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_33900 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | GCCTCCTGAGATAATCCTATTTGGTTATGATAGGCTCTTCTTTTCATGTAATGCTTAATTTTATGAATTGTTACTTTAATTAAGAGTTTAACAGCTGTATTTGTAAATGATAGTGGGTTTTAACTTAAACAGGCCTTGGAATCATGGCTACTTTTGCTTTATAGAATGAATTAGGTGACCTTTTTACTTTTTCCTATGATCTGTAACAGTTTGTATAATATAGAATAATCTGTTCCTTTAGAGTTGGAGAGAATTCCCTGTTAAATCCATCAAGTGAACCCAGCTCCTTTTTGGGGTAAGTTTCTCAATTTTCTCCTTGG... | GCCTCCTGAGATAATCCTATTTGGTTATGATAGGCTCTTCTTTTCATGTAATGCTTAATTTTATGAATTGTTACTTTAATTAAGAGTTTAACAGCTGTATTTGTAAATGATAGTGGGTTTTAACTTAAACAGGCCTTGGAATCATGGCTACTTTTGCTTTATAGAATGAATTAGGTGACCTTTTTACTTTTTCCTATGATCTGTAACAGTTTGTATAATATAGAATAATCTGTTCCTTTAGAGTTGGAGAGAATTCCCTGTTAAATCCATCAAGTGAACCCAGCTCCTTTTTGGGGTAAGTTTCTCAATTTTCTCCTTGG... |
Task1_train_33901 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCACTCTTCCTTTTCTTTCTGGGCTTTACGTTCTGCCTCCCTTTGTTGCTGCTCCATCAAGGCTTGGCGTCGCTTTTCCAGCTCCATGTTCCCTCGCTCATAGTTGGCTTTCCGTTTGTCCTCAAAAGTAACTGAACAAGGTATGCCTATCAGCATCCACACACATTAACAGCCTACAGAACCTGTAATCTAGTTTCTATATACTTATGCCTTGTGATCATTTGAGTGCTATCAGTATTTGAATACTTCTCCTAAGGATAATTTTAACTCAAATCTAAGTGGAAAAATATCTACTTTCTTCAAGGATATTCAATTTTAGA... | CCACTCTTCCTTTTCTTTCTGGGCTTTACGTTCTGCCTCCCTTTGTTGCTGCTCCATCAAGGCTTGGCGTCGCTTTTCCAGCTCCATGTTCCCTCGCTCATAGTTGGCTTTCCGTTTGTCCTCAAAAGTAACTGAACAAGGTATGCCTATCAGCATCCACACACATTAACAGCCTACAGAACCTGTAATCTAGTTTCTATATACTTATGCCTTGTGATCATTTGAGTGCTATCAGTATTTGAATACTTCTCCTAAGGATAATTTTAACTCAAATCTAAGTGGAAAAATATCTACTTTCTTCAAGGATATTCAATTTTAGA... |
Task1_train_33902 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TTAATAAACATCTGTTGAACAAGGCATACCAACAGGCCGCTATGCTAAGATTCAGAGGAAAAGAGGGTTTCGTGAAGGTGGTGATCAGTAGGAGCATATAGTGCTGGGAGGTGAGATAAGGGAGCTTGAAAAATGTCCTTTGGGTTCAGCAACATGGATATCACTGTTGATCTTAGAGTGGTTTTGTAAAATAATGGGAACAGAAGTGAGTTTCAAGTGGGTTGAGGTATGAGTCACAGGCAAGAAAATGGAGAAAGTGAGTACAAGTTGAGCACTGAAGATCCAAAATCTGAAATACTCCAAAATCTGAAGCTTTTTGA... | TTAATAAACATCTGTTGAACAAGGCATACCAACAGGCCGCTATGCTAAGATTCAGAGGAAAAGAGGGTTTCGTGAAGGTGGTGATCAGTAGGAGCATATAGTGCTGGGAGGTGAGATAAGGGAGCTTGAAAAATGTCCTTTGGGTTCAGCAACATGGATATCACTGTTGATCTTAGAGTGGTTTTGTAAAATAATGGGAACAGAAGTGAGTTTCAAGTGGGTTGAGGTATGAGTCACAGGCAAGAAAATGGAGAAAGTGAGTACAAGTTGAGCACTGAAGATCCAAAATCTGAAATACTCCAAAATCTGAAGCTTTTTGA... |
Task1_train_33903 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GCAGTGAGCTGAGATCGCGCCATTGCACTCCAGCCTGGCAACAAAGCAAGACTCCGTCTCAAAAAAAAAAAGAACCTGGGACTGGCTAATGCATGGCCTGAAGAGATATGACTGGTGTTTCCACCTAGTCAATGACCAGAAACTCACAGCCCCCTCTACAGAGATTTGGGGTGGGGACGGCAGGGCAGCACATAGCCACTGTCTCCAGGAGGTGGGGTGGGAAGCAAAGCTCCTGCTCTCAGGCAGCTCTCAGTGCTCCAAGGAACATACACAAATGAGCCCTGGGCTGGGGGTCAATGCCTGGGCTCCCGTCCTGTTTC... | GCAGTGAGCTGAGATCGCGCCATTGCACTCCAGCCTGGCAACAAAGCAAGACTCCGTCTCAAAAAAAAAAAGAACCTGGGACTGGCTAATGCATGGCCTGAAGAGATATGACTGGTGTTTCCACCTAGTCAATGACCAGAAACTCACAGCCCCCTCTACAGAGATTTGGGGTGGGGACGGCAGGGCAGCACATAGCCACTGTCTCCAGGAGGTGGGGTGGGAAGCAAAGCTCCTGCTCTCAGGCAGCTCTCAGTGCTCCAAGGAACATACACAAATGAGCCCTGGGCTGGGGGTCAATGCCTGGGCTCCCGTCCTGTTTC... |
Task1_train_33904 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CTTTGAACCCAGAAGGCGGAGGTTGCAGTGAGCCGAGATCGCTCCACTGTACTCCAGCCTGGGCAACAGTGTGAGACTATGTCTCAAAACAAAAAAAGACAAGACACAGAAAATATTTGCAAAAGACATATGATAAAGGATTGTTACTCAAAATATACAAAGAACTCTTAAAGCTCAACAATAAGAAAACACACAACCTGATTTTAAAATAAGTCAAAGAACTGATGAGACATCTCACGAAAGAAGATATGTAGATGGCAAACAAGTAAATGAAAAGGTGCTCCACAACATATGTCATTAGGGAAATGCAAATTAAAACA... | CTTTGAACCCAGAAGGCGGAGGTTGCAGTGAGCCGAGATCGCTCCACTGTACTCCAGCCTGGGCAACAGTGTGAGACTATGTCTCAAAACAAAAAAAGACAAGACACAGAAAATATTTGCAAAAGACATATGATAAAGGATTGTTACTCAAAATATACAAAGAACTCTTAAAGCTCAACAATAAGAAAACACACAACCTGATTTTAAAATAAGTCAAAGAACTGATGAGACATCTCACGAAAGAAGATATGTAGATGGCAAACAAGTAAATGAAAAGGTGCTCCACAACATATGTCATTAGGGAAATGCAAATTAAAACA... |
Task1_train_33905 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | TTCAGCAGCGTGGAGGAGGTGGCCAGTGTCTTCCCTGACCGCATCTTCGTGATGGAAGCCATCACCTTCAGCGTCAAGGTCAGTCACTCCCTCACCAGGTGTGGTGTCCCCACACTACTCCTTGCCTCAGGGGCAACCCTGACTCTGGTTGGAAGGTTGCCCTCAGGATCCAAGAAGGAGAGCGGCTCCTGGGGACCCCTTAGGGGTCTTTGGCACAATCAAGCCATGTCAGAAGGGTGGGGAATAGGACCCACTGGGCTGAAGGACTTCCTATGAAAGGTAGTGAAGCAGGAGCGGGTGTCTGGAAGGGTCATGTTCTG... | TTCAGCAGCGTGGAGGAGGTGGCCAGTGTCTTCCCTGACCGCATCTTCGTGATGGAAGCCATCACCTTCAGCGTCAAGGTCAGTCACTCCCTCACCAGGTGTGGTGTCCCCACACTACTCCTTGCCTCAGGGGCAACCCTGACTCTGGTTGGAAGGTTGCCCTCAGGATCCAAGAAGGAGAGCGGCTCCTGGGGACCCCTTAGGGGTCTTTGGCACAATCAAGCCATGTCAGAAGGGTGGGGAATAGGACCCACTGGGCTGAAGGACTTCCTATGAAAGGTAGTGAAGCAGGAGCGGGTGTCTGGAAGGGTCATGTTCTG... |
Task1_train_33906 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ACTGGTGGGGAGCTGGAACCGGAAAACTGTTCATTCTAAAAAACAACCCCAATCTTCTCTCAGCTTCTGGCTGTGCCCATGTCCTCTGAGGAGGGCCATGGAATGCCTTCTGACATGCTCTTGGATGCACAGCTGAGGATCTGAAGGCAGCAACTCACCAGGGAGATGGTGGAGCTGGGGGCTTGGGCGCGGCAGAAGCGTTTGCGCAAAGCTTCTTGTATCTGCGGGAGAGGTAAATGCTCTGCTTATGCCAGCCACGGCCCCGGCCTGCGGGCTGCAAGTGAGGCAGGGGGTTAGGTGGGCAGACTTACCTTCCTGTC... | ACTGGTGGGGAGCTGGAACCGGAAAACTGTTCATTCTAAAAAACAACCCCAATCTTCTCTCAGCTTCTGGCTGTGCCCATGTCCTCTGAGGAGGGCCATGGAATGCCTTCTGACATGCTCTTGGATGCACAGCTGAGGATCTGAAGGCAGCAACTCACCAGGGAGATGGTGGAGCTGGGGGCTTGGGCGCGGCAGAAGCGTTTGCGCAAAGCTTCTTGTATCTGCGGGAGAGGTAAATGCTCTGCTTATGCCAGCCACGGCCCCGGCCTGCGGGCTGCAAGTGAGGCAGGGGGTTAGGTGGGCAGACTTACCTTCCTGTC... |
Task1_train_33907 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TGTGCCCATGTCCTCTGAGGAGGGCCATGGAATGCCTTCTGACATGCTCTTGGATGCACAGCTGAGGATCTGAAGGCAGCAACTCACCAGGGAGATGGTGGAGCTGGGGGCTTGGGCGCGGCAGAAGCGTTTGCGCAAAGCTTCTTGTATCTGCGGGAGAGGTAAATGCTCTGCTTATGCCAGCCACGGCCCCGGCCTGCGGGCTGCAAGTGAGGCAGGGGGTTAGGTGGGCAGACTTACCTTCCTGTCCATGAGGCAACCAAACAATAGGATGAAGACGCCCTGAGAAGAGGGACATGGGGATAAGCTGGTCAAGGAGG... | TGTGCCCATGTCCTCTGAGGAGGGCCATGGAATGCCTTCTGACATGCTCTTGGATGCACAGCTGAGGATCTGAAGGCAGCAACTCACCAGGGAGATGGTGGAGCTGGGGGCTTGGGCGCGGCAGAAGCGTTTGCGCAAAGCTTCTTGTATCTGCGGGAGAGGTAAATGCTCTGCTTATGCCAGCCACGGCCCCGGCCTGCGGGCTGCAAGTGAGGCAGGGGGTTAGGTGGGCAGACTTACCTTCCTGTCCATGAGGCAACCAAACAATAGGATGAAGACGCCCTGAGAAGAGGGACATGGGGATAAGCTGGTCAAGGAGG... |
Task1_train_33908 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | CTCATTACCTCTTAAAGGTCCTGCCTCTTAATATTATCACATTGACAACACTGAATTTTGGAGGAGTTACATTCAAGCCGTAGCAACCTATGACCCCAGGATTGGACAAAAACTTCCCACAGTAGGATACTGATGATGCCCTTCTAGCCAAGCGCAGTGGCTTCTCCTCAGGCCTCATCTATTATGATTGGATACTGGATTTTCTTCTTTGGTTTAAATGACCCTAAAATATTTGCTCTTCTTTCTTAATGTATTTGTTTCCTTTGGTGGTTCTGCTTTTCCTTGCTTGATATGTCTTGAGTATCTAGATAAGACAATCT... | CTCATTACCTCTTAAAGGTCCTGCCTCTTAATATTATCACATTGACAACACTGAATTTTGGAGGAGTTACATTCAAGCCGTAGCAACCTATGACCCCAGGATTGGACAAAAACTTCCCACAGTAGGATACTGATGATGCCCTTCTAGCCAAGCGCAGTGGCTTCTCCTCAGGCCTCATCTATTATGATTGGATACTGGATTTTCTTCTTTGGTTTAAATGACCCTAAAATATTTGCTCTTCTTTCTTAATGTATTTGTTTCCTTTGGTGGTTCTGCTTTTCCTTGCTTGATATGTCTTGAGTATCTAGATAAGACAATCT... |
Task1_train_33909 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CGTAGCCTCCTAGTGCCTCTCCCCATCCCATCCCCCTTCTTCCCACTCTTTCTCCTGTTTCTGTCCCTGTGTAAATGTCTCCCTGGGCAAGCTGTCACTTTCTGTAAACTTTTCTGGTTTTTCTTCTTCCTGCCTCTCTCTCCATGCTCATGCTCGTGTGTCCCCAGCCCACAGTTGTCCGTGCATCTTTCTCCAGATCAAGCCCTGCAGTCAGGCGAGCATGGAGAAGGCGAGCATGGAGGAGACAAGCACGAGGTCAGAATTGGAGCTGGCAGAGCAGACGGAGATGGAGGGAGAAAAGGAAGAAAGCCTGGTGGAAG... | CGTAGCCTCCTAGTGCCTCTCCCCATCCCATCCCCCTTCTTCCCACTCTTTCTCCTGTTTCTGTCCCTGTGTAAATGTCTCCCTGGGCAAGCTGTCACTTTCTGTAAACTTTTCTGGTTTTTCTTCTTCCTGCCTCTCTCTCCATGCTCATGCTCGTGTGTCCCCAGCCCACAGTTGTCCGTGCATCTTTCTCCAGATCAAGCCCTGCAGTCAGGCGAGCATGGAGAAGGCGAGCATGGAGGAGACAAGCACGAGGTCAGAATTGGAGCTGGCAGAGCAGACGGAGATGGAGGGAGAAAAGGAAGAAAGCCTGGTGGAAG... |
Task1_train_33910 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ACCGGGGCACTGGCTGACCTGTGGCTCCAGGCCCCACAGGCTCACAGGCCCCACAGGCTCCAGTCCCCACAGGCTCACAGGCTTCTGGTGCTCTCAAAGCCAGAGCCACTCCCTCCTCCCAGGCCCTCACCTCTGTGCACTGACTCTGATTGATGAAGAAGACGCGGGCAAAGGGGTCTGAGAGTCCGCTGCTGTCGGCGGCAAAGAGGCTGCGGGCCTGGTACATGTGCGCTCGGAGCTGGAACGCCTGCTTCTCTGTGGGGAAGGGCAGCCTGAGGTTCCAGGATGGGCAGCCCCTCCGGCCCCCTCCCAGGTGAGGC... | ACCGGGGCACTGGCTGACCTGTGGCTCCAGGCCCCACAGGCTCACAGGCCCCACAGGCTCCAGTCCCCACAGGCTCACAGGCTTCTGGTGCTCTCAAAGCCAGAGCCACTCCCTCCTCCCAGGCCCTCACCTCTGTGCACTGACTCTGATTGATGAAGAAGACGCGGGCAAAGGGGTCTGAGAGTCCGCTGCTGTCGGCGGCAAAGAGGCTGCGGGCCTGGTACATGTGCGCTCGGAGCTGGAACGCCTGCTTCTCTGTGGGGAAGGGCAGCCTGAGGTTCCAGGATGGGCAGCCCCTCCGGCCCCCTCCCAGGTGAGGC... |
Task1_train_33911 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | GAATGAGCTGAAAGTGGCCTCCGGGAGAGGAGCCCAGGGCCCAGGCTCACACTCACCCTTCCTACCCTGGAGAGGGAGGGAATCTTGGGAGCTGCCCTAGGGTTTTCCTCTGGCAAAAAGTAGAGCACTCAACCGGGCTCAGGCTTAGCAGTGGAGAGTCATGATTGGGCTTCCTGCTCTGCGTCCTGGAGCCATTACTTTCTTGCAGCTCTAGTTTCCCCCCCAGTGCACAGGGATCACCCTTCCTCACTGGTCTAGAGGTGACTTGGTCCTGTGCCCCAGACAGGCGGCCCTCACTCAGTGCTTGGATGCTCCAGCAC... | GAATGAGCTGAAAGTGGCCTCCGGGAGAGGAGCCCAGGGCCCAGGCTCACACTCACCCTTCCTACCCTGGAGAGGGAGGGAATCTTGGGAGCTGCCCTAGGGTTTTCCTCTGGCAAAAAGTAGAGCACTCAACCGGGCTCAGGCTTAGCAGTGGAGAGTCATGATTGGGCTTCCTGCTCTGCGTCCTGGAGCCATTACTTTCTTGCAGCTCTAGTTTCCCCCCCAGTGCACAGGGATCACCCTTCCTCACTGGTCTAGAGGTGACTTGGTCCTGTGCCCCAGACAGGCGGCCCTCACTCAGTGCTTGGATGCTCCAGCAC... |
Task1_train_33912 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | AGAGATATTAGTACAAAAAGATCCCACTATAGGAGAGAGAGAGAGGATAAAAACCATCAAAGGACTAAAGCCATTATGTTGTACTTTTTTCTAACGATGTGTTTCAATTTTAGATGCCATGGGTTGACTCTGATTTAAAGAGATTCTTAGTAAGTGCACCCCCATCTCCCCTCCACCCACCCCCCAATTTTGGTTGCTTAAATTAGTTTTACTTTGACAGGTTTTATAACATTTACATTCCATTCTGTAACTAGCATTCACCTAGTTGCTATTCCTGGTTCTGCACTTCAATAGATTTGAAGCTCACCACCACTCATTCT... | AGAGATATTAGTACAAAAAGATCCCACTATAGGAGAGAGAGAGAGGATAAAAACCATCAAAGGACTAAAGCCATTATGTTGTACTTTTTTCTAACGATGTGTTTCAATTTTAGATGCCATGGGTTGACTCTGATTTAAAGAGATTCTTAGTAAGTGCACCCCCATCTCCCCTCCACCCACCCCCCAATTTTGGTTGCTTAAATTAGTTTTACTTTGACAGGTTTTATAACATTTACATTCCATTCTGTAACTAGCATTCACCTAGTTGCTATTCCTGGTTCTGCACTTCAATAGATTTGAAGCTCACCACCACTCATTCT... |
Task1_train_33913 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCGCTTCCTTGCCTTTTTCCTGAAGACAGAAAAGAAGGAAACCATGCATTGCTATCTAATTCCAGGCAGCGCCCGTTCTGTTGGTGAGGAGACCGAGGCCCAAGGCACAGGGAAAGACCCCAGAAGAGGTGAGAGTAGGGGACGGAGTTACATCTAGATGGCTGCGATGACTCTGCAGGACTGGGATGTAGAGGAGGTGATGGGGCTGGAGAGCTGGGCCCGGGTCAGATCACAGATGGCCTCGAATGCCACGCCGAGGATCTGACTCTGGACTAAAGTTCAGTCTGCTGGAGAAGGGATTGCAGGGGCAGGGGTCTGGT... | TCGCTTCCTTGCCTTTTTCCTGAAGACAGAAAAGAAGGAAACCATGCATTGCTATCTAATTCCAGGCAGCGCCCGTTCTGTTGGTGAGGAGACCGAGGCCCAAGGCACAGGGAAAGACCCCAGAAGAGGTGAGAGTAGGGGACGGAGTTACATCTAGATGGCTGCGATGACTCTGCAGGACTGGGATGTAGAGGAGGTGATGGGGCTGGAGAGCTGGGCCCGGGTCAGATCACAGATGGCCTCGAATGCCACGCCGAGGATCTGACTCTGGACTAAAGTTCAGTCTGCTGGAGAAGGGATTGCAGGGGCAGGGGTCTGGT... |
Task1_train_33914 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGGACGGAGTTACATCTAGATGGCTGCGATGACTCTGCAGGACTGGGATGTAGAGGAGGTGATGGGGCTGGAGAGCTGGGCCCGGGTCAGATCACAGATGGCCTCGAATGCCACGCCGAGGATCTGACTCTGGACTAAAGTTCAGTCTGCTGGAGAAGGGATTGCAGGGGCAGGGGTCTGGTGCAGTTAGAACAGTGAGGTTGTTATGACCACAGGCCAGGTACAAGGGCACATGGCTGGGCTCAGGTGGTGCAGATGGAGCTACAGGACTTGGTGACTGACTAGATGTGGGTGAGGTGGATGCCTCAGTTTCTGACTTG... | GGGACGGAGTTACATCTAGATGGCTGCGATGACTCTGCAGGACTGGGATGTAGAGGAGGTGATGGGGCTGGAGAGCTGGGCCCGGGTCAGATCACAGATGGCCTCGAATGCCACGCCGAGGATCTGACTCTGGACTAAAGTTCAGTCTGCTGGAGAAGGGATTGCAGGGGCAGGGGTCTGGTGCAGTTAGAACAGTGAGGTTGTTATGACCACAGGCCAGGTACAAGGGCACATGGCTGGGCTCAGGTGGTGCAGATGGAGCTACAGGACTTGGTGACTGACTAGATGTGGGTGAGGTGGATGCCTCAGTTTCTGACTTG... |
Task1_train_33915 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCTGGTCTGGAGAGAGGAGCATCTAGGCAAAGACCTCTGTGGGGAGGGAGAGGCCCAGAGCCCCTTGGACTTGGCCATCCCCAAAGACCTGAGCAGGTCAGTGCACCTGGGGAAGCCTCTTAGGGCCAAAGATGGCCACCGGGCTCCCCTGACTCTGCCCTTCATCTTTTTTTTTCTTAATTGTTATTATGTTTTTATGTAGAGACAGAGTCTCACTGTGTTGCCCAGGCTGGTCTCAGAACTCCTGGGCTCAGGTGTTCTTCCCTCCTCAGCTTTCCAACATGCTGGGATTACAGGCATGAGCCACAGCATCCTCCACT... | CCTGGTCTGGAGAGAGGAGCATCTAGGCAAAGACCTCTGTGGGGAGGGAGAGGCCCAGAGCCCCTTGGACTTGGCCATCCCCAAAGACCTGAGCAGGTCAGTGCACCTGGGGAAGCCTCTTAGGGCCAAAGATGGCCACCGGGCTCCCCTGACTCTGCCCTTCATCTTTTTTTTTCTTAATTGTTATTATGTTTTTATGTAGAGACAGAGTCTCACTGTGTTGCCCAGGCTGGTCTCAGAACTCCTGGGCTCAGGTGTTCTTCCCTCCTCAGCTTTCCAACATGCTGGGATTACAGGCATGAGCCACAGCATCCTCCACT... |
Task1_train_33916 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | AGACTAGCCCCCGAGAACCTGAAGACCTACCAGACCTTCCCATCAGGGAAGAGGGTCTCTCCACAGGAGCGGAAAAAGAGAGACTGCTACTTTGAGTTCAGAGCATGAGACTTTTAGTTCAGAGCAGAGCCTGATGCCTGAGATCCTGGGTCGTGACCAGCCTGGCTTGCTTGGAATAAAATCTTTAGCCATGACCATGCTACCCATCTCTCCTCTGGATCCCAGGGACACTCGGCCACAGCAGGAAATGCCCCCTGAAGGTCACACAGCATTGTGTCCTGAGGGCCTGCGGAAAGCTCTGTCCCAGGGACTCAAGCCAA... | AGACTAGCCCCCGAGAACCTGAAGACCTACCAGACCTTCCCATCAGGGAAGAGGGTCTCTCCACAGGAGCGGAAAAAGAGAGACTGCTACTTTGAGTTCAGAGCATGAGACTTTTAGTTCAGAGCAGAGCCTGATGCCTGAGATCCTGGGTCGTGACCAGCCTGGCTTGCTTGGAATAAAATCTTTAGCCATGACCATGCTACCCATCTCTCCTCTGGATCCCAGGGACACTCGGCCACAGCAGGAAATGCCCCCTGAAGGTCACACAGCATTGTGTCCTGAGGGCCTGCGGAAAGCTCTGTCCCAGGGACTCAAGCCAA... |
Task1_train_33917 | 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 | TGTCTGGTCCTAGCACTCACATTGAGGCCTATGGGCCTTAGATTATCCCTACAGCCTGGTGAGCCGGGAGCTACGTGGGATCATCCGAGGGCTGCTGGCGAAGGCAGCAGGGTCTCTGGAGCTCTTTTTTGACCACTGTCTGTTCACCATGTTGCAAGAGCTGGATAAGACACCAGGTGAAAGGGGCACGGGAGGGATGACCATCTTGGGAGCCTCCTCCTTTTTTTCCTGCTTCCAGTACCACTCAGTGGTTCTGTTTCCAGCAGAGAAATGTGCTAACCTTAACACTTTTTGGAAAGTGTGGAGGAAGTTAGGAGTCA... | TGTCTGGTCCTAGCACTCACATTGAGGCCTATGGGCCTTAGATTATCCCTACAGCCTGGTGAGCCGGGAGCTACGTGGGATCATCCGAGGGCTGCTGGCGAAGGCAGCAGGGTCTCTGGAGCTCTTTTTTGACCACTGTCTGTTCACCATGTTGCAAGAGCTGGATAAGACACCAGGTGAAAGGGGCACGGGAGGGATGACCATCTTGGGAGCCTCCTCCTTTTTTTCCTGCTTCCAGTACCACTCAGTGGTTCTGTTTCCAGCAGAGAAATGTGCTAACCTTAACACTTTTTGGAAAGTGTGGAGGAAGTTAGGAGTCA... |
Task1_train_33918 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TAACTATTGATCAAGTCAGATCCCTCGAGATTCCTCCTTTTTTTTCATATCTTTTCGTAAAAATTTCTGTAAAGCTGTAAAGCTCAGCTTGAAAATCTTTTTTTTCTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTGGAGACAAAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAAAGATTCTCCTGCCTCAGCCTCCCGAGTAGCAGGGATTACAGGCACCTGCCACCACACCCGGCTCATTTTTGTATTTTTAGTAGAGACAGGGTTTCAACA... | TAACTATTGATCAAGTCAGATCCCTCGAGATTCCTCCTTTTTTTTCATATCTTTTCGTAAAAATTTCTGTAAAGCTGTAAAGCTCAGCTTGAAAATCTTTTTTTTCTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTGGAGACAAAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAAAGATTCTCCTGCCTCAGCCTCCCGAGTAGCAGGGATTACAGGCACCTGCCACCACACCCGGCTCATTTTTGTATTTTTAGTAGAGACAGGGTTTCAACA... |
Task1_train_33919 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CTTTATCAGAGGTAAGAAGGGACAGAACAGGGTGAACATGAAACCCCAGGTATCTAGGGAAAAACCTATCTACCACTTTTAAAATGTAGGTAATCTGCCTCATCTACATCCCTGTGTTGAGGGTTCAATGACAATGGATGTTATATGGAAGGGCTATATAATTGCACGGCCACCAGGTCATCTTTTATGTCCCCATCACACATTGTCAAGCCTTACTGTTTTACATGAAGAACACCCTCAGATGATGCTGACGGGAAGTGATAAGACTTGTTTGTGGGTGGGGCAGGGGGCAAAGCTTTTGAATTACATTAAGTTCTTAA... | CTTTATCAGAGGTAAGAAGGGACAGAACAGGGTGAACATGAAACCCCAGGTATCTAGGGAAAAACCTATCTACCACTTTTAAAATGTAGGTAATCTGCCTCATCTACATCCCTGTGTTGAGGGTTCAATGACAATGGATGTTATATGGAAGGGCTATATAATTGCACGGCCACCAGGTCATCTTTTATGTCCCCATCACACATTGTCAAGCCTTACTGTTTTACATGAAGAACACCCTCAGATGATGCTGACGGGAAGTGATAAGACTTGTTTGTGGGTGGGGCAGGGGGCAAAGCTTTTGAATTACATTAAGTTCTTAA... |
Task1_train_33920 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AAAAATACAAAGGGCGTGGTGGCGTGCGCCTGTAATCCCAGCTACTCGGGAGCCTGAGGCAGGAGAATCACTTGAACCTGGGAAGTAGAGGTTGCAGTGAGCCGAGATCGCGCCATTGCCATTGCTCTTCAGCCTGGGCAACAAGCAACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAATCCTCTGCCAGGCACGGTGGTTCATGCCTGTAATCCTCCTGTAATCCCAACACTTTCGGAAAGTCCGAGAGAGGAGGATGGCTTGAGCCCAGGCTTTCGAGACAGCCTGGGCAACATGGGGATCCGTCCCTACGAAATA... | AAAAATACAAAGGGCGTGGTGGCGTGCGCCTGTAATCCCAGCTACTCGGGAGCCTGAGGCAGGAGAATCACTTGAACCTGGGAAGTAGAGGTTGCAGTGAGCCGAGATCGCGCCATTGCCATTGCTCTTCAGCCTGGGCAACAAGCAACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAATCCTCTGCCAGGCACGGTGGTTCATGCCTGTAATCCTCCTGTAATCCCAACACTTTCGGAAAGTCCGAGAGAGGAGGATGGCTTGAGCCCAGGCTTTCGAGACAGCCTGGGCAACATGGGGATCCGTCCCTACGAAATA... |
Task1_train_33921 | 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 | CTGCTCCACAGTGGACCCGGTCATGGCCCTGGTTTCTTGGATCCACATTTGCCCCGTCTCTTAAGTGTCCATCTCAGAGGTGGAGGATGGAGACAGTGAGGTGGAAAACGTGCTTGCTCTACACAAAGACAAATGGATCTTCTATTCCCAGAGGACCAGGGACACCAAAACCTCCCTCTTCAGAATGGAGGTAGACAGATAAAAATGAGAGGGGCTTGAGTGTCACAGACAATCTGAAAGTAATAATAGGGGCTCACTGTGGCTGGCAGAACTGGTACTGAAATGGGGACTACAGGGGAAGCAGCTTCCAGTTTTATGGT... | CTGCTCCACAGTGGACCCGGTCATGGCCCTGGTTTCTTGGATCCACATTTGCCCCGTCTCTTAAGTGTCCATCTCAGAGGTGGAGGATGGAGACAGTGAGGTGGAAAACGTGCTTGCTCTACACAAAGACAAATGGATCTTCTATTCCCAGAGGACCAGGGACACCAAAACCTCCCTCTTCAGAATGGAGGTAGACAGATAAAAATGAGAGGGGCTTGAGTGTCACAGACAATCTGAAAGTAATAATAGGGGCTCACTGTGGCTGGCAGAACTGGTACTGAAATGGGGACTACAGGGGAAGCAGCTTCCAGTTTTATGGT... |
Task1_train_33922 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CGCATCTCTCCAGAAAGAGGGCGGCCAAAAGCAAGAGCTAGCTGTTGTTTCACTACAACTATAACATGCCAAGGCACAAACAGCAGATTGTGGGACCCCCCCCCCTTTTTTTTTGGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGACACGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATGTGCTACCGCGCCCAGCTAATTTTTTTTTTTTTTTTTTGTATTTTTAGTAGAGACGAGATTTCACCATATTGGCCA... | CGCATCTCTCCAGAAAGAGGGCGGCCAAAAGCAAGAGCTAGCTGTTGTTTCACTACAACTATAACATGCCAAGGCACAAACAGCAGATTGTGGGACCCCCCCCCCTTTTTTTTTGGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGACACGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATGTGCTACCGCGCCCAGCTAATTTTTTTTTTTTTTTTTTGTATTTTTAGTAGAGACGAGATTTCACCATATTGGCCA... |
Task1_train_33923 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GAGTAAGACTGTCTCAAAAAAGGAAAATGTTCCGTATCTGTACTAACCAGTACAGTAGCTACTAACGTGGTTATTCCATTTGCACTTGAAATACGGCTAGTGCAAATGAGACACTGAATTTTTAGGTTAAATTAATTTTCTTCTATAGAGTCAGGGTCTCATTCATATTGCCCAGGCTGGTCTTGAATTCCTAGGTTCAAGTGATCCTCCCCCGCTTGGCCTCCTAAAGTGCTGGGATTACAGGAGTGAGTCACTACACCCAGCCTAAGGTACATTAATTTAAATTTAAGTAGTTACATGTGGCAAGTGGCGATTCTATT... | GAGTAAGACTGTCTCAAAAAAGGAAAATGTTCCGTATCTGTACTAACCAGTACAGTAGCTACTAACGTGGTTATTCCATTTGCACTTGAAATACGGCTAGTGCAAATGAGACACTGAATTTTTAGGTTAAATTAATTTTCTTCTATAGAGTCAGGGTCTCATTCATATTGCCCAGGCTGGTCTTGAATTCCTAGGTTCAAGTGATCCTCCCCCGCTTGGCCTCCTAAAGTGCTGGGATTACAGGAGTGAGTCACTACACCCAGCCTAAGGTACATTAATTTAAATTTAAGTAGTTACATGTGGCAAGTGGCGATTCTATT... |
Task1_train_33924 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGCGTGAGCCATCTTGCCTAGCTGATTTTTCTTTTTTTTTCTTTTTTTTTTTTTTTGATGGAGTCTTGCTCTGTCGCTCAGGCTGGAGTGCAGTTGCATGATCATAGTTCATTGCAGCCTCAACCTCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGAACCACAGACATACACCACCACACGTAGCTAATTTATTTTTATTTTTAATTTTTTTTGTAGAGACAGGGTGTCACTATGTTGACCAGGCTGGTCTTGAACTCCTGGCCTCAAGCGATCCTCCTGCCTCAGCCTCTCAAAGTGCTGGGAT... | GGCGTGAGCCATCTTGCCTAGCTGATTTTTCTTTTTTTTTCTTTTTTTTTTTTTTTGATGGAGTCTTGCTCTGTCGCTCAGGCTGGAGTGCAGTTGCATGATCATAGTTCATTGCAGCCTCAACCTCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGAACCACAGACATACACCACCACACGTAGCTAATTTATTTTTATTTTTAATTTTTTTTGTAGAGACAGGGTGTCACTATGTTGACCAGGCTGGTCTTGAACTCCTGGCCTCAAGCGATCCTCCTGCCTCAGCCTCTCAAAGTGCTGGGAT... |
Task1_train_33925 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | GAGTAAAGTCAGAGAGGGCCACAGGGATGGGGAGCTGTGGTGCCCGACTCACCTTCCATGAGGATTCGAAGAACGTCTCGGAGGGTGGGAGCGGTGGATCCAAGGGCACAGATGGAGAAGAGGAAGGTGCTGATGGGGTCGGCTGCCTTGTATTGAGGCTGCAGAGAAAGAGACCCCTAAGCCCAACAACCAGGGACCTTTCAGAGGAAGATCTAGGGGTATCTTGAACAAACATGACCTGAGAGGCCCCTCAAAACCCTGAAGAGGGGACAGGGAACATGACTCATGTCTGGGAGAGTCCTGGGAGGTGGGAGGGAGGA... | GAGTAAAGTCAGAGAGGGCCACAGGGATGGGGAGCTGTGGTGCCCGACTCACCTTCCATGAGGATTCGAAGAACGTCTCGGAGGGTGGGAGCGGTGGATCCAAGGGCACAGATGGAGAAGAGGAAGGTGCTGATGGGGTCGGCTGCCTTGTATTGAGGCTGCAGAGAAAGAGACCCCTAAGCCCAACAACCAGGGACCTTTCAGAGGAAGATCTAGGGGTATCTTGAACAAACATGACCTGAGAGGCCCCTCAAAACCCTGAAGAGGGGACAGGGAACATGACTCATGTCTGGGAGAGTCCTGGGAGGTGGGAGGGAGGA... |
Task1_train_33926 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CAATACTGCTGATTAAAATCTGCTAGAACCTCAAAACCAATCATCAGCCCCTCTCTTTCTACTTCTCTCCCTCTAACTTCTAGGGGTTATTGAGTTTTAAGACCTCAAAAGGCCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTTGTGGATCATGAGGTCAGGAGATGGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAAAATACAAAAAAATTAGCCCGGCATGATGGTGGGCACCTGTAGTCCCAGCTACTCAGGAGGCTGTGGCAGGAGAATGGCCTAAACCCA... | CAATACTGCTGATTAAAATCTGCTAGAACCTCAAAACCAATCATCAGCCCCTCTCTTTCTACTTCTCTCCCTCTAACTTCTAGGGGTTATTGAGTTTTAAGACCTCAAAAGGCCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTTGTGGATCATGAGGTCAGGAGATGGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAAAATACAAAAAAATTAGCCCGGCATGATGGTGGGCACCTGTAGTCCCAGCTACTCAGGAGGCTGTGGCAGGAGAATGGCCTAAACCCA... |
Task1_train_33927 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CCATCTACCTTGTCAGCCTAGCATCTCCCACTACTTAGCAAAAGTGCACCTGACAATCATGACATGCTGATCTCGGTGATGTTCCCACTTGCCTGAAATACTCTTTCTTCACCTAAAAGTCTTGTGCTGATTCTTTAAACTCCAGTACAAATGCAACTTCTTGAATAATTCTCTTCCCTTCTCTCTTAGGAAGTTAATCACCGTCCTCTATATTCCCTGATATTTATATGTTTGTTACGGCATTTACATGTGGTTATGGATGCCAACTGTATCAATATCTGATACATGAGATGTATCAATATCTGATATCTAAAAGGTGA... | CCATCTACCTTGTCAGCCTAGCATCTCCCACTACTTAGCAAAAGTGCACCTGACAATCATGACATGCTGATCTCGGTGATGTTCCCACTTGCCTGAAATACTCTTTCTTCACCTAAAAGTCTTGTGCTGATTCTTTAAACTCCAGTACAAATGCAACTTCTTGAATAATTCTCTTCCCTTCTCTCTTAGGAAGTTAATCACCGTCCTCTATATTCCCTGATATTTATATGTTTGTTACGGCATTTACATGTGGTTATGGATGCCAACTGTATCAATATCTGATACATGAGATGTATCAATATCTGATATCTAAAAGGTGA... |
Task1_train_33928 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CCCCAAACTCAGTTATCTATGCCCATTCATCAAAACACTGAGCAAAATATCAACAACAAATCCTCAGACCTTCCATCATTTCAGCTCCATGTGAATGCTGGAGTGGGATCTGGATCAAATAGCACAGAAACAAAACTTTCACAGTCACTTATCTCAGATAAGCAGTTACAACCTGGGGATGGCCCTCAAATCCTTGGATTCAAGCCTTTAGTTACATCAATGGGCAGTCTACCTCCAAGAAGTTTAGAACTTAATGTAATTCAAGAGGAAACTCCTTTACTGAAGAATGATCCAAAACATGTGCTAGAGCTTAGTATAGA... | CCCCAAACTCAGTTATCTATGCCCATTCATCAAAACACTGAGCAAAATATCAACAACAAATCCTCAGACCTTCCATCATTTCAGCTCCATGTGAATGCTGGAGTGGGATCTGGATCAAATAGCACAGAAACAAAACTTTCACAGTCACTTATCTCAGATAAGCAGTTACAACCTGGGGATGGCCCTCAAATCCTTGGATTCAAGCCTTTAGTTACATCAATGGGCAGTCTACCTCCAAGAAGTTTAGAACTTAATGTAATTCAAGAGGAAACTCCTTTACTGAAGAATGATCCAAAACATGTGCTAGAGCTTAGTATAGA... |
Task1_train_33929 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | CCAAGTGGAAAAATCTATTGGGTTGACACAACCATCTTTAGGAACTAGCCCAGGGCCACTGAGCCAAACTTCAGAATCTGTGGAGATGAGCTCAGTGTCATTCCAAGACATTCTCAAGACAATGCACCAACTTGGAAAAGCAATGGGGGAAACTCCAGTATCACAACACACAACAAAAGAATCTCTGGATTTGATACCAGGATCAGAAATGCAAAGTGTGAAATCAGAGGGGGTGACCACAGAGCCACAGCCCCATGATATGAAGTTTGTTTACTGCAATCTAGGGCCATGTTCAGAAGTTACTGAGTTGTCAGAGATAC... | CCAAGTGGAAAAATCTATTGGGTTGACACAACCATCTTTAGGAACTAGCCCAGGGCCACTGAGCCAAACTTCAGAATCTGTGGAGATGAGCTCAGTGTCATTCCAAGACATTCTCAAGACAATGCACCAACTTGGAAAAGCAATGGGGGAAACTCCAGTATCACAACACACAACAAAAGAATCTCTGGATTTGATACCAGGATCAGAAATGCAAAGTGTGAAATCAGAGGGGGTGACCACAGAGCCACAGCCCCATGATATGAAGTTTGTTTACTGCAATCTAGGGCCATGTTCAGAAGTTACTGAGTTGTCAGAGATAC... |
Task1_train_33930 | Located on Chromosome 2, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GGGGTGACCACAGAGCCACAGCCCCATGATATGAAGTTTGTTTACTGCAATCTAGGGCCATGTTCAGAAGTTACTGAGTTGTCAGAGATACCCCCCATGTCAGAATATAAAGAAACTGTGGGGTTGGCATTGCCTCAAGTTGCTAAGACCCAGGGGGTCATCCCAGTACCACCACATTCAGAAACAGGATTTTTGGAGTTGACTCTAGGACCAGGCACTCAATATGAGAAATCAGAGCCACTACTGCAAAATTTGAAATCTATGGAGTTAACCAGTGAGTCATCTCCATTATTGATAGGATCTAAAAAGTTAATTACAGA... | GGGGTGACCACAGAGCCACAGCCCCATGATATGAAGTTTGTTTACTGCAATCTAGGGCCATGTTCAGAAGTTACTGAGTTGTCAGAGATACCCCCCATGTCAGAATATAAAGAAACTGTGGGGTTGGCATTGCCTCAAGTTGCTAAGACCCAGGGGGTCATCCCAGTACCACCACATTCAGAAACAGGATTTTTGGAGTTGACTCTAGGACCAGGCACTCAATATGAGAAATCAGAGCCACTACTGCAAAATTTGAAATCTATGGAGTTAACCAGTGAGTCATCTCCATTATTGATAGGATCTAAAAAGTTAATTACAGA... |
Task1_train_33931 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AGAGATACCCCCCATGTCAGAATATAAAGAAACTGTGGGGTTGGCATTGCCTCAAGTTGCTAAGACCCAGGGGGTCATCCCAGTACCACCACATTCAGAAACAGGATTTTTGGAGTTGACTCTAGGACCAGGCACTCAATATGAGAAATCAGAGCCACTACTGCAAAATTTGAAATCTATGGAGTTAACCAGTGAGTCATCTCCATTATTGATAGGATCTAAAAAGTTAATTACAGAACAAAAACCACATGTTATGGACCTGACCCCAGGGCCACAGCTCCAGGGAGAAAAGTCTAAGCAGCTGGGTCTAGAGTCACAGT... | AGAGATACCCCCCATGTCAGAATATAAAGAAACTGTGGGGTTGGCATTGCCTCAAGTTGCTAAGACCCAGGGGGTCATCCCAGTACCACCACATTCAGAAACAGGATTTTTGGAGTTGACTCTAGGACCAGGCACTCAATATGAGAAATCAGAGCCACTACTGCAAAATTTGAAATCTATGGAGTTAACCAGTGAGTCATCTCCATTATTGATAGGATCTAAAAAGTTAATTACAGAACAAAAACCACATGTTATGGACCTGACCCCAGGGCCACAGCTCCAGGGAGAAAAGTCTAAGCAGCTGGGTCTAGAGTCACAGT... |
Task1_train_33932 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GAAAGGGTCTGAGTCAGAAGGTGTAATGTCTTTGGAGTTAATTCCAGAGCCAAAATCTGAAGGTATAAAATCGGTAGACCTCAAGTCTGACCTACAGTCGAAAGGTATAAAATCATCTGAATTGACTCCAGAATCAAATATGCAAGATGTAAAAGCTAAAGAGTTCAAACATGAACCACAGTTGCAAAGTATGAAATCTCCCAAGTTGACCCCAGGACCACAGTTGCACCAAGTGAAACCCTTGGGCTCGACTGTAGAGCCACAGATTCAAAGTGTGAAAATTGTGGAGTTAAACAAAGAGCTAGAGCTTGGAAGAATGA... | GAAAGGGTCTGAGTCAGAAGGTGTAATGTCTTTGGAGTTAATTCCAGAGCCAAAATCTGAAGGTATAAAATCGGTAGACCTCAAGTCTGACCTACAGTCGAAAGGTATAAAATCATCTGAATTGACTCCAGAATCAAATATGCAAGATGTAAAAGCTAAAGAGTTCAAACATGAACCACAGTTGCAAAGTATGAAATCTCCCAAGTTGACCCCAGGACCACAGTTGCACCAAGTGAAACCCTTGGGCTCGACTGTAGAGCCACAGATTCAAAGTGTGAAAATTGTGGAGTTAAACAAAGAGCTAGAGCTTGGAAGAATGA... |
Task1_train_33933 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TTCAGGGTTGACATCATGCTTTGGGTCACAATGCGTTAAATCTGTGGCCTTTGCATCGAAGCCATGCTTTCAAGATGTAAAACCTATGGAGCTGACACCAGGGGCCCAACAGCAAGGTATAAATTATCAAGAGTTGACTTCAGGATGGCAAGATGTGAAATCAATGATGTTGGTACCAGAGCCAACTAGGAAGTTCCCATCAGGACCACTGTTGACTAGTGTCAGATTTTCAAATTTGTCTCCAGAATCACAGCAACAGGATGTGAAATCTTTGGAGTTTACTGTAGAGCCAAAGTTGCAAAGCGTAAAACATGTGAAAT... | TTCAGGGTTGACATCATGCTTTGGGTCACAATGCGTTAAATCTGTGGCCTTTGCATCGAAGCCATGCTTTCAAGATGTAAAACCTATGGAGCTGACACCAGGGGCCCAACAGCAAGGTATAAATTATCAAGAGTTGACTTCAGGATGGCAAGATGTGAAATCAATGATGTTGGTACCAGAGCCAACTAGGAAGTTCCCATCAGGACCACTGTTGACTAGTGTCAGATTTTCAAATTTGTCTCCAGAATCACAGCAACAGGATGTGAAATCTTTGGAGTTTACTGTAGAGCCAAAGTTGCAAAGCGTAAAACATGTGAAAT... |
Task1_train_33934 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | ATGCTTTGGGTCACAATGCGTTAAATCTGTGGCCTTTGCATCGAAGCCATGCTTTCAAGATGTAAAACCTATGGAGCTGACACCAGGGGCCCAACAGCAAGGTATAAATTATCAAGAGTTGACTTCAGGATGGCAAGATGTGAAATCAATGATGTTGGTACCAGAGCCAACTAGGAAGTTCCCATCAGGACCACTGTTGACTAGTGTCAGATTTTCAAATTTGTCTCCAGAATCACAGCAACAGGATGTGAAATCTTTGGAGTTTACTGTAGAGCCAAAGTTGCAAAGCGTAAAACATGTGAAATTATCTTCAGTGTCTC... | ATGCTTTGGGTCACAATGCGTTAAATCTGTGGCCTTTGCATCGAAGCCATGCTTTCAAGATGTAAAACCTATGGAGCTGACACCAGGGGCCCAACAGCAAGGTATAAATTATCAAGAGTTGACTTCAGGATGGCAAGATGTGAAATCAATGATGTTGGTACCAGAGCCAACTAGGAAGTTCCCATCAGGACCACTGTTGACTAGTGTCAGATTTTCAAATTTGTCTCCAGAATCACAGCAACAGGATGTGAAATCTTTGGAGTTTACTGTAGAGCCAAAGTTGCAAAGCGTAAAACATGTGAAATTATCTTCAGTGTCTC... |
Task1_train_33935 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GCTGACACCAGGGGCCCAACAGCAAGGTATAAATTATCAAGAGTTGACTTCAGGATGGCAAGATGTGAAATCAATGATGTTGGTACCAGAGCCAACTAGGAAGTTCCCATCAGGACCACTGTTGACTAGTGTCAGATTTTCAAATTTGTCTCCAGAATCACAGCAACAGGATGTGAAATCTTTGGAGTTTACTGTAGAGCCAAAGTTGCAAAGCGTAAAACATGTGAAATTATCTTCAGTGTCTCTGCAGCAAACTATAAAATCTGTGGAATTAGCACCAGGGTCACTGCCTCAAAGAGTGAAATATGGGGAGCAAACTC... | GCTGACACCAGGGGCCCAACAGCAAGGTATAAATTATCAAGAGTTGACTTCAGGATGGCAAGATGTGAAATCAATGATGTTGGTACCAGAGCCAACTAGGAAGTTCCCATCAGGACCACTGTTGACTAGTGTCAGATTTTCAAATTTGTCTCCAGAATCACAGCAACAGGATGTGAAATCTTTGGAGTTTACTGTAGAGCCAAAGTTGCAAAGCGTAAAACATGTGAAATTATCTTCAGTGTCTCTGCAGCAAACTATAAAATCTGTGGAATTAGCACCAGGGTCACTGCCTCAAAGAGTGAAATATGGGGAGCAAACTC... |
Task1_train_33936 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTGGGTGTGGTCTTTGGAACATCCTGTCTATTTAGGCACTGATTATGACTTCCTTGCAGTCTCTGCCTCGCCTGGATTAAGGACTCCAGATACCACTGTTCCTGCTGCAGCTGCTGCTTCCTGTTTTCTAAGTGGCTTTGAGTAGCCGTTAGTTTCTGGGCTTGCTCAATTAGCTGCAGTAATTCCTTCTTGAACTGCTGGTTCTCTCTGTTGATGCCACAGGAGTATTCAAAAATAAACCGCTTTGCTGCCAACTTCAAGGCCTGGGCCTTCATATTAAGCTCTCTTCTTTTTCTCTTTCCCAGTAGCCTCCTGTCTGG... | CTGGGTGTGGTCTTTGGAACATCCTGTCTATTTAGGCACTGATTATGACTTCCTTGCAGTCTCTGCCTCGCCTGGATTAAGGACTCCAGATACCACTGTTCCTGCTGCAGCTGCTGCTTCCTGTTTTCTAAGTGGCTTTGAGTAGCCGTTAGTTTCTGGGCTTGCTCAATTAGCTGCAGTAATTCCTTCTTGAACTGCTGGTTCTCTCTGTTGATGCCACAGGAGTATTCAAAAATAAACCGCTTTGCTGCCAACTTCAAGGCCTGGGCCTTCATATTAAGCTCTCTTCTTTTTCTCTTTCCCAGTAGCCTCCTGTCTGG... |
Task1_train_33937 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | TCGCGCCATTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCCCCCCAAAAAAAAAAGGTCAAGCTGATAGACTTTTCTTACCTTTCCCTTTTCACAGACTAGCTCAAATATATGCAATCGCAGCAGAGTTTGGGGCCAGGGGTTGAGATAAAGGCTGATCTAAAATGTAAATGATCTAAAATGTAAAATCTCAGTTGAGATTTTGCACCAGGTTGATTTCACTCAACAGTCAGATTCTGTTTAATTCTGTGTTGGAGAAAGAGATCAATCAAGGACCGAGCAGATGCAGAGAGGACTGCCTGACATCTGTCCCCTT... | TCGCGCCATTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCCCCCCAAAAAAAAAAGGTCAAGCTGATAGACTTTTCTTACCTTTCCCTTTTCACAGACTAGCTCAAATATATGCAATCGCAGCAGAGTTTGGGGCCAGGGGTTGAGATAAAGGCTGATCTAAAATGTAAATGATCTAAAATGTAAAATCTCAGTTGAGATTTTGCACCAGGTTGATTTCACTCAACAGTCAGATTCTGTTTAATTCTGTGTTGGAGAAAGAGATCAATCAAGGACCGAGCAGATGCAGAGAGGACTGCCTGACATCTGTCCCCTT... |
Task1_train_33938 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TACTTGGATTACAGGCATGAGCCACTGCACCTGGCCTTTTTTTGTTTTTAAGATGGGGTTTCACTCTGTCACCTAGGCTGAGTGCTATGGCATGATCTCAGTTCACTGCAACCTTCACCTCCCAGGTTTAAGCAATCATCCCACCTCAGCCTCCCTAGTAGTTGGGACTACAGGCATGTACCACTATACCTGGCTAATTTTTCTGTAATTTTTGTAGAGATGGGGTTTTACCATGTTGCCCAGGTTGGTCTCAACCTCCTGGACTCAAGCAATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCA... | TACTTGGATTACAGGCATGAGCCACTGCACCTGGCCTTTTTTTGTTTTTAAGATGGGGTTTCACTCTGTCACCTAGGCTGAGTGCTATGGCATGATCTCAGTTCACTGCAACCTTCACCTCCCAGGTTTAAGCAATCATCCCACCTCAGCCTCCCTAGTAGTTGGGACTACAGGCATGTACCACTATACCTGGCTAATTTTTCTGTAATTTTTGTAGAGATGGGGTTTTACCATGTTGCCCAGGTTGGTCTCAACCTCCTGGACTCAAGCAATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCA... |
Task1_train_33939 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TAGGGCCCATTCCCCACCCAGAGCCATGTGTAATAATTACTACTCACTTCCTCCCCTCCCTTCATTAAAAACAAAAGGCTTAGGCCCGACACAATGGCTCACGTCTGGTGTCCCAGCTACTCAGGAGGCTGAGATGGGAGGACAGCTTGAGCCCAGGAGTTGGAGGCTGCTGTTAGCTATGATGATGCCATTGTACTCTGCCTAGACAACAGCGTGAGACCCTATCTCAAAAAAAAAAAAAAGAAAAAAAGAAAAAGGCTTAGCCCTGCCCTACTTAACTCTACCTCAAATTCTCCTTGCCCTCTCTCTGCCCCCTTCCA... | TAGGGCCCATTCCCCACCCAGAGCCATGTGTAATAATTACTACTCACTTCCTCCCCTCCCTTCATTAAAAACAAAAGGCTTAGGCCCGACACAATGGCTCACGTCTGGTGTCCCAGCTACTCAGGAGGCTGAGATGGGAGGACAGCTTGAGCCCAGGAGTTGGAGGCTGCTGTTAGCTATGATGATGCCATTGTACTCTGCCTAGACAACAGCGTGAGACCCTATCTCAAAAAAAAAAAAAAGAAAAAAAGAAAAAGGCTTAGCCCTGCCCTACTTAACTCTACCTCAAATTCTCCTTGCCCTCTCTCTGCCCCCTTCCA... |
Task1_train_33940 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GCATTTCCATTCTGCAAACTGACCCTCCTTCATTCACAAGGCAAGTCTGCTTCCCTCCTCTAAGGAGCTTCCCCTGCCTGAACTTCACCCGCGGACATCTCCCCATATCACATTCAGTCTGTACTTGATGGGCCCTAAAAGCCCCAAAGGGTTCTCATGTTTTCACATCTTGGCTCATTTTTCCAGATGGATGATAAACTCCTTGAAGATAAGTACATCTAGTCTGTTCCTTTTACATTCCATGCTTGGGTACTTAAATCCAGCCACCGTGGACTCTCCTCCCGCAAAGTTCATGGGCATTTTGGGAGCTGGTGTTGAGA... | GCATTTCCATTCTGCAAACTGACCCTCCTTCATTCACAAGGCAAGTCTGCTTCCCTCCTCTAAGGAGCTTCCCCTGCCTGAACTTCACCCGCGGACATCTCCCCATATCACATTCAGTCTGTACTTGATGGGCCCTAAAAGCCCCAAAGGGTTCTCATGTTTTCACATCTTGGCTCATTTTTCCAGATGGATGATAAACTCCTTGAAGATAAGTACATCTAGTCTGTTCCTTTTACATTCCATGCTTGGGTACTTAAATCCAGCCACCGTGGACTCTCCTCCCGCAAAGTTCATGGGCATTTTGGGAGCTGGTGTTGAGA... |
Task1_train_33941 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CATTCTGCAAACTGACCCTCCTTCATTCACAAGGCAAGTCTGCTTCCCTCCTCTAAGGAGCTTCCCCTGCCTGAACTTCACCCGCGGACATCTCCCCATATCACATTCAGTCTGTACTTGATGGGCCCTAAAAGCCCCAAAGGGTTCTCATGTTTTCACATCTTGGCTCATTTTTCCAGATGGATGATAAACTCCTTGAAGATAAGTACATCTAGTCTGTTCCTTTTACATTCCATGCTTGGGTACTTAAATCCAGCCACCGTGGACTCTCCTCCCGCAAAGTTCATGGGCATTTTGGGAGCTGGTGTTGAGATGCTCCC... | CATTCTGCAAACTGACCCTCCTTCATTCACAAGGCAAGTCTGCTTCCCTCCTCTAAGGAGCTTCCCCTGCCTGAACTTCACCCGCGGACATCTCCCCATATCACATTCAGTCTGTACTTGATGGGCCCTAAAAGCCCCAAAGGGTTCTCATGTTTTCACATCTTGGCTCATTTTTCCAGATGGATGATAAACTCCTTGAAGATAAGTACATCTAGTCTGTTCCTTTTACATTCCATGCTTGGGTACTTAAATCCAGCCACCGTGGACTCTCCTCCCGCAAAGTTCATGGGCATTTTGGGAGCTGGTGTTGAGATGCTCCC... |
Task1_train_33942 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | GTCAATAGAGTGAAGAATAGGAGAAAATATTTGCAAACTATCCATCCGACAAAGGATTAATAACCAGAATATATAAGGAACTCAAACAACTCAGTAACAAAAACAGAGAATCTGCTTTAAAAACTGGCAAAAGATGGAAGGCTTCTTAAAGGAGCGCATGCCTTAGCTGAACTTCCCCTCCTCTTTCCTGACTCCTGCTCCCTGTATGCTCTCAGCTCAGTGGTCCCTCCCTCTGGGAAGCTTTTTCTGTCCCCATCTCTGGCCGGGCTCCCAGGCCCCGCACTGTCATTGCTTCTTAATCATTGTGTTCTCCGCCAGAC... | GTCAATAGAGTGAAGAATAGGAGAAAATATTTGCAAACTATCCATCCGACAAAGGATTAATAACCAGAATATATAAGGAACTCAAACAACTCAGTAACAAAAACAGAGAATCTGCTTTAAAAACTGGCAAAAGATGGAAGGCTTCTTAAAGGAGCGCATGCCTTAGCTGAACTTCCCCTCCTCTTTCCTGACTCCTGCTCCCTGTATGCTCTCAGCTCAGTGGTCCCTCCCTCTGGGAAGCTTTTTCTGTCCCCATCTCTGGCCGGGCTCCCAGGCCCCGCACTGTCATTGCTTCTTAATCATTGTGTTCTCCGCCAGAC... |
Task1_train_33943 | 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 | ACAAGAGCAATAAGAAGTCTTGAGGTCTTAGGAAGAAAGGGGAAGTGCTCTCAAGAGGCACGTGGTTGCTGCCGTCAAGCCTGGGGTTGTGGTTGGCTGTTCTTCCCCTCCCCTGTGCAGACTGCTCCACCTGCTGAGCCTCTCCCTGGAGCCGTGGGGTGTCTCCAGCTCCCGGGGAGCCCAGGACAATGCCAGGGAGCCTCTGGGAGGAATTGTCCTGGCTGCACATTATGGAGGCAGAAGGTGGGGTTGGAATGCCCGAGAAGCTTCCTTAGAACTTCCAGTAGGTACAACTCCTAGAGCTGCCAGACCAACAACTC... | ACAAGAGCAATAAGAAGTCTTGAGGTCTTAGGAAGAAAGGGGAAGTGCTCTCAAGAGGCACGTGGTTGCTGCCGTCAAGCCTGGGGTTGTGGTTGGCTGTTCTTCCCCTCCCCTGTGCAGACTGCTCCACCTGCTGAGCCTCTCCCTGGAGCCGTGGGGTGTCTCCAGCTCCCGGGGAGCCCAGGACAATGCCAGGGAGCCTCTGGGAGGAATTGTCCTGGCTGCACATTATGGAGGCAGAAGGTGGGGTTGGAATGCCCGAGAAGCTTCCTTAGAACTTCCAGTAGGTACAACTCCTAGAGCTGCCAGACCAACAACTC... |
Task1_train_33944 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TCAAGCGATTCTCCTGCCTCAGCCTCCCCGGTAGCTGGGACTACAGGCATGTGCCACCACGCCCGGCTAATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTTCTGACCTCCAGTGATCCTCCCGTTCTCGGCCTCCCAAAGTGTGTGGGATTACAGGCGTGAGCCACTGCGCCTGGCCTGACTTGGCTGTTTTGATGCAGTGGTTTTGTTGAGGCCAGAATGAAAGTTAAAATGCTAGTCTTTTTTTTTTTTTTATTCCTCATCACTGATATTTACAAAGATAACCCTGAGCTCTTGGCCC... | TCAAGCGATTCTCCTGCCTCAGCCTCCCCGGTAGCTGGGACTACAGGCATGTGCCACCACGCCCGGCTAATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTTCTGACCTCCAGTGATCCTCCCGTTCTCGGCCTCCCAAAGTGTGTGGGATTACAGGCGTGAGCCACTGCGCCTGGCCTGACTTGGCTGTTTTGATGCAGTGGTTTTGTTGAGGCCAGAATGAAAGTTAAAATGCTAGTCTTTTTTTTTTTTTTATTCCTCATCACTGATATTTACAAAGATAACCCTGAGCTCTTGGCCC... |
Task1_train_33945 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | GGGTGAGGGGTGGCTCTTTTTTGGTCCTGCCTACGTGAAAGGCAGCTCCTTCCCAGCCCTTCTTGGCTGCCTCCTCCTCATCTCCCCGGCCTCTGGATGCTGGAACTCCCCCAGCGCTCAGCCCTCTGGCCTCTCGTCTATTTATACTGACCCGCTAGGTCCTCATCCAGTCCAGACATTAAGTACCATCTCTATGCTGAGGACTCCCACACCTCCCTCGCCAGCCTAGACCTTCCCTTGACCTCCAGACTAACATGTTTAGCTGCTGCTCAATATCTCTGCTTAAGTGCCTAATTATACTTCCAACTGACTGTGTCTAA... | GGGTGAGGGGTGGCTCTTTTTTGGTCCTGCCTACGTGAAAGGCAGCTCCTTCCCAGCCCTTCTTGGCTGCCTCCTCCTCATCTCCCCGGCCTCTGGATGCTGGAACTCCCCCAGCGCTCAGCCCTCTGGCCTCTCGTCTATTTATACTGACCCGCTAGGTCCTCATCCAGTCCAGACATTAAGTACCATCTCTATGCTGAGGACTCCCACACCTCCCTCGCCAGCCTAGACCTTCCCTTGACCTCCAGACTAACATGTTTAGCTGCTGCTCAATATCTCTGCTTAAGTGCCTAATTATACTTCCAACTGACTGTGTCTAA... |
Task1_train_33946 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TCTTGAACTCCTGATCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACTGTGCCCGGCTGTGCGTCCACTTTCAGTAAAGGGCTTCCTCTCCACTCAGACTTGCCTAGGACCTCCAGATGTACTGTGGTGAAAATCATCCTGGTGGAGGTGAAGCTCGGGAGAAAACTCGCCAGGAAGGAAGATGTGGTAGTGAGAGCTCTGGACTGGGAGGGGGATCTTCTTGTCCTGGCTGTGCTGACAGAGGAGCCGAGGGGCTGTGGAGGGTCCCCCACCCTCTCTGGGCCTCTGGGACCT... | TCTTGAACTCCTGATCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACTGTGCCCGGCTGTGCGTCCACTTTCAGTAAAGGGCTTCCTCTCCACTCAGACTTGCCTAGGACCTCCAGATGTACTGTGGTGAAAATCATCCTGGTGGAGGTGAAGCTCGGGAGAAAACTCGCCAGGAAGGAAGATGTGGTAGTGAGAGCTCTGGACTGGGAGGGGGATCTTCTTGTCCTGGCTGTGCTGACAGAGGAGCCGAGGGGCTGTGGAGGGTCCCCCACCCTCTCTGGGCCTCTGGGACCT... |
Task1_train_33947 | 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 | ACCTTCACCTCTGAGGATCCTGTGACCCTCGGAGGTTCCCTGCAAGAGCCCCAAGGGTGCAGCCTCAAAGCCAACATTCCTTGATAAATGTCACCAAGAGAGTGTCAGGCTGACCAGAGGGTGGCCCAGGGCATCTTCCCTGGTTCCTCCTTATTCCAGGCTGGCTTTGAAATCAGAGGGACCCGTGGGGCTCTAAGGGGAAGGTATCCTAGGGGATTAGATGATGTGGTCCTGATGAAGGAAGGACAAATTGCAGTTTCATGAAAAATAAAACAAGGTGGCTCACCTATGATCCCAGCACTTTGGGAGGTCAAGATGGG... | ACCTTCACCTCTGAGGATCCTGTGACCCTCGGAGGTTCCCTGCAAGAGCCCCAAGGGTGCAGCCTCAAAGCCAACATTCCTTGATAAATGTCACCAAGAGAGTGTCAGGCTGACCAGAGGGTGGCCCAGGGCATCTTCCCTGGTTCCTCCTTATTCCAGGCTGGCTTTGAAATCAGAGGGACCCGTGGGGCTCTAAGGGGAAGGTATCCTAGGGGATTAGATGATGTGGTCCTGATGAAGGAAGGACAAATTGCAGTTTCATGAAAAATAAAACAAGGTGGCTCACCTATGATCCCAGCACTTTGGGAGGTCAAGATGGG... |
Task1_train_33948 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | CTGAGGATCCTGTGACCCTCGGAGGTTCCCTGCAAGAGCCCCAAGGGTGCAGCCTCAAAGCCAACATTCCTTGATAAATGTCACCAAGAGAGTGTCAGGCTGACCAGAGGGTGGCCCAGGGCATCTTCCCTGGTTCCTCCTTATTCCAGGCTGGCTTTGAAATCAGAGGGACCCGTGGGGCTCTAAGGGGAAGGTATCCTAGGGGATTAGATGATGTGGTCCTGATGAAGGAAGGACAAATTGCAGTTTCATGAAAAATAAAACAAGGTGGCTCACCTATGATCCCAGCACTTTGGGAGGTCAAGATGGGCAGATTGCTT... | CTGAGGATCCTGTGACCCTCGGAGGTTCCCTGCAAGAGCCCCAAGGGTGCAGCCTCAAAGCCAACATTCCTTGATAAATGTCACCAAGAGAGTGTCAGGCTGACCAGAGGGTGGCCCAGGGCATCTTCCCTGGTTCCTCCTTATTCCAGGCTGGCTTTGAAATCAGAGGGACCCGTGGGGCTCTAAGGGGAAGGTATCCTAGGGGATTAGATGATGTGGTCCTGATGAAGGAAGGACAAATTGCAGTTTCATGAAAAATAAAACAAGGTGGCTCACCTATGATCCCAGCACTTTGGGAGGTCAAGATGGGCAGATTGCTT... |
Task1_train_33949 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | CGCAAAGGCTCTTTTGGGCTCTTAATAACTTTAAAGGGTTTAAAGCCATCCTGGGACCAAATAGCTTGAGAACCTCCCAACTAGATGCTGGTCTCCTGCGGGGAACCAGAAACATGGGGAGCCAGGCTGCTGGTTTGAGACACGGCACCAGTGAGCCAGCCACAGGGGCAAGCCTTTTCATCTCAGTTTCCCCAGCTGTAAAACATGGGGTGTGTGGGGTTGAACTAACTTGAGTGTTTTGAACTTTACTATTTTATTTTTTTGAGATATATATATATATTTTTAAGTTCTGGGATACATGTGCAGAACGTGCAGGTTTG... | CGCAAAGGCTCTTTTGGGCTCTTAATAACTTTAAAGGGTTTAAAGCCATCCTGGGACCAAATAGCTTGAGAACCTCCCAACTAGATGCTGGTCTCCTGCGGGGAACCAGAAACATGGGGAGCCAGGCTGCTGGTTTGAGACACGGCACCAGTGAGCCAGCCACAGGGGCAAGCCTTTTCATCTCAGTTTCCCCAGCTGTAAAACATGGGGTGTGTGGGGTTGAACTAACTTGAGTGTTTTGAACTTTACTATTTTATTTTTTTGAGATATATATATATATTTTTAAGTTCTGGGATACATGTGCAGAACGTGCAGGTTTG... |
Task1_train_33950 | This variant is present on Chromosome 2. Is the change likely to result in a pathogenic outcome? | Benign | CTCTTGTTTCCTTGTGCTCCTGAGAAGGGGACATTGGGGGTGATGGGGAGGGAATCGAGAAAGGGGGGCTTGCTTCTGGGTGCTGGGTTGGGGGGCTGGGGACCTTGCACTGAGCAGGTGCACTCTCGGGGGGAGGGTTGGGCAACTTGGGCTGGTGCGGTGGGGAAGTTCGCCGCTTTGTGGTGGGTGGGCTTAGCACCCTGGGGCTCACAGGTGGGCTGGGGGGCGTCTGCACAGCAGAGGGGCTTGGCTGGGCAGGTCTGTAAGAGGAGGGAAGGCTCCGGCGCCTCTTGTCTGCTTGAGGCACCCAGTGTGTCCTC... | CTCTTGTTTCCTTGTGCTCCTGAGAAGGGGACATTGGGGGTGATGGGGAGGGAATCGAGAAAGGGGGGCTTGCTTCTGGGTGCTGGGTTGGGGGGCTGGGGACCTTGCACTGAGCAGGTGCACTCTCGGGGGGAGGGTTGGGCAACTTGGGCTGGTGCGGTGGGGAAGTTCGCCGCTTTGTGGTGGGTGGGCTTAGCACCCTGGGGCTCACAGGTGGGCTGGGGGGCGTCTGCACAGCAGAGGGGCTTGGCTGGGCAGGTCTGTAAGAGGAGGGAAGGCTCCGGCGCCTCTTGTCTGCTTGAGGCACCCAGTGTGTCCTC... |
Task1_train_33951 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTCGTCCTCAGGATGGGGATTGCATTTCTGCAAGATGCTCTTGTCCTGACTAGGCAAAATACTGAAGTTCTTGGTGAGGGATGCCTTGAGCCTGCTGGTGGTGTTGCTTGGACTGACCCTGCAGGTGCCATTGGGCCACACGGCGGCTGCTCTGGGCTGCAGAATTTGCTCCTGGCTCTGCCCCTGCCCTTTGGCACCCAGGGCATAAAATGCCTCCAGCTTCTGACTGAGGTCCCTCTGGACCCTTCGCAGCTCCTGAAAGGTGGGGTCCTCCACGTGACTCTGGAGACACGACTCTGACTGGGACCTCGTCTGCCTCT... | TTCGTCCTCAGGATGGGGATTGCATTTCTGCAAGATGCTCTTGTCCTGACTAGGCAAAATACTGAAGTTCTTGGTGAGGGATGCCTTGAGCCTGCTGGTGGTGTTGCTTGGACTGACCCTGCAGGTGCCATTGGGCCACACGGCGGCTGCTCTGGGCTGCAGAATTTGCTCCTGGCTCTGCCCCTGCCCTTTGGCACCCAGGGCATAAAATGCCTCCAGCTTCTGACTGAGGTCCCTCTGGACCCTTCGCAGCTCCTGAAAGGTGGGGTCCTCCACGTGACTCTGGAGACACGACTCTGACTGGGACCTCGTCTGCCTCT... |
Task1_train_33952 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | ATTGATGTTTCATCTTCATGCATCTCTGATGAAAATATTTTTGGCAGTTAAGCAGATAAGGAAGGTAGCCTCTAGCCATCAGTGCTTTTACAGTTGTACACTCTAACTCCAGGGAAAGGCAACTGCCTTCAGAGAAAGGAAGAGTTGTCTGGTGTTGGCTTTTAACATAATGGCTTTCCCACGCTGAAAGTGATGCTTTTGACGCAGGTGAAACTGAGAAGGTCAGAAAAAGGTATGTATATATATACTTTTTATAATATACACACACATAGTCCTTTTGTTTGGTAATGTTTAGTAACTAGCAAGTAATAAGAGAATTG... | ATTGATGTTTCATCTTCATGCATCTCTGATGAAAATATTTTTGGCAGTTAAGCAGATAAGGAAGGTAGCCTCTAGCCATCAGTGCTTTTACAGTTGTACACTCTAACTCCAGGGAAAGGCAACTGCCTTCAGAGAAAGGAAGAGTTGTCTGGTGTTGGCTTTTAACATAATGGCTTTCCCACGCTGAAAGTGATGCTTTTGACGCAGGTGAAACTGAGAAGGTCAGAAAAAGGTATGTATATATATACTTTTTATAATATACACACACATAGTCCTTTTGTTTGGTAATGTTTAGTAACTAGCAAGTAATAAGAGAATTG... |
Task1_train_33953 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AAGGCAACTGCCTTCAGAGAAAGGAAGAGTTGTCTGGTGTTGGCTTTTAACATAATGGCTTTCCCACGCTGAAAGTGATGCTTTTGACGCAGGTGAAACTGAGAAGGTCAGAAAAAGGTATGTATATATATACTTTTTATAATATACACACACATAGTCCTTTTGTTTGGTAATGTTTAGTAACTAGCAAGTAATAAGAGAATTGCTTTCCTCTTGAATGCTTTGGTGTAGCTACCAACAGGAAAGAAAGTGGGCGTGAGGCTAGAGGAGAAGCAGAAAGAGGATGAAATGAGGACTTACTGATAAAGCATTCTAAGCAT... | AAGGCAACTGCCTTCAGAGAAAGGAAGAGTTGTCTGGTGTTGGCTTTTAACATAATGGCTTTCCCACGCTGAAAGTGATGCTTTTGACGCAGGTGAAACTGAGAAGGTCAGAAAAAGGTATGTATATATATACTTTTTATAATATACACACACATAGTCCTTTTGTTTGGTAATGTTTAGTAACTAGCAAGTAATAAGAGAATTGCTTTCCTCTTGAATGCTTTGGTGTAGCTACCAACAGGAAAGAAAGTGGGCGTGAGGCTAGAGGAGAAGCAGAAAGAGGATGAAATGAGGACTTACTGATAAAGCATTCTAAGCAT... |
Task1_train_33954 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | AGGTCTGAGGAGGATGCCAGCTGATGAGGGCTCTTATGAGACAGACAGGTGTAGTCTTTATCTCCCTGCTCCCTGCCCAGTCCTCCTGCCAGGTATGCTCAGGTGCACACAAATTCCTCTTCTCAAGGGGTAAGACAGTATTCTTCTTAGATACTGAGATGCGTCACCCAGTGGCTAAGGTGAAGGTATTTTACATGGATCCTGACTGAAGGTGGAGATCAGAATAGCTATGACCTTGCAGGGCTTCCATCACCACTTTGAGTCCCTTTGAGCAGTGTGGTCAGGTTGGGCTTTCTGGAACCACTGGCTGTCAGTCTTCC... | AGGTCTGAGGAGGATGCCAGCTGATGAGGGCTCTTATGAGACAGACAGGTGTAGTCTTTATCTCCCTGCTCCCTGCCCAGTCCTCCTGCCAGGTATGCTCAGGTGCACACAAATTCCTCTTCTCAAGGGGTAAGACAGTATTCTTCTTAGATACTGAGATGCGTCACCCAGTGGCTAAGGTGAAGGTATTTTACATGGATCCTGACTGAAGGTGGAGATCAGAATAGCTATGACCTTGCAGGGCTTCCATCACCACTTTGAGTCCCTTTGAGCAGTGTGGTCAGGTTGGGCTTTCTGGAACCACTGGCTGTCAGTCTTCC... |
Task1_train_33955 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AATCATTTTTTAAAAAGTGAATACAACCTAACCTGTTCAGTGGAAAGGGTAAATGTGGGATAAGGTGGGGGAATTGCTTCCTATCTTTATTACTGCTATTGAGGTAAAATGTAAAGAGTGAAATGTGCATGTCTTAAATGTGCAATCTGATTTTTCTGACATATGTAAGCATCATGTAATCCACACCTGAATCTAGAATGTGTCACCCAGAAAATTTCCTTATGCTCCCTTCTCATCGTTTCCCACCCTCACAGGCAACGACTGTTCTGATTTCTATCAGCACAGATTAGTTTTGTCTGCATCATATGGTTCTGTAAGTA... | AATCATTTTTTAAAAAGTGAATACAACCTAACCTGTTCAGTGGAAAGGGTAAATGTGGGATAAGGTGGGGGAATTGCTTCCTATCTTTATTACTGCTATTGAGGTAAAATGTAAAGAGTGAAATGTGCATGTCTTAAATGTGCAATCTGATTTTTCTGACATATGTAAGCATCATGTAATCCACACCTGAATCTAGAATGTGTCACCCAGAAAATTTCCTTATGCTCCCTTCTCATCGTTTCCCACCCTCACAGGCAACGACTGTTCTGATTTCTATCAGCACAGATTAGTTTTGTCTGCATCATATGGTTCTGTAAGTA... |
Task1_train_33956 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTGGGATGCCCCTTGGGGACACTTACTTGCCATGGCTTCAAGCCGCATCAGGAAGCAGACCAGGCTGGGGAAGCTGACCCTGCCGACGCTGTCGCTGTACCTGAGGGTCACCAGATGCAGCAGCTCACGGCTGATGAAGATCCCTCTGAGGAAGTCTGGGGCCACAGGTGAACGAGTGAGTGAGAGGAGGCTAGGGCTCGGGGGTTCCTCTGCCTCTCAGGGTCTGAGACACCTGTTCAGAGGGCCCGGCCACCTCCCACCAACTCCTCCCACTCAGCCCCCTCCCTTCAGTGTCTTCTCTTTCCTGTTGGTTGTTAGGC... | CTGGGATGCCCCTTGGGGACACTTACTTGCCATGGCTTCAAGCCGCATCAGGAAGCAGACCAGGCTGGGGAAGCTGACCCTGCCGACGCTGTCGCTGTACCTGAGGGTCACCAGATGCAGCAGCTCACGGCTGATGAAGATCCCTCTGAGGAAGTCTGGGGCCACAGGTGAACGAGTGAGTGAGAGGAGGCTAGGGCTCGGGGGTTCCTCTGCCTCTCAGGGTCTGAGACACCTGTTCAGAGGGCCCGGCCACCTCCCACCAACTCCTCCCACTCAGCCCCCTCCCTTCAGTGTCTTCTCTTTCCTGTTGGTTGTTAGGC... |
Task1_train_33957 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TGGACCAATCTGCAGACGAGTTTTAACAGACACATAAAGCTGTAAGCAGACATGACTGTTCTAAATTTATTAGGTATGAATTTTACAAACGTTACTTATATCTGTGATAACATTAGAGCTGGAGAATATTGCACCTTCTCCAAGTTGCATGGTGAGAACCACCAATAGCGTGGTAGAACTTACGGCCCTTTCCAAGGCCATGGCTCTTGCAGCCTGAGGATGTCAGCCCACACATCTCCCCATGCTTGTGGATAGATTTGGTGATCTGCTGGGTGTCAAGATTTCCTCTGATAGTTTTATGGAATGGATCAATGAGGATA... | TGGACCAATCTGCAGACGAGTTTTAACAGACACATAAAGCTGTAAGCAGACATGACTGTTCTAAATTTATTAGGTATGAATTTTACAAACGTTACTTATATCTGTGATAACATTAGAGCTGGAGAATATTGCACCTTCTCCAAGTTGCATGGTGAGAACCACCAATAGCGTGGTAGAACTTACGGCCCTTTCCAAGGCCATGGCTCTTGCAGCCTGAGGATGTCAGCCCACACATCTCCCCATGCTTGTGGATAGATTTGGTGATCTGCTGGGTGTCAAGATTTCCTCTGATAGTTTTATGGAATGGATCAATGAGGATA... |
Task1_train_33958 | This variant is present on Chromosome 2. Is the change likely to result in a pathogenic outcome? | Benign | ACTCAAGGTTTACACTAAATTTCTACAAGGGAAAGCCCTGAAGCAGGCTGCCTTACCAGAATCACTTGGAAATCGAGTGGAAATTTTGCATCTTCTGCTTTCAAATTTGATGGTGTGACAGCAACTGTGACGCACACGACAACATTGGTGCCTTCCATTGGCTCTTGCACAGAGAAGTTGAATTGAGCATCATTCCGAGGTCCTCCTGCATCAGAAAGAGCTGTTACTAGAGCTCAGCTCCACTCCTGGGACTCCTGGGCAGGGCCATGTCCAGTGCAGAGAGTTCTGTGGGGTTGTGTTGTGAACTCTGGATTGGAGAC... | ACTCAAGGTTTACACTAAATTTCTACAAGGGAAAGCCCTGAAGCAGGCTGCCTTACCAGAATCACTTGGAAATCGAGTGGAAATTTTGCATCTTCTGCTTTCAAATTTGATGGTGTGACAGCAACTGTGACGCACACGACAACATTGGTGCCTTCCATTGGCTCTTGCACAGAGAAGTTGAATTGAGCATCATTCCGAGGTCCTCCTGCATCAGAAAGAGCTGTTACTAGAGCTCAGCTCCACTCCTGGGACTCCTGGGCAGGGCCATGTCCAGTGCAGAGAGTTCTGTGGGGTTGTGTTGTGAACTCTGGATTGGAGAC... |
Task1_train_33959 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGCCTGGTTTCTGGTGCAAAGTGGCGACCCTCAGCAGTCAGCCAAGGTACAATACGAGATCCAACAGAACAGGTTCTGCTAGATCCGTCTCCCCCAGTCCCTGCTCTGCAAACATCACGGCCATGTTCAAAAGCCTTCATTTATGCCCATGCCTGCAGGGGATAAATCCAGACTTCCGGCATCAGGCTGTCCTGTGTCAGCTCCCAGCACTCTCTCTCCCAGTTTCCTCTGCCTCAGGCCGGCTTGTTGGCCCGGAACAGACTATCAATGTTCCCAGCTGGGTGCAATAGCCTATGCGTCCCCCTCCTATCTAGTGATCT... | AGCCTGGTTTCTGGTGCAAAGTGGCGACCCTCAGCAGTCAGCCAAGGTACAATACGAGATCCAACAGAACAGGTTCTGCTAGATCCGTCTCCCCCAGTCCCTGCTCTGCAAACATCACGGCCATGTTCAAAAGCCTTCATTTATGCCCATGCCTGCAGGGGATAAATCCAGACTTCCGGCATCAGGCTGTCCTGTGTCAGCTCCCAGCACTCTCTCTCCCAGTTTCCTCTGCCTCAGGCCGGCTTGTTGGCCCGGAACAGACTATCAATGTTCCCAGCTGGGTGCAATAGCCTATGCGTCCCCCTCCTATCTAGTGATCT... |
Task1_train_33960 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | AATGGTGGGTCAAAGAAGTTACATGTCATTTTAAGATCCCACAGCTAGTTGGTGGCAGCCCAGGATAAGGGCACAGGTCTCCCATCTCCCTGTCTTCTTTGTCCACTCTGCCACAGGTGCCCCCCACCCCATGCCCCTATTCCGTGAAGAGCTCAGCTTAGCCCTGAGCCAACAAAAGAAGAAAAGAGCAAGAGATGTCCAGAGACAACTTCTAAGTTTCTCTTTATTTCTTTTGGAAACAACCTCCATTCTTCATCTCTCAATGTAGTCCTGGCCTAGTGAAAAAGAAGGCTTTTCTTTCTGGCCTCCAGAGACTGCTT... | AATGGTGGGTCAAAGAAGTTACATGTCATTTTAAGATCCCACAGCTAGTTGGTGGCAGCCCAGGATAAGGGCACAGGTCTCCCATCTCCCTGTCTTCTTTGTCCACTCTGCCACAGGTGCCCCCCACCCCATGCCCCTATTCCGTGAAGAGCTCAGCTTAGCCCTGAGCCAACAAAAGAAGAAAAGAGCAAGAGATGTCCAGAGACAACTTCTAAGTTTCTCTTTATTTCTTTTGGAAACAACCTCCATTCTTCATCTCTCAATGTAGTCCTGGCCTAGTGAAAAAGAAGGCTTTTCTTTCTGGCCTCCAGAGACTGCTT... |
Task1_train_33961 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ACAGCTTTATGTGGGTTTGATGAACAACCCCTCTAACTCATATAGAGGGGACCTCTGGGGAAACCACTCCCCAGGCCAATCCCTCAGAATGATAAAGCTGAGAATAGTGAAGTTACCAATGGTGTCAGAGAAAGCCTCAGCGTGAAATCCAACAAGGTGGCTGCCATTCCCTGCAGACCTTGGGTGGTCCTGATCCTCACTGAGCCACAGATGGTCAGAGCTGGAGGCAATCTCAGAGACCATCTAGTTCCACTCATTTCACCTGTGGGGCAGCTGAGGCCCAGAGATTTAATGTAATTTGCCTAAGGCCCCACAGCTAA... | ACAGCTTTATGTGGGTTTGATGAACAACCCCTCTAACTCATATAGAGGGGACCTCTGGGGAAACCACTCCCCAGGCCAATCCCTCAGAATGATAAAGCTGAGAATAGTGAAGTTACCAATGGTGTCAGAGAAAGCCTCAGCGTGAAATCCAACAAGGTGGCTGCCATTCCCTGCAGACCTTGGGTGGTCCTGATCCTCACTGAGCCACAGATGGTCAGAGCTGGAGGCAATCTCAGAGACCATCTAGTTCCACTCATTTCACCTGTGGGGCAGCTGAGGCCCAGAGATTTAATGTAATTTGCCTAAGGCCCCACAGCTAA... |
Task1_train_33962 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTATAAATCTTGGCTTCATAGAAAGAAGAAGCAATCATCTAACTTTGGCAGCAAATACTCTGGTTGTTTTACTTTTTTTACTTTGAAGTTCATTCGTCTCCCTGAAGAAATCAGCCTATTTCTTCTGTGTTCTTCTCACTCCAAATATATGTATAAAATATTTTATATGGACTTTAAGCCTTTCTAATAATTTACCCCAGGCTTCATATGAAAGCCTCACGCTACTCATTTGCAATTCTTCTAGGTGGTGTGCTCTCTCCTTCCAGAGTTTTGTTGCTTGATCAATTTAACATGAGTTCATCAGACAGTTCCCTGGGTAG... | TTATAAATCTTGGCTTCATAGAAAGAAGAAGCAATCATCTAACTTTGGCAGCAAATACTCTGGTTGTTTTACTTTTTTTACTTTGAAGTTCATTCGTCTCCCTGAAGAAATCAGCCTATTTCTTCTGTGTTCTTCTCACTCCAAATATATGTATAAAATATTTTATATGGACTTTAAGCCTTTCTAATAATTTACCCCAGGCTTCATATGAAAGCCTCACGCTACTCATTTGCAATTCTTCTAGGTGGTGTGCTCTCTCCTTCCAGAGTTTTGTTGCTTGATCAATTTAACATGAGTTCATCAGACAGTTCCCTGGGTAG... |
Task1_train_33963 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TTTTTCAGATCACATAATCCACCTTGTGTAAAATATAGCCAGAGTTGAGACCAGTGCTCAGTAATTCACACATCCCACCAAGGGAAAGAGAAACAAAGCCAGAGTTTAGAAAAGTTGCATCCCCTCTGAGTCCTACAGAATGGCTCTAAAACACTTACTTGACCAGGTCATCTGGTTCAGGAGGTTCTGAAGTTGAACTGCATTAATCTCTGGATGCTAAATAGAAAGCAGATTGGCAAGAAAAAATAACTGTTACTGAAGGCTCATTAGATGGCAGAGGGGTCATATGACTGGCCATGAAATTAAACTGGGATTTCCTA... | TTTTTCAGATCACATAATCCACCTTGTGTAAAATATAGCCAGAGTTGAGACCAGTGCTCAGTAATTCACACATCCCACCAAGGGAAAGAGAAACAAAGCCAGAGTTTAGAAAAGTTGCATCCCCTCTGAGTCCTACAGAATGGCTCTAAAACACTTACTTGACCAGGTCATCTGGTTCAGGAGGTTCTGAAGTTGAACTGCATTAATCTCTGGATGCTAAATAGAAAGCAGATTGGCAAGAAAAAATAACTGTTACTGAAGGCTCATTAGATGGCAGAGGGGTCATATGACTGGCCATGAAATTAAACTGGGATTTCCTA... |
Task1_train_33964 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | CTTATGGACACAGATACAGATGGACCACGACCACCTCCCCACCTACACCACACAGCTACACACAGATAAGCTGGACATTCCGCATCATCTCAGGGAAAACACCCTTGTAAAGGACAAAGAGAACTGGGCAAGAGCTCAGAAGACCAAAATCAGGGCTCTGGTTCCGACATTTCTTGGGTATCTGCTTTATCTGATTCATATTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTGCCTCCTTTGTTTCTCCATCTCTCCCTATTTTTCTCTCTTGCTTACTCTCCCCTTTGTTCTCACTCAGGGCTATAGAGGGAGAGGAGA... | CTTATGGACACAGATACAGATGGACCACGACCACCTCCCCACCTACACCACACAGCTACACACAGATAAGCTGGACATTCCGCATCATCTCAGGGAAAACACCCTTGTAAAGGACAAAGAGAACTGGGCAAGAGCTCAGAAGACCAAAATCAGGGCTCTGGTTCCGACATTTCTTGGGTATCTGCTTTATCTGATTCATATTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTGCCTCCTTTGTTTCTCCATCTCTCCCTATTTTTCTCTCTTGCTTACTCTCCCCTTTGTTCTCACTCAGGGCTATAGAGGGAGAGGAGA... |
Task1_train_33965 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | GACACCACAGTGCTCCGGGTCTCCTTGCCTCCAAAGCCTCCTCCCATTCTCTTCACTCGAACCACAATCCGGTTTGCTGGAACCCCCAACATTTTTGCAACAAAGCTCTGTGAGTGAAAGACAGAACATTCGCACTGAATGCATTACCTGAACTTATTTCAGGCCTAAGGCAGAGCCTGTCCAACATGCATGGACCTAATTACTGCTGCGAATTCTGAAATTCCTTGATTGAAAATCCCATGCAGCTTTGTGGTTAGTGATGCTGGGGCCTGCCAGACTGAATTCAGCATTGGTTTTTAACCAGAGGGCAAGCAGTTGGT... | GACACCACAGTGCTCCGGGTCTCCTTGCCTCCAAAGCCTCCTCCCATTCTCTTCACTCGAACCACAATCCGGTTTGCTGGAACCCCCAACATTTTTGCAACAAAGCTCTGTGAGTGAAAGACAGAACATTCGCACTGAATGCATTACCTGAACTTATTTCAGGCCTAAGGCAGAGCCTGTCCAACATGCATGGACCTAATTACTGCTGCGAATTCTGAAATTCCTTGATTGAAAATCCCATGCAGCTTTGTGGTTAGTGATGCTGGGGCCTGCCAGACTGAATTCAGCATTGGTTTTTAACCAGAGGGCAAGCAGTTGGT... |
Task1_train_33966 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AAAGAAAGAATTCAAAAAAGAGGAAAGACAAACATCAGATCCCGATGCCTCAGGAACAAGTAGCTCAAGAGTTGTACTTCCAGTGGGCAATTTTCCCTCAGGCAGAATGAATCTCCAAGTCCTTTACTAATATTTTAAAATTTCCTCTGAAGAAGGACAATATGTAGATATTTGTTTTATGCATAATTACTCCTTTGGGTTTTTTTTTAAATGCACCGGTCATAATGTATTGTGCAAAGTGCCTTTTGATTTCAAAAACAAGCCTAAAGATTACATTAATATGATTGTCACAAAACACTAATCATTAAGATGAAATGACC... | AAAGAAAGAATTCAAAAAAGAGGAAAGACAAACATCAGATCCCGATGCCTCAGGAACAAGTAGCTCAAGAGTTGTACTTCCAGTGGGCAATTTTCCCTCAGGCAGAATGAATCTCCAAGTCCTTTACTAATATTTTAAAATTTCCTCTGAAGAAGGACAATATGTAGATATTTGTTTTATGCATAATTACTCCTTTGGGTTTTTTTTTAAATGCACCGGTCATAATGTATTGTGCAAAGTGCCTTTTGATTTCAAAAACAAGCCTAAAGATTACATTAATATGATTGTCACAAAACACTAATCATTAAGATGAAATGACC... |
Task1_train_33967 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TAGGTCAGAGTGAAGAAGGGGTAGAGATAGTAGGTAGAACCGAATAAAATTACAGATGCTTCTCTTATGGAGAGTTCACAACCCATTTCAATAGAGAAATTTGAGTTTTTACATCTTCCTTATGTTAAATTGAATTCTTTCAGTCTGCAATCTTCATTTGTTTCTTGCTTTAGAGGGTATCAAAAGAAGGGAAAAAAGAAAAACAGAAGGAATGGTCTAGTGTTCTATAATCTCAGTATTGGTACACAAATATTCTTGTATCTTATCTCCCAGGCAATATGGGGATCCCTTTTGTAGGGTCCAGTGTCTGCATGATTAGA... | TAGGTCAGAGTGAAGAAGGGGTAGAGATAGTAGGTAGAACCGAATAAAATTACAGATGCTTCTCTTATGGAGAGTTCACAACCCATTTCAATAGAGAAATTTGAGTTTTTACATCTTCCTTATGTTAAATTGAATTCTTTCAGTCTGCAATCTTCATTTGTTTCTTGCTTTAGAGGGTATCAAAAGAAGGGAAAAAAGAAAAACAGAAGGAATGGTCTAGTGTTCTATAATCTCAGTATTGGTACACAAATATTCTTGTATCTTATCTCCCAGGCAATATGGGGATCCCTTTTGTAGGGTCCAGTGTCTGCATGATTAGA... |
Task1_train_33968 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | ATGAACTAGGTTTCTAGTTTCCTCACTTTTAATCTATCTCTTTTCCTTAGCTTTTCATTGGGTTGAAATTATACCAGCTAATAACAACCAACTTTTACTGCATACTTAATATGATGCATATATTTTATTCTGCATTCCACACATATTCTCTTATTTTATTGCAACAATTTTTAAAAATATCTGTTTTACACGTGAGGAAGCTAAGTCACAGAGAGGTTAAGTGGAGTCAGATGGAGCCAGCCAGGGGATTACAGATGATTTATCTACTATTGTTATTTTAACCAGTTTTCTGTCCTCTCTTTCATGGATCATACACATAG... | ATGAACTAGGTTTCTAGTTTCCTCACTTTTAATCTATCTCTTTTCCTTAGCTTTTCATTGGGTTGAAATTATACCAGCTAATAACAACCAACTTTTACTGCATACTTAATATGATGCATATATTTTATTCTGCATTCCACACATATTCTCTTATTTTATTGCAACAATTTTTAAAAATATCTGTTTTACACGTGAGGAAGCTAAGTCACAGAGAGGTTAAGTGGAGTCAGATGGAGCCAGCCAGGGGATTACAGATGATTTATCTACTATTGTTATTTTAACCAGTTTTCTGTCCTCTCTTTCATGGATCATACACATAG... |
Task1_train_33969 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TCTCAGGCCAAATGAGACCACTTTTCTACCTTCTTTCACTTCTGACATTTGCATTAAAACTAAGTGGTGTATTTAGGCAGCCAAGCCACACTCTCATCTGTGTTAAAACAACAACAAACCACCCAAAAAAGGGGAAGGAGTATTCTCCCCTTGAGCAATATCCCCCTCCCGGGCAAAGTGTCGTATTATTGGTCCCCAAGGAAGAGGAACAGTTAACCAGCTGTGAACTTTCAGGATGGGTGGAAAAGAGCATTTTCAATGACCCGACTTCCCCACCTTCCCACACACATTTGGGTAAATACATCTCCACATTGCACTCC... | TCTCAGGCCAAATGAGACCACTTTTCTACCTTCTTTCACTTCTGACATTTGCATTAAAACTAAGTGGTGTATTTAGGCAGCCAAGCCACACTCTCATCTGTGTTAAAACAACAACAAACCACCCAAAAAAGGGGAAGGAGTATTCTCCCCTTGAGCAATATCCCCCTCCCGGGCAAAGTGTCGTATTATTGGTCCCCAAGGAAGAGGAACAGTTAACCAGCTGTGAACTTTCAGGATGGGTGGAAAAGAGCATTTTCAATGACCCGACTTCCCCACCTTCCCACACACATTTGGGTAAATACATCTCCACATTGCACTCC... |
Task1_train_33970 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CTCTAATTGATTTAAGTCAGCTACTCTTGAAAAACCCAAATACATAATACATCTACACTAATTTTTAAATCCAGAATGTGTCCTGGGTTTAGTGATTCAGAGTATCTAAATCTACATATACATAAAATTATCTTCTCTTTGGGAACAGGCTTCCAAAAATGTCATCTTTTGCTACTGACGGCATGCATGTGTGTATAAAATCCAATTATAAGTGTTTCCCTTCTCTACACCTGGGCAGAACACTGTACTGAGGAACCAATAAAAGGAGATGGTCTCCAAACACAGGTGGGCCTGCACCACTGCTCAGCCATGTTTACAGG... | CTCTAATTGATTTAAGTCAGCTACTCTTGAAAAACCCAAATACATAATACATCTACACTAATTTTTAAATCCAGAATGTGTCCTGGGTTTAGTGATTCAGAGTATCTAAATCTACATATACATAAAATTATCTTCTCTTTGGGAACAGGCTTCCAAAAATGTCATCTTTTGCTACTGACGGCATGCATGTGTGTATAAAATCCAATTATAAGTGTTTCCCTTCTCTACACCTGGGCAGAACACTGTACTGAGGAACCAATAAAAGGAGATGGTCTCCAAACACAGGTGGGCCTGCACCACTGCTCAGCCATGTTTACAGG... |
Task1_train_33971 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCTTGATCCTCCCGCTTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGGGCCACTGCGCCCGGCCCTACCTTCATCTCTTGAGCTCTGTAGCCATCCATTTTCAGCTGACTGACTTTTCTCCACCTGATGTTCTACCAGAACCTTAAATCCCACCTATAACAAGCCAAGTTCATCATCCTTCCCGCTGAACTGTTTCCTCCTCTGGACTTTACATGAATGACCACACACCCATCCCAGAGGGCAGTGTCACCCCAGAACTCCTCA... | TTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCTTGATCCTCCCGCTTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGGGCCACTGCGCCCGGCCCTACCTTCATCTCTTGAGCTCTGTAGCCATCCATTTTCAGCTGACTGACTTTTCTCCACCTGATGTTCTACCAGAACCTTAAATCCCACCTATAACAAGCCAAGTTCATCATCCTTCCCGCTGAACTGTTTCCTCCTCTGGACTTTACATGAATGACCACACACCCATCCCAGAGGGCAGTGTCACCCCAGAACTCCTCA... |
Task1_train_33972 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AGGTATGCACGGCTCTCCCAGGCACCCAGAAGATGCTGGAAATAGTGACAACACTGTGGGGGACTCGGGGGGAGGTGCCAGGGCAGGAAGGCTACATCCAGGCTCTGCCCTCTGTTTCATGGCCATTTTGCTTACCCTACTCAGACCAGCCTGAAGGTGGCGCGAGAATAGGCTATTGTAGAGTAAGGTCAAGCACCTGCTGACCAGCTGTCCACAACCCAAATCAAGACCCACCACCCCGGGCAGTCTCCCAGTTTTCCCACTAAGATTGGATGCCTTATCTCTGAATCCCATCCTCTCCTCCCTGGGTCATCTTCTCC... | AGGTATGCACGGCTCTCCCAGGCACCCAGAAGATGCTGGAAATAGTGACAACACTGTGGGGGACTCGGGGGGAGGTGCCAGGGCAGGAAGGCTACATCCAGGCTCTGCCCTCTGTTTCATGGCCATTTTGCTTACCCTACTCAGACCAGCCTGAAGGTGGCGCGAGAATAGGCTATTGTAGAGTAAGGTCAAGCACCTGCTGACCAGCTGTCCACAACCCAAATCAAGACCCACCACCCCGGGCAGTCTCCCAGTTTTCCCACTAAGATTGGATGCCTTATCTCTGAATCCCATCCTCTCCTCCCTGGGTCATCTTCTCC... |
Task1_train_33973 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTGAAAATATGATGCCTCAATGGGTGAGTTGCAAAATTCAGTAAAGAAAATCTTCATCTCCATTAAAAAACAACAACAAAAAAAACCCTGCACCCTGCATCCCCCAAAACTCTCTACTTAACATACTTTGTTTACCACCGCTCCCCTCTCTGCCACCTCCTCCAATATGAATGTGAGCGCCTCCAGGGGTGGGATTTCTGTTCGCTGTGCCTCCTGTGCACCTAGAGCATGGCACCATACTGCAGGCACTCAGAAAATACTTGTTGAATGAGTTACTGTGTGAATGCATTCAACTGTGTGAAAGACAGCAGGGAAAAGAT... | CTGAAAATATGATGCCTCAATGGGTGAGTTGCAAAATTCAGTAAAGAAAATCTTCATCTCCATTAAAAAACAACAACAAAAAAAACCCTGCACCCTGCATCCCCCAAAACTCTCTACTTAACATACTTTGTTTACCACCGCTCCCCTCTCTGCCACCTCCTCCAATATGAATGTGAGCGCCTCCAGGGGTGGGATTTCTGTTCGCTGTGCCTCCTGTGCACCTAGAGCATGGCACCATACTGCAGGCACTCAGAAAATACTTGTTGAATGAGTTACTGTGTGAATGCATTCAACTGTGTGAAAGACAGCAGGGAAAAGAT... |
Task1_train_33974 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | ACCACAATGATACATCCATCTTTTAATTTATCAGATGAGCAAAGATACACTGCAAGATGAGCAAGATACAATGACAGGTGATGCTGGGGAAGGGGTGGCGGAAACGGCACTTTCATACATGGTTGATGTGAGTGTAAACTGACACAACCTCCATGGAGGACAATTTGTCAACTCCAATCACAACTATTTAATACAAGGCACACATCTGTTGGCCCAGCAGCTTCATTTCTAAAAATTAACTAACTGATTGAGACATGGTCTCGCTCTGTTGTCCAGGCTTGAGTACAGTGGCATGACCATGGCTGAACTGCAGCCTCAAC... | ACCACAATGATACATCCATCTTTTAATTTATCAGATGAGCAAAGATACACTGCAAGATGAGCAAGATACAATGACAGGTGATGCTGGGGAAGGGGTGGCGGAAACGGCACTTTCATACATGGTTGATGTGAGTGTAAACTGACACAACCTCCATGGAGGACAATTTGTCAACTCCAATCACAACTATTTAATACAAGGCACACATCTGTTGGCCCAGCAGCTTCATTTCTAAAAATTAACTAACTGATTGAGACATGGTCTCGCTCTGTTGTCCAGGCTTGAGTACAGTGGCATGACCATGGCTGAACTGCAGCCTCAAC... |
Task1_train_33975 | 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 | AATGGCTGGTTAGATAAATTAAGACAGACAAAATGATTTATGCAGCCATAGCAATGACACAGAACGTTATGCACTGATATAGAAGGATTTCTAAGACAGAAAAGAAAGCAAAATGTAGAGATAGGTGTATATATATGGTACCATTTATGTAAAAAAGATACACCCGTATTTCATACACATAAATGAGTATGTATATGCTTGAAAAGGTATATAGTATCCCTGAAAGATATAAAATGCAGTTGTAAAAATAATTGCTTCCTATCAGGGCAATGGTTATGGCTGAGATAAAAGTGGAAACAATTTGACTTCACTATGTATCT... | AATGGCTGGTTAGATAAATTAAGACAGACAAAATGATTTATGCAGCCATAGCAATGACACAGAACGTTATGCACTGATATAGAAGGATTTCTAAGACAGAAAAGAAAGCAAAATGTAGAGATAGGTGTATATATATGGTACCATTTATGTAAAAAAGATACACCCGTATTTCATACACATAAATGAGTATGTATATGCTTGAAAAGGTATATAGTATCCCTGAAAGATATAAAATGCAGTTGTAAAAATAATTGCTTCCTATCAGGGCAATGGTTATGGCTGAGATAAAAGTGGAAACAATTTGACTTCACTATGTATCT... |
Task1_train_33976 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTCTTTAGTGTTTGATAGAAGGAAATAGTAACTAACACATTGAATATTTACTATGGCAGTTTACATATGTTAGTTCACTTAATTCTATTTACCCTAGGATTCAGGTATTACTACCTCTGTTTTACAGATGAGGAAATTGAGCCTTAATGAGGTTTAGTAACCTGGAAAGATTTACAGCTAGTAGGTGGTGGGGTGCTGAGTTGAGAGGCTGAGTTGAGAGGGTCTGTCTGATCCTATAGCCCATGCTCTTTGCATGGTAAGTACTGGAAAGTAAACAGCCATCTCGGAGTATAGATGAGTGTAAATAATTAGGCAATAAG... | CTCTTTAGTGTTTGATAGAAGGAAATAGTAACTAACACATTGAATATTTACTATGGCAGTTTACATATGTTAGTTCACTTAATTCTATTTACCCTAGGATTCAGGTATTACTACCTCTGTTTTACAGATGAGGAAATTGAGCCTTAATGAGGTTTAGTAACCTGGAAAGATTTACAGCTAGTAGGTGGTGGGGTGCTGAGTTGAGAGGCTGAGTTGAGAGGGTCTGTCTGATCCTATAGCCCATGCTCTTTGCATGGTAAGTACTGGAAAGTAAACAGCCATCTCGGAGTATAGATGAGTGTAAATAATTAGGCAATAAG... |
Task1_train_33977 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GAGAAAGAAAAGGAGAATAACTTTGTACTACCACCCTACCCAAAACAAAACAAAACAAAACAAAGCAAACTCTTGGCAGGCATCAGGGAAAGATGAAAATGAGATTGATCTTTATTGTAGAATCCAGGCCAGGGGGCTGCTTTGAAGGCAAGAATTTCATGCTAGAAATTCCTTACTAGCCACACAAACTTCTTGGAGCAAGATAGACTTGTATTACTTCTAACAGTGGGAAAAACACTGCCATCATAACTCACACTTTTGCCATGAGTAAAGAATTTGTCTAGAATCTTAGAGAAACTTCTGCTTGAACTTTAGGTGCA... | GAGAAAGAAAAGGAGAATAACTTTGTACTACCACCCTACCCAAAACAAAACAAAACAAAACAAAGCAAACTCTTGGCAGGCATCAGGGAAAGATGAAAATGAGATTGATCTTTATTGTAGAATCCAGGCCAGGGGGCTGCTTTGAAGGCAAGAATTTCATGCTAGAAATTCCTTACTAGCCACACAAACTTCTTGGAGCAAGATAGACTTGTATTACTTCTAACAGTGGGAAAAACACTGCCATCATAACTCACACTTTTGCCATGAGTAAAGAATTTGTCTAGAATCTTAGAGAAACTTCTGCTTGAACTTTAGGTGCA... |
Task1_train_33978 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | GTGGAAGGCAGCTGGTGAGAGAGATGGTCCAAGGTGAGAGAGATGGTCCAAGGTAAAGGATTGTACAGCTGTCATATATGTTATTGTCCTTATCCAGCTGTTTTCCCACCCCTGGATTTGTTGGATGACTCCTCCAACAGTGAAGGTAGAAACACATTCCACAGCCATGTGAATTCCAACTTCGGAGAAAGGTGAGCTACAGAACAGTTCTAATATAAACTGATGTCATGAGATTCTAGAGTCTGCTGTCATCACATTCTGTGTTATTGCCATGTTAACTCCACATGCAGCTTGAGCATTCAGTCTTCTGACCTGTTCCA... | GTGGAAGGCAGCTGGTGAGAGAGATGGTCCAAGGTGAGAGAGATGGTCCAAGGTAAAGGATTGTACAGCTGTCATATATGTTATTGTCCTTATCCAGCTGTTTTCCCACCCCTGGATTTGTTGGATGACTCCTCCAACAGTGAAGGTAGAAACACATTCCACAGCCATGTGAATTCCAACTTCGGAGAAAGGTGAGCTACAGAACAGTTCTAATATAAACTGATGTCATGAGATTCTAGAGTCTGCTGTCATCACATTCTGTGTTATTGCCATGTTAACTCCACATGCAGCTTGAGCATTCAGTCTTCTGACCTGTTCCA... |
Task1_train_33979 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTTAGCACTTAGGACACTGTAGAACTTTCTTTGGAAGTTTAATTGCAATGAACTTTAAAACTTGAAACTTCAATTCACTTTTCTAAATGTGAATGCATACATTTCATTTGAGCTTTATGCTTTCCCAGCTACCAAAGTAATTGCCATCTTAAAAAACACAACTGACCTCATCTCCACTGTCTTTTCCAAACAGCTTCCAAGACTATCTTCTGATTCTGACTTTCCAAAAAGCAGGCATTAATGTTAACTTTCAAAAAATCATCTAGAAGAGAAACTTGGTCAGTTGTAATGGGAGTTCTGTCCCCAACTCTTGTCACCTC... | CTTAGCACTTAGGACACTGTAGAACTTTCTTTGGAAGTTTAATTGCAATGAACTTTAAAACTTGAAACTTCAATTCACTTTTCTAAATGTGAATGCATACATTTCATTTGAGCTTTATGCTTTCCCAGCTACCAAAGTAATTGCCATCTTAAAAAACACAACTGACCTCATCTCCACTGTCTTTTCCAAACAGCTTCCAAGACTATCTTCTGATTCTGACTTTCCAAAAAGCAGGCATTAATGTTAACTTTCAAAAAATCATCTAGAAGAGAAACTTGGTCAGTTGTAATGGGAGTTCTGTCCCCAACTCTTGTCACCTC... |
Task1_train_33980 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TATTGTGGTTCTAATGAAAAACAAAGGCCGTTTCAAAAGTTAAAATGCCTATCTGCGGATGCACAAAAACCTATGGAACCTATTCCGGGATTTCCTTTTCCCTGATCTCTGGTTGACTTTTCTTTATTCGATTTCTGCCTCTCCCTCACCCACCATGGGTGTTTCTATGATTTTAATACTAAAAAGCCATTTTAAGTATACAGAAACTTTTAATTTGTGAAGGTAGCTGTACAGTATCTAAGGAAATATAGATTGCAGTGGATTTTAATAAGGAAAGAGTCATTCTCTGCCTTCCAAACACCTTTCTGTGGCGCCTGCAG... | TATTGTGGTTCTAATGAAAAACAAAGGCCGTTTCAAAAGTTAAAATGCCTATCTGCGGATGCACAAAAACCTATGGAACCTATTCCGGGATTTCCTTTTCCCTGATCTCTGGTTGACTTTTCTTTATTCGATTTCTGCCTCTCCCTCACCCACCATGGGTGTTTCTATGATTTTAATACTAAAAAGCCATTTTAAGTATACAGAAACTTTTAATTTGTGAAGGTAGCTGTACAGTATCTAAGGAAATATAGATTGCAGTGGATTTTAATAAGGAAAGAGTCATTCTCTGCCTTCCAAACACCTTTCTGTGGCGCCTGCAG... |
Task1_train_33981 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | TTAAAAATACTGTCTAATTTTTCTTCTTGTTATTGTTGGATGACAGTCTCTGTCGCTGTGCTGATGAAAGAGCACGGTGAACCATTCGACGTCTAGTAACTTCAAACAGTTTGGAAAACACCTAAAACATGAAGTGATTTGTTAGGAGAATGAATCAGAGTGCCTCGAAGCTAAAGAGTTTAAGACTACAAGAATTTGAGACTGTAGGTTTCTCACCTTCCTGGGACTCCTCTGAAGCAAAAGAAAAGAGAAATGCAAAGAAATTTAGACAAGGTTTGTTGACACAGCACAGATCTCTGACTAGCTGATTACCTTACCTA... | TTAAAAATACTGTCTAATTTTTCTTCTTGTTATTGTTGGATGACAGTCTCTGTCGCTGTGCTGATGAAAGAGCACGGTGAACCATTCGACGTCTAGTAACTTCAAACAGTTTGGAAAACACCTAAAACATGAAGTGATTTGTTAGGAGAATGAATCAGAGTGCCTCGAAGCTAAAGAGTTTAAGACTACAAGAATTTGAGACTGTAGGTTTCTCACCTTCCTGGGACTCCTCTGAAGCAAAAGAAAAGAGAAATGCAAAGAAATTTAGACAAGGTTTGTTGACACAGCACAGATCTCTGACTAGCTGATTACCTTACCTA... |
Task1_train_33982 | Located on Chromosome 2, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ATGCTTATCAGAAACACATAATCATTTAATTTCATAAAACTTACAACTGAAAAAGTAGACATGTATAAAAGTTGTTCCAACAAAGTTTTCCAGTATAACCAAATCAAATATTAATCATTTTCCACTCATATTTGTATCCATACTAACAAAACTGTTAATGTAAATAAAATTAAATAAAACTGAAAATTAAGTTCTTCAGTCACACCATTCAAACTGCTTTAATACTCATTTCTTTCACTAACAACCATTTCTATACATGTTTCCTCTTGTATGAACGGTCTATTCACAATCTAGATAGTTTTAAAGAAATGTTTAAATTA... | ATGCTTATCAGAAACACATAATCATTTAATTTCATAAAACTTACAACTGAAAAAGTAGACATGTATAAAAGTTGTTCCAACAAAGTTTTCCAGTATAACCAAATCAAATATTAATCATTTTCCACTCATATTTGTATCCATACTAACAAAACTGTTAATGTAAATAAAATTAAATAAAACTGAAAATTAAGTTCTTCAGTCACACCATTCAAACTGCTTTAATACTCATTTCTTTCACTAACAACCATTTCTATACATGTTTCCTCTTGTATGAACGGTCTATTCACAATCTAGATAGTTTTAAAGAAATGTTTAAATTA... |
Task1_train_33983 | 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 | TCTGTCGTGTTTAGACATGCATTCTCATGGTCTCTAAAATCTTGACCTTTCTTTTCAGAATTACTCAGTTGGATTGTGTGGGCCAGTCTTTCAGACCATAGAATCTGTTTCCAGCTAACCTGTCCTAACCCTGTCTCAAAAAAACCAGTCGGCCGGGCACAGTGCCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACCTGAGGTCAGGAGTTTAAGACTAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAAGTGTGGTGGCACACGCTTGTAATCCCAGC... | TCTGTCGTGTTTAGACATGCATTCTCATGGTCTCTAAAATCTTGACCTTTCTTTTCAGAATTACTCAGTTGGATTGTGTGGGCCAGTCTTTCAGACCATAGAATCTGTTTCCAGCTAACCTGTCCTAACCCTGTCTCAAAAAAACCAGTCGGCCGGGCACAGTGCCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACCTGAGGTCAGGAGTTTAAGACTAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAAGTGTGGTGGCACACGCTTGTAATCCCAGC... |
Task1_train_33984 | Located on Chromosome 2, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CTCAATTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACCTTAGGTGTGAGGCATCACGCCTGGCTAATTTTTTTTTTTTTTTTTCTGTATCCCCAGTAGAATGACTACTGGCTATTTTTTGTTTTGTTTTGTTTTTTTTACTTTTCGTGGAAACATGGTCTCACTATGTTGCCCAGGTGGGGCTCCAACTCCTGAGCTCAAGCGATCCTCCCACCTTGGCCTCCCAAAGTGCAGGGATTATGGGTGTGAGCCATTGCGCCCGGCCATACTTCAGTTTTGAATTTAAATTGTCATCTTACAGAGATATGATCTTTGA... | CTCAATTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACCTTAGGTGTGAGGCATCACGCCTGGCTAATTTTTTTTTTTTTTTTTCTGTATCCCCAGTAGAATGACTACTGGCTATTTTTTGTTTTGTTTTGTTTTTTTTACTTTTCGTGGAAACATGGTCTCACTATGTTGCCCAGGTGGGGCTCCAACTCCTGAGCTCAAGCGATCCTCCCACCTTGGCCTCCCAAAGTGCAGGGATTATGGGTGTGAGCCATTGCGCCCGGCCATACTTCAGTTTTGAATTTAAATTGTCATCTTACAGAGATATGATCTTTGA... |
Task1_train_33985 | Located on Chromosome 2, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAGAGCTTTTAAAATCAAAATTCCAATGCCTTGGAAACCTATGGGATCTGTCAATCTTCCTGGCCCTTGAGTCTCAATTGTTACAAGATGTTCTGTGTCCATGGATTTTCTCATCTCTGGTCTCACTGGTTTCAGTGCTAGGGAGCCAAAGAAACCCATGAGGTGTAGTTGCGATTAGGCCCAGACATAACTATTCTCATTTATAATCTTCAGTTTTTCTCCTCTGTTTAGATGGTGACTGTACAAGAACATCTTCTGGAATCTACGAGAGAAATGGAATAGGTATTCATACCACTCCTAATGGGATTGTCTACACAGGA... | AAGAGCTTTTAAAATCAAAATTCCAATGCCTTGGAAACCTATGGGATCTGTCAATCTTCCTGGCCCTTGAGTCTCAATTGTTACAAGATGTTCTGTGTCCATGGATTTTCTCATCTCTGGTCTCACTGGTTTCAGTGCTAGGGAGCCAAAGAAACCCATGAGGTGTAGTTGCGATTAGGCCCAGACATAACTATTCTCATTTATAATCTTCAGTTTTTCTCCTCTGTTTAGATGGTGACTGTACAAGAACATCTTCTGGAATCTACGAGAGAAATGGAATAGGTATTCATACCACTCCTAATGGGATTGTCTACACAGGA... |
Task1_train_33986 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ACAACCTGAGAACTGTTATTTCCATTCTGTTAGGTCATCCATGGCGAAGCTGTACAAAGGGCTGGCTTCCCAGTGTGCCAATGCTGGGCAAGATGCTTCCCCCACTGCAGGTCCTGAGGCTGTCCGTGACACTGGGATCCACTCAGAAGAGTTGCTGCAACCCTACCCTTCTGCTCCCAGTTCTGGCCCTGCCATCACGTAAGCACCTGTTGCTGTGGGAAGGTTAATGCCAATGCCTTTGGGACCCAGCCAGTCTGTGCGGGTTAGCAGGGCAGCCTAGATTCCTCCATCCCCTTTCCCCATCAGGCCTATATGTGCCA... | ACAACCTGAGAACTGTTATTTCCATTCTGTTAGGTCATCCATGGCGAAGCTGTACAAAGGGCTGGCTTCCCAGTGTGCCAATGCTGGGCAAGATGCTTCCCCCACTGCAGGTCCTGAGGCTGTCCGTGACACTGGGATCCACTCAGAAGAGTTGCTGCAACCCTACCCTTCTGCTCCCAGTTCTGGCCCTGCCATCACGTAAGCACCTGTTGCTGTGGGAAGGTTAATGCCAATGCCTTTGGGACCCAGCCAGTCTGTGCGGGTTAGCAGGGCAGCCTAGATTCCTCCATCCCCTTTCCCCATCAGGCCTATATGTGCCA... |
Task1_train_33987 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TTATTCTAAAGATACGACATGTTCATATATCAAATGTTATTAAGAATAGCCTCTCCCACTATAAATGTTTTCCTATCAATTTTGCAGAAGGAAATTTGTTGAGATTTGATTCCTCTGTCAATTTTTTAGTCACAAATTTTACTACGTGTGATTTTTGTGTTGCCAATTTTGTGTTAATTATTTGTATCCATAATAGCTATTATTAATTGCATTAAATGGCTGATAGGAATTGAATTTGCTATATTTATTTATGAGATAATCTATGAGAAAAACAATTCTGAGACAATGAGATGGACTCAGGGAGATGGGGACGAGAAAGC... | TTATTCTAAAGATACGACATGTTCATATATCAAATGTTATTAAGAATAGCCTCTCCCACTATAAATGTTTTCCTATCAATTTTGCAGAAGGAAATTTGTTGAGATTTGATTCCTCTGTCAATTTTTTAGTCACAAATTTTACTACGTGTGATTTTTGTGTTGCCAATTTTGTGTTAATTATTTGTATCCATAATAGCTATTATTAATTGCATTAAATGGCTGATAGGAATTGAATTTGCTATATTTATTTATGAGATAATCTATGAGAAAAACAATTCTGAGACAATGAGATGGACTCAGGGAGATGGGGACGAGAAAGC... |
Task1_train_33988 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGGCTGGAGATCAGGGACTCAGCTCTCTCCTCGGTCCTTCCATGTCCAAAGGAACAGGGCAGAAATTCCTGTCCCTTTCTCATCACAGACACTGCATTCTGTAGGAACGCCAGACCTCTTCAGGGAAAATCTCCCCTCCCTGGATACCCCCCCACCCACCCCCACCCCCAGAAAAAAGGCTGTGGACCCTTCTCCTCCCTGACCCCTCCCCAGCCAATCCCTGACACTGTGAGGAGGACAGAGATTAACCTGGCCCAGAGGGAGGCAGGAAGCTGCCCAGGAAGGTGAGAGGATCTAGGTGGGCAGTTTCAGAGTGGCGG... | AGGCTGGAGATCAGGGACTCAGCTCTCTCCTCGGTCCTTCCATGTCCAAAGGAACAGGGCAGAAATTCCTGTCCCTTTCTCATCACAGACACTGCATTCTGTAGGAACGCCAGACCTCTTCAGGGAAAATCTCCCCTCCCTGGATACCCCCCCACCCACCCCCACCCCCAGAAAAAAGGCTGTGGACCCTTCTCCTCCCTGACCCCTCCCCAGCCAATCCCTGACACTGTGAGGAGGACAGAGATTAACCTGGCCCAGAGGGAGGCAGGAAGCTGCCCAGGAAGGTGAGAGGATCTAGGTGGGCAGTTTCAGAGTGGCGG... |
Task1_train_33989 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCATTCTGTAGGAACGCCAGACCTCTTCAGGGAAAATCTCCCCTCCCTGGATACCCCCCCACCCACCCCCACCCCCAGAAAAAAGGCTGTGGACCCTTCTCCTCCCTGACCCCTCCCCAGCCAATCCCTGACACTGTGAGGAGGACAGAGATTAACCTGGCCCAGAGGGAGGCAGGAAGCTGCCCAGGAAGGTGAGAGGATCTAGGTGGGCAGTTTCAGAGTGGCGGGGAAGAGGAGAGCTGCGAGGGGGAGGGGCAGCGGCTTATCTCTCCCAGGAGGGGGGAGCTCACTCCAAACAGCTAGTGCACTGGCGTGTGAAA... | GCATTCTGTAGGAACGCCAGACCTCTTCAGGGAAAATCTCCCCTCCCTGGATACCCCCCCACCCACCCCCACCCCCAGAAAAAAGGCTGTGGACCCTTCTCCTCCCTGACCCCTCCCCAGCCAATCCCTGACACTGTGAGGAGGACAGAGATTAACCTGGCCCAGAGGGAGGCAGGAAGCTGCCCAGGAAGGTGAGAGGATCTAGGTGGGCAGTTTCAGAGTGGCGGGGAAGAGGAGAGCTGCGAGGGGGAGGGGCAGCGGCTTATCTCTCCCAGGAGGGGGGAGCTCACTCCAAACAGCTAGTGCACTGGCGTGTGAAA... |
Task1_train_33990 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | GTTCTGTGTGCTATTGGTGTTTATTTGCATCCACCTGTCCAGTTGCTCTGCTGTCTTGTGTTTTTGCAGCCTCTACAACCCCACGTCAGAGTGTGGGATTCTGTTACTCTATCCACACTGCAGATTATTGGACTTGGCACTTTTGAGCGTGGAGTAGGATGCCTGGATTTTTCAAAAGCAGTAAGTAACAATTTTTAGAGAAGTAAGCAAGCTGAACAAAAAAGCAGGAAAGAAGTTAAGCTCAGTTTTGTGTTTATGTGGCCATGAAGTGATAATCCTGAGTTGAAAAATGAGATGCTAGCTATTGCTAACATATTAGC... | GTTCTGTGTGCTATTGGTGTTTATTTGCATCCACCTGTCCAGTTGCTCTGCTGTCTTGTGTTTTTGCAGCCTCTACAACCCCACGTCAGAGTGTGGGATTCTGTTACTCTATCCACACTGCAGATTATTGGACTTGGCACTTTTGAGCGTGGAGTAGGATGCCTGGATTTTTCAAAAGCAGTAAGTAACAATTTTTAGAGAAGTAAGCAAGCTGAACAAAAAAGCAGGAAAGAAGTTAAGCTCAGTTTTGTGTTTATGTGGCCATGAAGTGATAATCCTGAGTTGAAAAATGAGATGCTAGCTATTGCTAACATATTAGC... |
Task1_train_33991 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | GCTGTCTTGTGTTTTTGCAGCCTCTACAACCCCACGTCAGAGTGTGGGATTCTGTTACTCTATCCACACTGCAGATTATTGGACTTGGCACTTTTGAGCGTGGAGTAGGATGCCTGGATTTTTCAAAAGCAGTAAGTAACAATTTTTAGAGAAGTAAGCAAGCTGAACAAAAAAGCAGGAAAGAAGTTAAGCTCAGTTTTGTGTTTATGTGGCCATGAAGTGATAATCCTGAGTTGAAAAATGAGATGCTAGCTATTGCTAACATATTAGCTATTGCTAAATGGCTAGCATTTTGACCTAAGTCCTAAAGTACTTTGGTT... | GCTGTCTTGTGTTTTTGCAGCCTCTACAACCCCACGTCAGAGTGTGGGATTCTGTTACTCTATCCACACTGCAGATTATTGGACTTGGCACTTTTGAGCGTGGAGTAGGATGCCTGGATTTTTCAAAAGCAGTAAGTAACAATTTTTAGAGAAGTAAGCAAGCTGAACAAAAAAGCAGGAAAGAAGTTAAGCTCAGTTTTGTGTTTATGTGGCCATGAAGTGATAATCCTGAGTTGAAAAATGAGATGCTAGCTATTGCTAACATATTAGCTATTGCTAAATGGCTAGCATTTTGACCTAAGTCCTAAAGTACTTTGGTT... |
Task1_train_33992 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | GTATGGAAGGGTGTGGGTGTGTGTGAAGGGGCGAGTGGAGACACTGTGTGTATCTCTAGATAAGAAGATATGCACCACGTTGAAAATACTCAGTGTAGATCTCTATGTGTATAGGTATCTGTATATCTTTCCTTTTGTTTACAACTGTTAAAAAACCTCAAAATAGTTCTCTTCAAAAGAAGAGAGATTCCAAGCAACCCATCTTTCTTCAGTATGTATGTTCTGTACATACTTATCGGAGCGCGCCAGTAAGTATCAGGCATATATATCTGTCTGTTAGCAATGATTATTACATCATCAGATCAGCATGTGCTATACTC... | GTATGGAAGGGTGTGGGTGTGTGTGAAGGGGCGAGTGGAGACACTGTGTGTATCTCTAGATAAGAAGATATGCACCACGTTGAAAATACTCAGTGTAGATCTCTATGTGTATAGGTATCTGTATATCTTTCCTTTTGTTTACAACTGTTAAAAAACCTCAAAATAGTTCTCTTCAAAAGAAGAGAGATTCCAAGCAACCCATCTTTCTTCAGTATGTATGTTCTGTACATACTTATCGGAGCGCGCCAGTAAGTATCAGGCATATATATCTGTCTGTTAGCAATGATTATTACATCATCAGATCAGCATGTGCTATACTC... |
Task1_train_33993 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ACCAACAGAATAAACTGTGATATATTTATAAAATGAAATCCCACAGAAGAATAAGAGGATAAAAGGAATTAACTACTGATACGTACAACACGGACTAACCTCAAAAATATTTTTTGAGCAGCCAGACACGGCGGCTCACATCTGTAATTCCAACATTTTCAGAGGCAAAAGCAGGACGATTACTTGAGCTCAGGAGTGAGTCTACAGTGAACTGTGACTGTGCCATTGCACTCCAGCCTGGGTCAGAGCTGGTTCCATTTACATGAAGTTCAAAAAAAGGCAAAACTATCTATTTATGATGATAAAAGTCAGAATAAGAA... | ACCAACAGAATAAACTGTGATATATTTATAAAATGAAATCCCACAGAAGAATAAGAGGATAAAAGGAATTAACTACTGATACGTACAACACGGACTAACCTCAAAAATATTTTTTGAGCAGCCAGACACGGCGGCTCACATCTGTAATTCCAACATTTTCAGAGGCAAAAGCAGGACGATTACTTGAGCTCAGGAGTGAGTCTACAGTGAACTGTGACTGTGCCATTGCACTCCAGCCTGGGTCAGAGCTGGTTCCATTTACATGAAGTTCAAAAAAAGGCAAAACTATCTATTTATGATGATAAAAGTCAGAATAAGAA... |
Task1_train_33994 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | CTACACTTAAACACAGTTTTCTTTCTCTTCCCACTCCTCTTCCTTCTCCCTTCCCTGCTCCACATAATAACTGCCTTCCTCACCAAGTGCTCTGGGCATATAGTTACTCCCATCCCCAGCCCCTGGAGCTGGGCAAGGGCCAGGATTACTATTCCTATTCACAGATGGAGAACTAAGTCCAGAGAAGGGTACAGTGGGCTGGGGCCATAGTTCGGACCAGGGAGTCAGTCCTACCTCCATGTGGCGGCAGCCTGAAGCCTGCTTCGCGAGGGAGCACCCAACCCCGTTTAGAGAAGGCCTTGCAAATGATGGAAAGGCGG... | CTACACTTAAACACAGTTTTCTTTCTCTTCCCACTCCTCTTCCTTCTCCCTTCCCTGCTCCACATAATAACTGCCTTCCTCACCAAGTGCTCTGGGCATATAGTTACTCCCATCCCCAGCCCCTGGAGCTGGGCAAGGGCCAGGATTACTATTCCTATTCACAGATGGAGAACTAAGTCCAGAGAAGGGTACAGTGGGCTGGGGCCATAGTTCGGACCAGGGAGTCAGTCCTACCTCCATGTGGCGGCAGCCTGAAGCCTGCTTCGCGAGGGAGCACCCAACCCCGTTTAGAGAAGGCCTTGCAAATGATGGAAAGGCGG... |
Task1_train_33995 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TCTATGCACATTGAATTCTTCCACCAGACAGGGGCTGTTGTCCCCATGTGCTTATGGAAACAGGCTTGGAGAGGTGACATGATGTGCCCTGTCCAAGATCCCGGGGTTAGTAAGCGGCAGAGAATTCCCCCAATGCAAGTTCATCTGCCTCTGGCCCCCCTGCACCTGCACGCTCCAAGAAAGGAGTGAGGTAGGTGGAGTATAGGTGGTAGGTGGCGCTGGGGAGTGGGGAGCCGGGCCAGGGAGCTGGAGGTACCCTGACCGCTATTGCAGAGGCAGAGCTCAGTGAGGAGGAAAGTGTGGTTTGGTAAGAGGTGTGA... | TCTATGCACATTGAATTCTTCCACCAGACAGGGGCTGTTGTCCCCATGTGCTTATGGAAACAGGCTTGGAGAGGTGACATGATGTGCCCTGTCCAAGATCCCGGGGTTAGTAAGCGGCAGAGAATTCCCCCAATGCAAGTTCATCTGCCTCTGGCCCCCCTGCACCTGCACGCTCCAAGAAAGGAGTGAGGTAGGTGGAGTATAGGTGGTAGGTGGCGCTGGGGAGTGGGGAGCCGGGCCAGGGAGCTGGAGGTACCCTGACCGCTATTGCAGAGGCAGAGCTCAGTGAGGAGGAAAGTGTGGTTTGGTAAGAGGTGTGA... |
Task1_train_33996 | 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 | GATTCTGTGAGGGTGCTATCTTGTATGCACCTAAGTAGCATGTATTTGTCTTAAGACATCTTCCCAGGAAGCTGTTTTTCTTACTTCGGTTCTATTTCACTACCAAAGGACATGTAAAACAGGTGGGGCGCATCTGGGCCTCCATCCAGAGCCAGCTGGGCCATGTTCTGGGGGAATATTTAAGCCTTAGCGATGTATTTGCATACTTAGTTCACTAGGTTGCAATCCTAAATACTTTTGGAATTGACATGCTTACTCCTCTTTAAATAAAGAGTCCAGCTAGAGAAATGGGGAAAAAACAAGGGGTTTGGGCATATGTG... | GATTCTGTGAGGGTGCTATCTTGTATGCACCTAAGTAGCATGTATTTGTCTTAAGACATCTTCCCAGGAAGCTGTTTTTCTTACTTCGGTTCTATTTCACTACCAAAGGACATGTAAAACAGGTGGGGCGCATCTGGGCCTCCATCCAGAGCCAGCTGGGCCATGTTCTGGGGGAATATTTAAGCCTTAGCGATGTATTTGCATACTTAGTTCACTAGGTTGCAATCCTAAATACTTTTGGAATTGACATGCTTACTCCTCTTTAAATAAAGAGTCCAGCTAGAGAAATGGGGAAAAAACAAGGGGTTTGGGCATATGTG... |
Task1_train_33997 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | TCTGTCCAGCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCCCCACACCAGCCTGTCTCAAGTTTACTTTCTAACTGAATATTGATAGACAAAACTCTCTGGGAGCCGCAACCCCTTTTAAGAGTGTAAAGAGGTCCTGAGACAAATTTGAAAACTGCCAACCTAGAACTTCAGTCCCACCCAAACCAGCAGTTCCCACTTGGGGGCTACCCACTGGGAGCCTTTATGTTGCTCTCTTTGCATGGGAGACTCCTTCCCTTTCTTTACTTGGCTAACTTCTTCAGTCTCTGCTTAGAGGTCACTTCCTCTGGGAC... | TCTGTCCAGCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCCCCACACCAGCCTGTCTCAAGTTTACTTTCTAACTGAATATTGATAGACAAAACTCTCTGGGAGCCGCAACCCCTTTTAAGAGTGTAAAGAGGTCCTGAGACAAATTTGAAAACTGCCAACCTAGAACTTCAGTCCCACCCAAACCAGCAGTTCCCACTTGGGGGCTACCCACTGGGAGCCTTTATGTTGCTCTCTTTGCATGGGAGACTCCTTCCCTTTCTTTACTTGGCTAACTTCTTCAGTCTCTGCTTAGAGGTCACTTCCTCTGGGAC... |
Task1_train_33998 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | TTCACTATACATTTCTGTATACTGAAATATTTCAAAGATACATAATAAAAATAATAAAGAAATGAACCCTGGGAGGGGAGAAGGAAAGCAAATTATCAACTAAAAAAGCTTAGAAGACTGGTCAGAGACAAAATTTTTAAATCTCACCAATTTCATAAAAATGATCACTAAAATGCCATTAATCACCTTGAAGTAGAGTAGGGCAATAATTATCCAGCACTCGTTAAAACCAAGCCCCATTATTTTTAGATGTTCTTATAAAAATAGCACAGGTAGAGCATCCCAAATCCAAAAATCTGAAATCAAAAAAGCTCCAAAAT... | TTCACTATACATTTCTGTATACTGAAATATTTCAAAGATACATAATAAAAATAATAAAGAAATGAACCCTGGGAGGGGAGAAGGAAAGCAAATTATCAACTAAAAAAGCTTAGAAGACTGGTCAGAGACAAAATTTTTAAATCTCACCAATTTCATAAAAATGATCACTAAAATGCCATTAATCACCTTGAAGTAGAGTAGGGCAATAATTATCCAGCACTCGTTAAAACCAAGCCCCATTATTTTTAGATGTTCTTATAAAAATAGCACAGGTAGAGCATCCCAAATCCAAAAATCTGAAATCAAAAAAGCTCCAAAAT... |
Task1_train_33999 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AGGTCACAACCTCTAAAAGCCACAGGTGTACCAGTAGGGAAAAAGTACCACAACCATGAGACTGACTCAGATTAAGACTCAAAGGACTAGTTTTCAAAACATGCATACCTATAACACAGACCAAGAAACCATGCATACATGAAAATTCACAATCTCAATCCAAAAAACAGCTTTTGTGTTTCCAAGTACCTGAGTTTTCACAAATGTCATTTTACCCCTTGCAAAAAGAAAGCAAACGAGATATGCATTGTTAAATCTACCAATGATCTAAGAGAAACTACAAAATAACTAGGCTGGGCATAATATCCACAATGATCCAT... | AGGTCACAACCTCTAAAAGCCACAGGTGTACCAGTAGGGAAAAAGTACCACAACCATGAGACTGACTCAGATTAAGACTCAAAGGACTAGTTTTCAAAACATGCATACCTATAACACAGACCAAGAAACCATGCATACATGAAAATTCACAATCTCAATCCAAAAAACAGCTTTTGTGTTTCCAAGTACCTGAGTTTTCACAAATGTCATTTTACCCCTTGCAAAAAGAAAGCAAACGAGATATGCATTGTTAAATCTACCAATGATCTAAGAGAAACTACAAAATAACTAGGCTGGGCATAATATCCACAATGATCCAT... |
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