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_34800 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | GTTTGTCTTTTTTATTATGATCATCCTAGTGAGTGTGATGTGGTATCTCATTGTGGTTTTGCTTTGCATTTCCCTAATGGCTGATGGGGTTGACTATCTTTTATATATAACTTAATTTTTCTATTAGGTAACATTTCACAATTATTTTTTAATATCAGCTGCCCATGATTGCACAGATGAGAAAATCTCTGTTCAATAATGCCCTAAAACTGAATGAAAAATGTTGTAATAGAAGGTGCATATGTTGCCAGTGTGGCCTCCTGAGCCACAGGGCACCTATCTCAGACTGTACCCCTAAGTAAGGATTCTGCCTCCACATT... | GTTTGTCTTTTTTATTATGATCATCCTAGTGAGTGTGATGTGGTATCTCATTGTGGTTTTGCTTTGCATTTCCCTAATGGCTGATGGGGTTGACTATCTTTTATATATAACTTAATTTTTCTATTAGGTAACATTTCACAATTATTTTTTAATATCAGCTGCCCATGATTGCACAGATGAGAAAATCTCTGTTCAATAATGCCCTAAAACTGAATGAAAAATGTTGTAATAGAAGGTGCATATGTTGCCAGTGTGGCCTCCTGAGCCACAGGGCACCTATCTCAGACTGTACCCCTAAGTAAGGATTCTGCCTCCACATT... |
Task1_train_34801 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | TTGCCCTGAAGTTTCAGAGCATCACAAATTTTCCTAGTTTCCTTTTCATAGAATATTATTCTGACTTGGTTCCCTTATCATACATTGAGAGCTCCAAAGGACATTTGCTCCTTTCTGCAGTGATAGGACAAGACCACGACTTTTCAGAATCCAGTGAGGAGGAGGCGCCCGCAGAAGCCTCGAGCGGGGCACTGAGAAGCAAGCATGGTGAGAAGGGTAAGAACAGCTCCCTTGACTTCAGGGCTCTGACTTCAGAGCACCTCTTCCCTGATGCACTGTGCTCTGAGCACACACAACAGCTATCCAGGAGCCAGTTCTCT... | TTGCCCTGAAGTTTCAGAGCATCACAAATTTTCCTAGTTTCCTTTTCATAGAATATTATTCTGACTTGGTTCCCTTATCATACATTGAGAGCTCCAAAGGACATTTGCTCCTTTCTGCAGTGATAGGACAAGACCACGACTTTTCAGAATCCAGTGAGGAGGAGGCGCCCGCAGAAGCCTCGAGCGGGGCACTGAGAAGCAAGCATGGTGAGAAGGGTAAGAACAGCTCCCTTGACTTCAGGGCTCTGACTTCAGAGCACCTCTTCCCTGATGCACTGTGCTCTGAGCACACACAACAGCTATCCAGGAGCCAGTTCTCT... |
Task1_train_34802 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GACGGCTGTTCTGCTGCGACACTTGTCCAAGATCCTTTCATGAGCACTGCCACATCCCATCCGTGGAAGCTAACAAGTGAGTAAGACATGTCCCCTTCCCTGAGCCCTTCCTTCTTGTGGTACAGCTCCTCCTGCCACTCATGAGTACTCTGCAGAGTTTCTGTACCTGGTTATGTGTTTCTTGATGCATAAGGAGCAGGCTCCTTAGCATCAAGATCCACAAGTATTATCCAGAGCTGTTGAACAGTGCTGGTAGCAGCAGATTAATGGGAAGCAAAAACTCTTCAAGTGGTTATTGAGTGCAATAGTAAGAGGTGTCA... | GACGGCTGTTCTGCTGCGACACTTGTCCAAGATCCTTTCATGAGCACTGCCACATCCCATCCGTGGAAGCTAACAAGTGAGTAAGACATGTCCCCTTCCCTGAGCCCTTCCTTCTTGTGGTACAGCTCCTCCTGCCACTCATGAGTACTCTGCAGAGTTTCTGTACCTGGTTATGTGTTTCTTGATGCATAAGGAGCAGGCTCCTTAGCATCAAGATCCACAAGTATTATCCAGAGCTGTTGAACAGTGCTGGTAGCAGCAGATTAATGGGAAGCAAAAACTCTTCAAGTGGTTATTGAGTGCAATAGTAAGAGGTGTCA... |
Task1_train_34803 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TGTGAGTGGTGTGTGGACAGAATTGTTAAGGCTGAGAGGATGATCTCTACCGGGAATGTGTCTGACTCTATGAGGGCAGAGCATTGCCCTTCCATAATGGAGGAGGCTAATGTGACCCACCTGCTCCCAGGGTGTCATCTCAGGGGATCAGCATAAACCTCTGCTTTTGACCAGTTGGCCAATCTGCAGAGGCAGAAGAAAAACCAGCTTTTTGGTTGAGCCCTTGTATAGCCCCTATCTCTGCACCAGAGATGCAAAGTGCTCTCAAAGGAGCACTTTGTAACAGGCTCCTTGAGCAAGCACTACATGGCCAAGGGGAT... | TGTGAGTGGTGTGTGGACAGAATTGTTAAGGCTGAGAGGATGATCTCTACCGGGAATGTGTCTGACTCTATGAGGGCAGAGCATTGCCCTTCCATAATGGAGGAGGCTAATGTGACCCACCTGCTCCCAGGGTGTCATCTCAGGGGATCAGCATAAACCTCTGCTTTTGACCAGTTGGCCAATCTGCAGAGGCAGAAGAAAAACCAGCTTTTTGGTTGAGCCCTTGTATAGCCCCTATCTCTGCACCAGAGATGCAAAGTGCTCTCAAAGGAGCACTTTGTAACAGGCTCCTTGAGCAAGCACTACATGGCCAAGGGGAT... |
Task1_train_34804 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGCCACTTGAACACAGCAACAGCGGGAGCTGCTCCTGAGAAGGCGACTCCTGTCCGTCCATGGCTCTTAGGCCAGCTGGGAAAGCTCTCAGGCAGGAAGCAGCTCAGCCAGGTTCCCCACCCACCCTGCACTCCCTGCAGGCTTCAAGCCTAGGGCCACGGCTCAGCTTCCCCTCCTTTTCCTCTTCCTCTTCCTCCTCCTCCTCCCCACAGGTCCAGGTTTATCCAAATGCTTCTCTTCTTCCCCTCAGGTCACCACCCCTCCCAAGCCCTTCAGCCCCCACTGAGCCCAGATCCTACAAGTAGACCTCAGTTGCTTTT... | TGCCACTTGAACACAGCAACAGCGGGAGCTGCTCCTGAGAAGGCGACTCCTGTCCGTCCATGGCTCTTAGGCCAGCTGGGAAAGCTCTCAGGCAGGAAGCAGCTCAGCCAGGTTCCCCACCCACCCTGCACTCCCTGCAGGCTTCAAGCCTAGGGCCACGGCTCAGCTTCCCCTCCTTTTCCTCTTCCTCTTCCTCCTCCTCCTCCCCACAGGTCCAGGTTTATCCAAATGCTTCTCTTCTTCCCCTCAGGTCACCACCCCTCCCAAGCCCTTCAGCCCCCACTGAGCCCAGATCCTACAAGTAGACCTCAGTTGCTTTT... |
Task1_train_34805 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | TATAATCGTGGTGTTTCAAGTGCATGCCCAGGAGTCTTGGTATTCATTCTGAACACCAGCTGACAGAGCTTCTGCCTTTAGTGCCACTTCTTACCTTTAGTGTCTCCCCCCACCCCACCATGCACAAAAAAAAGCCCCTGCAAGGGCTGGACCCAGGGAACCCTAGGGATGGCTTAACTCCAGCCTGGTCATCCCCTCCCTGAGGTCACACTGAGGCTGGCAGCCCTGCCATCTGGATCATCCCCTCCCTGAGGTCGCACTGAGACTGGTAGTCCCACCACCTCTCTCTGCTCCTCTCCCCGTTCCATGGCTTCAGTGTG... | TATAATCGTGGTGTTTCAAGTGCATGCCCAGGAGTCTTGGTATTCATTCTGAACACCAGCTGACAGAGCTTCTGCCTTTAGTGCCACTTCTTACCTTTAGTGTCTCCCCCCACCCCACCATGCACAAAAAAAAGCCCCTGCAAGGGCTGGACCCAGGGAACCCTAGGGATGGCTTAACTCCAGCCTGGTCATCCCCTCCCTGAGGTCACACTGAGGCTGGCAGCCCTGCCATCTGGATCATCCCCTCCCTGAGGTCGCACTGAGACTGGTAGTCCCACCACCTCTCTCTGCTCCTCTCCCCGTTCCATGGCTTCAGTGTG... |
Task1_train_34806 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CATCTGGATCATCCCCTCCCTGAGGTCGCACTGAGACTGGTAGTCCCACCACCTCTCTCTGCTCCTCTCCCCGTTCCATGGCTTCAGTGTGCCAGGGGCTGATTAAAGGTAGTCCAACGTGTCAGACAGTTAGTACAAGGGTTCTTCAATGACTGTCCGACTGCAGGTTGAACTGACAATGAACAAGACAGCACACTAGGGCTCCTTTACCCCAGTCAGGAGGGACAGAGTAGCTCAAATCCATGTTTTGGGAGTCTGGAACCTCTATTCCTTCCTGGTACTCCCCAGTTTAGGATATGTTGATAAAAGCTGGTTTAGAG... | CATCTGGATCATCCCCTCCCTGAGGTCGCACTGAGACTGGTAGTCCCACCACCTCTCTCTGCTCCTCTCCCCGTTCCATGGCTTCAGTGTGCCAGGGGCTGATTAAAGGTAGTCCAACGTGTCAGACAGTTAGTACAAGGGTTCTTCAATGACTGTCCGACTGCAGGTTGAACTGACAATGAACAAGACAGCACACTAGGGCTCCTTTACCCCAGTCAGGAGGGACAGAGTAGCTCAAATCCATGTTTTGGGAGTCTGGAACCTCTATTCCTTCCTGGTACTCCCCAGTTTAGGATATGTTGATAAAAGCTGGTTTAGAG... |
Task1_train_34807 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | ATGTTGTAAAGATTGTGATCATCAGCCAGTGAGAGAAACATTTCTGGGTTATGATCTTCAGAACTGGCATCTTCAGTACTGGTAGAAAGCAAGACTTTCCATTCCCAAGTCTTTTAATGAACACATGTGACTCATACTCAGAGAAGAATTTGGCCCATTGAACAGGCAAAGCAAGAAAGCAAGAAATGGTGGTGGCTCGCCAGTGGTTACAGCAGACACCCTATACTTCTTCCAAAGGAATTCTCTGCGTAGAAAGGAATGTTGGAGATGAAGGATGAGGGCCTGCAAGTAAAGCGTGCCATTTTCTAAAATCCAAGCCT... | ATGTTGTAAAGATTGTGATCATCAGCCAGTGAGAGAAACATTTCTGGGTTATGATCTTCAGAACTGGCATCTTCAGTACTGGTAGAAAGCAAGACTTTCCATTCCCAAGTCTTTTAATGAACACATGTGACTCATACTCAGAGAAGAATTTGGCCCATTGAACAGGCAAAGCAAGAAAGCAAGAAATGGTGGTGGCTCGCCAGTGGTTACAGCAGACACCCTATACTTCTTCCAAAGGAATTCTCTGCGTAGAAAGGAATGTTGGAGATGAAGGATGAGGGCCTGCAAGTAAAGCGTGCCATTTTCTAAAATCCAAGCCT... |
Task1_train_34808 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TCTTCAGAACTGGCATCTTCAGTACTGGTAGAAAGCAAGACTTTCCATTCCCAAGTCTTTTAATGAACACATGTGACTCATACTCAGAGAAGAATTTGGCCCATTGAACAGGCAAAGCAAGAAAGCAAGAAATGGTGGTGGCTCGCCAGTGGTTACAGCAGACACCCTATACTTCTTCCAAAGGAATTCTCTGCGTAGAAAGGAATGTTGGAGATGAAGGATGAGGGCCTGCAAGTAAAGCGTGCCATTTTCTAAAATCCAAGCCTTTTTGTGTGCAGAAATATTGTAGCTCAAGAAAATGCCAGTCTTCCACTAGGATG... | TCTTCAGAACTGGCATCTTCAGTACTGGTAGAAAGCAAGACTTTCCATTCCCAAGTCTTTTAATGAACACATGTGACTCATACTCAGAGAAGAATTTGGCCCATTGAACAGGCAAAGCAAGAAAGCAAGAAATGGTGGTGGCTCGCCAGTGGTTACAGCAGACACCCTATACTTCTTCCAAAGGAATTCTCTGCGTAGAAAGGAATGTTGGAGATGAAGGATGAGGGCCTGCAAGTAAAGCGTGCCATTTTCTAAAATCCAAGCCTTTTTGTGTGCAGAAATATTGTAGCTCAAGAAAATGCCAGTCTTCCACTAGGATG... |
Task1_train_34809 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | TTTTTTGAGACAGAGTTTCGCTCTTGATGCCCAGGCTGGAGTGCAATGGCACGATCTCAGCTCACCAAAACCTCCACCTCCTGGGTTCAAGCCATTCTCCTGCCTTAGCCTCCCAAGTAGCTGGGACTACAGGCATGCACCACCATGCCTGGCTAATTTTGTATTTTTAGTAGAGACTGGGTTTCTCCATGTTGGTCAGGCTGGCCTCCAATCCCCGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACACAAGCCACAGCGCCCGGCCCCAGAAGTCTAATTATTTTTCCCAGTGAATTC... | TTTTTTGAGACAGAGTTTCGCTCTTGATGCCCAGGCTGGAGTGCAATGGCACGATCTCAGCTCACCAAAACCTCCACCTCCTGGGTTCAAGCCATTCTCCTGCCTTAGCCTCCCAAGTAGCTGGGACTACAGGCATGCACCACCATGCCTGGCTAATTTTGTATTTTTAGTAGAGACTGGGTTTCTCCATGTTGGTCAGGCTGGCCTCCAATCCCCGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACACAAGCCACAGCGCCCGGCCCCAGAAGTCTAATTATTTTTCCCAGTGAATTC... |
Task1_train_34810 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TCCTCCCAGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCTGAGGAGCTGGAATTACAGGTGCCCGCCACCGCGCCCGGCTAATTTTTGAATTTTTAGTAGTGACGGGGCTTCACCATGTTGGCCAGGCTGGTCTCTAACTCCTGACTTCAGGTGATTTGTCCGCCTTGGCCTCTCAGAGTGCTGGGATTATAGGCGGGAGCCACCACACCCGGCCCCTCCTGTGGTTTCTAATGCTGTAGTAGCTGGGACTCCAGGTTGCACGTTTTGTTCTAGGGAATGTGCATCAGCCTTCACCTGCAAGCCCCGGGCCCCCTGCACTC... | TCCTCCCAGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCTGAGGAGCTGGAATTACAGGTGCCCGCCACCGCGCCCGGCTAATTTTTGAATTTTTAGTAGTGACGGGGCTTCACCATGTTGGCCAGGCTGGTCTCTAACTCCTGACTTCAGGTGATTTGTCCGCCTTGGCCTCTCAGAGTGCTGGGATTATAGGCGGGAGCCACCACACCCGGCCCCTCCTGTGGTTTCTAATGCTGTAGTAGCTGGGACTCCAGGTTGCACGTTTTGTTCTAGGGAATGTGCATCAGCCTTCACCTGCAAGCCCCGGGCCCCCTGCACTC... |
Task1_train_34811 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ATAGGCGGGAGCCACCACACCCGGCCCCTCCTGTGGTTTCTAATGCTGTAGTAGCTGGGACTCCAGGTTGCACGTTTTGTTCTAGGGAATGTGCATCAGCCTTCACCTGCAAGCCCCGGGCCCCCTGCACTCCAGAGATGCTGGACTGGAACCCACCCAAGGCAAAGGCGTCAGTTCTGGCCCCTCTGTTCTCTTCGTGTGGCCCCCAGCAGGCCAGCCGCCCCGGCTCCACAGCGTCCTCCACAAGGGGCCTGCCGAGTAAGTCAGCCTGGGCCCCACTGGCGTGGGAGCCTGGCCACCCGCCAACCTGCAGGGAAGGG... | ATAGGCGGGAGCCACCACACCCGGCCCCTCCTGTGGTTTCTAATGCTGTAGTAGCTGGGACTCCAGGTTGCACGTTTTGTTCTAGGGAATGTGCATCAGCCTTCACCTGCAAGCCCCGGGCCCCCTGCACTCCAGAGATGCTGGACTGGAACCCACCCAAGGCAAAGGCGTCAGTTCTGGCCCCTCTGTTCTCTTCGTGTGGCCCCCAGCAGGCCAGCCGCCCCGGCTCCACAGCGTCCTCCACAAGGGGCCTGCCGAGTAAGTCAGCCTGGGCCCCACTGGCGTGGGAGCCTGGCCACCCGCCAACCTGCAGGGAAGGG... |
Task1_train_34812 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CCCTGGAACCCCTAGGGCTGGCAGGGCCGGATCCGGAGCCCTCCGTTTCCTCCCCGGAGAGCTGGACCTTGGGTCACACCCCCCAGCCTGCACCTAAGGTGCCCCTGTCTTCCTCCAACCACATGCCCCAGCAACCTGGGGACCCTATGGGGAAAATGTCGCTCTATGGGGCTCAGCCTGCATTCACCCTGGGGCCTGGACCTGCAACCGGACCAGCCCTCAGGGCAACCCAGGCGTCTCCACGGGCTGCCTGTCTCTCCTGGCACCCTGCTCCTCCCCCTTGGAGGTCAGCGCCATCTCTCTGCTAGGCTGGCCCTGGA... | CCCTGGAACCCCTAGGGCTGGCAGGGCCGGATCCGGAGCCCTCCGTTTCCTCCCCGGAGAGCTGGACCTTGGGTCACACCCCCCAGCCTGCACCTAAGGTGCCCCTGTCTTCCTCCAACCACATGCCCCAGCAACCTGGGGACCCTATGGGGAAAATGTCGCTCTATGGGGCTCAGCCTGCATTCACCCTGGGGCCTGGACCTGCAACCGGACCAGCCCTCAGGGCAACCCAGGCGTCTCCACGGGCTGCCTGTCTCTCCTGGCACCCTGCTCCTCCCCCTTGGAGGTCAGCGCCATCTCTCTGCTAGGCTGGCCCTGGA... |
Task1_train_34813 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | GTTTTGGTGGAACTGCTTCCCTGGCCAAAGCTCAGGGGCCAGTCAGACCCTTCTCCCCAGGACTTGGGCGCATCACCTCCTCCTGGAAGCCTTCCCTCGGCTGGGGCAGGTGCCTCTCTTCGATGCCTGAGTTCCAGCTGTCAAAGCACTTATATGCCAGTATGTTTATCTGCCCTCTCCTTCACCCCGCCTCAGCCTTGAAAAGTGCCTGGCACATGGTTGGTGCTCAATAAATGTTGGATGAATGATGCCTGTGTTGCTTAGAGCTGAAGAAGGGGCTTGAATGTTAGATTAAAAGATTCCAGAAACTCTTGTGGATG... | GTTTTGGTGGAACTGCTTCCCTGGCCAAAGCTCAGGGGCCAGTCAGACCCTTCTCCCCAGGACTTGGGCGCATCACCTCCTCCTGGAAGCCTTCCCTCGGCTGGGGCAGGTGCCTCTCTTCGATGCCTGAGTTCCAGCTGTCAAAGCACTTATATGCCAGTATGTTTATCTGCCCTCTCCTTCACCCCGCCTCAGCCTTGAAAAGTGCCTGGCACATGGTTGGTGCTCAATAAATGTTGGATGAATGATGCCTGTGTTGCTTAGAGCTGAAGAAGGGGCTTGAATGTTAGATTAAAAGATTCCAGAAACTCTTGTGGATG... |
Task1_train_34814 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CGGCTGGACATGAGGCTATAGAGCACGGGGTTGGCCGCCGAGCCCAGGTAGAAGAAGATGCCGGAGATGACGTGCACGTGCTGGAAGGCCAGGTGCAGGCCATCTGTCCACTGTGACACGACGCTCCACATGACGCGGTCGGCGTGGAACGGGGCCCAGCAGATGCCAAACACCACGACCAGGACAACTGCAGGGACAGAGAAGGGAGGCCGAGTGCCCGCCCGAGGCCCCTCAGCTGCCTTCCCGGGCTTCAGTTTGGGTCACCCATTTTCACATCCTCTCCTATCCCACAGGCCACCCTCACCTATCACCCAGGTGGA... | CGGCTGGACATGAGGCTATAGAGCACGGGGTTGGCCGCCGAGCCCAGGTAGAAGAAGATGCCGGAGATGACGTGCACGTGCTGGAAGGCCAGGTGCAGGCCATCTGTCCACTGTGACACGACGCTCCACATGACGCGGTCGGCGTGGAACGGGGCCCAGCAGATGCCAAACACCACGACCAGGACAACTGCAGGGACAGAGAAGGGAGGCCGAGTGCCCGCCCGAGGCCCCTCAGCTGCCTTCCCGGGCTTCAGTTTGGGTCACCCATTTTCACATCCTCTCCTATCCCACAGGCCACCCTCACCTATCACCCAGGTGGA... |
Task1_train_34815 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | GGGGCTACAGGTGCACACCACCATGCCCAGCTAATTTTTGTTTTATTTTTTGTAGAGACAGGGTCATACTACGTTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAAGCGATCCTCCCACCTTGGCCTTTTAAAGTTCTGGGATTACAGGCATGAGCCACCATGCCCAGTCCCTCATTCAACGTTTTTAATATCCCTCCTGGGTATGAGAGAGTGCTGGAAAGCTTAGTATTGAAGCCAGACAGGGTTCAAATCCCAGATTCAGCTCTTATTAATAGTGTGGCTTTGAGTAAGTCGCTTATTCTCTGTGAGGCTCAGCATG... | GGGGCTACAGGTGCACACCACCATGCCCAGCTAATTTTTGTTTTATTTTTTGTAGAGACAGGGTCATACTACGTTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAAGCGATCCTCCCACCTTGGCCTTTTAAAGTTCTGGGATTACAGGCATGAGCCACCATGCCCAGTCCCTCATTCAACGTTTTTAATATCCCTCCTGGGTATGAGAGAGTGCTGGAAAGCTTAGTATTGAAGCCAGACAGGGTTCAAATCCCAGATTCAGCTCTTATTAATAGTGTGGCTTTGAGTAAGTCGCTTATTCTCTGTGAGGCTCAGCATG... |
Task1_train_34816 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GGGCACCGCCCGGGGCGAGCGCGGCCCAGCACCCCGCCTTCCCCTCCCCCGCGCTGGCAGCCGTCGTGTGCCCGCCGCCCCCTCTTCCCTCCCCCTCCTTCCGAGCAGCCGCGGGGAGGGCGGGAGAGGGAGGGAAGGGGGTTGGGCGGGCAGCTTTGCCGCGCTTTGGCTTTCTGCGTCAGCAGCCCCAGCAAAACAGCTGCGGGAGCGCGCGTCCGGAACGCGCTCGCGCACCCCTCCCCCGCGCCCTCGGCCCTGCTGAGACCCGGCAAACTCCGGCCTTGAATGACAGTGCGATCGGCGACTGCGCAGCGCGGGAC... | GGGCACCGCCCGGGGCGAGCGCGGCCCAGCACCCCGCCTTCCCCTCCCCCGCGCTGGCAGCCGTCGTGTGCCCGCCGCCCCCTCTTCCCTCCCCCTCCTTCCGAGCAGCCGCGGGGAGGGCGGGAGAGGGAGGGAAGGGGGTTGGGCGGGCAGCTTTGCCGCGCTTTGGCTTTCTGCGTCAGCAGCCCCAGCAAAACAGCTGCGGGAGCGCGCGTCCGGAACGCGCTCGCGCACCCCTCCCCCGCGCCCTCGGCCCTGCTGAGACCCGGCAAACTCCGGCCTTGAATGACAGTGCGATCGGCGACTGCGCAGCGCGGGAC... |
Task1_train_34817 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GACCCTCATCTAAAGGAGGACTTGGCCATTCCCTGGGCTGTCCCACAGCACCTGCCGGCCAGGGCCCGGGCACAGAGCGAGACTGTCTTTTCCTCAAGGAGACACCGTGGGGGAGGGAGGGAGAGGTAGACACCACCAACCTCATTCCATGACCAGGGCCTGGCGATGCTCAGAAGCCAGTGAGTGTGTCCCTGCCCTGAAGGGTCAGTGCTGGCCCCCTGGACCTAGGGGGAAGATGGTGCAGGCAGTGGCCCAGCCTGAGGAAGGAGCTGAAGCTCTCAAGAGTTTGCAGCCACCCTCCTGGGGAGAGACTGACGCCT... | GACCCTCATCTAAAGGAGGACTTGGCCATTCCCTGGGCTGTCCCACAGCACCTGCCGGCCAGGGCCCGGGCACAGAGCGAGACTGTCTTTTCCTCAAGGAGACACCGTGGGGGAGGGAGGGAGAGGTAGACACCACCAACCTCATTCCATGACCAGGGCCTGGCGATGCTCAGAAGCCAGTGAGTGTGTCCCTGCCCTGAAGGGTCAGTGCTGGCCCCCTGGACCTAGGGGGAAGATGGTGCAGGCAGTGGCCCAGCCTGAGGAAGGAGCTGAAGCTCTCAAGAGTTTGCAGCCACCCTCCTGGGGAGAGACTGACGCCT... |
Task1_train_34818 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TCTTGGCCTCCCAAAGTGGCCGGGCAGGGCTGAATTCGCCCCCTCACCAGCTACTGCCAACCACGGATGAATGGCTTCTGCCTGCCTCCTGCCCTCCAGATCTTACCAGGGCATTTCACTGGGAAATATGGCAACAGCCCTTGCCACTCAGGGGACAGCATGGCAGGGGCTGGGAACGAATGTTGTTGCCAAACGACAAGACCCAGCTGGGCCCAGTGGCTCACACTTGTGATCCCAGTGGTCTGAGAGGCTGAGGCAGGAGGATCACTTGAAGCCAGGAGTTTGAGAGCAGCCTGGGCAACACAGTGAGACTCTACAAA... | TCTTGGCCTCCCAAAGTGGCCGGGCAGGGCTGAATTCGCCCCCTCACCAGCTACTGCCAACCACGGATGAATGGCTTCTGCCTGCCTCCTGCCCTCCAGATCTTACCAGGGCATTTCACTGGGAAATATGGCAACAGCCCTTGCCACTCAGGGGACAGCATGGCAGGGGCTGGGAACGAATGTTGTTGCCAAACGACAAGACCCAGCTGGGCCCAGTGGCTCACACTTGTGATCCCAGTGGTCTGAGAGGCTGAGGCAGGAGGATCACTTGAAGCCAGGAGTTTGAGAGCAGCCTGGGCAACACAGTGAGACTCTACAAA... |
Task1_train_34819 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CTGAGGCAGTGAGCCATGATCATGCCACCGCAGTCCAGCCTGGTGACAAATGAGACCCTGCCTCAAAAAAAAAAAAAAAAAAAAAAGAGGAAGGTGAGCGCAGTGGCTCATGTCTGTAAATCCAGACACTTTGGGAGGCTGAGGTGGAGGTTCGAGACCAGCCTGGGCAACATAGCAAAACCATGTCTTTACACAAAATAAAAAATGAGTCAGGTGTGGTGGCACATGCCATTGGTGCCAGCTACGTGAGAGGCTGAGGTGGGAAGATTGCTTGAGCCTGGGAGGTCCGAAGCTGCAGGGAGCCGTAACTCAGGCATCAC... | CTGAGGCAGTGAGCCATGATCATGCCACCGCAGTCCAGCCTGGTGACAAATGAGACCCTGCCTCAAAAAAAAAAAAAAAAAAAAAAGAGGAAGGTGAGCGCAGTGGCTCATGTCTGTAAATCCAGACACTTTGGGAGGCTGAGGTGGAGGTTCGAGACCAGCCTGGGCAACATAGCAAAACCATGTCTTTACACAAAATAAAAAATGAGTCAGGTGTGGTGGCACATGCCATTGGTGCCAGCTACGTGAGAGGCTGAGGTGGGAAGATTGCTTGAGCCTGGGAGGTCCGAAGCTGCAGGGAGCCGTAACTCAGGCATCAC... |
Task1_train_34820 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CCACGTGCCCCTTTCCCACAGGGCCCAGGCTCCTGGCATCAGGAGGCTGAACCCAGGCCCTGGCCCAGACTGTGTGCTTCCAGCCTCCCCTCCTCTCGACACCAGAACACAGCCTGGCCCCAGCTTCTGGGAAATATAGAAAAAAATGGGTGAATGATCCAGTGACAGGGTGTCTTGTTCCACACAAGACACAGTGAGCAGGGGTTGGGGGAGGGGCTCCTGGCTGCGGGAGGCACACCACACTCACCCAAATGGCATCTGTACTCAATACCGCACCCTTCCCTGGGGGACACCTGGTCCCAACCTGAGCTGCCTTTCTC... | CCACGTGCCCCTTTCCCACAGGGCCCAGGCTCCTGGCATCAGGAGGCTGAACCCAGGCCCTGGCCCAGACTGTGTGCTTCCAGCCTCCCCTCCTCTCGACACCAGAACACAGCCTGGCCCCAGCTTCTGGGAAATATAGAAAAAAATGGGTGAATGATCCAGTGACAGGGTGTCTTGTTCCACACAAGACACAGTGAGCAGGGGTTGGGGGAGGGGCTCCTGGCTGCGGGAGGCACACCACACTCACCCAAATGGCATCTGTACTCAATACCGCACCCTTCCCTGGGGGACACCTGGTCCCAACCTGAGCTGCCTTTCTC... |
Task1_train_34821 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | ACGACACGCGGCAACGAGGTCATCTCCGTGATGAATCGGGCCAAGAAAGCAGGTGAGCTGGGGCCCGCTGTGGGGTCAGGGCCAGGTGACAGACCTCTATCGCATATCCTGACCTCTATCACCCTCAGGAAAGTCAGTGGGAGTGGTAACCACCACACGGGTGCAGCATGCCTCGCCAGCCGGCGCCTACGCCCACACGGTGAACCGCAACTGGTACTCGGATGCCGACGTGCCTGCCTCGGCCCGCCAGGAGGGGTGCCAGGACATCGCCACGCAGCTCATCTCCAACATGGACATTGATGTGCGACCCCCGGGCCAAG... | ACGACACGCGGCAACGAGGTCATCTCCGTGATGAATCGGGCCAAGAAAGCAGGTGAGCTGGGGCCCGCTGTGGGGTCAGGGCCAGGTGACAGACCTCTATCGCATATCCTGACCTCTATCACCCTCAGGAAAGTCAGTGGGAGTGGTAACCACCACACGGGTGCAGCATGCCTCGCCAGCCGGCGCCTACGCCCACACGGTGAACCGCAACTGGTACTCGGATGCCGACGTGCCTGCCTCGGCCCGCCAGGAGGGGTGCCAGGACATCGCCACGCAGCTCATCTCCAACATGGACATTGATGTGCGACCCCCGGGCCAAG... |
Task1_train_34822 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CGACACGCGGCAACGAGGTCATCTCCGTGATGAATCGGGCCAAGAAAGCAGGTGAGCTGGGGCCCGCTGTGGGGTCAGGGCCAGGTGACAGACCTCTATCGCATATCCTGACCTCTATCACCCTCAGGAAAGTCAGTGGGAGTGGTAACCACCACACGGGTGCAGCATGCCTCGCCAGCCGGCGCCTACGCCCACACGGTGAACCGCAACTGGTACTCGGATGCCGACGTGCCTGCCTCGGCCCGCCAGGAGGGGTGCCAGGACATCGCCACGCAGCTCATCTCCAACATGGACATTGATGTGCGACCCCCGGGCCAAGG... | CGACACGCGGCAACGAGGTCATCTCCGTGATGAATCGGGCCAAGAAAGCAGGTGAGCTGGGGCCCGCTGTGGGGTCAGGGCCAGGTGACAGACCTCTATCGCATATCCTGACCTCTATCACCCTCAGGAAAGTCAGTGGGAGTGGTAACCACCACACGGGTGCAGCATGCCTCGCCAGCCGGCGCCTACGCCCACACGGTGAACCGCAACTGGTACTCGGATGCCGACGTGCCTGCCTCGGCCCGCCAGGAGGGGTGCCAGGACATCGCCACGCAGCTCATCTCCAACATGGACATTGATGTGCGACCCCCGGGCCAAGG... |
Task1_train_34823 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACGCTTAAACAATAATAAACAAAGTAATGTTATGAGGTGGGATTTTAATGTGGCTTCTAAGAGGTAACCTGTGCGAGCGGATGAAATTGAGCCAGACTTGGTTGGGTGGGTCCATACAGAAGAGAGGAGAGGGCTCGGGACCCAGCTGTGGGCACAGGAATCAGAGAACAGGAGAATGGGGTTAAGCAGAATTGCAGTCCACGCAGAAAGTTCCCTCCATTTTCTTTGGCAGTGGCTGGATTCTCACCCTGCCTCCCACCTGAAGACCAGAGGCAGGAGGGAGGCCCAGGGGCTCTGTGTGGGCTTGCTGTGGCCTGGCC... | ACGCTTAAACAATAATAAACAAAGTAATGTTATGAGGTGGGATTTTAATGTGGCTTCTAAGAGGTAACCTGTGCGAGCGGATGAAATTGAGCCAGACTTGGTTGGGTGGGTCCATACAGAAGAGAGGAGAGGGCTCGGGACCCAGCTGTGGGCACAGGAATCAGAGAACAGGAGAATGGGGTTAAGCAGAATTGCAGTCCACGCAGAAAGTTCCCTCCATTTTCTTTGGCAGTGGCTGGATTCTCACCCTGCCTCCCACCTGAAGACCAGAGGCAGGAGGGAGGCCCAGGGGCTCTGTGTGGGCTTGCTGTGGCCTGGCC... |
Task1_train_34824 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TCCCAGCACTTCGGGAGGCCGAGGTGGGAGGATCGTCTGAGGCTAGGAGTTCACAACCAGCCTAGCCAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGTGCAGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGGGAATCACTTGAACCCAGGAGGCAGGGACTGCAGTGAGCCGAGATCATGCCATTGCACTCCAGCCTGGGAAACAAGAATGAAACTCCATCTCAAAAAAAAAAAAAGTTTTTAAAATATAAAATTAAAAAAAGTTTAATTACACAAAATTTTTGACC... | TCCCAGCACTTCGGGAGGCCGAGGTGGGAGGATCGTCTGAGGCTAGGAGTTCACAACCAGCCTAGCCAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGTGCAGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGGGAATCACTTGAACCCAGGAGGCAGGGACTGCAGTGAGCCGAGATCATGCCATTGCACTCCAGCCTGGGAAACAAGAATGAAACTCCATCTCAAAAAAAAAAAAAGTTTTTAAAATATAAAATTAAAAAAAGTTTAATTACACAAAATTTTTGACC... |
Task1_train_34825 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | GGAGGCAGAGGTTGCAGTGAGCCGAGATCGAGCCATTGCACTCCAGCCTGAGCAACAGAGCAAGACTGCATCTCAAAAAAAAAAAGGTTGGCCAATTTATTTATTTAAAAGTTTGTTCTTTGGAAGCCTGAAGATTAATTAATTCAGGTCACATTTTGAATCTGGAGGAGGAGGGTGGATTATTCAACAAATGATGCAAGGATTACTAACCAACCATTTGGAAGAAAATAAGGTTAATGATTAACCTCACATGATAAATAAAAATAAATTTCAGAGATTAAATATTTACATGGTTAAAAAAAAAAAGAAGCCATAAAAGT... | GGAGGCAGAGGTTGCAGTGAGCCGAGATCGAGCCATTGCACTCCAGCCTGAGCAACAGAGCAAGACTGCATCTCAAAAAAAAAAAGGTTGGCCAATTTATTTATTTAAAAGTTTGTTCTTTGGAAGCCTGAAGATTAATTAATTCAGGTCACATTTTGAATCTGGAGGAGGAGGGTGGATTATTCAACAAATGATGCAAGGATTACTAACCAACCATTTGGAAGAAAATAAGGTTAATGATTAACCTCACATGATAAATAAAAATAAATTTCAGAGATTAAATATTTACATGGTTAAAAAAAAAAAGAAGCCATAAAAGT... |
Task1_train_34826 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | TCTTCTTTATTTTCTTTTCCTTTTGGTCAAATAGTAGAAAAATGTGACTTGCTGCTGAGCCCTGCTCTTCACACCTGCTTGCCTTTACTCAGCTAGTATTTATTTCAAGAGATGATTCCTGCCTAGGTCATCACCAGTGGGGAAGGTTAATCTTTCATTTTTCCCACAGAAACCTGAATAAGGGAAATTTCAGAAAAGAACAGCCACAAATCTGTTTGAAACCTGATAGGGTGACTTTTTTGGTTTTTGTTTTGTTTTAAGGACAGTTTCTCTTTTTTTTATTGAAATGAAAATCATGCAAATGATCATCTTAAACTGGA... | TCTTCTTTATTTTCTTTTCCTTTTGGTCAAATAGTAGAAAAATGTGACTTGCTGCTGAGCCCTGCTCTTCACACCTGCTTGCCTTTACTCAGCTAGTATTTATTTCAAGAGATGATTCCTGCCTAGGTCATCACCAGTGGGGAAGGTTAATCTTTCATTTTTCCCACAGAAACCTGAATAAGGGAAATTTCAGAAAAGAACAGCCACAAATCTGTTTGAAACCTGATAGGGTGACTTTTTTGGTTTTTGTTTTGTTTTAAGGACAGTTTCTCTTTTTTTTATTGAAATGAAAATCATGCAAATGATCATCTTAAACTGGA... |
Task1_train_34827 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GCCCTGCCTTCTCAGGGGCTGGAGGCCTGCCACTCCTCGGCTGATTCCCGCAGATGCCACCCGGCTCAGCTGGGCCTGGTACCCAGAAGCCCTGCCGCGGCCTCCAGATGCAGGGAGGTGCCTACCTGCCAGTCTGTCTTGGGTGTGTCATTTGTCCATTTCTTTGGACATGTTCAGGCAGTCAGTGAGCCTAGACCCTGGTGCCTGCCAGGCGGTGGGCGCACTCAGGCCTTTTACCTGCCCAGCCCCCAGAAGCCTGAGGCAGCACGCCAGGGGCCTGGGGCCTTCCATGGGGACTGCAAGGCTGCAGACCCCTGCCT... | GCCCTGCCTTCTCAGGGGCTGGAGGCCTGCCACTCCTCGGCTGATTCCCGCAGATGCCACCCGGCTCAGCTGGGCCTGGTACCCAGAAGCCCTGCCGCGGCCTCCAGATGCAGGGAGGTGCCTACCTGCCAGTCTGTCTTGGGTGTGTCATTTGTCCATTTCTTTGGACATGTTCAGGCAGTCAGTGAGCCTAGACCCTGGTGCCTGCCAGGCGGTGGGCGCACTCAGGCCTTTTACCTGCCCAGCCCCCAGAAGCCTGAGGCAGCACGCCAGGGGCCTGGGGCCTTCCATGGGGACTGCAAGGCTGCAGACCCCTGCCT... |
Task1_train_34828 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GCAGCTGGAGGTTATCGAAAATCTGTTGTAAGGAGCATTGTTAACTTAGAATAAAAATCGAATCCAAAACACGCTTTTGCAATACCCCCTCCCGATATCCACCGAGGCAAAGGCAGAATTAAGAAGCAGGGTCTTGAGATGTAGGAAAGGAGAATGAACCCCACGCGGGAAGAGGACAGGCCGCCCTGACTTTGGTCCACTCAGCCAGGGGGTGAGCACCACCTGTCTTGGTGAATGACTCTGAGCCCATCTCAGGTGTGGCTGCAGGTGACACATCTTCTCTTCCTGTCCACCCCCCAGCCCCATGGCGTCCCTTCCTG... | GCAGCTGGAGGTTATCGAAAATCTGTTGTAAGGAGCATTGTTAACTTAGAATAAAAATCGAATCCAAAACACGCTTTTGCAATACCCCCTCCCGATATCCACCGAGGCAAAGGCAGAATTAAGAAGCAGGGTCTTGAGATGTAGGAAAGGAGAATGAACCCCACGCGGGAAGAGGACAGGCCGCCCTGACTTTGGTCCACTCAGCCAGGGGGTGAGCACCACCTGTCTTGGTGAATGACTCTGAGCCCATCTCAGGTGTGGCTGCAGGTGACACATCTTCTCTTCCTGTCCACCCCCCAGCCCCATGGCGTCCCTTCCTG... |
Task1_train_34829 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | TCATATTTTATTGCTTCAAGTGGGAACTGTGTTTATACCTAAAAGGATCAAAAGCTCACTTTTAAATTTATTCTCAGTTGAAATTCTGGATTTGATTTGAACAGGTTAAATGTTTATTGTAGTGTTGTTCAGAACATGGCAGCTCTTCCTTTTTCTCCAAAGAATCTTTAACGCATTGCTGTCATAGCCAAGTGGTTTAGGATCTAACTAGAAAATGACATTAGCATTTGCGGAACCGATTAATCACAGAACTGTTCAGGAGAATCAAAGAATGTCTTGCCTTTCTTTCCAGGGATGATGACATTGAGGTCATTGTGGAT... | TCATATTTTATTGCTTCAAGTGGGAACTGTGTTTATACCTAAAAGGATCAAAAGCTCACTTTTAAATTTATTCTCAGTTGAAATTCTGGATTTGATTTGAACAGGTTAAATGTTTATTGTAGTGTTGTTCAGAACATGGCAGCTCTTCCTTTTTCTCCAAAGAATCTTTAACGCATTGCTGTCATAGCCAAGTGGTTTAGGATCTAACTAGAAAATGACATTAGCATTTGCGGAACCGATTAATCACAGAACTGTTCAGGAGAATCAAAGAATGTCTTGCCTTTCTTTCCAGGGATGATGACATTGAGGTCATTGTGGAT... |
Task1_train_34830 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TTTCTTTCTTTCTTATAATGAACATGGATTACATGTGTAATTAAAAACATGCGCAGTTTTTAAAGTAGGTGTCTGGTTTCTTTCATCTTCTCCACCCTCACTGCTCTCTCCCTCTTTTGCCTTAGATGGTGTCGTGTTGGTTGATCCTGATCTTGTGAAGGGAAAGAAAGGTGAGATGAAGCCCCTTGTCTCAGGCTGGTTTCTGGGCGGAGTGGACTGCTCTCTGGGCGGCTCTGGGAAGGGGCATTTACATGGAAGGAGAGACAGGAAGGCAGAGGCAGCGCTCTTGCACATGGAACCAGTGCCAGGCCCACTGACCC... | TTTCTTTCTTTCTTATAATGAACATGGATTACATGTGTAATTAAAAACATGCGCAGTTTTTAAAGTAGGTGTCTGGTTTCTTTCATCTTCTCCACCCTCACTGCTCTCTCCCTCTTTTGCCTTAGATGGTGTCGTGTTGGTTGATCCTGATCTTGTGAAGGGAAAGAAAGGTGAGATGAAGCCCCTTGTCTCAGGCTGGTTTCTGGGCGGAGTGGACTGCTCTCTGGGCGGCTCTGGGAAGGGGCATTTACATGGAAGGAGAGACAGGAAGGCAGAGGCAGCGCTCTTGCACATGGAACCAGTGCCAGGCCCACTGACCC... |
Task1_train_34831 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ATTGTCCCCTGTCAAGGGCATCTTTACTGAATCCGAAGATGCTGATTTGATTCTTCCTTGTTGTCTACCTCTGCAAGGCTGATGGTCCCGCTTAGTGTAATTTCTTCGCTGAGCACTGTGGGCCGCAGGGTATTTCTTGCTCAGGGGATGTTTTGACAAGCTAGCCTCTCTAGGGCCCCTGTACGTAGCGACCCTCATAGACACTCCCTCCCAGTGCTGGCTTCCAGGTGGGCACCAGAGGCGAGAGTAGGGGCTCACCATCAAATCGCCGCTGTGCTCCCCAAAACTAGGTGGGCAGAAAGCTAAAAAAGTACAAAAAC... | ATTGTCCCCTGTCAAGGGCATCTTTACTGAATCCGAAGATGCTGATTTGATTCTTCCTTGTTGTCTACCTCTGCAAGGCTGATGGTCCCGCTTAGTGTAATTTCTTCGCTGAGCACTGTGGGCCGCAGGGTATTTCTTGCTCAGGGGATGTTTTGACAAGCTAGCCTCTCTAGGGCCCCTGTACGTAGCGACCCTCATAGACACTCCCTCCCAGTGCTGGCTTCCAGGTGGGCACCAGAGGCGAGAGTAGGGGCTCACCATCAAATCGCCGCTGTGCTCCCCAAAACTAGGTGGGCAGAAAGCTAAAAAAGTACAAAAAC... |
Task1_train_34832 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TTGTCCCCTGTCAAGGGCATCTTTACTGAATCCGAAGATGCTGATTTGATTCTTCCTTGTTGTCTACCTCTGCAAGGCTGATGGTCCCGCTTAGTGTAATTTCTTCGCTGAGCACTGTGGGCCGCAGGGTATTTCTTGCTCAGGGGATGTTTTGACAAGCTAGCCTCTCTAGGGCCCCTGTACGTAGCGACCCTCATAGACACTCCCTCCCAGTGCTGGCTTCCAGGTGGGCACCAGAGGCGAGAGTAGGGGCTCACCATCAAATCGCCGCTGTGCTCCCCAAAACTAGGTGGGCAGAAAGCTAAAAAAGTACAAAAACC... | TTGTCCCCTGTCAAGGGCATCTTTACTGAATCCGAAGATGCTGATTTGATTCTTCCTTGTTGTCTACCTCTGCAAGGCTGATGGTCCCGCTTAGTGTAATTTCTTCGCTGAGCACTGTGGGCCGCAGGGTATTTCTTGCTCAGGGGATGTTTTGACAAGCTAGCCTCTCTAGGGCCCCTGTACGTAGCGACCCTCATAGACACTCCCTCCCAGTGCTGGCTTCCAGGTGGGCACCAGAGGCGAGAGTAGGGGCTCACCATCAAATCGCCGCTGTGCTCCCCAAAACTAGGTGGGCAGAAAGCTAAAAAAGTACAAAAACC... |
Task1_train_34833 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | CTCCTTCTCTTGGTGGGACGTCCTGCAGCCTGGCCTTTTGAATCCCTGGGATGTCATTCATTTGTCCTGTTGAGTTCAGTTTATTGCCCTGCTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATCCTCCCAACTCAGCCTCCCAAGTAGCTGGGATTACAGGTACATGCCACCACGTCCAGCTATTTTTTGTATTTTTAGTTAGAGATGGAGTTTTACCATGTTGGCCAGGCTGGTCTCGAAC... | CTCCTTCTCTTGGTGGGACGTCCTGCAGCCTGGCCTTTTGAATCCCTGGGATGTCATTCATTTGTCCTGTTGAGTTCAGTTTATTGCCCTGCTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATCCTCCCAACTCAGCCTCCCAAGTAGCTGGGATTACAGGTACATGCCACCACGTCCAGCTATTTTTTGTATTTTTAGTTAGAGATGGAGTTTTACCATGTTGGCCAGGCTGGTCTCGAAC... |
Task1_train_34834 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACATAATTTGTTGCCACATTTTTCACAGAGAACTTCTGTAAGTAAACAGTTGCTGGCTTCTGCCTGCACCCTGCAAATCACTAGGGGAGCTTTAAAAGAGCACCTATGCCAGGAGCCTACCCCACTGGATCTAGATTTCATTTAACAACAGGGCAGCCATGTGCAGTCTGTAGACTGACACTGCACAAAAGGGCCACATCTAAGGAGTGTCACACATGGCATATATATTGTATACTGCATTTCTACATAGAGTTTTGTTTTATAATTGCAGCCGGCAGTAGAGTATCTTGTTCTAACATTTTCCCACAGATAGTAGTAAA... | ACATAATTTGTTGCCACATTTTTCACAGAGAACTTCTGTAAGTAAACAGTTGCTGGCTTCTGCCTGCACCCTGCAAATCACTAGGGGAGCTTTAAAAGAGCACCTATGCCAGGAGCCTACCCCACTGGATCTAGATTTCATTTAACAACAGGGCAGCCATGTGCAGTCTGTAGACTGACACTGCACAAAAGGGCCACATCTAAGGAGTGTCACACATGGCATATATATTGTATACTGCATTTCTACATAGAGTTTTGTTTTATAATTGCAGCCGGCAGTAGAGTATCTTGTTCTAACATTTTCCCACAGATAGTAGTAAA... |
Task1_train_34835 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GTAGTAGGTGGGGAAGGACTGACAAAGAGTAGAAAATCGCAGGTGAGCCGGACAAAAATGTAGATATATAGAGTGAGTTGCTATGTTTTCATATTTATCTTACCGCCAAGTGACTGGTAAATGTGAAGTCCTGCTGGTACAAGCTTTGCAACACTAAGAACCATGTCTCCTTCCCAAAATTCTAACAGCTGAAGAATATTAATGAAGGAAAAGAGAATGTTGAAAAGTGACATATACATATCACCTTTCCAGGTTACTGTGCCAACTCACATATGAAGATGACACAGAGAGCAAGCAAATGAATACTCTCACCCCCACCC... | GTAGTAGGTGGGGAAGGACTGACAAAGAGTAGAAAATCGCAGGTGAGCCGGACAAAAATGTAGATATATAGAGTGAGTTGCTATGTTTTCATATTTATCTTACCGCCAAGTGACTGGTAAATGTGAAGTCCTGCTGGTACAAGCTTTGCAACACTAAGAACCATGTCTCCTTCCCAAAATTCTAACAGCTGAAGAATATTAATGAAGGAAAAGAGAATGTTGAAAAGTGACATATACATATCACCTTTCCAGGTTACTGTGCCAACTCACATATGAAGATGACACAGAGAGCAAGCAAATGAATACTCTCACCCCCACCC... |
Task1_train_34836 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ACCCTTCAGAGTTTACCATTAAAGGCAATATAACAGTATTCCTATCGTTTGCTCTTTAACTTCTGTGACAGTTGCCTATACCTGTCTTTGCAGGATTACATCCATCTATTCCATATAAAAATGGTAGACTGGGATTTGTTTGGATTTGTATAGCTATAACAGCTCATCAATATGTGCAACAAGCACCTTTACTCATTGCTGACAAGTGTGTAGTGTTCGTATACAGTAGAATGCCTTTTAGAACTCAAACAGGAAAGTGAGAGAAAGCCCACATACAACAAGATTCATAAAGAAAATGGAGAAGGTCAGGAGAAAGTCAG... | ACCCTTCAGAGTTTACCATTAAAGGCAATATAACAGTATTCCTATCGTTTGCTCTTTAACTTCTGTGACAGTTGCCTATACCTGTCTTTGCAGGATTACATCCATCTATTCCATATAAAAATGGTAGACTGGGATTTGTTTGGATTTGTATAGCTATAACAGCTCATCAATATGTGCAACAAGCACCTTTACTCATTGCTGACAAGTGTGTAGTGTTCGTATACAGTAGAATGCCTTTTAGAACTCAAACAGGAAAGTGAGAGAAAGCCCACATACAACAAGATTCATAAAGAAAATGGAGAAGGTCAGGAGAAAGTCAG... |
Task1_train_34837 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | TTATGCCCTGAGGTTGGCTGTTGAATCCCTCACGAAATGCTCCTCAGTGTGTTGCCTAACACACACTGCTGAGCTCACCCATTAAAATCTGCATGATGGAATTCAGCCCAATGCAATGAGAATTCCCATGGACTTCCTCTGTGCAAGGCAAAGCATGGGTGCTGTGGAAGGAGGATGAAAACAGGTAGAAGATGTAATCTCATCCTCAAGGGGTGCTCGGTAGAATGGAGGAAACAATACATAGATTCCTGAAGATGAGCACCAAAGTGATTGGGGTGGGCCCATAGCAAAGGCCTGCAGCTCTGTTCAGAATGCAGAAG... | TTATGCCCTGAGGTTGGCTGTTGAATCCCTCACGAAATGCTCCTCAGTGTGTTGCCTAACACACACTGCTGAGCTCACCCATTAAAATCTGCATGATGGAATTCAGCCCAATGCAATGAGAATTCCCATGGACTTCCTCTGTGCAAGGCAAAGCATGGGTGCTGTGGAAGGAGGATGAAAACAGGTAGAAGATGTAATCTCATCCTCAAGGGGTGCTCGGTAGAATGGAGGAAACAATACATAGATTCCTGAAGATGAGCACCAAAGTGATTGGGGTGGGCCCATAGCAAAGGCCTGCAGCTCTGTTCAGAATGCAGAAG... |
Task1_train_34838 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AACTCGCGTGCCAGCCAGGTGTGCATGACTAGCTCTGGGCAAGTCTGTTCTAGTAATTCAAGGTACCACCTCTCACTGGGACAGCCTAGTTTCTACACAGGTCTTGCTCTGGGACCGCCCTCAGCAGTGTGGTTAGCAGGCAGGGCCAGTGTGACCCTCCCTTTCTGGGCCTCAGTTGAGAAACCTGAAGCTCAGGAGAGGAGTCACTCCCCTGGCAGATGGGTGGCTGGGCCAGAAGCAGATACCAGGCTTTCTGACTCCTGCTCTAGGATTCTCACCACGTACTGGCTAGACTTATACTTCTCAAATCTTAATTTCCT... | AACTCGCGTGCCAGCCAGGTGTGCATGACTAGCTCTGGGCAAGTCTGTTCTAGTAATTCAAGGTACCACCTCTCACTGGGACAGCCTAGTTTCTACACAGGTCTTGCTCTGGGACCGCCCTCAGCAGTGTGGTTAGCAGGCAGGGCCAGTGTGACCCTCCCTTTCTGGGCCTCAGTTGAGAAACCTGAAGCTCAGGAGAGGAGTCACTCCCCTGGCAGATGGGTGGCTGGGCCAGAAGCAGATACCAGGCTTTCTGACTCCTGCTCTAGGATTCTCACCACGTACTGGCTAGACTTATACTTCTCAAATCTTAATTTCCT... |
Task1_train_34839 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | CAGCCAGGTGTGCATGACTAGCTCTGGGCAAGTCTGTTCTAGTAATTCAAGGTACCACCTCTCACTGGGACAGCCTAGTTTCTACACAGGTCTTGCTCTGGGACCGCCCTCAGCAGTGTGGTTAGCAGGCAGGGCCAGTGTGACCCTCCCTTTCTGGGCCTCAGTTGAGAAACCTGAAGCTCAGGAGAGGAGTCACTCCCCTGGCAGATGGGTGGCTGGGCCAGAAGCAGATACCAGGCTTTCTGACTCCTGCTCTAGGATTCTCACCACGTACTGGCTAGACTTATACTTCTCAAATCTTAATTTCCTAAAGGCAAGTA... | CAGCCAGGTGTGCATGACTAGCTCTGGGCAAGTCTGTTCTAGTAATTCAAGGTACCACCTCTCACTGGGACAGCCTAGTTTCTACACAGGTCTTGCTCTGGGACCGCCCTCAGCAGTGTGGTTAGCAGGCAGGGCCAGTGTGACCCTCCCTTTCTGGGCCTCAGTTGAGAAACCTGAAGCTCAGGAGAGGAGTCACTCCCCTGGCAGATGGGTGGCTGGGCCAGAAGCAGATACCAGGCTTTCTGACTCCTGCTCTAGGATTCTCACCACGTACTGGCTAGACTTATACTTCTCAAATCTTAATTTCCTAAAGGCAAGTA... |
Task1_train_34840 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TGCAGCCCAGACCCCTCCTCATCTCCAGACCCTGGAAGCTGATGCCTTGGGCTGCTCCTCCTATTTCCTGGGCACCAGGAATATGAGCTACTCCCTCCCCACAGTCCTGCTCTCCCCAGTGCTCCCATGTCGCTGAAGGCACCACCATCTTCCAAGATACATGGGCCTCCCCAGGGTCTAGGAGTCCTAGACGTGGGAGTAGAAATTAGATGACATTGGTGTCTAAACAAAACACCACTGCATGGAGATAGAACAGGGGAGCCCCCTGAATGTGGTGAGAGCACCCTCCCAGGTGTGTTCCACCCTCACCCCGGGCTCAT... | TGCAGCCCAGACCCCTCCTCATCTCCAGACCCTGGAAGCTGATGCCTTGGGCTGCTCCTCCTATTTCCTGGGCACCAGGAATATGAGCTACTCCCTCCCCACAGTCCTGCTCTCCCCAGTGCTCCCATGTCGCTGAAGGCACCACCATCTTCCAAGATACATGGGCCTCCCCAGGGTCTAGGAGTCCTAGACGTGGGAGTAGAAATTAGATGACATTGGTGTCTAAACAAAACACCACTGCATGGAGATAGAACAGGGGAGCCCCCTGAATGTGGTGAGAGCACCCTCCCAGGTGTGTTCCACCCTCACCCCGGGCTCAT... |
Task1_train_34841 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CTGATGCCTTGGGCTGCTCCTCCTATTTCCTGGGCACCAGGAATATGAGCTACTCCCTCCCCACAGTCCTGCTCTCCCCAGTGCTCCCATGTCGCTGAAGGCACCACCATCTTCCAAGATACATGGGCCTCCCCAGGGTCTAGGAGTCCTAGACGTGGGAGTAGAAATTAGATGACATTGGTGTCTAAACAAAACACCACTGCATGGAGATAGAACAGGGGAGCCCCCTGAATGTGGTGAGAGCACCCTCCCAGGTGTGTTCCACCCTCACCCCGGGCTCATCAGGAGGGTGCTTAGGATGCATACAGTTTTAAGGGGGT... | CTGATGCCTTGGGCTGCTCCTCCTATTTCCTGGGCACCAGGAATATGAGCTACTCCCTCCCCACAGTCCTGCTCTCCCCAGTGCTCCCATGTCGCTGAAGGCACCACCATCTTCCAAGATACATGGGCCTCCCCAGGGTCTAGGAGTCCTAGACGTGGGAGTAGAAATTAGATGACATTGGTGTCTAAACAAAACACCACTGCATGGAGATAGAACAGGGGAGCCCCCTGAATGTGGTGAGAGCACCCTCCCAGGTGTGTTCCACCCTCACCCCGGGCTCATCAGGAGGGTGCTTAGGATGCATACAGTTTTAAGGGGGT... |
Task1_train_34842 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | GTGAGAGCACCCTCCCAGGTGTGTTCCACCCTCACCCCGGGCTCATCAGGAGGGTGCTTAGGATGCATACAGTTTTAAGGGGGTTGGAGGAATAGTTCAGAGGCTGAGATGTTGCACCCACAGCTGAGAATCCCTTTCTAGCGCTCTGTGTCCTCACAACTCCCCGGGAATCATCCTCCCCTGGAGAGTTCCCAAAGCCCTTGCAGGCCTGCCTTCTCTGTGCCTTCCTGCCTGCGCCCTCTGGTGGACAGCTCCATTCGCTGCCTGTCCCATGGGTTCTGTCCAAAGGTGGAATCTATTATCAATGTGGATTTCTAATG... | GTGAGAGCACCCTCCCAGGTGTGTTCCACCCTCACCCCGGGCTCATCAGGAGGGTGCTTAGGATGCATACAGTTTTAAGGGGGTTGGAGGAATAGTTCAGAGGCTGAGATGTTGCACCCACAGCTGAGAATCCCTTTCTAGCGCTCTGTGTCCTCACAACTCCCCGGGAATCATCCTCCCCTGGAGAGTTCCCAAAGCCCTTGCAGGCCTGCCTTCTCTGTGCCTTCCTGCCTGCGCCCTCTGGTGGACAGCTCCATTCGCTGCCTGTCCCATGGGTTCTGTCCAAAGGTGGAATCTATTATCAATGTGGATTTCTAATG... |
Task1_train_34843 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGCTCCATTCGCTGCCTGTCCCATGGGTTCTGTCCAAAGGTGGAATCTATTATCAATGTGGATTTCTAATGGGGGTAACTTCCTCCCTAAGGGAAGCCTCAGCTTCACCAGCAATGGCAGACACGGCCAGGCATGTAGACACAGAGGAAGTGAGATAGAAAGTGTGCACAGCCCAGAGAGCCTGCCCACATCATCCTGGGGCGACCAGGACAAGGAGGCGTCAGCAATCTTGCCAAGCACAAGTATGAGTGACTTTCTGGAGCAGGACGAGTCTCATGGGCGTGAGACCATTGTGAGTGCTCAGGGTCTCTCCATTAGAA... | AGCTCCATTCGCTGCCTGTCCCATGGGTTCTGTCCAAAGGTGGAATCTATTATCAATGTGGATTTCTAATGGGGGTAACTTCCTCCCTAAGGGAAGCCTCAGCTTCACCAGCAATGGCAGACACGGCCAGGCATGTAGACACAGAGGAAGTGAGATAGAAAGTGTGCACAGCCCAGAGAGCCTGCCCACATCATCCTGGGGCGACCAGGACAAGGAGGCGTCAGCAATCTTGCCAAGCACAAGTATGAGTGACTTTCTGGAGCAGGACGAGTCTCATGGGCGTGAGACCATTGTGAGTGCTCAGGGTCTCTCCATTAGAA... |
Task1_train_34844 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TGGGGGTAACTTCCTCCCTAAGGGAAGCCTCAGCTTCACCAGCAATGGCAGACACGGCCAGGCATGTAGACACAGAGGAAGTGAGATAGAAAGTGTGCACAGCCCAGAGAGCCTGCCCACATCATCCTGGGGCGACCAGGACAAGGAGGCGTCAGCAATCTTGCCAAGCACAAGTATGAGTGACTTTCTGGAGCAGGACGAGTCTCATGGGCGTGAGACCATTGTGAGTGCTCAGGGTCTCTCCATTAGAAAGGCACACGTTTAATTCTCCATTTTGAAATTTGAACTAGAGCCCCCACAAATTATTCTGTTCTGGAGGA... | TGGGGGTAACTTCCTCCCTAAGGGAAGCCTCAGCTTCACCAGCAATGGCAGACACGGCCAGGCATGTAGACACAGAGGAAGTGAGATAGAAAGTGTGCACAGCCCAGAGAGCCTGCCCACATCATCCTGGGGCGACCAGGACAAGGAGGCGTCAGCAATCTTGCCAAGCACAAGTATGAGTGACTTTCTGGAGCAGGACGAGTCTCATGGGCGTGAGACCATTGTGAGTGCTCAGGGTCTCTCCATTAGAAAGGCACACGTTTAATTCTCCATTTTGAAATTTGAACTAGAGCCCCCACAAATTATTCTGTTCTGGAGGA... |
Task1_train_34845 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGGTAACTTCCTCCCTAAGGGAAGCCTCAGCTTCACCAGCAATGGCAGACACGGCCAGGCATGTAGACACAGAGGAAGTGAGATAGAAAGTGTGCACAGCCCAGAGAGCCTGCCCACATCATCCTGGGGCGACCAGGACAAGGAGGCGTCAGCAATCTTGCCAAGCACAAGTATGAGTGACTTTCTGGAGCAGGACGAGTCTCATGGGCGTGAGACCATTGTGAGTGCTCAGGGTCTCTCCATTAGAAAGGCACACGTTTAATTCTCCATTTTGAAATTTGAACTAGAGCCCCCACAAATTATTCTGTTCTGGAGGAACC... | GGGTAACTTCCTCCCTAAGGGAAGCCTCAGCTTCACCAGCAATGGCAGACACGGCCAGGCATGTAGACACAGAGGAAGTGAGATAGAAAGTGTGCACAGCCCAGAGAGCCTGCCCACATCATCCTGGGGCGACCAGGACAAGGAGGCGTCAGCAATCTTGCCAAGCACAAGTATGAGTGACTTTCTGGAGCAGGACGAGTCTCATGGGCGTGAGACCATTGTGAGTGCTCAGGGTCTCTCCATTAGAAAGGCACACGTTTAATTCTCCATTTTGAAATTTGAACTAGAGCCCCCACAAATTATTCTGTTCTGGAGGAACC... |
Task1_train_34846 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | CTTCACCAGCAATGGCAGACACGGCCAGGCATGTAGACACAGAGGAAGTGAGATAGAAAGTGTGCACAGCCCAGAGAGCCTGCCCACATCATCCTGGGGCGACCAGGACAAGGAGGCGTCAGCAATCTTGCCAAGCACAAGTATGAGTGACTTTCTGGAGCAGGACGAGTCTCATGGGCGTGAGACCATTGTGAGTGCTCAGGGTCTCTCCATTAGAAAGGCACACGTTTAATTCTCCATTTTGAAATTTGAACTAGAGCCCCCACAAATTATTCTGTTCTGGAGGAACCATTCTTATCAGAACTTGGTGCTGGATTGAC... | CTTCACCAGCAATGGCAGACACGGCCAGGCATGTAGACACAGAGGAAGTGAGATAGAAAGTGTGCACAGCCCAGAGAGCCTGCCCACATCATCCTGGGGCGACCAGGACAAGGAGGCGTCAGCAATCTTGCCAAGCACAAGTATGAGTGACTTTCTGGAGCAGGACGAGTCTCATGGGCGTGAGACCATTGTGAGTGCTCAGGGTCTCTCCATTAGAAAGGCACACGTTTAATTCTCCATTTTGAAATTTGAACTAGAGCCCCCACAAATTATTCTGTTCTGGAGGAACCATTCTTATCAGAACTTGGTGCTGGATTGAC... |
Task1_train_34847 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | GTCTGTGAGATTGGCAGAGGGGAACAAGACCACACAGGTCAGTCTTTCAGGATGCTTTTTTCTGTCTCTGGACTTTGCTGGGGTGACCTCACTGACACCCATGGCTTCCACATATGCGGATGGCTCCAAGTCTATCTGTGCAGCCCAGACCCCTCCTCATCTCCAGACCCTGGAAGCTGATGACTTGGGCAGCTCCTTCTGTTTCCCAGGCACCAGGAGCTCCTCCCTCCCCATAGTTCTGCTATCCTTAGGGCCCCTAGGTCTCTGGAGTACCACCGTCTTCCAAGATACATGGGCCTCCTCAGGGTCTGGGAGTCCCA... | GTCTGTGAGATTGGCAGAGGGGAACAAGACCACACAGGTCAGTCTTTCAGGATGCTTTTTTCTGTCTCTGGACTTTGCTGGGGTGACCTCACTGACACCCATGGCTTCCACATATGCGGATGGCTCCAAGTCTATCTGTGCAGCCCAGACCCCTCCTCATCTCCAGACCCTGGAAGCTGATGACTTGGGCAGCTCCTTCTGTTTCCCAGGCACCAGGAGCTCCTCCCTCCCCATAGTTCTGCTATCCTTAGGGCCCCTAGGTCTCTGGAGTACCACCGTCTTCCAAGATACATGGGCCTCCTCAGGGTCTGGGAGTCCCA... |
Task1_train_34848 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AAGACACACATGGCTCCGGTGCTCAGAAAGGACCAACAGGCAAACAAGGAAATAGACGTTTATAACAGGAGGTGACGGGTATGAAGAGAGCAGCCAAATGGGCGTTTGAGATCTGGCTAAGGGAGGGGACCTCATCTCTGCAGCCCTTGTTGAGGTAGCGATATTTCAGCTAAGACCTGAAGGCAGAGAGGAGGATGTCTGTGTGAAGCATAGGACCGGGAGAGCATTCCACACGGAGAGAACATTGCAGAGGCTCTGGGGCAGAGAAGAGCTTGGAATCTCTGAAGAGTTGAGAAGTGGCTGTGGCTGGAGTTAAGGAG... | AAGACACACATGGCTCCGGTGCTCAGAAAGGACCAACAGGCAAACAAGGAAATAGACGTTTATAACAGGAGGTGACGGGTATGAAGAGAGCAGCCAAATGGGCGTTTGAGATCTGGCTAAGGGAGGGGACCTCATCTCTGCAGCCCTTGTTGAGGTAGCGATATTTCAGCTAAGACCTGAAGGCAGAGAGGAGGATGTCTGTGTGAAGCATAGGACCGGGAGAGCATTCCACACGGAGAGAACATTGCAGAGGCTCTGGGGCAGAGAAGAGCTTGGAATCTCTGAAGAGTTGAGAAGTGGCTGTGGCTGGAGTTAAGGAG... |
Task1_train_34849 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AAGGGGTCCAGTGAGATAAGGCTGGAGAAGGCGGGAGGTGGAAGAGCTTCACGGCTTGCTGGGGATAAAGGCCTGGATGGAGTGGGAGGGGAGGAAGGGAAGGCAGGCCTGGAAAGAGGACAAGGGACAGCAGCGAGGGGGATTATTATGAAGTCTGAAGATGGGGGTGCACTCAGGGTGGGTGAAGTGGAGGGGCCTGCCTCCTGTTGCAGGGTGGCCTGTTACGGCTCCCTTCCTTCATCCGTCTGCTCTTTTTCTCTGCTGGCCTCGTGCCTTCTCTCAGTTCCTTGCTCTCACCTGCTGTCTCCCTGCTTCTGTGT... | AAGGGGTCCAGTGAGATAAGGCTGGAGAAGGCGGGAGGTGGAAGAGCTTCACGGCTTGCTGGGGATAAAGGCCTGGATGGAGTGGGAGGGGAGGAAGGGAAGGCAGGCCTGGAAAGAGGACAAGGGACAGCAGCGAGGGGGATTATTATGAAGTCTGAAGATGGGGGTGCACTCAGGGTGGGTGAAGTGGAGGGGCCTGCCTCCTGTTGCAGGGTGGCCTGTTACGGCTCCCTTCCTTCATCCGTCTGCTCTTTTTCTCTGCTGGCCTCGTGCCTTCTCTCAGTTCCTTGCTCTCACCTGCTGTCTCCCTGCTTCTGTGT... |
Task1_train_34850 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | GGTTGAGACTACAGGCGCCTGCCAACACGCCCGGCCAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCAACCGTGTTAGCCAGGATGACCTCGATCTCCTGACCTCGTGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGACACCGTGCCCTTCTAGCTCACTTTTTAATGCTTTTCTGACTCCTGGACTATTTCCTGGGCCCCAGCCAGGACAGAGGGCTAAGCCAGCTCTGGACTGTTAGGGGTTGGAGGTGGAGGGCAGCAGGGTTGTCCTCTCTGCCTTCTCTCTGCTCACCCCCAGCCC... | GGTTGAGACTACAGGCGCCTGCCAACACGCCCGGCCAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCAACCGTGTTAGCCAGGATGACCTCGATCTCCTGACCTCGTGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGACACCGTGCCCTTCTAGCTCACTTTTTAATGCTTTTCTGACTCCTGGACTATTTCCTGGGCCCCAGCCAGGACAGAGGGCTAAGCCAGCTCTGGACTGTTAGGGGTTGGAGGTGGAGGGCAGCAGGGTTGTCCTCTCTGCCTTCTCTCTGCTCACCCCCAGCCC... |
Task1_train_34851 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | GCTTCCAGCCCCTCTGGCGCCAAGTGCATTCCCCTGTTGCTGTTGGTAGCCATGGAGACCTTCTGTGAGACGGTGCAGTTTTATCTGAAGCACCTGGAGGAGAGCGTGTACCCCGTGATGACTGAGGAGGAGTTTGCCCTGAAGGTGTTCCCCATGTATCGCTACTTCGTGACAGTGTGGCTGAGGCACTACAACCCCGAGGTGAGATGCACCCCTCTTAGGAGGGCCTGGTGGTCCCCAGGCCACAGCTCCCCAGCCTGTGGGGCCGGGAGGTGCTGAGGGACCGTCGGGTCCACACTTACTCCCAGGACCCTAGAGGG... | GCTTCCAGCCCCTCTGGCGCCAAGTGCATTCCCCTGTTGCTGTTGGTAGCCATGGAGACCTTCTGTGAGACGGTGCAGTTTTATCTGAAGCACCTGGAGGAGAGCGTGTACCCCGTGATGACTGAGGAGGAGTTTGCCCTGAAGGTGTTCCCCATGTATCGCTACTTCGTGACAGTGTGGCTGAGGCACTACAACCCCGAGGTGAGATGCACCCCTCTTAGGAGGGCCTGGTGGTCCCCAGGCCACAGCTCCCCAGCCTGTGGGGCCGGGAGGTGCTGAGGGACCGTCGGGTCCACACTTACTCCCAGGACCCTAGAGGG... |
Task1_train_34852 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTAAGCTTCCTGCTTTAGTTGGGTGTGCTGTCATCAGTTGTACAACTAGCAAACACTTGCCCAGCCCTTACGGTGTGCCAGACTCTGTGTTAACTCTGTGAGAGAGGCACTGTCATTATCCACACTTTACAGGCGAGGAAACTGAGGCGCAGAGGGGCTACGTAATTCACTTTACGTCCCACAGCTGGGATGTGGTGGAGCCAGGATTTGAACCCAGGGAAGGCCTGGTGTCAGGACCCATGCTCTTCACGGTGGTGCTTTGCAACCTCTGTGTGCCCACTGCATGCCCACTTCATGCCCAGTGCTCTGTGCCCAGCTGC... | TTAAGCTTCCTGCTTTAGTTGGGTGTGCTGTCATCAGTTGTACAACTAGCAAACACTTGCCCAGCCCTTACGGTGTGCCAGACTCTGTGTTAACTCTGTGAGAGAGGCACTGTCATTATCCACACTTTACAGGCGAGGAAACTGAGGCGCAGAGGGGCTACGTAATTCACTTTACGTCCCACAGCTGGGATGTGGTGGAGCCAGGATTTGAACCCAGGGAAGGCCTGGTGTCAGGACCCATGCTCTTCACGGTGGTGCTTTGCAACCTCTGTGTGCCCACTGCATGCCCACTTCATGCCCAGTGCTCTGTGCCCAGCTGC... |
Task1_train_34853 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | CAGATCTGCTAAAAATTTGCAAGGATAGTGCAAAGATACTCTTCATGCAGATTCACAGTTCTTAATACTTTGTCACATTTTCTTTCTCGGTTTTCTTCTGCCTCTGTCCTTCCACACACACACATCTTTTGAACCACGGATAGCTGCAGACATCCAGAGTAACAGTACTCTCTTATATAACAACAGTACCATGATCAAATTCAGGACATTTAATGTTGACACGATGCATGTATTAAAACTGATGGCCCATATTCAAATTTCATGAATTGCCCCAGTAATGTCCTTTAGAGCTGTTTTCTCCTCGATCCAGGATATAATCC... | CAGATCTGCTAAAAATTTGCAAGGATAGTGCAAAGATACTCTTCATGCAGATTCACAGTTCTTAATACTTTGTCACATTTTCTTTCTCGGTTTTCTTCTGCCTCTGTCCTTCCACACACACACATCTTTTGAACCACGGATAGCTGCAGACATCCAGAGTAACAGTACTCTCTTATATAACAACAGTACCATGATCAAATTCAGGACATTTAATGTTGACACGATGCATGTATTAAAACTGATGGCCCATATTCAAATTTCATGAATTGCCCCAGTAATGTCCTTTAGAGCTGTTTTCTCCTCGATCCAGGATATAATCC... |
Task1_train_34854 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTCATGATGGGGCCTGTCTAGAACCACAAGGAAGCATTGAAAGTCGATCTGAGTAGGAGGGTGAGGTGGGCAAAAGCTGGCCAGGAAAGGGCTGGCCCCAGGATTTTAACACCCACTTTGGTGTTCTGGGCTCTACCCATAGCTCCTGGAAAAGTGGATCTTGTCGGAGAAAGAATGGGAGCGGGAAAAGGCCGTGAGCCTCCATCTCTATCTCATGTGGATTTATGTCCACAGCACTGCTGTCTGTGTGAGTCCAGGAGTCCCCAGCCCCCAGCCTGCTGCTCTGACATGCACAGAAAAATTCCTGTGTCTATCTGGAA... | TTCATGATGGGGCCTGTCTAGAACCACAAGGAAGCATTGAAAGTCGATCTGAGTAGGAGGGTGAGGTGGGCAAAAGCTGGCCAGGAAAGGGCTGGCCCCAGGATTTTAACACCCACTTTGGTGTTCTGGGCTCTACCCATAGCTCCTGGAAAAGTGGATCTTGTCGGAGAAAGAATGGGAGCGGGAAAAGGCCGTGAGCCTCCATCTCTATCTCATGTGGATTTATGTCCACAGCACTGCTGTCTGTGTGAGTCCAGGAGTCCCCAGCCCCCAGCCTGCTGCTCTGACATGCACAGAAAAATTCCTGTGTCTATCTGGAA... |
Task1_train_34855 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GGAGTCAGGGTCTGGGGCGCAGGGATGGGCGTCTGGTGCAGGGAGAGAAGTGGGCTGGGCAGGAGGACCCTGGTCCTGGGCACCTGGATGGAGGTGGGGATGAAGGCTCAGCAAAATGAGGCAGGGGCCAAGTCCAACACTCAGTAACATGTGAGGCCAGAGGCTGTGTGGAAGGCTTCACCTGGGCTCTCATGACATTCCCTGCAAGAGGAGGTGCCATCATCATCTCCACTGTGCAGACAGGAAACATGAGACTGAGAGGCAGAGTACCCTGCCTGGACTGCTCAGCTAGTGAGCAGGAAGCTCTGATTTGATCCCCA... | GGAGTCAGGGTCTGGGGCGCAGGGATGGGCGTCTGGTGCAGGGAGAGAAGTGGGCTGGGCAGGAGGACCCTGGTCCTGGGCACCTGGATGGAGGTGGGGATGAAGGCTCAGCAAAATGAGGCAGGGGCCAAGTCCAACACTCAGTAACATGTGAGGCCAGAGGCTGTGTGGAAGGCTTCACCTGGGCTCTCATGACATTCCCTGCAAGAGGAGGTGCCATCATCATCTCCACTGTGCAGACAGGAAACATGAGACTGAGAGGCAGAGTACCCTGCCTGGACTGCTCAGCTAGTGAGCAGGAAGCTCTGATTTGATCCCCA... |
Task1_train_34856 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGGACTTGGAAACCAGGAAGGCCCTTTTCCAACTGTAGTTTGGCAGGTGGCCTGACTGCTGCAAGCCTCACTTCCCTCTTCTGTGGAATAGGGAGACAAAATACCTTCCTCAAAGATGTGTTGGGAGGGTTAGGTGATATAATATCAGAAAGCTACCGACAACCAACCTGATGCAAATTGGGCACTAGGAGGTATTGTGGGACATGTCCGTACAGTCATCAAACAGGTGGGGGTCTCTGTGGTCATCTAGCAGTGGAGGTGGGGCTTCCGTGGGGGCCATGGCTTTCCCAAAGGTACCGTGAGCCCGTGCAGAGAAAGGG... | TGGACTTGGAAACCAGGAAGGCCCTTTTCCAACTGTAGTTTGGCAGGTGGCCTGACTGCTGCAAGCCTCACTTCCCTCTTCTGTGGAATAGGGAGACAAAATACCTTCCTCAAAGATGTGTTGGGAGGGTTAGGTGATATAATATCAGAAAGCTACCGACAACCAACCTGATGCAAATTGGGCACTAGGAGGTATTGTGGGACATGTCCGTACAGTCATCAAACAGGTGGGGGTCTCTGTGGTCATCTAGCAGTGGAGGTGGGGCTTCCGTGGGGGCCATGGCTTTCCCAAAGGTACCGTGAGCCCGTGCAGAGAAAGGG... |
Task1_train_34857 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGGAAACCAGGAAGGCCCTTTTCCAACTGTAGTTTGGCAGGTGGCCTGACTGCTGCAAGCCTCACTTCCCTCTTCTGTGGAATAGGGAGACAAAATACCTTCCTCAAAGATGTGTTGGGAGGGTTAGGTGATATAATATCAGAAAGCTACCGACAACCAACCTGATGCAAATTGGGCACTAGGAGGTATTGTGGGACATGTCCGTACAGTCATCAAACAGGTGGGGGTCTCTGTGGTCATCTAGCAGTGGAGGTGGGGCTTCCGTGGGGGCCATGGCTTTCCCAAAGGTACCGTGAGCCCGTGCAGAGAAAGGGGGTTGA... | TGGAAACCAGGAAGGCCCTTTTCCAACTGTAGTTTGGCAGGTGGCCTGACTGCTGCAAGCCTCACTTCCCTCTTCTGTGGAATAGGGAGACAAAATACCTTCCTCAAAGATGTGTTGGGAGGGTTAGGTGATATAATATCAGAAAGCTACCGACAACCAACCTGATGCAAATTGGGCACTAGGAGGTATTGTGGGACATGTCCGTACAGTCATCAAACAGGTGGGGGTCTCTGTGGTCATCTAGCAGTGGAGGTGGGGCTTCCGTGGGGGCCATGGCTTTCCCAAAGGTACCGTGAGCCCGTGCAGAGAAAGGGGGTTGA... |
Task1_train_34858 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | AGCAATGCCCAGCCCCTTGAGGGCTACGTGATCCCTGCCAAAGGAGAGACTACACCCTGACGGAATGATCCAGAAGGCTCTGCAGGGACCAAGGCATTGGGTATTCCTTGGAGAATGGCTGGGGTTTTGCTGGGCTTCCTGCTGCCTGCATGTCAGCCTGTGTCCATCCTGGCCACAGGAGAGCGAGCTGCTGCGTCTGAAAGCCTTCATCCTCTTTGGAAAGCTGGCAAGGGTGGTCGGGATGTCCAAGAAGCATTTCTTCAAAGGGGAGGTGAAGAAGGCCTGGATCCCCCTCATGCTGCACTCCCAGGACCCCTGCT... | AGCAATGCCCAGCCCCTTGAGGGCTACGTGATCCCTGCCAAAGGAGAGACTACACCCTGACGGAATGATCCAGAAGGCTCTGCAGGGACCAAGGCATTGGGTATTCCTTGGAGAATGGCTGGGGTTTTGCTGGGCTTCCTGCTGCCTGCATGTCAGCCTGTGTCCATCCTGGCCACAGGAGAGCGAGCTGCTGCGTCTGAAAGCCTTCATCCTCTTTGGAAAGCTGGCAAGGGTGGTCGGGATGTCCAAGAAGCATTTCTTCAAAGGGGAGGTGAAGAAGGCCTGGATCCCCCTCATGCTGCACTCCCAGGACCCCTGCT... |
Task1_train_34859 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GGCTACGTGATCCCTGCCAAAGGAGAGACTACACCCTGACGGAATGATCCAGAAGGCTCTGCAGGGACCAAGGCATTGGGTATTCCTTGGAGAATGGCTGGGGTTTTGCTGGGCTTCCTGCTGCCTGCATGTCAGCCTGTGTCCATCCTGGCCACAGGAGAGCGAGCTGCTGCGTCTGAAAGCCTTCATCCTCTTTGGAAAGCTGGCAAGGGTGGTCGGGATGTCCAAGAAGCATTTCTTCAAAGGGGAGGTGAAGAAGGCCTGGATCCCCCTCATGCTGCACTCCCAGGACCCCTGCTCCAATGCAGCCCAAGTAAGAT... | GGCTACGTGATCCCTGCCAAAGGAGAGACTACACCCTGACGGAATGATCCAGAAGGCTCTGCAGGGACCAAGGCATTGGGTATTCCTTGGAGAATGGCTGGGGTTTTGCTGGGCTTCCTGCTGCCTGCATGTCAGCCTGTGTCCATCCTGGCCACAGGAGAGCGAGCTGCTGCGTCTGAAAGCCTTCATCCTCTTTGGAAAGCTGGCAAGGGTGGTCGGGATGTCCAAGAAGCATTTCTTCAAAGGGGAGGTGAAGAAGGCCTGGATCCCCCTCATGCTGCACTCCCAGGACCCCTGCTCCAATGCAGCCCAAGTAAGAT... |
Task1_train_34860 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGATCCCATGGAGGGCTGGGTCCCAGGCAGGGCTGCTGAGGGCACGAAGGTGCTGGCTGAGGGGGCGGGTGGGGCTGCATCTGCCCCCAAGGGGCTTTCTATAAATGTACCTGCAGCCATGTTCAAGCTGGCAGGGGCCCAGGTCCCAGGTGGCCTCCCAGGAGCCACCAGCCCTGCCTTTCTTTGGCTTGGTGAGGCTTTTCTGGGGCTGCCCTCTGGCTTCCTGCCAGCCTCACCCCTCTGGGGAACCACGTGGCCTGGCTGATGGCTCTGCTGCCGTCCTGTGTCCCTGCAGGCCTGTATGGCTACCATGTTTCAGT... | TGATCCCATGGAGGGCTGGGTCCCAGGCAGGGCTGCTGAGGGCACGAAGGTGCTGGCTGAGGGGGCGGGTGGGGCTGCATCTGCCCCCAAGGGGCTTTCTATAAATGTACCTGCAGCCATGTTCAAGCTGGCAGGGGCCCAGGTCCCAGGTGGCCTCCCAGGAGCCACCAGCCCTGCCTTTCTTTGGCTTGGTGAGGCTTTTCTGGGGCTGCCCTCTGGCTTCCTGCCAGCCTCACCCCTCTGGGGAACCACGTGGCCTGGCTGATGGCTCTGCTGCCGTCCTGTGTCCCTGCAGGCCTGTATGGCTACCATGTTTCAGT... |
Task1_train_34861 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AAAGGAAGAGCTGGGGCACTATCTGAGAAAAAGCAGTTAGGTTTAGACAAGCAGGACGAGCAGAGCAGAGGAGCTCTGATGTGTGGGAGACCAGGAGAAACCTCAGATCTCTCTCTGGGCCGGACAGTTGTTTTTGGTGAAATTCTCCCCTTTCAACTGAGAAGGAGACTCTTGAGAGGTCATCTGTTAAACAGAACGCATAAACTTTGCCTCAAAGCAGCCTCCATGAAGTGTCTGCCATGAAGATGTAGCTGAGATTCTTGAAGGCTTCACTAACTGTGGCTGAAAGTCACCCGGCTGGTGGTTTGGTCTGAAAAAGC... | AAAGGAAGAGCTGGGGCACTATCTGAGAAAAAGCAGTTAGGTTTAGACAAGCAGGACGAGCAGAGCAGAGGAGCTCTGATGTGTGGGAGACCAGGAGAAACCTCAGATCTCTCTCTGGGCCGGACAGTTGTTTTTGGTGAAATTCTCCCCTTTCAACTGAGAAGGAGACTCTTGAGAGGTCATCTGTTAAACAGAACGCATAAACTTTGCCTCAAAGCAGCCTCCATGAAGTGTCTGCCATGAAGATGTAGCTGAGATTCTTGAAGGCTTCACTAACTGTGGCTGAAAGTCACCCGGCTGGTGGTTTGGTCTGAAAAAGC... |
Task1_train_34862 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | GAAACCTCAGATCTCTCTCTGGGCCGGACAGTTGTTTTTGGTGAAATTCTCCCCTTTCAACTGAGAAGGAGACTCTTGAGAGGTCATCTGTTAAACAGAACGCATAAACTTTGCCTCAAAGCAGCCTCCATGAAGTGTCTGCCATGAAGATGTAGCTGAGATTCTTGAAGGCTTCACTAACTGTGGCTGAAAGTCACCCGGCTGGTGGTTTGGTCTGAAAAAGCCCCAAGTGGGCACAGGAGTGGGCATCAGGCACACAGTTGGAGACCAAGACCCGAGGGAAAGACTGCTGTTAGCCGTGCACTGCCAGGGGAGGAGCT... | GAAACCTCAGATCTCTCTCTGGGCCGGACAGTTGTTTTTGGTGAAATTCTCCCCTTTCAACTGAGAAGGAGACTCTTGAGAGGTCATCTGTTAAACAGAACGCATAAACTTTGCCTCAAAGCAGCCTCCATGAAGTGTCTGCCATGAAGATGTAGCTGAGATTCTTGAAGGCTTCACTAACTGTGGCTGAAAGTCACCCGGCTGGTGGTTTGGTCTGAAAAAGCCCCAAGTGGGCACAGGAGTGGGCATCAGGCACACAGTTGGAGACCAAGACCCGAGGGAAAGACTGCTGTTAGCCGTGCACTGCCAGGGGAGGAGCT... |
Task1_train_34863 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | ACAGATGACAACCAAGGCTTGTTTCATCTGCTTCTGGTTAGCTCACACAGTATGACTTTATACACGAAAATAACTTTGAAAACCAAAACATCCAACAAAACCTGGGAGCTTCTAGAACTGAGCCAAGGAGCCTGAGCCGCTAACCCATGAGACTGGTCTGTGTCCAGACAGCTCCCCACTGCAGCACCCACCATGTGCAGCCCCTGGGAGGGTGGGGGTTACCTGCACGGAGCAGGCAGCTGAGCGGTGGGTGGAGTCTAGGGAGGATGTCCGAGGATGCAATAGCAAAGAACTGGGGAGTAGGGGGAGAATGCCAGTGA... | ACAGATGACAACCAAGGCTTGTTTCATCTGCTTCTGGTTAGCTCACACAGTATGACTTTATACACGAAAATAACTTTGAAAACCAAAACATCCAACAAAACCTGGGAGCTTCTAGAACTGAGCCAAGGAGCCTGAGCCGCTAACCCATGAGACTGGTCTGTGTCCAGACAGCTCCCCACTGCAGCACCCACCATGTGCAGCCCCTGGGAGGGTGGGGGTTACCTGCACGGAGCAGGCAGCTGAGCGGTGGGTGGAGTCTAGGGAGGATGTCCGAGGATGCAATAGCAAAGAACTGGGGAGTAGGGGGAGAATGCCAGTGA... |
Task1_train_34864 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GATGACAACCAAGGCTTGTTTCATCTGCTTCTGGTTAGCTCACACAGTATGACTTTATACACGAAAATAACTTTGAAAACCAAAACATCCAACAAAACCTGGGAGCTTCTAGAACTGAGCCAAGGAGCCTGAGCCGCTAACCCATGAGACTGGTCTGTGTCCAGACAGCTCCCCACTGCAGCACCCACCATGTGCAGCCCCTGGGAGGGTGGGGGTTACCTGCACGGAGCAGGCAGCTGAGCGGTGGGTGGAGTCTAGGGAGGATGTCCGAGGATGCAATAGCAAAGAACTGGGGAGTAGGGGGAGAATGCCAGTGAAAG... | GATGACAACCAAGGCTTGTTTCATCTGCTTCTGGTTAGCTCACACAGTATGACTTTATACACGAAAATAACTTTGAAAACCAAAACATCCAACAAAACCTGGGAGCTTCTAGAACTGAGCCAAGGAGCCTGAGCCGCTAACCCATGAGACTGGTCTGTGTCCAGACAGCTCCCCACTGCAGCACCCACCATGTGCAGCCCCTGGGAGGGTGGGGGTTACCTGCACGGAGCAGGCAGCTGAGCGGTGGGTGGAGTCTAGGGAGGATGTCCGAGGATGCAATAGCAAAGAACTGGGGAGTAGGGGGAGAATGCCAGTGAAAG... |
Task1_train_34865 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CCTGTGAGAATACTGTGCTCGTGGCTCTCCCAGGCCACTCTTGCTCTTTCCCTACCAGGAATCCAGAAATAGGAAGTCATTCGCTTTAGATCACTTTCGCCTTACAACAGCTATTTTCTGAGTGTCAGATGAAGAGGTTAGAAATGAAGGTTTGACAAAGACGAATAAAGCGTAGTAAGTGAGGATTTGCAGGAAAAAAGCCTCTGAATGCATTCTAATGGAAAGTGTGAAACTTCTGCAAGAGCACTTTCTGCTTTACCTCGATGCATCTTACACAGGGACACATTCTTGATAGAGACGCTGACTTTACAGGAAGGAAA... | CCTGTGAGAATACTGTGCTCGTGGCTCTCCCAGGCCACTCTTGCTCTTTCCCTACCAGGAATCCAGAAATAGGAAGTCATTCGCTTTAGATCACTTTCGCCTTACAACAGCTATTTTCTGAGTGTCAGATGAAGAGGTTAGAAATGAAGGTTTGACAAAGACGAATAAAGCGTAGTAAGTGAGGATTTGCAGGAAAAAAGCCTCTGAATGCATTCTAATGGAAAGTGTGAAACTTCTGCAAGAGCACTTTCTGCTTTACCTCGATGCATCTTACACAGGGACACATTCTTGATAGAGACGCTGACTTTACAGGAAGGAAA... |
Task1_train_34866 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | GAGAAAAAGTGCCCCGTGGTGGCCTCTGCGTAAGCTCAGAGGTTGGGCATACCCACACCTTTATTCATATGAATACTCCTCCACAGCAAGGTTATTTGGCAATAAAATTTGACACTAAATACCTGGATCTCTCCTTCGTTTCTTTCCTTTATTAGTCTTCCACCCCAAATTCTCAATCCTGAAGAAAAGAAACAAAAATGACCATTTACATAATCCTGAACGCTGAACTTCTGCTCAATCTGTGTTCACCAGATGCCAAAGTGACAGGCAAAAAAAAGGTACAATATTAAAACCAAGCCAGGTTTCTGATACCCTGCGAT... | GAGAAAAAGTGCCCCGTGGTGGCCTCTGCGTAAGCTCAGAGGTTGGGCATACCCACACCTTTATTCATATGAATACTCCTCCACAGCAAGGTTATTTGGCAATAAAATTTGACACTAAATACCTGGATCTCTCCTTCGTTTCTTTCCTTTATTAGTCTTCCACCCCAAATTCTCAATCCTGAAGAAAAGAAACAAAAATGACCATTTACATAATCCTGAACGCTGAACTTCTGCTCAATCTGTGTTCACCAGATGCCAAAGTGACAGGCAAAAAAAAGGTACAATATTAAAACCAAGCCAGGTTTCTGATACCCTGCGAT... |
Task1_train_34867 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GCTTTGAACTAAGACCTCCATCACCACCTTTCCCAGGCAGCTGCAGCCTCAAAAGCTCACCTTCTAATTTCCAAATCCAAGGGCTCTTTTTGCCACCTTCAAACAGCCAGACCCTGAGACTTCGTCTCCCACCCAGCGGAGCCTCTGCAGTTCCAGATCCTTATTTCCAAACGTTGCCAGGGAAACCCATCATTGCCTCAAACTCAGTCTAATGGAAACCAGACTTGCTCCCTTGGCTAGAAGGGGCCCTTCTCACCAAGCTCCAGCTGGGCTCGCCAGTGCTTGTAACCTTGAAATTACAGGGTTATTTACTTTTTAAA... | GCTTTGAACTAAGACCTCCATCACCACCTTTCCCAGGCAGCTGCAGCCTCAAAAGCTCACCTTCTAATTTCCAAATCCAAGGGCTCTTTTTGCCACCTTCAAACAGCCAGACCCTGAGACTTCGTCTCCCACCCAGCGGAGCCTCTGCAGTTCCAGATCCTTATTTCCAAACGTTGCCAGGGAAACCCATCATTGCCTCAAACTCAGTCTAATGGAAACCAGACTTGCTCCCTTGGCTAGAAGGGGCCCTTCTCACCAAGCTCCAGCTGGGCTCGCCAGTGCTTGTAACCTTGAAATTACAGGGTTATTTACTTTTTAAA... |
Task1_train_34868 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | ATTTCACAGGAGGAGGTAGGTGGGGCTTCAAGGCCCAGGGATGCTCCCAGCTAAGCGCATCTCTGTAACCCAGTTAATGTAAATGAATAGAAACTGTCTACCTGATTTCCTAACACTTTCCCAAGGAAGTGTGATTATTTCCTTTCAAAGGAAAAGGAAACTGGCAGGTGATTTTCTGGGGTCGGGGGGGCAATTTGATAGAATACGATGACTGTGGACTTCATCACATTAGAAAAGATGTAGGTTTAGTTTAACTAAAAACGGATTCCTTTCTTTGGTCATTTGCTTTGGCAACTTAAAAAAAAAAAAGAAAGAAAGAA... | ATTTCACAGGAGGAGGTAGGTGGGGCTTCAAGGCCCAGGGATGCTCCCAGCTAAGCGCATCTCTGTAACCCAGTTAATGTAAATGAATAGAAACTGTCTACCTGATTTCCTAACACTTTCCCAAGGAAGTGTGATTATTTCCTTTCAAAGGAAAAGGAAACTGGCAGGTGATTTTCTGGGGTCGGGGGGGCAATTTGATAGAATACGATGACTGTGGACTTCATCACATTAGAAAAGATGTAGGTTTAGTTTAACTAAAAACGGATTCCTTTCTTTGGTCATTTGCTTTGGCAACTTAAAAAAAAAAAAGAAAGAAAGAA... |
Task1_train_34869 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GAAGTGTGATTATTTCCTTTCAAAGGAAAAGGAAACTGGCAGGTGATTTTCTGGGGTCGGGGGGGCAATTTGATAGAATACGATGACTGTGGACTTCATCACATTAGAAAAGATGTAGGTTTAGTTTAACTAAAAACGGATTCCTTTCTTTGGTCATTTGCTTTGGCAACTTAAAAAAAAAAAAGAAAGAAAGAAAGAAAGAAACGTTTCCTTTCTTTCTTTCAATTGTTTATTACGGGAAGCCAGAATGTCAGCAGACTCCGTAAGTGAGGCAGTTTGGGAGGTGGGGGAGGGGAGTCCTGGGGAGAAGTATATGTGCT... | GAAGTGTGATTATTTCCTTTCAAAGGAAAAGGAAACTGGCAGGTGATTTTCTGGGGTCGGGGGGGCAATTTGATAGAATACGATGACTGTGGACTTCATCACATTAGAAAAGATGTAGGTTTAGTTTAACTAAAAACGGATTCCTTTCTTTGGTCATTTGCTTTGGCAACTTAAAAAAAAAAAAGAAAGAAAGAAAGAAAGAAACGTTTCCTTTCTTTCTTTCAATTGTTTATTACGGGAAGCCAGAATGTCAGCAGACTCCGTAAGTGAGGCAGTTTGGGAGGTGGGGGAGGGGAGTCCTGGGGAGAAGTATATGTGCT... |
Task1_train_34870 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TTTCTAGTCACCCTTCGTCTTTATGCCATCCCATCATTGGGGGTGGTGACTTCACACACATTTGAGATTTGAAAGCATGATGACTGTACTTCAAAGTTGGGGAATTCCATGGCCCACCCCACAACCCACTCATGTCAAGTGCATTCCAGGGAGCAATGGGTTTCCAGGTCCAAGTCCATCTGGGGGATTGTGGTCTGTGGTGGGCAGGGGCTGACTAACCTGCCCAAGGGGTTTAGCAAGGGAATGGCTGTTCCGGGACCTGGCCCAGCATCCTCCCACTGTACACAGCCTCCCTGCACAACCTACAGAGGGGGCTCCCA... | TTTCTAGTCACCCTTCGTCTTTATGCCATCCCATCATTGGGGGTGGTGACTTCACACACATTTGAGATTTGAAAGCATGATGACTGTACTTCAAAGTTGGGGAATTCCATGGCCCACCCCACAACCCACTCATGTCAAGTGCATTCCAGGGAGCAATGGGTTTCCAGGTCCAAGTCCATCTGGGGGATTGTGGTCTGTGGTGGGCAGGGGCTGACTAACCTGCCCAAGGGGTTTAGCAAGGGAATGGCTGTTCCGGGACCTGGCCCAGCATCCTCCCACTGTACACAGCCTCCCTGCACAACCTACAGAGGGGGCTCCCA... |
Task1_train_34871 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GTCGGCTGTGGCATGGGCCTTTCTCTTTGAGGGAGTGAGTTGTGTGTCCTTGGAAGGCATTTCCCATTGCCCAGTTTCATTCTCTTTAAGAGCCCCTGTTGGGCAAATGGGAGGGTTGCGACAAGATTGAAATCCCTTTTCCATGGTCACAGCCCTCAGTGTGTAACAGGACATCTCCGCAACCCTCAAACAGGTTAATCCCACACAGGGGCCTGGCTGACTTTCCCTCTTCTCTGGATTCCAACTAGGGATAGAGAAGTGGAGGTATGACCTTAGCACAGAGGCGTTGCCACTTTGGGAAGAAGAAAGTGCCTCACGGC... | GTCGGCTGTGGCATGGGCCTTTCTCTTTGAGGGAGTGAGTTGTGTGTCCTTGGAAGGCATTTCCCATTGCCCAGTTTCATTCTCTTTAAGAGCCCCTGTTGGGCAAATGGGAGGGTTGCGACAAGATTGAAATCCCTTTTCCATGGTCACAGCCCTCAGTGTGTAACAGGACATCTCCGCAACCCTCAAACAGGTTAATCCCACACAGGGGCCTGGCTGACTTTCCCTCTTCTCTGGATTCCAACTAGGGATAGAGAAGTGGAGGTATGACCTTAGCACAGAGGCGTTGCCACTTTGGGAAGAAGAAAGTGCCTCACGGC... |
Task1_train_34872 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGGGTGCATGCAATGAAGGGTGACGCTTCCGACTGTGCAGAGAGGGGCGAGGGGTCTCTGCCTTAGGGCGGCCAGGAACGTACATCAGGGTGTTCTTGGGACCGTATGTATTTCTCAGATACCTTAAATTGTGTGTTTGTACATTTCTCAACATATGATAAAATTTCCTAGAACTTCACAAAATAAAAATATTTTCAATTCATTTTGATTTCCATTATCTTTGTATTTGAAATCATGTCACTGTTCTGCTCAGAACCCTGCATGGCTCCCCATTCCCCCCAAAGCACAGGCGAGGGTCCTCACGGTGGCCCGCAAGCCCC... | AGGGTGCATGCAATGAAGGGTGACGCTTCCGACTGTGCAGAGAGGGGCGAGGGGTCTCTGCCTTAGGGCGGCCAGGAACGTACATCAGGGTGTTCTTGGGACCGTATGTATTTCTCAGATACCTTAAATTGTGTGTTTGTACATTTCTCAACATATGATAAAATTTCCTAGAACTTCACAAAATAAAAATATTTTCAATTCATTTTGATTTCCATTATCTTTGTATTTGAAATCATGTCACTGTTCTGCTCAGAACCCTGCATGGCTCCCCATTCCCCCCAAAGCACAGGCGAGGGTCCTCACGGTGGCCCGCAAGCCCC... |
Task1_train_34873 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GTTGTGAGGAGGGGTGGGGCAGTGGCCAGCCCACAAGAGGCCGAGTGAAACGTTGGCCACAGGGGTCTTTTGGGTTTCGCCCTGGAACAGGCTAGTGACTTTGGTTGTGCTGCGTCCATGGTCAGGAGGTAGAGGCCTGGTTGTCAGTGATCCGGAGGTGCAGAAGCAGAGGGAGCCAGTGGGGAGGTGGGCTGTGCAGACACAAAGGGAGAGGCACAGGCGAGGAGGGGTCCACGCCAGCTGTGTGCCATGCCTCCACCCTCCACAGCCCCAGGCCAGGGCCTCCTCTGTGTCCCCGCTGCCCTCTTCCTTCTCGTGCC... | GTTGTGAGGAGGGGTGGGGCAGTGGCCAGCCCACAAGAGGCCGAGTGAAACGTTGGCCACAGGGGTCTTTTGGGTTTCGCCCTGGAACAGGCTAGTGACTTTGGTTGTGCTGCGTCCATGGTCAGGAGGTAGAGGCCTGGTTGTCAGTGATCCGGAGGTGCAGAAGCAGAGGGAGCCAGTGGGGAGGTGGGCTGTGCAGACACAAAGGGAGAGGCACAGGCGAGGAGGGGTCCACGCCAGCTGTGTGCCATGCCTCCACCCTCCACAGCCCCAGGCCAGGGCCTCCTCTGTGTCCCCGCTGCCCTCTTCCTTCTCGTGCC... |
Task1_train_34874 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CTGCCTTCTCTGGGAAATGCTAAATCCCCAACCCAGCCCCACCCTACCCTAGCGCTCAGTAAACCCACCCTGGATTCCTGAGTCTTCTCAGGGACTGATGGGGAGAAGCCATAGGTGGGGATCTAGCTCAGCCACAGTGTGGGCCAGCACCGTCTCCAGGTCCTTGGCGATGCAGTCAGGAAGTCTGAATCAGCTTTCTGTAACTCCCGCCCTCTGGTCCCAGTTCTGCCACCAGGAGGGACGTGAATTAAGGCTCAGGAAGCCGGAATCAGCTTTCTGTAACTCCCGCCCTCTGGTCCCAGTTCTGCCACCAGGAGGGA... | CTGCCTTCTCTGGGAAATGCTAAATCCCCAACCCAGCCCCACCCTACCCTAGCGCTCAGTAAACCCACCCTGGATTCCTGAGTCTTCTCAGGGACTGATGGGGAGAAGCCATAGGTGGGGATCTAGCTCAGCCACAGTGTGGGCCAGCACCGTCTCCAGGTCCTTGGCGATGCAGTCAGGAAGTCTGAATCAGCTTTCTGTAACTCCCGCCCTCTGGTCCCAGTTCTGCCACCAGGAGGGACGTGAATTAAGGCTCAGGAAGCCGGAATCAGCTTTCTGTAACTCCCGCCCTCTGGTCCCAGTTCTGCCACCAGGAGGGA... |
Task1_train_34875 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GGACTATCTGGTCCCTAGTATTATTCAAGTCTGCTGTTTCCTTATTGATTTTCTGTCTGGATGATACATTCATTACTGAGAGTGGGATAGTGAGTTCTCCTACTATTATTGTATTGCTGTCTATTTCTCCCTTCAGATATGTTAATATTTACTTCATATATTTAGGTGCTTTGATTAAAGGTGTATATATAATTGTTATATCTTCCTATTGAATTGACCCTTTTATCATTAGTTAATGATCTTTTTGGTTTCTTGTGATAGTTTTTGATTTGACGTCTATTTTGTCTAAGTATAGCCATTTCTTCTCTCTTTTGCTTATT... | GGACTATCTGGTCCCTAGTATTATTCAAGTCTGCTGTTTCCTTATTGATTTTCTGTCTGGATGATACATTCATTACTGAGAGTGGGATAGTGAGTTCTCCTACTATTATTGTATTGCTGTCTATTTCTCCCTTCAGATATGTTAATATTTACTTCATATATTTAGGTGCTTTGATTAAAGGTGTATATATAATTGTTATATCTTCCTATTGAATTGACCCTTTTATCATTAGTTAATGATCTTTTTGGTTTCTTGTGATAGTTTTTGATTTGACGTCTATTTTGTCTAAGTATAGCCATTTCTTCTCTCTTTTGCTTATT... |
Task1_train_34876 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CGATACACCAAAAAATAATGAATTGTCCCCTAGTTAGCAGAAAGCTTTTGCTTCAGGTGTATAAAACAGTATTATATCTAAATTCCCATGGCATTTCCATTTTTTATGTTAGTACCATCATTCTTTGCTGAACACTCTTAAGCAAAGCCTATCAACTATTTTAATAATCAGTTTCTCACCGATGAACAAGCCAAGTCCACATTCTGCTGAATGAGAGATTCCAGGTCTCTCAGAGTTTCACTGCCCAAGAACAAAAGCAAGTAACAGCTGTCAGTTCCTGAATTACACCTAACCAGTCACTAACTTAGCATAGACTATGC... | CGATACACCAAAAAATAATGAATTGTCCCCTAGTTAGCAGAAAGCTTTTGCTTCAGGTGTATAAAACAGTATTATATCTAAATTCCCATGGCATTTCCATTTTTTATGTTAGTACCATCATTCTTTGCTGAACACTCTTAAGCAAAGCCTATCAACTATTTTAATAATCAGTTTCTCACCGATGAACAAGCCAAGTCCACATTCTGCTGAATGAGAGATTCCAGGTCTCTCAGAGTTTCACTGCCCAAGAACAAAAGCAAGTAACAGCTGTCAGTTCCTGAATTACACCTAACCAGTCACTAACTTAGCATAGACTATGC... |
Task1_train_34877 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | GAAATGGGGGGGCCCCTGGGGACAACAGCCAGCCAAGGGCAGAGCCCAACTATGGTGAGATCAGGGCAGGGAGACTCAGCTATCGACATCCTCCACCCCCGGGGCGGTGAGACTTCAGGGACACCTCCATTACTCCCTAAGGAGCCAGTGACTGGCTGGTGTTTTCCTGAACATGGAAACCTGGACGGGGTGGTGGGCAACCAGGAGCCCTCACCGGGAGACGTGGCCATCTTTCCCGGGTGCAATGTTGGAAAGGGCTGTGCTCAGGCGACGTGGATCTGGCTTCCTCCAAAAAGTAGCCCAGGACCCAGAGGGCAGGA... | GAAATGGGGGGGCCCCTGGGGACAACAGCCAGCCAAGGGCAGAGCCCAACTATGGTGAGATCAGGGCAGGGAGACTCAGCTATCGACATCCTCCACCCCCGGGGCGGTGAGACTTCAGGGACACCTCCATTACTCCCTAAGGAGCCAGTGACTGGCTGGTGTTTTCCTGAACATGGAAACCTGGACGGGGTGGTGGGCAACCAGGAGCCCTCACCGGGAGACGTGGCCATCTTTCCCGGGTGCAATGTTGGAAAGGGCTGTGCTCAGGCGACGTGGATCTGGCTTCCTCCAAAAAGTAGCCCAGGACCCAGAGGGCAGGA... |
Task1_train_34878 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | GGACGGGGTGGTGGGCAACCAGGAGCCCTCACCGGGAGACGTGGCCATCTTTCCCGGGTGCAATGTTGGAAAGGGCTGTGCTCAGGCGACGTGGATCTGGCTTCCTCCAAAAAGTAGCCCAGGACCCAGAGGGCAGGACTGCATCCCACATGGAATCCCATTTCCATTCTGTGTTTTATAAGCTTAGGCTGCCACCAAAGCACCCAGGCTGAGTTGTTTTGTTGTTGTTGCTGTTGTTGTTTTTTGAATTTGTGGTTATTTCAGAATAGATTCAATAAGTAAGTGTCTCCTTTGTGTCCTATTTGATACTCTACATAGAA... | GGACGGGGTGGTGGGCAACCAGGAGCCCTCACCGGGAGACGTGGCCATCTTTCCCGGGTGCAATGTTGGAAAGGGCTGTGCTCAGGCGACGTGGATCTGGCTTCCTCCAAAAAGTAGCCCAGGACCCAGAGGGCAGGACTGCATCCCACATGGAATCCCATTTCCATTCTGTGTTTTATAAGCTTAGGCTGCCACCAAAGCACCCAGGCTGAGTTGTTTTGTTGTTGTTGCTGTTGTTGTTTTTTGAATTTGTGGTTATTTCAGAATAGATTCAATAAGTAAGTGTCTCCTTTGTGTCCTATTTGATACTCTACATAGAA... |
Task1_train_34879 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | CACTCAGCTCTGAGCACGGGGCTACGGACTCAAATATAAACATGCACAGAAATGGCATGCACAAATTTAAAACATGAGTATTACCTCTCAGTGCCAGTTTTCACAAATTAATGCATGTTGCAGTTATTAATGTACATATCCTAGGTTCCTGACAGGACGGCAAGCTCCCAGATTTTATGTGACTTTATTCTGCCTCCCTTTTCACACCCTCACAGTGAGCACCTGGTACATATGGGCATGTTAAAGCCTGTTAGGTGAATGAATAAACTGATGGATGAAATTAACTCTTAAAATGTGGTACAGTCTACGCAACCCACAAA... | CACTCAGCTCTGAGCACGGGGCTACGGACTCAAATATAAACATGCACAGAAATGGCATGCACAAATTTAAAACATGAGTATTACCTCTCAGTGCCAGTTTTCACAAATTAATGCATGTTGCAGTTATTAATGTACATATCCTAGGTTCCTGACAGGACGGCAAGCTCCCAGATTTTATGTGACTTTATTCTGCCTCCCTTTTCACACCCTCACAGTGAGCACCTGGTACATATGGGCATGTTAAAGCCTGTTAGGTGAATGAATAAACTGATGGATGAAATTAACTCTTAAAATGTGGTACAGTCTACGCAACCCACAAA... |
Task1_train_34880 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AAGTCTTTAGGAGACAGGTGCTGCTGGCAGGGGAAGTGGCGCATCAGAGAGGGTGTTTAAGAGAGAAGAAGCAATGCATTTTATCATGGATGGAACCATCCAGCACAGTGGAGAAAGGGTGACACAAGAGCAAGAAAGGGAACTGCAGATGGTGCCACTGAGCAGGTGAGAGGAAAGGGAGCTGAGGAAGCGGAGACAGGCCACCCAAGGAACCACGGGATGACGTGGCCGGGGACAGCTCTCTTTGGGTTTACTTGCATTTTCTTGGAGAAATAGGACTCAAGATTACCAGCTGAGAGTCAGGTGGGTCAGGAGAGGTG... | AAGTCTTTAGGAGACAGGTGCTGCTGGCAGGGGAAGTGGCGCATCAGAGAGGGTGTTTAAGAGAGAAGAAGCAATGCATTTTATCATGGATGGAACCATCCAGCACAGTGGAGAAAGGGTGACACAAGAGCAAGAAAGGGAACTGCAGATGGTGCCACTGAGCAGGTGAGAGGAAAGGGAGCTGAGGAAGCGGAGACAGGCCACCCAAGGAACCACGGGATGACGTGGCCGGGGACAGCTCTCTTTGGGTTTACTTGCATTTTCTTGGAGAAATAGGACTCAAGATTACCAGCTGAGAGTCAGGTGGGTCAGGAGAGGTG... |
Task1_train_34881 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GAGAACATGACTTAGCTCTAGGCCTCATTCACACTCCACAGCTCCAGGGTCTTCCTACTGCCCAATAAGCACAATCCTGCAGACATGGTCAGACCTGTTGGTAACATTGATTGGTAACATTGGCAACTGATTGGTAATGTTGATGCAGATTACCGGTTTTTATACTGTAATTCAGACCAGCTCTAAGTGATGTTTGGATAGGTATACGAAAGGCCAGCAGAGAGCCTTCGCTGGATGTTTCTCAGTGAGTAGATGGATTGTGGGAGAGGGAGAGATGAATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGAT... | GAGAACATGACTTAGCTCTAGGCCTCATTCACACTCCACAGCTCCAGGGTCTTCCTACTGCCCAATAAGCACAATCCTGCAGACATGGTCAGACCTGTTGGTAACATTGATTGGTAACATTGGCAACTGATTGGTAATGTTGATGCAGATTACCGGTTTTTATACTGTAATTCAGACCAGCTCTAAGTGATGTTTGGATAGGTATACGAAAGGCCAGCAGAGAGCCTTCGCTGGATGTTTCTCAGTGAGTAGATGGATTGTGGGAGAGGGAGAGATGAATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGAT... |
Task1_train_34882 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTGCCCAATAAGCACAATCCTGCAGACATGGTCAGACCTGTTGGTAACATTGATTGGTAACATTGGCAACTGATTGGTAATGTTGATGCAGATTACCGGTTTTTATACTGTAATTCAGACCAGCTCTAAGTGATGTTTGGATAGGTATACGAAAGGCCAGCAGAGAGCCTTCGCTGGATGTTTCTCAGTGAGTAGATGGATTGTGGGAGAGGGAGAGATGAATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGTAGGATGGATGGATGGATGGATGGATGATAGGATGGATGGATGGGTGGATG... | CTGCCCAATAAGCACAATCCTGCAGACATGGTCAGACCTGTTGGTAACATTGATTGGTAACATTGGCAACTGATTGGTAATGTTGATGCAGATTACCGGTTTTTATACTGTAATTCAGACCAGCTCTAAGTGATGTTTGGATAGGTATACGAAAGGCCAGCAGAGAGCCTTCGCTGGATGTTTCTCAGTGAGTAGATGGATTGTGGGAGAGGGAGAGATGAATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGTAGGATGGATGGATGGATGGATGGATGATAGGATGGATGGATGGGTGGATG... |
Task1_train_34883 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | TTTGGTTAAACTATAGCTACAGCATGCAAACCCCATAATTTAGGGTTTAAGGATAACAGGAAGATGGGCGCAAGATGTATAAGTATTAACGTATTTTCTCGTGTAAAGAAGGTTTAATACTGTTAATATACAAGTGTCCCTCGTTGTGTTGTGATTAGCATATATAGGGAGTAAAGGGCTGTAATTAGTATATTAAGTCCTATAAGCATAACAGTGATAGTTGATCAGGAGAACGAGGCCATAGTCACAAAGAGTTCTCCTACTAGATTACTGATAGCGGGTAAAGCAAGATTAGTAAGATTTGCTAGAAGTCATCAAGA... | TTTGGTTAAACTATAGCTACAGCATGCAAACCCCATAATTTAGGGTTTAAGGATAACAGGAAGATGGGCGCAAGATGTATAAGTATTAACGTATTTTCTCGTGTAAAGAAGGTTTAATACTGTTAATATACAAGTGTCCCTCGTTGTGTTGTGATTAGCATATATAGGGAGTAAAGGGCTGTAATTAGTATATTAAGTCCTATAAGCATAACAGTGATAGTTGATCAGGAGAACGAGGCCATAGTCACAAAGAGTTCTCCTACTAGATTACTGATAGCGGGTAAAGCAAGATTAGTAAGATTTGCTAGAAGTCATCAAGA... |
Task1_train_34884 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TAGTATATTAAGTCCTATAAGCATAACAGTGATAGTTGATCAGGAGAACGAGGCCATAGTCACAAAGAGTTCTCCTACTAGATTACTGATAGCGGGTAAAGCAAGATTAGTAAGATTTGCTAGAAGTCATCAAGAGGCTATTTACTGGGAGCAGTGTTTGAAGGCCTCGGGTAAGTAATATGGTTCGGCCTAGGGTTAAAATAGTTACTAATACAAGGCCTGTGCTGATTATTAGTGTCAGGTGGGTTGTTTGAAGGGCTCATGGCAGGAGTAGTAGTAGAGTGATCTCTAAGTCGAACAGGAGGAACGTGATGGCTACT... | TAGTATATTAAGTCCTATAAGCATAACAGTGATAGTTGATCAGGAGAACGAGGCCATAGTCACAAAGAGTTCTCCTACTAGATTACTGATAGCGGGTAAAGCAAGATTAGTAAGATTTGCTAGAAGTCATCAAGAGGCTATTTACTGGGAGCAGTGTTTGAAGGCCTCGGGTAAGTAATATGGTTCGGCCTAGGGTTAAAATAGTTACTAATACAAGGCCTGTGCTGATTATTAGTGTCAGGTGGGTTGTTTGAAGGGCTCATGGCAGGAGTAGTAGTAGAGTGATCTCTAAGTCGAACAGGAGGAACGTGATGGCTACT... |
Task1_train_34885 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCCATAAAAGTGTCACCAGTGACATATTTTGTTGGTTTGCTTTAATCCCTAGCTAGTGTCTGTATTGCATTTGTAAACTCTAAACTTTGGTATTGTCGCGAGTTGAAAGCTCAAGGGGTTCCTACCTAGTATTCTGTCCGTACATATCTAAGTAATGTGATAATCCTGATGACTGGTGCCCACACAGGGTCAGATGCCCACGTCTGAGTGATGCTACTCCCACCAGAGCAGTTGTTACTGTTGGAGAAATATAATTTTTAGAAAAACCCGAAATCTTTTCATTACCCAGAAAATCTCTCCATAAGGGTAGCAGAGGAAGA... | CCCATAAAAGTGTCACCAGTGACATATTTTGTTGGTTTGCTTTAATCCCTAGCTAGTGTCTGTATTGCATTTGTAAACTCTAAACTTTGGTATTGTCGCGAGTTGAAAGCTCAAGGGGTTCCTACCTAGTATTCTGTCCGTACATATCTAAGTAATGTGATAATCCTGATGACTGGTGCCCACACAGGGTCAGATGCCCACGTCTGAGTGATGCTACTCCCACCAGAGCAGTTGTTACTGTTGGAGAAATATAATTTTTAGAAAAACCCGAAATCTTTTCATTACCCAGAAAATCTCTCCATAAGGGTAGCAGAGGAAGA... |
Task1_train_34886 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AACACGGGGGTCCCCCAAATGTGGGACTCGAAGCAGGGACAGACGACTGAGGTTTACACCCAAGGCGACAGGACGGATGGGTCTTGGGGCTTCCTGAGGGGTTACAGGGGTGACAAGGTCACGGGAGGGTGAGGGGAGGAAAGCCTTCTGGTTATGCAGATAAAAATCTCTCGGGTAACCAGGAGCTGCCCTCGAAGAATCGGCAGCAGTCCATGCTGGCGGCGTCGCTGTCCGACGTGTCACTGTCAGGCATCAGTGTCCTTTTAAGGCCGCTGAGGGGGTCTCAGAGAAAGCCTGTCTGCCTGGTGTTCAGCTCACCC... | AACACGGGGGTCCCCCAAATGTGGGACTCGAAGCAGGGACAGACGACTGAGGTTTACACCCAAGGCGACAGGACGGATGGGTCTTGGGGCTTCCTGAGGGGTTACAGGGGTGACAAGGTCACGGGAGGGTGAGGGGAGGAAAGCCTTCTGGTTATGCAGATAAAAATCTCTCGGGTAACCAGGAGCTGCCCTCGAAGAATCGGCAGCAGTCCATGCTGGCGGCGTCGCTGTCCGACGTGTCACTGTCAGGCATCAGTGTCCTTTTAAGGCCGCTGAGGGGGTCTCAGAGAAAGCCTGTCTGCCTGGTGTTCAGCTCACCC... |
Task1_train_34887 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GAGGTGGAGGAAGGTACAGAAAAATAAATCAAGGCAGAAGGTCCCTGGGGTGAGGGTGACATTTCAAACAGGACAGTCAGGGCGCCTCACTGAGCGTGGGATTTGCCCAAAGAGCTGGCAGAGGTGCCGGGGCTGCCGTGTGGCTGTCTAAGGTCAAGTGTTGCAGCCCCTCCTAAGGTCCCAAGGAGGGAGCCGCTGCAGGAGACAGCCCGGCCAAGATGGGCGAGGCAGGGGCGGGTGGGCGCGCAGAGGCTGGAGCCGGACGTAGTGGCAGAGTCAGACAGAACGGAGCCTCCCAGGCCATGGTCCAGGCTCTGCCT... | GAGGTGGAGGAAGGTACAGAAAAATAAATCAAGGCAGAAGGTCCCTGGGGTGAGGGTGACATTTCAAACAGGACAGTCAGGGCGCCTCACTGAGCGTGGGATTTGCCCAAAGAGCTGGCAGAGGTGCCGGGGCTGCCGTGTGGCTGTCTAAGGTCAAGTGTTGCAGCCCCTCCTAAGGTCCCAAGGAGGGAGCCGCTGCAGGAGACAGCCCGGCCAAGATGGGCGAGGCAGGGGCGGGTGGGCGCGCAGAGGCTGGAGCCGGACGTAGTGGCAGAGTCAGACAGAACGGAGCCTCCCAGGCCATGGTCCAGGCTCTGCCT... |
Task1_train_34888 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGAAGCCTCAGGCACAGAGCTCTTTCCCCTTCTGTGTGATGAGAAGCTCAGCGTCAAACGGGAGGTATTTTGCTTTCTCCTTCCTTGATCCTTACAGCAGCCAATACAGTGATGCCACTTTTTCCAGGTGGATAACAATGTCTTATTGTTTAAAACTTACACCTGCTTATCATAGGGACAAGGATGAAAACCAATATCACCTTCCAAAAAGTGGCCACCTTTGAAATAACCTTGCCACATCAGGTGTCCAGATAGAGACCCAACAGGAAAACATCATGTGGGGTTTACCTCCCAAAACAGGGTCTGGGTTGCTGCAGTTT... | GGAAGCCTCAGGCACAGAGCTCTTTCCCCTTCTGTGTGATGAGAAGCTCAGCGTCAAACGGGAGGTATTTTGCTTTCTCCTTCCTTGATCCTTACAGCAGCCAATACAGTGATGCCACTTTTTCCAGGTGGATAACAATGTCTTATTGTTTAAAACTTACACCTGCTTATCATAGGGACAAGGATGAAAACCAATATCACCTTCCAAAAAGTGGCCACCTTTGAAATAACCTTGCCACATCAGGTGTCCAGATAGAGACCCAACAGGAAAACATCATGTGGGGTTTACCTCCCAAAACAGGGTCTGGGTTGCTGCAGTTT... |
Task1_train_34889 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | TTTCCCCTTCTGTGTGATGAGAAGCTCAGCGTCAAACGGGAGGTATTTTGCTTTCTCCTTCCTTGATCCTTACAGCAGCCAATACAGTGATGCCACTTTTTCCAGGTGGATAACAATGTCTTATTGTTTAAAACTTACACCTGCTTATCATAGGGACAAGGATGAAAACCAATATCACCTTCCAAAAAGTGGCCACCTTTGAAATAACCTTGCCACATCAGGTGTCCAGATAGAGACCCAACAGGAAAACATCATGTGGGGTTTACCTCCCAAAACAGGGTCTGGGTTGCTGCAGTTTGGATATTTGTCCCTTCCAAACC... | TTTCCCCTTCTGTGTGATGAGAAGCTCAGCGTCAAACGGGAGGTATTTTGCTTTCTCCTTCCTTGATCCTTACAGCAGCCAATACAGTGATGCCACTTTTTCCAGGTGGATAACAATGTCTTATTGTTTAAAACTTACACCTGCTTATCATAGGGACAAGGATGAAAACCAATATCACCTTCCAAAAAGTGGCCACCTTTGAAATAACCTTGCCACATCAGGTGTCCAGATAGAGACCCAACAGGAAAACATCATGTGGGGTTTACCTCCCAAAACAGGGTCTGGGTTGCTGCAGTTTGGATATTTGTCCCTTCCAAACC... |
Task1_train_34890 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATTTCTTCCTGGCACCACCACCTCCATCTGGCCTGCTCCCCAACCCCCCAGAAGCAGGTGGGCCCAGGCTCCAGGCCAGTGCCCCCATCAAGATCAGACGTAAGGCATCTTCCCACCGTCGCTGTGCTGCGGGGACTTTTCCAATCCTTCCTTCCTCTCTGTCCAGAGGCTGCCAGGCTGAGGGGGCCACCGTCCAGGTGGAACAGGCACAGGCATCGGGGAATCAGATGGTATCAGTGGGGATAGGGCACAGCACTTTCCTGGGAGCCATGTGACGCCAGATCTTCCTCTGGCAGTTCCCACTGGCTGTGGGAAGTGGT... | ATTTCTTCCTGGCACCACCACCTCCATCTGGCCTGCTCCCCAACCCCCCAGAAGCAGGTGGGCCCAGGCTCCAGGCCAGTGCCCCCATCAAGATCAGACGTAAGGCATCTTCCCACCGTCGCTGTGCTGCGGGGACTTTTCCAATCCTTCCTTCCTCTCTGTCCAGAGGCTGCCAGGCTGAGGGGGCCACCGTCCAGGTGGAACAGGCACAGGCATCGGGGAATCAGATGGTATCAGTGGGGATAGGGCACAGCACTTTCCTGGGAGCCATGTGACGCCAGATCTTCCTCTGGCAGTTCCCACTGGCTGTGGGAAGTGGT... |
Task1_train_34891 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GTATCAGTGGGGATAGGGCACAGCACTTTCCTGGGAGCCATGTGACGCCAGATCTTCCTCTGGCAGTTCCCACTGGCTGTGGGAAGTGGTTTTCATAAAGGGGGCCAACTTCCAGGAACATCTAGGGCTCGGGAGCAACCCAGCATTGACAGTGAATCAGAATCCACCTAGAGCTGGCCATGGCCCAGGCAGGGGGTGTCTTCCCCACAGCCCCCAGGAGTGGCTGCACCTAGTGGGCGCAGCATTTGGCCTGCCTCGCGGGCCCCTTGTTCAGAGCCACAGCTGCATCCCCCCGTAGAGCCTGGCCCTCCTCGTCGCTT... | GTATCAGTGGGGATAGGGCACAGCACTTTCCTGGGAGCCATGTGACGCCAGATCTTCCTCTGGCAGTTCCCACTGGCTGTGGGAAGTGGTTTTCATAAAGGGGGCCAACTTCCAGGAACATCTAGGGCTCGGGAGCAACCCAGCATTGACAGTGAATCAGAATCCACCTAGAGCTGGCCATGGCCCAGGCAGGGGGTGTCTTCCCCACAGCCCCCAGGAGTGGCTGCACCTAGTGGGCGCAGCATTTGGCCTGCCTCGCGGGCCCCTTGTTCAGAGCCACAGCTGCATCCCCCCGTAGAGCCTGGCCCTCCTCGTCGCTT... |
Task1_train_34892 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | GTGGGCGCAGCATTTGGCCTGCCTCGCGGGCCCCTTGTTCAGAGCCACAGCTGCATCCCCCCGTAGAGCCTGGCCCTCCTCGTCGCTTCTCTGCAGTAGCTCTTGGGCTGTGAACAGCAAGAGGAGGGGGCTGGCTAGGGAGGGAAGTCGCCCAGCCCAGCACAGCCCTGCAGACCAGCCACCCCAGGACCCGCCCCTCCTGTGTTTACCCTGAACCATAGAACAAGGGCCTCCTGCCCCTCCTGGTCACCATCCAGTCCCTAAAGACATTCTATGGGATACCACGTCACCAGCAACAGGGACCCAGGGAAGTTGGTCAG... | GTGGGCGCAGCATTTGGCCTGCCTCGCGGGCCCCTTGTTCAGAGCCACAGCTGCATCCCCCCGTAGAGCCTGGCCCTCCTCGTCGCTTCTCTGCAGTAGCTCTTGGGCTGTGAACAGCAAGAGGAGGGGGCTGGCTAGGGAGGGAAGTCGCCCAGCCCAGCACAGCCCTGCAGACCAGCCACCCCAGGACCCGCCCCTCCTGTGTTTACCCTGAACCATAGAACAAGGGCCTCCTGCCCCTCCTGGTCACCATCCAGTCCCTAAAGACATTCTATGGGATACCACGTCACCAGCAACAGGGACCCAGGGAAGTTGGTCAG... |
Task1_train_34893 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTCTCCCAGGAAGAGGAGCCTGTGGTGGATCCCAGAGGGCACAGCTCAGGCTCCTGACTGTCCAGCCAGACATGGAGCTGGCAGCAGGTGTGGCCGGCCATGCCCCCAGCTCTCGCACCATCCACCATCGTGAGTGCACTCCTCCTGTCCTGGCCCGGAGATCCCTCGGCCGGCCCTGCATTTGTCCCCACTGAGCTCCCCAGCCAGCTCCCCAGACAGACGCTCCAAACCCACCCTGGCCGCCCACTGCCCCTCCAAGCCTTGAGTAACCTCGTGCCCATGTTTTTGTGCCTGCCCAAGCACACAGCCCATGTAGTCAC... | CTCTCCCAGGAAGAGGAGCCTGTGGTGGATCCCAGAGGGCACAGCTCAGGCTCCTGACTGTCCAGCCAGACATGGAGCTGGCAGCAGGTGTGGCCGGCCATGCCCCCAGCTCTCGCACCATCCACCATCGTGAGTGCACTCCTCCTGTCCTGGCCCGGAGATCCCTCGGCCGGCCCTGCATTTGTCCCCACTGAGCTCCCCAGCCAGCTCCCCAGACAGACGCTCCAAACCCACCCTGGCCGCCCACTGCCCCTCCAAGCCTTGAGTAACCTCGTGCCCATGTTTTTGTGCCTGCCCAAGCACACAGCCCATGTAGTCAC... |
Task1_train_34894 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GATGCTCGGACCCTGGCTTGCTGGAATGAAAGGAACTAGGGCCTCGCGCCTCATTGTCGGGGCCTCCATCCCCCTCACCTGTAAAATACAGAATGCCCGGCACCACCCTGAAGCTTCACAGACCCCACACATCACCCCCCCACCCCCACCCAAGAAAGGTGGGTGCTCTGTGGGTACAGCTCTCTGTGGGCTGAGCACGTCCAAGCACGTCTCAATGAATCCAAAGCACCCTCCTACGCTCCAACCGGGCATCTCGGAATCTCTCAGCCCTGCTTGCGCTCACCTAGTGAGTGCCTTTGGGCGCTGGCTCCTGCAGGCTC... | GATGCTCGGACCCTGGCTTGCTGGAATGAAAGGAACTAGGGCCTCGCGCCTCATTGTCGGGGCCTCCATCCCCCTCACCTGTAAAATACAGAATGCCCGGCACCACCCTGAAGCTTCACAGACCCCACACATCACCCCCCCACCCCCACCCAAGAAAGGTGGGTGCTCTGTGGGTACAGCTCTCTGTGGGCTGAGCACGTCCAAGCACGTCTCAATGAATCCAAAGCACCCTCCTACGCTCCAACCGGGCATCTCGGAATCTCTCAGCCCTGCTTGCGCTCACCTAGTGAGTGCCTTTGGGCGCTGGCTCCTGCAGGCTC... |
Task1_train_34895 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | TGTCATAATTTGTCATAAGAGTTGGCTTTGGGAGAAACCTTCAGATTCTGGCGTGCAGCCTGAAGTTGCAGCGTGCAAGTGAGGCCTCATCTGTCACTGGTCACCCTCTGCGTTCCAGTGTTTTACAAAGAGGCTGGAATAAGGTCAGGGTCCGTGACTTTTCATTTTAATGTAGAAGCTTTCATCTTATTTCTTTTTATTTATGGAAATGTAGACACCTCCAGGCCCCATCTTCTCAGGCCTCGCATTCCAGGGAGGTACCTCATTCATTATCTTTATGACTATTAAAGAAACACAGCTCTTTTCAATTGTGTAAAAAA... | TGTCATAATTTGTCATAAGAGTTGGCTTTGGGAGAAACCTTCAGATTCTGGCGTGCAGCCTGAAGTTGCAGCGTGCAAGTGAGGCCTCATCTGTCACTGGTCACCCTCTGCGTTCCAGTGTTTTACAAAGAGGCTGGAATAAGGTCAGGGTCCGTGACTTTTCATTTTAATGTAGAAGCTTTCATCTTATTTCTTTTTATTTATGGAAATGTAGACACCTCCAGGCCCCATCTTCTCAGGCCTCGCATTCCAGGGAGGTACCTCATTCATTATCTTTATGACTATTAAAGAAACACAGCTCTTTTCAATTGTGTAAAAAA... |
Task1_train_34896 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTTTCTCAGGAAAACAATAGTTGAGTGGCAGAAGATAGATTTCCTTTCATATGAGCTATTTCAAAAGCATCTTCCTTGAGACTGACCTTGAGGCTGCATTTCTAAAAGTGCACTGAATATTCTTTTTAAAAATTACTTGAAAGCTGCTTTTAGGGCTGTGTGACATGGAGTGCAGTTTGACAGCTGCAAAAGTACAAGTTGTCAAGTTGTTCATTGAGAAGTGAGAGTGGGGAATTGAACCTTCAGTCTGTTCCTAAACCCATCATTGTGGATTGTTTGGCTGCCTGATCCAGAGTTCTTTCTATTTGTTGAAACTTAAC... | TTTTCTCAGGAAAACAATAGTTGAGTGGCAGAAGATAGATTTCCTTTCATATGAGCTATTTCAAAAGCATCTTCCTTGAGACTGACCTTGAGGCTGCATTTCTAAAAGTGCACTGAATATTCTTTTTAAAAATTACTTGAAAGCTGCTTTTAGGGCTGTGTGACATGGAGTGCAGTTTGACAGCTGCAAAAGTACAAGTTGTCAAGTTGTTCATTGAGAAGTGAGAGTGGGGAATTGAACCTTCAGTCTGTTCCTAAACCCATCATTGTGGATTGTTTGGCTGCCTGATCCAGAGTTCTTTCTATTTGTTGAAACTTAAC... |
Task1_train_34897 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTTGCCTGTAATCTTATACGCCTTTTTAATTCCTCCTTTCTCAACCGTTTTAAGAGTTGACTGCATTCTTCATTTTTTCATATCCCATCTTTGCATTCTAACTTCCATGCCTCTCCCATCACTGAGACTTCTCTCGCTAGTTTATCAGTGCCTCCTAATTGTTACGCACAGTAGACTTCGGATTGCCTCTCAGCCACACTTTACACTATTATGTGTCTTCTTGACTTTTTTGACATTCCTTCTCAATTCCCTTTCCTTTCCTCCTCTTTTGACTGTTCTCATGCTCCTGTGCATCCATTTGCTTCTTAAATGTTGGTGGG... | CTTGCCTGTAATCTTATACGCCTTTTTAATTCCTCCTTTCTCAACCGTTTTAAGAGTTGACTGCATTCTTCATTTTTTCATATCCCATCTTTGCATTCTAACTTCCATGCCTCTCCCATCACTGAGACTTCTCTCGCTAGTTTATCAGTGCCTCCTAATTGTTACGCACAGTAGACTTCGGATTGCCTCTCAGCCACACTTTACACTATTATGTGTCTTCTTGACTTTTTTGACATTCCTTCTCAATTCCCTTTCCTTTCCTCCTCTTTTGACTGTTCTCATGCTCCTGTGCATCCATTTGCTTCTTAAATGTTGGTGGG... |
Task1_train_34898 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TCAAACTTGTCAAAGCCTTGTACCTATTGAGTGATTTTTTTTTTTTTTTTTAATTGAGATGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAGTCTTGGCTCACTGCAACATCCACTGCCCGGGTTCAAACGATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACGTGCCACCACGTCCAGCTAATTTTATTGTATTTTTAGTAGAGATGGGGTTTCGCCGTGTTGGCCAGGCTGACCTTGAACTCCTGACCTCAGGTGATCTGCCCGCCTTGGCCTCCCAAAGTGCCGGGATTACAGGCG... | TCAAACTTGTCAAAGCCTTGTACCTATTGAGTGATTTTTTTTTTTTTTTTTAATTGAGATGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAGTCTTGGCTCACTGCAACATCCACTGCCCGGGTTCAAACGATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACGTGCCACCACGTCCAGCTAATTTTATTGTATTTTTAGTAGAGATGGGGTTTCGCCGTGTTGGCCAGGCTGACCTTGAACTCCTGACCTCAGGTGATCTGCCCGCCTTGGCCTCCCAAAGTGCCGGGATTACAGGCG... |
Task1_train_34899 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TGCGAGATAGTTTCTCTGTCTTTGGCTTTCAACATTTTCATTATCATGTGTCTGGGAGTGAATGTCTTTGTGTTTTATCCCACCCAGAATTCACTGAGCCTCTTAGGTATGTAGATTAGTGTTTTCCATTACATTTGAGATGTTTTCAGCCATTATTTTTCAGAGACATTTTTCTGCCCCTTTCTCTTGCTCCTGCCCTTCTGCTACTCCTGTTTTCCCTATTTGGTGCCTTATGGTGTCCCACATTTCTCTGAGGCTCTGTTTATCTTTCTCATGTTTTTCCTGTCTTATATTTGGATTTCGTAATCTCTGTAAATCTA... | TGCGAGATAGTTTCTCTGTCTTTGGCTTTCAACATTTTCATTATCATGTGTCTGGGAGTGAATGTCTTTGTGTTTTATCCCACCCAGAATTCACTGAGCCTCTTAGGTATGTAGATTAGTGTTTTCCATTACATTTGAGATGTTTTCAGCCATTATTTTTCAGAGACATTTTTCTGCCCCTTTCTCTTGCTCCTGCCCTTCTGCTACTCCTGTTTTCCCTATTTGGTGCCTTATGGTGTCCCACATTTCTCTGAGGCTCTGTTTATCTTTCTCATGTTTTTCCTGTCTTATATTTGGATTTCGTAATCTCTGTAAATCTA... |
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