCATTTTTTAAAAGTTAAAAACAATTTTAAATACAAGTAGATATGAGGTTTCATTATGTTGCCTAGGCTGGTCTTGAACTCCTGGGCTCAAGCAATCTTCCCGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGCGAGCTACCACGCCAGACCCTAATTGTGCACTTTTGCAAAGGCCCTATGGGCAGGAGGGAACTCTACCTCAGAATGGGGA... |
Task1_train_41045 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TTGTTTGTGGCTGGCTCTTTGCTGTTCTAAGTGACAGGATTCAGTGCCTGGCAGGGTGAGGTAGAAGGAGGGTCTGCAGGAGGATCTCCAGGAGTCCTTTGAAGGTGACAGCTGTAGTACCAGCCATACCCAGAGAGAACACAGCCCAATCTGGAAGGGAGCTTAAACAGGTCACCGTCTTTCTGGCTGTAAAGGAGCTCTGTGCTCTGGATATATCTCTGATGTTGAGATGGCCCCAGAAAGCCAGAGGCTCTGACTCACAGCCCCAGCCCTCTGACTCTCACCTAGTGGCTGTGCCCGGTCCACAGCCTGCATGTCCA... | TTGTTTGTGGCTGGCTCTTTGCTGTTCTAAGTGACAGGATTCAGTGCCTGGCAGGGTGAGGTAGAAGGAGGGTCTGCAGGAGGATCTCCAGGAGTCCTTTGAAGGTGACAGCTGTAGTACCAGCCATACCCAGAGAGAACACAGCCCAATCTGGAAGGGAGCTTAAACAGGTCACCGTCTTTCTGGCTGTAAAGGAGCTCTGTGCTCTGGATATATCTCTGATGTTGAGATGGCCCCAGAAAGCCAGAGGCTCTGACTCACAGCCCCAGCCCTCTGACTCTCACCTAGTGGCTGTGCCCGGTCCACAGCCTGCATGTCCA... |
Task1_train_41046 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | AAACAAAACTCAGAAATAAACTAGATGCAAAGGCTGATGGAGAACTCTGTCATCCATAAATCTGATTCCCATGATCACAACCACCAACGTGGTCTCATTATTCTCACTGATTGAGCTCAATCATGAGCAAATGTTATATTTGAACCTATAAAATTGATATACATTAACAAATGTTTTCTATATTAGGGCTCCAACTAAGATTTCCCTGGAAGAAAAAGATGTCCTGCTGCCTAAGGTTTGCAAACCACTGGCCTATTCCTCCCACCGTTGCTGCGCATGTGGCATGGCTCTGCCCCTCTCCATGGGGCCTTGTTCCCTAC... | AAACAAAACTCAGAAATAAACTAGATGCAAAGGCTGATGGAGAACTCTGTCATCCATAAATCTGATTCCCATGATCACAACCACCAACGTGGTCTCATTATTCTCACTGATTGAGCTCAATCATGAGCAAATGTTATATTTGAACCTATAAAATTGATATACATTAACAAATGTTTTCTATATTAGGGCTCCAACTAAGATTTCCCTGGAAGAAAAAGATGTCCTGCTGCCTAAGGTTTGCAAACCACTGGCCTATTCCTCCCACCGTTGCTGCGCATGTGGCATGGCTCTGCCCCTCTCCATGGGGCCTTGTTCCCTAC... |
Task1_train_41047 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCAAGTGCTTACTGTAGAAAGGGGTGGTGAGACGGGAGAACCCAAGGGTCTCCGGTCTGATCCCAAATGAAACCTTTAGGTACCAGGTAAAGTTTCCAGCCCTTGGTAACGCCCAGACAAAGGTCCTTCCCCTCTCCTGGCACCCAGAAGAGGCCACTGGCAGCAGCAGCAGCAGCAAGTCCGCAGCCTCTTTCCCCATGGGACGGGTCTACAGTGAACTCCTTCCAGGCCTCCCCCTGGTTCCAGAGGATGGGGACCCAAGGCCTCGAACTAGAAGAACCCTAGAGCCAGCAAAAAAAGCCTTCTACCTTCCGCTTTCC... | CCAAGTGCTTACTGTAGAAAGGGGTGGTGAGACGGGAGAACCCAAGGGTCTCCGGTCTGATCCCAAATGAAACCTTTAGGTACCAGGTAAAGTTTCCAGCCCTTGGTAACGCCCAGACAAAGGTCCTTCCCCTCTCCTGGCACCCAGAAGAGGCCACTGGCAGCAGCAGCAGCAGCAAGTCCGCAGCCTCTTTCCCCATGGGACGGGTCTACAGTGAACTCCTTCCAGGCCTCCCCCTGGTTCCAGAGGATGGGGACCCAAGGCCTCGAACTAGAAGAACCCTAGAGCCAGCAAAAAAAGCCTTCTACCTTCCGCTTTCC... |
Task1_train_41048 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | TTGGCCCCCTCGATCCCTTGCAAACAAACAGGAAGGAGCCTGTCTCGGATACCTCCCCCACCCAGCCTCACCTCCTTCAGCCTCTTCAGCCAGGGCTTCTGGGCCTTGCGGAAGCCGTCCTCGGCCGCCCGGCTCTCGCGGAAGCCGCCCAGCACAGGCCGGTGGAAAGCCCCCCGCTGCCAGGCGCGCACCCGCTCACTGTCCTGCCCTTGCAGCTTCTCCCGCACCTCCAGGTGCAGCGCGCTCAGCCGCTCAGCCGCCGTGAAAAAGGCATGCCAGGCCTTCTCCAGTGTGCCATACTGGGGGCCTGCAGGGAGGGA... | TTGGCCCCCTCGATCCCTTGCAAACAAACAGGAAGGAGCCTGTCTCGGATACCTCCCCCACCCAGCCTCACCTCCTTCAGCCTCTTCAGCCAGGGCTTCTGGGCCTTGCGGAAGCCGTCCTCGGCCGCCCGGCTCTCGCGGAAGCCGCCCAGCACAGGCCGGTGGAAAGCCCCCCGCTGCCAGGCGCGCACCCGCTCACTGTCCTGCCCTTGCAGCTTCTCCCGCACCTCCAGGTGCAGCGCGCTCAGCCGCTCAGCCGCCGTGAAAAAGGCATGCCAGGCCTTCTCCAGTGTGCCATACTGGGGGCCTGCAGGGAGGGA... |
Task1_train_41049 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CACAGCACGCTAGGGAGCGCAGGCACTCACCGCAGAGTAAACCAGCAGCTTGGGGAGCTGGGAGGTGGTCGCCATTAGGGTCAGGTTCTTCCTTATCTGAGCCAGCAGGACTCCTGAAGGAGAAAAGTCCCCGGTGTTGCTGGCTACAGCCACCTCTGCCTTCTAATTAGACCTATCTGTGCTCCTTTCACCCTCTGCCAGGCCTGGGCCTCATCACCTACACGGAGAACTCTTTAGTGTCATAGGGACCATGTAAGAACTCTGTGGCACCCCTCCTCTCTAAGAACTGTCAAATGTACAGAAGGAAGCAAGACAAAACA... | CACAGCACGCTAGGGAGCGCAGGCACTCACCGCAGAGTAAACCAGCAGCTTGGGGAGCTGGGAGGTGGTCGCCATTAGGGTCAGGTTCTTCCTTATCTGAGCCAGCAGGACTCCTGAAGGAGAAAAGTCCCCGGTGTTGCTGGCTACAGCCACCTCTGCCTTCTAATTAGACCTATCTGTGCTCCTTTCACCCTCTGCCAGGCCTGGGCCTCATCACCTACACGGAGAACTCTTTAGTGTCATAGGGACCATGTAAGAACTCTGTGGCACCCCTCCTCTCTAAGAACTGTCAAATGTACAGAAGGAAGCAAGACAAAACA... |
Task1_train_41050 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AGCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGATGAAATCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCACACACCTGTAATCCCAGCTACTTGGGAGGCTGAGACAGGAGAATCGCTTGAACCTAGGAGGTGGAGGTTGCAGTGAGCCAAGACCATGTCACTGCACTCCAGCCTGAGCAACACAGCAAGACTCTGTCTCAAAAAAAAAAATTTTTTTTGAAGAGCTTATTCAGAGATAGTGGCTCATGAAAAGGGAGGAGGAAACTGGGGAAGGACAAGCTCAGGACAGAGCTGGGCCT... | AGCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGATGAAATCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCACACACCTGTAATCCCAGCTACTTGGGAGGCTGAGACAGGAGAATCGCTTGAACCTAGGAGGTGGAGGTTGCAGTGAGCCAAGACCATGTCACTGCACTCCAGCCTGAGCAACACAGCAAGACTCTGTCTCAAAAAAAAAAATTTTTTTTGAAGAGCTTATTCAGAGATAGTGGCTCATGAAAAGGGAGGAGGAAACTGGGGAAGGACAAGCTCAGGACAGAGCTGGGCCT... |
Task1_train_41051 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | TGTCCTCAGTGTTGGAGTGAGGGGGAAGGGGCCCAAGAGAAGCAGGGCAGATGCACCCAAACATTCCCTGCTGGCCTGGAGGGGACTTTGGGGGAGAAAAGCCGGCACGGTGGCTGGGAGCCCAGACTTTGGAGTCAGAGGAGGGTTGGAGTCTTGACTCTACCGCCGCCTAACTGTGTGACCATAGTTACTTAATCTCTTTGAACCTCAGTTTGCTTATCTGTAAAATGAGTTTAAGAATAGTCCTGAGCCAGGAGCAGTAGCGTGCGCCCATAATCTCAGATACTCAGGAAGCTGAAACCTGATTGCTTCAGCCCAGT... | TGTCCTCAGTGTTGGAGTGAGGGGGAAGGGGCCCAAGAGAAGCAGGGCAGATGCACCCAAACATTCCCTGCTGGCCTGGAGGGGACTTTGGGGGAGAAAAGCCGGCACGGTGGCTGGGAGCCCAGACTTTGGAGTCAGAGGAGGGTTGGAGTCTTGACTCTACCGCCGCCTAACTGTGTGACCATAGTTACTTAATCTCTTTGAACCTCAGTTTGCTTATCTGTAAAATGAGTTTAAGAATAGTCCTGAGCCAGGAGCAGTAGCGTGCGCCCATAATCTCAGATACTCAGGAAGCTGAAACCTGATTGCTTCAGCCCAGT... |
Task1_train_41052 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CAGCAAAAAGGTTTTAAAGGTGAGGAGGCTCTCACTAGCCCTTCTTTAGCACAGAGAAGGCAAAGTCTCATAGGCTTCCCATATCAGTGTTTTTAATTTTATTTTATTTTATTTATTTATTTTTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGACGCAATCTCGGCTCACTGCCAGCTCCGCCTCCCGGCTTCATGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAG... | CAGCAAAAAGGTTTTAAAGGTGAGGAGGCTCTCACTAGCCCTTCTTTAGCACAGAGAAGGCAAAGTCTCATAGGCTTCCCATATCAGTGTTTTTAATTTTATTTTATTTTATTTATTTATTTTTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGACGCAATCTCGGCTCACTGCCAGCTCCGCCTCCCGGCTTCATGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAG... |
Task1_train_41053 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTTTAGCACAGAGAAGGCAAAGTCTCATAGGCTTCCCATATCAGTGTTTTTAATTTTATTTTATTTTATTTATTTATTTTTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGACGCAATCTCGGCTCACTGCCAGCTCCGCCTCCCGGCTTCATGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGATCTCGATCTCCTGACCTTGTGATCTGCCCGCCTCGGCC... | CTTTAGCACAGAGAAGGCAAAGTCTCATAGGCTTCCCATATCAGTGTTTTTAATTTTATTTTATTTTATTTATTTATTTTTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGACGCAATCTCGGCTCACTGCCAGCTCCGCCTCCCGGCTTCATGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGATCTCGATCTCCTGACCTTGTGATCTGCCCGCCTCGGCC... |
Task1_train_41054 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | AGCTTGCAGTGAGACGGGATTGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGATCCGTCTCAAAAAGAAGAACAGATAACTTCACCTGAAAGAGAATGTTGAACAAGAAGGTGTCAAAGATATTTGCTTTTTAATTTATATCATCCTGTATTGTATCATTTTTATGTAATAAGCATTGTTCATGTGTCACTTGTGTAATTAATTTTTAAAAATATTTTTATAGAAAAAGGGTAGACCCAGGATTAGAAAGTGCATCAGCTCCATTTTTCTCCTTGGTTAAGTCTGTCATGATCTCCTACCTTTGTGTTTGTCAACA... | AGCTTGCAGTGAGACGGGATTGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGATCCGTCTCAAAAAGAAGAACAGATAACTTCACCTGAAAGAGAATGTTGAACAAGAAGGTGTCAAAGATATTTGCTTTTTAATTTATATCATCCTGTATTGTATCATTTTTATGTAATAAGCATTGTTCATGTGTCACTTGTGTAATTAATTTTTAAAAATATTTTTATAGAAAAAGGGTAGACCCAGGATTAGAAAGTGCATCAGCTCCATTTTTCTCCTTGGTTAAGTCTGTCATGATCTCCTACCTTTGTGTTTGTCAACA... |
Task1_train_41055 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GACCAAGGAGCTGTAGCCACCCCTGTCCCTCTGCCCCTTCCCTTCTGGTGGGGCAGCTGGAGCTGCTCTGGGTCCCAGGCCAGGCAGGACTGGGGGCCAAGGGAGCTGAAGAGGGGCTGGGGATCTGGAGGGGCTCCTGGCAGAATTAGGGGTGATGAGGGTGCTGTGCTATGTTGGGCACTCACCTCGGGGTCCGGAAACTGCTGCTCCAGGGGTGGGGGTGGGAGAAAGGGTAGGTGGCACATGAGAGGTATGGCCACCTTCCCTCAAAGACCTGGACCCCACCCATGGGCCTTTACTTCCTCCCTATTTTCCGCACT... | GACCAAGGAGCTGTAGCCACCCCTGTCCCTCTGCCCCTTCCCTTCTGGTGGGGCAGCTGGAGCTGCTCTGGGTCCCAGGCCAGGCAGGACTGGGGGCCAAGGGAGCTGAAGAGGGGCTGGGGATCTGGAGGGGCTCCTGGCAGAATTAGGGGTGATGAGGGTGCTGTGCTATGTTGGGCACTCACCTCGGGGTCCGGAAACTGCTGCTCCAGGGGTGGGGGTGGGAGAAAGGGTAGGTGGCACATGAGAGGTATGGCCACCTTCCCTCAAAGACCTGGACCCCACCCATGGGCCTTTACTTCCTCCCTATTTTCCGCACT... |
Task1_train_41056 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTTGCCCATTCATGACCCCATGAGGCTGGGCATCTGCCCCAGGATCTCACCTTCCCAGCCTTTCCCAGGGTCAAGGTACCAGGCAGGTGGGACGGTTTATTGTCCCCAATTCCCACCCATCTCTCAACTCACCTTCACCCATCGCCCAAACATTCAGACAGTGCCAGGCCATGGGCCAGGAGCCGTGACACCAAGATGATAAAACAGAGTCCCACCCAGATGAGACCCGGACTCAGCCCTAAGCCCCCACGCCTACCCTGCAAGCCTTGGGGTTTCTCTCACACCCTGTGTGTGCAGCACTGGGCACGTGGCCAGCACTC... | CTTGCCCATTCATGACCCCATGAGGCTGGGCATCTGCCCCAGGATCTCACCTTCCCAGCCTTTCCCAGGGTCAAGGTACCAGGCAGGTGGGACGGTTTATTGTCCCCAATTCCCACCCATCTCTCAACTCACCTTCACCCATCGCCCAAACATTCAGACAGTGCCAGGCCATGGGCCAGGAGCCGTGACACCAAGATGATAAAACAGAGTCCCACCCAGATGAGACCCGGACTCAGCCCTAAGCCCCCACGCCTACCCTGCAAGCCTTGGGGTTTCTCTCACACCCTGTGTGTGCAGCACTGGGCACGTGGCCAGCACTC... |
Task1_train_41057 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TCACTCACACATATCCACTCACATATGATCGCACCTACCCACACCTCACACACACTTGCACGCACACACCTGCTTACACACATCTCACGTTACTCAGCCCCACACGCACACACCTGCTCACACACATCTCACATTACTCAGCTACACACACACGCCCCTGCTCACACACTTGTGCTCACACACCTCACACCATTCACTCACGCACACACCCACTCACACATGCTCACGTCTGCTCACACACATGCTCACCTATCCATACACACACTTCCTCACACACCTCACACCAAGTCTCACACACACTTATGCTTACAAACTCATGC... | TCACTCACACATATCCACTCACATATGATCGCACCTACCCACACCTCACACACACTTGCACGCACACACCTGCTTACACACATCTCACGTTACTCAGCCCCACACGCACACACCTGCTCACACACATCTCACATTACTCAGCTACACACACACGCCCCTGCTCACACACTTGTGCTCACACACCTCACACCATTCACTCACGCACACACCCACTCACACATGCTCACGTCTGCTCACACACATGCTCACCTATCCATACACACACTTCCTCACACACCTCACACCAAGTCTCACACACACTTATGCTTACAAACTCATGC... |
Task1_train_41058 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GCACTTCCCCTTTCCCTTGCTCATGGAGGAGCCAGGCCGGGCTGACTCAGAGCAGGAGCGCACAGTAGTCCTCCCAGCCCGACCTGGGCGGCGTGGTCTGGCGGCCGGGCGCGCCCCCGTGCGGCCACGGGCAGACTGCGGCCCTGGACGGGAAGCGGCGGCCAGATCCGCAAGCCCCGCAGCCTGGTCGATCGCGGTCCCCGCAGAGCCGCCGCTTCCGTCCCTGCCCAGCCTGGCTGAGCGCGGTGCGTGTGGCTCTCTCACTTCCGACCGACCCTCCCCTCCGGCCCGCAGCCCTGCCCAAACGGAAGTGCGCCCTC... | GCACTTCCCCTTTCCCTTGCTCATGGAGGAGCCAGGCCGGGCTGACTCAGAGCAGGAGCGCACAGTAGTCCTCCCAGCCCGACCTGGGCGGCGTGGTCTGGCGGCCGGGCGCGCCCCCGTGCGGCCACGGGCAGACTGCGGCCCTGGACGGGAAGCGGCGGCCAGATCCGCAAGCCCCGCAGCCTGGTCGATCGCGGTCCCCGCAGAGCCGCCGCTTCCGTCCCTGCCCAGCCTGGCTGAGCGCGGTGCGTGTGGCTCTCTCACTTCCGACCGACCCTCCCCTCCGGCCCGCAGCCCTGCCCAAACGGAAGTGCGCCCTC... |
Task1_train_41059 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CTCAAGCTCTGATGCCTCACACAAACCTTCACCAATTTGGATGCCTCCTTACTCTGGTGAGGTCCCAATGGCCCACGCCAGGCTGCCCCTCCTTGGGCTTGGTCTCTGACACTTCAAAACAACCCAACCCCATGTGTGGATTCTGTCCTCTCTCCACACAGGTTCTGACCTCTCACCCCAGGCCTTGCCCTGTGTGGACACTCTTCAGCCTGCTTAGATTCCAGTGCCTCACACCAGGTCACCCCTCCACACAGATGCTTGTCTTGCTCTGTCCCACTTAATGGTTTTAGAACTGGTTTAGGGAAGGGGGTGAACATGAG... | CTCAAGCTCTGATGCCTCACACAAACCTTCACCAATTTGGATGCCTCCTTACTCTGGTGAGGTCCCAATGGCCCACGCCAGGCTGCCCCTCCTTGGGCTTGGTCTCTGACACTTCAAAACAACCCAACCCCATGTGTGGATTCTGTCCTCTCTCCACACAGGTTCTGACCTCTCACCCCAGGCCTTGCCCTGTGTGGACACTCTTCAGCCTGCTTAGATTCCAGTGCCTCACACCAGGTCACCCCTCCACACAGATGCTTGTCTTGCTCTGTCCCACTTAATGGTTTTAGAACTGGTTTAGGGAAGGGGGTGAACATGAG... |
Task1_train_41060 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | AAACACAAAAATTAGCCGGGCGTGGTGGTATACGCCTGTAGTCCCAGCTACTTGGGAGGCTGGGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATGGCACCACTGCACTCCAGCCTGGGTGACAAGAGCAAAACTCCGCCCCTGCCCCCGCCAAAAAATACCCAGGATCAGAACCTGCTGTGGCTGATCCTATCAGTTCCTTCACAGTTGGCCCTCCTCCTCTCACCTCCCTACCTCCGCACACACCTGAGACACGCCTGGCAGCCATGCTGGCCTCTGTCCTTCCTGGAACATTCCAGGA... | AAACACAAAAATTAGCCGGGCGTGGTGGTATACGCCTGTAGTCCCAGCTACTTGGGAGGCTGGGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATGGCACCACTGCACTCCAGCCTGGGTGACAAGAGCAAAACTCCGCCCCTGCCCCCGCCAAAAAATACCCAGGATCAGAACCTGCTGTGGCTGATCCTATCAGTTCCTTCACAGTTGGCCCTCCTCCTCTCACCTCCCTACCTCCGCACACACCTGAGACACGCCTGGCAGCCATGCTGGCCTCTGTCCTTCCTGGAACATTCCAGGA... |
Task1_train_41061 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGCTCTAGCCACTTTTCTCTGACTAGAGCCAACTTCTTCTTTTTTATTTTTTTTTGAGACAGAGTCTTGCTCTGTCTCCAGGCTGGAGTACAGTGGCGTGATCTTGGCTCACTGCAACCTCCGCCCCCTGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCACACCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTTGGCCAGGATGGTCTCGAACTCCTGACCTCGTGATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGC... | TGCTCTAGCCACTTTTCTCTGACTAGAGCCAACTTCTTCTTTTTTATTTTTTTTTGAGACAGAGTCTTGCTCTGTCTCCAGGCTGGAGTACAGTGGCGTGATCTTGGCTCACTGCAACCTCCGCCCCCTGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCACACCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTTGGCCAGGATGGTCTCGAACTCCTGACCTCGTGATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGC... |
Task1_train_41062 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGGCGGATGTCTCTGACTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGGAAAAAAAAATATTTCTCATAGATTTATTTTTCCCTTATCTACTCCCAAGCCACCCCCTGCCAGAAGAAAGGTTCTACAAAAGCAGAGGGTTTTTTTTTTTTTTGTCTGTTTGATGTACTGCTAAATCCTAAGCCCCTAGGGAGAGTATCTGACAAATATATTAGATATTGATAAGACCAATTTTTATCCCCGTTTTTCTTTTTTTTTTTTAAGACAAAGTTTCACTTTTGTCACCCAGGCTGGAATGCAGTGG... | TGGCGGATGTCTCTGACTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGGAAAAAAAAATATTTCTCATAGATTTATTTTTCCCTTATCTACTCCCAAGCCACCCCCTGCCAGAAGAAAGGTTCTACAAAAGCAGAGGGTTTTTTTTTTTTTTGTCTGTTTGATGTACTGCTAAATCCTAAGCCCCTAGGGAGAGTATCTGACAAATATATTAGATATTGATAAGACCAATTTTTATCCCCGTTTTTCTTTTTTTTTTTTAAGACAAAGTTTCACTTTTGTCACCCAGGCTGGAATGCAGTGG... |
Task1_train_41063 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TAGTTGTGCAGAAAGGGTTAACATAGCAGGCCTGAGGCTGCTCTCCTTAGAAAGTCTTGCTTGTACTCTGGGAGGCCGAAGTGGGCAGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCCAATATGGTGGGCACTGTGCCTCTAGCAAGCTTTCCTGGGAAACAACATTTTACACACATCATCACAATTCAGTGCTGGAAGAATTAAGCATGTCCTGTGAGACTCTACTGGGAGGGGACTCTTAGACGATTGTGTCTGGCTTCAGACTTCACTCCATGTGCCTTTTCCCTTTTTTCACTTTGCTTTGTATCTTTTCAC... | TAGTTGTGCAGAAAGGGTTAACATAGCAGGCCTGAGGCTGCTCTCCTTAGAAAGTCTTGCTTGTACTCTGGGAGGCCGAAGTGGGCAGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCCAATATGGTGGGCACTGTGCCTCTAGCAAGCTTTCCTGGGAAACAACATTTTACACACATCATCACAATTCAGTGCTGGAAGAATTAAGCATGTCCTGTGAGACTCTACTGGGAGGGGACTCTTAGACGATTGTGTCTGGCTTCAGACTTCACTCCATGTGCCTTTTCCCTTTTTTCACTTTGCTTTGTATCTTTTCAC... |
Task1_train_41064 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | ATCTATTATAGCTGCAAACTTAGCTTTTTTTTTAAGCTGAAAAGAACCAAACATTTTAAAAAACAGGTGGAGAAACTTTTTTAAGGTGAGGAGAACCAAAAATTGAAGAAAGAGGTCCTCTGTTAGTTTTCTGATCTAGGGGGCTGGGGAGTGTGATCTCAGGGGCTGGAGTCGGCCATGGGCGCCTGAGCTCTTGGAGCCCACGGCTGGAGGTGAACGAGGTCCAGCGTGGAGCAGCAAATATGAAACCAGTGGCTTCCGACATTTTAAGTCAGGAAACTATTTCTTTAAACAAAACCTTGCCCAGGAGCCCAAAAAGT... | ATCTATTATAGCTGCAAACTTAGCTTTTTTTTTAAGCTGAAAAGAACCAAACATTTTAAAAAACAGGTGGAGAAACTTTTTTAAGGTGAGGAGAACCAAAAATTGAAGAAAGAGGTCCTCTGTTAGTTTTCTGATCTAGGGGGCTGGGGAGTGTGATCTCAGGGGCTGGAGTCGGCCATGGGCGCCTGAGCTCTTGGAGCCCACGGCTGGAGGTGAACGAGGTCCAGCGTGGAGCAGCAAATATGAAACCAGTGGCTTCCGACATTTTAAGTCAGGAAACTATTTCTTTAAACAAAACCTTGCCCAGGAGCCCAAAAAGT... |
Task1_train_41065 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCTGCCCTGGGGATTTGGCTGGATGCCCTGAAGGGGTCATTGTGAGCTAGGTGGGTTTCCCAGGATCTGCTGTCTCTGCTCCTCACCAGTTTCCTTCCCTGCCTTTTGCTTCTGGATTTGCTGTTTTGCACGAGCCCAGCATGTAGCTTCCAGAGTAAGATCTTGAGGAGGTTGCTGAAGCATGTTCTCTACCTAATGTGTTGCTTTGGTTTTCAATATTGGGTGATCATGTTTTGTTTTGTTTTGTTTTAGATCCCCCTCCTCCAGATGGATCCCCTAATATTACATCTGTCAGTCACAATTCAGTAAAGGTCAAGTTC... | CCTGCCCTGGGGATTTGGCTGGATGCCCTGAAGGGGTCATTGTGAGCTAGGTGGGTTTCCCAGGATCTGCTGTCTCTGCTCCTCACCAGTTTCCTTCCCTGCCTTTTGCTTCTGGATTTGCTGTTTTGCACGAGCCCAGCATGTAGCTTCCAGAGTAAGATCTTGAGGAGGTTGCTGAAGCATGTTCTCTACCTAATGTGTTGCTTTGGTTTTCAATATTGGGTGATCATGTTTTGTTTTGTTTTGTTTTAGATCCCCCTCCTCCAGATGGATCCCCTAATATTACATCTGTCAGTCACAATTCAGTAAAGGTCAAGTTC... |
Task1_train_41066 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AATGAGGGGATGACTGTAAGATGCTTATCACAGTCTAGCACACAGTAGACCCGGAATACACAGCAGCAGCATCTGCAGTTGTTGTGGTTGTTAGGAAGACAATGACAATGAAGATGGTAAACATCTGGTAACCACCATGTTCACCATCTTCATCATCATCCTAACAACCACATGATGGCAAACATGAGCTAACAAGATGCTCTAGTTCCTCCAGGCCACCAGACCCCTTGGCAGCCTTCTTGTGTTGTTTTTGAAGCTTCCCTTATTTCTATTCCTCTACACCGGTAAGAGAGTCCCATCTTGCTTTCTCTTTCCCTTTC... | AATGAGGGGATGACTGTAAGATGCTTATCACAGTCTAGCACACAGTAGACCCGGAATACACAGCAGCAGCATCTGCAGTTGTTGTGGTTGTTAGGAAGACAATGACAATGAAGATGGTAAACATCTGGTAACCACCATGTTCACCATCTTCATCATCATCCTAACAACCACATGATGGCAAACATGAGCTAACAAGATGCTCTAGTTCCTCCAGGCCACCAGACCCCTTGGCAGCCTTCTTGTGTTGTTTTTGAAGCTTCCCTTATTTCTATTCCTCTACACCGGTAAGAGAGTCCCATCTTGCTTTCTCTTTCCCTTTC... |
Task1_train_41067 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TAAGGTGAATAAGAGATACTTCAAAATAATTTTATTTTATTTAATATTTTTTGAGACGGAGTTTTGCTCTTGTCACCCAGGCTGGAGTGCAATGGTGAGATCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGTGATTATCCTGTCTCAGCCTCCTGAGTAGGTGGGATTACAGGTGCCCACCAGCATGCCCGGTTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCCGATCTTGAACTCCTGACCTCAGTTGATCCACCCACCTCGGCCTCCTAAAGTGCTGGGATTACAGGCCTGAG... | TAAGGTGAATAAGAGATACTTCAAAATAATTTTATTTTATTTAATATTTTTTGAGACGGAGTTTTGCTCTTGTCACCCAGGCTGGAGTGCAATGGTGAGATCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGTGATTATCCTGTCTCAGCCTCCTGAGTAGGTGGGATTACAGGTGCCCACCAGCATGCCCGGTTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCCGATCTTGAACTCCTGACCTCAGTTGATCCACCCACCTCGGCCTCCTAAAGTGCTGGGATTACAGGCCTGAG... |
Task1_train_41068 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TTAAAATCAGAAGACTAAAGTGGTCCTTACAAATCCTTTGAGGGGACCTCTCATTGACACTCCAAACCAGAAGTAATTATAGAACATTTGCTTTCAAGCTAAATTTCACAGAAAATACTCACCTAGTGATAGAGTCATTGTTTCCGTGAGGATGAAACCTCCCCATGTAAGATTCCTGCCTTCTGCATAAACATCCTGTGTGTGAAAGATTGGTATATGGCAGAAGGATCAGCTGGGTACACAGAGGAGCATGGTGGGGAGCTAAAGGGAGGGCACAACAACGAGGGGATGGCATTATGGCTGTTTTATAGATCAGGAAA... | TTAAAATCAGAAGACTAAAGTGGTCCTTACAAATCCTTTGAGGGGACCTCTCATTGACACTCCAAACCAGAAGTAATTATAGAACATTTGCTTTCAAGCTAAATTTCACAGAAAATACTCACCTAGTGATAGAGTCATTGTTTCCGTGAGGATGAAACCTCCCCATGTAAGATTCCTGCCTTCTGCATAAACATCCTGTGTGTGAAAGATTGGTATATGGCAGAAGGATCAGCTGGGTACACAGAGGAGCATGGTGGGGAGCTAAAGGGAGGGCACAACAACGAGGGGATGGCATTATGGCTGTTTTATAGATCAGGAAA... |
Task1_train_41069 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CCAGGCCACACAACTCTTCTTTGGACCAAGGTCTGTATTTTCGAGATGTACATGCTTCTACCACATCACTCACTTCTGCAGAGTACCTTATAGTGGTTCATCATATCAATCTTGCCTTATACTATCACGTGGAATGAGTTTTCTACACCGAGTGCTAACATTTCTCAACCCCAACCTCAAATCTGTGAAGCTAACCAGGTTCCCTAATAGGCATAAGAAAGAAACTGAGAAGAGGAAAGGAAAATCACAAAGCCTCAACCACTGTTCTTGGAGGAAGGTATGGAGAAGGGGAAATTTATGAGGCAGTAACAAGTCAGAAG... | CCAGGCCACACAACTCTTCTTTGGACCAAGGTCTGTATTTTCGAGATGTACATGCTTCTACCACATCACTCACTTCTGCAGAGTACCTTATAGTGGTTCATCATATCAATCTTGCCTTATACTATCACGTGGAATGAGTTTTCTACACCGAGTGCTAACATTTCTCAACCCCAACCTCAAATCTGTGAAGCTAACCAGGTTCCCTAATAGGCATAAGAAAGAAACTGAGAAGAGGAAAGGAAAATCACAAAGCCTCAACCACTGTTCTTGGAGGAAGGTATGGAGAAGGGGAAATTTATGAGGCAGTAACAAGTCAGAAG... |
Task1_train_41070 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATGCTATTTGAGAATCAAGATAATTGCAAATGTTACGTTAACTGTTATAAGTCCTTTAAAAGATAAAGTTAGTTGTGTCATTAGTCAGCATAAGCTGCATTTTGCTGTGGTAACATATGAATTCTGAACTCTCAGTGGTTTAACACATACAATTTTATTTCCTGTTCAAGCCAAATCTGCTGAGCTGTGGGTTGGGTGATCCTCTAGGGAACTGTTCTCCATGTAGTTACTCAGCAATCCAGACTGTTGCTTCTGTATAGCTGTTTCATATCAGTTTGTGTCTCCCAGGTTTGCTGCAGCAGAGAAAAATAAAGCTGGGG... | ATGCTATTTGAGAATCAAGATAATTGCAAATGTTACGTTAACTGTTATAAGTCCTTTAAAAGATAAAGTTAGTTGTGTCATTAGTCAGCATAAGCTGCATTTTGCTGTGGTAACATATGAATTCTGAACTCTCAGTGGTTTAACACATACAATTTTATTTCCTGTTCAAGCCAAATCTGCTGAGCTGTGGGTTGGGTGATCCTCTAGGGAACTGTTCTCCATGTAGTTACTCAGCAATCCAGACTGTTGCTTCTGTATAGCTGTTTCATATCAGTTTGTGTCTCCCAGGTTTGCTGCAGCAGAGAAAAATAAAGCTGGGG... |
Task1_train_41071 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ATAAGCTGCATTTTGCTGTGGTAACATATGAATTCTGAACTCTCAGTGGTTTAACACATACAATTTTATTTCCTGTTCAAGCCAAATCTGCTGAGCTGTGGGTTGGGTGATCCTCTAGGGAACTGTTCTCCATGTAGTTACTCAGCAATCCAGACTGTTGCTTCTGTATAGCTGTTTCATATCAGTTTGTGTCTCCCAGGTTTGCTGCAGCAGAGAAAAATAAAGCTGGGGAGTAGCTTGCTGGCTCCTAAATGGTTATGCCTCAATGTGACATATATCACTTCTGCAAATGTGGCTCTCCTTAAAAAGGAGTGGGCTGG... | ATAAGCTGCATTTTGCTGTGGTAACATATGAATTCTGAACTCTCAGTGGTTTAACACATACAATTTTATTTCCTGTTCAAGCCAAATCTGCTGAGCTGTGGGTTGGGTGATCCTCTAGGGAACTGTTCTCCATGTAGTTACTCAGCAATCCAGACTGTTGCTTCTGTATAGCTGTTTCATATCAGTTTGTGTCTCCCAGGTTTGCTGCAGCAGAGAAAAATAAAGCTGGGGAGTAGCTTGCTGGCTCCTAAATGGTTATGCCTCAATGTGACATATATCACTTCTGCAAATGTGGCTCTCCTTAAAAAGGAGTGGGCTGG... |
Task1_train_41072 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | TTGTCTATCTATTATCTATCTTCTTCATCATCATCTATCACTTTCTACCTAAATTATTTTCTAAAACCAGAGTGTTATAGACACTTTGAGAAAAATGAAGCATTTTCTACATGCATATTAAACATATGGTTTATGTAAAAGCCCAGTAAATAAGGCTTTTGGTTTTCACAGCATCTAAAATAAGGCTGTTGATTAGAGATAAGTCAACTAGCTCAATGGAGACTTCCTCAGGGAAAGTTCAGTATCATTGAGAAGAAAATTAGAAAGTTCTTGGCCAGTATTTATATACTATTTATCATTAATAGATTAAAATAGAGTTA... | TTGTCTATCTATTATCTATCTTCTTCATCATCATCTATCACTTTCTACCTAAATTATTTTCTAAAACCAGAGTGTTATAGACACTTTGAGAAAAATGAAGCATTTTCTACATGCATATTAAACATATGGTTTATGTAAAAGCCCAGTAAATAAGGCTTTTGGTTTTCACAGCATCTAAAATAAGGCTGTTGATTAGAGATAAGTCAACTAGCTCAATGGAGACTTCCTCAGGGAAAGTTCAGTATCATTGAGAAGAAAATTAGAAAGTTCTTGGCCAGTATTTATATACTATTTATCATTAATAGATTAAAATAGAGTTA... |
Task1_train_41073 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGAAAGAAAATATTTCCAGGTTATCATTGAGTCGTTTTACTCCAAGATTTTTCATGAAGCCCAAGATCTCTACTTTCTTCCATTGATTTTAATTTCATTTAGACAACTTTGTCATCTATTATTTTACTTTGTGACGTTCAGAAATAATTTAAAAGCAGAGAATATATTCTATGCCATACATCATGGGTAATGATTTTCCAAAAATAATTAAAAAAGGAACCAATACACACAGTTTTAGTGTTTCCACCATATTTAATAGAAACACTATAAATGAGTTTTGATGACATTAGAATGCAAATAAAGACATTAAATATAACTTA... | AGAAAGAAAATATTTCCAGGTTATCATTGAGTCGTTTTACTCCAAGATTTTTCATGAAGCCCAAGATCTCTACTTTCTTCCATTGATTTTAATTTCATTTAGACAACTTTGTCATCTATTATTTTACTTTGTGACGTTCAGAAATAATTTAAAAGCAGAGAATATATTCTATGCCATACATCATGGGTAATGATTTTCCAAAAATAATTAAAAAAGGAACCAATACACACAGTTTTAGTGTTTCCACCATATTTAATAGAAACACTATAAATGAGTTTTGATGACATTAGAATGCAAATAAAGACATTAAATATAACTTA... |
Task1_train_41074 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | ATTGGACTATAAACAGAAACACAGATATAAAAGTGTTGTATCGTCATATGGTTCACTTCCTGCTGAAATGAAATAAAGATTTGACGAAGGGTAAAATATTACCCCCATGATTCTAACAAGAAGTAATACATTGTGGGAATTTTGCCAATGGGCTGACACTCACCTCTGAATCCCTTGAGCCTGTCCATCAGTCCAATGATGGGCCCTGCACTGAACTCTGGATTCACAGGCTCAGACACTTGCAGCAGCAGGGACTCATACCTGCAAGGAGAAAGATAGAGTTACCATATCAACAGCCAAAAAAATACATAAGAATCACC... | ATTGGACTATAAACAGAAACACAGATATAAAAGTGTTGTATCGTCATATGGTTCACTTCCTGCTGAAATGAAATAAAGATTTGACGAAGGGTAAAATATTACCCCCATGATTCTAACAAGAAGTAATACATTGTGGGAATTTTGCCAATGGGCTGACACTCACCTCTGAATCCCTTGAGCCTGTCCATCAGTCCAATGATGGGCCCTGCACTGAACTCTGGATTCACAGGCTCAGACACTTGCAGCAGCAGGGACTCATACCTGCAAGGAGAAAGATAGAGTTACCATATCAACAGCCAAAAAAATACATAAGAATCACC... |
Task1_train_41075 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | AAGTATTTTAGCAGTGAAAAAGTGTTGATGTTTTGTTTTTTATACATATATACATATCAGTTAACAGTTCTGAAAAATAGATCGAAAAAAACTGGAGTGTTAGAACTGTATAAGTCTCTAGGGAAGTTCTTTGCTAAAAGGGGAGAGAACAAGTTTCCATTCTTTATCTTGAGAAGGAAGCAGTGGAAGCATCAGTCTCCCCAGAACCCCGCTATTTCAGACAAAGATGTCAGGGGAGTCTGCCAAGAAGTGGAACTCAGAATTTCGTTTCTAAATATTCTCAAGGCCATAAAGCTAAGGAACCTTACACATTTGGGGCA... | AAGTATTTTAGCAGTGAAAAAGTGTTGATGTTTTGTTTTTTATACATATATACATATCAGTTAACAGTTCTGAAAAATAGATCGAAAAAAACTGGAGTGTTAGAACTGTATAAGTCTCTAGGGAAGTTCTTTGCTAAAAGGGGAGAGAACAAGTTTCCATTCTTTATCTTGAGAAGGAAGCAGTGGAAGCATCAGTCTCCCCAGAACCCCGCTATTTCAGACAAAGATGTCAGGGGAGTCTGCCAAGAAGTGGAACTCAGAATTTCGTTTCTAAATATTCTCAAGGCCATAAAGCTAAGGAACCTTACACATTTGGGGCA... |
Task1_train_41076 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AAAAATTTCCCAAAGATTACCAAAGTATGCAGTAATAAATGACTGGAAAAATGTAATGGTGGAAGTCACACAGCATGTGTCACTTAGCTTAGAGCAGTGACATATGCTGATGACATTTGCATGTCCTGGCAGCATTGTCCAGCAAAGGCTTCCTGTCTCTGAGGATGGACCCTCCCTCCTCACCTGGAGCAGCTCCACGTCAGGCATGTGGTATGTCTCCCACAGCTCTCTGTACATGTCTTTCATCCCTTCTAAATGTTGGGTCATTCTCACTTGACTGTCTTGTAGTTGTTGGAAAAGCTCTTTTGCTTCTCTTTCCA... | AAAAATTTCCCAAAGATTACCAAAGTATGCAGTAATAAATGACTGGAAAAATGTAATGGTGGAAGTCACACAGCATGTGTCACTTAGCTTAGAGCAGTGACATATGCTGATGACATTTGCATGTCCTGGCAGCATTGTCCAGCAAAGGCTTCCTGTCTCTGAGGATGGACCCTCCCTCCTCACCTGGAGCAGCTCCACGTCAGGCATGTGGTATGTCTCCCACAGCTCTCTGTACATGTCTTTCATCCCTTCTAAATGTTGGGTCATTCTCACTTGACTGTCTTGTAGTTGTTGGAAAAGCTCTTTTGCTTCTCTTTCCA... |
Task1_train_41077 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TGTAATGGTGGAAGTCACACAGCATGTGTCACTTAGCTTAGAGCAGTGACATATGCTGATGACATTTGCATGTCCTGGCAGCATTGTCCAGCAAAGGCTTCCTGTCTCTGAGGATGGACCCTCCCTCCTCACCTGGAGCAGCTCCACGTCAGGCATGTGGTATGTCTCCCACAGCTCTCTGTACATGTCTTTCATCCCTTCTAAATGTTGGGTCATTCTCACTTGACTGTCTTGTAGTTGTTGGAAAAGCTCTTTTGCTTCTCTTTCCAGTGCCTGCAGATGCCGTTGCTCCTCCTCATCGAGAAATATATGCATCTTTT... | TGTAATGGTGGAAGTCACACAGCATGTGTCACTTAGCTTAGAGCAGTGACATATGCTGATGACATTTGCATGTCCTGGCAGCATTGTCCAGCAAAGGCTTCCTGTCTCTGAGGATGGACCCTCCCTCCTCACCTGGAGCAGCTCCACGTCAGGCATGTGGTATGTCTCCCACAGCTCTCTGTACATGTCTTTCATCCCTTCTAAATGTTGGGTCATTCTCACTTGACTGTCTTGTAGTTGTTGGAAAAGCTCTTTTGCTTCTCTTTCCAGTGCCTGCAGATGCCGTTGCTCCTCCTCATCGAGAAATATATGCATCTTTT... |
Task1_train_41078 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ATAGTATAATCTTCCAGGTACACTCCACCAGAAAAAGGAAGAGAGACTCAGATGGGCCTGTGTATACTTCCCTAAACACATTGCGGGTGCTCTTTTCCCAAGGGTTAGGAGGGCTGGGCAGCCCACCCTAAGAGAAGAATCATGGGAAAGAGGCAAGCGTAAAGAAGTCCTACGATCACAGTTAAGTGGGGCACTTGGCCTTCTCTCACCTTCATGTGCCTGCTTGGCTCTCTTCCAAGCACACCTTCCTTTCTTTCCTGTTATAAGGCCTTTTAAAATAAACTTCCATTCCTGCTCTGAAACTTGCCTTGGTCTCTTTT... | ATAGTATAATCTTCCAGGTACACTCCACCAGAAAAAGGAAGAGAGACTCAGATGGGCCTGTGTATACTTCCCTAAACACATTGCGGGTGCTCTTTTCCCAAGGGTTAGGAGGGCTGGGCAGCCCACCCTAAGAGAAGAATCATGGGAAAGAGGCAAGCGTAAAGAAGTCCTACGATCACAGTTAAGTGGGGCACTTGGCCTTCTCTCACCTTCATGTGCCTGCTTGGCTCTCTTCCAAGCACACCTTCCTTTCTTTCCTGTTATAAGGCCTTTTAAAATAAACTTCCATTCCTGCTCTGAAACTTGCCTTGGTCTCTTTT... |
Task1_train_41079 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGTGTGTCTGAGCAGCTGCTCTGTGGAGACTACACAGCTGTGTGTATCGGACCCAAGGCCCTGGTAGCCTGGGCTCACGAGGGGATTTCCTGATCCACGGGTTACAAAGATCCATGGGAAAATCATGGTTTTCTGGGGTTGCACATTCCCTTACTGCATCGTGGGGGTTCCCTTGGCTCCCTGCTGCTCCTGGGTGAGCCATACCGCTGTGCTGCTTTTCTTCATTCTCTGTGGGTGGAGTTGTTTCCCTGATCTGTCCCAAATGTGAGTACCTGGATCTTTCAGTTGAAGATGCTGTATCACTTGTCCTTTTCTTTCCT... | TGTGTGTCTGAGCAGCTGCTCTGTGGAGACTACACAGCTGTGTGTATCGGACCCAAGGCCCTGGTAGCCTGGGCTCACGAGGGGATTTCCTGATCCACGGGTTACAAAGATCCATGGGAAAATCATGGTTTTCTGGGGTTGCACATTCCCTTACTGCATCGTGGGGGTTCCCTTGGCTCCCTGCTGCTCCTGGGTGAGCCATACCGCTGTGCTGCTTTTCTTCATTCTCTGTGGGTGGAGTTGTTTCCCTGATCTGTCCCAAATGTGAGTACCTGGATCTTTCAGTTGAAGATGCTGTATCACTTGTCCTTTTCTTTCCT... |
Task1_train_41080 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | GATCCATGGGAAAATCATGGTTTTCTGGGGTTGCACATTCCCTTACTGCATCGTGGGGGTTCCCTTGGCTCCCTGCTGCTCCTGGGTGAGCCATACCGCTGTGCTGCTTTTCTTCATTCTCTGTGGGTGGAGTTGTTTCCCTGATCTGTCCCAAATGTGAGTACCTGGATCTTTCAGTTGAAGATGCTGTATCACTTGTCCTTTTCTTTCCTCTCCGTGAGTGCCACGGATCTCAGCTGCTTCTAATCGGCAATCTTGGCCCCCTCCCAAAAACAGCTTTTAATAATAAAATGTTACCAAAAAGTAAACTGATTGACAGA... | GATCCATGGGAAAATCATGGTTTTCTGGGGTTGCACATTCCCTTACTGCATCGTGGGGGTTCCCTTGGCTCCCTGCTGCTCCTGGGTGAGCCATACCGCTGTGCTGCTTTTCTTCATTCTCTGTGGGTGGAGTTGTTTCCCTGATCTGTCCCAAATGTGAGTACCTGGATCTTTCAGTTGAAGATGCTGTATCACTTGTCCTTTTCTTTCCTCTCCGTGAGTGCCACGGATCTCAGCTGCTTCTAATCGGCAATCTTGGCCCCCTCCCAAAAACAGCTTTTAATAATAAAATGTTACCAAAAAGTAAACTGATTGACAGA... |
Task1_train_41081 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ATTCCCTTACTGCATCGTGGGGGTTCCCTTGGCTCCCTGCTGCTCCTGGGTGAGCCATACCGCTGTGCTGCTTTTCTTCATTCTCTGTGGGTGGAGTTGTTTCCCTGATCTGTCCCAAATGTGAGTACCTGGATCTTTCAGTTGAAGATGCTGTATCACTTGTCCTTTTCTTTCCTCTCCGTGAGTGCCACGGATCTCAGCTGCTTCTAATCGGCAATCTTGGCCCCCTCCCAAAAACAGCTTTTAATAATAAAATGTTACCAAAAAGTAAACTGATTGACAGAGGAATAGAAAATAAATAGCTCATAATCATAAGATAA... | ATTCCCTTACTGCATCGTGGGGGTTCCCTTGGCTCCCTGCTGCTCCTGGGTGAGCCATACCGCTGTGCTGCTTTTCTTCATTCTCTGTGGGTGGAGTTGTTTCCCTGATCTGTCCCAAATGTGAGTACCTGGATCTTTCAGTTGAAGATGCTGTATCACTTGTCCTTTTCTTTCCTCTCCGTGAGTGCCACGGATCTCAGCTGCTTCTAATCGGCAATCTTGGCCCCCTCCCAAAAACAGCTTTTAATAATAAAATGTTACCAAAAAGTAAACTGATTGACAGAGGAATAGAAAATAAATAGCTCATAATCATAAGATAA... |
Task1_train_41082 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | GGGTGGAGTTGTTTCCCTGATCTGTCCCAAATGTGAGTACCTGGATCTTTCAGTTGAAGATGCTGTATCACTTGTCCTTTTCTTTCCTCTCCGTGAGTGCCACGGATCTCAGCTGCTTCTAATCGGCAATCTTGGCCCCCTCCCAAAAACAGCTTTTAATAATAAAATGTTACCAAAAAGTAAACTGATTGACAGAGGAATAGAAAATAAATAGCTCATAATCATAAGATAAAATGTTGCTGAAAGCAGAAAAATTTCAAGATTAGCTATTTGTTCATATGCTAGGAATTTGCTTCTATTTCTTCTGTATTCTTCAGCGT... | GGGTGGAGTTGTTTCCCTGATCTGTCCCAAATGTGAGTACCTGGATCTTTCAGTTGAAGATGCTGTATCACTTGTCCTTTTCTTTCCTCTCCGTGAGTGCCACGGATCTCAGCTGCTTCTAATCGGCAATCTTGGCCCCCTCCCAAAAACAGCTTTTAATAATAAAATGTTACCAAAAAGTAAACTGATTGACAGAGGAATAGAAAATAAATAGCTCATAATCATAAGATAAAATGTTGCTGAAAGCAGAAAAATTTCAAGATTAGCTATTTGTTCATATGCTAGGAATTTGCTTCTATTTCTTCTGTATTCTTCAGCGT... |
Task1_train_41083 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | TACCTTCCTTAATAATTCTATTAAATCATTCGAGGTTTATCACGTACCAGACATTGTGCTACCTTGTGGCAATTATTGTTATCTAGTAGGCAAGTACTTTATGGGCCATGATTGTATATTTAACTAATAGAAATTTCAGCCTGAAATTCAAATGCTCTTTCAATGAAGCCATCACCCTTTCTGATGGGTTTTCAGCATAATATGGGTGACTTGAGCAATACAAAATCGTTCAGAAGCCTACACTGACATTTGGAAACATGATATAAACTTCATTACCTACCCATGAGAGGTTATGGCCTATTGTTATTACAGTCTTAAAG... | TACCTTCCTTAATAATTCTATTAAATCATTCGAGGTTTATCACGTACCAGACATTGTGCTACCTTGTGGCAATTATTGTTATCTAGTAGGCAAGTACTTTATGGGCCATGATTGTATATTTAACTAATAGAAATTTCAGCCTGAAATTCAAATGCTCTTTCAATGAAGCCATCACCCTTTCTGATGGGTTTTCAGCATAATATGGGTGACTTGAGCAATACAAAATCGTTCAGAAGCCTACACTGACATTTGGAAACATGATATAAACTTCATTACCTACCCATGAGAGGTTATGGCCTATTGTTATTACAGTCTTAAAG... |
Task1_train_41084 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGTCCCATTAACCTTCTTATTGCTTGTGGATACTCATTTGTTAACTATGATTTCTCTGTTTTCTTATTTTAGTCTTCTTTTCATTCCCTGAGCTCCCTCTGATGGTGGGTCCAAATTTTTACTATACTTCTGCTTGCTTTTCACTAAGATACGTTCCATCACAGGTAAAATTACTACTCACATAATTAAATCATTATTTTCTAAGACATAGAGTTTTATTGTTTGGCCATAACAGGCTTTCCTGAATTGTACGTATCTTATCCTTTTTTTTTCCTGGACTACGTCTATAAATCTTTTCAAGTTGACAGAGATCTGAATAA... | TGTCCCATTAACCTTCTTATTGCTTGTGGATACTCATTTGTTAACTATGATTTCTCTGTTTTCTTATTTTAGTCTTCTTTTCATTCCCTGAGCTCCCTCTGATGGTGGGTCCAAATTTTTACTATACTTCTGCTTGCTTTTCACTAAGATACGTTCCATCACAGGTAAAATTACTACTCACATAATTAAATCATTATTTTCTAAGACATAGAGTTTTATTGTTTGGCCATAACAGGCTTTCCTGAATTGTACGTATCTTATCCTTTTTTTTTCCTGGACTACGTCTATAAATCTTTTCAAGTTGACAGAGATCTGAATAA... |
Task1_train_41085 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGGCACTTTACTTTGTTTTAATAAAACGACAACTCTAATAGGTAAGGGTTGTTGGACTCCTCATTTTAAAAATGATGCAAGTAAGGGATAGAGAGCTTTAGTAAATGGCCCAAACTCTCATAAAAAGTGGTGAACTTGAGGTTGTAGCTGAAGCAGTGTGGCTCCAGTGTCCACATTATTCACCACATGCTACACTTTCTCTCCAAAGATGTCTTGGATCTTAAATAGGTACATGCTGAATGAGACACGTATAGTCACTATTTATTCACTGTAATCATGAAACCCCATGTCCCACTGACTACCATTTTTCATGTAAACGT... | AGGCACTTTACTTTGTTTTAATAAAACGACAACTCTAATAGGTAAGGGTTGTTGGACTCCTCATTTTAAAAATGATGCAAGTAAGGGATAGAGAGCTTTAGTAAATGGCCCAAACTCTCATAAAAAGTGGTGAACTTGAGGTTGTAGCTGAAGCAGTGTGGCTCCAGTGTCCACATTATTCACCACATGCTACACTTTCTCTCCAAAGATGTCTTGGATCTTAAATAGGTACATGCTGAATGAGACACGTATAGTCACTATTTATTCACTGTAATCATGAAACCCCATGTCCCACTGACTACCATTTTTCATGTAAACGT... |
Task1_train_41086 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | ATTATTCACCACATGCTACACTTTCTCTCCAAAGATGTCTTGGATCTTAAATAGGTACATGCTGAATGAGACACGTATAGTCACTATTTATTCACTGTAATCATGAAACCCCATGTCCCACTGACTACCATTTTTCATGTAAACGTCATGAGCTTGGAAATTTTTATTTAATTATAAATTTATAAAAAATGAAAAACAAATTGTCAGCAGAATATCATAAAAGAGAGGTGCATGAATAGTTCTGTAGATAATTGACTAGAAAGGATTCTGAATTTCTCAAATTTAATCCCATTGTTTTCCAGTGAGCAAACTGAGGCAGA... | ATTATTCACCACATGCTACACTTTCTCTCCAAAGATGTCTTGGATCTTAAATAGGTACATGCTGAATGAGACACGTATAGTCACTATTTATTCACTGTAATCATGAAACCCCATGTCCCACTGACTACCATTTTTCATGTAAACGTCATGAGCTTGGAAATTTTTATTTAATTATAAATTTATAAAAAATGAAAAACAAATTGTCAGCAGAATATCATAAAAGAGAGGTGCATGAATAGTTCTGTAGATAATTGACTAGAAAGGATTCTGAATTTCTCAAATTTAATCCCATTGTTTTCCAGTGAGCAAACTGAGGCAGA... |
Task1_train_41087 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CAAGGGCTCTGGTTCCTTTCATAAACCTGCCTCTAGTCTTCCCCACCTTTCTCTGTTCCTATCCCCTCTCTAATTGCTGGATGAGGCTGTGCTGCTGCAGCCAACTGTCTGGCCCCTGAGCATTACATCCCCGTACTCCAGGCCTTTATTCATCACCAAAACAGCATGGTACTGGTATAAAAATAGGCACATAGACCAGTGGAACAGAATAGAGAACCCAGAAATGAACCCAAATACTTACAACCAACTGATCTTTGACAAAGCAAACAAAAACATAAAGTAGGGAGAGGACACCCTATTCAACAAATGGTGCTGGGATC... | CAAGGGCTCTGGTTCCTTTCATAAACCTGCCTCTAGTCTTCCCCACCTTTCTCTGTTCCTATCCCCTCTCTAATTGCTGGATGAGGCTGTGCTGCTGCAGCCAACTGTCTGGCCCCTGAGCATTACATCCCCGTACTCCAGGCCTTTATTCATCACCAAAACAGCATGGTACTGGTATAAAAATAGGCACATAGACCAGTGGAACAGAATAGAGAACCCAGAAATGAACCCAAATACTTACAACCAACTGATCTTTGACAAAGCAAACAAAAACATAAAGTAGGGAGAGGACACCCTATTCAACAAATGGTGCTGGGATC... |
Task1_train_41088 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TAGTTGTCTTTCAAATTGCCCTCATCTGGCCAGTGTATTAGGAATATTGAATCCAAAATGCCAGTTTTCATCCTAGGGTGGCAGAATTAGGCTTCTGTGGGAGTCTCCAGTGTGCATAACTTCCCATAGTAGACACTTCTGAAAACAACTGGGCATTAAGGTTATTGGGTTTCCATGGCATTGTGTGAGTAACTTCCCATTATAAATCTCCCAGAGTTATTGTTACTTCTTTGTGTTACTAGGATGTGAAAGAGATGTTATATTTGGTAATGTTTCTAAAATGTCTCTGTTGGTCATGGACCAAGTTGTTCCAAGGAACT... | TAGTTGTCTTTCAAATTGCCCTCATCTGGCCAGTGTATTAGGAATATTGAATCCAAAATGCCAGTTTTCATCCTAGGGTGGCAGAATTAGGCTTCTGTGGGAGTCTCCAGTGTGCATAACTTCCCATAGTAGACACTTCTGAAAACAACTGGGCATTAAGGTTATTGGGTTTCCATGGCATTGTGTGAGTAACTTCCCATTATAAATCTCCCAGAGTTATTGTTACTTCTTTGTGTTACTAGGATGTGAAAGAGATGTTATATTTGGTAATGTTTCTAAAATGTCTCTGTTGGTCATGGACCAAGTTGTTCCAAGGAACT... |
Task1_train_41089 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGTCTTTCAAATTGCCCTCATCTGGCCAGTGTATTAGGAATATTGAATCCAAAATGCCAGTTTTCATCCTAGGGTGGCAGAATTAGGCTTCTGTGGGAGTCTCCAGTGTGCATAACTTCCCATAGTAGACACTTCTGAAAACAACTGGGCATTAAGGTTATTGGGTTTCCATGGCATTGTGTGAGTAACTTCCCATTATAAATCTCCCAGAGTTATTGTTACTTCTTTGTGTTACTAGGATGTGAAAGAGATGTTATATTTGGTAATGTTTCTAAAATGTCTCTGTTGGTCATGGACCAAGTTGTTCCAAGGAACTTGCC... | TGTCTTTCAAATTGCCCTCATCTGGCCAGTGTATTAGGAATATTGAATCCAAAATGCCAGTTTTCATCCTAGGGTGGCAGAATTAGGCTTCTGTGGGAGTCTCCAGTGTGCATAACTTCCCATAGTAGACACTTCTGAAAACAACTGGGCATTAAGGTTATTGGGTTTCCATGGCATTGTGTGAGTAACTTCCCATTATAAATCTCCCAGAGTTATTGTTACTTCTTTGTGTTACTAGGATGTGAAAGAGATGTTATATTTGGTAATGTTTCTAAAATGTCTCTGTTGGTCATGGACCAAGTTGTTCCAAGGAACTTGCC... |
Task1_train_41090 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TGAGTAACTTCCCATTATAAATCTCCCAGAGTTATTGTTACTTCTTTGTGTTACTAGGATGTGAAAGAGATGTTATATTTGGTAATGTTTCTAAAATGTCTCTGTTGGTCATGGACCAAGTTGTTCCAAGGAACTTGCCTTATTACTTCAAACTCTGTATTTTGGCTAGACTGATGAATCACACTAGACACTGATATTTACTGTCACTCCCATATCACAAGGTCAGGAGATCAAGACCATCCTGACTAACATGATGAAACCCTGTCTCTGTTAAAGATACAAAAATTAGCTGAGTGTGGTGGCACGCACCTGTAGTCCTA... | TGAGTAACTTCCCATTATAAATCTCCCAGAGTTATTGTTACTTCTTTGTGTTACTAGGATGTGAAAGAGATGTTATATTTGGTAATGTTTCTAAAATGTCTCTGTTGGTCATGGACCAAGTTGTTCCAAGGAACTTGCCTTATTACTTCAAACTCTGTATTTTGGCTAGACTGATGAATCACACTAGACACTGATATTTACTGTCACTCCCATATCACAAGGTCAGGAGATCAAGACCATCCTGACTAACATGATGAAACCCTGTCTCTGTTAAAGATACAAAAATTAGCTGAGTGTGGTGGCACGCACCTGTAGTCCTA... |
Task1_train_41091 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | TTTCTTACATTGAACTTGGAATTTATCCTTCAGTATTTTTTTGTTTTTAGTCTGGATGCTGAGGTTGTATTTTTGAGCACTCTTAGTACCTGAACAACATTATAAATAAAACTATGTTTCACCATTTTTTACCTCTCTTTTCATTGTATATTTTCTCCTCTCTCACTATCCAGTTCACTGTATGAGTTCTGCCAAAAAAGCAAACAAAAAAACCCTCTAGTTGCTGATGTAATAGCTGGTGACAGGGATGAGTTAGTTTAGTTCAGTTTAAAACTATGCTGAAATTAGAATAGTAAATGTGTTTGGAATTGTGGTATAGG... | TTTCTTACATTGAACTTGGAATTTATCCTTCAGTATTTTTTTGTTTTTAGTCTGGATGCTGAGGTTGTATTTTTGAGCACTCTTAGTACCTGAACAACATTATAAATAAAACTATGTTTCACCATTTTTTACCTCTCTTTTCATTGTATATTTTCTCCTCTCTCACTATCCAGTTCACTGTATGAGTTCTGCCAAAAAAGCAAACAAAAAAACCCTCTAGTTGCTGATGTAATAGCTGGTGACAGGGATGAGTTAGTTTAGTTCAGTTTAAAACTATGCTGAAATTAGAATAGTAAATGTGTTTGGAATTGTGGTATAGG... |
Task1_train_41092 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TGACCTACCCTAAAGTTTAAAATCTGATTTTCTTATTTTTCTTTGGCCCAAATGTATAAAGATTCCTAGAAGCAAGTGCTGATACTGATGCTGAGTTACCTTTCTGGCCACCTCCTGATTGACAGCTCTGGGAATCTGATATTCTTCTGCTCTCAACTAATTCAGTTCCCTCACCCAAAATGCTTACCAATATTTCATTCAGCTTGTGGCCTTTACTTATTTCCATATGCCTTTACTAAGTTATCTCTTATTTTATTTATGTCTACACTTTTACTCTCCCTCTGATCCTTAAAGATGTCTTGGCTTGCTTTGATGCATAG... | TGACCTACCCTAAAGTTTAAAATCTGATTTTCTTATTTTTCTTTGGCCCAAATGTATAAAGATTCCTAGAAGCAAGTGCTGATACTGATGCTGAGTTACCTTTCTGGCCACCTCCTGATTGACAGCTCTGGGAATCTGATATTCTTCTGCTCTCAACTAATTCAGTTCCCTCACCCAAAATGCTTACCAATATTTCATTCAGCTTGTGGCCTTTACTTATTTCCATATGCCTTTACTAAGTTATCTCTTATTTTATTTATGTCTACACTTTTACTCTCCCTCTGATCCTTAAAGATGTCTTGGCTTGCTTTGATGCATAG... |
Task1_train_41093 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | ATTGAAAAACACATTTCAATTATATATATATAGGTGAAGACAGAATTATCCTTTAAAGCTGTGTCTGCCTGTGGAAATGAAGTCAAAAGTTGGAGAGTAATTATCTAGATGACTCATGAAAAAGCTTTTTGTAGATAAGGTGGCTGACTTTTTAAGTGAGTAAATACAATTGGTAAGAGCACTTTATTATAAGTAAAATTTTCACATTTTCAAATCTGACCATCATCATAATCCTGAGACATGAGCAGGTAAGCTATATATAAACACCTCTGCTACACAATAATGCATATAAAGTTGAAATATACACTTCTTTTAGGAAT... | ATTGAAAAACACATTTCAATTATATATATATAGGTGAAGACAGAATTATCCTTTAAAGCTGTGTCTGCCTGTGGAAATGAAGTCAAAAGTTGGAGAGTAATTATCTAGATGACTCATGAAAAAGCTTTTTGTAGATAAGGTGGCTGACTTTTTAAGTGAGTAAATACAATTGGTAAGAGCACTTTATTATAAGTAAAATTTTCACATTTTCAAATCTGACCATCATCATAATCCTGAGACATGAGCAGGTAAGCTATATATAAACACCTCTGCTACACAATAATGCATATAAAGTTGAAATATACACTTCTTTTAGGAAT... |
Task1_train_41094 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | ATTATCTAGATGACTCATGAAAAAGCTTTTTGTAGATAAGGTGGCTGACTTTTTAAGTGAGTAAATACAATTGGTAAGAGCACTTTATTATAAGTAAAATTTTCACATTTTCAAATCTGACCATCATCATAATCCTGAGACATGAGCAGGTAAGCTATATATAAACACCTCTGCTACACAATAATGCATATAAAGTTGAAATATACACTTCTTTTAGGAATTAAACTTCATTAGACCTGATTACTTTATATAAATAATTGGAAAATAATTAATAAAGCCTCAAGATTCCGGTTTATATTCAATATATTGTTTCTCTTCCT... | ATTATCTAGATGACTCATGAAAAAGCTTTTTGTAGATAAGGTGGCTGACTTTTTAAGTGAGTAAATACAATTGGTAAGAGCACTTTATTATAAGTAAAATTTTCACATTTTCAAATCTGACCATCATCATAATCCTGAGACATGAGCAGGTAAGCTATATATAAACACCTCTGCTACACAATAATGCATATAAAGTTGAAATATACACTTCTTTTAGGAATTAAACTTCATTAGACCTGATTACTTTATATAAATAATTGGAAAATAATTAATAAAGCCTCAAGATTCCGGTTTATATTCAATATATTGTTTCTCTTCCT... |
Task1_train_41095 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | AAGTTCCTCTTCAAAGACTTTACTCCCCATCTAATTAGGAATAAATAGTAACTTCTCTTCGAAGCAAATTTTGTTTAAAGACCTGCACTCCTAAATATTTGCCCTGGCATGCTTATACTGATCCAAGCAAGCATTAGGTCATAGCCTGTTCCTCTTTCTTATTTAAAAGTGTTTTTACCTTTGTCAGCATTCCACAAGTTACTTCCTGCTTCCTTTTTCTCCTCTGCCTTTGCCTCTTTTAAAAACTTCTGAGTTGCTAGCCAATATGGACAAATACAGAATGAGGTCCTGTTCCAGCCAATGGAAAACGGACACAGCAG... | AAGTTCCTCTTCAAAGACTTTACTCCCCATCTAATTAGGAATAAATAGTAACTTCTCTTCGAAGCAAATTTTGTTTAAAGACCTGCACTCCTAAATATTTGCCCTGGCATGCTTATACTGATCCAAGCAAGCATTAGGTCATAGCCTGTTCCTCTTTCTTATTTAAAAGTGTTTTTACCTTTGTCAGCATTCCACAAGTTACTTCCTGCTTCCTTTTTCTCCTCTGCCTTTGCCTCTTTTAAAAACTTCTGAGTTGCTAGCCAATATGGACAAATACAGAATGAGGTCCTGTTCCAGCCAATGGAAAACGGACACAGCAG... |
Task1_train_41096 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTACTTGCATATTATGTACTGTCTAGTGTCATCTTGACAACAAAAATGTAGAGAATTTATTTTTCTTGAAAGAGAAGCCTTGTGATAATATTAGTTTCCATATATTCTTAAAAACTGATCTTCACTGGGAAAAGTGACATTTCAAAGTTGAAGCACTGACTTTTCCATGATAGAAAATAAATTGAATGAAGAAGGTATTTAGTATCTACTCTCTCTTCTCTAAAACCACATCACCTTCTTTCCTCCAAATCTCTGCTCTGTTCCAGGAATGTGCAGTTTTTGAATATCAGGATAATGAAAACTCTTCTGGGGATTACAAA... | CTACTTGCATATTATGTACTGTCTAGTGTCATCTTGACAACAAAAATGTAGAGAATTTATTTTTCTTGAAAGAGAAGCCTTGTGATAATATTAGTTTCCATATATTCTTAAAAACTGATCTTCACTGGGAAAAGTGACATTTCAAAGTTGAAGCACTGACTTTTCCATGATAGAAAATAAATTGAATGAAGAAGGTATTTAGTATCTACTCTCTCTTCTCTAAAACCACATCACCTTCTTTCCTCCAAATCTCTGCTCTGTTCCAGGAATGTGCAGTTTTTGAATATCAGGATAATGAAAACTCTTCTGGGGATTACAAA... |
Task1_train_41097 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GACAGAGCCAGTCCTGCTGATACTCATCTAGGAAACCATCCTTATACTGCAGATGAGAAAACCAGGTTTCGGAGATGCCAGCAGCATGCTCAAATACAGATTAAGTTAGTGATGCAAAGTGGAATAAAATCTACTTGTCATTTATTGACTCCCAAGCCAGCGTTCCTTTAACTTCACAAGGATTGTTGCAAGAAAGTACTCAGTCCTGGGGCTAGGGAGGAGAGGATGAGATTAAGTAATATATGGCACTTCCACAGTTTCCTGTGGTTGTTCTGCATTCAGTGTAAGGGATGGGGGTGGAGTGGGCTACTGAAAAGCAG... | GACAGAGCCAGTCCTGCTGATACTCATCTAGGAAACCATCCTTATACTGCAGATGAGAAAACCAGGTTTCGGAGATGCCAGCAGCATGCTCAAATACAGATTAAGTTAGTGATGCAAAGTGGAATAAAATCTACTTGTCATTTATTGACTCCCAAGCCAGCGTTCCTTTAACTTCACAAGGATTGTTGCAAGAAAGTACTCAGTCCTGGGGCTAGGGAGGAGAGGATGAGATTAAGTAATATATGGCACTTCCACAGTTTCCTGTGGTTGTTCTGCATTCAGTGTAAGGGATGGGGGTGGAGTGGGCTACTGAAAAGCAG... |
Task1_train_41098 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AAATGATATCAATTCTGATTTTCTCATTCGGCTCCCACCATGTACTCAGCAATGAAATCAATACTTTGGCAGATAAAGAAGAATAAAGCAAAATTGGCCTTATCTTTAAACTTTCTATACTTTCTGAGGAGATAAGCGAGACTAATAACCAAATCTGTAAATGATAGGATATGGTTTATGGTAACTGTGAGTTATAAGCACTAATGTTTGCAATATATACAGAGGAGAAGAAACAATGAGTAATCTTTACAAGAGTAGATGGTAAAATAAAGCATTATAAAAGTGAGAATAGATAGAAAGCAAACTTTATGTAAATGAGC... | AAATGATATCAATTCTGATTTTCTCATTCGGCTCCCACCATGTACTCAGCAATGAAATCAATACTTTGGCAGATAAAGAAGAATAAAGCAAAATTGGCCTTATCTTTAAACTTTCTATACTTTCTGAGGAGATAAGCGAGACTAATAACCAAATCTGTAAATGATAGGATATGGTTTATGGTAACTGTGAGTTATAAGCACTAATGTTTGCAATATATACAGAGGAGAAGAAACAATGAGTAATCTTTACAAGAGTAGATGGTAAAATAAAGCATTATAAAAGTGAGAATAGATAGAAAGCAAACTTTATGTAAATGAGC... |
Task1_train_41099 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | GATTTTCTCATTCGGCTCCCACCATGTACTCAGCAATGAAATCAATACTTTGGCAGATAAAGAAGAATAAAGCAAAATTGGCCTTATCTTTAAACTTTCTATACTTTCTGAGGAGATAAGCGAGACTAATAACCAAATCTGTAAATGATAGGATATGGTTTATGGTAACTGTGAGTTATAAGCACTAATGTTTGCAATATATACAGAGGAGAAGAAACAATGAGTAATCTTTACAAGAGTAGATGGTAAAATAAAGCATTATAAAAGTGAGAATAGATAGAAAGCAAACTTTATGTAAATGAGCATGTGCTTTATAATAA... | GATTTTCTCATTCGGCTCCCACCATGTACTCAGCAATGAAATCAATACTTTGGCAGATAAAGAAGAATAAAGCAAAATTGGCCTTATCTTTAAACTTTCTATACTTTCTGAGGAGATAAGCGAGACTAATAACCAAATCTGTAAATGATAGGATATGGTTTATGGTAACTGTGAGTTATAAGCACTAATGTTTGCAATATATACAGAGGAGAAGAAACAATGAGTAATCTTTACAAGAGTAGATGGTAAAATAAAGCATTATAAAAGTGAGAATAGATAGAAAGCAAACTTTATGTAAATGAGCATGTGCTTTATAATAA... |
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