ID stringlengths 13 17 | question stringlengths 88 1.13k | answer stringlengths 6 156 | reference_sequence stringlengths 4.1k 4.1k | variant_sequence stringlengths 4.1k 4.1k |
|---|---|---|---|---|
Task1_train_41800 | Assess the clinical impact of this variant found on Chromosome 12. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GATTGCGCCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAGTATATTTACAGTGTTGTGCAAGCATCACCATTGTCAAATTCCAGAACGTTTTCATCATCTTTGAAACAAATTATACTGGCCAGACGCAGTGGCTCACGCCTCTAATCCCAACACTTTGGGAGACCGGGGTAGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCTTGACCAACACAGTGAAACCCCATCTCTAATAAAAATACAAAAATTAGCAGGGCTTGATGGCATGCACCTGTATCC... | GATTGCGCCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAGTATATTTACAGTGTTGTGCAAGCATCACCATTGTCAAATTCCAGAACGTTTTCATCATCTTTGAAACAAATTATACTGGCCAGACGCAGTGGCTCACGCCTCTAATCCCAACACTTTGGGAGACCGGGGTAGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCTTGACCAACACAGTGAAACCCCATCTCTAATAAAAATACAAAAATTAGCAGGGCTTGATGGCATGCACCTGTATCC... |
Task1_train_41801 | Assess the clinical impact of this variant found on Chromosome 12. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CGTTTAATCAATATTAATTTCATGCACAATCTTCACAAAGTTTCTTTTCCCCTCCTCCGACTCAGAGCTCAGGCTCCGGTTATCCTGCTTTGCCCTTCCCTTCCACCCTCACAGCCCTGCAGTCACTCAACACTACTGAGGCTCTCTCCATTAAAGATGAACAACAGATCATTTTTCATTGCATGGCAACCCTAAGAGCTCTCTAGCTTAGCAGAGCATGATGGGAGTCTTTCCATCCCCCCCCCCACCCCCCGCCCGCTCGTTCCTCTTCTTTTTTTTTTTTTTTTCCTTCCTTTCCTTCTTCCACAATTAATCCCTAA... | CGTTTAATCAATATTAATTTCATGCACAATCTTCACAAAGTTTCTTTTCCCCTCCTCCGACTCAGAGCTCAGGCTCCGGTTATCCTGCTTTGCCCTTCCCTTCCACCCTCACAGCCCTGCAGTCACTCAACACTACTGAGGCTCTCTCCATTAAAGATGAACAACAGATCATTTTTCATTGCATGGCAACCCTAAGAGCTCTCTAGCTTAGCAGAGCATGATGGGAGTCTTTCCATCCCCCCCCCCACCCCCCGCCCGCTCGTTCCTCTTCTTTTTTTTTTTTTTTTCCTTCCTTTCCTTCTTCCACAATTAATCCCTAA... |
Task1_train_41802 | A mutation found on Chromosome 12 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GATAGGTAGAACTAGTAGAATGCATTCCGAAGTCATTTTGAAAAGTCTGTAAGATTGAGTGACTCCCAGTTTGTATAAGCATCATTCATTAAGAATGACAAGTTATGTTTCTACATATTGGTACATTAGCCTTTGATCAGTTATCTGGATGAACTCTATAAACAGACATAGGACCATGAATTGTTTTTACTTTGAAGAGAGTTTTCCTGATCAAATACTAGTAGGAAGCCTTTGATGTATTATTATTTGAAGTATGTCTAAAAGATCACTCTTCCATAAGGAAACCCTTCCCCAAATTTATGCTTGCCATAGTGCCCAAA... | GATAGGTAGAACTAGTAGAATGCATTCCGAAGTCATTTTGAAAAGTCTGTAAGATTGAGTGACTCCCAGTTTGTATAAGCATCATTCATTAAGAATGACAAGTTATGTTTCTACATATTGGTACATTAGCCTTTGATCAGTTATCTGGATGAACTCTATAAACAGACATAGGACCATGAATTGTTTTTACTTTGAAGAGAGTTTTCCTGATCAAATACTAGTAGGAAGCCTTTGATGTATTATTATTTGAAGTATGTCTAAAAGATCACTCTTCCATAAGGAAACCCTTCCCCAAATTTATGCTTGCCATAGTGCCCAAA... |
Task1_train_41803 | A variant has been detected on Chromosome 12. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TCCCTTGCTCCCTCAGTACCCTGTCTCTCAGATTCCCATATCAACTCCTCATGTGTCTACGGCTCAGACAGGTTTCTCATCCCTTCCCATCACAATGGCAGCTGGCATTACTCAGCCTCTGCTCACGTTGGCTTCATCTGCTACAACAGCTGCGATCCCGGGGGTATCAACTGTGGTTCCTAGTCAGCTTCCAACCCTTCTGCAGCCTGTGACTCAGCTGCCAAGTCAGGTTCACCCACAGCTCCTACAACCAGCAGTTCAGTCCATGGGAATACCAGCTAACCTTGGACAAGCTGCTGAGGTTCCACTTTCCTCTGGAG... | TCCCTTGCTCCCTCAGTACCCTGTCTCTCAGATTCCCATATCAACTCCTCATGTGTCTACGGCTCAGACAGGTTTCTCATCCCTTCCCATCACAATGGCAGCTGGCATTACTCAGCCTCTGCTCACGTTGGCTTCATCTGCTACAACAGCTGCGATCCCGGGGGTATCAACTGTGGTTCCTAGTCAGCTTCCAACCCTTCTGCAGCCTGTGACTCAGCTGCCAAGTCAGGTTCACCCACAGCTCCTACAACCAGCAGTTCAGTCCATGGGAATACCAGCTAACCTTGGACAAGCTGCTGAGGTTCCACTTTCCTCTGGAG... |
Task1_train_41804 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ATTTGCTCTTCAGTACGCAGTCTTTATATTTAGCGTCTCACGGACTTGATTTTCCCTTTGTTGTCTGTAGGTGCTGCCAGTGGGTACTGAACTTCCAGCAGGTACTCTACCCAGCGAGCAGCTGCCACCTTTTCCAGGACCTTCTCTAACCCAGGTGCCTCAAGACTTGACAAATTTCTTCCTGTGCCCTACTTTCTTTGACAAAGCTTGCTGAAGTTCTCCACTACGTGGTCTTGGCTTTTGCCTATTTGTCTTTGACTTAGTAACACCTTTCTTTTAAAATGTTATAACCAATGACCCAGTTCCTACTTAAGTAAGAA... | ATTTGCTCTTCAGTACGCAGTCTTTATATTTAGCGTCTCACGGACTTGATTTTCCCTTTGTTGTCTGTAGGTGCTGCCAGTGGGTACTGAACTTCCAGCAGGTACTCTACCCAGCGAGCAGCTGCCACCTTTTCCAGGACCTTCTCTAACCCAGGTGCCTCAAGACTTGACAAATTTCTTCCTGTGCCCTACTTTCTTTGACAAAGCTTGCTGAAGTTCTCCACTACGTGGTCTTGGCTTTTGCCTATTTGTCTTTGACTTAGTAACACCTTTCTTTTAAAATGTTATAACCAATGACCCAGTTCCTACTTAAGTAAGAA... |
Task1_train_41805 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CAACAAGAGAGAAACTCTGTCTCAAAAACGAAAAAAAAAAAAAAAGAAAATGTGTAACATATACACCATGGAATACTATGCAGCCATAAAAAAGGATGAGTTCATGTCCTTTGCAGGGACATGGATGAAGCTGGAAACCATCATTCTCAGCAAACTAACACAGGAACAGAAAACCAAACACCGCATGTTCTCACTCATAAGTGGGAGCTGAACCGTGAGAACACATGGACACAGGGAGGGGAACATCACACACGGCCTGTCGGGGGATCAGGGGCTAGGAAAGGGATAGCATTAGGAGAAATACCTAATGTAGATGATGG... | CAACAAGAGAGAAACTCTGTCTCAAAAACGAAAAAAAAAAAAAAAGAAAATGTGTAACATATACACCATGGAATACTATGCAGCCATAAAAAAGGATGAGTTCATGTCCTTTGCAGGGACATGGATGAAGCTGGAAACCATCATTCTCAGCAAACTAACACAGGAACAGAAAACCAAACACCGCATGTTCTCACTCATAAGTGGGAGCTGAACCGTGAGAACACATGGACACAGGGAGGGGAACATCACACACGGCCTGTCGGGGGATCAGGGGCTAGGAAAGGGATAGCATTAGGAGAAATACCTAATGTAGATGATGG... |
Task1_train_41806 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TACTGTATAGGCCTAAACTGAACTCTGATCTTTTTAGCAAGCTGAAGATTGTTTTAGCCACTAAGCCCTTGCTCTTTATTCTCTTTTAATTATTTCCTGGAAATAGTATTAGAAACAAAGGAAATGTGCTATATGTATTATGCAGCCATGAAAAACATAGTTTCGGTCATATATAATGTAGTGAACAGTACTGACAATATAATGTTAAATAGATAATGTATCAAGCAAAATGTGAGGTGTGATACTGTTAGAAGCTGATTTATATAAATTTATTAAAAGACTTGGCAGGAAAATTTCCAAAATGTTACAAATGATTACTT... | TACTGTATAGGCCTAAACTGAACTCTGATCTTTTTAGCAAGCTGAAGATTGTTTTAGCCACTAAGCCCTTGCTCTTTATTCTCTTTTAATTATTTCCTGGAAATAGTATTAGAAACAAAGGAAATGTGCTATATGTATTATGCAGCCATGAAAAACATAGTTTCGGTCATATATAATGTAGTGAACAGTACTGACAATATAATGTTAAATAGATAATGTATCAAGCAAAATGTGAGGTGTGATACTGTTAGAAGCTGATTTATATAAATTTATTAAAAGACTTGGCAGGAAAATTTCCAAAATGTTACAAATGATTACTT... |
Task1_train_41807 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CCACAGCCTCCTAGTCACTACTACTAAAGAATAGAGACCCTGACTCCCACTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCACCCGGCTGGAGTGCAGTTGTGCTATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGCGACTGCAGGCATGTGCCACCACATCTGGCTAATTTTTATACTTTTTTATTACAGGTGAGCTTTCACCATGTTGGCCGGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCACCTTGGCCCCCCGAAGAGCCCCGCA... | CCACAGCCTCCTAGTCACTACTACTAAAGAATAGAGACCCTGACTCCCACTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCACCCGGCTGGAGTGCAGTTGTGCTATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGCGACTGCAGGCATGTGCCACCACATCTGGCTAATTTTTATACTTTTTTATTACAGGTGAGCTTTCACCATGTTGGCCGGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCACCTTGGCCCCCCGAAGAGCCCCGCA... |
Task1_train_41808 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTGTCTCCTGTGCTCAGGTGCAGGTGGGAAGGTACCTGCTGGCCCGGCACTCACCTTTGTTGTTGCATGCAATCCACTTCATGCGGTCAGCAAAAGACACTTCTCTCCCAATGAGGTAAGTGAAAACTCGGACCTAACCCACAAGACACAGAGGCACTCAGCAGCAAAATTCCCGGCCATAAGTAATGTTAACATTGTTTATATGAGTCTTAGATGTTGGCCCCAGTGCCTCTCAGTCTTCGGGTTCTCCAATTTCACCCCCTGAGGCCCAGGCAGCAACACAATTCGCCCAGGGCCATGGGGACTGCGGGTAGGTGCAA... | CTGTCTCCTGTGCTCAGGTGCAGGTGGGAAGGTACCTGCTGGCCCGGCACTCACCTTTGTTGTTGCATGCAATCCACTTCATGCGGTCAGCAAAAGACACTTCTCTCCCAATGAGGTAAGTGAAAACTCGGACCTAACCCACAAGACACAGAGGCACTCAGCAGCAAAATTCCCGGCCATAAGTAATGTTAACATTGTTTATATGAGTCTTAGATGTTGGCCCCAGTGCCTCTCAGTCTTCGGGTTCTCCAATTTCACCCCCTGAGGCCCAGGCAGCAACACAATTCGCCCAGGGCCATGGGGACTGCGGGTAGGTGCAA... |
Task1_train_41809 | An alteration has been detected on Chromosome 12. Is it pathogenic, and if so, what disease is involved? | Benign | TTCACCCAGGCTGGAGTCCGATGGCACGAACTTGGCTCACTACAACCCCCATCTCCCAGGTTCAAGCAACTCCTATGCCTCAGCCTTCCAAGTAGCTGGGATTACAGGTGTTCACCACCATACCTGGCTAATTTTTGTATTTTTTAGTAGAGATGGGGTTTTGCCATATTACCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCATTGCGCCTGGCCTCTTTCTTTACTCCTAATCCATGATTTGAGAGACTCAAACCAGCCAGAAAGACTC... | TTCACCCAGGCTGGAGTCCGATGGCACGAACTTGGCTCACTACAACCCCCATCTCCCAGGTTCAAGCAACTCCTATGCCTCAGCCTTCCAAGTAGCTGGGATTACAGGTGTTCACCACCATACCTGGCTAATTTTTGTATTTTTTAGTAGAGATGGGGTTTTGCCATATTACCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCATTGCGCCTGGCCTCTTTCTTTACTCCTAATCCATGATTTGAGAGACTCAAACCAGCCAGAAAGACTC... |
Task1_train_41810 | This alteration occurs on Chromosome 12. Is it associated with a disease or is it a benign variant? | Benign | CTGCAGGAAAGGTTCTTCCATATGAGATGGGTGACTGGGCCCTCTGAGTGATCTTTGCCGGTTACTGGCCATTCTTCTGGGCCTCAGAGCCAGGAGGGGCGGCTTTGTGGGGAAGCCCTTTCTGGCACCATTGTTTACTCCTGGGGTTGCTATGGTGATGCTGCTTGAGTGGTGATGCAGAGAAGAGGCCCTCACCTGTCCCTGGAGCCTCTTGTGACCCTTGGGCCCCTGGCTACTTTTCAGGTTAGACAGGCAGGGGATAGCACTTTCTTCAAGTTCTGACTGCAAAAAACTGTAACAGGAGCTGCTGCCGGGCAGAA... | CTGCAGGAAAGGTTCTTCCATATGAGATGGGTGACTGGGCCCTCTGAGTGATCTTTGCCGGTTACTGGCCATTCTTCTGGGCCTCAGAGCCAGGAGGGGCGGCTTTGTGGGGAAGCCCTTTCTGGCACCATTGTTTACTCCTGGGGTTGCTATGGTGATGCTGCTTGAGTGGTGATGCAGAGAAGAGGCCCTCACCTGTCCCTGGAGCCTCTTGTGACCCTTGGGCCCCTGGCTACTTTTCAGGTTAGACAGGCAGGGGATAGCACTTTCTTCAAGTTCTGACTGCAAAAAACTGTAACAGGAGCTGCTGCCGGGCAGAA... |
Task1_train_41811 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TGCCTGTGCAAGTGCTCCAACTGCTGCTTTGGGTGAACTTCAGGCCTTGCCTCTTCCCTATCACCATCGTCTCCATCAACACCCTCTTTCTTTTCCAGCCTCTCCTGGTGCCTTAGGAATCAGACGCCAATAAACCACAGAGCCCAGCATGTCCACCTTCGCTTTTATTGAGTAGTTAGTGTTCTCAAGCTGGCTCACACCCATGCGGTCAGCTGGGGCCTAGGGTGGCTCTTTGCAAAGCTGAGGGGCAAGCTAAGGAAGCCAGGCAGGTCAGGGGCCCTTTCGGCCTTCTCAAGCCTCCACCTGAGTTCTCGTCAATG... | TGCCTGTGCAAGTGCTCCAACTGCTGCTTTGGGTGAACTTCAGGCCTTGCCTCTTCCCTATCACCATCGTCTCCATCAACACCCTCTTTCTTTTCCAGCCTCTCCTGGTGCCTTAGGAATCAGACGCCAATAAACCACAGAGCCCAGCATGTCCACCTTCGCTTTTATTGAGTAGTTAGTGTTCTCAAGCTGGCTCACACCCATGCGGTCAGCTGGGGCCTAGGGTGGCTCTTTGCAAAGCTGAGGGGCAAGCTAAGGAAGCCAGGCAGGTCAGGGGCCCTTTCGGCCTTCTCAAGCCTCCACCTGAGTTCTCGTCAATG... |
Task1_train_41812 | Chromosome 12 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AAAAAGGAAAGGGGAGAAAACCCACTGCATGAAAACCCAAACAGGGCACATGCTACGGCCACATGAATGAATTTACGCTAAATTATGTATGTGTGGTATAATTTTGTGTGTAATATGTTTTATTTATAATTAAAGAAAATGTTTTTTAGAGACAGGGTCTCATTTTGTTGCCTAAGCTAGAATGCAGTGGCACGATTATAGCTCATTGCAGCCTCCAGCTCTGGAGCTCAAGTAATCCTTCTGCCTCAGCCTCCCAAGTGGCTGGGACAACAGGTATACATGAAAATGCCTGGCTAATTAAAAAAAAATTTTTTTTTTTT... | AAAAAGGAAAGGGGAGAAAACCCACTGCATGAAAACCCAAACAGGGCACATGCTACGGCCACATGAATGAATTTACGCTAAATTATGTATGTGTGGTATAATTTTGTGTGTAATATGTTTTATTTATAATTAAAGAAAATGTTTTTTAGAGACAGGGTCTCATTTTGTTGCCTAAGCTAGAATGCAGTGGCACGATTATAGCTCATTGCAGCCTCCAGCTCTGGAGCTCAAGTAATCCTTCTGCCTCAGCCTCCCAAGTGGCTGGGACAACAGGTATACATGAAAATGCCTGGCTAATTAAAAAAAAATTTTTTTTTTTT... |
Task1_train_41813 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | TCTCTCCAAACCACTGACATTTGATCAAGCCAGTTCATTGTGAAGGGCAGAGAAAGACAGACTCTTCAGTGCTGTTAAAATTGGCCTTGGGGTTTTGAAAGCTCTTAGAGGTCACCTGGTCTGAGTCAGTGCATGATCAAGCCCCAGTTGGCGCTGTGTGAACACCTGCCAGGGTGGACCTCAGGTGGCTCATATGATTGTGGGACAGCTCTAATTCTTGGTAAATTAAAAATCTGCCTTCTAATCATGCCTAGTGACTAGCCTTTGTTCTGCCCCCAAAGCCATGATAAGGCCACATGTAAGTCTTTCCATGTGACAGC... | TCTCTCCAAACCACTGACATTTGATCAAGCCAGTTCATTGTGAAGGGCAGAGAAAGACAGACTCTTCAGTGCTGTTAAAATTGGCCTTGGGGTTTTGAAAGCTCTTAGAGGTCACCTGGTCTGAGTCAGTGCATGATCAAGCCCCAGTTGGCGCTGTGTGAACACCTGCCAGGGTGGACCTCAGGTGGCTCATATGATTGTGGGACAGCTCTAATTCTTGGTAAATTAAAAATCTGCCTTCTAATCATGCCTAGTGACTAGCCTTTGTTCTGCCCCCAAAGCCATGATAAGGCCACATGTAAGTCTTTCCATGTGACAGC... |
Task1_train_41814 | A mutation located on Chromosome 12 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TCCCGCACATGACACACACAACACACACGTGCATGCGCGCACACACACACACACACACACACACACATTGGAGGGCCACCTCTGGGTGACCCATGCATCCCCTCTCCCTGCCTCATCCTATTAGTGGGACCACCACCACTGCTCTTCCCTAGGGGAAGGGAGTTTCCTGTGAATTCTCTTTAACCTTGGACTGGGGTCCAGGGCCAGCCTATGATGGAAAATAAATATGTCATCCTGTGCATCTGAGCAAGAGCTCAAAGCATCGGATACCCCATCCCCTCATTTTACTGATGTGGTGAGGACCAAGGAGGGAGCGGGCT... | TCCCGCACATGACACACACAACACACACGTGCATGCGCGCACACACACACACACACACACACACACATTGGAGGGCCACCTCTGGGTGACCCATGCATCCCCTCTCCCTGCCTCATCCTATTAGTGGGACCACCACCACTGCTCTTCCCTAGGGGAAGGGAGTTTCCTGTGAATTCTCTTTAACCTTGGACTGGGGTCCAGGGCCAGCCTATGATGGAAAATAAATATGTCATCCTGTGCATCTGAGCAAGAGCTCAAAGCATCGGATACCCCATCCCCTCATTTTACTGATGTGGTGAGGACCAAGGAGGGAGCGGGCT... |
Task1_train_41815 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TGTGGCAGATGATGACAAAGATGATGATGATGATGACCAAGTATTAAGTAAAGATGCCATTTACAGATGGACATAATCCCTGTCCTCACAGAATACTTGATTTAGTGGGGGACTAAAGCAATAATGACACAAATAAATACATCCTTTACAAATTGTGAGACTGCTGTGAAGGAGAAGGAAAGGTTGTGAAGAAACGTGTCTCAGACTCAGATTTTAATAAAGCGCCCCCGATTAACATTAGCAGATGACCTTGGCTCTGCCCCCAGCGCCAGCCCTTACTCACTGTGTGTCCTTAGGTAGGACACTCCAACTCTTCAGAC... | TGTGGCAGATGATGACAAAGATGATGATGATGATGACCAAGTATTAAGTAAAGATGCCATTTACAGATGGACATAATCCCTGTCCTCACAGAATACTTGATTTAGTGGGGGACTAAAGCAATAATGACACAAATAAATACATCCTTTACAAATTGTGAGACTGCTGTGAAGGAGAAGGAAAGGTTGTGAAGAAACGTGTCTCAGACTCAGATTTTAATAAAGCGCCCCCGATTAACATTAGCAGATGACCTTGGCTCTGCCCCCAGCGCCAGCCCTTACTCACTGTGTGTCCTTAGGTAGGACACTCCAACTCTTCAGAC... |
Task1_train_41816 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GCTAGCTGGTTGCAAAGCCACACATGACTCAAAACCAGAAACTCCTGATTCCGAGCCTCCCACTTCCCAAAGTTACACACTAAGCACCTGGACACCCTGCTAAAATGCAGATTCGGTGGGGCTGGGGGCAAGACTCTGCATTCCTAAGATGTTTCCAGGTGACGCCAATGTTGCGGGTCCATGGACTACACTTTCAACAGCAAGTCTCTACACTGTTGTCTGGAAGGATACAGGGATCCTTAAACTTAGCCTCTGATTATATTCAGGCTCAAACTCTCCACTTCAGCCAGACAAATCCTCTAAGATTAACAAAGATACTT... | GCTAGCTGGTTGCAAAGCCACACATGACTCAAAACCAGAAACTCCTGATTCCGAGCCTCCCACTTCCCAAAGTTACACACTAAGCACCTGGACACCCTGCTAAAATGCAGATTCGGTGGGGCTGGGGGCAAGACTCTGCATTCCTAAGATGTTTCCAGGTGACGCCAATGTTGCGGGTCCATGGACTACACTTTCAACAGCAAGTCTCTACACTGTTGTCTGGAAGGATACAGGGATCCTTAAACTTAGCCTCTGATTATATTCAGGCTCAAACTCTCCACTTCAGCCAGACAAATCCTCTAAGATTAACAAAGATACTT... |
Task1_train_41817 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | TGAACTACTTAGTCATGGCAACAACAACTTGCCCCAGATTTCTGGAGAAGGGACAAGTCTTTCAACTTTTGATGAAAAACAAGCCAAAGCTCACTAAGCTGCCAAATCGCTTAGCCAATCGGACCACCAAGAAAAGTCAAAGTGCAGATGCCCAGTCTCGAACTTCTAGAACACACCAAGGCCACCCCTCCTGGGAGGATATGGGAGTATAGGCTAGAAAGGATTCTGGGAGGTTTATCAATCCATTTCACTGCTTCCAGAACAACACACAAATCATTTTGGTGAGCAAAATCTTTAAAGAGCCCTCAAATATTCATAGC... | TGAACTACTTAGTCATGGCAACAACAACTTGCCCCAGATTTCTGGAGAAGGGACAAGTCTTTCAACTTTTGATGAAAAACAAGCCAAAGCTCACTAAGCTGCCAAATCGCTTAGCCAATCGGACCACCAAGAAAAGTCAAAGTGCAGATGCCCAGTCTCGAACTTCTAGAACACACCAAGGCCACCCCTCCTGGGAGGATATGGGAGTATAGGCTAGAAAGGATTCTGGGAGGTTTATCAATCCATTTCACTGCTTCCAGAACAACACACAAATCATTTTGGTGAGCAAAATCTTTAAAGAGCCCTCAAATATTCATAGC... |
Task1_train_41818 | Consider a variant on Chromosome 12. Determine its clinical classification and disease relevance. | Benign | AACAAGCCAAAGCTCACTAAGCTGCCAAATCGCTTAGCCAATCGGACCACCAAGAAAAGTCAAAGTGCAGATGCCCAGTCTCGAACTTCTAGAACACACCAAGGCCACCCCTCCTGGGAGGATATGGGAGTATAGGCTAGAAAGGATTCTGGGAGGTTTATCAATCCATTTCACTGCTTCCAGAACAACACACAAATCATTTTGGTGAGCAAAATCTTTAAAGAGCCCTCAAATATTCATAGCCTTTTCTATTTCCCTATCTGAGGTCTCACAGCCGTGAATGTTTCCCTCATGCTGCAATCTAAGCCCACTTCAGTGAG... | AACAAGCCAAAGCTCACTAAGCTGCCAAATCGCTTAGCCAATCGGACCACCAAGAAAAGTCAAAGTGCAGATGCCCAGTCTCGAACTTCTAGAACACACCAAGGCCACCCCTCCTGGGAGGATATGGGAGTATAGGCTAGAAAGGATTCTGGGAGGTTTATCAATCCATTTCACTGCTTCCAGAACAACACACAAATCATTTTGGTGAGCAAAATCTTTAAAGAGCCCTCAAATATTCATAGCCTTTTCTATTTCCCTATCTGAGGTCTCACAGCCGTGAATGTTTCCCTCATGCTGCAATCTAAGCCCACTTCAGTGAG... |
Task1_train_41819 | A mutation on Chromosome 12 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TCCCTGTGTCTATTCCAAAGCACATTTTAGGAAAAAAAATGGTGGAGGGGTAGTTATGTTTTGTTTGAGATCTCAGCCATCTACAATTTTCCAAGTAGTGGCCTGCTAAAAACTGCTTCATTTCCCACCTTGGCTTCCTGCACAAGCCTGGTTTGCCGAGGATACCGTGTGCAAATGCTTCCACATGATGGGTTTTGGCCAGGAAGGCACCCACAGCTGGGGCAGCTGGGAGGCACCGTAGCTCTAGAGACCCAGGAGAGGTAAAGATGCTGGGGAGCTGATGGTGATAGGAAGCCTTAGGGAGAACTCCATGAAAAACC... | TCCCTGTGTCTATTCCAAAGCACATTTTAGGAAAAAAAATGGTGGAGGGGTAGTTATGTTTTGTTTGAGATCTCAGCCATCTACAATTTTCCAAGTAGTGGCCTGCTAAAAACTGCTTCATTTCCCACCTTGGCTTCCTGCACAAGCCTGGTTTGCCGAGGATACCGTGTGCAAATGCTTCCACATGATGGGTTTTGGCCAGGAAGGCACCCACAGCTGGGGCAGCTGGGAGGCACCGTAGCTCTAGAGACCCAGGAGAGGTAAAGATGCTGGGGAGCTGATGGTGATAGGAAGCCTTAGGGAGAACTCCATGAAAAACC... |
Task1_train_41820 | Consider this mutation on Chromosome 12. Is this a benign change or a disease-causing variant? | Benign | AGTGAGGACTGGGGAGGAAGGTTGAGTCAGTATTTCTGGGACTTAATGTTTCTGACTATATTTCAAGTCAAATACAAGCGATTTCTTTAAAACTTTATACCTAGTTTCAATTCTCCATGCCTCCTCATCCCTTCATTAAAGAGTGGAGCTCAATGAGAGTTAATTAGGTTATATACAGCAAGAGTGCTGAGTTGCACAGTACTTGTGGCCCAGAGTTGACCTCCATAAACATGAATTTCCTTTTCTTTCTGTCTAGAGGGAATAATCAAAAGTTAAGCCTGATTTTGAAACTACTAACACCAACCACCGCTACTGCAGAC... | AGTGAGGACTGGGGAGGAAGGTTGAGTCAGTATTTCTGGGACTTAATGTTTCTGACTATATTTCAAGTCAAATACAAGCGATTTCTTTAAAACTTTATACCTAGTTTCAATTCTCCATGCCTCCTCATCCCTTCATTAAAGAGTGGAGCTCAATGAGAGTTAATTAGGTTATATACAGCAAGAGTGCTGAGTTGCACAGTACTTGTGGCCCAGAGTTGACCTCCATAAACATGAATTTCCTTTTCTTTCTGTCTAGAGGGAATAATCAAAAGTTAAGCCTGATTTTGAAACTACTAACACCAACCACCGCTACTGCAGAC... |
Task1_train_41821 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ATCTTTTTTTCAATTTTGCCTTCTCTGGATTTCCCTAATGTTCCCCTCCCATAATCCTTTTTATTCTTATATTCCGACATGCTTTTAAGTAGTACTACAAAGAGGATAAGCTAACAGAAGCTGAGATAAATTTTATTTTTATTTTAAACAGAAGAAAGGAAAAAGGGGTTACATTTTTATAAATATCTATAAATATAGAAGGATAGGCAAACTTCCAAATAAATAAATAAATACTGCCACATGACGAGGGATATAAGAAATTGTAGGAGCTATTTTGGCTTTGCCATAAAGAAAACCCCTGATGGTAGTGTTGAGTTTGT... | ATCTTTTTTTCAATTTTGCCTTCTCTGGATTTCCCTAATGTTCCCCTCCCATAATCCTTTTTATTCTTATATTCCGACATGCTTTTAAGTAGTACTACAAAGAGGATAAGCTAACAGAAGCTGAGATAAATTTTATTTTTATTTTAAACAGAAGAAAGGAAAAAGGGGTTACATTTTTATAAATATCTATAAATATAGAAGGATAGGCAAACTTCCAAATAAATAAATAAATACTGCCACATGACGAGGGATATAAGAAATTGTAGGAGCTATTTTGGCTTTGCCATAAAGAAAACCCCTGATGGTAGTGTTGAGTTTGT... |
Task1_train_41822 | This is a variant located on Chromosome 12. Is this mutation a likely cause of disease or not? | Benign | AATAAGCCAAATGATGGGCCGAGGGCTGCAGGAAAGAGTAGGTCAGTGAGAGCAGAGGTTTTCGTCAATGTGCTTAGAAGCTGGTTGCATTAACCCAAGTGCCAGCATTGGCACTCCCAGAGGTGACCTATGGGGGTGGGGATGGGAATGGGTGGGACTGGTACCAGCCTAAAGTGTATAACGGGTAGGCTGCTTCTCTAGCGTACGTGATCGGAGACCAGAGGATTGAAAACCCTAGTGCAGAATCTCAGCACACTGATGAGGATGAAAATAGCCTCCCATTCCACTCCTCCTGCTGCGCACGAGGCTGGGGCATCTTG... | AATAAGCCAAATGATGGGCCGAGGGCTGCAGGAAAGAGTAGGTCAGTGAGAGCAGAGGTTTTCGTCAATGTGCTTAGAAGCTGGTTGCATTAACCCAAGTGCCAGCATTGGCACTCCCAGAGGTGACCTATGGGGGTGGGGATGGGAATGGGTGGGACTGGTACCAGCCTAAAGTGTATAACGGGTAGGCTGCTTCTCTAGCGTACGTGATCGGAGACCAGAGGATTGAAAACCCTAGTGCAGAATCTCAGCACACTGATGAGGATGAAAATAGCCTCCCATTCCACTCCTCCTGCTGCGCACGAGGCTGGGGCATCTTG... |
Task1_train_41823 | A mutation on Chromosome 12 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AGATATAGAACTTGGATCAAAAGATCACCAACTTTCCACTGAGTGCCTACTTCAAGTATAACTATAGTACTGAAATTTAACAATAGTTTTCACTCAGAACCTTGAAGAAAATCATCCTCTTAAAAAAGAAAATTAGGCACAGAGTCCAAGCTTCTGAAGATCTGGGTATATATCCAAAGGAATAGAAATCATTCTATATAAAGATACATGCACACGCATGGTCTTCGCAGTACTATTCACAATAGCAAAGACGTGGAATCAACCTGAATGCCCATCAATGATAGACTGGATAAAGAAAATGTGGCACATATACATCATGG... | AGATATAGAACTTGGATCAAAAGATCACCAACTTTCCACTGAGTGCCTACTTCAAGTATAACTATAGTACTGAAATTTAACAATAGTTTTCACTCAGAACCTTGAAGAAAATCATCCTCTTAAAAAAGAAAATTAGGCACAGAGTCCAAGCTTCTGAAGATCTGGGTATATATCCAAAGGAATAGAAATCATTCTATATAAAGATACATGCACACGCATGGTCTTCGCAGTACTATTCACAATAGCAAAGACGTGGAATCAACCTGAATGCCCATCAATGATAGACTGGATAAAGAAAATGTGGCACATATACATCATGG... |
Task1_train_41824 | A mutation on Chromosome 12 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CTTAAAAATATACTAATATTCAGTGCGTCTATTTATTAGTTGAAGTTTGAACATGCTGCTTCTCATTCCTTCTACTCTTAGAGGGAGTCAATAAAATAGATGACTGGCTTTATCTTTAGAGTAGACAAAGGTGTGTGTGTGTGTGTATATAAAAGTGGGGGACTGCAAGTCTATTGTCCTATTTTAGATACATGTTTCAATTTAAAATAATCTAAAACAACACATTCCAATACAAAAAAAGTCTAAAGCCAGAATGTATTATGTATGTTATATATGAGGGGTTTGATTTCAAAGATGGCTACAAAAGGCTTTCTCACACA... | CTTAAAAATATACTAATATTCAGTGCGTCTATTTATTAGTTGAAGTTTGAACATGCTGCTTCTCATTCCTTCTACTCTTAGAGGGAGTCAATAAAATAGATGACTGGCTTTATCTTTAGAGTAGACAAAGGTGTGTGTGTGTGTGTATATAAAAGTGGGGGACTGCAAGTCTATTGTCCTATTTTAGATACATGTTTCAATTTAAAATAATCTAAAACAACACATTCCAATACAAAAAAAGTCTAAAGCCAGAATGTATTATGTATGTTATATATGAGGGGTTTGATTTCAAAGATGGCTACAAAAGGCTTTCTCACACA... |
Task1_train_41825 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TGTTTCAATTTAAAATAATCTAAAACAACACATTCCAATACAAAAAAAGTCTAAAGCCAGAATGTATTATGTATGTTATATATGAGGGGTTTGATTTCAAAGATGGCTACAAAAGGCTTTCTCACACATTACACACCTGAAAGCTATGCTTACTTTTAGATTTTTTTCATCAGTTTAAATTTTCTTCAGCATATAGCCTCCCACTCCCCACCTCTACTAATTGCTATATACTGTAAAATAGTTGTCTGTTTCACGGATTGGAAACCCTGCGTGGAGACAGAGCTTGCCAACGACCCTTAGGAATAGATCTAATATTGGAA... | TGTTTCAATTTAAAATAATCTAAAACAACACATTCCAATACAAAAAAAGTCTAAAGCCAGAATGTATTATGTATGTTATATATGAGGGGTTTGATTTCAAAGATGGCTACAAAAGGCTTTCTCACACATTACACACCTGAAAGCTATGCTTACTTTTAGATTTTTTTCATCAGTTTAAATTTTCTTCAGCATATAGCCTCCCACTCCCCACCTCTACTAATTGCTATATACTGTAAAATAGTTGTCTGTTTCACGGATTGGAAACCCTGCGTGGAGACAGAGCTTGCCAACGACCCTTAGGAATAGATCTAATATTGGAA... |
Task1_train_41826 | Given this context: Chromosome 12 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TAAGTAGCACGTGTAGTCTTTTTAAGACCAAAGTCAAAGACCATACAGTTTCTTGTTTAGGCTTGATATAGCCTAATCTGGATGCTCTGTAATCGTGTGTTTTCCCAGTCATCAGATAAATATAGCGACCCAGTTGCAAGCGTTGCTAATACCATGTAAATACCACTTAATTAAGCAGAGAAAGCCTGTTTTTCCTTATCTTCTGATTCCTATGATGATGAAATTTTCTAAATAATTCTAGCCTCTTGTGCCACCCTTTGCTACTTAATGATTAACAGCAGTTGGTCCACTTTTCTCAATCAAGAGGAGACAATCAAAAG... | TAAGTAGCACGTGTAGTCTTTTTAAGACCAAAGTCAAAGACCATACAGTTTCTTGTTTAGGCTTGATATAGCCTAATCTGGATGCTCTGTAATCGTGTGTTTTCCCAGTCATCAGATAAATATAGCGACCCAGTTGCAAGCGTTGCTAATACCATGTAAATACCACTTAATTAAGCAGAGAAAGCCTGTTTTTCCTTATCTTCTGATTCCTATGATGATGAAATTTTCTAAATAATTCTAGCCTCTTGTGCCACCCTTTGCTACTTAATGATTAACAGCAGTTGGTCCACTTTTCTCAATCAAGAGGAGACAATCAAAAG... |
Task1_train_41827 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCTGGATCCCTTCATCATCACCAGCAAAATACAAAATAGGGACATTGAGCTCAGAGGCAGCTACCCATTGAAGGACGGCTTGGAGTTGCTTGTTCTGAACTGTGTCCGTTAGGTTGTGATTGCTGACAATCACCGTGGGTGCTGCACACCCTTCAGGGGGCTGTCCTGATGTGCCTCTCATTTCATTATGGATAGCTTGATAGGCATTCTGCAGGACAGCTTCTGCTGACCCTGTGCCCTTGGCTGGTAAGCACTCATATAAACTATCTGGGAAGGCCGAAGTTAGCCTACTGGCATCTCCAGACTTGTCATCTCCCAGC... | CCTGGATCCCTTCATCATCACCAGCAAAATACAAAATAGGGACATTGAGCTCAGAGGCAGCTACCCATTGAAGGACGGCTTGGAGTTGCTTGTTCTGAACTGTGTCCGTTAGGTTGTGATTGCTGACAATCACCGTGGGTGCTGCACACCCTTCAGGGGGCTGTCCTGATGTGCCTCTCATTTCATTATGGATAGCTTGATAGGCATTCTGCAGGACAGCTTCTGCTGACCCTGTGCCCTTGGCTGGTAAGCACTCATATAAACTATCTGGGAAGGCCGAAGTTAGCCTACTGGCATCTCCAGACTTGTCATCTCCCAGC... |
Task1_train_41828 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TTGAATCCAGCCTGGACAACATAGTGAGACCCTGTCTCTGGAACAAAAAAAAAAAAAAGAAAGAAAAGAAAAACCTACTGCCCTGAGGTAACTGTTGATGGGAGCTCCTTTCTCGTCCTAGGTTTTATATTGTCCTGATTTGAACCAAATAAAATAAAATCTTGAACTTACCATGTCACACCCTAGTGGTCTGGTTAAGGAGACTGTCACATCCATTGTGCCACAAACTGATCTTCATTTGGGTTTTCATCCATTCATTCAACAAATGTTTATTGAATGCCTACTATGTCTTAGATAATGTACTAGGTACTCAGAAGGTT... | TTGAATCCAGCCTGGACAACATAGTGAGACCCTGTCTCTGGAACAAAAAAAAAAAAAAGAAAGAAAAGAAAAACCTACTGCCCTGAGGTAACTGTTGATGGGAGCTCCTTTCTCGTCCTAGGTTTTATATTGTCCTGATTTGAACCAAATAAAATAAAATCTTGAACTTACCATGTCACACCCTAGTGGTCTGGTTAAGGAGACTGTCACATCCATTGTGCCACAAACTGATCTTCATTTGGGTTTTCATCCATTCATTCAACAAATGTTTATTGAATGCCTACTATGTCTTAGATAATGTACTAGGTACTCAGAAGGTT... |
Task1_train_41829 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AAAAGAAAGCACGGTGTGGGGGTGTGGGGTGTGGTGATCTAAGGAGGGTTCCTGGAGGAGGCAGGCTCGGATTGGGACTTGAAGGCGTCATAGGATTTGAGACAGCAGAGAAAATGAGGGAAGACTGGGAAACTGGGTCGGGGTGGAGAGCTAGGGAGCGCCGAAGGAATGGTGTGAACAAAAGTGAGGAATCCGGAAGCGCCCTGAGCTGACCAGCCTGGGATAGCAGGCTTTGGGGAGGAGACCGGTAGGAGGGCAAAGCTGGGAAGGGAGCATAGGTTGTCTTCAGAAAACCCGTCGAGGCGTCCTTAATCTTTGTG... | AAAAGAAAGCACGGTGTGGGGGTGTGGGGTGTGGTGATCTAAGGAGGGTTCCTGGAGGAGGCAGGCTCGGATTGGGACTTGAAGGCGTCATAGGATTTGAGACAGCAGAGAAAATGAGGGAAGACTGGGAAACTGGGTCGGGGTGGAGAGCTAGGGAGCGCCGAAGGAATGGTGTGAACAAAAGTGAGGAATCCGGAAGCGCCCTGAGCTGACCAGCCTGGGATAGCAGGCTTTGGGGAGGAGACCGGTAGGAGGGCAAAGCTGGGAAGGGAGCATAGGTTGTCTTCAGAAAACCCGTCGAGGCGTCCTTAATCTTTGTG... |
Task1_train_41830 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | CCTAGAAGAGAAAGTCTGGAAGGACTCCTAGGGTCAGGAGCCAGGTTAACACTGGGATCACTAGGTCTGGAGATTGTAAAAATGTGCAGAAATGCCTGAGCCTTCTTTATCATTTAAAGATACCAAAATGCTTCCTTTCCTAATCCAAGCTGCCAATAACCTCTTACAGTTGGATCATTGTTTGAAGAGAGATGGGTAAGAGTTGATTCTGATGTCCCAGTATACCAAGGTATGATAGGAAAACAAGTACCCTCCAGGACATCCCTAGCTTTTTTATTTCCACACAGTCATATTGTGACTGTCCCAAGCTGTACAAAGAA... | CCTAGAAGAGAAAGTCTGGAAGGACTCCTAGGGTCAGGAGCCAGGTTAACACTGGGATCACTAGGTCTGGAGATTGTAAAAATGTGCAGAAATGCCTGAGCCTTCTTTATCATTTAAAGATACCAAAATGCTTCCTTTCCTAATCCAAGCTGCCAATAACCTCTTACAGTTGGATCATTGTTTGAAGAGAGATGGGTAAGAGTTGATTCTGATGTCCCAGTATACCAAGGTATGATAGGAAAACAAGTACCCTCCAGGACATCCCTAGCTTTTTTATTTCCACACAGTCATATTGTGACTGTCCCAAGCTGTACAAAGAA... |
Task1_train_41831 | Consider this mutation on Chromosome 12. Is this a benign change or a disease-causing variant? | Benign | TCTAGATCAGATGGACTTCCCCAGTAATGTTTTCTTTGGGCTTATATAAAAATTACGGTGCATTCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCGGAGGCAGGCGGATCACGAGGTCAGGAGATCGAGATTGAGACCATCCTGGCCAACACGGTGAAACCCCGTCTCTGCTAAAAATACAAAAATTAGCCGGGTGTGGTAGCGGGCGCCTGTAATCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATCATTTGAACCCCGGGAGTCGGAGGTTGCAGTGAGCCAAGATCGCCATTGCACCCAGCCTGGCGAC... | TCTAGATCAGATGGACTTCCCCAGTAATGTTTTCTTTGGGCTTATATAAAAATTACGGTGCATTCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCGGAGGCAGGCGGATCACGAGGTCAGGAGATCGAGATTGAGACCATCCTGGCCAACACGGTGAAACCCCGTCTCTGCTAAAAATACAAAAATTAGCCGGGTGTGGTAGCGGGCGCCTGTAATCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATCATTTGAACCCCGGGAGTCGGAGGTTGCAGTGAGCCAAGATCGCCATTGCACCCAGCCTGGCGAC... |
Task1_train_41832 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | TGCAGCTGTATTATTCTTTTTGAGGGGAGTAGAGAATGTAATCCTAGTTGTATGCCATATTTTTTGTATTGTTCAAGTTGCATTTTGTTGGGCCTGTAATATTGAAGAAAATGTCACTTGTATGCAGAATAGGAGGGAGATTCCTTATGCTGTAGAGGAACCATTTTCCTAGGATAGTACAATTCCTTAGAGTCATCTCTAAGGGTGAGCAGCAAAGCTAGAATCCCTCTCTTGGCTTTGACCTTGAAGGAGTCAGTTTTCCCAAAGACTAGTTCCCATGGAAAGAAGATGGTCTCCTTATCACAGCAGCAAGAGGAGGC... | TGCAGCTGTATTATTCTTTTTGAGGGGAGTAGAGAATGTAATCCTAGTTGTATGCCATATTTTTTGTATTGTTCAAGTTGCATTTTGTTGGGCCTGTAATATTGAAGAAAATGTCACTTGTATGCAGAATAGGAGGGAGATTCCTTATGCTGTAGAGGAACCATTTTCCTAGGATAGTACAATTCCTTAGAGTCATCTCTAAGGGTGAGCAGCAAAGCTAGAATCCCTCTCTTGGCTTTGACCTTGAAGGAGTCAGTTTTCCCAAAGACTAGTTCCCATGGAAAGAAGATGGTCTCCTTATCACAGCAGCAAGAGGAGGC... |
Task1_train_41833 | This mutation occurs on Chromosome 12. Does this change lead to a known medical condition, or is it benign? | Benign | ACAAACAAAAAAAGTCTATCATTGTTATTCCAGGTGGCAATGCTGAGTGTGATGAAGAAAAGTAAGGCAGGATCGAGGGACAGAGAGGGACGGGGTGGGGGTATTTTGGCTAGGATGGTCAGGGAAGATGTCAGGAAGGAGGTGACATTTGAGCAGAGAGCTGAAGAGAGGGAATGTGATGCACAGGTCTGAGGAAGAGTGCCCAAAGCACAGAGGGCAACAGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAGAGGGCAACGGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAAAGGGCAATAGCACAAAG... | ACAAACAAAAAAAGTCTATCATTGTTATTCCAGGTGGCAATGCTGAGTGTGATGAAGAAAAGTAAGGCAGGATCGAGGGACAGAGAGGGACGGGGTGGGGGTATTTTGGCTAGGATGGTCAGGGAAGATGTCAGGAAGGAGGTGACATTTGAGCAGAGAGCTGAAGAGAGGGAATGTGATGCACAGGTCTGAGGAAGAGTGCCCAAAGCACAGAGGGCAACAGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAGAGGGCAACGGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAAAGGGCAATAGCACAAAG... |
Task1_train_41834 | A mutation on Chromosome 12 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TTTGGCTAGGATGGTCAGGGAAGATGTCAGGAAGGAGGTGACATTTGAGCAGAGAGCTGAAGAGAGGGAATGTGATGCACAGGTCTGAGGAAGAGTGCCCAAAGCACAGAGGGCAACAGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAGAGGGCAACGGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAAAGGGCAATAGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAGAGGGCAACAGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAGAGGGCAACAGCACAAAGACCTGAGGTCAAGG... | TTTGGCTAGGATGGTCAGGGAAGATGTCAGGAAGGAGGTGACATTTGAGCAGAGAGCTGAAGAGAGGGAATGTGATGCACAGGTCTGAGGAAGAGTGCCCAAAGCACAGAGGGCAACAGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAGAGGGCAACGGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAAAGGGCAATAGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAGAGGGCAACAGCACAAAGACCTGAGGTCAAGGTGCCCAAAGCAGAGAGGGCAACAGCACAAAGACCTGAGGTCAAGG... |
Task1_train_41835 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | GGCCTCTTCAGGGACACAGCTGCCTTCCAACATGACTTTATCTGGAGGGCAGAAACAGCCTTCGGAGGGATGGTCCCCACAGGAGCTCACGTTGCCATCACAGTGCCGGGGACAGCCATGCTCACAGTGGTTGTAGACCAGAGATGGTGGGCATGACATAGCTGTAGACAGAGAAGGAGGTCACTTGCAAAGGCCCACACCAGCCAGAGTGAAATGGGCACAGCTGATTCAACATGGTTAATCATCAGACAAACTTGCCAGGGCAGAGACGGCTATTTTCCACCAATCTTCATCCTCCCCACCTTCCATAGAAACAGAAC... | GGCCTCTTCAGGGACACAGCTGCCTTCCAACATGACTTTATCTGGAGGGCAGAAACAGCCTTCGGAGGGATGGTCCCCACAGGAGCTCACGTTGCCATCACAGTGCCGGGGACAGCCATGCTCACAGTGGTTGTAGACCAGAGATGGTGGGCATGACATAGCTGTAGACAGAGAAGGAGGTCACTTGCAAAGGCCCACACCAGCCAGAGTGAAATGGGCACAGCTGATTCAACATGGTTAATCATCAGACAAACTTGCCAGGGCAGAGACGGCTATTTTCCACCAATCTTCATCCTCCCCACCTTCCATAGAAACAGAAC... |
Task1_train_41836 | Assess the clinical impact of this variant found on Chromosome 12. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CGGATTATTTTGAATCAAGTAGAGCCACAAAAAGAGCCTCTTCGTCACCTGCTGCTTCAGGTGCCTCGCTCACCCACCTATATTGGCTTTTGAAATGAAAGCCTTGGCGAAACTCTTCATTTCATCAAAATAAGAAGCTGGGAAACTGGAGGAGCCATCCAGGAGAAGGATCACGTCCAGGGGCTGGCTGCAGTCTGCAAAGACAACCAGGAAGGTGAGCACACAGGTGCCAGCAGGGACAATGGCCACCAGGCCTACAACCTGACATCCAATAGGATCTGCAGGGCGTGCTGACCACGTGGCACCACCAAGGGGGGCGG... | CGGATTATTTTGAATCAAGTAGAGCCACAAAAAGAGCCTCTTCGTCACCTGCTGCTTCAGGTGCCTCGCTCACCCACCTATATTGGCTTTTGAAATGAAAGCCTTGGCGAAACTCTTCATTTCATCAAAATAAGAAGCTGGGAAACTGGAGGAGCCATCCAGGAGAAGGATCACGTCCAGGGGCTGGCTGCAGTCTGCAAAGACAACCAGGAAGGTGAGCACACAGGTGCCAGCAGGGACAATGGCCACCAGGCCTACAACCTGACATCCAATAGGATCTGCAGGGCGTGCTGACCACGTGGCACCACCAAGGGGGGCGG... |
Task1_train_41837 | Given this context: Chromosome 12 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TGCAAAAGGAAATGGAGCGGCAGCCCCTCCCTGGACAATGAGCTGCTGTGTCCTCAGATCTTGCAGGGCAGGTGAACATACTGTGATTCTTCCAGCTATAAATGCCTAGTGCTCCTGTTAGTGTCTGAGCACATCTGAGATTTGATGAAATGATGTAATTGTTGTTTTCCTCAGCAGAAATATTACAAGAATTTAAATAAATCTATGGCCGTGAATAAAAACAAAAACAAAGAAACAAAAGTACTGACAAGTGTGTGACTCAAAAGATACTAAAAGAAGGCTTATTATTCTGGGATGGTCCCAAACACACCGAATAAAGA... | TGCAAAAGGAAATGGAGCGGCAGCCCCTCCCTGGACAATGAGCTGCTGTGTCCTCAGATCTTGCAGGGCAGGTGAACATACTGTGATTCTTCCAGCTATAAATGCCTAGTGCTCCTGTTAGTGTCTGAGCACATCTGAGATTTGATGAAATGATGTAATTGTTGTTTTCCTCAGCAGAAATATTACAAGAATTTAAATAAATCTATGGCCGTGAATAAAAACAAAAACAAAGAAACAAAAGTACTGACAAGTGTGTGACTCAAAAGATACTAAAAGAAGGCTTATTATTCTGGGATGGTCCCAAACACACCGAATAAAGA... |
Task1_train_41838 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATGCATACACTCAAACACACATATACATACATCTATGTACTCATACACACACTCACACACGTGCTCACACATACACAGATGCACACACATACACCCATGTACTCATACACACACACACGCATACACATACATACACACACGTAGCCATACACACACACGCGCTCACGCATACACACACATACACCCATGTACTCATACACAGTCACACACACGCACATGCATACACCCACACACACGCACATGCATACACCCACACAGACATGCTCATGCATACACACATGCACACATACATGCATACATATGTCCATACAACACACACA... | ATGCATACACTCAAACACACATATACATACATCTATGTACTCATACACACACTCACACACGTGCTCACACATACACAGATGCACACACATACACCCATGTACTCATACACACACACACGCATACACATACATACACACACGTAGCCATACACACACACGCGCTCACGCATACACACACATACACCCATGTACTCATACACAGTCACACACACGCACATGCATACACCCACACACACGCACATGCATACACCCACACAGACATGCTCATGCATACACACATGCACACATACATGCATACATATGTCCATACAACACACACA... |
Task1_train_41839 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CCTTCACAAGGGACAGACTGGACAGAGGAACACCCCGAGGGATGATGTCTGCACCATCAGATGGGCCCAAACAGGGTGTTTCCAGGCCCAGCTCCATTTTCTTTGTGTTATGGCCAAGAACACGTGTCCCGTGCTGCAGGCGGCACGCTGCGCACCCTTAATAAATTACACGGACTTCTCTGCTCTCTCGAATCTGGCCGCAATAATTTGCACACTCGCCGGCATCGTAAGGAAGCAGTTGTGAAAATAACCGAATCTCTTACAATATGAACCTGCAAGTTAGAATCCCCTGTGGCTGAAGTGCGAGTCACCTCGTCACG... | CCTTCACAAGGGACAGACTGGACAGAGGAACACCCCGAGGGATGATGTCTGCACCATCAGATGGGCCCAAACAGGGTGTTTCCAGGCCCAGCTCCATTTTCTTTGTGTTATGGCCAAGAACACGTGTCCCGTGCTGCAGGCGGCACGCTGCGCACCCTTAATAAATTACACGGACTTCTCTGCTCTCTCGAATCTGGCCGCAATAATTTGCACACTCGCCGGCATCGTAAGGAAGCAGTTGTGAAAATAACCGAATCTCTTACAATATGAACCTGCAAGTTAGAATCCCCTGTGGCTGAAGTGCGAGTCACCTCGTCACG... |
Task1_train_41840 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TTACATTGAATCAGGATGCATTGCAGAAATTTCCAGACCCAGGCTTGAAAAGACCTGAGTTTGGGTGCTAAAAAGGAGTTTTAATGGACCCAACAGAATCATTCCTAAATGGTTACAACTAATGTGGGGAGAGAAGGCCATCTGACCACAATGGCTTTAAAAGAGATCTCTGCTCGCGTCAGCCCCTGCCCAGCCACTCCATGCGAATTTGCAACACCCGCAACACTCCATCCCTGGACACTCCAATCTCCCCTCCCTGCTGCTTCCCCTCTGATATCCTATATATGTTCTTCTCACCATCTGATATACTACACATCTCA... | TTACATTGAATCAGGATGCATTGCAGAAATTTCCAGACCCAGGCTTGAAAAGACCTGAGTTTGGGTGCTAAAAAGGAGTTTTAATGGACCCAACAGAATCATTCCTAAATGGTTACAACTAATGTGGGGAGAGAAGGCCATCTGACCACAATGGCTTTAAAAGAGATCTCTGCTCGCGTCAGCCCCTGCCCAGCCACTCCATGCGAATTTGCAACACCCGCAACACTCCATCCCTGGACACTCCAATCTCCCCTCCCTGCTGCTTCCCCTCTGATATCCTATATATGTTCTTCTCACCATCTGATATACTACACATCTCA... |
Task1_train_41841 | A variant on Chromosome 12 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTATTAAAAATACAAAAATTAGCTGGGCATGATGGTGGGCACCTGTAATCTCAGCTACTCGGGAGGTTGAGGCAGGAGAATCGCTTCAGCCTGGAAGGCGGAGGTTGTGGTGAGCCAAGATCGTGCCACTGCCCTCCAGCCTGGGCAACAGAGTGAGACCCTCTCTCAAAAAACAAAACAAACAAAAAGAAAGTGAACTGGCTAACGTGAAGCACCCCCTTGAAGACCGGGGTGCAGGAGGCAAGACTGGTCAGGAACCAGGAGACCCGAGTTC... | GTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTATTAAAAATACAAAAATTAGCTGGGCATGATGGTGGGCACCTGTAATCTCAGCTACTCGGGAGGTTGAGGCAGGAGAATCGCTTCAGCCTGGAAGGCGGAGGTTGTGGTGAGCCAAGATCGTGCCACTGCCCTCCAGCCTGGGCAACAGAGTGAGACCCTCTCTCAAAAAACAAAACAAACAAAAAGAAAGTGAACTGGCTAACGTGAAGCACCCCCTTGAAGACCGGGGTGCAGGAGGCAAGACTGGTCAGGAACCAGGAGACCCGAGTTC... |
Task1_train_41842 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AAAGGCATGAGGCAGAGAACTAATCCTCGCTCTGCCATGACACGGTTGGTGGGGGTCAGAGTGGGATCAGTCCTCTGATCAGAGGAGTCTATCCTAGCCCTGGAAGTTCTGGAGTGCTGCACCATCCCTCCACTTCCTGTGCCCTGGTTGCCTCATTTATAAAATGGCAGTAATATTTGCACTGTCCACCTGCCAGGGTCATTTCCAGAGAAACAGTGAAAAGTATGGATTGCTATCCAGTGTGATTCCAGGACCACCAAGAACAAGAGGAAGTGGCCCACACATGCAGAGTCCCAGTGTCCAGGGGAAGAATCTGGTGG... | AAAGGCATGAGGCAGAGAACTAATCCTCGCTCTGCCATGACACGGTTGGTGGGGGTCAGAGTGGGATCAGTCCTCTGATCAGAGGAGTCTATCCTAGCCCTGGAAGTTCTGGAGTGCTGCACCATCCCTCCACTTCCTGTGCCCTGGTTGCCTCATTTATAAAATGGCAGTAATATTTGCACTGTCCACCTGCCAGGGTCATTTCCAGAGAAACAGTGAAAAGTATGGATTGCTATCCAGTGTGATTCCAGGACCACCAAGAACAAGAGGAAGTGGCCCACACATGCAGAGTCCCAGTGTCCAGGGGAAGAATCTGGTGG... |
Task1_train_41843 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | ACTCAGATACCAAGAAGTCAAATTCCTACCCCACACACAGTGAGTGGCAGAGAGCAAGAGAGCGATATGGAAATGGGTAGCTCCCAGCCCAGAAGTGTGGTGGGCGGTGGCCGACTGAGAACCTGGGGGCTCAGTGCACACAGAAGGCTGCTAAGATAGCAAAGGGAGGAGGCCTGGGGACCAAACGAGTTGTCCCTGCTGTGCAGGAGACTGGCAAAGCCAGCCAGAGGTGACATCCAGGGGTGCTTCTTGAGATGACAGAAGCCAGGCTGGGCCTGGCCTACTGCAGGGACCAAGGGAGGGCAGACTGGTGTGAGTTT... | ACTCAGATACCAAGAAGTCAAATTCCTACCCCACACACAGTGAGTGGCAGAGAGCAAGAGAGCGATATGGAAATGGGTAGCTCCCAGCCCAGAAGTGTGGTGGGCGGTGGCCGACTGAGAACCTGGGGGCTCAGTGCACACAGAAGGCTGCTAAGATAGCAAAGGGAGGAGGCCTGGGGACCAAACGAGTTGTCCCTGCTGTGCAGGAGACTGGCAAAGCCAGCCAGAGGTGACATCCAGGGGTGCTTCTTGAGATGACAGAAGCCAGGCTGGGCCTGGCCTACTGCAGGGACCAAGGGAGGGCAGACTGGTGTGAGTTT... |
Task1_train_41844 | A mutation on Chromosome 12 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCCTGCCTGCTTAGGGGTCTAGGCCGAGGCAGGGGGAGGACCGGACGGCCGGCCACTCGCCGCGACCAGCAGGAGAGAGGGGTGCCTGCCACAGGTTGTCACCCTCGCCGCCTCCCCCGGCGGCGCCCCGCCCCTTACTCAGCCCTCATTACTGCAGCGCCTCGCGGGGGTCTGGCCCGGAGTGGAGGGCGCGCGGTCCCAGCCCTCCCGCTCGGCCGGCGGGTGTCGAGTTCAGGTGCGACCGAAAAGGGGAAAGGAGGGCACCGCCACGTGAGCTGTCCTCTCCGGGGAAGGCGGTGGCTGCGTGAGGGCGGGGGCTG... | CCCTGCCTGCTTAGGGGTCTAGGCCGAGGCAGGGGGAGGACCGGACGGCCGGCCACTCGCCGCGACCAGCAGGAGAGAGGGGTGCCTGCCACAGGTTGTCACCCTCGCCGCCTCCCCCGGCGGCGCCCCGCCCCTTACTCAGCCCTCATTACTGCAGCGCCTCGCGGGGGTCTGGCCCGGAGTGGAGGGCGCGCGGTCCCAGCCCTCCCGCTCGGCCGGCGGGTGTCGAGTTCAGGTGCGACCGAAAAGGGGAAAGGAGGGCACCGCCACGTGAGCTGTCCTCTCCGGGGAAGGCGGTGGCTGCGTGAGGGCGGGGGCTG... |
Task1_train_41845 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GGTACCCCCTCCATAGGAGCAAGGCTTCTGAGCCAACTCTTAGGTCGCCACCCCACCCCCAGGGTGAAATGGGATCTGCAATGTCCTGACAACGGTCCAGCTGAATTATCGATGGTGGGAGAGTAAGTCCAGAGCAGCAGGCCCCAGTAGCACTGTGGATAGAGGGAGCTCAGAGAGCTCTGGGTCAGTGTCGGGACCTCAGGCTCCTTCGTGGAATCCAGAGAAAGGGGCGTAGCCTCGAGAGCATTCCTGGGAGGATCCTGGGAGGGAGGGACTGTCAGGAGCTGGGCTAAGGGCCCCTGCGAGGCTCTCTTCACCTG... | GGTACCCCCTCCATAGGAGCAAGGCTTCTGAGCCAACTCTTAGGTCGCCACCCCACCCCCAGGGTGAAATGGGATCTGCAATGTCCTGACAACGGTCCAGCTGAATTATCGATGGTGGGAGAGTAAGTCCAGAGCAGCAGGCCCCAGTAGCACTGTGGATAGAGGGAGCTCAGAGAGCTCTGGGTCAGTGTCGGGACCTCAGGCTCCTTCGTGGAATCCAGAGAAAGGGGCGTAGCCTCGAGAGCATTCCTGGGAGGATCCTGGGAGGGAGGGACTGTCAGGAGCTGGGCTAAGGGCCCCTGCGAGGCTCTCTTCACCTG... |
Task1_train_41846 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GCTGTGTAGAAAATGTGAAAAGCAGTCAGGGTCAGGGTGTAAATTCCAGTTCATTCCTTGGCTAGCAGTGTGAATCTAGGCAAGCCATTAACCCCCAAGCCTCGGTTTCCTCATCACCACAGGGATCGCCCACCTCTCAGGATTGAGGATTAAGCAAAATCATTATGCCTCATTTAATAAGTGCTTGAGAAGGTAGCCAGCTAGCTGTTATGGGATTGTTGTTTCATCACTGTTTTGCTGATAAGAATCCTTTGGCAAAGAGAGGTTAAAGGGCTTTTTCTTAAATGACACTGCTAGTTACAGTACCTGACTTCGGGGAG... | GCTGTGTAGAAAATGTGAAAAGCAGTCAGGGTCAGGGTGTAAATTCCAGTTCATTCCTTGGCTAGCAGTGTGAATCTAGGCAAGCCATTAACCCCCAAGCCTCGGTTTCCTCATCACCACAGGGATCGCCCACCTCTCAGGATTGAGGATTAAGCAAAATCATTATGCCTCATTTAATAAGTGCTTGAGAAGGTAGCCAGCTAGCTGTTATGGGATTGTTGTTTCATCACTGTTTTGCTGATAAGAATCCTTTGGCAAAGAGAGGTTAAAGGGCTTTTTCTTAAATGACACTGCTAGTTACAGTACCTGACTTCGGGGAG... |
Task1_train_41847 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ATCTTCTAATATTTTCTTCCTGCTCCCCAGGGAAGTGTTGTGTACCCCACCCAGCCCCTCCAGAGCCTGCCCAGCTAAGCGCCCTGGGCACTGAGCAGGGAAGCTGTGGGCAGAGCATGCACTGAAACCTTAGGAGCCATTGAGGAACCGCTGGAGGTTTTCTCACGTGCTCTTCCTTCCTTCTGCTGCAGGTTGTTTTTATTTTTATTTTTATTTATTTATTTTATTTATTTATTTTTTTTTGAGACCGAGTCTCGCTGTCACCCAGGCTGGAGTGCAATGGCGTGATCTCAGCTCACTGCAGGCTCCGCCTCCCGGGT... | ATCTTCTAATATTTTCTTCCTGCTCCCCAGGGAAGTGTTGTGTACCCCACCCAGCCCCTCCAGAGCCTGCCCAGCTAAGCGCCCTGGGCACTGAGCAGGGAAGCTGTGGGCAGAGCATGCACTGAAACCTTAGGAGCCATTGAGGAACCGCTGGAGGTTTTCTCACGTGCTCTTCCTTCCTTCTGCTGCAGGTTGTTTTTATTTTTATTTTTATTTATTTATTTTATTTATTTATTTTTTTTTGAGACCGAGTCTCGCTGTCACCCAGGCTGGAGTGCAATGGCGTGATCTCAGCTCACTGCAGGCTCCGCCTCCCGGGT... |
Task1_train_41848 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GTTCGACAAGTTTCTTCCTAAAGGTCCCCAGTTCCTCATGATTCTTCTGAGGGTCTCATCCACCCTCCCAGGGCCTGCAGTCAGCTAGCCACCCCACTGCCCCATGCCTGCAGTGAACACATTTACCACAACCTGGAAATGGCTGGTGACAGAAAAGTCCTCACGGCCACAACACTCTCTGCGGTGGGAATTCAGGTGCCTTGCCTGATGGTGACAAAGCTGGTTTTGCATAAACAGCTCTCTGAATCACACCCAAATGTGGCTTCTGACTTGAGTGGACCCCCATGAAGAGCTGCAGAGGGGGCTGGGAAAAGACAAGA... | GTTCGACAAGTTTCTTCCTAAAGGTCCCCAGTTCCTCATGATTCTTCTGAGGGTCTCATCCACCCTCCCAGGGCCTGCAGTCAGCTAGCCACCCCACTGCCCCATGCCTGCAGTGAACACATTTACCACAACCTGGAAATGGCTGGTGACAGAAAAGTCCTCACGGCCACAACACTCTCTGCGGTGGGAATTCAGGTGCCTTGCCTGATGGTGACAAAGCTGGTTTTGCATAAACAGCTCTCTGAATCACACCCAAATGTGGCTTCTGACTTGAGTGGACCCCCATGAAGAGCTGCAGAGGGGGCTGGGAAAAGACAAGA... |
Task1_train_41849 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TGCCCACGCCTGGAATCTCACTGAAACCCACCAGCTCCACTTCACCAGCCTTGGTCCTACCCCTTCTCTCCCCTTAGCTGGCGTGCTCCTGACACCCCTCCCCCAAGCGCACCCGCCTCTACCCATCTCCTTCTCCCGTCTCCCCCTGCCCCCACTGCTGGCCAAGACTCATCGGATCTCCTTCTGCAGACAAAGGAGAAAGTCCTGTGGAGCCTGCAGAGCCTTGTCATTACAGCTGCCCCAGGGAGGAGGAGGGCAGCACCATCCCCATCCAGGAGGATTACCGAAAACCGGAGCCTGCCTGCTCCCCCTGAGCCAGC... | TGCCCACGCCTGGAATCTCACTGAAACCCACCAGCTCCACTTCACCAGCCTTGGTCCTACCCCTTCTCTCCCCTTAGCTGGCGTGCTCCTGACACCCCTCCCCCAAGCGCACCCGCCTCTACCCATCTCCTTCTCCCGTCTCCCCCTGCCCCCACTGCTGGCCAAGACTCATCGGATCTCCTTCTGCAGACAAAGGAGAAAGTCCTGTGGAGCCTGCAGAGCCTTGTCATTACAGCTGCCCCAGGGAGGAGGAGGGCAGCACCATCCCCATCCAGGAGGATTACCGAAAACCGGAGCCTGCCTGCTCCCCCTGAGCCAGC... |
Task1_train_41850 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CGCCTGCGCTGCAGGAGGGCGGGGGCTCTGGTTGTAAAACACACTTCCTGCTGCGAAAGACCCACATGCTACAAGACGGGCAAAATAAAGTGACAGATGACCACCCTGCAGCTCTCCAGCTTCCTCTCTGAAATCCCAGTCCCAAAATCCAGTTTCCTGGCCGCCTCCTGGCTCAGGTCAGGATCTGGCAGAGGAGGTTTCTCAGCCGGTTATGTTGGGGCCTGCTTAAGGGCGGGGGTGAGAAAGGTCCCCAGGCTACTGTGGATCCTGTGTCTGACTTCAGATCCCCTTTTCCCACAGTTATAGCTCCACTTTTTTGG... | CGCCTGCGCTGCAGGAGGGCGGGGGCTCTGGTTGTAAAACACACTTCCTGCTGCGAAAGACCCACATGCTACAAGACGGGCAAAATAAAGTGACAGATGACCACCCTGCAGCTCTCCAGCTTCCTCTCTGAAATCCCAGTCCCAAAATCCAGTTTCCTGGCCGCCTCCTGGCTCAGGTCAGGATCTGGCAGAGGAGGTTTCTCAGCCGGTTATGTTGGGGCCTGCTTAAGGGCGGGGGTGAGAAAGGTCCCCAGGCTACTGTGGATCCTGTGTCTGACTTCAGATCCCCTTTTCCCACAGTTATAGCTCCACTTTTTTGG... |
Task1_train_41851 | A variant has been detected on Chromosome 12. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CCCAGACTGGAGTGCAATGGCGCGATCTTGGCTCACTGCAACCTCCACCTCCCGGATTCAAGCAATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGAATTACAGGCACCTGCCACCATGCCCGGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCCACCTCGGCCCCCCAAAGTGCTGGGATTACCGGCATGAGCCACCGCACCCAGCCACCACGTACTTTTTAAACTATTGTTTCTAGTCTTCACAGCATCCTTGCTTAAGCAGGTGA... | CCCAGACTGGAGTGCAATGGCGCGATCTTGGCTCACTGCAACCTCCACCTCCCGGATTCAAGCAATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGAATTACAGGCACCTGCCACCATGCCCGGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCCACCTCGGCCCCCCAAAGTGCTGGGATTACCGGCATGAGCCACCGCACCCAGCCACCACGTACTTTTTAAACTATTGTTTCTAGTCTTCACAGCATCCTTGCTTAAGCAGGTGA... |
Task1_train_41852 | Consider this mutation on Chromosome 12. Is this a benign change or a disease-causing variant? | Benign | CAGGTCAGCGAGATGGCGGTGCTGCTCATCGACCCCGAGCCTCAGATTGCTGCCCTGGCCAAGAACTTCTTCAATGAGCTCTCCCACAAGGTGAGAGGCAGAGAGGCACTGAGGGCTGGCTGCAGAGGGAATCTGTAGGTCACCTCATCTCCTTAACATGGCTCTCTCTGTCTTACAGGGCAACGCAATCTATAATCTCCTTCCAGATATCATCAGCCGCCTGTCAGACCCCGAGCTGGGGGTGGAGGAAGAGCCTTTCCACACCATCATGAAGTATTGCTCCCCGGGCCCTGGGGCACATTTTCCACATAGCACGGGCT... | CAGGTCAGCGAGATGGCGGTGCTGCTCATCGACCCCGAGCCTCAGATTGCTGCCCTGGCCAAGAACTTCTTCAATGAGCTCTCCCACAAGGTGAGAGGCAGAGAGGCACTGAGGGCTGGCTGCAGAGGGAATCTGTAGGTCACCTCATCTCCTTAACATGGCTCTCTCTGTCTTACAGGGCAACGCAATCTATAATCTCCTTCCAGATATCATCAGCCGCCTGTCAGACCCCGAGCTGGGGGTGGAGGAAGAGCCTTTCCACACCATCATGAAGTATTGCTCCCCGGGCCCTGGGGCACATTTTCCACATAGCACGGGCT... |
Task1_train_41853 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AAGGGAGAACGTGTCTTTTTCCCAGAGACACATGGCAAACTGCTAGGAACACAGCAGAGAGAACCGTTCACACAAAAGTGGCAGAGTTAATTTACAATCAGAGGAGGCAGCCTGAGTCCTGACATGCTGACAGTGGTATGTGGGTAAACTGAGCTAAGTTATTTGGGGCCTGTGGTTTAACCTTTTGGATCACTCTGTGATATGGAGAAAACTGGCTGACTTTTCCCTGCTTTCATCTGCAGTGGAACTAAAGAGTATCAATCAAAGTGATGAAAAAGAAGCACTTGGCTGGGTGCGGTGGCTCATGCCTGTAATCCCAG... | AAGGGAGAACGTGTCTTTTTCCCAGAGACACATGGCAAACTGCTAGGAACACAGCAGAGAGAACCGTTCACACAAAAGTGGCAGAGTTAATTTACAATCAGAGGAGGCAGCCTGAGTCCTGACATGCTGACAGTGGTATGTGGGTAAACTGAGCTAAGTTATTTGGGGCCTGTGGTTTAACCTTTTGGATCACTCTGTGATATGGAGAAAACTGGCTGACTTTTCCCTGCTTTCATCTGCAGTGGAACTAAAGAGTATCAATCAAAGTGATGAAAAAGAAGCACTTGGCTGGGTGCGGTGGCTCATGCCTGTAATCCCAG... |
Task1_train_41854 | A variant was discovered on Chromosome 12. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TTTTTCCCAGAGACACATGGCAAACTGCTAGGAACACAGCAGAGAGAACCGTTCACACAAAAGTGGCAGAGTTAATTTACAATCAGAGGAGGCAGCCTGAGTCCTGACATGCTGACAGTGGTATGTGGGTAAACTGAGCTAAGTTATTTGGGGCCTGTGGTTTAACCTTTTGGATCACTCTGTGATATGGAGAAAACTGGCTGACTTTTCCCTGCTTTCATCTGCAGTGGAACTAAAGAGTATCAATCAAAGTGATGAAAAAGAAGCACTTGGCTGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGAAGGCCA... | TTTTTCCCAGAGACACATGGCAAACTGCTAGGAACACAGCAGAGAGAACCGTTCACACAAAAGTGGCAGAGTTAATTTACAATCAGAGGAGGCAGCCTGAGTCCTGACATGCTGACAGTGGTATGTGGGTAAACTGAGCTAAGTTATTTGGGGCCTGTGGTTTAACCTTTTGGATCACTCTGTGATATGGAGAAAACTGGCTGACTTTTCCCTGCTTTCATCTGCAGTGGAACTAAAGAGTATCAATCAAAGTGATGAAAAAGAAGCACTTGGCTGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGAAGGCCA... |
Task1_train_41855 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | TGGTGTGTCAGGGGTGAGGGTGTTAGGGGAGCATTTTGTATTTTATTTAAGATTGTCCTTCTAATGATGCTGTTTTTGAAGTGGGAATACTTTTATTTATTTTGCTTTAGAACCAGCCTCTTAGAGGAAGTGATTTAGGAATGGGAGTGGAGGGCAGGTGGGCTAGGGCAGGGGGAAAAGGAGGGAAGATTTTTGGAAGCCCTTCTCTACTACGGAGCGTCACAAATCCTGGCCTGATCTCCGCGGCCCCAGTGTATCCCATATGCAGTGTTGCTGGAGGCTCTTGCCCTGCGTAATGTGCGGCAGCTGGAAGACCTTGT... | TGGTGTGTCAGGGGTGAGGGTGTTAGGGGAGCATTTTGTATTTTATTTAAGATTGTCCTTCTAATGATGCTGTTTTTGAAGTGGGAATACTTTTATTTATTTTGCTTTAGAACCAGCCTCTTAGAGGAAGTGATTTAGGAATGGGAGTGGAGGGCAGGTGGGCTAGGGCAGGGGGAAAAGGAGGGAAGATTTTTGGAAGCCCTTCTCTACTACGGAGCGTCACAAATCCTGGCCTGATCTCCGCGGCCCCAGTGTATCCCATATGCAGTGTTGCTGGAGGCTCTTGCCCTGCGTAATGTGCGGCAGCTGGAAGACCTTGT... |
Task1_train_41856 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TGCAGTGAGCTGAGATCACGCCACTGCTTGGGTGACACAGCAATACTCCATCTCAAAAAAAAAAAAGATAAAAAGATGAGGGCCATGGCTGCTGAGTTCCATCATCCACAGTTCAGAGCCCAGGTGGTGGTGAATAATCCACACTAGATTGACTTCTGGGATTCCTGGATTCTTTCACCACTGGGTTCCCTTGACCCGGTCATGCATCTTCACCAGCCTAGCCTACTTACTGAGATTTAGTAACTGCACTGGACTAGGACACCAGTGCCTGGTTGTTGAGCTCAACTTCATCTCTCTGCTTGTTGAGTCACTGGACAAAT... | TGCAGTGAGCTGAGATCACGCCACTGCTTGGGTGACACAGCAATACTCCATCTCAAAAAAAAAAAAGATAAAAAGATGAGGGCCATGGCTGCTGAGTTCCATCATCCACAGTTCAGAGCCCAGGTGGTGGTGAATAATCCACACTAGATTGACTTCTGGGATTCCTGGATTCTTTCACCACTGGGTTCCCTTGACCCGGTCATGCATCTTCACCAGCCTAGCCTACTTACTGAGATTTAGTAACTGCACTGGACTAGGACACCAGTGCCTGGTTGTTGAGCTCAACTTCATCTCTCTGCTTGTTGAGTCACTGGACAAAT... |
Task1_train_41857 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | GTCTGGGAAGTTAGAAGGAAAGGTGACAAAAATTCTGAATGGTTCGAAAGAGGTAGAATATATTTCTAGAATCCTTGTCTACTTTGCAGCCAGGGCTTGGGTTAGAGTTGCAGGAAGTGGCCTGGATTTGGGAGGAGTGAATAAATCCGTCCCTTGGTCAGCAAATATTTACTGAGCAAGGGTTTTCCAAGACAGTATAAAACAAACACAGAAAAAAGAATACTCAGAGAGTATGTGTTGACTGGTTGATAACTATCGGCCATGACAGATTAGCCATGTCTGCAGCACGCACCTGCGGCCACTCAGTAGTAGCACCCCAC... | GTCTGGGAAGTTAGAAGGAAAGGTGACAAAAATTCTGAATGGTTCGAAAGAGGTAGAATATATTTCTAGAATCCTTGTCTACTTTGCAGCCAGGGCTTGGGTTAGAGTTGCAGGAAGTGGCCTGGATTTGGGAGGAGTGAATAAATCCGTCCCTTGGTCAGCAAATATTTACTGAGCAAGGGTTTTCCAAGACAGTATAAAACAAACACAGAAAAAAGAATACTCAGAGAGTATGTGTTGACTGGTTGATAACTATCGGCCATGACAGATTAGCCATGTCTGCAGCACGCACCTGCGGCCACTCAGTAGTAGCACCCCAC... |
Task1_train_41858 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | AAGGAAACTTTCCCCTGATCATCAAGAATCTTAAGATAGAAGACTCAGATACTTACATCTGTGAAGTGGAGGACCAGAAGGAGGAGGTGCAATTGCTAGTGTTCGGATGTGAGTGGGGCAGGTGGGGATGAGGATACCTCCTGCCTGGTTCCCTTCCCCACTACTCCCACCCCTGCACCAAATCCAGCCTGAGCTGGTGATACCGCAGCAGCCCCAAGAGGACCAGGCTGTCAAACTGGCCTCCAAATGTCTTAAAACCCTTCTTGATCAGGTGAGGGATGCTGGTGGGCGGAGGAGGGAAGAGGCCTTGGGAAAAGGAA... | AAGGAAACTTTCCCCTGATCATCAAGAATCTTAAGATAGAAGACTCAGATACTTACATCTGTGAAGTGGAGGACCAGAAGGAGGAGGTGCAATTGCTAGTGTTCGGATGTGAGTGGGGCAGGTGGGGATGAGGATACCTCCTGCCTGGTTCCCTTCCCCACTACTCCCACCCCTGCACCAAATCCAGCCTGAGCTGGTGATACCGCAGCAGCCCCAAGAGGACCAGGCTGTCAAACTGGCCTCCAAATGTCTTAAAACCCTTCTTGATCAGGTGAGGGATGCTGGTGGGCGGAGGAGGGAAGAGGCCTTGGGAAAAGGAA... |
Task1_train_41859 | A variant on Chromosome 12 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TGGTGAGATCGGGGTCCTCCCCACCTGTTCTCCCCAATATCCAGGCCCCAGCATCATCACCTGACCTCCAACTTCATCAGCCATACAGCAGCTCCGTCATCTCTCCTCCAGTTCCATCATCCATCTTCCTCTCCTCTGTCCATCCCCCACTCCATTTGTGGCCCCCATCTTGATCATCTGTCTTTTAGTTCCCACTACCCTGTTTACCCCAGCTCCAGCATCTGCTTCAGTTCCCACTCCTCAGCTCCATCACCGTCCTTCAGTTCCACGACCTGTCCTCCAGCTCCGTCATCCATCCTGCAGCTCCACGGTTCAGCCGC... | TGGTGAGATCGGGGTCCTCCCCACCTGTTCTCCCCAATATCCAGGCCCCAGCATCATCACCTGACCTCCAACTTCATCAGCCATACAGCAGCTCCGTCATCTCTCCTCCAGTTCCATCATCCATCTTCCTCTCCTCTGTCCATCCCCCACTCCATTTGTGGCCCCCATCTTGATCATCTGTCTTTTAGTTCCCACTACCCTGTTTACCCCAGCTCCAGCATCTGCTTCAGTTCCCACTCCTCAGCTCCATCACCGTCCTTCAGTTCCACGACCTGTCCTCCAGCTCCGTCATCCATCCTGCAGCTCCACGGTTCAGCCGC... |
Task1_train_41860 | This variant is located on Chromosome 12. Evaluate its biological effect and specify any disease association. | Benign | CCAGGCGGCGCTGGGCCGGGTGCGGCTGGATTGCGGGGCGAGCTGCGCGGCCGATCCGGGCGCCGCGCTCCCCGCCGTGCTTCTCGGGGCCCCGGAGCCCGACTCCGGGCCGGGACCCACGCAGGGGTCCTGGGAGCGACAGCTTCTCCGTGCAGCGCTCCGCCGCGCAGACTGCCTGACCCAGTGCGCAGCACGGAGGCTGGGCCCCGGGGGCGCGGCGCGGCTTCGCGTGGGGAGCGCGCTCCGGGACGCCTTCCGCCGTCGGGAGCCCTACAACTACCTGCAGAGGGCCTATTACCAGGTGGGGAGCGGGCCGGGCA... | CCAGGCGGCGCTGGGCCGGGTGCGGCTGGATTGCGGGGCGAGCTGCGCGGCCGATCCGGGCGCCGCGCTCCCCGCCGTGCTTCTCGGGGCCCCGGAGCCCGACTCCGGGCCGGGACCCACGCAGGGGTCCTGGGAGCGACAGCTTCTCCGTGCAGCGCTCCGCCGCGCAGACTGCCTGACCCAGTGCGCAGCACGGAGGCTGGGCCCCGGGGGCGCGGCGCGGCTTCGCGTGGGGAGCGCGCTCCGGGACGCCTTCCGCCGTCGGGAGCCCTACAACTACCTGCAGAGGGCCTATTACCAGGTGGGGAGCGGGCCGGGCA... |
Task1_train_41861 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | TGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGCTGTCTCTAAAAGAAAGAAAGGAATCAGAGGTGATTCCTGTTCCTAAGGGGCTCACAGTCTGGCTCCAACTCTTTTTTCCTCACCCTATCCTATATAAGTTTCCACTGCCCTTCTCCATTTCCTCGGTCCCAATTCACCTTCCCATTTCCTGCCTCTCTTCTCCTGAGCCCCACCTGTAAGGGATGACCTTTTTACTGATTAAAAAAACACAAGATGTGCTCAGATTTGAGGAGAGAAGGACATTTGTAAGAAAATCTTTTGGTAGAAAGGCACTGAAGATCAGCA... | TGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGCTGTCTCTAAAAGAAAGAAAGGAATCAGAGGTGATTCCTGTTCCTAAGGGGCTCACAGTCTGGCTCCAACTCTTTTTTCCTCACCCTATCCTATATAAGTTTCCACTGCCCTTCTCCATTTCCTCGGTCCCAATTCACCTTCCCATTTCCTGCCTCTCTTCTCCTGAGCCCCACCTGTAAGGGATGACCTTTTTACTGATTAAAAAAACACAAGATGTGCTCAGATTTGAGGAGAGAAGGACATTTGTAAGAAAATCTTTTGGTAGAAAGGCACTGAAGATCAGCA... |
Task1_train_41862 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TAAGTACAGAGGGGCCCATATTGGATTTTAATTTAAGGAGAGAAACCTGCCCAGAATTACTGAACTGTTTTCAAGCCTTTCAGCTGGGCAGGAGCAAAAGCCAGCACTTCCCCCCTTCCCTTGGTTTCTGAATTCCCTAGAAGTGCCCAAATGTATCAGTCAAGAGAAGAAAATAGGATGGAGAATCAGAAGCTGCTGTGCTCTGAGGGGTCACGTGGATGTGATAAGGCAAGCTAGGAGCGGCTCCTAGAGAAGGCAACGGGTGCTAAATGTGCACCTGGCACAGCCCTGTGCCCGCGAAGGTTGTTCAGTGCTGGCTG... | TAAGTACAGAGGGGCCCATATTGGATTTTAATTTAAGGAGAGAAACCTGCCCAGAATTACTGAACTGTTTTCAAGCCTTTCAGCTGGGCAGGAGCAAAAGCCAGCACTTCCCCCCTTCCCTTGGTTTCTGAATTCCCTAGAAGTGCCCAAATGTATCAGTCAAGAGAAGAAAATAGGATGGAGAATCAGAAGCTGCTGTGCTCTGAGGGGTCACGTGGATGTGATAAGGCAAGCTAGGAGCGGCTCCTAGAGAAGGCAACGGGTGCTAAATGTGCACCTGGCACAGCCCTGTGCCCGCGAAGGTTGTTCAGTGCTGGCTG... |
Task1_train_41863 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GCATAAAAAAAGGCAGAATATAGACAACCTATTTCTCTTAGGCTCACCCCATCCACCCCTACTTCACCCCCTTACCTACCACTGTTTTCAGGGTTAAAGCAATTTTAGCAACCCTTTACTAGGAACTGTGGGGAGATAGCTTGTATTTTCAGTAAGTTGGCGGTGGGGGGCAGGGACAAACTCCAAACAAACTCTGGAAAACGAATGTAGGAAGTTTTTATGTTCCTTGTCATTTGGCTGTCCCTTTTCTCCTTCCTCGCACAACCCTGTATCAGTGGGGCAGCACTTCCTTCTCAGACCGCTTGTCCCAGGGTCCCTGC... | GCATAAAAAAAGGCAGAATATAGACAACCTATTTCTCTTAGGCTCACCCCATCCACCCCTACTTCACCCCCTTACCTACCACTGTTTTCAGGGTTAAAGCAATTTTAGCAACCCTTTACTAGGAACTGTGGGGAGATAGCTTGTATTTTCAGTAAGTTGGCGGTGGGGGGCAGGGACAAACTCCAAACAAACTCTGGAAAACGAATGTAGGAAGTTTTTATGTTCCTTGTCATTTGGCTGTCCCTTTTCTCCTTCCTCGCACAACCCTGTATCAGTGGGGCAGCACTTCCTTCTCAGACCGCTTGTCCCAGGGTCCCTGC... |
Task1_train_41864 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GTGGTGCAGGCAAGGGAGGGTTGTAATAGGAGCAAAGAGGTTGGTAGTCTCCATTCTTCTGGACCCAGGACACCCACCCAATCCTCCTGATGGAGCTGGAAGCACCTTGGAGTAAAGAACAATGCATCAGGTGAACTCGACTTGATGCAACATTCAAATGTGAGCTCCACAAAGGCTGTGTGACTATGTGGGTTTCTTTTTACTGAACCTCCCACATCTAGGACAGTGCCTGACAGTAGACACTTAAAGTGTGCATTAAATGAATTAACTGTGACTTAAGGACATATCCTAGGTCTCTTCTTTGATTCTGATTAAGTGTT... | GTGGTGCAGGCAAGGGAGGGTTGTAATAGGAGCAAAGAGGTTGGTAGTCTCCATTCTTCTGGACCCAGGACACCCACCCAATCCTCCTGATGGAGCTGGAAGCACCTTGGAGTAAAGAACAATGCATCAGGTGAACTCGACTTGATGCAACATTCAAATGTGAGCTCCACAAAGGCTGTGTGACTATGTGGGTTTCTTTTTACTGAACCTCCCACATCTAGGACAGTGCCTGACAGTAGACACTTAAAGTGTGCATTAAATGAATTAACTGTGACTTAAGGACATATCCTAGGTCTCTTCTTTGATTCTGATTAAGTGTT... |
Task1_train_41865 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CTGGAAGCACCTTGGAGTAAAGAACAATGCATCAGGTGAACTCGACTTGATGCAACATTCAAATGTGAGCTCCACAAAGGCTGTGTGACTATGTGGGTTTCTTTTTACTGAACCTCCCACATCTAGGACAGTGCCTGACAGTAGACACTTAAAGTGTGCATTAAATGAATTAACTGTGACTTAAGGACATATCCTAGGTCTCTTCTTTGATTCTGATTAAGTGTTCCATGTGGACCTGTTGAACAACGATGGGATGTCCAGTCTTGGGTCTCTGTCCAGAGACAGAGATTTTTAGTTTACCAGCTTTTGTGAGATTGATC... | CTGGAAGCACCTTGGAGTAAAGAACAATGCATCAGGTGAACTCGACTTGATGCAACATTCAAATGTGAGCTCCACAAAGGCTGTGTGACTATGTGGGTTTCTTTTTACTGAACCTCCCACATCTAGGACAGTGCCTGACAGTAGACACTTAAAGTGTGCATTAAATGAATTAACTGTGACTTAAGGACATATCCTAGGTCTCTTCTTTGATTCTGATTAAGTGTTCCATGTGGACCTGTTGAACAACGATGGGATGTCCAGTCTTGGGTCTCTGTCCAGAGACAGAGATTTTTAGTTTACCAGCTTTTGTGAGATTGATC... |
Task1_train_41866 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | TTTGAATCCTGCCATTTTTTAGAGATAAATTTAACCTTTGACCATATAGCAACTTGACTCTTGATGCTAACAAATTACCTCTCTTCTCTCTTTTATGGTGTTTATTTTCTATTTCCATTGAACAGTTGTATTTTATTTGTGTCTTTCACTGTAAATCACCTCCAATCTTTTTTTTTTGGGGGGGATGAAGTCTTGGTCTGTCCGCAGGCTGGAGTGCAGTGGCGTGATCTTAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACGTGTCACCACG... | TTTGAATCCTGCCATTTTTTAGAGATAAATTTAACCTTTGACCATATAGCAACTTGACTCTTGATGCTAACAAATTACCTCTCTTCTCTCTTTTATGGTGTTTATTTTCTATTTCCATTGAACAGTTGTATTTTATTTGTGTCTTTCACTGTAAATCACCTCCAATCTTTTTTTTTTGGGGGGGATGAAGTCTTGGTCTGTCCGCAGGCTGGAGTGCAGTGGCGTGATCTTAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACGTGTCACCACG... |
Task1_train_41867 | This mutation occurs on Chromosome 12. Does this change lead to a known medical condition, or is it benign? | Benign | CTTCCTCATTTGTAACATCTCCCACTACCACCTGCCCTCCAAACCATCCCCAAAGCACTGCGAGTGTTCAGGCTACCCTTAGAGTTTTCCGTGGATCAGATTGGGTTAAGAAGGCAATGCTTTCGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCGAGATGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACCCGGTGAAACCCCGTCTCTACTAAAAAATACAAAAAAAAATTAGCCGGCCGTGGTGGCGGGCGCCTGTAGTCCCAGCTATTCGGGAGGCTGAGGCAGGAG... | CTTCCTCATTTGTAACATCTCCCACTACCACCTGCCCTCCAAACCATCCCCAAAGCACTGCGAGTGTTCAGGCTACCCTTAGAGTTTTCCGTGGATCAGATTGGGTTAAGAAGGCAATGCTTTCGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCGAGATGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACCCGGTGAAACCCCGTCTCTACTAAAAAATACAAAAAAAAATTAGCCGGCCGTGGTGGCGGGCGCCTGTAGTCCCAGCTATTCGGGAGGCTGAGGCAGGAG... |
Task1_train_41868 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGCTATAGGAAAACAGCACCTAGCACAGACTTGCCAACTGGCAACCCAGGGGCTGATTCTGGCCCATGGCTATACTTGGTTTGACTTGCACAGTGTTTTATTTTTTATTTTTAGTTTTTTTAAAACATTTGAGTTCGTTTTCACTGATCAGATTGACAACACTCAAAGAGTTTGAAGATAACTGTGACAAGCAGGGTAGGGGGGAACAGGCACTTCCATATATGTTTGATAGGTATGTAAATTAGCAAAACCGTTTTGGAGAAAATTTTAGCAATATCAAAATTTAAAATGCAAATATTTTTTAACCTACTCCATTTCTA... | AGCTATAGGAAAACAGCACCTAGCACAGACTTGCCAACTGGCAACCCAGGGGCTGATTCTGGCCCATGGCTATACTTGGTTTGACTTGCACAGTGTTTTATTTTTTATTTTTAGTTTTTTTAAAACATTTGAGTTCGTTTTCACTGATCAGATTGACAACACTCAAAGAGTTTGAAGATAACTGTGACAAGCAGGGTAGGGGGGAACAGGCACTTCCATATATGTTTGATAGGTATGTAAATTAGCAAAACCGTTTTGGAGAAAATTTTAGCAATATCAAAATTTAAAATGCAAATATTTTTTAACCTACTCCATTTCTA... |
Task1_train_41869 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | GATAGGAAGACAGTGAATTTGAATTTGACCTTGGCATTCAAATGGAAATTGGTTCCAGGACCCCCACCTCACTAAATCTGCTGAATAAAATGGCTTAGTATCTGTAGAGAAACTACATACATCCCCCTGTGTACTTTATTATTATCATTTTGATACAGAGTCTTGCTCTGTCACCCAGACTAGAATGCAATGGCATGATCTTGGCTCACTGCAACCTCTGGCTCCCGGGTTCAAGTAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCGCCACCATGCCCGGCTAATTTTTGTACTTTTGTATTTT... | GATAGGAAGACAGTGAATTTGAATTTGACCTTGGCATTCAAATGGAAATTGGTTCCAGGACCCCCACCTCACTAAATCTGCTGAATAAAATGGCTTAGTATCTGTAGAGAAACTACATACATCCCCCTGTGTACTTTATTATTATCATTTTGATACAGAGTCTTGCTCTGTCACCCAGACTAGAATGCAATGGCATGATCTTGGCTCACTGCAACCTCTGGCTCCCGGGTTCAAGTAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCGCCACCATGCCCGGCTAATTTTTGTACTTTTGTATTTT... |
Task1_train_41870 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | GATGATGAGGGTATTATGTATCTACTCATATCAAATTTTGATGACTGCCAGAATCACCTGGGGAGCTTTAAAAACTCTCGGCACCTAAATTATACCCTAGAATGTCTAGGGGGTGGGAGCCACGTGTCAGTGGTTTTTAAAAATCCCATGTAATCTTTAAAAGTTTGGGAATAATTTTCCTCTTTTGTTTCCTACAAGTATCTGAAGCTTTGCAGAAAGAGTTACAAAGCAATAGGACAAAAAGAAAATGAATGAGGAAGTAAGGAGGAACAGGTAATGATGAAATAAGGATCCAATGAAGCCAGGGAATAAAGTCAGCT... | GATGATGAGGGTATTATGTATCTACTCATATCAAATTTTGATGACTGCCAGAATCACCTGGGGAGCTTTAAAAACTCTCGGCACCTAAATTATACCCTAGAATGTCTAGGGGGTGGGAGCCACGTGTCAGTGGTTTTTAAAAATCCCATGTAATCTTTAAAAGTTTGGGAATAATTTTCCTCTTTTGTTTCCTACAAGTATCTGAAGCTTTGCAGAAAGAGTTACAAAGCAATAGGACAAAAAGAAAATGAATGAGGAAGTAAGGAGGAACAGGTAATGATGAAATAAGGATCCAATGAAGCCAGGGAATAAAGTCAGCT... |
Task1_train_41871 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | TCTGTAAAGTGGGTCTACTAATATCTATTTAATAGGGGTATTAAGAAGATTAAAAACATTGAGATACATAAAGTGTTTTACACAACACCTGGATTTTAGTAAACATCAGTTATTATTATTAGCATTCTTCCAAGATCTGCACACAAAGTGAGTTACGGCTAATCAGTTGATAAACTCCTAGCAGAGCAGAAGGTTATGTGTGTTGTGATGTTTAAGTGGTACTGGGAAACTCTGGTTGCCTTGAGGTTCTGAAATTCTACTGTATCAGATGGGTTCCTTTAAACATTGCTCTCTCTAGGGGGTCCTCTTTTTAAAAGTAT... | TCTGTAAAGTGGGTCTACTAATATCTATTTAATAGGGGTATTAAGAAGATTAAAAACATTGAGATACATAAAGTGTTTTACACAACACCTGGATTTTAGTAAACATCAGTTATTATTATTAGCATTCTTCCAAGATCTGCACACAAAGTGAGTTACGGCTAATCAGTTGATAAACTCCTAGCAGAGCAGAAGGTTATGTGTGTTGTGATGTTTAAGTGGTACTGGGAAACTCTGGTTGCCTTGAGGTTCTGAAATTCTACTGTATCAGATGGGTTCCTTTAAACATTGCTCTCTCTAGGGGGTCCTCTTTTTAAAAGTAT... |
Task1_train_41872 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | ATCACATGGTTATTTATGTTCACATGATAAAATATTGTATGCCATTTGAAGGCTATTCATTGAAATTAGAATATATTTACAGTATACTTTTACATATAAAAGTAGGATACAGATATCCTAAATATAGTGTAACACTACATTACATGCATATATATCATACTATATATACATATACATATATAGTATCTATATTTCATATACACATTTCATATACACAATCATAACTTTAAGTTTTTGTACAAAAGGAAGACTAATAGTTAATGTTTCTGAATATTAGTAATGGTTATTTTTGATAATCAGATTAAACGTGGAATGCATTT... | ATCACATGGTTATTTATGTTCACATGATAAAATATTGTATGCCATTTGAAGGCTATTCATTGAAATTAGAATATATTTACAGTATACTTTTACATATAAAAGTAGGATACAGATATCCTAAATATAGTGTAACACTACATTACATGCATATATATCATACTATATATACATATACATATATAGTATCTATATTTCATATACACATTTCATATACACAATCATAACTTTAAGTTTTTGTACAAAAGGAAGACTAATAGTTAATGTTTCTGAATATTAGTAATGGTTATTTTTGATAATCAGATTAAACGTGGAATGCATTT... |
Task1_train_41873 | This alteration occurs on Chromosome 12. Is it associated with a disease or is it a benign variant? | Benign | CTATTTAATAAATGGTGCTGGGAAAACTGGCTAGCCATATGTAGAAAGCTGAAACTGGATCCCTTCCTTACACCTTACACAAAAATTAATTCAAGATGAATTAAAGACTTCAATGTTAGACCTAAAAGCATAAAAACCCTAGAAGAAAACCTAGGCAATACCATTCAGGACATAAGCATGGGCAAGGACTTCATGACTAAAACACCAAAAGCAATGGCAACAAAAGCCAAAATTGACAAATGGGATCTAATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTATCATCAGAGTCAACAGGCAACCTACAGAATGGGA... | CTATTTAATAAATGGTGCTGGGAAAACTGGCTAGCCATATGTAGAAAGCTGAAACTGGATCCCTTCCTTACACCTTACACAAAAATTAATTCAAGATGAATTAAAGACTTCAATGTTAGACCTAAAAGCATAAAAACCCTAGAAGAAAACCTAGGCAATACCATTCAGGACATAAGCATGGGCAAGGACTTCATGACTAAAACACCAAAAGCAATGGCAACAAAAGCCAAAATTGACAAATGGGATCTAATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTATCATCAGAGTCAACAGGCAACCTACAGAATGGGA... |
Task1_train_41874 | Given this context: Chromosome 12 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGTGCTGGGAAAACTGGCTAGCCATATGTAGAAAGCTGAAACTGGATCCCTTCCTTACACCTTACACAAAAATTAATTCAAGATGAATTAAAGACTTCAATGTTAGACCTAAAAGCATAAAAACCCTAGAAGAAAACCTAGGCAATACCATTCAGGACATAAGCATGGGCAAGGACTTCATGACTAAAACACCAAAAGCAATGGCAACAAAAGCCAAAATTGACAAATGGGATCTAATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTATCATCAGAGTCAACAGGCAACCTACAGAATGGGAGAAAATTTTTACA... | GGTGCTGGGAAAACTGGCTAGCCATATGTAGAAAGCTGAAACTGGATCCCTTCCTTACACCTTACACAAAAATTAATTCAAGATGAATTAAAGACTTCAATGTTAGACCTAAAAGCATAAAAACCCTAGAAGAAAACCTAGGCAATACCATTCAGGACATAAGCATGGGCAAGGACTTCATGACTAAAACACCAAAAGCAATGGCAACAAAAGCCAAAATTGACAAATGGGATCTAATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTATCATCAGAGTCAACAGGCAACCTACAGAATGGGAGAAAATTTTTACA... |
Task1_train_41875 | A change on Chromosome 12 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AAACTAGAGTCCTCTAGTCTTTCTTTCTCTGCACAGGGAATATAGGTTGTATGTGTCTCCTTGGTGAAGGCCGTTGTATAACAATTGTTTTCATCATTCTTTCAGTAGAGACATTATGATTCTCTGAGAATCCCCACCAGATCCCTGTGCTGATAAATCCGGTTTTTACACAACACACATCACTGCCCAACCCCTCTTTGCTGCCAGAGATTCCAAGCTCAATCCAGGCTTCTGGCACTTACCTGTGCAATTCACTGCAGCGTCTTCCTTGTGCCCACACTCACTATGGCCCCAGCGTCTGGCAGGACAATCCCACAAGG... | AAACTAGAGTCCTCTAGTCTTTCTTTCTCTGCACAGGGAATATAGGTTGTATGTGTCTCCTTGGTGAAGGCCGTTGTATAACAATTGTTTTCATCATTCTTTCAGTAGAGACATTATGATTCTCTGAGAATCCCCACCAGATCCCTGTGCTGATAAATCCGGTTTTTACACAACACACATCACTGCCCAACCCCTCTTTGCTGCCAGAGATTCCAAGCTCAATCCAGGCTTCTGGCACTTACCTGTGCAATTCACTGCAGCGTCTTCCTTGTGCCCACACTCACTATGGCCCCAGCGTCTGGCAGGACAATCCCACAAGG... |
Task1_train_41876 | A mutation on Chromosome 12 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CATAGTTTGGATTTTTTCCCAAAAATATTCTCCTTTTTTTGCAACTGTCTTTGATAGTTAAAATTGTTAGACACTCAGGCACTAAAATCAATGTTTTGTGTACATCTCTTAAAATGACAGTTCATTTGCTGACACTTCACAGTTTTGCAGTGCATGTCTTCTACCAGATTTATGTCATTAAAATAGGAATAAATCACTTCTGAGATACAGAGTTTTTCACTTCCTTAAGTTACTGAATCATAGTTCTGTTCCCCATAATACATATGAAATAGTACATTTTTAAATTTCAGAATGTTTTCTAAAACTCACCATGTATACAA... | CATAGTTTGGATTTTTTCCCAAAAATATTCTCCTTTTTTTGCAACTGTCTTTGATAGTTAAAATTGTTAGACACTCAGGCACTAAAATCAATGTTTTGTGTACATCTCTTAAAATGACAGTTCATTTGCTGACACTTCACAGTTTTGCAGTGCATGTCTTCTACCAGATTTATGTCATTAAAATAGGAATAAATCACTTCTGAGATACAGAGTTTTTCACTTCCTTAAGTTACTGAATCATAGTTCTGTTCCCCATAATACATATGAAATAGTACATTTTTAAATTTCAGAATGTTTTCTAAAACTCACCATGTATACAA... |
Task1_train_41877 | This variant is located on Chromosome 12. Evaluate its biological effect and specify any disease association. | Benign | AATCTTATACCTCTATTGATCTAAAAATTACTCAAAAACCAAAGTGAGCAAAACCCAAACACTTCTATCTAAAGTGCAACATGAATTGTAAACTTATCTGACTCTCCCAGTGGAATTTGTGTAGATATTTCCTGGTTTCTTGAGAGTGATCTAGTCATAAGGACCAATGTTTCTTTTCAATTTCAAAGGTAGTACTGGAAATTTACACCCTTCTTCTTAACAAGTTGATTGAAAGTCATACCTGAGCAGGTAATTTTGGCTTCTTCATAGTGATCACAGGTAAGTCCACCCCATTGCCAGTTCTTGCAGTCCCAAAGAGA... | AATCTTATACCTCTATTGATCTAAAAATTACTCAAAAACCAAAGTGAGCAAAACCCAAACACTTCTATCTAAAGTGCAACATGAATTGTAAACTTATCTGACTCTCCCAGTGGAATTTGTGTAGATATTTCCTGGTTTCTTGAGAGTGATCTAGTCATAAGGACCAATGTTTCTTTTCAATTTCAAAGGTAGTACTGGAAATTTACACCCTTCTTCTTAACAAGTTGATTGAAAGTCATACCTGAGCAGGTAATTTTGGCTTCTTCATAGTGATCACAGGTAAGTCCACCCCATTGCCAGTTCTTGCAGTCCCAAAGAGA... |
Task1_train_41878 | This alteration occurs on Chromosome 12. Is it associated with a disease or is it a benign variant? | Benign | TAAACGTTCTCTGAAGTAAATTATGGTATATCTAAACAAGCACATACAGTTGCAGCCATTAAATTAACTAACTAGGGCTAGGCGCAGTGGCTTACACCTGCACTCCCAGCACTTTGGGAGGCCAAGGCTGGTGGATCACCTGAGGTCAGAAGTTCAAGACCAGCCTGGCCAACATGGTGAAATCCCGTCTCTACTAAAAATACAAAAATTAGCCCGGCGCCGGGCGAGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGTGGGCGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGA... | TAAACGTTCTCTGAAGTAAATTATGGTATATCTAAACAAGCACATACAGTTGCAGCCATTAAATTAACTAACTAGGGCTAGGCGCAGTGGCTTACACCTGCACTCCCAGCACTTTGGGAGGCCAAGGCTGGTGGATCACCTGAGGTCAGAAGTTCAAGACCAGCCTGGCCAACATGGTGAAATCCCGTCTCTACTAAAAATACAAAAATTAGCCCGGCGCCGGGCGAGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGTGGGCGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGA... |
Task1_train_41879 | This genomic variant is located on Chromosome 12. Can you determine its pathogenicity and name any linked disease? | Benign | CAACACCTTCGACTGCCCGATGCTGGGAGGTCTGGGAACTGGGCCGCTGGCGCGCTGACGCCCTCTGCGCCTGGTCTTAGCTGTGTCCCCTGCGTCCAGAAGAAAGAATGCTGGTCTATATATCCGAGTGGGAAAGAAAAATGAACGTACCCCCAGTCTCTCCCTTTCCTTGCGTCTGCCTTAGTACCTCACAGTTCCACAAAGGATCCTCGTTTCTATGTGCACAGGTCCCTAGACTTTGAGAATCGATCTCGAACTTTGATATTGTTTAATACTTTCACATATAGGGGGCAAAAAACAAAACAAAACACACATACACG... | CAACACCTTCGACTGCCCGATGCTGGGAGGTCTGGGAACTGGGCCGCTGGCGCGCTGACGCCCTCTGCGCCTGGTCTTAGCTGTGTCCCCTGCGTCCAGAAGAAAGAATGCTGGTCTATATATCCGAGTGGGAAAGAAAAATGAACGTACCCCCAGTCTCTCCCTTTCCTTGCGTCTGCCTTAGTACCTCACAGTTCCACAAAGGATCCTCGTTTCTATGTGCACAGGTCCCTAGACTTTGAGAATCGATCTCGAACTTTGATATTGTTTAATACTTTCACATATAGGGGGCAAAAAACAAAACAAAACACACATACACG... |
Task1_train_41880 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | GTTTCATTCTTGAAATAATTGTTTGATGCCCTTTGGGTCCATATTTCCTTCCTGCAAAGGATTAAGGCCATAGAGGCATTTCTGGGGTGGAACTTGTCTCCCTCCGGCTCTGCATACGACGCTGTAGGCAGTCCCTGATCCTGGACACAGCCGACCAATTATCCCTGAGGAGGTGAGTAGGCCTGGACTAGGGAGCAACAGTTTGGCCTCACTCTAGGCCATATTTCATGGTTTGATTTTACCATCAATAAAGCTGATAATTTTATTTTATTTATTATCTTTTTTTTAGACAGGGTCTCACTTTGTCACCCGGGCTGGAG... | GTTTCATTCTTGAAATAATTGTTTGATGCCCTTTGGGTCCATATTTCCTTCCTGCAAAGGATTAAGGCCATAGAGGCATTTCTGGGGTGGAACTTGTCTCCCTCCGGCTCTGCATACGACGCTGTAGGCAGTCCCTGATCCTGGACACAGCCGACCAATTATCCCTGAGGAGGTGAGTAGGCCTGGACTAGGGAGCAACAGTTTGGCCTCACTCTAGGCCATATTTCATGGTTTGATTTTACCATCAATAAAGCTGATAATTTTATTTTATTTATTATCTTTTTTTTAGACAGGGTCTCACTTTGTCACCCGGGCTGGAG... |
Task1_train_41881 | Given this context: Chromosome 12 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CATGTTGGCCAGGCTGGTCTCGAACTCCAGACCTCAAATGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGCACTCGGTCTTCAGTGATTCTTTAAAATTCTCTTCTCTGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTCGGAGGCTGAGGCAGACGGATCACGAGGTCAGGAGATTGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAACTACAAAAAATTATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTTCCAGCTACTTGGGAGGATGAGGCA... | CATGTTGGCCAGGCTGGTCTCGAACTCCAGACCTCAAATGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGCACTCGGTCTTCAGTGATTCTTTAAAATTCTCTTCTCTGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTCGGAGGCTGAGGCAGACGGATCACGAGGTCAGGAGATTGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAACTACAAAAAATTATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTTCCAGCTACTTGGGAGGATGAGGCA... |
Task1_train_41882 | A variant was discovered on Chromosome 12. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CAGCTTCCCAAGTCGCTGGGATTACAGGCGCTGACCCACTCTGCATGGCTATTCACCCAGTTTTTCTAAACTATGCATTAATGTTCTTGCCTTTATAATTTCTTTCTTTCTTTCTTTCTTTTTTTTTTTTTGAGACAGGGTCTCATTCTGTTGCCCACGCGGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCCGCCTCCTAGGTTCAGGTGATTTCTCCTGTCTCAGTCTCTCGAGTAGCAGGTATTACAGATGTATGCCACCACGCCTAGCTAATTTTTGTAGTTCTTAGTAGAGAAGGGGTTTCGGTGTGTT... | CAGCTTCCCAAGTCGCTGGGATTACAGGCGCTGACCCACTCTGCATGGCTATTCACCCAGTTTTTCTAAACTATGCATTAATGTTCTTGCCTTTATAATTTCTTTCTTTCTTTCTTTCTTTTTTTTTTTTTGAGACAGGGTCTCATTCTGTTGCCCACGCGGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCCGCCTCCTAGGTTCAGGTGATTTCTCCTGTCTCAGTCTCTCGAGTAGCAGGTATTACAGATGTATGCCACCACGCCTAGCTAATTTTTGTAGTTCTTAGTAGAGAAGGGGTTTCGGTGTGTT... |
Task1_train_41883 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ACTCTAAGTGCTTGGTTCTTCTTTTATTTTTCTTCCTCTTTCCGCAACCCTTTGAGTTCCCACTTTTATTGCATTTGCTTGCATTTGTTTCAAGGCTGTGATTCTCACTATACTGGTCCTGAGGAAAGGGCTTCTGTGAACTGCGGTTTTTAGTTTTTATTGTGGTTCTTAGTTCTCATGAGACCCCTCTTGAGGATATGTGCCTATCTGGTGCCTCTGCTCTCCACTAGTTGAGTGAAAGGAAGGAGGTAATTTACCACCATGTTTGGTTCCTGTTTATAAGATGTTTTAAGAAAGATCTGAAACAGATTTTCTGAAGA... | ACTCTAAGTGCTTGGTTCTTCTTTTATTTTTCTTCCTCTTTCCGCAACCCTTTGAGTTCCCACTTTTATTGCATTTGCTTGCATTTGTTTCAAGGCTGTGATTCTCACTATACTGGTCCTGAGGAAAGGGCTTCTGTGAACTGCGGTTTTTAGTTTTTATTGTGGTTCTTAGTTCTCATGAGACCCCTCTTGAGGATATGTGCCTATCTGGTGCCTCTGCTCTCCACTAGTTGAGTGAAAGGAAGGAGGTAATTTACCACCATGTTTGGTTCCTGTTTATAAGATGTTTTAAGAAAGATCTGAAACAGATTTTCTGAAGA... |
Task1_train_41884 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AGAAATATTTCAGGAAGAGTTCTCCACTGGCTTTTACTCTGATTATTCCTGCCCTGCTCAAGACTGTGTGGGATCTAAAAGTCAATTTTGCAAATTAGGTGGATTGCTGCGTATCTTTGGCTTTCAGCATTTGTTGAGTTTTATTCCCCCTGGTTCTGTCACCCAGGCTGGAGTGCATTGGTGCAATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTCTCCCACCCCAGCCTCCCAAGTAGCTGGGATTACAGGTGTGCATCACTATGCTCAGCTAATTTTTTTTTTTTTTTTTTTTGTATTTTTAGTA... | AGAAATATTTCAGGAAGAGTTCTCCACTGGCTTTTACTCTGATTATTCCTGCCCTGCTCAAGACTGTGTGGGATCTAAAAGTCAATTTTGCAAATTAGGTGGATTGCTGCGTATCTTTGGCTTTCAGCATTTGTTGAGTTTTATTCCCCCTGGTTCTGTCACCCAGGCTGGAGTGCATTGGTGCAATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTCTCCCACCCCAGCCTCCCAAGTAGCTGGGATTACAGGTGTGCATCACTATGCTCAGCTAATTTTTTTTTTTTTTTTTTTTGTATTTTTAGTA... |
Task1_train_41885 | The following genetic variant occurs on Chromosome 12. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TATTCTCTAAAGCCCAAATCTTATTTTGATATTCGAGGAAGAGCTTACATGGTAATAATATTAAGGGTTACAGCTGGTTTCACCGAAGCTTTGTAGGCCTTCTCTAATATCTTATTTTTTTGAAGGAATAGCTGTTCTGCTTGAATTATAGACTACATAATACATGTACTGTCAGGTACATTCATGGAAGGCAGATGGAGTCATATGTTACTGGAGTCCTGATGAACAGATGTAGAAAATAGTCCAAGGAATAAGAAAAAAGTTGATATTGAAAAGTGCTTGTTGAAGTCTGTAAATGTGCATTAAATGTGGCAGTAAAA... | TATTCTCTAAAGCCCAAATCTTATTTTGATATTCGAGGAAGAGCTTACATGGTAATAATATTAAGGGTTACAGCTGGTTTCACCGAAGCTTTGTAGGCCTTCTCTAATATCTTATTTTTTTGAAGGAATAGCTGTTCTGCTTGAATTATAGACTACATAATACATGTACTGTCAGGTACATTCATGGAAGGCAGATGGAGTCATATGTTACTGGAGTCCTGATGAACAGATGTAGAAAATAGTCCAAGGAATAAGAAAAAAGTTGATATTGAAAAGTGCTTGTTGAAGTCTGTAAATGTGCATTAAATGTGGCAGTAAAA... |
Task1_train_41886 | A mutation on Chromosome 12 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TGTTTTGAATTTCCTTTTCCTGATGGCCCTTTTGTTTAGATTTATTTTCCAGTCTCATGTTGGGTCAGAAAAGTCCTGGGGAGTTTTCTGTGTTCTAGGTCTTGTGGCCTGAGCTGACCTTCACTGTTTTTATTCTTCCTTGATAGCCTGCCTTACACTTGGTGATAATGCACATTTATTGACAGTGAACTCAAAACACATGTATTCTTTCCACTAACAGGGTACCAGATAAGCAAATCCTATATAATTTTGCAGCTGGAGCAAGGAAAAGAGCTGTGGCGGGAAGGAAGAGAATTTCTTCAAGACCAGAATCCAGGTAA... | TGTTTTGAATTTCCTTTTCCTGATGGCCCTTTTGTTTAGATTTATTTTCCAGTCTCATGTTGGGTCAGAAAAGTCCTGGGGAGTTTTCTGTGTTCTAGGTCTTGTGGCCTGAGCTGACCTTCACTGTTTTTATTCTTCCTTGATAGCCTGCCTTACACTTGGTGATAATGCACATTTATTGACAGTGAACTCAAAACACATGTATTCTTTCCACTAACAGGGTACCAGATAAGCAAATCCTATATAATTTTGCAGCTGGAGCAAGGAAAAGAGCTGTGGCGGGAAGGAAGAGAATTTCTTCAAGACCAGAATCCAGGTAA... |
Task1_train_41887 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | GGCCCTTTTGTTTAGATTTATTTTCCAGTCTCATGTTGGGTCAGAAAAGTCCTGGGGAGTTTTCTGTGTTCTAGGTCTTGTGGCCTGAGCTGACCTTCACTGTTTTTATTCTTCCTTGATAGCCTGCCTTACACTTGGTGATAATGCACATTTATTGACAGTGAACTCAAAACACATGTATTCTTTCCACTAACAGGGTACCAGATAAGCAAATCCTATATAATTTTGCAGCTGGAGCAAGGAAAAGAGCTGTGGCGGGAAGGAAGAGAATTTCTTCAAGACCAGAATCCAGGTAAGCAACAGGGTCCTGTGCTCTAATA... | GGCCCTTTTGTTTAGATTTATTTTCCAGTCTCATGTTGGGTCAGAAAAGTCCTGGGGAGTTTTCTGTGTTCTAGGTCTTGTGGCCTGAGCTGACCTTCACTGTTTTTATTCTTCCTTGATAGCCTGCCTTACACTTGGTGATAATGCACATTTATTGACAGTGAACTCAAAACACATGTATTCTTTCCACTAACAGGGTACCAGATAAGCAAATCCTATATAATTTTGCAGCTGGAGCAAGGAAAAGAGCTGTGGCGGGAAGGAAGAGAATTTCTTCAAGACCAGAATCCAGGTAAGCAACAGGGTCCTGTGCTCTAATA... |
Task1_train_41888 | This variant is located on Chromosome 12. Evaluate its biological effect and specify any disease association. | Benign | CCAGTCTCATGTTGGGTCAGAAAAGTCCTGGGGAGTTTTCTGTGTTCTAGGTCTTGTGGCCTGAGCTGACCTTCACTGTTTTTATTCTTCCTTGATAGCCTGCCTTACACTTGGTGATAATGCACATTTATTGACAGTGAACTCAAAACACATGTATTCTTTCCACTAACAGGGTACCAGATAAGCAAATCCTATATAATTTTGCAGCTGGAGCAAGGAAAAGAGCTGTGGCGGGAAGGAAGAGAATTTCTTCAAGACCAGAATCCAGGTAAGCAACAGGGTCCTGTGCTCTAATAGGAGGAGGTGCTTTGTCAATGAAT... | CCAGTCTCATGTTGGGTCAGAAAAGTCCTGGGGAGTTTTCTGTGTTCTAGGTCTTGTGGCCTGAGCTGACCTTCACTGTTTTTATTCTTCCTTGATAGCCTGCCTTACACTTGGTGATAATGCACATTTATTGACAGTGAACTCAAAACACATGTATTCTTTCCACTAACAGGGTACCAGATAAGCAAATCCTATATAATTTTGCAGCTGGAGCAAGGAAAAGAGCTGTGGCGGGAAGGAAGAGAATTTCTTCAAGACCAGAATCCAGGTAAGCAACAGGGTCCTGTGCTCTAATAGGAGGAGGTGCTTTGTCAATGAAT... |
Task1_train_41889 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ACAGTGAACTCAAAACACATGTATTCTTTCCACTAACAGGGTACCAGATAAGCAAATCCTATATAATTTTGCAGCTGGAGCAAGGAAAAGAGCTGTGGCGGGAAGGAAGAGAATTTCTTCAAGACCAGAATCCAGGTAAGCAACAGGGTCCTGTGCTCTAATAGGAGGAGGTGCTTTGTCAATGAATAATATCAGTTGAATATTAATTAGTGGTTTTATTAAATGAGTGATAATTTCTAAAATGTAGGTTAGGCTACTGGAGCAGAATTCCTTAGATGTTATTGTCATTTTGTTCATGTGTCAGATGCTACTCTTGTGTC... | ACAGTGAACTCAAAACACATGTATTCTTTCCACTAACAGGGTACCAGATAAGCAAATCCTATATAATTTTGCAGCTGGAGCAAGGAAAAGAGCTGTGGCGGGAAGGAAGAGAATTTCTTCAAGACCAGAATCCAGGTAAGCAACAGGGTCCTGTGCTCTAATAGGAGGAGGTGCTTTGTCAATGAATAATATCAGTTGAATATTAATTAGTGGTTTTATTAAATGAGTGATAATTTCTAAAATGTAGGTTAGGCTACTGGAGCAGAATTCCTTAGATGTTATTGTCATTTTGTTCATGTGTCAGATGCTACTCTTGTGTC... |
Task1_train_41890 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | AAGCCCTTGGATGTAGGGAAAAGAAAGAGAGATCAGACTGTCACTGTGTCTATGTAGAAAGGGAAGACATGAGACTCCATTTTGAAAAAGACCTGTACTTTAAACAATTGCTTTGCTGAGATGTTGTTCATTTGTAGCTTTGCCCCAGCCACTTTGCCCCAGCCGCTTTGACCCAACTTGGAGCTCACAAAAACCTGTGTTGTATAAAATCAAGGTTTAAGGGATCTAGGGCCGTGCAGGACGTGCCTTGTTAACCACATGTTTACAAGCAGTATACTTGGTAAAAGACATTGCCATTCTCTAGTCTCAATAAACCAGGG... | AAGCCCTTGGATGTAGGGAAAAGAAAGAGAGATCAGACTGTCACTGTGTCTATGTAGAAAGGGAAGACATGAGACTCCATTTTGAAAAAGACCTGTACTTTAAACAATTGCTTTGCTGAGATGTTGTTCATTTGTAGCTTTGCCCCAGCCACTTTGCCCCAGCCGCTTTGACCCAACTTGGAGCTCACAAAAACCTGTGTTGTATAAAATCAAGGTTTAAGGGATCTAGGGCCGTGCAGGACGTGCCTTGTTAACCACATGTTTACAAGCAGTATACTTGGTAAAAGACATTGCCATTCTCTAGTCTCAATAAACCAGGG... |
Task1_train_41891 | Consider a variant on Chromosome 12. Determine its clinical classification and disease relevance. | Benign | CAGGACGTGCCTTGTTAACCACATGTTTACAAGCAGTATACTTGGTAAAAGACATTGCCATTCTCTAGTCTCAATAAACCAGGGGCACAATGCACCGTGGAAAGCCGCAGGGACCTCTGCCCTTGAAAGCAGGGTATTGTCCAAGGTTTCTCCCCATGTGATAGTCTGAAATATGGCCTCATGGGATGAGAAAGACCTGACTGTCCCCCAGCCTGACACCCGTAAAGGGTCTGTGCTGAGGTGGATTAGTCAAAGAGGAAAGCCTCTTGCAGTTGAGATGGAGGAAGGCCACTGTCTCCTGCTCGCCCCTGGGAACTGAA... | CAGGACGTGCCTTGTTAACCACATGTTTACAAGCAGTATACTTGGTAAAAGACATTGCCATTCTCTAGTCTCAATAAACCAGGGGCACAATGCACCGTGGAAAGCCGCAGGGACCTCTGCCCTTGAAAGCAGGGTATTGTCCAAGGTTTCTCCCCATGTGATAGTCTGAAATATGGCCTCATGGGATGAGAAAGACCTGACTGTCCCCCAGCCTGACACCCGTAAAGGGTCTGTGCTGAGGTGGATTAGTCAAAGAGGAAAGCCTCTTGCAGTTGAGATGGAGGAAGGCCACTGTCTCCTGCTCGCCCCTGGGAACTGAA... |
Task1_train_41892 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ACGTGCCTTGTTAACCACATGTTTACAAGCAGTATACTTGGTAAAAGACATTGCCATTCTCTAGTCTCAATAAACCAGGGGCACAATGCACCGTGGAAAGCCGCAGGGACCTCTGCCCTTGAAAGCAGGGTATTGTCCAAGGTTTCTCCCCATGTGATAGTCTGAAATATGGCCTCATGGGATGAGAAAGACCTGACTGTCCCCCAGCCTGACACCCGTAAAGGGTCTGTGCTGAGGTGGATTAGTCAAAGAGGAAAGCCTCTTGCAGTTGAGATGGAGGAAGGCCACTGTCTCCTGCTCGCCCCTGGGAACTGAATGTC... | ACGTGCCTTGTTAACCACATGTTTACAAGCAGTATACTTGGTAAAAGACATTGCCATTCTCTAGTCTCAATAAACCAGGGGCACAATGCACCGTGGAAAGCCGCAGGGACCTCTGCCCTTGAAAGCAGGGTATTGTCCAAGGTTTCTCCCCATGTGATAGTCTGAAATATGGCCTCATGGGATGAGAAAGACCTGACTGTCCCCCAGCCTGACACCCGTAAAGGGTCTGTGCTGAGGTGGATTAGTCAAAGAGGAAAGCCTCTTGCAGTTGAGATGGAGGAAGGCCACTGTCTCCTGCTCGCCCCTGGGAACTGAATGTC... |
Task1_train_41893 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTAGTCTCAATAAACCAGGGGCACAATGCACCGTGGAAAGCCGCAGGGACCTCTGCCCTTGAAAGCAGGGTATTGTCCAAGGTTTCTCCCCATGTGATAGTCTGAAATATGGCCTCATGGGATGAGAAAGACCTGACTGTCCCCCAGCCTGACACCCGTAAAGGGTCTGTGCTGAGGTGGATTAGTCAAAGAGGAAAGCCTCTTGCAGTTGAGATGGAGGAAGGCCACTGTCTCCTGCTCGCCCCTGGGAACTGAATGTCTCGGTGTAAAACCCGATCGTACATTTATTCAACTCTGAGCTAGGAGAAAAGCTGCCCTGT... | CTAGTCTCAATAAACCAGGGGCACAATGCACCGTGGAAAGCCGCAGGGACCTCTGCCCTTGAAAGCAGGGTATTGTCCAAGGTTTCTCCCCATGTGATAGTCTGAAATATGGCCTCATGGGATGAGAAAGACCTGACTGTCCCCCAGCCTGACACCCGTAAAGGGTCTGTGCTGAGGTGGATTAGTCAAAGAGGAAAGCCTCTTGCAGTTGAGATGGAGGAAGGCCACTGTCTCCTGCTCGCCCCTGGGAACTGAATGTCTCGGTGTAAAACCCGATCGTACATTTATTCAACTCTGAGCTAGGAGAAAAGCTGCCCTGT... |
Task1_train_41894 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTCGTCTAGAGAGCAAATACACAGTAATTCCCCCGTTTCCTATTGACGTCCCAGCGGAAGTCTGACTCCTGCGCGTCATGCAGTTTCTGAGGCAACGAATCACTGGCACGGAAGCTTTTCCTGGCGCGTTTCCAGAGAACCATGCGAACTACAATGTCCCTCACCAGAATTCAACGTGGCAGAGTCCCTGCATCTGCTCCCTGCCTGGCCTGGGCTCCCACATCCACAGAAGGGCCACAGCCGGGGAGCTTCGGAGTCACCGCACAGAGTCTGCTCTCTGCTCTGTGCTCCTCAGTCCCACAGTCCCCTCCAAGTCACGG... | GTCGTCTAGAGAGCAAATACACAGTAATTCCCCCGTTTCCTATTGACGTCCCAGCGGAAGTCTGACTCCTGCGCGTCATGCAGTTTCTGAGGCAACGAATCACTGGCACGGAAGCTTTTCCTGGCGCGTTTCCAGAGAACCATGCGAACTACAATGTCCCTCACCAGAATTCAACGTGGCAGAGTCCCTGCATCTGCTCCCTGCCTGGCCTGGGCTCCCACATCCACAGAAGGGCCACAGCCGGGGAGCTTCGGAGTCACCGCACAGAGTCTGCTCTCTGCTCTGTGCTCCTCAGTCCCACAGTCCCCTCCAAGTCACGG... |
Task1_train_41895 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | AAGAATATAACTGCCTTTGAAAATATAATATTCACAAAAAGAATTTAAAAAGAGGGGACATTTACTAAATTTTTATTGGGCATAACAATTATTTCTTTTAGGGCGTTGCTAAATTTTTTGTCTAAATGAAAAAAAAAACAAATTGAGAAATTCCACATTTCACACTGATCTAGTGATCTCAACATACTTGTGGGTTTCTACTAACTGTTGTTTGGTATTGCTTTCTCAATTTCCTTTTTTTTTTTTTTTCGCCTCATCTCCCGGAATGTATCAAAGGAAACCCCTGTCTTTGAAAAAGACTTCTTTTGAGCTAACTTTCT... | AAGAATATAACTGCCTTTGAAAATATAATATTCACAAAAAGAATTTAAAAAGAGGGGACATTTACTAAATTTTTATTGGGCATAACAATTATTTCTTTTAGGGCGTTGCTAAATTTTTTGTCTAAATGAAAAAAAAAACAAATTGAGAAATTCCACATTTCACACTGATCTAGTGATCTCAACATACTTGTGGGTTTCTACTAACTGTTGTTTGGTATTGCTTTCTCAATTTCCTTTTTTTTTTTTTTTCGCCTCATCTCCCGGAATGTATCAAAGGAAACCCCTGTCTTTGAAAAAGACTTCTTTTGAGCTAACTTTCT... |
Task1_train_41896 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GCCTACCTGCACCTGCGACCCTTCTACAGCACAACCCGCAGCTTCCTTGGCATCCACCGGCTAAACGGCCCCTTGAAATGTGGCCAGCCCCAGGAAGTGCTGGTGGATTATTACATCGACCCGGCCGATGCAAGCCCTGACCAAGAGATCAGCTTCTCCTACTATGTGAGACCGGGAAACGGGGACGGGTGAGAGTATGCTGGGAAGGAAAGAGAATGAGAAGAGTCAGCCAGAGGGTGCACCTAGGCTATCTGAATTGCAGATGCACATCTAATTAAAAACAATTTTAAAGCCACACTAAAAAAGTAAAAGAACAGTTG... | GCCTACCTGCACCTGCGACCCTTCTACAGCACAACCCGCAGCTTCCTTGGCATCCACCGGCTAAACGGCCCCTTGAAATGTGGCCAGCCCCAGGAAGTGCTGGTGGATTATTACATCGACCCGGCCGATGCAAGCCCTGACCAAGAGATCAGCTTCTCCTACTATGTGAGACCGGGAAACGGGGACGGGTGAGAGTATGCTGGGAAGGAAAGAGAATGAGAAGAGTCAGCCAGAGGGTGCACCTAGGCTATCTGAATTGCAGATGCACATCTAATTAAAAACAATTTTAAAGCCACACTAAAAAAGTAAAAGAACAGTTG... |
Task1_train_41897 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | AGCCACTGCACCCGGCAGCAGGAGATTTTCATAGGCAAAAGGAGGAATGCATAGTACCAGAAGGAATAGGAGAGTCTGAAGTGCCATTCCTCATGGGGCTGATTAACTGGGAGGCAGGAGGAAGAAGAGAAAGTGTGCAGCACGATGATGACTCTCTGTGGAATTTATTTTCAGCAAGATCACTATGAATAGTACCCAGTGCTTTCTGCATCCCAGAGAAAGCACCGAGTACAGAAATCCCTGGATTATAGAAAGTTCTTCTAAAATTTTGTCTTGAGAACCCCTGCCATTCCCCATCTTCTATTGTGTCACCTTTTTTT... | AGCCACTGCACCCGGCAGCAGGAGATTTTCATAGGCAAAAGGAGGAATGCATAGTACCAGAAGGAATAGGAGAGTCTGAAGTGCCATTCCTCATGGGGCTGATTAACTGGGAGGCAGGAGGAAGAAGAGAAAGTGTGCAGCACGATGATGACTCTCTGTGGAATTTATTTTCAGCAAGATCACTATGAATAGTACCCAGTGCTTTCTGCATCCCAGAGAAAGCACCGAGTACAGAAATCCCTGGATTATAGAAAGTTCTTCTAAAATTTTGTCTTGAGAACCCCTGCCATTCCCCATCTTCTATTGTGTCACCTTTTTTT... |
Task1_train_41898 | This is a variant located on Chromosome 12. Is this mutation a likely cause of disease or not? | Benign | GCACTGCTTTCTTCTGTTCACTACCTTGTCTGTACCTGTCCCAAGCAGAGGGCGAGGCGTAGATCCTGCAGGATAACTTGTTCAATTCAGGACACACTCAGTGCAAGAAAGACTTGTATAAACTTTTCTAGAGAGATCACTTACATTGCTATTCCAGGGCAAGGATTAAAAATCTTGAGTGTTAAAAAAAAAATCTATTTATAGGATTCATTAGTCTTCCTCTGCAGGATCTTATTAGTCTCCCCTAAGTTTTTGTCTTCTTCTTCTCTTATACACTGTATGAAATATGCGTGGGGGCCAGGCGCAGTGGCTCATGCTTG... | GCACTGCTTTCTTCTGTTCACTACCTTGTCTGTACCTGTCCCAAGCAGAGGGCGAGGCGTAGATCCTGCAGGATAACTTGTTCAATTCAGGACACACTCAGTGCAAGAAAGACTTGTATAAACTTTTCTAGAGAGATCACTTACATTGCTATTCCAGGGCAAGGATTAAAAATCTTGAGTGTTAAAAAAAAAATCTATTTATAGGATTCATTAGTCTTCCTCTGCAGGATCTTATTAGTCTCCCCTAAGTTTTTGTCTTCTTCTTCTCTTATACACTGTATGAAATATGCGTGGGGGCCAGGCGCAGTGGCTCATGCTTG... |
Task1_train_41899 | An alteration has been detected on Chromosome 12. Is it pathogenic, and if so, what disease is involved? | Benign | TGTCCAAATCACTTTGATGAGGCTACAGAAATAACTAAGAAAATATATTTCTTGTTCTCATGAAGATTATATTCTGATTTGTTGAAATTAGCCAATTTCACTGAAGATATAACATGTAAATCAGACCTGAAAGAATGAACATCTTTTAATAGGTTGCATGTTTGGTAAAAATGTTAAAAGCACCAAGTTTAGGCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACGAGGTCAGGAGATCGAGACCACGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGGG... | TGTCCAAATCACTTTGATGAGGCTACAGAAATAACTAAGAAAATATATTTCTTGTTCTCATGAAGATTATATTCTGATTTGTTGAAATTAGCCAATTTCACTGAAGATATAACATGTAAATCAGACCTGAAAGAATGAACATCTTTTAATAGGTTGCATGTTTGGTAAAAATGTTAAAAGCACCAAGTTTAGGCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACGAGGTCAGGAGATCGAGACCACGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGGG... |
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