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_45800 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | GAGGTGAACGTTGGCGCCATCAGGGGCCACTCCCTGGATGGAAGATAGTGCTCGGGCCCTCACGACGTCCACAGCAGCATTCTCAGCAAGGAGCCACTGCAGGGTGGCACAGCACAGGGGCACGCCTGGAGGGGAGGCATCAGCCGAGAGCTCAGCCTGATCCTACCAGGTGGGCTCAGCCGATCCTACCAGGTGGGCATCTGCATACCTGCCCCAAAGTGCCCTTCCCAGAGCCATCTAAGCATCCCAGCTGTCCCCAGCCCCACCCTAAGCTGCGGCGTGGCCAGCTGACCCAGAGGAAGGAGGCCACTGCTCAACTT... | GAGGTGAACGTTGGCGCCATCAGGGGCCACTCCCTGGATGGAAGATAGTGCTCGGGCCCTCACGACGTCCACAGCAGCATTCTCAGCAAGGAGCCACTGCAGGGTGGCACAGCACAGGGGCACGCCTGGAGGGGAGGCATCAGCCGAGAGCTCAGCCTGATCCTACCAGGTGGGCTCAGCCGATCCTACCAGGTGGGCATCTGCATACCTGCCCCAAAGTGCCCTTCCCAGAGCCATCTAAGCATCCCAGCTGTCCCCAGCCCCACCCTAAGCTGCGGCGTGGCCAGCTGACCCAGAGGAAGGAGGCCACTGCTCAACTT... |
Task1_train_45801 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TTTTTATCTTAAAAAAAAATAAATAAAAGTCTTCTGGGCAGGAATTACTGATAACTGTTATTATAACCAATGCAGACTTTAAAATCCCACCTGGACATCGGGTGAGAGGAGGAGGGCAGGCAGCAAACCGACCTGCAGACCTGCAGAGGGGAGCCGTGTCCAGGGCCACTGCGTCCCCACCAGACAACAGCTACTAGAAGAGGAAAGTGGCCCTCACAGGCAGGGTGCCTGCCACCAAGCAGTCAGACAAGGGGGTAACCAAGAGCTCCCAGCCAGAAAAACATGGGGGCAGGGAGGCCAAACAAAAAGCACTGAAAATA... | TTTTTATCTTAAAAAAAAATAAATAAAAGTCTTCTGGGCAGGAATTACTGATAACTGTTATTATAACCAATGCAGACTTTAAAATCCCACCTGGACATCGGGTGAGAGGAGGAGGGCAGGCAGCAAACCGACCTGCAGACCTGCAGAGGGGAGCCGTGTCCAGGGCCACTGCGTCCCCACCAGACAACAGCTACTAGAAGAGGAAAGTGGCCCTCACAGGCAGGGTGCCTGCCACCAAGCAGTCAGACAAGGGGGTAACCAAGAGCTCCCAGCCAGAAAAACATGGGGGCAGGGAGGCCAAACAAAAAGCACTGAAAATA... |
Task1_train_45802 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CAGCCTGCTTCATAGTTTTACCTTTTACCATTAGGCCTATGACCCATCCTGAGCTGATCTTTGTGTCTTGTGTATACACGTCTGTAATCCCAGCACTTTGGGAGACCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCCAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATATAAAAATTAGCCAGGCGTGGGTGCACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGTATCACTTGAACCCAGGACGTGGAGGTTGCAGTAAGTGGAGATCATGAGATTGCACTGCAGCCTGGGTGA... | CAGCCTGCTTCATAGTTTTACCTTTTACCATTAGGCCTATGACCCATCCTGAGCTGATCTTTGTGTCTTGTGTATACACGTCTGTAATCCCAGCACTTTGGGAGACCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCCAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATATAAAAATTAGCCAGGCGTGGGTGCACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGTATCACTTGAACCCAGGACGTGGAGGTTGCAGTAAGTGGAGATCATGAGATTGCACTGCAGCCTGGGTGA... |
Task1_train_45803 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ACCATTAGGCCTATGACCCATCCTGAGCTGATCTTTGTGTCTTGTGTATACACGTCTGTAATCCCAGCACTTTGGGAGACCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCCAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATATAAAAATTAGCCAGGCGTGGGTGCACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGTATCACTTGAACCCAGGACGTGGAGGTTGCAGTAAGTGGAGATCATGAGATTGCACTGCAGCCTGGGTGACAGGGTGAGATTCCGTCTCAAAACAA... | ACCATTAGGCCTATGACCCATCCTGAGCTGATCTTTGTGTCTTGTGTATACACGTCTGTAATCCCAGCACTTTGGGAGACCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCCAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATATAAAAATTAGCCAGGCGTGGGTGCACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGTATCACTTGAACCCAGGACGTGGAGGTTGCAGTAAGTGGAGATCATGAGATTGCACTGCAGCCTGGGTGACAGGGTGAGATTCCGTCTCAAAACAA... |
Task1_train_45804 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | CCGAGACCTCACATGTTTTTTCTTCTGTGCACACATTCCTCGTGTCTCTCCATGTGTCCCACCGTGTGTCCCAATTTTCTTGTAAGGATGTTGGATTAGGGCCCACGCTAATGGCACTTATTTATTTATTTAGGGATGGAGTCTTGCTCTGTCACCAGGCTGGAGTGCAGCGGCACCATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTCCCAGCAATTCCCCTGCCTCAGCCTCCCATGTAGCTGGGATTACAGGCATGCGCCACGATGCCCAGCTAATTTTTTGTACTTTTAGTAGAGACAGGGTCACACCATGTTG... | CCGAGACCTCACATGTTTTTTCTTCTGTGCACACATTCCTCGTGTCTCTCCATGTGTCCCACCGTGTGTCCCAATTTTCTTGTAAGGATGTTGGATTAGGGCCCACGCTAATGGCACTTATTTATTTATTTAGGGATGGAGTCTTGCTCTGTCACCAGGCTGGAGTGCAGCGGCACCATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTCCCAGCAATTCCCCTGCCTCAGCCTCCCATGTAGCTGGGATTACAGGCATGCGCCACGATGCCCAGCTAATTTTTTGTACTTTTAGTAGAGACAGGGTCACACCATGTTG... |
Task1_train_45805 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AATTTTAAAAAATTACCGGGACGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTTAGGAGATCGAGACCATCCCGGCTAAAACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAA... | AATTTTAAAAAATTACCGGGACGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTTAGGAGATCGAGACCATCCCGGCTAAAACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAA... |
Task1_train_45806 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCGGGACGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTTAGGAGATCGAGACCATCCCGGCTAAAACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAATTACCAGG... | CCGGGACGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTTAGGAGATCGAGACCATCCCGGCTAAAACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAATTACCAGG... |
Task1_train_45807 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAATTACCAGGACATGGTTGCAGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGAGGAAGGATGGCTTGAGCCCAGGAGTTTGAGGCTGCAGTGAGCTGAGAGCCTGATGCTGTGATCAGCTTCTTCCTGGTGAAACTGGATTGGAATGGGAT... | CGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAATTACCAGGACATGGTTGCAGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGAGGAAGGATGGCTTGAGCCCAGGAGTTTGAGGCTGCAGTGAGCTGAGAGCCTGATGCTGTGATCAGCTTCTTCCTGGTGAAACTGGATTGGAATGGGAT... |
Task1_train_45808 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TCAGCTTTTTCACTTCCTGTGACTTTAGACATGTTATTTCACCTCTCTAGACTCAGTTTCCCCACTGTGCAATGGAAGTCATGGGTATGACACGGTGTGATTCACAAGAAGTGCCAGGATCAGGGCCTGGCGCCGGGTGTGCACTCAAGCACATGGTGGGGGGTGGGGGAGGCACTCGACACCTCCAGCTAAGATGGCTGCTCTGTGGACACCAGTATGCGAGAGGTGTAACCCTGTAAGCTCCTGGCCAGCCCAGCACCTCTACCAGTATAACCAAGCCCCACCACCTCTGAGGGACCAACCGGAAGAATCGCACCACC... | TCAGCTTTTTCACTTCCTGTGACTTTAGACATGTTATTTCACCTCTCTAGACTCAGTTTCCCCACTGTGCAATGGAAGTCATGGGTATGACACGGTGTGATTCACAAGAAGTGCCAGGATCAGGGCCTGGCGCCGGGTGTGCACTCAAGCACATGGTGGGGGGTGGGGGAGGCACTCGACACCTCCAGCTAAGATGGCTGCTCTGTGGACACCAGTATGCGAGAGGTGTAACCCTGTAAGCTCCTGGCCAGCCCAGCACCTCTACCAGTATAACCAAGCCCCACCACCTCTGAGGGACCAACCGGAAGAATCGCACCACC... |
Task1_train_45809 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | AAGAGTGCTGAAGCAATGGTAGAGAGAAGTGGGTGGAGTCAGGAGCTGAAGGAGGAAATTCCATCAGGCCCCTCTGAGAAGTCTTGCCTTCCTCCCCCAAGTCTGGGTAGGGTGTCCACATGTCCACCGCTGCAACCCAGAGGTAACACTCTGGGCATGTTGGGAAACGGAGTCCACTGTGTGTATATTTTGCTTATAGACACATTTCTCTTCCCAAACGTGGCACTGGTTTTACAGCAAAGCTGTTTTATAATTTGTGTATAAACTGTAGGCTTCTTGTTGGGGGTTATATGGCTGCCAAAGGGATAGTGAGATAGAGG... | AAGAGTGCTGAAGCAATGGTAGAGAGAAGTGGGTGGAGTCAGGAGCTGAAGGAGGAAATTCCATCAGGCCCCTCTGAGAAGTCTTGCCTTCCTCCCCCAAGTCTGGGTAGGGTGTCCACATGTCCACCGCTGCAACCCAGAGGTAACACTCTGGGCATGTTGGGAAACGGAGTCCACTGTGTGTATATTTTGCTTATAGACACATTTCTCTTCCCAAACGTGGCACTGGTTTTACAGCAAAGCTGTTTTATAATTTGTGTATAAACTGTAGGCTTCTTGTTGGGGGTTATATGGCTGCCAAAGGGATAGTGAGATAGAGG... |
Task1_train_45810 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GACACATTTCTCTTCCCAAACGTGGCACTGGTTTTACAGCAAAGCTGTTTTATAATTTGTGTATAAACTGTAGGCTTCTTGTTGGGGGTTATATGGCTGCCAAAGGGATAGTGAGATAGAGGTGAGGAAGGTGCAGGGAGGAGGCGCACTGGCCTGGGTAGCACATGGCACGTTCTGAACCGTGCTGCATTGAATTGGCACCTTTGTTTGTTTGTTTATTTATTTATTTATTGAGATGGAGTCTTGCTTCCTCGCCCAGGCTGGAGTGCAGTGGCGTGATCTGGGCTCACTGCAACCTCCACCTCCTGGGTTTAAGCAGT... | GACACATTTCTCTTCCCAAACGTGGCACTGGTTTTACAGCAAAGCTGTTTTATAATTTGTGTATAAACTGTAGGCTTCTTGTTGGGGGTTATATGGCTGCCAAAGGGATAGTGAGATAGAGGTGAGGAAGGTGCAGGGAGGAGGCGCACTGGCCTGGGTAGCACATGGCACGTTCTGAACCGTGCTGCATTGAATTGGCACCTTTGTTTGTTTGTTTATTTATTTATTTATTGAGATGGAGTCTTGCTTCCTCGCCCAGGCTGGAGTGCAGTGGCGTGATCTGGGCTCACTGCAACCTCCACCTCCTGGGTTTAAGCAGT... |
Task1_train_45811 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | TTTTTTCTGTGTTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTGAATCTCCTGACCTTGTGATCTGCCCATCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCAGGTCTGCCCACGTTTCTCTGTGTAGCTCCACTGGGCTTCTTTCGGCAGCTGTGCAATGGAGTCTGTGGGTGATCAGAGGAGAATTCATTCAACCAGCCACCTAGGGGTGGACATTAGGTTGTTTCTGCTTTCCTTTTTCAGCTGTGCTGCAGTGGACATCTGTGACAGGTGCCATTGGGCTGGGGG... | TTTTTTCTGTGTTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTGAATCTCCTGACCTTGTGATCTGCCCATCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCAGGTCTGCCCACGTTTCTCTGTGTAGCTCCACTGGGCTTCTTTCGGCAGCTGTGCAATGGAGTCTGTGGGTGATCAGAGGAGAATTCATTCAACCAGCCACCTAGGGGTGGACATTAGGTTGTTTCTGCTTTCCTTTTTCAGCTGTGCTGCAGTGGACATCTGTGACAGGTGCCATTGGGCTGGGGG... |
Task1_train_45812 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GGGAGGGGTCTGCCCTGGGAGCCGGAGGGAAGACATTGGGTTCCCATGACGGCCCTCTGCAGGTACCCTGTTTCATAGCCATGGGGCAGCCTGGATTCAGGGAGACCAAGCCAGAGCCCTGGGAGTTGGCGAGTCGGAGCATCCAGCTGGGAGCCAGTGAGGGTGTGGCCTCCAGGAGGCTGCGGAACCTGGGAACTCTGCGGAGACCTCGCTTGGTCCTTGCTTTCACAGGAAAAGCACCAGAAAGCCCTAGCCCTGTGGGAATCAGCCCTGAGGGGGTCGGTCTGAGGGTGACGTGCCCAGGGGTTCTGTTTCCATTA... | GGGAGGGGTCTGCCCTGGGAGCCGGAGGGAAGACATTGGGTTCCCATGACGGCCCTCTGCAGGTACCCTGTTTCATAGCCATGGGGCAGCCTGGATTCAGGGAGACCAAGCCAGAGCCCTGGGAGTTGGCGAGTCGGAGCATCCAGCTGGGAGCCAGTGAGGGTGTGGCCTCCAGGAGGCTGCGGAACCTGGGAACTCTGCGGAGACCTCGCTTGGTCCTTGCTTTCACAGGAAAAGCACCAGAAAGCCCTAGCCCTGTGGGAATCAGCCCTGAGGGGGTCGGTCTGAGGGTGACGTGCCCAGGGGTTCTGTTTCCATTA... |
Task1_train_45813 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | GAGGGTGTGGCCTCCAGGAGGCTGCGGAACCTGGGAACTCTGCGGAGACCTCGCTTGGTCCTTGCTTTCACAGGAAAAGCACCAGAAAGCCCTAGCCCTGTGGGAATCAGCCCTGAGGGGGTCGGTCTGAGGGTGACGTGCCCAGGGGTTCTGTTTCCATTAGAACAGAATGTCTCTCGTCCAAGAGACTACACCTTCCTAATTCTCTAAAAGCTTTGGCCGAGTACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTAGCCAACACGGTGA... | GAGGGTGTGGCCTCCAGGAGGCTGCGGAACCTGGGAACTCTGCGGAGACCTCGCTTGGTCCTTGCTTTCACAGGAAAAGCACCAGAAAGCCCTAGCCCTGTGGGAATCAGCCCTGAGGGGGTCGGTCTGAGGGTGACGTGCCCAGGGGTTCTGTTTCCATTAGAACAGAATGTCTCTCGTCCAAGAGACTACACCTTCCTAATTCTCTAAAAGCTTTGGCCGAGTACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTAGCCAACACGGTGA... |
Task1_train_45814 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | ACTCCGTCTCAAAAAAAAAAAAAAAATCCATGAGTTAATTCCAGTACTTGCAATTTTAATCCAATAGCACAGTTTTCTTTTGCATTGTTTTCAATATACTCAATTGCTCAGCCCTAGAATACACAAAAAGTAGTTTTAAGAATGCTAACCTGGCCCACTGTGGAGACGATGCCTCCTAACTGGAGTGTAACATTTGTCTGTAGTTCTTGTCATTTGTAGCCTGAGGCCGTGGAGTCCAGATTTTGGGTTCAGAAGTTACTGGAATTCACTATCCCATCCCATTGGTCAGACCATGTCACTCATTTCAAATACAGTTTGGT... | ACTCCGTCTCAAAAAAAAAAAAAAAATCCATGAGTTAATTCCAGTACTTGCAATTTTAATCCAATAGCACAGTTTTCTTTTGCATTGTTTTCAATATACTCAATTGCTCAGCCCTAGAATACACAAAAAGTAGTTTTAAGAATGCTAACCTGGCCCACTGTGGAGACGATGCCTCCTAACTGGAGTGTAACATTTGTCTGTAGTTCTTGTCATTTGTAGCCTGAGGCCGTGGAGTCCAGATTTTGGGTTCAGAAGTTACTGGAATTCACTATCCCATCCCATTGGTCAGACCATGTCACTCATTTCAAATACAGTTTGGT... |
Task1_train_45815 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | TCCTGGGAAGGGAGTCGGGTGATGGGAACGGTGGGAGCTCAGCGCTCCGAGTCTGCGGCCGGGGGCCAGCGGGGCTGAAACGCGCCTCCTGAGTGTTGAAAGCGGCAGGCGCCGGCCTTTGCACCCAGAGGCCAGGGCGTCTCACTCACCTTCACATCCAGGCCTCTTAGGGGAGCGCGGCTTTGGCTTTTCCAGGAAGGAATGGACTCCAACGGACAGGGAAAGAAGAAGTGTGGAGAGACGGGCAGGATAAGCAGGCACTGGGCCCAAGCCGCCCTTGGAGGCTCTGCCTGTTCTGATCTGAAGGCGGAGGCTCAGCC... | TCCTGGGAAGGGAGTCGGGTGATGGGAACGGTGGGAGCTCAGCGCTCCGAGTCTGCGGCCGGGGGCCAGCGGGGCTGAAACGCGCCTCCTGAGTGTTGAAAGCGGCAGGCGCCGGCCTTTGCACCCAGAGGCCAGGGCGTCTCACTCACCTTCACATCCAGGCCTCTTAGGGGAGCGCGGCTTTGGCTTTTCCAGGAAGGAATGGACTCCAACGGACAGGGAAAGAAGAAGTGTGGAGAGACGGGCAGGATAAGCAGGCACTGGGCCCAAGCCGCCCTTGGAGGCTCTGCCTGTTCTGATCTGAAGGCGGAGGCTCAGCC... |
Task1_train_45816 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GTTCAAGACCAGCCTGGGCAACATACTGAAACCCTGTCTCTACCAAAATTACAAAAATTAGGGGCCAGGTGCGGTGGCTCATGCCTATCATCCCAGCACTTTGGGAGGTCGAGGCAAGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCCTCTCTACTAAAAATACAAAAAATTGGCTGGGTGTGGTGGCGTGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCATTGCACCCCAGCCT... | GTTCAAGACCAGCCTGGGCAACATACTGAAACCCTGTCTCTACCAAAATTACAAAAATTAGGGGCCAGGTGCGGTGGCTCATGCCTATCATCCCAGCACTTTGGGAGGTCGAGGCAAGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCCTCTCTACTAAAAATACAAAAAATTGGCTGGGTGTGGTGGCGTGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCATTGCACCCCAGCCT... |
Task1_train_45817 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCAGATGGGCGTGGGGGAGGAGGTGAGTGCTGCGGGCCTCTGGGAGGGACGGGCATGAGCCACAGGCCCGTCGGAGCCAGGCTGGCCTGTCACCCCTGTGAGGCAGAAGACGCTGCCTGCCCCTTCCCCAGGAGGCTGCTCAGACCCTCAGGAGCCCAGCCTGCCCTGACTGTGATCCCAGGCCACTTCCTTCCTCAGCCTTCCCCCAGAGCACGCTAGGAGGGGCCGCCAGGAGGGGCAAGTGCCCACAGTCCCCTCAGAAGAGACTGCTGGTCCAGAGGCAGGGTACGTATAAATGTCAGCATTTATTTCCTGCTCAA... | CCAGATGGGCGTGGGGGAGGAGGTGAGTGCTGCGGGCCTCTGGGAGGGACGGGCATGAGCCACAGGCCCGTCGGAGCCAGGCTGGCCTGTCACCCCTGTGAGGCAGAAGACGCTGCCTGCCCCTTCCCCAGGAGGCTGCTCAGACCCTCAGGAGCCCAGCCTGCCCTGACTGTGATCCCAGGCCACTTCCTTCCTCAGCCTTCCCCCAGAGCACGCTAGGAGGGGCCGCCAGGAGGGGCAAGTGCCCACAGTCCCCTCAGAAGAGACTGCTGGTCCAGAGGCAGGGTACGTATAAATGTCAGCATTTATTTCCTGCTCAA... |
Task1_train_45818 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTGTCAGAGTCGGGGCCTGGGTGGGAAAGGGATGCCCCTCCCCCAGGATTGAGGACGTGAAAAATAAAGGCCACGAAACAAAAGAAAACACGTCAAACCCACACACGTGGCCGAGTCCCCAGGTGTCGGGGCTGGGCCTGTCCTGGGTGTGGCACCTTGGGCTTTTCTGCTTGGTCTGTTCTCATTTCAGGGAGGCAAGTCCTGCCCTTTTTTTTGTTTTGTTTTGTTTTGTTTGTGTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTCCACCTCCTGGGTT... | CTGTCAGAGTCGGGGCCTGGGTGGGAAAGGGATGCCCCTCCCCCAGGATTGAGGACGTGAAAAATAAAGGCCACGAAACAAAAGAAAACACGTCAAACCCACACACGTGGCCGAGTCCCCAGGTGTCGGGGCTGGGCCTGTCCTGGGTGTGGCACCTTGGGCTTTTCTGCTTGGTCTGTTCTCATTTCAGGGAGGCAAGTCCTGCCCTTTTTTTTGTTTTGTTTTGTTTTGTTTGTGTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTCCACCTCCTGGGTT... |
Task1_train_45819 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTGTCAGGTGCCTCCTTTTGGTGGTTGTGGGGCGCAGTGGGGCTGAGGTCTGTGGCCTGGGCCTGGGCCTGGGACGCTGTCCTGGGTGGGTGCTGGGTGAGGGCCCCACACCTTTGCTTTCCGAGTCTCCTGCCCCAGGGCCTCCGTGGCACTGGTTGAGCTGCCCTGGGGTACCTGATGGTTTCTTTCCTCTCCTCCCAGGGAGTGCCTGCAGCACCCCGGCGGGGCCACCCCAGTCTGCGTGTACACGAGGGATGAGGTAGGCGGCCTGCTCTTGCTCACCCAGTCCCCGCTCACTTTCAGCCCACTTTCCAACTGGA... | CTGTCAGGTGCCTCCTTTTGGTGGTTGTGGGGCGCAGTGGGGCTGAGGTCTGTGGCCTGGGCCTGGGCCTGGGACGCTGTCCTGGGTGGGTGCTGGGTGAGGGCCCCACACCTTTGCTTTCCGAGTCTCCTGCCCCAGGGCCTCCGTGGCACTGGTTGAGCTGCCCTGGGGTACCTGATGGTTTCTTTCCTCTCCTCCCAGGGAGTGCCTGCAGCACCCCGGCGGGGCCACCCCAGTCTGCGTGTACACGAGGGATGAGGTAGGCGGCCTGCTCTTGCTCACCCAGTCCCCGCTCACTTTCAGCCCACTTTCCAACTGGA... |
Task1_train_45820 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGTTGGCAGCAGAGAGGCGGCTGGATTTGGGGCCCCAGTGTCCTGGGCGGCAGCTAGGGAGGGGCCGGCTCCAGGCCCTCAGGCTGTGTCAGGGCAGGGCGGGCACCCCCACTTCTCCCTGTCAGCCGAGGGAGCCAGGCAGGGGCAGCCTGAGACATCCTGGGACAGTGCTGGTGGGGAGAGGCCCCTCAGCCTGTGCCTCCCTCAAAGGCCCTTCCCGGGCCCTGCTCTGGCTGGGGGGACGGTGTGACCCACTTTCCCTTTCCAGCCCCAGCTTGGTGACCGGGTGGCTCCATTCACCCTGGGTCCCTCGCTGAAAC... | GGTTGGCAGCAGAGAGGCGGCTGGATTTGGGGCCCCAGTGTCCTGGGCGGCAGCTAGGGAGGGGCCGGCTCCAGGCCCTCAGGCTGTGTCAGGGCAGGGCGGGCACCCCCACTTCTCCCTGTCAGCCGAGGGAGCCAGGCAGGGGCAGCCTGAGACATCCTGGGACAGTGCTGGTGGGGAGAGGCCCCTCAGCCTGTGCCTCCCTCAAAGGCCCTTCCCGGGCCCTGCTCTGGCTGGGGGGACGGTGTGACCCACTTTCCCTTTCCAGCCCCAGCTTGGTGACCGGGTGGCTCCATTCACCCTGGGTCCCTCGCTGAAAC... |
Task1_train_45821 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | GGGCACAGCATTTGCCTCAGCATTGTGCAGTGCCCCTTGACCTTTGGGATGGTGGCCAGATGCCCCAGGATGGCCCTTGCCTTTTGCGGTGGAGCAGCTCCCACCACCTCTGCCCCACATGTGCACGCGCTCCCCAACACCAGGCGGCTCTTGCTCACAGCCCGAACCCCACAAAGCACTTCCACCCCCATGCACTGAGGGGGCACCCCTGACTTGCCGGGTGAGACGCTGCCCCACACGGCATAGATTCCCAAGCAGCCAGCCGCTGGGTGCAGGGCTGGTGGCCACCAGCTACTCCTGAGGCTAAGCAGCCCCGGGGT... | GGGCACAGCATTTGCCTCAGCATTGTGCAGTGCCCCTTGACCTTTGGGATGGTGGCCAGATGCCCCAGGATGGCCCTTGCCTTTTGCGGTGGAGCAGCTCCCACCACCTCTGCCCCACATGTGCACGCGCTCCCCAACACCAGGCGGCTCTTGCTCACAGCCCGAACCCCACAAAGCACTTCCACCCCCATGCACTGAGGGGGCACCCCTGACTTGCCGGGTGAGACGCTGCCCCACACGGCATAGATTCCCAAGCAGCCAGCCGCTGGGTGCAGGGCTGGTGGCCACCAGCTACTCCTGAGGCTAAGCAGCCCCGGGGT... |
Task1_train_45822 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | ACCATGGGGGCTGATGGGGTGCCGTGGTGGTGGTCACAGCTCTCAGAATGGAGGGTTCTGAGGGCTCTGGCTGCTGGGGATGGGCCTTGACTAGGAGGCCCTGGGAGGTCTCCAGGTTCCCTGGCTGCGTGTTTGTTCCTGGTATCTCCCCACCAAATCCGCCCCTGGTCACCCCTTGAAGGAAGAAGAGCCAAGTGTAGCTCTGGAACAGTGGGGAAAGTCCCTGAGGGCCGTGACTTGCTCAGGTGGGGCTGGGGTAGCCGACTCCGGGCCTAGGGATCAGAGCGTCTGTCCCTGCAGTGGTACCCGGAGGTGCGGCA... | ACCATGGGGGCTGATGGGGTGCCGTGGTGGTGGTCACAGCTCTCAGAATGGAGGGTTCTGAGGGCTCTGGCTGCTGGGGATGGGCCTTGACTAGGAGGCCCTGGGAGGTCTCCAGGTTCCCTGGCTGCGTGTTTGTTCCTGGTATCTCCCCACCAAATCCGCCCCTGGTCACCCCTTGAAGGAAGAAGAGCCAAGTGTAGCTCTGGAACAGTGGGGAAAGTCCCTGAGGGCCGTGACTTGCTCAGGTGGGGCTGGGGTAGCCGACTCCGGGCCTAGGGATCAGAGCGTCTGTCCCTGCAGTGGTACCCGGAGGTGCGGCA... |
Task1_train_45823 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CTCCCTGATGTGGTGGCACAGGAGCCTGGGTGGGGGCGGGGGTGACTGGGAGGGCACACCTGGGGGACAGCAGCGGCGGGAGTGTGGTCCGACTGGCCTGGAAGATCTTGGGCAGAGCTGACCTCAGAGAACAGTGCGGGTCTCTCGCCCTCCTGGGGCAGTCCCCAGGACGAGGTGCCAGGTGCCTGGCCCATGTTGCAGGGGGCCGTGGAGCCCATGCAGATCGACGTGGACCCCCAGGAAGACCCGCAGAATGCACCTGACGTCAACTACGTGGTGGAGAACCCCAGCCTGGTACGGAGCCCAGTGGGGGGACCTTG... | CTCCCTGATGTGGTGGCACAGGAGCCTGGGTGGGGGCGGGGGTGACTGGGAGGGCACACCTGGGGGACAGCAGCGGCGGGAGTGTGGTCCGACTGGCCTGGAAGATCTTGGGCAGAGCTGACCTCAGAGAACAGTGCGGGTCTCTCGCCCTCCTGGGGCAGTCCCCAGGACGAGGTGCCAGGTGCCTGGCCCATGTTGCAGGGGGCCGTGGAGCCCATGCAGATCGACGTGGACCCCCAGGAAGACCCGCAGAATGCACCTGACGTCAACTACGTGGTGGAGAACCCCAGCCTGGTACGGAGCCCAGTGGGGGGACCTTG... |
Task1_train_45824 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | GGCAGGCAGGGACTGCTGGCACCAGCCTGATGTGGCAGCTGCTCTTGGACTGGCCAGCGCCCTGGGGGTTACATGGGAAGGTTTCAGGGTTATCGCTGGTCTCCCCTGCAGCTTGTAAAGTTGTCAGAGATCTGGGAGGCTGCCACCTGTTGAGGGCCCAGATGGGCTGGCCCAGGATACGGCGGCGACCAGGGGTCTCAGGGGAGACAGCACTAGGCTGAGGCCTTGCCACTGGTGGCTAAGAGAGGGGCGAGCAGCCTCGTCCCGTGCCTTTGGCCCAGCAACAAGACCCATGCACACACTCCCGGGGACCCCAGCCT... | GGCAGGCAGGGACTGCTGGCACCAGCCTGATGTGGCAGCTGCTCTTGGACTGGCCAGCGCCCTGGGGGTTACATGGGAAGGTTTCAGGGTTATCGCTGGTCTCCCCTGCAGCTTGTAAAGTTGTCAGAGATCTGGGAGGCTGCCACCTGTTGAGGGCCCAGATGGGCTGGCCCAGGATACGGCGGCGACCAGGGGTCTCAGGGGAGACAGCACTAGGCTGAGGCCTTGCCACTGGTGGCTAAGAGAGGGGCGAGCAGCCTCGTCCCGTGCCTTTGGCCCAGCAACAAGACCCATGCACACACTCCCGGGGACCCCAGCCT... |
Task1_train_45825 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGCTGGCCCCGCACTGCTGTCCCCACTGCGGGGGTTCTTCTGATTCAGGGTGAGGCCCTGTGTCAGCCTCAGGCGTGCGGGCACGCAGCTCCGGCTCTCCATGCTCCAAACCTCCCAGGTGGCCCTGGCTGCCAGTGCTGGTGATCAGCGGCCAGCGGGGCCCTGCTCTCTGCAGCCTGTCGAGGGCTGGGCCAGCTACAGGGGAGCCCTGGCTGGCTCCCAAGGAGGTTGGAGACTCGTCCAGCACCCTGAGGGCTTCCACAGAAAGTGAGCGGCAGCGGCCGGGCTTGGTGGCTCACGCCTGTAATCCCAGCACTTTG... | GGCTGGCCCCGCACTGCTGTCCCCACTGCGGGGGTTCTTCTGATTCAGGGTGAGGCCCTGTGTCAGCCTCAGGCGTGCGGGCACGCAGCTCCGGCTCTCCATGCTCCAAACCTCCCAGGTGGCCCTGGCTGCCAGTGCTGGTGATCAGCGGCCAGCGGGGCCCTGCTCTCTGCAGCCTGTCGAGGGCTGGGCCAGCTACAGGGGAGCCCTGGCTGGCTCCCAAGGAGGTTGGAGACTCGTCCAGCACCCTGAGGGCTTCCACAGAAAGTGAGCGGCAGCGGCCGGGCTTGGTGGCTCACGCCTGTAATCCCAGCACTTTG... |
Task1_train_45826 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | GAAAAAACAAATACATGCAAATAACCAAGAAAACCCTGAGAGAGAAGGATAAAGAGGAGATCCTACATCAGCCAGACATGTAAAAGGACCAGGAAGTGACACTGATTCTGACCCAATGGAACTGCCTGTGAACAGACTGAGAGTGGCCGAACGAACCGTCCGGATATAGCTCCAAAAGCACATGGAACATTTAGCACCATGACAAAGGTGGGAGTCCGAATATGCGGGAAGTGTGAGCGATGGAAAACTGGGAGCCGTTGCCACTTTGGGGGTTAATAAGAAGTGGTTCTGGCCAGGCACGGTGGCTCACCCCTGTAATC... | GAAAAAACAAATACATGCAAATAACCAAGAAAACCCTGAGAGAGAAGGATAAAGAGGAGATCCTACATCAGCCAGACATGTAAAAGGACCAGGAAGTGACACTGATTCTGACCCAATGGAACTGCCTGTGAACAGACTGAGAGTGGCCGAACGAACCGTCCGGATATAGCTCCAAAAGCACATGGAACATTTAGCACCATGACAAAGGTGGGAGTCCGAATATGCGGGAAGTGTGAGCGATGGAAAACTGGGAGCCGTTGCCACTTTGGGGGTTAATAAGAAGTGGTTCTGGCCAGGCACGGTGGCTCACCCCTGTAATC... |
Task1_train_45827 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CAAATCAATAAGAAAGACCACAATCTAATACACAAATGGGCAGGTAACTGAAGAACAGGGAAAGGAAGTGGCTCCTAAACACACACGAAGATGCACGACCTCCCAGCAGAGGCGCTGATGCCAATCCTGCTGCCACCGGCAAAAGTTCCGTGTGGCTACAGGACTCTCAGACACTGCTGCTGGGAGCAGCCTCTGGGTGGGTGGCGGAGGCTGAGGCGATGCTGTCCACCACACGTGGCACGCGGGCAGCCTTGACTACGCAAGCCCCTGGGGCACGTACACGTGTGTTTTCACACACACTGCAGCCTGTAAGGTTACTA... | CAAATCAATAAGAAAGACCACAATCTAATACACAAATGGGCAGGTAACTGAAGAACAGGGAAAGGAAGTGGCTCCTAAACACACACGAAGATGCACGACCTCCCAGCAGAGGCGCTGATGCCAATCCTGCTGCCACCGGCAAAAGTTCCGTGTGGCTACAGGACTCTCAGACACTGCTGCTGGGAGCAGCCTCTGGGTGGGTGGCGGAGGCTGAGGCGATGCTGTCCACCACACGTGGCACGCGGGCAGCCTTGACTACGCAAGCCCCTGGGGCACGTACACGTGTGTTTTCACACACACTGCAGCCTGTAAGGTTACTA... |
Task1_train_45828 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | ATCAATAAGAAAGACCACAATCTAATACACAAATGGGCAGGTAACTGAAGAACAGGGAAAGGAAGTGGCTCCTAAACACACACGAAGATGCACGACCTCCCAGCAGAGGCGCTGATGCCAATCCTGCTGCCACCGGCAAAAGTTCCGTGTGGCTACAGGACTCTCAGACACTGCTGCTGGGAGCAGCCTCTGGGTGGGTGGCGGAGGCTGAGGCGATGCTGTCCACCACACGTGGCACGCGGGCAGCCTTGACTACGCAAGCCCCTGGGGCACGTACACGTGTGTTTTCACACACACTGCAGCCTGTAAGGTTACTATTC... | ATCAATAAGAAAGACCACAATCTAATACACAAATGGGCAGGTAACTGAAGAACAGGGAAAGGAAGTGGCTCCTAAACACACACGAAGATGCACGACCTCCCAGCAGAGGCGCTGATGCCAATCCTGCTGCCACCGGCAAAAGTTCCGTGTGGCTACAGGACTCTCAGACACTGCTGCTGGGAGCAGCCTCTGGGTGGGTGGCGGAGGCTGAGGCGATGCTGTCCACCACACGTGGCACGCGGGCAGCCTTGACTACGCAAGCCCCTGGGGCACGTACACGTGTGTTTTCACACACACTGCAGCCTGTAAGGTTACTATTC... |
Task1_train_45829 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | AAGAAAGACCACAATCTAATACACAAATGGGCAGGTAACTGAAGAACAGGGAAAGGAAGTGGCTCCTAAACACACACGAAGATGCACGACCTCCCAGCAGAGGCGCTGATGCCAATCCTGCTGCCACCGGCAAAAGTTCCGTGTGGCTACAGGACTCTCAGACACTGCTGCTGGGAGCAGCCTCTGGGTGGGTGGCGGAGGCTGAGGCGATGCTGTCCACCACACGTGGCACGCGGGCAGCCTTGACTACGCAAGCCCCTGGGGCACGTACACGTGTGTTTTCACACACACTGCAGCCTGTAAGGTTACTATTCTAACAG... | AAGAAAGACCACAATCTAATACACAAATGGGCAGGTAACTGAAGAACAGGGAAAGGAAGTGGCTCCTAAACACACACGAAGATGCACGACCTCCCAGCAGAGGCGCTGATGCCAATCCTGCTGCCACCGGCAAAAGTTCCGTGTGGCTACAGGACTCTCAGACACTGCTGCTGGGAGCAGCCTCTGGGTGGGTGGCGGAGGCTGAGGCGATGCTGTCCACCACACGTGGCACGCGGGCAGCCTTGACTACGCAAGCCCCTGGGGCACGTACACGTGTGTTTTCACACACACTGCAGCCTGTAAGGTTACTATTCTAACAG... |
Task1_train_45830 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | CTCACGCCCTCACCTGTCTACCCCCACAGCCACACGTCCTCACTACCTGCTTCTTTACTTGATTACCAATAAACAGTGTGGGCTCCCAGAGCTGGGGGCCTTTGCAGCCTCCATACACCAGCGTGGGCCCCCTGGACCCACCCTATGTACTCTTGTCTCATTCCTTTGACTCTGCTGGACTTCGTAGCCCCCATGACCTGGTGTTGGGTCTGATCACCCCAACGGTACAACTCCCTTTTTTTGGAGTTTTACTTGCTTCCAACAAGGAAGGCAAGTTTCTCCTGCTTCATGATGATGGAAGGCAGGTAACTCCTTTATGG... | CTCACGCCCTCACCTGTCTACCCCCACAGCCACACGTCCTCACTACCTGCTTCTTTACTTGATTACCAATAAACAGTGTGGGCTCCCAGAGCTGGGGGCCTTTGCAGCCTCCATACACCAGCGTGGGCCCCCTGGACCCACCCTATGTACTCTTGTCTCATTCCTTTGACTCTGCTGGACTTCGTAGCCCCCATGACCTGGTGTTGGGTCTGATCACCCCAACGGTACAACTCCCTTTTTTTGGAGTTTTACTTGCTTCCAACAAGGAAGGCAAGTTTCTCCTGCTTCATGATGATGGAAGGCAGGTAACTCCTTTATGG... |
Task1_train_45831 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AAGTCAGCACCCGCACGGCGGGCAAGTGGGCCTCAGCTGTCCAAGCACTGCACGCACCTGCACGGACTCGGCGCCCAGACGAGGTGCAGGCTGAGCACCAGCCTTCATGCTGGGGACGGGAGCTTCCAGACACCCTCCCTCCACTCAGGGAGAAGCTGACCTCCAGCTCAACTCTCTCTTTCCCTGGACACTGGGCAGGTGGCACACGGGTGTCTACCACATTAGCAAGCAGCACTGCGTGGGTCAAATGACTGCTGACTGGCACTTTTTATCCACGCCGCGAGATGCGATAGAGAGAGGGACCATCAACACTGTGGGCT... | AAGTCAGCACCCGCACGGCGGGCAAGTGGGCCTCAGCTGTCCAAGCACTGCACGCACCTGCACGGACTCGGCGCCCAGACGAGGTGCAGGCTGAGCACCAGCCTTCATGCTGGGGACGGGAGCTTCCAGACACCCTCCCTCCACTCAGGGAGAAGCTGACCTCCAGCTCAACTCTCTCTTTCCCTGGACACTGGGCAGGTGGCACACGGGTGTCTACCACATTAGCAAGCAGCACTGCGTGGGTCAAATGACTGCTGACTGGCACTTTTTATCCACGCCGCGAGATGCGATAGAGAGAGGGACCATCAACACTGTGGGCT... |
Task1_train_45832 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGCCTTCATGCTGGGGACGGGAGCTTCCAGACACCCTCCCTCCACTCAGGGAGAAGCTGACCTCCAGCTCAACTCTCTCTTTCCCTGGACACTGGGCAGGTGGCACACGGGTGTCTACCACATTAGCAAGCAGCACTGCGTGGGTCAAATGACTGCTGACTGGCACTTTTTATCCACGCCGCGAGATGCGATAGAGAGAGGGACCATCAACACTGTGGGCTTCCCAGAAGACGGTGGCGCTCAGGGTACATCTGCTGCAGGGACTGCAGACGCGATCCCTGCGGGCTGCTACAGGAGATACTGGCTGCACAATACTGGTT... | AGCCTTCATGCTGGGGACGGGAGCTTCCAGACACCCTCCCTCCACTCAGGGAGAAGCTGACCTCCAGCTCAACTCTCTCTTTCCCTGGACACTGGGCAGGTGGCACACGGGTGTCTACCACATTAGCAAGCAGCACTGCGTGGGTCAAATGACTGCTGACTGGCACTTTTTATCCACGCCGCGAGATGCGATAGAGAGAGGGACCATCAACACTGTGGGCTTCCCAGAAGACGGTGGCGCTCAGGGTACATCTGCTGCAGGGACTGCAGACGCGATCCCTGCGGGCTGCTACAGGAGATACTGGCTGCACAATACTGGTT... |
Task1_train_45833 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ATCTTGCGCAGAGACCCTGGAGCACCCTAGCAAGGCTGTGGCTCGAGGCGGTGGGTAACAGCACTTGCCGGAGCAGCCCCTCCTCTGGCCTTTGCTCCATGCATGCATTGGGTCACCAACGTTCACCGGGCGTCTTTATGCCAGCGTCTGTGCCAGGAGCAGGGGGCAGTGTGGACCAGGAGCCCTCCCGCCTGGAGCTGACCTCAGGGAGGCCAGGTGGACAGCCAGCAGGACACAGGGTGTGGGTGTGGCCCTCAAAGGCCAACCCAGGAACGGGCCGTGGGTGAAACCAACTGGGGCCCCGGGGAACAGCATTCCAC... | ATCTTGCGCAGAGACCCTGGAGCACCCTAGCAAGGCTGTGGCTCGAGGCGGTGGGTAACAGCACTTGCCGGAGCAGCCCCTCCTCTGGCCTTTGCTCCATGCATGCATTGGGTCACCAACGTTCACCGGGCGTCTTTATGCCAGCGTCTGTGCCAGGAGCAGGGGGCAGTGTGGACCAGGAGCCCTCCCGCCTGGAGCTGACCTCAGGGAGGCCAGGTGGACAGCCAGCAGGACACAGGGTGTGGGTGTGGCCCTCAAAGGCCAACCCAGGAACGGGCCGTGGGTGAAACCAACTGGGGCCCCGGGGAACAGCATTCCAC... |
Task1_train_45834 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CAGCTTGGACGAAGGCATTTCCTATCAACTCCCTCCCCTGTATATTTCCACTGGGGTGGGTGAAGTCAGAGCCTCAGGTGTGTGCCGGGCGGCTGCGCTGTGGCAGGAGTGCTGCCACTGACCTGCCGAATCACCCTCCTCGTGGGAAGCAGTGGCCAGGCCCCACCGCCCCCAGCTCCCTCCTGTTTCTCCAAGGCCTAGGCCAGGTGCAGGTGCTCGGCTGCGTGAGGAAGGGCAGGGCTTCTGCAGACACCCACAGGCCAGCCTCAGAGGCAAGCAGAGCAGACATGGGTTCCAGCCTGTCCTTGTGGGGCCCAGCC... | CAGCTTGGACGAAGGCATTTCCTATCAACTCCCTCCCCTGTATATTTCCACTGGGGTGGGTGAAGTCAGAGCCTCAGGTGTGTGCCGGGCGGCTGCGCTGTGGCAGGAGTGCTGCCACTGACCTGCCGAATCACCCTCCTCGTGGGAAGCAGTGGCCAGGCCCCACCGCCCCCAGCTCCCTCCTGTTTCTCCAAGGCCTAGGCCAGGTGCAGGTGCTCGGCTGCGTGAGGAAGGGCAGGGCTTCTGCAGACACCCACAGGCCAGCCTCAGAGGCAAGCAGAGCAGACATGGGTTCCAGCCTGTCCTTGTGGGGCCCAGCC... |
Task1_train_45835 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CGAAGGCATTTCCTATCAACTCCCTCCCCTGTATATTTCCACTGGGGTGGGTGAAGTCAGAGCCTCAGGTGTGTGCCGGGCGGCTGCGCTGTGGCAGGAGTGCTGCCACTGACCTGCCGAATCACCCTCCTCGTGGGAAGCAGTGGCCAGGCCCCACCGCCCCCAGCTCCCTCCTGTTTCTCCAAGGCCTAGGCCAGGTGCAGGTGCTCGGCTGCGTGAGGAAGGGCAGGGCTTCTGCAGACACCCACAGGCCAGCCTCAGAGGCAAGCAGAGCAGACATGGGTTCCAGCCTGTCCTTGTGGGGCCCAGCCTGCTTGTGC... | CGAAGGCATTTCCTATCAACTCCCTCCCCTGTATATTTCCACTGGGGTGGGTGAAGTCAGAGCCTCAGGTGTGTGCCGGGCGGCTGCGCTGTGGCAGGAGTGCTGCCACTGACCTGCCGAATCACCCTCCTCGTGGGAAGCAGTGGCCAGGCCCCACCGCCCCCAGCTCCCTCCTGTTTCTCCAAGGCCTAGGCCAGGTGCAGGTGCTCGGCTGCGTGAGGAAGGGCAGGGCTTCTGCAGACACCCACAGGCCAGCCTCAGAGGCAAGCAGAGCAGACATGGGTTCCAGCCTGTCCTTGTGGGGCCCAGCCTGCTTGTGC... |
Task1_train_45836 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ACCTTGGCCCGGCTGCTGGCTACGGGAACGCTGGGTCCTCGATGCCATGGTCGGGGTTGCAGCTGAAGGCGATGGTGATGGCGTAACGGGTGCCCCAGTGGACCTTCTCCACGCGGTGTAGGTTCTCGGACCCCGAGGTGAAGAAGGAGACGCGACCTGGGAGAGGAGAAGAGAGAGAGGTGGCCATAGAGCCACACCCACGGCCACAGCCTTCAGAGGGTCTGCGGTCACCTGAAAGAGCAACTATAACCAATCAACACAACCAACCAGGCAGGCTGGAGAAATTGCCCCTCTGGGAACTGCTTCTGCAGGAAGGAGGA... | ACCTTGGCCCGGCTGCTGGCTACGGGAACGCTGGGTCCTCGATGCCATGGTCGGGGTTGCAGCTGAAGGCGATGGTGATGGCGTAACGGGTGCCCCAGTGGACCTTCTCCACGCGGTGTAGGTTCTCGGACCCCGAGGTGAAGAAGGAGACGCGACCTGGGAGAGGAGAAGAGAGAGAGGTGGCCATAGAGCCACACCCACGGCCACAGCCTTCAGAGGGTCTGCGGTCACCTGAAAGAGCAACTATAACCAATCAACACAACCAACCAGGCAGGCTGGAGAAATTGCCCCTCTGGGAACTGCTTCTGCAGGAAGGAGGA... |
Task1_train_45837 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ATTTGTGCACACGAGCGTGGGTCAGGAGAAATACCCACAACGTTGTGAAAAGGGACCAAAAATCCCACGCATTTCCAAATCTTTTAAATTTCCAAGTAATTCATGAGTTAAAAAACAATAATAATAAAAATTAGAGGCCAGGCGCAGTGGCTCATGCCTGTAACCCCAGGGCCTTAGGAGGCCAAGGCAGGTGGATCACCTGAGGTCAGCAGTTTGAGATCAGCCTGGGCAACATAGGCAAAACACCGTCTCTACTAAAATTACAAAAATTAGCCAGACATGGTGGCAGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTG... | ATTTGTGCACACGAGCGTGGGTCAGGAGAAATACCCACAACGTTGTGAAAAGGGACCAAAAATCCCACGCATTTCCAAATCTTTTAAATTTCCAAGTAATTCATGAGTTAAAAAACAATAATAATAAAAATTAGAGGCCAGGCGCAGTGGCTCATGCCTGTAACCCCAGGGCCTTAGGAGGCCAAGGCAGGTGGATCACCTGAGGTCAGCAGTTTGAGATCAGCCTGGGCAACATAGGCAAAACACCGTCTCTACTAAAATTACAAAAATTAGCCAGACATGGTGGCAGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTG... |
Task1_train_45838 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | ATTTGATAAATTCTGCATGTGGGCCCTGAGAGTCAGAGTCTGTGAACTGGATCCTACTTTCCAGTTCATTTGCACATCTCAAAATTTTTGGTTGAGAACTGAACATTTCAGTTAATACATTATAGCAAAGCTGAATGTTTACTCTTTTCCCCAGTGGCTGGTGGTGGTCTTTTTGTTGTTTTCTAGCAAATGGCCTGCATTTAACCTGCAGGACCTGCCCCTGGCTGTGTGCACTCACTGATGTCTGTGCTGAGATTTTTTGGTTCTTATTTTTACATTTTAGCCTGGCTTCCTAGGGTCATCCCTCTGTCTTCATAGTT... | ATTTGATAAATTCTGCATGTGGGCCCTGAGAGTCAGAGTCTGTGAACTGGATCCTACTTTCCAGTTCATTTGCACATCTCAAAATTTTTGGTTGAGAACTGAACATTTCAGTTAATACATTATAGCAAAGCTGAATGTTTACTCTTTTCCCCAGTGGCTGGTGGTGGTCTTTTTGTTGTTTTCTAGCAAATGGCCTGCATTTAACCTGCAGGACCTGCCCCTGGCTGTGTGCACTCACTGATGTCTGTGCTGAGATTTTTTGGTTCTTATTTTTACATTTTAGCCTGGCTTCCTAGGGTCATCCCTCTGTCTTCATAGTT... |
Task1_train_45839 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | AAAACTATAACCTCAGAGGTTCTCCACTGTGTGGGGATTCTAGACCTAAATTAGGAGGAAATCCTAAGTTAGACAAAGCTAGACTCCCCTGAAGTCAGGTGGCCCCTATTTCTGGGCTTGGCAGGCAGTGCTGGGGCTGGACACCGAAGCAGATCGCGAGTGGGCTTTGCCTTATTTCCAAGAACGAGGTGATGAGACCGGGGCTCCCAGAGGCCAGCGATAACTGCAGCCGTTGCTCTCGTAGGTGAAGATCCCGGATCTGTTTTGTGGCCTAGAGATTGTCCCCGCGTTGCTCCACGGGGATCTCTGGTCGGGAAACG... | AAAACTATAACCTCAGAGGTTCTCCACTGTGTGGGGATTCTAGACCTAAATTAGGAGGAAATCCTAAGTTAGACAAAGCTAGACTCCCCTGAAGTCAGGTGGCCCCTATTTCTGGGCTTGGCAGGCAGTGCTGGGGCTGGACACCGAAGCAGATCGCGAGTGGGCTTTGCCTTATTTCCAAGAACGAGGTGATGAGACCGGGGCTCCCAGAGGCCAGCGATAACTGCAGCCGTTGCTCTCGTAGGTGAAGATCCCGGATCTGTTTTGTGGCCTAGAGATTGTCCCCGCGTTGCTCCACGGGGATCTCTGGTCGGGAAACG... |
Task1_train_45840 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGCAGAGTAAGCCAGAACATTCACTGTAACATTATAAGCAAGTAGAATAAATTGATAATACCTTCACCAGTAATGCACTTTCCCTAGTGGAAATAAATTATTTGTATAAATAGCCTCTTGATGTTTGTGTGTTATTTAGTTATACAAATCACATTTTTCTTTTTTACATATGGCACTTTAATGTTAGTACTGAAAATGTTTTTTCTGACATTTTTTCAGTAATTGTCATTTACATCAAATATGCAGCTAGAGCTAATAGAAAAACAGTTAAAACAATTTGTTGTAATGGTGAGATATTTATAAGGAAACATTTATAAAAG... | GGCAGAGTAAGCCAGAACATTCACTGTAACATTATAAGCAAGTAGAATAAATTGATAATACCTTCACCAGTAATGCACTTTCCCTAGTGGAAATAAATTATTTGTATAAATAGCCTCTTGATGTTTGTGTGTTATTTAGTTATACAAATCACATTTTTCTTTTTTACATATGGCACTTTAATGTTAGTACTGAAAATGTTTTTTCTGACATTTTTTCAGTAATTGTCATTTACATCAAATATGCAGCTAGAGCTAATAGAAAAACAGTTAAAACAATTTGTTGTAATGGTGAGATATTTATAAGGAAACATTTATAAAAG... |
Task1_train_45841 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | TGCCACACGACACTCCCTGGTCTCTAGGTGGCTCGCACCTGCCACACGACACTCCCTGGTCTCTAGGTGGCTCGCACCTGCCACACGACACTCCCTGGTCTCTAGGTGGCTCGCACCTGCCACACGACACTCCCTGGTCTCTAGGTGGCTCGCACCTGCCACACGACACTCCCTGGTCTCTGGTTGGCATGCACCTGCCACACGACACTCCTTGGTCTCTAGGTGGCTTCCATCTGCCACACGACACTCCCTGGTCTCTGGTTGGCATGCACCTGCCACACGACACTCCTTGGTCTCTAGGTGGCTTGCACCTGCCACAT... | TGCCACACGACACTCCCTGGTCTCTAGGTGGCTCGCACCTGCCACACGACACTCCCTGGTCTCTAGGTGGCTCGCACCTGCCACACGACACTCCCTGGTCTCTAGGTGGCTCGCACCTGCCACACGACACTCCCTGGTCTCTAGGTGGCTCGCACCTGCCACACGACACTCCCTGGTCTCTGGTTGGCATGCACCTGCCACACGACACTCCTTGGTCTCTAGGTGGCTTCCATCTGCCACACGACACTCCCTGGTCTCTGGTTGGCATGCACCTGCCACACGACACTCCTTGGTCTCTAGGTGGCTTGCACCTGCCACAT... |
Task1_train_45842 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | CCCCATCGGGGTTCACATTCCCTCTCCCTAGAGCACACTCCCTTGGATTTCCTCGAGTGGGGTCTGCTGCGGTGAAGCTTTCCCATTTTATGTGCAGATTATTTTCAGAGGGTATATAGAATTCAGGCAGCTGTTTCGTTGTAGCACATTAAAAATATTTTCCCACTTCCTCCTTGCTTCTGTTGTTGCTTTTGAGTGTTACCTCTGAGTCTGCCTGTGCTCCCTGGAAACGGCCCGGGTTTCCCACCCCCTGCCCAGGTTTGCTCCTTCCCTGGTTTTTCTGTCATTATCACGCTCACGTGTTTCCCTCGGTCACCCCC... | CCCCATCGGGGTTCACATTCCCTCTCCCTAGAGCACACTCCCTTGGATTTCCTCGAGTGGGGTCTGCTGCGGTGAAGCTTTCCCATTTTATGTGCAGATTATTTTCAGAGGGTATATAGAATTCAGGCAGCTGTTTCGTTGTAGCACATTAAAAATATTTTCCCACTTCCTCCTTGCTTCTGTTGTTGCTTTTGAGTGTTACCTCTGAGTCTGCCTGTGCTCCCTGGAAACGGCCCGGGTTTCCCACCCCCTGCCCAGGTTTGCTCCTTCCCTGGTTTTTCTGTCATTATCACGCTCACGTGTTTCCCTCGGTCACCCCC... |
Task1_train_45843 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | ACTTCCTCCTTGCTTCTGTTGTTGCTTTTGAGTGTTACCTCTGAGTCTGCCTGTGCTCCCTGGAAACGGCCCGGGTTTCCCACCCCCTGCCCAGGTTTGCTCCTTCCCTGGTTTTTCTGTCATTATCACGCTCACGTGTTTCCCTCGGTCACCCCCTCTGCAATTTTCACACGTCTTTTCCCTCTCTCTTTGCTTCATTACCTTTGGCCCGCCTGCCAGCTGCTGATTCTCTCTGAAGATGTCTCTAAATGACTTTTAACTGTGATTTGTGGAATTCTTATTGTGGAGTTTTGCGTCTTTTCAGGTGTAGGTTTTTTGTC... | ACTTCCTCCTTGCTTCTGTTGTTGCTTTTGAGTGTTACCTCTGAGTCTGCCTGTGCTCCCTGGAAACGGCCCGGGTTTCCCACCCCCTGCCCAGGTTTGCTCCTTCCCTGGTTTTTCTGTCATTATCACGCTCACGTGTTTCCCTCGGTCACCCCCTCTGCAATTTTCACACGTCTTTTCCCTCTCTCTTTGCTTCATTACCTTTGGCCCGCCTGCCAGCTGCTGATTCTCTCTGAAGATGTCTCTAAATGACTTTTAACTGTGATTTGTGGAATTCTTATTGTGGAGTTTTGCGTCTTTTCAGGTGTAGGTTTTTTGTC... |
Task1_train_45844 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCTTATCTCAATCTATCTCCCCTGAAGTGGCCTGAATTAATACTACCTGTATGATCCCCAAAACTCCTAAAGTGGAAAATTTGATTGACTTGGCCCTGACCAGTGGTATTCCCAGACAAGGGCAGAAGATGCAAATACAAAACCTCTCTGGTAGAATGTAGGCTATAATATGAGTACATTTTTGAAAAGGGCTAGAAATGATCAAGAAGAGATTAGAAAAAAACAGAGCCCCTAGAAATGTAAGAAGTGAAATGAAAAGCTCAATGGATAGCTTAGACACAGCTGAAGAGAGAATTAGAAAACTGGAAGATCTGAAAACA... | TCTTATCTCAATCTATCTCCCCTGAAGTGGCCTGAATTAATACTACCTGTATGATCCCCAAAACTCCTAAAGTGGAAAATTTGATTGACTTGGCCCTGACCAGTGGTATTCCCAGACAAGGGCAGAAGATGCAAATACAAAACCTCTCTGGTAGAATGTAGGCTATAATATGAGTACATTTTTGAAAAGGGCTAGAAATGATCAAGAAGAGATTAGAAAAAAACAGAGCCCCTAGAAATGTAAGAAGTGAAATGAAAAGCTCAATGGATAGCTTAGACACAGCTGAAGAGAGAATTAGAAAACTGGAAGATCTGAAAACA... |
Task1_train_45845 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGCAGTGCTGTCAGAGGTGACCAGAGCCCGCTCCCTCGACCTTCAGGACTCCCCGAGAGGGAGGCAACGTGTCAGGACGGTGTATGTGGAGAGAGGGTCGAGGCTCGGTGCCTGAGCACGGGCAGGAGGACAGTGGCCTCGATGCCAGAGACGGGAGGGAGAGACGTGACGATGAGGCTGCATAAGAAGAGAGCTGACTGTAGCTGAGTGTATCAGCCACTCACCGAGTCCAGTTTCCACACAGCACGATCATCGTGCCCTTGCCCACACACGTGTTAGATGAGCTTGTGTGAGCTTTATGGGCTGTAATTTGTGAGTCT... | GGCAGTGCTGTCAGAGGTGACCAGAGCCCGCTCCCTCGACCTTCAGGACTCCCCGAGAGGGAGGCAACGTGTCAGGACGGTGTATGTGGAGAGAGGGTCGAGGCTCGGTGCCTGAGCACGGGCAGGAGGACAGTGGCCTCGATGCCAGAGACGGGAGGGAGAGACGTGACGATGAGGCTGCATAAGAAGAGAGCTGACTGTAGCTGAGTGTATCAGCCACTCACCGAGTCCAGTTTCCACACAGCACGATCATCGTGCCCTTGCCCACACACGTGTTAGATGAGCTTGTGTGAGCTTTATGGGCTGTAATTTGTGAGTCT... |
Task1_train_45846 | Mutation context: Chromosome 18. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CAGGGGACCTGGGGTAGAGCCTGTTCATCTGCCCACCCCCAGGCTATGCTGGCTTCATCTTATCTGTGCGATAGGGCTGGGGGTGGGGGTGGGAATTACCAGGAGACCATCACACAGGCCGTGGACAAGTTCTACAAGAGCCAGGGAGAAGAACACTGTCCGTGCATGCGTCCCAGCACCCAGCTCACACATCTCTCATTTGACAGCTTCCCCAAAGCAGGCTTTGCAGTCCAGGCTCCCCAAGAAGCCAGGGGAGGAGACTCTGCCAGGCTGAAGGGTCTGTCCCCAAAGGTGCCACCCTCACCAGGCTCATCCTGACA... | CAGGGGACCTGGGGTAGAGCCTGTTCATCTGCCCACCCCCAGGCTATGCTGGCTTCATCTTATCTGTGCGATAGGGCTGGGGGTGGGGGTGGGAATTACCAGGAGACCATCACACAGGCCGTGGACAAGTTCTACAAGAGCCAGGGAGAAGAACACTGTCCGTGCATGCGTCCCAGCACCCAGCTCACACATCTCTCATTTGACAGCTTCCCCAAAGCAGGCTTTGCAGTCCAGGCTCCCCAAGAAGCCAGGGGAGGAGACTCTGCCAGGCTGAAGGGTCTGTCCCCAAAGGTGCCACCCTCACCAGGCTCATCCTGACA... |
Task1_train_45847 | A variant was discovered on Chromosome 18. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCTGAAGTTTTGGAGTGGGGGACAGGGAGAGAGCAGACAGTACTCATTAGCCACCTTTCCAGAGAGCATCAGCCCTCCAGACTGGGGCAGGTCAGACCTCCACTCAGGCATTTTTCTCACTGGTTGCCAGTTGGGGGAAGCAGTATTTGTGAGCACCTGCCTGTCTCCCCAGGTCCTGTTCAGAAACCCCATCTGTGCCTTTGGAGGGACTGCCCTGCGCACACAGGCCCAGCAACCACCATCTACGGCCCCCAGGACCTAATCCCCTTCTACTTGGGATTCAGTGCATGTTAGCAGACACTGGGCTTGATTCCTGCCTA... | CCTGAAGTTTTGGAGTGGGGGACAGGGAGAGAGCAGACAGTACTCATTAGCCACCTTTCCAGAGAGCATCAGCCCTCCAGACTGGGGCAGGTCAGACCTCCACTCAGGCATTTTTCTCACTGGTTGCCAGTTGGGGGAAGCAGTATTTGTGAGCACCTGCCTGTCTCCCCAGGTCCTGTTCAGAAACCCCATCTGTGCCTTTGGAGGGACTGCCCTGCGCACACAGGCCCAGCAACCACCATCTACGGCCCCCAGGACCTAATCCCCTTCTACTTGGGATTCAGTGCATGTTAGCAGACACTGGGCTTGATTCCTGCCTA... |
Task1_train_45848 | A mutation located on Chromosome 18 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GGGGACAGGGAGAGAGCAGACAGTACTCATTAGCCACCTTTCCAGAGAGCATCAGCCCTCCAGACTGGGGCAGGTCAGACCTCCACTCAGGCATTTTTCTCACTGGTTGCCAGTTGGGGGAAGCAGTATTTGTGAGCACCTGCCTGTCTCCCCAGGTCCTGTTCAGAAACCCCATCTGTGCCTTTGGAGGGACTGCCCTGCGCACACAGGCCCAGCAACCACCATCTACGGCCCCCAGGACCTAATCCCCTTCTACTTGGGATTCAGTGCATGTTAGCAGACACTGGGCTTGATTCCTGCCTAGTCCCTGCCAGATATCC... | GGGGACAGGGAGAGAGCAGACAGTACTCATTAGCCACCTTTCCAGAGAGCATCAGCCCTCCAGACTGGGGCAGGTCAGACCTCCACTCAGGCATTTTTCTCACTGGTTGCCAGTTGGGGGAAGCAGTATTTGTGAGCACCTGCCTGTCTCCCCAGGTCCTGTTCAGAAACCCCATCTGTGCCTTTGGAGGGACTGCCCTGCGCACACAGGCCCAGCAACCACCATCTACGGCCCCCAGGACCTAATCCCCTTCTACTTGGGATTCAGTGCATGTTAGCAGACACTGGGCTTGATTCCTGCCTAGTCCCTGCCAGATATCC... |
Task1_train_45849 | Here is a genetic alteration on Chromosome 18. Based on the data, is it a benign variant or a cause of disease? | Benign | TTGCCAGTTGGGGGAAGCAGTATTTGTGAGCACCTGCCTGTCTCCCCAGGTCCTGTTCAGAAACCCCATCTGTGCCTTTGGAGGGACTGCCCTGCGCACACAGGCCCAGCAACCACCATCTACGGCCCCCAGGACCTAATCCCCTTCTACTTGGGATTCAGTGCATGTTAGCAGACACTGGGCTTGATTCCTGCCTAGTCCCTGCCAGATATCCCATGCCCACCTCATTAAGAGAATGAGGCCACACAAACACACCCAGGCCATCGTGATGATGGAGTGCCTGGGGTCCCACTTGCCCACCCTTCATTGCTGGTTCAGAG... | TTGCCAGTTGGGGGAAGCAGTATTTGTGAGCACCTGCCTGTCTCCCCAGGTCCTGTTCAGAAACCCCATCTGTGCCTTTGGAGGGACTGCCCTGCGCACACAGGCCCAGCAACCACCATCTACGGCCCCCAGGACCTAATCCCCTTCTACTTGGGATTCAGTGCATGTTAGCAGACACTGGGCTTGATTCCTGCCTAGTCCCTGCCAGATATCCCATGCCCACCTCATTAAGAGAATGAGGCCACACAAACACACCCAGGCCATCGTGATGATGGAGTGCCTGGGGTCCCACTTGCCCACCCTTCATTGCTGGTTCAGAG... |
Task1_train_45850 | A variant has been detected on Chromosome 18. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GGCTTGCCTTCAGCAACAGGTTTTCCACCACATCACTGCCCAAGGCCCAGGGCATCACCAAGTTCATGTGAAGCCTGCCTGCCATGTCCACAGCCCATACCGACCCCTCCTGGAGCCACTGGAATGCTTGTTCCTGGGCATGTGATGAACCCAGACAGCTTCCGCCTTGCAGGACAACTATGCGCATCTGGCAGCAGTAGCCAGAGGGCCCATAGAAAGAAGATGGAGGCAAAACCAGATGCTGTGAGAATACTTTATTAGTCAAAACCGCATACTATAAAAATGCTTTAAAACGCAGCAGGAGATGTGAAGACACAAAT... | GGCTTGCCTTCAGCAACAGGTTTTCCACCACATCACTGCCCAAGGCCCAGGGCATCACCAAGTTCATGTGAAGCCTGCCTGCCATGTCCACAGCCCATACCGACCCCTCCTGGAGCCACTGGAATGCTTGTTCCTGGGCATGTGATGAACCCAGACAGCTTCCGCCTTGCAGGACAACTATGCGCATCTGGCAGCAGTAGCCAGAGGGCCCATAGAAAGAAGATGGAGGCAAAACCAGATGCTGTGAGAATACTTTATTAGTCAAAACCGCATACTATAAAAATGCTTTAAAACGCAGCAGGAGATGTGAAGACACAAAT... |
Task1_train_45851 | This mutation is located on Chromosome 18. Is it associated with a disease or is it a benign polymorphism? | Benign | GTTTGACTTAAACCATAACATTCTTTAATTCTGACCACCCCTTCTTGTCTTACATGTCACTTTTATCAAGTTTACCTTTTAAAATAACCCTAAATAATAATTATTACTATTTTATAACAGTGAATTCTTGATAAGATTTATTCAGATTTCTTCATGTTTACCAAAGTGTCTACACAGTAATCCTTTCTGCAATTTACTCCTTTCTGGGTTCAGTTTCCTTAAGACAGCTTTTTTACTGGGGACTGTTGATAATTTCTCATAGTTTTAGTCAATCACTCAACCACAACTGTTTAACTTGTTACAGAATTTTTTAGTTGAAA... | GTTTGACTTAAACCATAACATTCTTTAATTCTGACCACCCCTTCTTGTCTTACATGTCACTTTTATCAAGTTTACCTTTTAAAATAACCCTAAATAATAATTATTACTATTTTATAACAGTGAATTCTTGATAAGATTTATTCAGATTTCTTCATGTTTACCAAAGTGTCTACACAGTAATCCTTTCTGCAATTTACTCCTTTCTGGGTTCAGTTTCCTTAAGACAGCTTTTTTACTGGGGACTGTTGATAATTTCTCATAGTTTTAGTCAATCACTCAACCACAACTGTTTAACTTGTTACAGAATTTTTTAGTTGAAA... |
Task1_train_45852 | A mutation found on Chromosome 18 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTCTGTCCCCACAGGTGCCTGGTGGCAGCCCTCAAGCTTCTCTGCATTATAATTATTTCAACAGCCACCAGAAGGAGCCACACATCTCCAGGCTTGATAGGCAATATCTTCCAGGAAGAATCATGAAGATACAATTCCAATGCCACGAATGCTTCTAGCCACTGGATGAAACCCAAATCTCTGTAATGTTGCCTCCCATGTTTACGTGACTAGGAATTCGTGATATCTCTGAATCCCCAACAAGCCTGCAATTTCCAGATGTAAACTATCCTTAAATTATAGTTTTCCCCAACCAAGTATGTGGCAGGCATACCTGTTCC... | CTCTGTCCCCACAGGTGCCTGGTGGCAGCCCTCAAGCTTCTCTGCATTATAATTATTTCAACAGCCACCAGAAGGAGCCACACATCTCCAGGCTTGATAGGCAATATCTTCCAGGAAGAATCATGAAGATACAATTCCAATGCCACGAATGCTTCTAGCCACTGGATGAAACCCAAATCTCTGTAATGTTGCCTCCCATGTTTACGTGACTAGGAATTCGTGATATCTCTGAATCCCCAACAAGCCTGCAATTTCCAGATGTAAACTATCCTTAAATTATAGTTTTCCCCAACCAAGTATGTGGCAGGCATACCTGTTCC... |
Task1_train_45853 | The following genetic variant occurs on Chromosome 18. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TTCCAGATGTAAACTATCCTTAAATTATAGTTTTCCCCAACCAAGTATGTGGCAGGCATACCTGTTCCTCTCTAGTGTTTATGAAAACAAGATGTGAAGACTTGTCTTCACAGAAAAGCTTTGCATCCTCAAAAATTTCTTTCTCAACTGAAAAATAGTAGCATTTGTCTGTGAAGTTCTTCCAGTGAGGCGGGCAGCCTAGGAATGCAAAAGTGGAAAACATTGATTAAAAGATCACAGAAAGCACTCTGCCTTTCTTCAGCTGTGTTTCAGAGGCCAAAACTGTGGTCCCGCTGGGAGCAGCCTGAGCGTCCCTGCAC... | TTCCAGATGTAAACTATCCTTAAATTATAGTTTTCCCCAACCAAGTATGTGGCAGGCATACCTGTTCCTCTCTAGTGTTTATGAAAACAAGATGTGAAGACTTGTCTTCACAGAAAAGCTTTGCATCCTCAAAAATTTCTTTCTCAACTGAAAAATAGTAGCATTTGTCTGTGAAGTTCTTCCAGTGAGGCGGGCAGCCTAGGAATGCAAAAGTGGAAAACATTGATTAAAAGATCACAGAAAGCACTCTGCCTTTCTTCAGCTGTGTTTCAGAGGCCAAAACTGTGGTCCCGCTGGGAGCAGCCTGAGCGTCCCTGCAC... |
Task1_train_45854 | Given this context: Chromosome 18 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CTTCACAGAAAAGCTTTGCATCCTCAAAAATTTCTTTCTCAACTGAAAAATAGTAGCATTTGTCTGTGAAGTTCTTCCAGTGAGGCGGGCAGCCTAGGAATGCAAAAGTGGAAAACATTGATTAAAAGATCACAGAAAGCACTCTGCCTTTCTTCAGCTGTGTTTCAGAGGCCAAAACTGTGGTCCCGCTGGGAGCAGCCTGAGCGTCCCTGCACGAGGCCCACAGCTGACGTTCACGGACGTGCTCGCAGCAAGCATGACCCAAAGTGGACTGCAGAGCACAAGCCAAAACCACATAATCTGGAAAAGATCTTTGACTG... | CTTCACAGAAAAGCTTTGCATCCTCAAAAATTTCTTTCTCAACTGAAAAATAGTAGCATTTGTCTGTGAAGTTCTTCCAGTGAGGCGGGCAGCCTAGGAATGCAAAAGTGGAAAACATTGATTAAAAGATCACAGAAAGCACTCTGCCTTTCTTCAGCTGTGTTTCAGAGGCCAAAACTGTGGTCCCGCTGGGAGCAGCCTGAGCGTCCCTGCACGAGGCCCACAGCTGACGTTCACGGACGTGCTCGCAGCAAGCATGACCCAAAGTGGACTGCAGAGCACAAGCCAAAACCACATAATCTGGAAAAGATCTTTGACTG... |
Task1_train_45855 | This alteration occurs on Chromosome 18. Is it associated with a disease or is it a benign variant? | Benign | ACTGTTTTGTTTTGTTGTTGTTTGTTTTTTTGGGGACAGAATCTCACTCTGTTGCCTAGGGTGGAGTGCAGGGGCACAATATCTGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCCCGTGCCTCATACTCCCAAGTAGCTGGGATTACAGTTGTGCGCAGCAACTCTCAGCTAATTTTCGTATTTTTCATAGAGACAGGGTTTCACCTTGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCTCCCGCCTTGGCCTCCCAAATTACTGGGATTACAGGTGTGACCCACTGCACCCAGCCATAAAA... | ACTGTTTTGTTTTGTTGTTGTTTGTTTTTTTGGGGACAGAATCTCACTCTGTTGCCTAGGGTGGAGTGCAGGGGCACAATATCTGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCCCGTGCCTCATACTCCCAAGTAGCTGGGATTACAGTTGTGCGCAGCAACTCTCAGCTAATTTTCGTATTTTTCATAGAGACAGGGTTTCACCTTGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCTCCCGCCTTGGCCTCCCAAATTACTGGGATTACAGGTGTGACCCACTGCACCCAGCCATAAAA... |
Task1_train_45856 | This mutation on Chromosome 18 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GCCCTGTGCCACCTATTACAGCTCACCTGCACCTTTGCATCTTTCAGAAAGGAGCACCTACAAGATAACCCACCCCCCACCTTTTTTTTTTTTTTTTTTAGTAGTACAGATTGCCTCTCATAGCATAATTGGGCTTCATTATTATCCTTAAAGACCCTCTTTCTGTGGCAGATTGGGATGGATAAAATAAAGAAGATCGAGAGGTTGAAGAACCCATCCTGTTTTGCCAGTGAGAAGGGGATAGAATTAAAAGGATTAGGAGGGCTCAGGCATGGTGGCTCCAGCGTGTCATCCCAGCTACTCAGGAGGCTGAGGCGGGA... | GCCCTGTGCCACCTATTACAGCTCACCTGCACCTTTGCATCTTTCAGAAAGGAGCACCTACAAGATAACCCACCCCCCACCTTTTTTTTTTTTTTTTTTAGTAGTACAGATTGCCTCTCATAGCATAATTGGGCTTCATTATTATCCTTAAAGACCCTCTTTCTGTGGCAGATTGGGATGGATAAAATAAAGAAGATCGAGAGGTTGAAGAACCCATCCTGTTTTGCCAGTGAGAAGGGGATAGAATTAAAAGGATTAGGAGGGCTCAGGCATGGTGGCTCCAGCGTGTCATCCCAGCTACTCAGGAGGCTGAGGCGGGA... |
Task1_train_45857 | A variant on Chromosome 18 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TATTCATTCAAATCTTTTTTTTTTTTTTCCCCATACGGCTCTGTCACCCAGACTGGAGTGCAGTGGCGCTTTCTCAGCTACTGCAAGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTACCTCAGCCTCCTGAGTACCTGGGGTTACAGGCGTGTGCCACCTCGCCCCACTAATTTTTGTATTTTCAGTAGAGAGGGTTTCACTATGTTGGCCAGGATGGTCTCAATCTCCTGACCTCGTGATCTGCCCGCCTCGACCTCCCAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCAGCCCTCTATTGATTCCAGA... | TATTCATTCAAATCTTTTTTTTTTTTTTCCCCATACGGCTCTGTCACCCAGACTGGAGTGCAGTGGCGCTTTCTCAGCTACTGCAAGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTACCTCAGCCTCCTGAGTACCTGGGGTTACAGGCGTGTGCCACCTCGCCCCACTAATTTTTGTATTTTCAGTAGAGAGGGTTTCACTATGTTGGCCAGGATGGTCTCAATCTCCTGACCTCGTGATCTGCCCGCCTCGACCTCCCAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCAGCCCTCTATTGATTCCAGA... |
Task1_train_45858 | This variant is found on Chromosome 18. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CACAAAATGAATGGCTTTGCATTTGCTTGTGTACTTTCAGAACGAGGGCTTGGATCCAAAATAATTTTTTTGTTGTTTTTTGAGACGGACTCTTGTTCTGTCACCCAGGTTGGAGGGCAGTGGCGTGATCTCGGCTCATTGCAACCCCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGACTACAGATACGCATTACCACGCCCAGATAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTTTTGAACTTCTGACCTCAGGTGATCCACCCACCTCAGCC... | CACAAAATGAATGGCTTTGCATTTGCTTGTGTACTTTCAGAACGAGGGCTTGGATCCAAAATAATTTTTTTGTTGTTTTTTGAGACGGACTCTTGTTCTGTCACCCAGGTTGGAGGGCAGTGGCGTGATCTCGGCTCATTGCAACCCCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGACTACAGATACGCATTACCACGCCCAGATAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTTTTGAACTTCTGACCTCAGGTGATCCACCCACCTCAGCC... |
Task1_train_45859 | A genomic variant on Chromosome 18 is under review. What is the biological outcome — benign or pathogenic? | Benign | AGCCGAGGGTCTGGCAGGCTCCGCGACTGCTCGGACGCCTCCCCCAGCCCTAGGCAGCTCAGGGTCCCGGGTAGAGCCAGTGAGCTTCTGGCCGCTGGAGAACCCCCCCTCCCCCAACCCGGCCCACAGGATGGGGGCAGGGCACGGCCCCTAGCTTGGTTTCTTTTACCTATTCTTGGGACGAGTTAGGAGAACTTCAGCTCTGGAGCCTGGCCGGGGGTTGAGCGTGAAGCTCCCTCGGACTTTGCTTTGTTACTGCTTGTTCTGGACTATCCGGGTGGGGTCTCTCTCTCTCCTCCACCCTTTCTTTTCATTTCATT... | AGCCGAGGGTCTGGCAGGCTCCGCGACTGCTCGGACGCCTCCCCCAGCCCTAGGCAGCTCAGGGTCCCGGGTAGAGCCAGTGAGCTTCTGGCCGCTGGAGAACCCCCCCTCCCCCAACCCGGCCCACAGGATGGGGGCAGGGCACGGCCCCTAGCTTGGTTTCTTTTACCTATTCTTGGGACGAGTTAGGAGAACTTCAGCTCTGGAGCCTGGCCGGGGGTTGAGCGTGAAGCTCCCTCGGACTTTGCTTTGTTACTGCTTGTTCTGGACTATCCGGGTGGGGTCTCTCTCTCTCCTCCACCCTTTCTTTTCATTTCATT... |
Task1_train_45860 | This is a variant located on Chromosome 18. Is this mutation a likely cause of disease or not? | Benign | CCTATCTGAAAACAAAGATACAATTTCAGAAAATACCTTCTCTATGTGATCACTTTAAAAACTAAACATGTTCTTCAAAACTCAAGTGATTTCACTACGGACACGAATATAATGGAATGCACCAAAGGGATCTGTATATAGCATTTATTCAAACAGAGTAATTTATCATTAAATATTAGATGTTTCCTTTACCTCTAGAATTGTATCATAATGTTACCTATTGCAATTGTTGCAGAGACTATCTGCAGATGACTACAGCTCAGTAAGCTGAACACTAATGATCTGTGAATTCCCTATGCGTCTTGGCAGCCATATTAATA... | CCTATCTGAAAACAAAGATACAATTTCAGAAAATACCTTCTCTATGTGATCACTTTAAAAACTAAACATGTTCTTCAAAACTCAAGTGATTTCACTACGGACACGAATATAATGGAATGCACCAAAGGGATCTGTATATAGCATTTATTCAAACAGAGTAATTTATCATTAAATATTAGATGTTTCCTTTACCTCTAGAATTGTATCATAATGTTACCTATTGCAATTGTTGCAGAGACTATCTGCAGATGACTACAGCTCAGTAAGCTGAACACTAATGATCTGTGAATTCCCTATGCGTCTTGGCAGCCATATTAATA... |
Task1_train_45861 | Consider this mutation on Chromosome 18. Is this a benign change or a disease-causing variant? | Benign | TGTATCATAATGTTACCTATTGCAATTGTTGCAGAGACTATCTGCAGATGACTACAGCTCAGTAAGCTGAACACTAATGATCTGTGAATTCCCTATGCGTCTTGGCAGCCATATTAATATAGTTCTAAGAAATCTAGGTCTTTTTTTTACTTTTTATTTTAAAATAATTTCAGCCTTTACAACTGACTTATTGGCCATAATAAAACTTCCCCAATTATTTACTAATGTACTTTTTCTGACCCAGGATCAAAGCCAGGATCAAACATTGCATTTAGCTGCCATCCCTCCTAACTCTCCTCCAACCTGGAAAAGTTCCTCGG... | TGTATCATAATGTTACCTATTGCAATTGTTGCAGAGACTATCTGCAGATGACTACAGCTCAGTAAGCTGAACACTAATGATCTGTGAATTCCCTATGCGTCTTGGCAGCCATATTAATATAGTTCTAAGAAATCTAGGTCTTTTTTTTACTTTTTATTTTAAAATAATTTCAGCCTTTACAACTGACTTATTGGCCATAATAAAACTTCCCCAATTATTTACTAATGTACTTTTTCTGACCCAGGATCAAAGCCAGGATCAAACATTGCATTTAGCTGCCATCCCTCCTAACTCTCCTCCAACCTGGAAAAGTTCCTCGG... |
Task1_train_45862 | Located on Chromosome 18, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TAAATGGTTAAAATTTTAGTTTACATCTGCTGTAGACAGTGTAGCTAACACATTCAGACCACTATTTCATTGTTACAAGTAAATAGTTGATTGAAAATTCTATACCTAGCTTTCAGACACGGTGGAGTCATCGCATTTTAAAATAAGGAGTGGCCAGGCATGGTGGCCATGCCTGTAATCCCAGCGCTTTGGGAGGCTTTGCTTGAGTCCAGGAGTTCAAGACCAGCCTGGGCAACGTGACAAGACCCTGACTCCACATTTTTTTAATTAGCCAGGCAGGCATGCAGACCAGGTGCAGTGGCTCACACCTGTAATCCCAG... | TAAATGGTTAAAATTTTAGTTTACATCTGCTGTAGACAGTGTAGCTAACACATTCAGACCACTATTTCATTGTTACAAGTAAATAGTTGATTGAAAATTCTATACCTAGCTTTCAGACACGGTGGAGTCATCGCATTTTAAAATAAGGAGTGGCCAGGCATGGTGGCCATGCCTGTAATCCCAGCGCTTTGGGAGGCTTTGCTTGAGTCCAGGAGTTCAAGACCAGCCTGGGCAACGTGACAAGACCCTGACTCCACATTTTTTTAATTAGCCAGGCAGGCATGCAGACCAGGTGCAGTGGCTCACACCTGTAATCCCAG... |
Task1_train_45863 | A variant on Chromosome 18 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GTTACCAAATAACCACATATCCCAAAGGCAGACAGTCTTCACAGTGTACTTTTACCTCATTGAAGTTGAAGCTGTTCCTTTACAATATTTTTCCACTTCAATGTGAAGTAGACTGTTAAGGTTTCATTAGGGGTTTAATTATGTGTCCTTTTAAAGAAAAAATGGTTTTGACAATTCTTCCACAATTCACAGTTCTCAGACAATAACTTTTTTTGTAAATCATATAGTCCAACTATGTTTTGAATAACCAGATGCTCTTTAGTAGACGAAATCTCTCAATGCAACTGTAATAAATAAGCATCTGTATCCTGATTCTTATT... | GTTACCAAATAACCACATATCCCAAAGGCAGACAGTCTTCACAGTGTACTTTTACCTCATTGAAGTTGAAGCTGTTCCTTTACAATATTTTTCCACTTCAATGTGAAGTAGACTGTTAAGGTTTCATTAGGGGTTTAATTATGTGTCCTTTTAAAGAAAAAATGGTTTTGACAATTCTTCCACAATTCACAGTTCTCAGACAATAACTTTTTTTGTAAATCATATAGTCCAACTATGTTTTGAATAACCAGATGCTCTTTAGTAGACGAAATCTCTCAATGCAACTGTAATAAATAAGCATCTGTATCCTGATTCTTATT... |
Task1_train_45864 | A variant has been detected on Chromosome 18. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTGGCTACAGAGCAAGATGCTGTCTCAAAAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAATAAATTTGGCAATCCGAAAAACCAACTTTCACTCTAGGTATATTTGCCCTAAAAAAAATATTTACACTATATG... | CTGGCTACAGAGCAAGATGCTGTCTCAAAAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAATAAATTTGGCAATCCGAAAAACCAACTTTCACTCTAGGTATATTTGCCCTAAAAAAAATATTTACACTATATG... |
Task1_train_45865 | This alteration occurs on Chromosome 18. Is it associated with a disease or is it a benign variant? | Benign | TGATAGTTACCAAGGTTTTTTTCTTTGTAATAAAGAAGTTCTGTAAAATTATTATTAAGCCTTTTTCTCTTCGTAAATCTTAATACTGAAGCTTTTTTTTTTTTTAAAAACTAAATATTAGGTCAAGACAATCAAGACACTTCCCCTCTTTTATGGAAGCATAGTAAGATTTTTTCTTTATGGCGATCATGATGGAGAAGTATATGCTACAGGAGGAGAGGTTCAAATTGCAATGGTAAGACAGCAAGTGATAAAACATACTGAAAGTTTCTTGATAACACTTTTGCATAATTGTTAAGATACAGTATATTTCGCTAGTG... | TGATAGTTACCAAGGTTTTTTTCTTTGTAATAAAGAAGTTCTGTAAAATTATTATTAAGCCTTTTTCTCTTCGTAAATCTTAATACTGAAGCTTTTTTTTTTTTTAAAAACTAAATATTAGGTCAAGACAATCAAGACACTTCCCCTCTTTTATGGAAGCATAGTAAGATTTTTTCTTTATGGCGATCATGATGGAGAAGTATATGCTACAGGAGGAGAGGTTCAAATTGCAATGGTAAGACAGCAAGTGATAAAACATACTGAAAGTTTCTTGATAACACTTTTGCATAATTGTTAAGATACAGTATATTTCGCTAGTG... |
Task1_train_45866 | Consider this mutation on Chromosome 18. Is this a benign change or a disease-causing variant? | Benign | GGCTGCGTCCAAGAATTGTTTTCTTGCAGTCCAGCCATGATGACTGTGTGTCTCCCAGAACTGAGTGCAGACTTACTTGGTCCATGGGGACTTGTTGAGGGGCCTGCTTTGTGCTAGAAGGAACCTATTCCTGACCTCCCCCTCCCTGTTTTCTTTTCTCCCATCCTTGCCTTTGGGACTTTTACCTCCCTGACCTGGTTCCGCTCTGGGTGACACAGGCCCTTGCACAAGGAACTGAGATTTCATGGCCTCTGTGAACCTTGGGATTTTATGATCAAGTCCCAGATGAGACATAAAACCCAAGGCAGCGTAGGCTAGAA... | GGCTGCGTCCAAGAATTGTTTTCTTGCAGTCCAGCCATGATGACTGTGTGTCTCCCAGAACTGAGTGCAGACTTACTTGGTCCATGGGGACTTGTTGAGGGGCCTGCTTTGTGCTAGAAGGAACCTATTCCTGACCTCCCCCTCCCTGTTTTCTTTTCTCCCATCCTTGCCTTTGGGACTTTTACCTCCCTGACCTGGTTCCGCTCTGGGTGACACAGGCCCTTGCACAAGGAACTGAGATTTCATGGCCTCTGTGAACCTTGGGATTTTATGATCAAGTCCCAGATGAGACATAAAACCCAAGGCAGCGTAGGCTAGAA... |
Task1_train_45867 | Chromosome 18 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGAACTGAGTGCAGACTTACTTGGTCCATGGGGACTTGTTGAGGGGCCTGCTTTGTGCTAGAAGGAACCTATTCCTGACCTCCCCCTCCCTGTTTTCTTTTCTCCCATCCTTGCCTTTGGGACTTTTACCTCCCTGACCTGGTTCCGCTCTGGGTGACACAGGCCCTTGCACAAGGAACTGAGATTTCATGGCCTCTGTGAACCTTGGGATTTTATGATCAAGTCCCAGATGAGACATAAAACCCAAGGCAGCGTAGGCTAGAACGTGGGAAGCAGGCGAGCTCTGGCTTGGTCAGGGAGAGCCAGGGCCAGGTCCTGGC... | AGAACTGAGTGCAGACTTACTTGGTCCATGGGGACTTGTTGAGGGGCCTGCTTTGTGCTAGAAGGAACCTATTCCTGACCTCCCCCTCCCTGTTTTCTTTTCTCCCATCCTTGCCTTTGGGACTTTTACCTCCCTGACCTGGTTCCGCTCTGGGTGACACAGGCCCTTGCACAAGGAACTGAGATTTCATGGCCTCTGTGAACCTTGGGATTTTATGATCAAGTCCCAGATGAGACATAAAACCCAAGGCAGCGTAGGCTAGAACGTGGGAAGCAGGCGAGCTCTGGCTTGGTCAGGGAGAGCCAGGGCCAGGTCCTGGC... |
Task1_train_45868 | A variant on Chromosome 18 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GGGGTGGTGTCAGAGTAGAGACAGGAGAAGGAAGTGAGCATTTGTGGGATACCCACCACGTGCCAGGGACTGAACCCTATCTGGATCTCCTGCAGCCCTCCCAATGGCACTGTGAAGCCAGTGTTGTTTTACAGATGAGGAAACTGAGATTTGTGGCTATAACAGATAAACAGATGACCCTGAATGGGGCAGGTCATGTCATCTGCCATAGATACATGCATAGAACAATGCAAACCAGTCAGTCCCCTCTGAGTCAGACCAGGCTGACCATCAGGGACATGCAGACACTGGCAGGGCTGGGGTTGTTCCCCATCGGTGAT... | GGGGTGGTGTCAGAGTAGAGACAGGAGAAGGAAGTGAGCATTTGTGGGATACCCACCACGTGCCAGGGACTGAACCCTATCTGGATCTCCTGCAGCCCTCCCAATGGCACTGTGAAGCCAGTGTTGTTTTACAGATGAGGAAACTGAGATTTGTGGCTATAACAGATAAACAGATGACCCTGAATGGGGCAGGTCATGTCATCTGCCATAGATACATGCATAGAACAATGCAAACCAGTCAGTCCCCTCTGAGTCAGACCAGGCTGACCATCAGGGACATGCAGACACTGGCAGGGCTGGGGTTGTTCCCCATCGGTGAT... |
Task1_train_45869 | Consider a variant on Chromosome 18. Determine its clinical classification and disease relevance. | Benign | CCTTAAAGGCTGTGGAGAGAGATTCAGAGCCAAAACTTTAGCATAAAAATTCTCAATGTAAGGTTAAATCTCAAATTCTTAGCTCTCAAAAATTCCCTTTCTGGTTGAAAGGAAATGGAAACAAGGTGAATTTGTCGACCCACTGATAATGAGTATTCTTTGAGGAAATAGTTCAATTTTATCAGGTTTTAAAAGATCCCTGCTTATTTTGATTTTTTTTCCCTTGAATTCTTTGTCACAATCGCCATATTTACATTCTAGAGAAAGGGCCACAAGAGATTTCTAGGAAGGTTCTTGGCTTTGGGATTCTCTTTCTTCTT... | CCTTAAAGGCTGTGGAGAGAGATTCAGAGCCAAAACTTTAGCATAAAAATTCTCAATGTAAGGTTAAATCTCAAATTCTTAGCTCTCAAAAATTCCCTTTCTGGTTGAAAGGAAATGGAAACAAGGTGAATTTGTCGACCCACTGATAATGAGTATTCTTTGAGGAAATAGTTCAATTTTATCAGGTTTTAAAAGATCCCTGCTTATTTTGATTTTTTTTCCCTTGAATTCTTTGTCACAATCGCCATATTTACATTCTAGAGAAAGGGCCACAAGAGATTTCTAGGAAGGTTCTTGGCTTTGGGATTCTCTTTCTTCTT... |
Task1_train_45870 | Chromosome 18 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTAGAATGTAATCAACTACAGTACCTCCATGATCTTGGAATAGAGAAGGCATTTCACCACAAAGGCACAAAAATCACTAAGGACAAAGCATATGTTAGTAAATATGACTACAATGAATTTGACATTAAAATTAAAGTCAGAGAAGATGTATGCGACTTACAGACCTGCAAAGGATTTCTACTCATAACATGTAAAGAACTTTGCAAGTCAACAAGAATGCATTAGAAAAATGGGCAAAAACCTTGAACAGGCATAAAAGAGGATATCAAAATGGACTGTGTACATAGGAAAGGATGTTCAAACTCATTTGACACTCAGAT... | TTAGAATGTAATCAACTACAGTACCTCCATGATCTTGGAATAGAGAAGGCATTTCACCACAAAGGCACAAAAATCACTAAGGACAAAGCATATGTTAGTAAATATGACTACAATGAATTTGACATTAAAATTAAAGTCAGAGAAGATGTATGCGACTTACAGACCTGCAAAGGATTTCTACTCATAACATGTAAAGAACTTTGCAAGTCAACAAGAATGCATTAGAAAAATGGGCAAAAACCTTGAACAGGCATAAAAGAGGATATCAAAATGGACTGTGTACATAGGAAAGGATGTTCAAACTCATTTGACACTCAGAT... |
Task1_train_45871 | A variant was discovered on Chromosome 18. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AAAGAAAGAAGAGAAAAGAAAGAAAGGGAAAGGAAGGAAGGAAGGGAGAGAGAGAAAGAAAGAAAGAGAAAGAAGGAAGGAAAGAAAGAGGAAGATAAAGAAAAAGAAAGAAAAAAGGAAAAGAGAGAAAGAAAGAAAAAGAAAAGAAAGAAGAAAGAAAAAAAGAAAGAAAGAAAGGAAGAAAGGCACATTGAGGCCTCAGCTCACATGAGGGGTAGAGATGGGAGTTTTAGTTAAAGGGAGTTTTGTAAAAGGCAGCATTGCTTCTGATCACAAAATCCTGCCATGTTGTGTAAAGTTCATTGCTGGAAGCTGATTTT... | AAAGAAAGAAGAGAAAAGAAAGAAAGGGAAAGGAAGGAAGGAAGGGAGAGAGAGAAAGAAAGAAAGAGAAAGAAGGAAGGAAAGAAAGAGGAAGATAAAGAAAAAGAAAGAAAAAAGGAAAAGAGAGAAAGAAAGAAAAAGAAAAGAAAGAAGAAAGAAAAAAAGAAAGAAAGAAAGGAAGAAAGGCACATTGAGGCCTCAGCTCACATGAGGGGTAGAGATGGGAGTTTTAGTTAAAGGGAGTTTTGTAAAAGGCAGCATTGCTTCTGATCACAAAATCCTGCCATGTTGTGTAAAGTTCATTGCTGGAAGCTGATTTT... |
Task1_train_45872 | This alteration on Chromosome 18 may affect genome function. Does it lead to a disease or is it benign? | Benign | AAGAAAGAAAAAAGGAAAAGAGAGAAAGAAAGAAAAAGAAAAGAAAGAAGAAAGAAAAAAAGAAAGAAAGAAAGGAAGAAAGGCACATTGAGGCCTCAGCTCACATGAGGGGTAGAGATGGGAGTTTTAGTTAAAGGGAGTTTTGTAAAAGGCAGCATTGCTTCTGATCACAAAATCCTGCCATGTTGTGTAAAGTTCATTGCTGGAAGCTGATTTTTACCTAACTTTTATCATCCGTAAGAGTTATAGACATATATTTGGTATGTTGGTACATATGTTGACTAAAATGCAATACTTCATATAAAATAAAGATCCATTTG... | AAGAAAGAAAAAAGGAAAAGAGAGAAAGAAAGAAAAAGAAAAGAAAGAAGAAAGAAAAAAAGAAAGAAAGAAAGGAAGAAAGGCACATTGAGGCCTCAGCTCACATGAGGGGTAGAGATGGGAGTTTTAGTTAAAGGGAGTTTTGTAAAAGGCAGCATTGCTTCTGATCACAAAATCCTGCCATGTTGTGTAAAGTTCATTGCTGGAAGCTGATTTTTACCTAACTTTTATCATCCGTAAGAGTTATAGACATATATTTGGTATGTTGGTACATATGTTGACTAAAATGCAATACTTCATATAAAATAAAGATCCATTTG... |
Task1_train_45873 | Here is a genetic alteration on Chromosome 18. Based on the data, is it a benign variant or a cause of disease? | Benign | GTTCATTGCTGGAAGCTGATTTTTACCTAACTTTTATCATCCGTAAGAGTTATAGACATATATTTGGTATGTTGGTACATATGTTGACTAAAATGCAATACTTCATATAAAATAAAGATCCATTTGTATAATAGGATTATAGAGTATTATCATGTAGCGTATATATGCAAGACTGTTTTTTCTTCCCATGCATACAAATTCATCTCAATGCCTACCCTTCTTCACTCTTTTAAAAACCTATACAATCTTGTAGATGTCTTCATTGACTCTTGCATATGGTTGTTCTGTGTGTTTCCACTAGAGGCGAACTTAACTTGGTG... | GTTCATTGCTGGAAGCTGATTTTTACCTAACTTTTATCATCCGTAAGAGTTATAGACATATATTTGGTATGTTGGTACATATGTTGACTAAAATGCAATACTTCATATAAAATAAAGATCCATTTGTATAATAGGATTATAGAGTATTATCATGTAGCGTATATATGCAAGACTGTTTTTTCTTCCCATGCATACAAATTCATCTCAATGCCTACCCTTCTTCACTCTTTTAAAAACCTATACAATCTTGTAGATGTCTTCATTGACTCTTGCATATGGTTGTTCTGTGTGTTTCCACTAGAGGCGAACTTAACTTGGTG... |
Task1_train_45874 | A mutation located on Chromosome 18 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CATTTTTAATTCATTTAGTATTAGGCATCTTTTGACCTTACTAAAGTACCAGTAGTAGAAAAATATTTTTGTGTGATGAAACTGAAAACATCAGTGGTCGTATTTAATAAAAGGTGACTAGTACTGCCCATTTAAAGTAGGTGTCTAACTTTGAATAAATGTGGATAGCAATGAATAAGAAATGACCATGCATGGTGTTAGCAGAAAATTTTAACATGTGTTTTACCTTTAGAATACTAACTGGGTTCAGCGTAGTATGTAATTTTCCTTCCTTATATCCATGAAAAAAAATGTACGAGTGCTCCCTTTCATTTCAAACC... | CATTTTTAATTCATTTAGTATTAGGCATCTTTTGACCTTACTAAAGTACCAGTAGTAGAAAAATATTTTTGTGTGATGAAACTGAAAACATCAGTGGTCGTATTTAATAAAAGGTGACTAGTACTGCCCATTTAAAGTAGGTGTCTAACTTTGAATAAATGTGGATAGCAATGAATAAGAAATGACCATGCATGGTGTTAGCAGAAAATTTTAACATGTGTTTTACCTTTAGAATACTAACTGGGTTCAGCGTAGTATGTAATTTTCCTTCCTTATATCCATGAAAAAAAATGTACGAGTGCTCCCTTTCATTTCAAACC... |
Task1_train_45875 | This alteration occurs on Chromosome 18. Is it associated with a disease or is it a benign variant? | Benign | CCCTGGTCATGATATCTAGGGGTTTGAAAATAGCCTTGGAAGTCTCATGGTTCCAAATAATGGTAAGATCCACGTACAAAATGAGCCAAACGGCAGAGTCTAGAAAACTTTGCTTAAGATATTTCAAAGCTGTATGTGTTTTATTTATAAATAACATTTAGACACAGAGGTCAATAAGATGTTCCAAAAATTCCCAATTTTTTAGTACAGACACATCAGAGAGGAAAAATAGTATGTTTATATGTTTCTGTCACTTGACAGCAAAAACAAAGGCTGGTCATATCCAGATATCTGAGTAGACATAGTACCAGATCACTTAC... | CCCTGGTCATGATATCTAGGGGTTTGAAAATAGCCTTGGAAGTCTCATGGTTCCAAATAATGGTAAGATCCACGTACAAAATGAGCCAAACGGCAGAGTCTAGAAAACTTTGCTTAAGATATTTCAAAGCTGTATGTGTTTTATTTATAAATAACATTTAGACACAGAGGTCAATAAGATGTTCCAAAAATTCCCAATTTTTTAGTACAGACACATCAGAGAGGAAAAATAGTATGTTTATATGTTTCTGTCACTTGACAGCAAAAACAAAGGCTGGTCATATCCAGATATCTGAGTAGACATAGTACCAGATCACTTAC... |
Task1_train_45876 | A variant found on Chromosome 18 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AAATGAGAGGAGAAATACACTATACATGGGAGAGGCAGAAAATTAAACTTAGCTCCACCTTTATGCTGATCTAAATTTCCAGGCATCCTATATCAGTTTTATTTTAGTGATAAAAGTAACATTTACTACTAGTTACCTCAAAATGAGGTTTTTGTTCCAAAGTTTCTGAAATGTGGATGGCTGCACTCTGCTCCTCTTGTCGCTCACGGGAAGCAGCGGCTGTCTCTTCCTGTTCCAGGACAGCTTTAGCGACCTCCTCCCCTCCTTCCTCTTTAGCCCCCTCCGTCAAGGCAGAGCCCTCTTTCCCTTTAATGCCTGTG... | AAATGAGAGGAGAAATACACTATACATGGGAGAGGCAGAAAATTAAACTTAGCTCCACCTTTATGCTGATCTAAATTTCCAGGCATCCTATATCAGTTTTATTTTAGTGATAAAAGTAACATTTACTACTAGTTACCTCAAAATGAGGTTTTTGTTCCAAAGTTTCTGAAATGTGGATGGCTGCACTCTGCTCCTCTTGTCGCTCACGGGAAGCAGCGGCTGTCTCTTCCTGTTCCAGGACAGCTTTAGCGACCTCCTCCCCTCCTTCCTCTTTAGCCCCCTCCGTCAAGGCAGAGCCCTCTTTCCCTTTAATGCCTGTG... |
Task1_train_45877 | This variant is found on Chromosome 18. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCACACGCCGCTCCTCCACCAACACGGTCTCCTGCACCACCTTCTCAGTGCTAAGCGGCAGGTGGTGCACGGTGGGTTCCGTCTCTATTCCACTGGACTCCGTCTTGGTTTCCATTTTCTGCATGGGAAGAGATTGTGGCATCAGTGTGACCATCCATAAACCAAAGGTCAGAAAATAACTAAAGCTGCCACTCGCCAGGATGTCTAAAGCCAGCAGCAAGTGCTTATAACCAGAAACACTGACGAAAAATATAAATTAGCTTTCATTTCTCCCACTGAAATCTCTGATGCCTGCCCCTGCCCCTGGTGCATGCACTTGA... | CCACACGCCGCTCCTCCACCAACACGGTCTCCTGCACCACCTTCTCAGTGCTAAGCGGCAGGTGGTGCACGGTGGGTTCCGTCTCTATTCCACTGGACTCCGTCTTGGTTTCCATTTTCTGCATGGGAAGAGATTGTGGCATCAGTGTGACCATCCATAAACCAAAGGTCAGAAAATAACTAAAGCTGCCACTCGCCAGGATGTCTAAAGCCAGCAGCAAGTGCTTATAACCAGAAACACTGACGAAAAATATAAATTAGCTTTCATTTCTCCCACTGAAATCTCTGATGCCTGCCCCTGCCCCTGGTGCATGCACTTGA... |
Task1_train_45878 | This is a variant located on Chromosome 18. Is this mutation a likely cause of disease or not? | Benign | ATTGTGTTCTTAACTGTAATATGTTCTAGTCCAACACTATTTGATAATATTGCCAATATGAGAAATAGTGATATTAAAGCCTAGGATTTCAAGTAGTTCTCAAAATATTTTCCATGTATAAAAAGTTATTTATATATCAGTTGGAGCAAATCGTTATATATAACTCAAGAACCTTGAAAATGTCTCTTATGCAAAATCTATTAAAAGTGTAGACTTTTACTTAAAACACCTGTGAGACCATTCACATTTTTTTCCTTCTGCTGCAAAGAAATGGTCATAATTCCACTAAATATAGATACTCGCACACCCTCAACATATAA... | ATTGTGTTCTTAACTGTAATATGTTCTAGTCCAACACTATTTGATAATATTGCCAATATGAGAAATAGTGATATTAAAGCCTAGGATTTCAAGTAGTTCTCAAAATATTTTCCATGTATAAAAAGTTATTTATATATCAGTTGGAGCAAATCGTTATATATAACTCAAGAACCTTGAAAATGTCTCTTATGCAAAATCTATTAAAAGTGTAGACTTTTACTTAAAACACCTGTGAGACCATTCACATTTTTTTCCTTCTGCTGCAAAGAAATGGTCATAATTCCACTAAATATAGATACTCGCACACCCTCAACATATAA... |
Task1_train_45879 | A genetic alteration is present on Chromosome 18. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CCAAAATGAAAACACAATCTATATATTATCTTCTCTCTACTCTTTTCCATTCGTAAATATTCATGGAATCTGCACACTTCAATGCCTCACTTTTCAAGCTTAAGAGAAATGTCTCAGTCTGTTTGGGCTGCTATGACAAAATGCCACAAACTGGGTAACCTATAAACAACAGAAATTTATTTCTCACAGTTTTGGTGGATGGGAAGTCCAAGAGCAAGCGCCATCAGATTTGGTGTCTGGTGAGGGCTCATTTCCTGGTTCACAGGTGGTGCCTTCTCACTGTGTCCACATACAGTGCAAGGGGTGAGGGGGTTCCCTTG... | CCAAAATGAAAACACAATCTATATATTATCTTCTCTCTACTCTTTTCCATTCGTAAATATTCATGGAATCTGCACACTTCAATGCCTCACTTTTCAAGCTTAAGAGAAATGTCTCAGTCTGTTTGGGCTGCTATGACAAAATGCCACAAACTGGGTAACCTATAAACAACAGAAATTTATTTCTCACAGTTTTGGTGGATGGGAAGTCCAAGAGCAAGCGCCATCAGATTTGGTGTCTGGTGAGGGCTCATTTCCTGGTTCACAGGTGGTGCCTTCTCACTGTGTCCACATACAGTGCAAGGGGTGAGGGGGTTCCCTTG... |
Task1_train_45880 | Chromosome 18 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTCCAGTTTTCTCTACTCCCTGACAAAATGACCAATCATACACATTTTCTAATAGCCATATTTATTTTTTAATCTTTAATATAAATAGCGGGTTTCAATACCTTTTAAAATCTCTAGCCTCTTTAGCAGTTCTCCAATGAAAGTCATATTTCCTTACTAATTGTGCTTCTTGCTATTCTTGATTAACCAGCTCTGCACTGGAAAATTCTATGTTCCCATGTGCTAGGTCTCACACTTTGCTTCCAAGTAACTCAGATAACTCTGAAGTCACAAATTAATTCTCACAGTGTGGTAGGTGAAAATTACTATTCTCCTTACAG... | TTCCAGTTTTCTCTACTCCCTGACAAAATGACCAATCATACACATTTTCTAATAGCCATATTTATTTTTTAATCTTTAATATAAATAGCGGGTTTCAATACCTTTTAAAATCTCTAGCCTCTTTAGCAGTTCTCCAATGAAAGTCATATTTCCTTACTAATTGTGCTTCTTGCTATTCTTGATTAACCAGCTCTGCACTGGAAAATTCTATGTTCCCATGTGCTAGGTCTCACACTTTGCTTCCAAGTAACTCAGATAACTCTGAAGTCACAAATTAATTCTCACAGTGTGGTAGGTGAAAATTACTATTCTCCTTACAG... |
Task1_train_45881 | A variant on Chromosome 18 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AGATTATATCATCTACCAGAGGCCCAGAGGGATTAAGTGATTTGTCTAAGGTTATACAGATAATAGGTGGATATCCCAGATTTCAGACTAGACTTTCTTGAGCTCAAGTTCAAGGAAGGTCCATTCTTCTACACTATGCATTCAGCAATATATTACAATGGTAATAATAATTACAATAACCCCCATCTATTGAATACATCCTGTGGGCCAAGGGTTCTGGTAAACTCCACACATATAAACCCTCCTCTGACCCTGACCCTGTTCTATTCCTCTCATAGCTCCATGAGATATGTCTGGTTCTCTTCATTTTACAGAAAGAT... | AGATTATATCATCTACCAGAGGCCCAGAGGGATTAAGTGATTTGTCTAAGGTTATACAGATAATAGGTGGATATCCCAGATTTCAGACTAGACTTTCTTGAGCTCAAGTTCAAGGAAGGTCCATTCTTCTACACTATGCATTCAGCAATATATTACAATGGTAATAATAATTACAATAACCCCCATCTATTGAATACATCCTGTGGGCCAAGGGTTCTGGTAAACTCCACACATATAAACCCTCCTCTGACCCTGACCCTGTTCTATTCCTCTCATAGCTCCATGAGATATGTCTGGTTCTCTTCATTTTACAGAAAGAT... |
Task1_train_45882 | This alteration occurs on Chromosome 18. Is it associated with a disease or is it a benign variant? | Benign | TGAGCGTCTGGCCCAGCAGCCACACCAGTGTTAGGACAGGGTCCCCTGAGGCCCCGCTGATGGTGGAGGGTCCTCAGAAGGGTCTCTCCAGCTTTTGGAAGTGCCCACCTGACCGTCCTCTCATTACTCCTGGCTACTCTCCTTTGTGGAGGCTCCAGGAAAGCTTGGGAGCACAACCAAGAAATGGTTAATGGAACAAAAAGGAGAATTAATGAATCATGAAAACATGTGCTTATTATTATTATTTTTTAGAGATTCACACTTTCCTGAGTAAAGTACACAAAAATCTCACATGAAGTCTTTTGAAAGCACCAGGCCTC... | TGAGCGTCTGGCCCAGCAGCCACACCAGTGTTAGGACAGGGTCCCCTGAGGCCCCGCTGATGGTGGAGGGTCCTCAGAAGGGTCTCTCCAGCTTTTGGAAGTGCCCACCTGACCGTCCTCTCATTACTCCTGGCTACTCTCCTTTGTGGAGGCTCCAGGAAAGCTTGGGAGCACAACCAAGAAATGGTTAATGGAACAAAAAGGAGAATTAATGAATCATGAAAACATGTGCTTATTATTATTATTTTTTAGAGATTCACACTTTCCTGAGTAAAGTACACAAAAATCTCACATGAAGTCTTTTGAAAGCACCAGGCCTC... |
Task1_train_45883 | This alteration on Chromosome 18 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCCCCTGAGGCCCCGCTGATGGTGGAGGGTCCTCAGAAGGGTCTCTCCAGCTTTTGGAAGTGCCCACCTGACCGTCCTCTCATTACTCCTGGCTACTCTCCTTTGTGGAGGCTCCAGGAAAGCTTGGGAGCACAACCAAGAAATGGTTAATGGAACAAAAAGGAGAATTAATGAATCATGAAAACATGTGCTTATTATTATTATTTTTTAGAGATTCACACTTTCCTGAGTAAAGTACACAAAAATCTCACATGAAGTCTTTTGAAAGCACCAGGCCTCTAGCTCTTAGACTAGCTGTGCTCCATGGCAGATCTGAGCCA... | TCCCCTGAGGCCCCGCTGATGGTGGAGGGTCCTCAGAAGGGTCTCTCCAGCTTTTGGAAGTGCCCACCTGACCGTCCTCTCATTACTCCTGGCTACTCTCCTTTGTGGAGGCTCCAGGAAAGCTTGGGAGCACAACCAAGAAATGGTTAATGGAACAAAAAGGAGAATTAATGAATCATGAAAACATGTGCTTATTATTATTATTTTTTAGAGATTCACACTTTCCTGAGTAAAGTACACAAAAATCTCACATGAAGTCTTTTGAAAGCACCAGGCCTCTAGCTCTTAGACTAGCTGTGCTCCATGGCAGATCTGAGCCA... |
Task1_train_45884 | This variant is present on Chromosome 18. Is the change likely to result in a pathogenic outcome? | Benign | ACTTCACCAGAATCACCCTCTTGTCATGGTCACCAGACAACTCGTCTGTTTTTAGAACTGCCTGAGTTGATCTTTCCCTCCTTTGAAGAACACTTTCTTCACCTGACTTCAAGGATGCCCTAAGCTTCTGACTGTCTTCCCACTTTTCCTAGCTGCGCTGCTGGAGACCCTGTGCCCCTTATTTCTTGTCCTCTCAGCCTTTCAAGGTTGGAGAACGGTAGGGTTCAGTCCTCGGAACTCTCCTGTATTTGCACTTGCCTTCCTTGGCGAGCTCAATCCATCTCACTGCTTTAAATACACCTGTATGTGGATGCCACTGA... | ACTTCACCAGAATCACCCTCTTGTCATGGTCACCAGACAACTCGTCTGTTTTTAGAACTGCCTGAGTTGATCTTTCCCTCCTTTGAAGAACACTTTCTTCACCTGACTTCAAGGATGCCCTAAGCTTCTGACTGTCTTCCCACTTTTCCTAGCTGCGCTGCTGGAGACCCTGTGCCCCTTATTTCTTGTCCTCTCAGCCTTTCAAGGTTGGAGAACGGTAGGGTTCAGTCCTCGGAACTCTCCTGTATTTGCACTTGCCTTCCTTGGCGAGCTCAATCCATCTCACTGCTTTAAATACACCTGTATGTGGATGCCACTGA... |
Task1_train_45885 | A genomic change on Chromosome 18 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTTTAACAAAGGTTAGTCCCTATGGGAGATTTAGAGATTTCACTAAGGCCTATTTTTTTTTCGTCAAATAAGTGAAAATTCAGAAAAATCTAGAAGTGCATAAAAGATTCAGTGTCGCTTTCCAAAGGTCCATAACTTACAGCGGTGCTGCTACCGAGGTAGAAGAGAAGATTATCGGGTTCCTGTGTCTTAACATTTAGTGTTAAGGTATTGTAGTTGGTAGAGGAAATCTGAGGCTGGTAGGCCCGGATGCAATCTCTGTCTGCAGACACGGCGACTTTAATCTGTAGAAGGAAAATGAAAGTGTCCCCATCATTTAG... | TTTTAACAAAGGTTAGTCCCTATGGGAGATTTAGAGATTTCACTAAGGCCTATTTTTTTTTCGTCAAATAAGTGAAAATTCAGAAAAATCTAGAAGTGCATAAAAGATTCAGTGTCGCTTTCCAAAGGTCCATAACTTACAGCGGTGCTGCTACCGAGGTAGAAGAGAAGATTATCGGGTTCCTGTGTCTTAACATTTAGTGTTAAGGTATTGTAGTTGGTAGAGGAAATCTGAGGCTGGTAGGCCCGGATGCAATCTCTGTCTGCAGACACGGCGACTTTAATCTGTAGAAGGAAAATGAAAGTGTCCCCATCATTTAG... |
Task1_train_45886 | A genetic alteration is present on Chromosome 18. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTGTCATATTACTGATGCTGAACACAAACTGAGGCTTGTCTGTTTGCTTTTTTTTCTTTTGGGCAGTGGTCAATGAACTAAGAGCTTCTTGTTTCTAATGGCAATATTAAAGCTGCATATCATATGCTCTACTATCCCCTTTTAGGGACAAATGAAATAATTTTTGTTAATACTTCTCTGGAATATGATTTCAATAAACAATGAGATCACAAAAGTAATGGCCAATCGCTGTGTGAGCTGTGTCTTACATCTTAATAAGCTGAACTTCTTTATTTGGGTCCTTTTCCATCACTCCTTTCTCAGCTTCATGAAACATGTCC... | TTGTCATATTACTGATGCTGAACACAAACTGAGGCTTGTCTGTTTGCTTTTTTTTCTTTTGGGCAGTGGTCAATGAACTAAGAGCTTCTTGTTTCTAATGGCAATATTAAAGCTGCATATCATATGCTCTACTATCCCCTTTTAGGGACAAATGAAATAATTTTTGTTAATACTTCTCTGGAATATGATTTCAATAAACAATGAGATCACAAAAGTAATGGCCAATCGCTGTGTGAGCTGTGTCTTACATCTTAATAAGCTGAACTTCTTTATTTGGGTCCTTTTCCATCACTCCTTTCTCAGCTTCATGAAACATGTCC... |
Task1_train_45887 | A mutation on Chromosome 18 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GGAAGCAGTACTCAATTTAGCGCATAATTTATGCAATATTCTATCTTATACGATTTTTAATTGCTTTTGTTGTGTGAACTAATCTTTTATGTCAGCATTTTTCCAATAAGGAGACACGCATCTTTCCCCTTCCACAGAACATGCACAAGAACATACATTTTCCCAGTGTGGTCAGACTTGTCACCCATAACGCATAGCAAATTTTAAAGAAAGAAATTTACCAATTAACTCACAGTATTATGTAAATCACTGATAACACCTAAAACTTTGGTTCCCACATTTGCAGCACATTAGAATCACCTGAGGGTTTTTAAAAAATC... | GGAAGCAGTACTCAATTTAGCGCATAATTTATGCAATATTCTATCTTATACGATTTTTAATTGCTTTTGTTGTGTGAACTAATCTTTTATGTCAGCATTTTTCCAATAAGGAGACACGCATCTTTCCCCTTCCACAGAACATGCACAAGAACATACATTTTCCCAGTGTGGTCAGACTTGTCACCCATAACGCATAGCAAATTTTAAAGAAAGAAATTTACCAATTAACTCACAGTATTATGTAAATCACTGATAACACCTAAAACTTTGGTTCCCACATTTGCAGCACATTAGAATCACCTGAGGGTTTTTAAAAAATC... |
Task1_train_45888 | This variant lies on Chromosome 18. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACATGCGTGAGCCACCACGCCCAGCCAATAATTCTACTTCTTAATATCTACCCTGAAAATAATCTGAAATACAGAAAAAGAAGAGATATATACAGTATAAATAAATATTTGATATTTCAATATAGAAAAAGATATAAAACATTTGAATAAGAAGTCCCTCACAACATAATTTAAAATAGCAAAATATTAAAGTTTAAATATCTCACATGACTATATCATTTCATTAGATTATAGTTTAGATAGTAACGTCCAGAGTAGAGTTTTAATAAAGTATCATGTAAC... | ATGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACATGCGTGAGCCACCACGCCCAGCCAATAATTCTACTTCTTAATATCTACCCTGAAAATAATCTGAAATACAGAAAAAGAAGAGATATATACAGTATAAATAAATATTTGATATTTCAATATAGAAAAAGATATAAAACATTTGAATAAGAAGTCCCTCACAACATAATTTAAAATAGCAAAATATTAAAGTTTAAATATCTCACATGACTATATCATTTCATTAGATTATAGTTTAGATAGTAACGTCCAGAGTAGAGTTTTAATAAAGTATCATGTAAC... |
Task1_train_45889 | A mutation on Chromosome 18 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CAACACCTAAGAAAAAAATGCCTTTTAGGCTAAACTACAAAAGAATTCAATAAAGAAAGACTTTATAAATACTAAAAATAAAGAAAAATAAAGTGCTTAATTTATGCCAACAGCCTTCTAATTTCTTGTATAATTTTATTTCAACCTTAAAACTTGATGAATACTTTACATAAACACAAAAAGTTATTTAAAGAAAACGGACAAGTGGTTTATTTAGAGCAAATCATTCAAAATGAGTTAAAATTTAAATCAAATATTTGTCTTATTTGATATATATAAAATAGTTATATCCCTGGGACCAAGACTGGCAGATATTATAC... | CAACACCTAAGAAAAAAATGCCTTTTAGGCTAAACTACAAAAGAATTCAATAAAGAAAGACTTTATAAATACTAAAAATAAAGAAAAATAAAGTGCTTAATTTATGCCAACAGCCTTCTAATTTCTTGTATAATTTTATTTCAACCTTAAAACTTGATGAATACTTTACATAAACACAAAAAGTTATTTAAAGAAAACGGACAAGTGGTTTATTTAGAGCAAATCATTCAAAATGAGTTAAAATTTAAATCAAATATTTGTCTTATTTGATATATATAAAATAGTTATATCCCTGGGACCAAGACTGGCAGATATTATAC... |
Task1_train_45890 | This is a variant located on Chromosome 18. Is this mutation a likely cause of disease or not? | Benign | ACTACAGTCATCCATCACTTAAAGATGGGGATACTGCCTGAGAAATGCATCCCTAGCTGATTTCGTCACGGTGTGAACGTCATAGAGTGCACTTATACAAACCTAGATGGCACAGCCTACTACACGCCTAGGCCATATGGTAGAGCCTATTGCTCCTGGGCCACAAACCTGTCCAGCATGTTACCGTACTGAATACTGTAGGCAGTTGCAACACAACAGGAAATATTTGTGCATCTAACTATAACTAACATAGAAAAGGTACAGTAAAAACACAGTATTATAGTCTTATCAGACCACTGTCCTATATGTGATCTGTTGTT... | ACTACAGTCATCCATCACTTAAAGATGGGGATACTGCCTGAGAAATGCATCCCTAGCTGATTTCGTCACGGTGTGAACGTCATAGAGTGCACTTATACAAACCTAGATGGCACAGCCTACTACACGCCTAGGCCATATGGTAGAGCCTATTGCTCCTGGGCCACAAACCTGTCCAGCATGTTACCGTACTGAATACTGTAGGCAGTTGCAACACAACAGGAAATATTTGTGCATCTAACTATAACTAACATAGAAAAGGTACAGTAAAAACACAGTATTATAGTCTTATCAGACCACTGTCCTATATGTGATCTGTTGTT... |
Task1_train_45891 | This variant is located on Chromosome 18. Evaluate its biological effect and specify any disease association. | Benign | TTCTATCTGCTATGGTTGCAAAGTTTAAATGATATATTTTTTTAAATGAACTCAATTGAGGGTAAATGTCACCACCACTATCACCATCATCATCTTCATTATTATCATCGTCATCATCCCCTCACCAGGTGCACGTAAGAATCAATTCAGTTGGGTAATTTACCCTCCCCATCGCTGGGGGGCCCACCCATCCCTACTGGTCGATATCCATTTTAACTGCCAGTGGCTGAGAACTTGATGGGGTCACAAGAGTCTTTGAACAGACGCAACCTATTCAGGAGACTCTGGTATTTGCAAGTCAATTTGCCAGTTTTTGAAAC... | TTCTATCTGCTATGGTTGCAAAGTTTAAATGATATATTTTTTTAAATGAACTCAATTGAGGGTAAATGTCACCACCACTATCACCATCATCATCTTCATTATTATCATCGTCATCATCCCCTCACCAGGTGCACGTAAGAATCAATTCAGTTGGGTAATTTACCCTCCCCATCGCTGGGGGGCCCACCCATCCCTACTGGTCGATATCCATTTTAACTGCCAGTGGCTGAGAACTTGATGGGGTCACAAGAGTCTTTGAACAGACGCAACCTATTCAGGAGACTCTGGTATTTGCAAGTCAATTTGCCAGTTTTTGAAAC... |
Task1_train_45892 | A variant was discovered on Chromosome 18. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TGTTCTCAACCTCGGCACTATTGATGTTTTGGACCAGATAATTCCTTCATGTGCAGTTTGCATAAAGAGTTGTGGGCTGTTTAGCAGTTTCCCTGGCCTCTATCCACAAGAAGCCAGGAGCAATTCATACTCTTCTCCCTACAGGTCGTGAAAACCAAAACTATCTCCGGACATTGCCAAATGTCCCTTGGAGGGCAAAAGTCCCTCCTGACAGAGGACAACTGATGTAGTGTATACACGTGTTCAAGGCATAGGCTCAGGTATTCAGAAAAATGTCATTTTTCCTTCTCTATATTTCAACCTAAGCTTCCTTTGAAGCC... | TGTTCTCAACCTCGGCACTATTGATGTTTTGGACCAGATAATTCCTTCATGTGCAGTTTGCATAAAGAGTTGTGGGCTGTTTAGCAGTTTCCCTGGCCTCTATCCACAAGAAGCCAGGAGCAATTCATACTCTTCTCCCTACAGGTCGTGAAAACCAAAACTATCTCCGGACATTGCCAAATGTCCCTTGGAGGGCAAAAGTCCCTCCTGACAGAGGACAACTGATGTAGTGTATACACGTGTTCAAGGCATAGGCTCAGGTATTCAGAAAAATGTCATTTTTCCTTCTCTATATTTCAACCTAAGCTTCCTTTGAAGCC... |
Task1_train_45893 | Located on Chromosome 18, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GATTACAAAATAGTCCTAGTGTAGGACTGCTGGAGTTCGGTAAGTTGTTCAAGTTGGTTGGGAAAGGCAGTCTGACATATTCAGACTCCATTGTTAGCAGAGAAAACTGTAGTCAAAACAAAGATTATCTGCTCTAGCTGTTTCAGGGACTCTTAGTCAATTTGAAGCAGAGCTCAAAAGAAATATCATCTGCCAGTTATTTTCAATAAAGTCGCAGCCACTGCCACAAGGTTTACAAAAGTTACAGCTCCTTTAATTACATTTTAAAAACTAACTTACTTGAAGAAATTGGAAACAAAAGTAAAATAGAATATTGGGGA... | GATTACAAAATAGTCCTAGTGTAGGACTGCTGGAGTTCGGTAAGTTGTTCAAGTTGGTTGGGAAAGGCAGTCTGACATATTCAGACTCCATTGTTAGCAGAGAAAACTGTAGTCAAAACAAAGATTATCTGCTCTAGCTGTTTCAGGGACTCTTAGTCAATTTGAAGCAGAGCTCAAAAGAAATATCATCTGCCAGTTATTTTCAATAAAGTCGCAGCCACTGCCACAAGGTTTACAAAAGTTACAGCTCCTTTAATTACATTTTAAAAACTAACTTACTTGAAGAAATTGGAAACAAAAGTAAAATAGAATATTGGGGA... |
Task1_train_45894 | A variant was discovered on Chromosome 18. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AGCCTCACCAGGCAGGGTTATGCTCCCGCCCTCCTCCTTGTAATTATTACCTGACCCTCTGCCTCCTGCAACGCCAGGGCTGGAGGACAGGCTGGCCCCTATTCCTATGGGCACTGGCCAACATCCAACGCCTGGGACATAAACTGCACCCAATGGTATGTGAACTGTACTTTACAGTTTGCACGGTGTGTTCTGGTATTTGCTAAATCTTCACACATGCTCAGGTGGCAGTACGTTTTAATGATACAGGCGAGGGAACTGGGGCTCAGAAAGGTCTAGTGCCTTGCGCATGGGAGACTCAAGTGGTAGAACCGGTGGCC... | AGCCTCACCAGGCAGGGTTATGCTCCCGCCCTCCTCCTTGTAATTATTACCTGACCCTCTGCCTCCTGCAACGCCAGGGCTGGAGGACAGGCTGGCCCCTATTCCTATGGGCACTGGCCAACATCCAACGCCTGGGACATAAACTGCACCCAATGGTATGTGAACTGTACTTTACAGTTTGCACGGTGTGTTCTGGTATTTGCTAAATCTTCACACATGCTCAGGTGGCAGTACGTTTTAATGATACAGGCGAGGGAACTGGGGCTCAGAAAGGTCTAGTGCCTTGCGCATGGGAGACTCAAGTGGTAGAACCGGTGGCC... |
Task1_train_45895 | This genomic variant is located on Chromosome 18. Can you determine its pathogenicity and name any linked disease? | Benign | TAGGAGGGGCAAAGCTAGGACTCCGGGCAGCATGTTTGACCCCAAGTCCAGCAGGCCTGGTTTTGTCCTCAGCTAAGAGATGACAGTGGGCGTGTCATCCTCCCGAGGACGCACAGATAGCGCCAGGGCAAGCTTTCCCTGTGGCAGTGGCTGCACACTTGGTCGTAGGTGTTGGGCTGAGCCTTCCTGGTCATATCGTTTTCCCCCTTTCCATGGGGTTTGTGGTGAGCAAGGAGGGACCAGGTAGAGTGGAAGGAGGAAAGTTGGGAGGCGCCGAGGGAGGCATTTCTCTTTCTGCCAAATGATGAGTGTGCGACCAG... | TAGGAGGGGCAAAGCTAGGACTCCGGGCAGCATGTTTGACCCCAAGTCCAGCAGGCCTGGTTTTGTCCTCAGCTAAGAGATGACAGTGGGCGTGTCATCCTCCCGAGGACGCACAGATAGCGCCAGGGCAAGCTTTCCCTGTGGCAGTGGCTGCACACTTGGTCGTAGGTGTTGGGCTGAGCCTTCCTGGTCATATCGTTTTCCCCCTTTCCATGGGGTTTGTGGTGAGCAAGGAGGGACCAGGTAGAGTGGAAGGAGGAAAGTTGGGAGGCGCCGAGGGAGGCATTTCTCTTTCTGCCAAATGATGAGTGTGCGACCAG... |
Task1_train_45896 | This alteration on Chromosome 18 may affect genome function. Does it lead to a disease or is it benign? | Benign | CAGCTTTTGAGGATCCTCCAGAACCCTCTGGAAGCCCTATGAGGACACTTCTTAGGTTTTGATACACTTGACTCTATCCAACACTTACCTCCTTGCCTTGGGTCTCTGGGTTTAATTTCCTGCTGTGTTATAGCAACTAAAGGGAAAGGAACGTAAGTAAAGGCTCTGAAGTTGCACTTGCATGGCAAGAGGCTGCAAGGAGCTCAGGTGTCTGGGTCTGCAGTACCCAGTGTGTACCCAGAGCTCGGTACTGACTCAGTACGTGCCTGGACTTCCAAACACCTTCATGCTCATACCTCATGTTTTTGTCATGTCATTCT... | CAGCTTTTGAGGATCCTCCAGAACCCTCTGGAAGCCCTATGAGGACACTTCTTAGGTTTTGATACACTTGACTCTATCCAACACTTACCTCCTTGCCTTGGGTCTCTGGGTTTAATTTCCTGCTGTGTTATAGCAACTAAAGGGAAAGGAACGTAAGTAAAGGCTCTGAAGTTGCACTTGCATGGCAAGAGGCTGCAAGGAGCTCAGGTGTCTGGGTCTGCAGTACCCAGTGTGTACCCAGAGCTCGGTACTGACTCAGTACGTGCCTGGACTTCCAAACACCTTCATGCTCATACCTCATGTTTTTGTCATGTCATTCT... |
Task1_train_45897 | A mutation on Chromosome 18 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTAATTTCCTGCTGTGTTATAGCAACTAAAGGGAAAGGAACGTAAGTAAAGGCTCTGAAGTTGCACTTGCATGGCAAGAGGCTGCAAGGAGCTCAGGTGTCTGGGTCTGCAGTACCCAGTGTGTACCCAGAGCTCGGTACTGACTCAGTACGTGCCTGGACTTCCAAACACCTTCATGCTCATACCTCATGTTTTTGTCATGTCATTCTTGTGGGACATTAGGGCTGGGGAGACCGGGATGGGGAGAAGCGAATTGCCCTGTCTCAGGTACCTTAGGAAACCAGGGGAAAGCTGAGCTCTCATTTGGGGTGGCCTGACTT... | TTAATTTCCTGCTGTGTTATAGCAACTAAAGGGAAAGGAACGTAAGTAAAGGCTCTGAAGTTGCACTTGCATGGCAAGAGGCTGCAAGGAGCTCAGGTGTCTGGGTCTGCAGTACCCAGTGTGTACCCAGAGCTCGGTACTGACTCAGTACGTGCCTGGACTTCCAAACACCTTCATGCTCATACCTCATGTTTTTGTCATGTCATTCTTGTGGGACATTAGGGCTGGGGAGACCGGGATGGGGAGAAGCGAATTGCCCTGTCTCAGGTACCTTAGGAAACCAGGGGAAAGCTGAGCTCTCATTTGGGGTGGCCTGACTT... |
Task1_train_45898 | Chromosome 18 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TCAGAATTGCTTTCAGAGTCTGAGTCAAAGCACATGAGAAAAGATATACTTTTTGATCAAGGATATAGTCATCCACCCACCTCATCCACTGGCCTTGACTCGAAGCCAGTAGTATCTGTTGTCAAATACAACAGATGTATCCCCATGAAAAGATGACAGGGAACACAGGGAGGGTCAATTCCCAGAAACGTGCTACAGGGGCAGCATCCCAGGACACCATGCCATGCAGCGACCACAGTGGCTTCTCGGGAAAGCGCAGCATCGTTTGCTTGTACATGCCGGTGTGTTACTAAGGAAAAGGTTGATTCCCTTGAATGCAG... | TCAGAATTGCTTTCAGAGTCTGAGTCAAAGCACATGAGAAAAGATATACTTTTTGATCAAGGATATAGTCATCCACCCACCTCATCCACTGGCCTTGACTCGAAGCCAGTAGTATCTGTTGTCAAATACAACAGATGTATCCCCATGAAAAGATGACAGGGAACACAGGGAGGGTCAATTCCCAGAAACGTGCTACAGGGGCAGCATCCCAGGACACCATGCCATGCAGCGACCACAGTGGCTTCTCGGGAAAGCGCAGCATCGTTTGCTTGTACATGCCGGTGTGTTACTAAGGAAAAGGTTGATTCCCTTGAATGCAG... |
Task1_train_45899 | A genomic change on Chromosome 18 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GAACTCCAGCCTGGGCAACAAGAGCGAAACTCCGTCTCCAAAAAAAAAAAAAGACACTTATTTAGGCTTTCCATATATCATGGTAATTTGCTTTCTAAAAGGCTATATGAATTTTTAAGTGTGCTTGTTTCTCTATATGCTCAACAGAATGGAATGCTATCTTAAAAGAAAAAAGATACTTGGTAGTTTGATAACTAGTAATGTTATTTTAAGTTGTATGTTTTTAGTTACTAGTAAGCAGTTTGAATTCTGTGAAACTTTTGTTCATGATCTTTACTCATTTTTTAAGTGCATTTATGATCTCTTCAGGCTATTAGCCT... | GAACTCCAGCCTGGGCAACAAGAGCGAAACTCCGTCTCCAAAAAAAAAAAAAGACACTTATTTAGGCTTTCCATATATCATGGTAATTTGCTTTCTAAAAGGCTATATGAATTTTTAAGTGTGCTTGTTTCTCTATATGCTCAACAGAATGGAATGCTATCTTAAAAGAAAAAAGATACTTGGTAGTTTGATAACTAGTAATGTTATTTTAAGTTGTATGTTTTTAGTTACTAGTAAGCAGTTTGAATTCTGTGAAACTTTTGTTCATGATCTTTACTCATTTTTTAAGTGCATTTATGATCTCTTCAGGCTATTAGCCT... |
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