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_33800 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TCTGAAATGAATCTGGTGTGAATCCAACGCAGTCATTTTCATGTTGTGCTCACCTCTGATTCCACAGGGCCTGATTATTCACTAGTTTTAAAACCCTTTTCATTATTTAGAAATGACAGAGTGGATTAAAGAAAAAACTGTGAGAGGGACAATTATAGGAACAGCATGAAAGTTTTAATGAACAGTTTCCAAATCAGCACCTGGAATAAGGCATGGGCGTCTTCTTCATCGCTCATGGAAATACACAGCGGCATCATCATCTTAATAAAAAGGCCAAAAATACATTTTAACTTCAGCCAACCTCACCTGCTTAATTATTA... | TCTGAAATGAATCTGGTGTGAATCCAACGCAGTCATTTTCATGTTGTGCTCACCTCTGATTCCACAGGGCCTGATTATTCACTAGTTTTAAAACCCTTTTCATTATTTAGAAATGACAGAGTGGATTAAAGAAAAAACTGTGAGAGGGACAATTATAGGAACAGCATGAAAGTTTTAATGAACAGTTTCCAAATCAGCACCTGGAATAAGGCATGGGCGTCTTCTTCATCGCTCATGGAAATACACAGCGGCATCATCATCTTAATAAAAAGGCCAAAAATACATTTTAACTTCAGCCAACCTCACCTGCTTAATTATTA... |
Task1_train_33801 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | CCCATGCACCTGGGACATAGCCAGGGCCTCCTTCCCGGCTGCCCTTGGTGCCTCCACAGGCACTGCCCCTTCCAGAGAGCTGGTGGATCCACAGACGTCCCGTGAGCTCCCAGAGCCGTGGCAGCACTCCCAGTTCCAGCACCCACCCGGTCTGGCAATCTCACCCGTGTACAGCCCCCTGGGGTCAGCGAAGTGGGTGGGAGCACACAGTGCCCACAGGGATGGGAAGAAACCATTAGAGTTCCCATTGGGTGCAGTTTTACTTATGCTGGGTGAGGTGTGGATTGCAGTGGCCGGTCCCTGGGCTGCCAGCCAGATAG... | CCCATGCACCTGGGACATAGCCAGGGCCTCCTTCCCGGCTGCCCTTGGTGCCTCCACAGGCACTGCCCCTTCCAGAGAGCTGGTGGATCCACAGACGTCCCGTGAGCTCCCAGAGCCGTGGCAGCACTCCCAGTTCCAGCACCCACCCGGTCTGGCAATCTCACCCGTGTACAGCCCCCTGGGGTCAGCGAAGTGGGTGGGAGCACACAGTGCCCACAGGGATGGGAAGAAACCATTAGAGTTCCCATTGGGTGCAGTTTTACTTATGCTGGGTGAGGTGTGGATTGCAGTGGCCGGTCCCTGGGCTGCCAGCCAGATAG... |
Task1_train_33802 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGAATTCATGTTTTAGAGACACATTTATATCCTCGTTTTATGCACATTCAGGAACAGAAAGTCCTGGCAATGAATTGGGAGTTTTTAGGGATCAGAAGCTTGGTCTCATTTATTTTATGTCTTCCATTCCATGTAAAACACAGAATGCATGTTTTGCAGGAAGCAGAGCCCCTGGGTTGTCCTGAATGTCTTGTGTTAAACTGACACAGGAGTCTGGCCTCAGGATGAAGGGAGTGCAGGAGGGCTGTGGGACTTCGGTGCTGGAGCCCAGGAGAGCATACCCTCTACCCCACGGAGCACAGCGCTGCCAGATAGGGCGG... | AGAATTCATGTTTTAGAGACACATTTATATCCTCGTTTTATGCACATTCAGGAACAGAAAGTCCTGGCAATGAATTGGGAGTTTTTAGGGATCAGAAGCTTGGTCTCATTTATTTTATGTCTTCCATTCCATGTAAAACACAGAATGCATGTTTTGCAGGAAGCAGAGCCCCTGGGTTGTCCTGAATGTCTTGTGTTAAACTGACACAGGAGTCTGGCCTCAGGATGAAGGGAGTGCAGGAGGGCTGTGGGACTTCGGTGCTGGAGCCCAGGAGAGCATACCCTCTACCCCACGGAGCACAGCGCTGCCAGATAGGGCGG... |
Task1_train_33803 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AACTTACGGCATTTCACCTTTAATCCTTTTGAAGTGAAACTGGAAACCTCAACCACTTCTGGTTGTCATGGTGTTGAGTAGGGCTTGGAGGATTTCTGATGAGCTGTGCAATAGACTCTGCCATCAATAATACATCATTGCAAAGTTTATTGAGCCTGGACAATGTGGCTTCTTATCATCAAGAGAATGCCTTTAAATACCTCTTTAATATTTTATAACATGTCATCTTCATGGAATTTAATATATAAAATATTTGAAGGTGGTGTTCACAAGTTGTAATAAAAATTCTTGCAGGCCATACATGCACTTAACATTTGTAG... | AACTTACGGCATTTCACCTTTAATCCTTTTGAAGTGAAACTGGAAACCTCAACCACTTCTGGTTGTCATGGTGTTGAGTAGGGCTTGGAGGATTTCTGATGAGCTGTGCAATAGACTCTGCCATCAATAATACATCATTGCAAAGTTTATTGAGCCTGGACAATGTGGCTTCTTATCATCAAGAGAATGCCTTTAAATACCTCTTTAATATTTTATAACATGTCATCTTCATGGAATTTAATATATAAAATATTTGAAGGTGGTGTTCACAAGTTGTAATAAAAATTCTTGCAGGCCATACATGCACTTAACATTTGTAG... |
Task1_train_33804 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GATCATATACTACATGTTTTCTAATATGATTGTTTATTTTTGACACCTAATAAAAATAAACTAAGTCTATTTTTCTCATTAAGAATTCTTGATATTGGGTTTTAAAAAATAATGGACTTTTATTTGTGATAGAAGAAAGATATAACTATTCACATTTCTGTTCTGGGATATGGATGACAAGATACCTATTCATCAGAAATAAATTTATAGAAATTTAGAGTGGAAGCGTGACTGTCAAATGTAAATTTATTGACTATTTACCTGTTAGCTCATTCAGTCAATGGTGGCTTGGATCTGCTGCCATTAGTCATGTGTCTCCT... | GATCATATACTACATGTTTTCTAATATGATTGTTTATTTTTGACACCTAATAAAAATAAACTAAGTCTATTTTTCTCATTAAGAATTCTTGATATTGGGTTTTAAAAAATAATGGACTTTTATTTGTGATAGAAGAAAGATATAACTATTCACATTTCTGTTCTGGGATATGGATGACAAGATACCTATTCATCAGAAATAAATTTATAGAAATTTAGAGTGGAAGCGTGACTGTCAAATGTAAATTTATTGACTATTTACCTGTTAGCTCATTCAGTCAATGGTGGCTTGGATCTGCTGCCATTAGTCATGTGTCTCCT... |
Task1_train_33805 | 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 | GTATAGGGATAATTAAAACCTTGCCACAGTATGCAGTCATTTATAATGAATTCCTACACAGGTTGCAGTAGTCTATGTAGACAAATGGTATTTCAGCAAAGCTAATATGAAATACACATCAGGTGATCAGAAGGTATTTCAGTGTCATTCTCGTGCATGCACCAAAGGTGAATCTCTTACCAGAAGTTAGAGCCCAACAGAAAAGGGTAACCATGAATGAATATCTGTAAAATTCAGCTCAGAGTTCAAATGTTCCAATATTGCCACTTTTGCTATTGAGCTATTGGCCATGGAATTAATAAATATAGAGAAACAATGTT... | GTATAGGGATAATTAAAACCTTGCCACAGTATGCAGTCATTTATAATGAATTCCTACACAGGTTGCAGTAGTCTATGTAGACAAATGGTATTTCAGCAAAGCTAATATGAAATACACATCAGGTGATCAGAAGGTATTTCAGTGTCATTCTCGTGCATGCACCAAAGGTGAATCTCTTACCAGAAGTTAGAGCCCAACAGAAAAGGGTAACCATGAATGAATATCTGTAAAATTCAGCTCAGAGTTCAAATGTTCCAATATTGCCACTTTTGCTATTGAGCTATTGGCCATGGAATTAATAAATATAGAGAAACAATGTT... |
Task1_train_33806 | 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 | AGATAAATATTATTGAATATGAAATGCTTCTAAATAATTATTTAAAATGTTACTTTCTCCGGTACCCACATGCCCTCTTATTAGTCATTATAAAAAAATCAAATAGATTCTGTGCCTACAAATACTTAGATTGGGAGTTACCATGCTTATATTCACAAGATAATTAGCACTTTTACACCACACTATCCTGTTAACTGAGGACATTTGTGTATTATTTCTGGGTCAAAACTAGACCATGACATGGCAACAATGCCTATTCACCAAACTCTTGCAAGGAAAGAGGTTCTGGACTTGGGAGGCCAACCCAACTCATTTGCAGG... | AGATAAATATTATTGAATATGAAATGCTTCTAAATAATTATTTAAAATGTTACTTTCTCCGGTACCCACATGCCCTCTTATTAGTCATTATAAAAAAATCAAATAGATTCTGTGCCTACAAATACTTAGATTGGGAGTTACCATGCTTATATTCACAAGATAATTAGCACTTTTACACCACACTATCCTGTTAACTGAGGACATTTGTGTATTATTTCTGGGTCAAAACTAGACCATGACATGGCAACAATGCCTATTCACCAAACTCTTGCAAGGAAAGAGGTTCTGGACTTGGGAGGCCAACCCAACTCATTTGCAGG... |
Task1_train_33807 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | CAAATGATGGATAATAGGTCCTTTTAAAGGCAGATGAGACTTACCTGAATCTAAGGGGCTGAAGTCACAGCCTTCACTTAACAGCTTTCAGAGAAGGTGCTTTGGCGCTGCCTAGGCAAGGTGGAATTGGTGTGGAGTGTGGGAAGAGGCTCTCCGGAGGCAGGTGCAGTGGGTGGAGCAGGGCAGGAGTGGCTCGGGCAGCTCCCTCACTGGGACAGGCCCTCCAGGCCAGCTGTGGCTGCCATCTGCTTCTGGGGCTTGCCTCAGTGCCCCAGTACTCACATCACGCTCTCTTCTGCTCGCGACAAGAATGGATACAC... | CAAATGATGGATAATAGGTCCTTTTAAAGGCAGATGAGACTTACCTGAATCTAAGGGGCTGAAGTCACAGCCTTCACTTAACAGCTTTCAGAGAAGGTGCTTTGGCGCTGCCTAGGCAAGGTGGAATTGGTGTGGAGTGTGGGAAGAGGCTCTCCGGAGGCAGGTGCAGTGGGTGGAGCAGGGCAGGAGTGGCTCGGGCAGCTCCCTCACTGGGACAGGCCCTCCAGGCCAGCTGTGGCTGCCATCTGCTTCTGGGGCTTGCCTCAGTGCCCCAGTACTCACATCACGCTCTCTTCTGCTCGCGACAAGAATGGATACAC... |
Task1_train_33808 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGGGTTCCCTGCTGGCCCCAAGTACTCACCTCGTCTACTCTAAGCCTCGCAGGCCTCCCTGAGGCTCTCAGTGGAAGCGCTTTTTTTTTTTCTTTTTTCTTTTTTTTGAGACGGAATCTCGCTCTGTCACCCAGGCAGGAGTACAGTGGCCCAATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCGCGCCCGGCTAATTTTTTGTATTTTAAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGA... | TGGGTTCCCTGCTGGCCCCAAGTACTCACCTCGTCTACTCTAAGCCTCGCAGGCCTCCCTGAGGCTCTCAGTGGAAGCGCTTTTTTTTTTTCTTTTTTCTTTTTTTTGAGACGGAATCTCGCTCTGTCACCCAGGCAGGAGTACAGTGGCCCAATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCGCGCCCGGCTAATTTTTTGTATTTTAAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGA... |
Task1_train_33809 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GCGCTTTTTTTTTTTCTTTTTTCTTTTTTTTGAGACGGAATCTCGCTCTGTCACCCAGGCAGGAGTACAGTGGCCCAATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCGCGCCCGGCTAATTTTTTGTATTTTAAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCGCCCACCTCGGCCTCCCAAATTGCTGGGCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGG... | GCGCTTTTTTTTTTTCTTTTTTCTTTTTTTTGAGACGGAATCTCGCTCTGTCACCCAGGCAGGAGTACAGTGGCCCAATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCGCGCCCGGCTAATTTTTTGTATTTTAAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCGCCCACCTCGGCCTCCCAAATTGCTGGGCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGG... |
Task1_train_33810 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AAGCCAGCCAGACCTGCATTCACATTCCGGCTCCACCATTCAACTCTTACGTAAGCCTGGTCAGGTTGTTTCTCCCACCCACAGCTTCTTTAACCTAGAACAGTGTTTTTATAACAATGAAGCAACTACGAAGCACGTAGCACTTAGAATGGGAGCTAGCACTGATTTTTCCTAGATCCAACCACACGAGCAAGCAGGCACCTAACTAAACAAATTGTGACACAATCGTGACAGCCCGGAGACTGCATCCCATCCCTCACGTCCCATGACAATGCCCGGGAAAGCGCAGAGGTGGACAGTGACTCAGGCGCAGACACAGG... | AAGCCAGCCAGACCTGCATTCACATTCCGGCTCCACCATTCAACTCTTACGTAAGCCTGGTCAGGTTGTTTCTCCCACCCACAGCTTCTTTAACCTAGAACAGTGTTTTTATAACAATGAAGCAACTACGAAGCACGTAGCACTTAGAATGGGAGCTAGCACTGATTTTTCCTAGATCCAACCACACGAGCAAGCAGGCACCTAACTAAACAAATTGTGACACAATCGTGACAGCCCGGAGACTGCATCCCATCCCTCACGTCCCATGACAATGCCCGGGAAAGCGCAGAGGTGGACAGTGACTCAGGCGCAGACACAGG... |
Task1_train_33811 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GGTAAACATGGAGCTGCTTACGTCCCTGCTGTGGGTCTGCCGTTTGCTGGTGTGAGGTGGGCTTCAATCAGATGCTCGCCACGGCCCAGGACGTGGCTCCTCCTCTCACTCAAGGCTCTGATGTCAGATGCCTGGCTTTGCTGGTTTTTGAAGTTCCACAGGTGGCCCCTCCAGCCCAAGTTTCTCAGAACCAAATCCAGCCGGAAATGTCAAACACCAATTCCAGAATGAATTTCCACGGCTGCCCTGTCCTGACTGCCCTGACCTGGCCTGTGCTTACCTGGAATTCCCACCCAGGCCTCGATCAGCTCAGCCTTCCC... | GGTAAACATGGAGCTGCTTACGTCCCTGCTGTGGGTCTGCCGTTTGCTGGTGTGAGGTGGGCTTCAATCAGATGCTCGCCACGGCCCAGGACGTGGCTCCTCCTCTCACTCAAGGCTCTGATGTCAGATGCCTGGCTTTGCTGGTTTTTGAAGTTCCACAGGTGGCCCCTCCAGCCCAAGTTTCTCAGAACCAAATCCAGCCGGAAATGTCAAACACCAATTCCAGAATGAATTTCCACGGCTGCCCTGTCCTGACTGCCCTGACCTGGCCTGTGCTTACCTGGAATTCCCACCCAGGCCTCGATCAGCTCAGCCTTCCC... |
Task1_train_33812 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | CTGGAGACCAGAAGAGCAAGTCACGGTGTTGGCAGGGCTTTGCTCCCCCCGAAGGTTGGAAGGACGAATGCGCCTTGCACATCCAGCCTTTGGTGCCCTGCTGGTGTTCACTGGCATTGCTTGGCCTACAGACTCCTCACGCCAACCTCTCCCTCTGTCTTTACCCGGCCTTCTCCCCTGCGTGTCTGTATTCAAATGCCCCTATTCCTATAAGGGCACCAGTCCTGCTGGATTCCAGGTTCCACCCTACCCCAGTATAGACTCACCCTAACTAATTACATCTGAAAAAAACCTTACTTCCAGGCAAGGTAACATTCCCA... | CTGGAGACCAGAAGAGCAAGTCACGGTGTTGGCAGGGCTTTGCTCCCCCCGAAGGTTGGAAGGACGAATGCGCCTTGCACATCCAGCCTTTGGTGCCCTGCTGGTGTTCACTGGCATTGCTTGGCCTACAGACTCCTCACGCCAACCTCTCCCTCTGTCTTTACCCGGCCTTCTCCCCTGCGTGTCTGTATTCAAATGCCCCTATTCCTATAAGGGCACCAGTCCTGCTGGATTCCAGGTTCCACCCTACCCCAGTATAGACTCACCCTAACTAATTACATCTGAAAAAAACCTTACTTCCAGGCAAGGTAACATTCCCA... |
Task1_train_33813 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | CGGCCACATTCCTCTCAAGGTGCAAAATGATCTCAACTTACAACAGCTTCACATCTGAATTATTTCATTTCACAGGGACTTTATACCAAGGTTCTCCACGTTGCACAAAGATCACTACACCTTCCAAAACCCTGCTCAGGACGTCTTAGTCATGCATTCACAATGGGAACTGGAAGTAAAAAGCATTGAGACTGTTCCACTGACAATTGTTTTACTTCTTTTTTATCTTCATTAGCAGGCATCAGGCAACTTTAACCAACCTTCTAGGCAGTTGTCAGTGATCATTGTCATATTAAAGTGCATGTTATAGATTATAAATT... | CGGCCACATTCCTCTCAAGGTGCAAAATGATCTCAACTTACAACAGCTTCACATCTGAATTATTTCATTTCACAGGGACTTTATACCAAGGTTCTCCACGTTGCACAAAGATCACTACACCTTCCAAAACCCTGCTCAGGACGTCTTAGTCATGCATTCACAATGGGAACTGGAAGTAAAAAGCATTGAGACTGTTCCACTGACAATTGTTTTACTTCTTTTTTATCTTCATTAGCAGGCATCAGGCAACTTTAACCAACCTTCTAGGCAGTTGTCAGTGATCATTGTCATATTAAAGTGCATGTTATAGATTATAAATT... |
Task1_train_33814 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AAAACTGTGTCTTAAACCCCAAAATGCAGATGTGACCTCAGTTTTACACACTCAAAATTGGAAAGACCATGAGTACAGATCAGAATTATTTTTTTTTTACCAAGATAGACTATAAGAAATATTTCTGCAACCCCAATTAGACATTAGTGATCTGTTGGAGAGGTGGGTCTAATTAGAGGCAATCCTTGGGAGAGGGAAAAAGATCTTTTAAAAAGAATAATGAGGGCAGAAAACACTGGGAGCAGCGCGTCATGAAAGCACGCCGGATCCCTCATGTCTGAACTGTAATGATCATTCGCTGGCTTTGGGGAAAGTCATTT... | AAAACTGTGTCTTAAACCCCAAAATGCAGATGTGACCTCAGTTTTACACACTCAAAATTGGAAAGACCATGAGTACAGATCAGAATTATTTTTTTTTTACCAAGATAGACTATAAGAAATATTTCTGCAACCCCAATTAGACATTAGTGATCTGTTGGAGAGGTGGGTCTAATTAGAGGCAATCCTTGGGAGAGGGAAAAAGATCTTTTAAAAAGAATAATGAGGGCAGAAAACACTGGGAGCAGCGCGTCATGAAAGCACGCCGGATCCCTCATGTCTGAACTGTAATGATCATTCGCTGGCTTTGGGGAAAGTCATTT... |
Task1_train_33815 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AACACTGGGAGCAGCGCGTCATGAAAGCACGCCGGATCCCTCATGTCTGAACTGTAATGATCATTCGCTGGCTTTGGGGAAAGTCATTTAATTATGAAGGAGACACAGACTGCTTTCTGGGACCTCAAGTTCTGTCTTGCCTCTGCACGAGGGTCTTCTTGGTGACCCTCCTATTGGGTAACCTTCACCCACGGCCCAGTGTTGGAGATCATGTATTACAGCTGCTCCATCCGCATCCATGTACCCACACACCCATCCACGCGTCCACCCACCCACCGTCCATCTACCTGACAGGCACACACTAAGAGCTTGCTGTGAGG... | AACACTGGGAGCAGCGCGTCATGAAAGCACGCCGGATCCCTCATGTCTGAACTGTAATGATCATTCGCTGGCTTTGGGGAAAGTCATTTAATTATGAAGGAGACACAGACTGCTTTCTGGGACCTCAAGTTCTGTCTTGCCTCTGCACGAGGGTCTTCTTGGTGACCCTCCTATTGGGTAACCTTCACCCACGGCCCAGTGTTGGAGATCATGTATTACAGCTGCTCCATCCGCATCCATGTACCCACACACCCATCCACGCGTCCACCCACCCACCGTCCATCTACCTGACAGGCACACACTAAGAGCTTGCTGTGAGG... |
Task1_train_33816 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCTTCATCTCAAGTGATCCACCCGCCTTGGCCTCCTGAAGTGCTGGGATTACATGCGTGAGCGACCACACCTGGCCTCTTCTTATTTCTTCTATTTTGATAACTTTGGTACCAATGGTTCTTCATTAATGTCATTACCAAATGGAAATGCCATTACTACATTCTGGCTAAGAGCAGGTACACAGTAATTTACTCATAACTATCATGCTTTCCATGGCCCCATTTTGTGTTGAATTCCTGGGTTTCTGCTGACTTCTGCTTTCTGAAGCTGC... | TTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCTTCATCTCAAGTGATCCACCCGCCTTGGCCTCCTGAAGTGCTGGGATTACATGCGTGAGCGACCACACCTGGCCTCTTCTTATTTCTTCTATTTTGATAACTTTGGTACCAATGGTTCTTCATTAATGTCATTACCAAATGGAAATGCCATTACTACATTCTGGCTAAGAGCAGGTACACAGTAATTTACTCATAACTATCATGCTTTCCATGGCCCCATTTTGTGTTGAATTCCTGGGTTTCTGCTGACTTCTGCTTTCTGAAGCTGC... |
Task1_train_33817 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AACCGAATGGCATCTGTTTCTGCAGTTTGAGGTGTTAAGGCACGTGCCTGCAGGAGGGAAGAAAAACACATGCACATTTATGAAGTTAGATTTAATAGAGATTATGAAGTTAGATTTAAAAAGGCAGTTTATCTCATCTACTGTTGATAAAGTATAAATTAGTACAGAGTGTCTGGAAAGCAATTTAGAAATATGTATTAAATGCCTTTGACTTTTGCACACTTTCAACACAATTCCACTTCAAATTTGCATATGGAAATCATTGTAAATGGGTACAAAATTAAGTAATAAAGATGTAAATTATCTACACATCAATGTTT... | AACCGAATGGCATCTGTTTCTGCAGTTTGAGGTGTTAAGGCACGTGCCTGCAGGAGGGAAGAAAAACACATGCACATTTATGAAGTTAGATTTAATAGAGATTATGAAGTTAGATTTAAAAAGGCAGTTTATCTCATCTACTGTTGATAAAGTATAAATTAGTACAGAGTGTCTGGAAAGCAATTTAGAAATATGTATTAAATGCCTTTGACTTTTGCACACTTTCAACACAATTCCACTTCAAATTTGCATATGGAAATCATTGTAAATGGGTACAAAATTAAGTAATAAAGATGTAAATTATCTACACATCAATGTTT... |
Task1_train_33818 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GAAACGAAGACAGTGATAGCAGCTGTCTCGAGGGGTGTTCTGAGAATCACACAGGCATATGTATATATAGCCAGGGGCATAGTATGTGCGGATAAATGTTAGCTAGTTGTGTTGTCAGCTTCAGCCATCAGTGCTTAGTGAGTGTGCTGTTTTCTTACTGTTTAAATTTTTCATGTCATTCGCACTGTATCAGATTTCCAGAGTCAGGCAGATAATATGAGCTGGGGCGTGGGGCGGGGGTAGGGGCGGACGGCATGGGGAAGTCAAGAGACTATTACAAATTGAAGAGTCTTGGGAGGGCTTCATGGAAGAGGAGGGAC... | GAAACGAAGACAGTGATAGCAGCTGTCTCGAGGGGTGTTCTGAGAATCACACAGGCATATGTATATATAGCCAGGGGCATAGTATGTGCGGATAAATGTTAGCTAGTTGTGTTGTCAGCTTCAGCCATCAGTGCTTAGTGAGTGTGCTGTTTTCTTACTGTTTAAATTTTTCATGTCATTCGCACTGTATCAGATTTCCAGAGTCAGGCAGATAATATGAGCTGGGGCGTGGGGCGGGGGTAGGGGCGGACGGCATGGGGAAGTCAAGAGACTATTACAAATTGAAGAGTCTTGGGAGGGCTTCATGGAAGAGGAGGGAC... |
Task1_train_33819 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GACCCAGGCCCGGAGCCCGCGGGCACCCCGAGTCCCAGCGGCGAGGCCGACGGCGACTGTGCCCCCGAGGACGCGGCACCCAGTAGCGGAGGGGCCCCGAGGCAGGACGCGGCCCGCGAGGTCCCAGGCAGCGAAGCCGCGCGCCCGGAGCAGGAGCCTCCCGTTGCGGAGCCGGTCCCGGTGTGCACCATCTTCAGCCAGCGCGCGCCCCCAGCCTCCGGGGACGGCTTCGAGCCGCAGATGGTGAAGTCGCCCAGCTTCGGTGGCGCCAGCGAGGCCTCGGCCAGGACACCGCCCCAGGTCGTGCAGCCCAGCCCCAG... | GACCCAGGCCCGGAGCCCGCGGGCACCCCGAGTCCCAGCGGCGAGGCCGACGGCGACTGTGCCCCCGAGGACGCGGCACCCAGTAGCGGAGGGGCCCCGAGGCAGGACGCGGCCCGCGAGGTCCCAGGCAGCGAAGCCGCGCGCCCGGAGCAGGAGCCTCCCGTTGCGGAGCCGGTCCCGGTGTGCACCATCTTCAGCCAGCGCGCGCCCCCAGCCTCCGGGGACGGCTTCGAGCCGCAGATGGTGAAGTCGCCCAGCTTCGGTGGCGCCAGCGAGGCCTCGGCCAGGACACCGCCCCAGGTCGTGCAGCCCAGCCCCAG... |
Task1_train_33820 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | GCGTCAGGCCTTGAATAAAATTAGTTTTAATGAGCTGTACTCGAAGGTACTAGACTGGAGAGAGTCGTTTTGGGTTTTTTTTGTTTTTTCCTTCCTACCAAACTGGAATTGTACTTGTCTGTCTTTCTTTGTAACATCCCAATTAGCAAGCCAGTAACTCCAGTCCCAGTTTGGAGGAAATGGAACATGTAGAAGAATAAAGAAATAAAAGTACCTCTGGGATTATACGATGAGTAAGTAAGAAGAAAAACACCATTGGTGGCCATAGTTACTGCTGACCGCGTGCTTATAGCTAAGTGCGAGAATGCAGGGGAGCATTT... | GCGTCAGGCCTTGAATAAAATTAGTTTTAATGAGCTGTACTCGAAGGTACTAGACTGGAGAGAGTCGTTTTGGGTTTTTTTTGTTTTTTCCTTCCTACCAAACTGGAATTGTACTTGTCTGTCTTTCTTTGTAACATCCCAATTAGCAAGCCAGTAACTCCAGTCCCAGTTTGGAGGAAATGGAACATGTAGAAGAATAAAGAAATAAAAGTACCTCTGGGATTATACGATGAGTAAGTAAGAAGAAAAACACCATTGGTGGCCATAGTTACTGCTGACCGCGTGCTTATAGCTAAGTGCGAGAATGCAGGGGAGCATTT... |
Task1_train_33821 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CCCAAGAATGATAGATTCACTGGCAGCTTGCACCCTGCACCTGCAAAAGCTATAGGCACTCAAAGCCATCCCATGAGAGCAACCTCAGGAGCCCCTGCAAAGCCACAGGGACAGAGCTGCCTAAGGCCTTGGGAGCCCATTCCTTGCACCAGTGTGCCCTAGATGTGGGACATGGAGTCAAAGGGTATTATTTTGGAGCTTTAAGATTTAGTGGCTGCCCTGCTGAGTTTTGAACTTTCATGGGTCCTGTAGCTCCTTTCTTTTGACCAATTTCCCCCTTTTGGAATGAGAATATTTACCTAATGCCTTTACCCGCTTTG... | CCCAAGAATGATAGATTCACTGGCAGCTTGCACCCTGCACCTGCAAAAGCTATAGGCACTCAAAGCCATCCCATGAGAGCAACCTCAGGAGCCCCTGCAAAGCCACAGGGACAGAGCTGCCTAAGGCCTTGGGAGCCCATTCCTTGCACCAGTGTGCCCTAGATGTGGGACATGGAGTCAAAGGGTATTATTTTGGAGCTTTAAGATTTAGTGGCTGCCCTGCTGAGTTTTGAACTTTCATGGGTCCTGTAGCTCCTTTCTTTTGACCAATTTCCCCCTTTTGGAATGAGAATATTTACCTAATGCCTTTACCCGCTTTG... |
Task1_train_33822 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGTGCTGGGCAGGCCCAGGCTCCGATCCTGGGGACAGGCAGAGGCTGCTGGGCCACGGGGAGCCCCGGCACCACGGAGGCGATGACCAGGTGTCACTCTTCACAGGAAGAAGGTTAGGGTCCGTCCAGGGACTAGGAACAAACTCGCAGCCGGAGGGAATCGGTTGGCAGAACTGGGAGGGCGGAGTGTAGCTCAGTTGATTAGCGAGAGAAGACTTAGGACAGCTGCGTGTTCTGGACACCGTGCCGTCTGCGAGGCATCAGAGGGACTTCCCGCCTAGCCACAGGGGCACAGATACTCGATTTTGGAGCCCAGACTGT... | GGTGCTGGGCAGGCCCAGGCTCCGATCCTGGGGACAGGCAGAGGCTGCTGGGCCACGGGGAGCCCCGGCACCACGGAGGCGATGACCAGGTGTCACTCTTCACAGGAAGAAGGTTAGGGTCCGTCCAGGGACTAGGAACAAACTCGCAGCCGGAGGGAATCGGTTGGCAGAACTGGGAGGGCGGAGTGTAGCTCAGTTGATTAGCGAGAGAAGACTTAGGACAGCTGCGTGTTCTGGACACCGTGCCGTCTGCGAGGCATCAGAGGGACTTCCCGCCTAGCCACAGGGGCACAGATACTCGATTTTGGAGCCCAGACTGT... |
Task1_train_33823 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | CTTCTGTAAATTACATTACAATATAGGTTCCTTCACACTATTATCCATGTAAAAACAATTTTGCTTTGCTTCAAACCCAGATTTCAGGAAAACAACAACAAAATTCTCCAAACTTTACTACTAAATGTGTGGAGTCATTTTGTTCTCTTAATTTTTTCAATAGCTGTATTAGTTATCTTTTATTTTAATTAACTTTTGTAGAGGTGAGGTCTTGCTATGTGGCCCAGGCTGGCCTTGAACTCCTGGGCTCAAGCGATCCTCCCACCTCTCCTGAATAGCTGGGACTGCAGGCAGGAGCCACCACACCCGGCTTGTATGAG... | CTTCTGTAAATTACATTACAATATAGGTTCCTTCACACTATTATCCATGTAAAAACAATTTTGCTTTGCTTCAAACCCAGATTTCAGGAAAACAACAACAAAATTCTCCAAACTTTACTACTAAATGTGTGGAGTCATTTTGTTCTCTTAATTTTTTCAATAGCTGTATTAGTTATCTTTTATTTTAATTAACTTTTGTAGAGGTGAGGTCTTGCTATGTGGCCCAGGCTGGCCTTGAACTCCTGGGCTCAAGCGATCCTCCCACCTCTCCTGAATAGCTGGGACTGCAGGCAGGAGCCACCACACCCGGCTTGTATGAG... |
Task1_train_33824 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | TAAAAACAATTTTGCTTTGCTTCAAACCCAGATTTCAGGAAAACAACAACAAAATTCTCCAAACTTTACTACTAAATGTGTGGAGTCATTTTGTTCTCTTAATTTTTTCAATAGCTGTATTAGTTATCTTTTATTTTAATTAACTTTTGTAGAGGTGAGGTCTTGCTATGTGGCCCAGGCTGGCCTTGAACTCCTGGGCTCAAGCGATCCTCCCACCTCTCCTGAATAGCTGGGACTGCAGGCAGGAGCCACCACACCCGGCTTGTATGAGTTATTTATTGCTGCCTAACAAATTACCCCAAAACTCAGTGGCCTAAGAA... | TAAAAACAATTTTGCTTTGCTTCAAACCCAGATTTCAGGAAAACAACAACAAAATTCTCCAAACTTTACTACTAAATGTGTGGAGTCATTTTGTTCTCTTAATTTTTTCAATAGCTGTATTAGTTATCTTTTATTTTAATTAACTTTTGTAGAGGTGAGGTCTTGCTATGTGGCCCAGGCTGGCCTTGAACTCCTGGGCTCAAGCGATCCTCCCACCTCTCCTGAATAGCTGGGACTGCAGGCAGGAGCCACCACACCCGGCTTGTATGAGTTATTTATTGCTGCCTAACAAATTACCCCAAAACTCAGTGGCCTAAGAA... |
Task1_train_33825 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CAAAATTCTCCAAACTTTACTACTAAATGTGTGGAGTCATTTTGTTCTCTTAATTTTTTCAATAGCTGTATTAGTTATCTTTTATTTTAATTAACTTTTGTAGAGGTGAGGTCTTGCTATGTGGCCCAGGCTGGCCTTGAACTCCTGGGCTCAAGCGATCCTCCCACCTCTCCTGAATAGCTGGGACTGCAGGCAGGAGCCACCACACCCGGCTTGTATGAGTTATTTATTGCTGCCTAACAAATTACCCCAAAACTCAGTGGCCTAAGAAAGATTGATTACCTCCCAGATCAGGAATCGGCACAGGGCTTAGCTCAGTC... | CAAAATTCTCCAAACTTTACTACTAAATGTGTGGAGTCATTTTGTTCTCTTAATTTTTTCAATAGCTGTATTAGTTATCTTTTATTTTAATTAACTTTTGTAGAGGTGAGGTCTTGCTATGTGGCCCAGGCTGGCCTTGAACTCCTGGGCTCAAGCGATCCTCCCACCTCTCCTGAATAGCTGGGACTGCAGGCAGGAGCCACCACACCCGGCTTGTATGAGTTATTTATTGCTGCCTAACAAATTACCCCAAAACTCAGTGGCCTAAGAAAGATTGATTACCTCCCAGATCAGGAATCGGCACAGGGCTTAGCTCAGTC... |
Task1_train_33826 | This variant is present on Chromosome 2. Is the change likely to result in a pathogenic outcome? | Benign | TCCAAACTTTACTACTAAATGTGTGGAGTCATTTTGTTCTCTTAATTTTTTCAATAGCTGTATTAGTTATCTTTTATTTTAATTAACTTTTGTAGAGGTGAGGTCTTGCTATGTGGCCCAGGCTGGCCTTGAACTCCTGGGCTCAAGCGATCCTCCCACCTCTCCTGAATAGCTGGGACTGCAGGCAGGAGCCACCACACCCGGCTTGTATGAGTTATTTATTGCTGCCTAACAAATTACCCCAAAACTCAGTGGCCTAAGAAAGATTGATTACCTCCCAGATCAGGAATCGGCACAGGGCTTAGCTCAGTCTTCTACTT... | TCCAAACTTTACTACTAAATGTGTGGAGTCATTTTGTTCTCTTAATTTTTTCAATAGCTGTATTAGTTATCTTTTATTTTAATTAACTTTTGTAGAGGTGAGGTCTTGCTATGTGGCCCAGGCTGGCCTTGAACTCCTGGGCTCAAGCGATCCTCCCACCTCTCCTGAATAGCTGGGACTGCAGGCAGGAGCCACCACACCCGGCTTGTATGAGTTATTTATTGCTGCCTAACAAATTACCCCAAAACTCAGTGGCCTAAGAAAGATTGATTACCTCCCAGATCAGGAATCGGCACAGGGCTTAGCTCAGTCTTCTACTT... |
Task1_train_33827 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CGGCCAGGCACAGTGGCTCACACATGTAATCCCAGCACTTTGGGAGGCCAAGGAGGGTGGATCACCTAAGGTCAGGAGTTTGAGACCAGCTTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATACAGTAATTCCGGCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACGAAGTCAGGAGATGGAGACCATCCTGGCCAGCATGGTAAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCAGGCGTGGTGGCAGGTTCTTGTAATCTCAGCTACTCGGGAGTC... | CGGCCAGGCACAGTGGCTCACACATGTAATCCCAGCACTTTGGGAGGCCAAGGAGGGTGGATCACCTAAGGTCAGGAGTTTGAGACCAGCTTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATACAGTAATTCCGGCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACGAAGTCAGGAGATGGAGACCATCCTGGCCAGCATGGTAAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCAGGCGTGGTGGCAGGTTCTTGTAATCTCAGCTACTCGGGAGTC... |
Task1_train_33828 | 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 | TCCTGGATCCCAGCCTGTGCATTTTCTCTTCTGGCTAGAACTGAGGATTTTCGTTGGGGAATGGTGGTCACATGTGGCCAGGTTATGAGAGATCCTACAGTCATATTAGCTAAGAACCGCCCTGAACAGTTTTTTCTGTGATGGACGGAATGGCCCCTGCTGTGGGTCAGGTGCATGTGGGGTGCACTGCCTCGCATGCAGCATCTGCTGTGTTGGCCCTAACGAGACTGCTCTTGTCCTCTGTGTTGCGCAGGTCACGACTGGTGTGTCCTCAGGCTGGGGATCCAAGGAGTCATCCGGGGCTTCGACGTGGACGTTTC... | TCCTGGATCCCAGCCTGTGCATTTTCTCTTCTGGCTAGAACTGAGGATTTTCGTTGGGGAATGGTGGTCACATGTGGCCAGGTTATGAGAGATCCTACAGTCATATTAGCTAAGAACCGCCCTGAACAGTTTTTTCTGTGATGGACGGAATGGCCCCTGCTGTGGGTCAGGTGCATGTGGGGTGCACTGCCTCGCATGCAGCATCTGCTGTGTTGGCCCTAACGAGACTGCTCTTGTCCTCTGTGTTGCGCAGGTCACGACTGGTGTGTCCTCAGGCTGGGGATCCAAGGAGTCATCCGGGGCTTCGACGTGGACGTTTC... |
Task1_train_33829 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TTCCACAAGTGTCTTCTTTGATTTAGAAAGAGGGTCAGGCTAGAGGTGAGAGCTGCTCCCATGTAAAGATAGGAAATAATCTCCGGGAGAGACCAAGATGGTCTCTTCCTTCATTTTCTTATCAATTTGCTTATGTATAATCAACTATTAGAAACAACTGATGGGCATTTAGGTTGCCCATCAATTGTTTATTGGGGCCTGCTTATTCATGTATTATTTGGGCATCCTATCCCTACTAGCAGATTTTCATGGAAAGCCCAATTATCATCAATTAATAACTTATTTTAAAGCCCCTTCGGTTAAGTCTAAGCCAAAGGTTT... | TTCCACAAGTGTCTTCTTTGATTTAGAAAGAGGGTCAGGCTAGAGGTGAGAGCTGCTCCCATGTAAAGATAGGAAATAATCTCCGGGAGAGACCAAGATGGTCTCTTCCTTCATTTTCTTATCAATTTGCTTATGTATAATCAACTATTAGAAACAACTGATGGGCATTTAGGTTGCCCATCAATTGTTTATTGGGGCCTGCTTATTCATGTATTATTTGGGCATCCTATCCCTACTAGCAGATTTTCATGGAAAGCCCAATTATCATCAATTAATAACTTATTTTAAAGCCCCTTCGGTTAAGTCTAAGCCAAAGGTTT... |
Task1_train_33830 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GAGACAGGGCGGACAGTGTGAGAAAGCTGTTGATGAGAGCTGCTGCCAAATAAAATCATCTTTCACCTGCCTACGGCCAGCCCCCACCACCCCAGAGTTCTTTCTGCTCATCCCCCCACTCCCTTCGGACCTCAGCATGACATTTTGTGTAGCTGTGAACCTGACACCGACCGTGCTGTGCTGGACTATGTGGCTGGTGGAGGCGTCACGCTATCCTGTAGCCATCCATCGCTGGATTTGTTTCTCCTTCCAGTTTCTGAACACAGGATTTGGAGTTAGAAACTCTGGCTTTAAATTGTGGACTGACCCTCACTGGTTAT... | GAGACAGGGCGGACAGTGTGAGAAAGCTGTTGATGAGAGCTGCTGCCAAATAAAATCATCTTTCACCTGCCTACGGCCAGCCCCCACCACCCCAGAGTTCTTTCTGCTCATCCCCCCACTCCCTTCGGACCTCAGCATGACATTTTGTGTAGCTGTGAACCTGACACCGACCGTGCTGTGCTGGACTATGTGGCTGGTGGAGGCGTCACGCTATCCTGTAGCCATCCATCGCTGGATTTGTTTCTCCTTCCAGTTTCTGAACACAGGATTTGGAGTTAGAAACTCTGGCTTTAAATTGTGGACTGACCCTCACTGGTTAT... |
Task1_train_33831 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AAATCTTGAAAATTTATAGATATTAGATATTAGTAAATATAGTGAAACTGCCTTTTCCTAACATGAAGCGTAGTTGATGAATGTTTGTTTTGTTAATGGTGAAACCGTTCTACATTTTTCTCTTTTAGGATTCTTTCTGCATGGGCCCATTAGTCACTGTTTTATAAATCAACTAGACTCTCCTGGGAACGTAGATGTTCTTTTGCTGATTTATACGAAGGGGGGCCTTCCTGTGTTCGCAGGGATGATCTCTGTGCTGTTCAGGTTGACTTTAGAGAGTTCCCCCATTGCCAGGTTTGCAGGCTGAGGAAACAAGGTAA... | AAATCTTGAAAATTTATAGATATTAGATATTAGTAAATATAGTGAAACTGCCTTTTCCTAACATGAAGCGTAGTTGATGAATGTTTGTTTTGTTAATGGTGAAACCGTTCTACATTTTTCTCTTTTAGGATTCTTTCTGCATGGGCCCATTAGTCACTGTTTTATAAATCAACTAGACTCTCCTGGGAACGTAGATGTTCTTTTGCTGATTTATACGAAGGGGGGCCTTCCTGTGTTCGCAGGGATGATCTCTGTGCTGTTCAGGTTGACTTTAGAGAGTTCCCCCATTGCCAGGTTTGCAGGCTGAGGAAACAAGGTAA... |
Task1_train_33832 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TCAGTGACTGATTTTTATCAAGGCGAGGACAGAATGGATGCAGGGCTGTGGGTAGGCCACCTCTTCATGCTGGCATCGTCATCAAAAGGCAGCGTGCGCATGACTCCTGGGGGCTCCAGGTCAGCCTCTGGTTACCCACTCTCTTAGTCATAATCTCCCTCTGCAAATTTTTATTTAAAAAGCAGCAGAGAGCTCTTCAAAGTCTTCTTCTCCAGCCATTAAGCTGCTCCTATTTCGTGCTGGCACTCAAATCGTAGCCACAGTTGTCCTGGGAATCGTGCGTTTCTCCTGCTCATGGCTGTTGGAGGCATGGCTTTGCT... | TCAGTGACTGATTTTTATCAAGGCGAGGACAGAATGGATGCAGGGCTGTGGGTAGGCCACCTCTTCATGCTGGCATCGTCATCAAAAGGCAGCGTGCGCATGACTCCTGGGGGCTCCAGGTCAGCCTCTGGTTACCCACTCTCTTAGTCATAATCTCCCTCTGCAAATTTTTATTTAAAAAGCAGCAGAGAGCTCTTCAAAGTCTTCTTCTCCAGCCATTAAGCTGCTCCTATTTCGTGCTGGCACTCAAATCGTAGCCACAGTTGTCCTGGGAATCGTGCGTTTCTCCTGCTCATGGCTGTTGGAGGCATGGCTTTGCT... |
Task1_train_33833 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CACCCCCTCAGTTGCTTGAGCTCTGGTAGTCAGGGTCTCCTCCTCGAATCTGGCTCATTTCTGCCTCTCATGTCCTTCGTCATGTGTCACTGGGCCCCATCTGCTGGGTGAGCTTTCAGGATCCTGCAGGTGCTTCCTTCTGGGCCAGACGTGTCTTCTCCCTCCTGGTAGAATTCTCCCTCCATGTGGAATTCACCAGGTGGGTGAATTCTCCCTTCTCCTTCCATGTGGAATTCACCAGGTGGGTTTTCCTAACTAAATATTAGCGCAGTGACACCCAGTGAGGTGTCAGTCGTAAAACTTGAGAAAGGGATGATGTA... | CACCCCCTCAGTTGCTTGAGCTCTGGTAGTCAGGGTCTCCTCCTCGAATCTGGCTCATTTCTGCCTCTCATGTCCTTCGTCATGTGTCACTGGGCCCCATCTGCTGGGTGAGCTTTCAGGATCCTGCAGGTGCTTCCTTCTGGGCCAGACGTGTCTTCTCCCTCCTGGTAGAATTCTCCCTCCATGTGGAATTCACCAGGTGGGTGAATTCTCCCTTCTCCTTCCATGTGGAATTCACCAGGTGGGTTTTCCTAACTAAATATTAGCGCAGTGACACCCAGTGAGGTGTCAGTCGTAAAACTTGAGAAAGGGATGATGTA... |
Task1_train_33834 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AAATTGCTTAAAACATTTGTTAAAGATCATGCAAAATAAACACTGTATTAAAATGCTAGATTACACTCAAACATCAAGGCAATGAAACACAAAAGAGCAACTATTTAGCACAATGACTGGCCCAGTAAATAACTTAATCAGCATATTAATAAAAACCCACTGAGTGATAAACATCGAAAATGTAACACTGAATCTAGATAATAGCGCATCTGCGATCTCACCATCTACCGTCCTAACTGTGACTTGGGGTAAACCACCAGAATTCATTCTACATAAATGAGCTATGTTAAAACGATAACAATATTTCATTGCATGATGAC... | AAATTGCTTAAAACATTTGTTAAAGATCATGCAAAATAAACACTGTATTAAAATGCTAGATTACACTCAAACATCAAGGCAATGAAACACAAAAGAGCAACTATTTAGCACAATGACTGGCCCAGTAAATAACTTAATCAGCATATTAATAAAAACCCACTGAGTGATAAACATCGAAAATGTAACACTGAATCTAGATAATAGCGCATCTGCGATCTCACCATCTACCGTCCTAACTGTGACTTGGGGTAAACCACCAGAATTCATTCTACATAAATGAGCTATGTTAAAACGATAACAATATTTCATTGCATGATGAC... |
Task1_train_33835 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | TTGACTGATTTCATACTTAACCTGCCTTAAAAAAAAAAAGCTGGAAGCAGTCTGCCCCAGCCTGCCTCTTCATCAAGCGGTCAGATGCCACATTCCCATTTGATGAGCAGTGATGAAGCAGGTTGCATAGTCCAAGGAAAAGCACAAGAGCAGGGGCTGGTGTGGAGTCCTAAGACTCATCCACGCTGCTCACCTGATTCTCAGCAGACAGCAGCCGTGGGCTTTGCAATTTAGAAATATGTGTGAAGAACCACTGGGTGCTTAGTTCTGCACACCTGAGCTGGGTTTGAACCATTGGTTTGTCCAGAACCTAGAAAGGG... | TTGACTGATTTCATACTTAACCTGCCTTAAAAAAAAAAAGCTGGAAGCAGTCTGCCCCAGCCTGCCTCTTCATCAAGCGGTCAGATGCCACATTCCCATTTGATGAGCAGTGATGAAGCAGGTTGCATAGTCCAAGGAAAAGCACAAGAGCAGGGGCTGGTGTGGAGTCCTAAGACTCATCCACGCTGCTCACCTGATTCTCAGCAGACAGCAGCCGTGGGCTTTGCAATTTAGAAATATGTGTGAAGAACCACTGGGTGCTTAGTTCTGCACACCTGAGCTGGGTTTGAACCATTGGTTTGTCCAGAACCTAGAAAGGG... |
Task1_train_33836 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TTCCTTTACTTTCATAAAGATATGAAACTTCATTTCAGGTTTTTTTTGAGACAGTCTTACTGTTCTGTCACCCAGGCTGGAGTGCAGTGGTACAATGATGGCTCACTGCAACTTTGACTTCCTGGGCTCAAGGAATCCCCCTGCCTTGGCCTTCTGAGTATCTGGGACTACCAGTGCATAACACCACACTCAGCTGATTTTTTAAAATGTTTTGTAGAGATGGGGGTCTTGCCCAGGCTGGTGTTTTGTTTTGTTTGAGACAGTCTCACTGTGTCACCCAGGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAGCC... | TTCCTTTACTTTCATAAAGATATGAAACTTCATTTCAGGTTTTTTTTGAGACAGTCTTACTGTTCTGTCACCCAGGCTGGAGTGCAGTGGTACAATGATGGCTCACTGCAACTTTGACTTCCTGGGCTCAAGGAATCCCCCTGCCTTGGCCTTCTGAGTATCTGGGACTACCAGTGCATAACACCACACTCAGCTGATTTTTTAAAATGTTTTGTAGAGATGGGGGTCTTGCCCAGGCTGGTGTTTTGTTTTGTTTGAGACAGTCTCACTGTGTCACCCAGGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAGCC... |
Task1_train_33837 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TTCATGCAAATACATATTTTTACATTCACATGTGACACCACAGGTTCACTACCATGATAGCAGTGATGTTTTTAAAGAACTCACTTATATCAAGGAGGAAGGACTACATTATAACCTCTCCCAAACCCTATATGCATAAATTCTAACATGCAGAAAATATTAGTTCAAGGGTAAAATGGGTTGTCACAAATTTGAAACTATAATTTCCATACAGTAACATAAAAACCTCAGAGAATATCCCTCAAATATTTTAGGGAAATAACAGAGTATCTGGAACAGATCTGGTTGCATTAAGTTTCATGGAATGTACCCACCCAAAT... | TTCATGCAAATACATATTTTTACATTCACATGTGACACCACAGGTTCACTACCATGATAGCAGTGATGTTTTTAAAGAACTCACTTATATCAAGGAGGAAGGACTACATTATAACCTCTCCCAAACCCTATATGCATAAATTCTAACATGCAGAAAATATTAGTTCAAGGGTAAAATGGGTTGTCACAAATTTGAAACTATAATTTCCATACAGTAACATAAAAACCTCAGAGAATATCCCTCAAATATTTTAGGGAAATAACAGAGTATCTGGAACAGATCTGGTTGCATTAAGTTTCATGGAATGTACCCACCCAAAT... |
Task1_train_33838 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TTTAGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAAGCGGAGGTTGCAGTGGGCTGAGATGGTGCCACTGCACTCCAGACTGGGTGAAAGAGCAAGACTGTCTTAAAAAAAAAAATTGGTGGAATTTTCACATTTATTGGCCTAGAGTTGTTCAGAATATGCCCTTATGATCTTTTTAATGTCTGTGGTATTTGCAGTGATGCCCCTACATATTGGTTAGTGATGCCACTGATATCAGTTTATTTTGATTTTCTTTGCTCCGTTGCTCAGACTGGAGCACAGTGGCCCGATTATAGCTCACTGCAGCCTTGAGCTC... | TTTAGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAAGCGGAGGTTGCAGTGGGCTGAGATGGTGCCACTGCACTCCAGACTGGGTGAAAGAGCAAGACTGTCTTAAAAAAAAAAATTGGTGGAATTTTCACATTTATTGGCCTAGAGTTGTTCAGAATATGCCCTTATGATCTTTTTAATGTCTGTGGTATTTGCAGTGATGCCCCTACATATTGGTTAGTGATGCCACTGATATCAGTTTATTTTGATTTTCTTTGCTCCGTTGCTCAGACTGGAGCACAGTGGCCCGATTATAGCTCACTGCAGCCTTGAGCTC... |
Task1_train_33839 | 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 | TTTTAAACATTTCCTTCATCCCATTATTTTTCAGTTTAATCTTTTTTCTAACTTCTTGGGATGTACGATTATATCAAAAATCCTCTTCTCAATGAGATCTCTCTTGAACATCACATTTCAGACTGAAATCACCTTGTTGTTCCCATTCTCCTCTCCTCTTTATTTTTCTCCTTGGAACTCACCACCACTTAACATACCACATATTTTCCTTATTTATTTTTGTCTCTCCCCATCAGAATACAATCTCCATGAAGGCAAGGACTTTTGTTTACTTTGTTCACTGCTGAATCCCCAGGACACAAACCAGTTCCTGTTTAATA... | TTTTAAACATTTCCTTCATCCCATTATTTTTCAGTTTAATCTTTTTTCTAACTTCTTGGGATGTACGATTATATCAAAAATCCTCTTCTCAATGAGATCTCTCTTGAACATCACATTTCAGACTGAAATCACCTTGTTGTTCCCATTCTCCTCTCCTCTTTATTTTTCTCCTTGGAACTCACCACCACTTAACATACCACATATTTTCCTTATTTATTTTTGTCTCTCCCCATCAGAATACAATCTCCATGAAGGCAAGGACTTTTGTTTACTTTGTTCACTGCTGAATCCCCAGGACACAAACCAGTTCCTGTTTAATA... |
Task1_train_33840 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | GCTCAATTTTGATACTGTTCTACCATATCAGAAATGTTGGTTTTCTGAAATCCTACATGCACATGTGTGTTGTACTATAGTTATTTATCCAAGCCTTCTATCTCCTTTCTCGATTGTCAACTGCTTAAGGAGATTGTCTTATTCATCTTTTTATTTCTGAGATTATCTTATTCATGTTTTTATTTCTCAAAGTACTTTGCACAATTCCTTGCATAGAATAGGCTCTAAACTAAATTTTATTTTATTTTATTTTATTTGAGACGGAGTCTGGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCTCACTGTAA... | GCTCAATTTTGATACTGTTCTACCATATCAGAAATGTTGGTTTTCTGAAATCCTACATGCACATGTGTGTTGTACTATAGTTATTTATCCAAGCCTTCTATCTCCTTTCTCGATTGTCAACTGCTTAAGGAGATTGTCTTATTCATCTTTTTATTTCTGAGATTATCTTATTCATGTTTTTATTTCTCAAAGTACTTTGCACAATTCCTTGCATAGAATAGGCTCTAAACTAAATTTTATTTTATTTTATTTTATTTGAGACGGAGTCTGGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCTCACTGTAA... |
Task1_train_33841 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GCCAGCCTCTTCACATTCAACACTAAAGCCTTGTTGGACTGTTTGCATTTCCTGAAAGCACCATCCCATGTTTGTCATAGCCTGTAGCATACTGCATTCTCATTAGGAAAAGGACTTGAGGAAGAGGACTGTGTCTGTGTCTTAAGTACCCAGAACACACTAGTTGCTCAATAAATGTTTGTTGGAAGAATAAAAGCCAAGTGAAAACCTGAGCCAAGCTACCAGAATCTGGTAGACAGAAAAATACTTTGATGCGATATTTTGAATTATCATTGTTATATGTGTTCTGTTTCTATGTTAACAAAGCATTTTTTAATCAG... | GCCAGCCTCTTCACATTCAACACTAAAGCCTTGTTGGACTGTTTGCATTTCCTGAAAGCACCATCCCATGTTTGTCATAGCCTGTAGCATACTGCATTCTCATTAGGAAAAGGACTTGAGGAAGAGGACTGTGTCTGTGTCTTAAGTACCCAGAACACACTAGTTGCTCAATAAATGTTTGTTGGAAGAATAAAAGCCAAGTGAAAACCTGAGCCAAGCTACCAGAATCTGGTAGACAGAAAAATACTTTGATGCGATATTTTGAATTATCATTGTTATATGTGTTCTGTTTCTATGTTAACAAAGCATTTTTTAATCAG... |
Task1_train_33842 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GATAAGTTTAGAGATGCTAAATTCATTTCTTTGTTCATTTATTCACCCAATTATTCTTCAACAAATGTTTAAATGAGTTCCTACTCTCTACCACTCCCTGACAACACTAGGGGCATAAGGATGGCTGAGACAGTCTCTGCCTTTAAGAACCTCCATAATTTGTCATTCAAGGTCATGCCACTAGAAAATGGTGGAGCCGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATTGAGACCATCCCGGCTAAAACGGTGAAACCCCGTCTCTACTAAAA... | GATAAGTTTAGAGATGCTAAATTCATTTCTTTGTTCATTTATTCACCCAATTATTCTTCAACAAATGTTTAAATGAGTTCCTACTCTCTACCACTCCCTGACAACACTAGGGGCATAAGGATGGCTGAGACAGTCTCTGCCTTTAAGAACCTCCATAATTTGTCATTCAAGGTCATGCCACTAGAAAATGGTGGAGCCGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATTGAGACCATCCCGGCTAAAACGGTGAAACCCCGTCTCTACTAAAA... |
Task1_train_33843 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GAGTTCCTACTCTCTACCACTCCCTGACAACACTAGGGGCATAAGGATGGCTGAGACAGTCTCTGCCTTTAAGAACCTCCATAATTTGTCATTCAAGGTCATGCCACTAGAAAATGGTGGAGCCGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATTGAGACCATCCCGGCTAAAACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATG... | GAGTTCCTACTCTCTACCACTCCCTGACAACACTAGGGGCATAAGGATGGCTGAGACAGTCTCTGCCTTTAAGAACCTCCATAATTTGTCATTCAAGGTCATGCCACTAGAAAATGGTGGAGCCGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATTGAGACCATCCCGGCTAAAACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATG... |
Task1_train_33844 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TAAAACTTTCAGAAAATTTAATTAACGTTTGGCTAGCCATGAAAAACTTTAAAAAGACACCTTTTAAATTGTCTTGTGTTTTATTATCAATCAAGGAATGAAACATATTTAAAGGAAGAATGATCATCACCCAGTATCCCATTATCGTGATGATTGCTTTATTCATTGTTTTGATGTGTATGCAAATTTTATGTAGCGTAGTTGTGTTCACAGATAGGATTTGGTAGTGTACTTTCTTCTACTTAGTTTGTTTCATAAACATTTTCTCTGTATTTTAATCTTCATAATTATCCTTTGGAAGAGGACTTGTGGCTTTTATC... | TAAAACTTTCAGAAAATTTAATTAACGTTTGGCTAGCCATGAAAAACTTTAAAAAGACACCTTTTAAATTGTCTTGTGTTTTATTATCAATCAAGGAATGAAACATATTTAAAGGAAGAATGATCATCACCCAGTATCCCATTATCGTGATGATTGCTTTATTCATTGTTTTGATGTGTATGCAAATTTTATGTAGCGTAGTTGTGTTCACAGATAGGATTTGGTAGTGTACTTTCTTCTACTTAGTTTGTTTCATAAACATTTTCTCTGTATTTTAATCTTCATAATTATCCTTTGGAAGAGGACTTGTGGCTTTTATC... |
Task1_train_33845 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGGGGCCGGGGCAACGACGGGAGGCGGGAGCGCCGCACTGCCTTGGAGGCGGGGCAACGCTTGGAGGCGGGAACGCGGCACGCGAGCGTTGGGGGCCCTAAGCGTCGCGACCTGGGGGCTTCGGGGAGGTAGCCGTGGACGTGGGCAGAGCGCGGGCCTCGTGGTGTGCGGGCACTGTGGGCCGGGCGAGCCCCTTCCCGCCCGTGTGGTGAGTCGGCCTCGGCGCCCGGTTCTGTGACATCACAGGGGGTTTAGTGGCGCAGCCTGCGGGACAGAGGCCGGGGATTTGAGGTGGCCTCGTCTTGTTTGATCTCGGGGAA... | AGGGGCCGGGGCAACGACGGGAGGCGGGAGCGCCGCACTGCCTTGGAGGCGGGGCAACGCTTGGAGGCGGGAACGCGGCACGCGAGCGTTGGGGGCCCTAAGCGTCGCGACCTGGGGGCTTCGGGGAGGTAGCCGTGGACGTGGGCAGAGCGCGGGCCTCGTGGTGTGCGGGCACTGTGGGCCGGGCGAGCCCCTTCCCGCCCGTGTGGTGAGTCGGCCTCGGCGCCCGGTTCTGTGACATCACAGGGGGTTTAGTGGCGCAGCCTGCGGGACAGAGGCCGGGGATTTGAGGTGGCCTCGTCTTGTTTGATCTCGGGGAA... |
Task1_train_33846 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | CCTGGCCATCATGGCAAAACCCCGTCTCTTCTAAAAATACAAAAATTGGGCGTGGTGGCAGGCACCTGTAATCCCAGATACTCAGAAGGCTGAGGCAAGAGAATCGCTTGAACCTGGGAGGCACAGGTTGCAGTGAGCCGGGATCACACCACTGGACTCTAGCCTGGGCAACAGAGTGAAACTCCGTTTCAAAAAAAAAAAAAAGAAAGAAAGAAAAAAGATACACACAGTTCACACCCAGAAGGGCAACTGCAGCTGGCTGACCTCCTCAACAATTCCTGAAACCATCTCCTCTGCAAGCCTCTCACCGCCACTGCCTT... | CCTGGCCATCATGGCAAAACCCCGTCTCTTCTAAAAATACAAAAATTGGGCGTGGTGGCAGGCACCTGTAATCCCAGATACTCAGAAGGCTGAGGCAAGAGAATCGCTTGAACCTGGGAGGCACAGGTTGCAGTGAGCCGGGATCACACCACTGGACTCTAGCCTGGGCAACAGAGTGAAACTCCGTTTCAAAAAAAAAAAAAAGAAAGAAAGAAAAAAGATACACACAGTTCACACCCAGAAGGGCAACTGCAGCTGGCTGACCTCCTCAACAATTCCTGAAACCATCTCCTCTGCAAGCCTCTCACCGCCACTGCCTT... |
Task1_train_33847 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTCTAGCCTGGGCAACAGAGTGAAACTCCGTTTCAAAAAAAAAAAAAAGAAAGAAAGAAAAAAGATACACACAGTTCACACCCAGAAGGGCAACTGCAGCTGGCTGACCTCCTCAACAATTCCTGAAACCATCTCCTCTGCAAGCCTCTCACCGCCACTGCCTTGGTTCAGGACTCGGCCACCTGGATCATTGCAGACTCCCCCACCCACTCACACAGGTGGTCATGTTATCCCTAGTCTGACTCTGTCCAGTTCATCCTCCCTACAGTTGTCGGTGTGACGTTCCTAAAACACAAACTGTCACAATCCTTACCTTTCAG... | CTCTAGCCTGGGCAACAGAGTGAAACTCCGTTTCAAAAAAAAAAAAAAGAAAGAAAGAAAAAAGATACACACAGTTCACACCCAGAAGGGCAACTGCAGCTGGCTGACCTCCTCAACAATTCCTGAAACCATCTCCTCTGCAAGCCTCTCACCGCCACTGCCTTGGTTCAGGACTCGGCCACCTGGATCATTGCAGACTCCCCCACCCACTCACACAGGTGGTCATGTTATCCCTAGTCTGACTCTGTCCAGTTCATCCTCCCTACAGTTGTCGGTGTGACGTTCCTAAAACACAAACTGTCACAATCCTTACCTTTCAG... |
Task1_train_33848 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GCGGGAGGGGAGGATGGCGACTTCACCCGGCCTTTAACAACACGTACGCATCTTTCGGCGTCTTCTACAATGGCTATGTTAATTACGTGGCCAGGAACTAAACTATCAATGAAGCCACCTCTGACTACTTCAGTTACAGTGAGTTTAACAGGAGCAAAAAAGCACGTGGCGCCCTAGGGCAACCGAAACGAGGGTTTTAGACGCTGATTATGGGAAATTGAAATCTGAGTTGAGTATGAGATGACACCAATAAATTATAATTTTGTTAGATAATAGCTTTATCAGCCATAAAGTAATCAATAAAAATACCAGTTTCCTGG... | GCGGGAGGGGAGGATGGCGACTTCACCCGGCCTTTAACAACACGTACGCATCTTTCGGCGTCTTCTACAATGGCTATGTTAATTACGTGGCCAGGAACTAAACTATCAATGAAGCCACCTCTGACTACTTCAGTTACAGTGAGTTTAACAGGAGCAAAAAAGCACGTGGCGCCCTAGGGCAACCGAAACGAGGGTTTTAGACGCTGATTATGGGAAATTGAAATCTGAGTTGAGTATGAGATGACACCAATAAATTATAATTTTGTTAGATAATAGCTTTATCAGCCATAAAGTAATCAATAAAAATACCAGTTTCCTGG... |
Task1_train_33849 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGAATTGTATGATTGCTGGGCTCCTTGGCACTTGCAAGAGGTACCTGCCAAGACCTGGGGAAAGCCCTGGATTTGAGAACTCAACAGATAGCTTGTGATGTCCCCAGGAATGCGCAGTCATCAAGTAAAACTGAAGCATTAACGATCACGAGAATCAGCTCAGCACGGGAAAGACGTCACTTTAGGAGGCATCTCTTCACCTTCATGCCTATCAACAGCTCTAGCAGAAAGGCCATGTTTCAGAAGGAAACCAAGTTTTGTTCACTTGGCCAGGTGCCTAGGTATGCGAGAGAGAGTAGAGAGCAGAGCTGCCCCTCCCT... | AGAATTGTATGATTGCTGGGCTCCTTGGCACTTGCAAGAGGTACCTGCCAAGACCTGGGGAAAGCCCTGGATTTGAGAACTCAACAGATAGCTTGTGATGTCCCCAGGAATGCGCAGTCATCAAGTAAAACTGAAGCATTAACGATCACGAGAATCAGCTCAGCACGGGAAAGACGTCACTTTAGGAGGCATCTCTTCACCTTCATGCCTATCAACAGCTCTAGCAGAAAGGCCATGTTTCAGAAGGAAACCAAGTTTTGTTCACTTGGCCAGGTGCCTAGGTATGCGAGAGAGAGTAGAGAGCAGAGCTGCCCCTCCCT... |
Task1_train_33850 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ATTGTATGATTGCTGGGCTCCTTGGCACTTGCAAGAGGTACCTGCCAAGACCTGGGGAAAGCCCTGGATTTGAGAACTCAACAGATAGCTTGTGATGTCCCCAGGAATGCGCAGTCATCAAGTAAAACTGAAGCATTAACGATCACGAGAATCAGCTCAGCACGGGAAAGACGTCACTTTAGGAGGCATCTCTTCACCTTCATGCCTATCAACAGCTCTAGCAGAAAGGCCATGTTTCAGAAGGAAACCAAGTTTTGTTCACTTGGCCAGGTGCCTAGGTATGCGAGAGAGAGTAGAGAGCAGAGCTGCCCCTCCCTGGC... | ATTGTATGATTGCTGGGCTCCTTGGCACTTGCAAGAGGTACCTGCCAAGACCTGGGGAAAGCCCTGGATTTGAGAACTCAACAGATAGCTTGTGATGTCCCCAGGAATGCGCAGTCATCAAGTAAAACTGAAGCATTAACGATCACGAGAATCAGCTCAGCACGGGAAAGACGTCACTTTAGGAGGCATCTCTTCACCTTCATGCCTATCAACAGCTCTAGCAGAAAGGCCATGTTTCAGAAGGAAACCAAGTTTTGTTCACTTGGCCAGGTGCCTAGGTATGCGAGAGAGAGTAGAGAGCAGAGCTGCCCCTCCCTGGC... |
Task1_train_33851 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTTCAACTCAGTACCTCCCGATTTAGAAACAGTGGGAAAAGGCTTGTATTTTCATGTTACTGCAAGGTAGGTGCTCACTCAACCCAGCAGAGGGGCCTCTGCAGGAGCTGAGGTGGCTGTGCTGCAGACCTGGGATCCTTCCAGGCTGTGCTGCTCCTGCCCCATTTGACATCACTTGAGTTTCAGAGGGAATCAACGAATGTTTCCAGGTATAAAGAAAATTGATAAGAAATTAGGAACAGGCACAATGAGGTCCCTCTGAATGTGTATTTGGCTTACGTAAGTGATAAATGTAAGAGGGCAAATTTGCTCTCAGCAGA... | CTTCAACTCAGTACCTCCCGATTTAGAAACAGTGGGAAAAGGCTTGTATTTTCATGTTACTGCAAGGTAGGTGCTCACTCAACCCAGCAGAGGGGCCTCTGCAGGAGCTGAGGTGGCTGTGCTGCAGACCTGGGATCCTTCCAGGCTGTGCTGCTCCTGCCCCATTTGACATCACTTGAGTTTCAGAGGGAATCAACGAATGTTTCCAGGTATAAAGAAAATTGATAAGAAATTAGGAACAGGCACAATGAGGTCCCTCTGAATGTGTATTTGGCTTACGTAAGTGATAAATGTAAGAGGGCAAATTTGCTCTCAGCAGA... |
Task1_train_33852 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | CACAACTACTAGAAAGGGAGCCTGGCACAGGTAATGCAGGTGCCATCATCTCTCCTGTGGGCTGCCACAGCCTGTGCTTGTTGCGTCCAGATTAGAGCCTGTTTAATGCATTCCCCTGCGGCAGCAAAAGTAATCTTTTCAGAACACAGGTCTGATCCTATCCCCCCGCTTACAACTCTTGTCAGGACTCCCTGCCCTACATCCCCACAGCCGGCTCACAAGACCCCTCCTAACCTGGCTTTCTACCTGCCCCCACAGGCTCGAATGCTCAGCCATGGGAGGTACTTGCTCCCGCAGCTCTGCACCCACTCTACTGTCAA... | CACAACTACTAGAAAGGGAGCCTGGCACAGGTAATGCAGGTGCCATCATCTCTCCTGTGGGCTGCCACAGCCTGTGCTTGTTGCGTCCAGATTAGAGCCTGTTTAATGCATTCCCCTGCGGCAGCAAAAGTAATCTTTTCAGAACACAGGTCTGATCCTATCCCCCCGCTTACAACTCTTGTCAGGACTCCCTGCCCTACATCCCCACAGCCGGCTCACAAGACCCCTCCTAACCTGGCTTTCTACCTGCCCCCACAGGCTCGAATGCTCAGCCATGGGAGGTACTTGCTCCCGCAGCTCTGCACCCACTCTACTGTCAA... |
Task1_train_33853 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTTCAGAAGAACTTCCAGATAAGAATTTCTGCCTGCAGCTCCTGATTTAAATAGACAAAGTTTTTTAAAGGTAAAGATAAAGGAGTCCATAAAATTAATCCATTTAGAAAGTATTCTCAGAGCATCTAGCATAGAACAGCTAAGGGAAATCATTTCCGTCTGTCTTACCAGTATCAAGGATATGGGGCAGCACAGCCACAACACAGAGCTGGTGCTCCTCACACGTCCTCTTGGCAATGTCCTCGTTGATAATCTGTGGGACCCAAAAGACAAGGGACAATCAGGAGGCTGCATGATACAACACCTAAAGGTAAGCTGGC... | CTTCAGAAGAACTTCCAGATAAGAATTTCTGCCTGCAGCTCCTGATTTAAATAGACAAAGTTTTTTAAAGGTAAAGATAAAGGAGTCCATAAAATTAATCCATTTAGAAAGTATTCTCAGAGCATCTAGCATAGAACAGCTAAGGGAAATCATTTCCGTCTGTCTTACCAGTATCAAGGATATGGGGCAGCACAGCCACAACACAGAGCTGGTGCTCCTCACACGTCCTCTTGGCAATGTCCTCGTTGATAATCTGTGGGACCCAAAAGACAAGGGACAATCAGGAGGCTGCATGATACAACACCTAAAGGTAAGCTGGC... |
Task1_train_33854 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | CAGACATGAGTACTTTATGTTATTAGCAGCAAGTCACTTGCCCTGCCTCAGCAGCTGATGGTGACGCTGTTACAACACGGCAGGTAGAACTATGGCTGCAAACCCCCTGTGTCTAATTAAGGGACTCCCAGGTGCCTATTCTGAGTTCTAGTCACTCAGGTCATCTTTCTGGGTTAGAATAAAGAACTGTCCCCAAGCACCAGAGTTGAGAGTGACTCTTGTTTTAGGGCTTGTGGAAGAGACTGCAAGCAATGAAAATCAAAGTTGCAGATTCTGGAAATTCCTCCACAGTCGCAGAACTGCAGCCAGGTATATACTGC... | CAGACATGAGTACTTTATGTTATTAGCAGCAAGTCACTTGCCCTGCCTCAGCAGCTGATGGTGACGCTGTTACAACACGGCAGGTAGAACTATGGCTGCAAACCCCCTGTGTCTAATTAAGGGACTCCCAGGTGCCTATTCTGAGTTCTAGTCACTCAGGTCATCTTTCTGGGTTAGAATAAAGAACTGTCCCCAAGCACCAGAGTTGAGAGTGACTCTTGTTTTAGGGCTTGTGGAAGAGACTGCAAGCAATGAAAATCAAAGTTGCAGATTCTGGAAATTCCTCCACAGTCGCAGAACTGCAGCCAGGTATATACTGC... |
Task1_train_33855 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | GTTACAACACGGCAGGTAGAACTATGGCTGCAAACCCCCTGTGTCTAATTAAGGGACTCCCAGGTGCCTATTCTGAGTTCTAGTCACTCAGGTCATCTTTCTGGGTTAGAATAAAGAACTGTCCCCAAGCACCAGAGTTGAGAGTGACTCTTGTTTTAGGGCTTGTGGAAGAGACTGCAAGCAATGAAAATCAAAGTTGCAGATTCTGGAAATTCCTCCACAGTCGCAGAACTGCAGCCAGGTATATACTGCCTGCCACACTTCACCACACAGCTCCCCCGGTGGGCGCCCAAGGCCTTGCCAATGGAATGGGAGAGGAG... | GTTACAACACGGCAGGTAGAACTATGGCTGCAAACCCCCTGTGTCTAATTAAGGGACTCCCAGGTGCCTATTCTGAGTTCTAGTCACTCAGGTCATCTTTCTGGGTTAGAATAAAGAACTGTCCCCAAGCACCAGAGTTGAGAGTGACTCTTGTTTTAGGGCTTGTGGAAGAGACTGCAAGCAATGAAAATCAAAGTTGCAGATTCTGGAAATTCCTCCACAGTCGCAGAACTGCAGCCAGGTATATACTGCCTGCCACACTTCACCACACAGCTCCCCCGGTGGGCGCCCAAGGCCTTGCCAATGGAATGGGAGAGGAG... |
Task1_train_33856 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACTCCTGACCTCGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACACCTGGCCGCTCTTTTTTCAGTAAATGTTTAAACTTAAATTTTATAATGTAATATTTAATTATCTACAAAACATACTTGCACTTCTGTTCCAGTTCCTCTTTGGCTTGCATCTCATTGCTAAGATGTTCTTCTAATGTATACAGTTTTTTCTGAATCTGTCAAAAAACAAGAAACTGTAATTACGTATTTTGGTCATATTTAAAGATGAGAGGCTTAAAGAAAACAATGATAAGCTTATTTTGTCTTTCCAC... | ACTCCTGACCTCGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACACCTGGCCGCTCTTTTTTCAGTAAATGTTTAAACTTAAATTTTATAATGTAATATTTAATTATCTACAAAACATACTTGCACTTCTGTTCCAGTTCCTCTTTGGCTTGCATCTCATTGCTAAGATGTTCTTCTAATGTATACAGTTTTTTCTGAATCTGTCAAAAAACAAGAAACTGTAATTACGTATTTTGGTCATATTTAAAGATGAGAGGCTTAAAGAAAACAATGATAAGCTTATTTTGTCTTTCCAC... |
Task1_train_33857 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | ATGTGCAACTGAGGACTGACTCTTGTGGAGTGGGCTGTTGGCTGAGTTGAGTGGGTATTTGACTGCCTGGGTCAAGCAGGTCTAGCCCCTTCCCTTCTCCAAGATGTGCAGAAGGGGAAGTCTCCCGGCCAGGTCATGGGCAGGCTCTTTGGCCGAGTGGAGCTGCTGTTTGACTGAAAGCCTGCCCTATTCAGAGACCATCGCAAGTTGGTATCACCATGGGACCAAACAGAATTCTAAGTTTTCACTGCTACCAAAACTACAGAAATTTAACTATAATGTTCACAGAAATATTCTAAACTACAGTAAGAGTTATGCTG... | ATGTGCAACTGAGGACTGACTCTTGTGGAGTGGGCTGTTGGCTGAGTTGAGTGGGTATTTGACTGCCTGGGTCAAGCAGGTCTAGCCCCTTCCCTTCTCCAAGATGTGCAGAAGGGGAAGTCTCCCGGCCAGGTCATGGGCAGGCTCTTTGGCCGAGTGGAGCTGCTGTTTGACTGAAAGCCTGCCCTATTCAGAGACCATCGCAAGTTGGTATCACCATGGGACCAAACAGAATTCTAAGTTTTCACTGCTACCAAAACTACAGAAATTTAACTATAATGTTCACAGAAATATTCTAAACTACAGTAAGAGTTATGCTG... |
Task1_train_33858 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AAATAAATGTTAAGAGGTAGACTCTCCATTGGTCATTAGATTTTCACATAATTTCCAAATAAATACAGTAAACACTGTGACTACTCATGGCCTACATCCCTCCAGCTCTTCAGAAGGCATGGACCACACTGGGCTGGGAGGGACCTAGGTCAGAGAGTTAGGGGACCCCCTGGGGATTGACCTTGACCTCAGGGAATTGACCTCCCTTTCCCAAGCCAATGCAAGGAACTGCCCTGTATTAGTCCATTTTCACACTGCTGATAAAGACATACCCAAGATTGGGCAATTTTCAAAAGAAACTGGTTTCCTAGACCCACAGT... | AAATAAATGTTAAGAGGTAGACTCTCCATTGGTCATTAGATTTTCACATAATTTCCAAATAAATACAGTAAACACTGTGACTACTCATGGCCTACATCCCTCCAGCTCTTCAGAAGGCATGGACCACACTGGGCTGGGAGGGACCTAGGTCAGAGAGTTAGGGGACCCCCTGGGGATTGACCTTGACCTCAGGGAATTGACCTCCCTTTCCCAAGCCAATGCAAGGAACTGCCCTGTATTAGTCCATTTTCACACTGCTGATAAAGACATACCCAAGATTGGGCAATTTTCAAAAGAAACTGGTTTCCTAGACCCACAGT... |
Task1_train_33859 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CAGCACTCCCCAGCTCCATGAATGCCTTGAAGTCCAACAACCACGCTGTGAGCAGGCGTCAGTTTCCACATTTTACTGATTGGGAAGGTGAGGCTCATTGAGGCTGGGTGCTTGCCTAGGACCTCGTGGGCCGGAGGAGGTGGAGGCAAGAGGTGACATTAGATGTGAACCCTGACGTACATGCTTGGCACTTCACCATGTTGCACAGACTTCCTAAGCATGGCGATTGTTATCACGGTGGACACCAGCCTTCCCGAGGACGCAGGAAGGTCGCTGGTTGTTTTCATGCCTCCTGCCCAGAGGGTCTGTAGAGGCACATT... | CAGCACTCCCCAGCTCCATGAATGCCTTGAAGTCCAACAACCACGCTGTGAGCAGGCGTCAGTTTCCACATTTTACTGATTGGGAAGGTGAGGCTCATTGAGGCTGGGTGCTTGCCTAGGACCTCGTGGGCCGGAGGAGGTGGAGGCAAGAGGTGACATTAGATGTGAACCCTGACGTACATGCTTGGCACTTCACCATGTTGCACAGACTTCCTAAGCATGGCGATTGTTATCACGGTGGACACCAGCCTTCCCGAGGACGCAGGAAGGTCGCTGGTTGTTTTCATGCCTCCTGCCCAGAGGGTCTGTAGAGGCACATT... |
Task1_train_33860 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTGTAATCCCAGCTACTCGGGAGACTGAGGCAGGAGAATCGCTTGAACTCAGGAGGCAGAGGTTGCAGTGAGCTGAGGCCGCGCCACTGCACTCCAGCCTGGGCAACAAGAGCGAGACTCTGTCTCGAAAAAAAAAATCACCAGGCTGGCTTACAAAGGATGGTGTTTTTTTACTGTCGTTTCCAGAGATGTGATTCTGGAGGTCAAGGCAGGGCCCAGGGACACACAGGTTTAATAGGCCCATGGGGGTTCTGTGCAGTGCCTCGGGTCACACCTGGAGAACCGTTGCTCTGATTGGTATTTCTCCACCCGGGCTGTGC... | TTGTAATCCCAGCTACTCGGGAGACTGAGGCAGGAGAATCGCTTGAACTCAGGAGGCAGAGGTTGCAGTGAGCTGAGGCCGCGCCACTGCACTCCAGCCTGGGCAACAAGAGCGAGACTCTGTCTCGAAAAAAAAAATCACCAGGCTGGCTTACAAAGGATGGTGTTTTTTTACTGTCGTTTCCAGAGATGTGATTCTGGAGGTCAAGGCAGGGCCCAGGGACACACAGGTTTAATAGGCCCATGGGGGTTCTGTGCAGTGCCTCGGGTCACACCTGGAGAACCGTTGCTCTGATTGGTATTTCTCCACCCGGGCTGTGC... |
Task1_train_33861 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | CGCTTGAACTCAGGAGGCAGAGGTTGCAGTGAGCTGAGGCCGCGCCACTGCACTCCAGCCTGGGCAACAAGAGCGAGACTCTGTCTCGAAAAAAAAAATCACCAGGCTGGCTTACAAAGGATGGTGTTTTTTTACTGTCGTTTCCAGAGATGTGATTCTGGAGGTCAAGGCAGGGCCCAGGGACACACAGGTTTAATAGGCCCATGGGGGTTCTGTGCAGTGCCTCGGGTCACACCTGGAGAACCGTTGCTCTGATTGGTATTTCTCCACCCGGGCTGTGCGTTAGAATCAAGAAGAAGCGTTGAGATATTGGGATGCCT... | CGCTTGAACTCAGGAGGCAGAGGTTGCAGTGAGCTGAGGCCGCGCCACTGCACTCCAGCCTGGGCAACAAGAGCGAGACTCTGTCTCGAAAAAAAAAATCACCAGGCTGGCTTACAAAGGATGGTGTTTTTTTACTGTCGTTTCCAGAGATGTGATTCTGGAGGTCAAGGCAGGGCCCAGGGACACACAGGTTTAATAGGCCCATGGGGGTTCTGTGCAGTGCCTCGGGTCACACCTGGAGAACCGTTGCTCTGATTGGTATTTCTCCACCCGGGCTGTGCGTTAGAATCAAGAAGAAGCGTTGAGATATTGGGATGCCT... |
Task1_train_33862 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TAGAGTAGAGAGGATTGTAGGAAAGTGAGAGAAGCACCCTACTGTTAATTAAGAAATAAGAAAGAGCATGTCTTTTTCCTAAAACACAAAAACTGGACGGGGTATTCAGGAAGTAGAGTGCAACTCTGAGTTTCGACCTTAGCATGACGCAGGACCAATGACCGAGGCAGTTCCACTGGGCCCCACTGTCTACCTCAAATGAAGACCAACATTCTTTCAGTCATGTTGTGTGTGTTTTTTTACGTGGCCATGGCGTGTCTGTGGTAGGCCCGAAGACCACGGTGCTCAGGAAACAGAGCTAGGACAGGGTGCAGGGCTTG... | TAGAGTAGAGAGGATTGTAGGAAAGTGAGAGAAGCACCCTACTGTTAATTAAGAAATAAGAAAGAGCATGTCTTTTTCCTAAAACACAAAAACTGGACGGGGTATTCAGGAAGTAGAGTGCAACTCTGAGTTTCGACCTTAGCATGACGCAGGACCAATGACCGAGGCAGTTCCACTGGGCCCCACTGTCTACCTCAAATGAAGACCAACATTCTTTCAGTCATGTTGTGTGTGTTTTTTTACGTGGCCATGGCGTGTCTGTGGTAGGCCCGAAGACCACGGTGCTCAGGAAACAGAGCTAGGACAGGGTGCAGGGCTTG... |
Task1_train_33863 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCTGTGAACGAACACTTGAGAGAGTGTTCTAGAGACAAAAGTTAAACATGTGACATCAGGCCTTTTACTTTTGGACTTTTAAAGCTATTTTCATTTTGTCTGACTTTTTTATGCAGTCTTCCCCCGCTACCCGCACCCAGTGTTTGGTTATCCATTTAATCGATATTTTCTTTCTTTCTTTCTCTCTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCGTTCTGTCATCCAGGCTGGAGTGCAACGGCATGATCTCGACTCACTGCAGCCTTTGTCTTACGGGTTCAAGCGATTCTCCTGCCTCAGCTACCCGAGTAG... | CCTGTGAACGAACACTTGAGAGAGTGTTCTAGAGACAAAAGTTAAACATGTGACATCAGGCCTTTTACTTTTGGACTTTTAAAGCTATTTTCATTTTGTCTGACTTTTTTATGCAGTCTTCCCCCGCTACCCGCACCCAGTGTTTGGTTATCCATTTAATCGATATTTTCTTTCTTTCTTTCTCTCTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCGTTCTGTCATCCAGGCTGGAGTGCAACGGCATGATCTCGACTCACTGCAGCCTTTGTCTTACGGGTTCAAGCGATTCTCCTGCCTCAGCTACCCGAGTAG... |
Task1_train_33864 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | CATATCTGTAGACACACACACACACACACACACACACTCACACACACAAGCAAAAGAGATAAATGAAGATTACAAATTGCTTCAAATTCAGATCCATTCTTGCTGACCTGAATTACTGTTTTTAAATAGCTTAAGAACTTTCTGCCTTCACCAGTTTCGCGGATGAAGACACAGACTCAGGGAGTTGAACCTGCCCAGGGTTCCCCTGCTCCCAGTGATGAGGTCGAGGAACCGGCTCTTCCGGCCCACGCCCCGGACCTCGCCCAAGCCTGCTTCCCGCGCCGTCTTATCTGCGTTTGGACTGGGAGCTGCTTCTTGCC... | CATATCTGTAGACACACACACACACACACACACACACTCACACACACAAGCAAAAGAGATAAATGAAGATTACAAATTGCTTCAAATTCAGATCCATTCTTGCTGACCTGAATTACTGTTTTTAAATAGCTTAAGAACTTTCTGCCTTCACCAGTTTCGCGGATGAAGACACAGACTCAGGGAGTTGAACCTGCCCAGGGTTCCCCTGCTCCCAGTGATGAGGTCGAGGAACCGGCTCTTCCGGCCCACGCCCCGGACCTCGCCCAAGCCTGCTTCCCGCGCCGTCTTATCTGCGTTTGGACTGGGAGCTGCTTCTTGCC... |
Task1_train_33865 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AGAGCTGCTCTATTTTGGGCAATAGCGTCAAGTATTACAAGGCTTTCTGGCTGGCCAGGGGGTGTCTGGGGCCAGGACCCCGGGTTTCCTATTTGCTTTGTGTGCTCTGGGTCCTGGCCTTCTTGTATTTTGCATGCAACCTTTCATTAAAATAACCTGTTCTATAGATTGAGTTGTGTTCCCCAAATTAGTATGTTAAAGCCCAAACTCCCAGTGTGACTGTATTTGGAGTAAGGGAGTAATTAAGGTTAAATGATGTTGTAAGGGTGGGGCCCTGATCCCATAGGATTAGTGTTCTTAAAGAGGAGACACCAGAGAGC... | AGAGCTGCTCTATTTTGGGCAATAGCGTCAAGTATTACAAGGCTTTCTGGCTGGCCAGGGGGTGTCTGGGGCCAGGACCCCGGGTTTCCTATTTGCTTTGTGTGCTCTGGGTCCTGGCCTTCTTGTATTTTGCATGCAACCTTTCATTAAAATAACCTGTTCTATAGATTGAGTTGTGTTCCCCAAATTAGTATGTTAAAGCCCAAACTCCCAGTGTGACTGTATTTGGAGTAAGGGAGTAATTAAGGTTAAATGATGTTGTAAGGGTGGGGCCCTGATCCCATAGGATTAGTGTTCTTAAAGAGGAGACACCAGAGAGC... |
Task1_train_33866 | 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 | ATTGAGTTAGATATCTGTGGAGGGAAGAGAGGAAGAAGCAAGGCTGCTTCCCTATTCAGAAGGATTCTATCATATTCCTACCTCTGCCACTGGGGGCTTGAGTTTTGGCTCATTCTCTGAGCCTCAGTTTCCATATCTGTAAAATGAAAGTATTGAATTAGAGACCACTGGGCAAAAGCTAGCTGTTTATTCTCTTAGTTGCTCATGTGTTGTATAATGCCTGTTTATGTGCATTTCTTTTTTTTTATTTTTGAAGGCAAATAAAGTGTTGTTGATGTCATTGAGGTGGATCACTTTCTCTCCAATTTTGCCTTAGTTCT... | ATTGAGTTAGATATCTGTGGAGGGAAGAGAGGAAGAAGCAAGGCTGCTTCCCTATTCAGAAGGATTCTATCATATTCCTACCTCTGCCACTGGGGGCTTGAGTTTTGGCTCATTCTCTGAGCCTCAGTTTCCATATCTGTAAAATGAAAGTATTGAATTAGAGACCACTGGGCAAAAGCTAGCTGTTTATTCTCTTAGTTGCTCATGTGTTGTATAATGCCTGTTTATGTGCATTTCTTTTTTTTTATTTTTGAAGGCAAATAAAGTGTTGTTGATGTCATTGAGGTGGATCACTTTCTCTCCAATTTTGCCTTAGTTCT... |
Task1_train_33867 | 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 | AGGCAAAAAAAAAAAAAAAAAAAAAGTTCTCTGAAGTTTCTTTTGTTAAGAAGGCTTTGTTATTCTGTGTCTCTAGAATAAAAAGTAAGATCTTGTTCTGTTTCTCCACTCCCTAATGTCTTCTTCAAACCTTAAAAAACAGTCTGTATTAGAGTAAGTCTCAAATTGGATTCTTCTGTAAACGTGGCTAGAAATTCACTAAGATGAAATACTGCCTTTTAATATTCTTGAGATGCCCCAGTGGGACAAGACTAAGAAGCCCCATTGAAAGGGGACTAAAACAGTACCTGTTGAGACCCTTTCATCTTGGGAGACCAGGA... | AGGCAAAAAAAAAAAAAAAAAAAAAGTTCTCTGAAGTTTCTTTTGTTAAGAAGGCTTTGTTATTCTGTGTCTCTAGAATAAAAAGTAAGATCTTGTTCTGTTTCTCCACTCCCTAATGTCTTCTTCAAACCTTAAAAAACAGTCTGTATTAGAGTAAGTCTCAAATTGGATTCTTCTGTAAACGTGGCTAGAAATTCACTAAGATGAAATACTGCCTTTTAATATTCTTGAGATGCCCCAGTGGGACAAGACTAAGAAGCCCCATTGAAAGGGGACTAAAACAGTACCTGTTGAGACCCTTTCATCTTGGGAGACCAGGA... |
Task1_train_33868 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CATACCAATTCCAAGAAGGATGTTTCAAAAGGAAGAGAGCGAGAAAAGAAGAGACAGAGAAAAAAAAAAACATGAAAGGAATAGAGAGATCATTAAATAGTTTTCACGACTGCAAGTAGTTCATGAGGGTGATGGAAAAAAAGAAAACAACAGAAAAGGAAATTATTCAATCCAGGAAAAACAGAGAGTTGTATTAAAAGGAAAATAAATCACACCTAGTTCCGCAGTATAAACAATATTTACGTAATCATAATGATGAAAACACTGGAGAATGGTAGGAGAAGTGGATATGGGAGAAGGGAAAGGACTTCCATAAAAGG... | CATACCAATTCCAAGAAGGATGTTTCAAAAGGAAGAGAGCGAGAAAAGAAGAGACAGAGAAAAAAAAAAACATGAAAGGAATAGAGAGATCATTAAATAGTTTTCACGACTGCAAGTAGTTCATGAGGGTGATGGAAAAAAAGAAAACAACAGAAAAGGAAATTATTCAATCCAGGAAAAACAGAGAGTTGTATTAAAAGGAAAATAAATCACACCTAGTTCCGCAGTATAAACAATATTTACGTAATCATAATGATGAAAACACTGGAGAATGGTAGGAGAAGTGGATATGGGAGAAGGGAAAGGACTTCCATAAAAGG... |
Task1_train_33869 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | TACTTCTTTTTAAATTTCAGGGAATACAAAAAGAAATAACAGGACTAGGCTATATAAAAGCATAAATAAAAAGAGATTCATCTTTGTTTACTGGAAATATGCTACACTAGTTCATTTTCACCTAACAAATTAATTGGGAATATATTTTGTACTCTGTGAATAAGCAATATGATATACACAAAGACTCAGTATGTGAAATACTTTGGATTAAATATACATTCAGACACTTCTTTCCTACTCAAATTTCCCAACATCAAAAACATGCTCAACTTTCAAGGTCTAGATCCAAATCTTACCTTTCCAAGAAGGCTTTCCTGATT... | TACTTCTTTTTAAATTTCAGGGAATACAAAAAGAAATAACAGGACTAGGCTATATAAAAGCATAAATAAAAAGAGATTCATCTTTGTTTACTGGAAATATGCTACACTAGTTCATTTTCACCTAACAAATTAATTGGGAATATATTTTGTACTCTGTGAATAAGCAATATGATATACACAAAGACTCAGTATGTGAAATACTTTGGATTAAATATACATTCAGACACTTCTTTCCTACTCAAATTTCCCAACATCAAAAACATGCTCAACTTTCAAGGTCTAGATCCAAATCTTACCTTTCCAAGAAGGCTTTCCTGATT... |
Task1_train_33870 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TTCATCAAATTCACCTACTTTTCAAGAACTTTGCTGAATTCTCTAAAAAAAAGTAAGCTCAACAAATACTTTAAATGTTACTGTTACAGTATAATAATAAATATACTTACTACTATCATATAGGGAATAGCAATTTAAAAATTAAAAAATAATGAAAAAAATTAACTGGATAGTCAAACTGAACATTTTAGGCACTTTTTAAAAAAGATATCATTAGAGAAACTAAGGCTAAGTATAAAAATAATAAATTGTATCTGTACAGACTTCTGCAATATATTACCTCAAAACATCACAGAACTCAGGCATATCAACATGACGTG... | TTCATCAAATTCACCTACTTTTCAAGAACTTTGCTGAATTCTCTAAAAAAAAGTAAGCTCAACAAATACTTTAAATGTTACTGTTACAGTATAATAATAAATATACTTACTACTATCATATAGGGAATAGCAATTTAAAAATTAAAAAATAATGAAAAAAATTAACTGGATAGTCAAACTGAACATTTTAGGCACTTTTTAAAAAAGATATCATTAGAGAAACTAAGGCTAAGTATAAAAATAATAAATTGTATCTGTACAGACTTCTGCAATATATTACCTCAAAACATCACAGAACTCAGGCATATCAACATGACGTG... |
Task1_train_33871 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TAAAATTATGATATAACAGGATTTAACATATAACAGGAGAACAAAGTGAAAATTCTTTGTGCATACTCGTGGTAGAGTAAGAAAACTAAATATCCATCTTCCACAAAGGGAAGTAAATAAACATTGTGTAAAATTGGAATCAAGAAGTACAATGTAAGCTTTTTATTTAAATGTATGAAAACAATCAAAAGAATCAATTAAAATAGCTAAAAGTGGTTACCTTTGGAAAGCAAGAAGTTGGGTGGAGGAGTCAGTTTTTAAAACTAAACACTTGAAATTATGTGCAAATACAACTCATAAAAATTAAATGTAAATATAAG... | TAAAATTATGATATAACAGGATTTAACATATAACAGGAGAACAAAGTGAAAATTCTTTGTGCATACTCGTGGTAGAGTAAGAAAACTAAATATCCATCTTCCACAAAGGGAAGTAAATAAACATTGTGTAAAATTGGAATCAAGAAGTACAATGTAAGCTTTTTATTTAAATGTATGAAAACAATCAAAAGAATCAATTAAAATAGCTAAAAGTGGTTACCTTTGGAAAGCAAGAAGTTGGGTGGAGGAGTCAGTTTTTAAAACTAAACACTTGAAATTATGTGCAAATACAACTCATAAAAATTAAATGTAAATATAAG... |
Task1_train_33872 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | ACTAGCACTGAGACTTATTCCATTTTGCGCACTGCTGTATTCCTTAGCAGTTAATATGCTTCCTGATACAGAGCAGACACTCGATAAATATTTATTCACTTTAACACAACTGTGCCATTTATCTAATTCACTGTTTACTGCAACTCAGAAAAAGCTAAGTGTCATAAACAGATTCCCGAAAAAAAGATTACAGTAAAAAATGCGTTGATTTAAAATGAAAAATACTGATTTGAAAAAAAGAAAAAAAACAAGACACCAACTAGAACTGACTAAAAGATGATCCTGACATCTGTGCCCATTCATATTGATACTGCTGAACT... | ACTAGCACTGAGACTTATTCCATTTTGCGCACTGCTGTATTCCTTAGCAGTTAATATGCTTCCTGATACAGAGCAGACACTCGATAAATATTTATTCACTTTAACACAACTGTGCCATTTATCTAATTCACTGTTTACTGCAACTCAGAAAAAGCTAAGTGTCATAAACAGATTCCCGAAAAAAAGATTACAGTAAAAAATGCGTTGATTTAAAATGAAAAATACTGATTTGAAAAAAAGAAAAAAAACAAGACACCAACTAGAACTGACTAAAAGATGATCCTGACATCTGTGCCCATTCATATTGATACTGCTGAACT... |
Task1_train_33873 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ACAACCTCCACCTCCTAGGCTCAAGCGATTCTCCCACCTCAGCCTTCCAAGTAGCTGGGACCACAGGCACACACGACCAAGCCTGGCTATTTTTTTGTATTTTTGGTAGACAGGTCTCCCCAAGTTGCCCAGGCTCGTCTTGAACTCCTGAGCTCAAGCAATCTGCCCGCCTTGGCCTACCAAAGTGCTGGGATTACAGGCATGAGCCCCTGTGCCTGGCCTACATTCATTTTTAAAGTATTAGCCAGTAGTTAGCAAAGAAGCCAGTTTGGGTACTGAGCTCCCTTGAAAAGACTTGTTAAGGTCATCAAAGAACACAA... | ACAACCTCCACCTCCTAGGCTCAAGCGATTCTCCCACCTCAGCCTTCCAAGTAGCTGGGACCACAGGCACACACGACCAAGCCTGGCTATTTTTTTGTATTTTTGGTAGACAGGTCTCCCCAAGTTGCCCAGGCTCGTCTTGAACTCCTGAGCTCAAGCAATCTGCCCGCCTTGGCCTACCAAAGTGCTGGGATTACAGGCATGAGCCCCTGTGCCTGGCCTACATTCATTTTTAAAGTATTAGCCAGTAGTTAGCAAAGAAGCCAGTTTGGGTACTGAGCTCCCTTGAAAAGACTTGTTAAGGTCATCAAAGAACACAA... |
Task1_train_33874 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CTTTGTAATATTTAGTGTGCAACAACAAAGATATTTAATATGCATTTGTCTTTTAATAGTAATGTTAAACATTTCATCTATTTTTAGTCTCCCTTTGGGTAATGGCTATCATCATGTCCTTTACCTACTTACCTCTTGAGGTTTTAATTTTTCTTTTGTGCAAGTTCTTTATGTATTAAGGATATAAGCTTCTATCATATTTGCTTTGAATTTGTTTTTCTTTTTAATTTTAGTTAAAAAATTATGCCATTTTTCTCCTCTTCTGAAATTTTATTTTCTACTCACTTTTAAAAATAGTTTTCAATTAGTGAATATTCCAC... | CTTTGTAATATTTAGTGTGCAACAACAAAGATATTTAATATGCATTTGTCTTTTAATAGTAATGTTAAACATTTCATCTATTTTTAGTCTCCCTTTGGGTAATGGCTATCATCATGTCCTTTACCTACTTACCTCTTGAGGTTTTAATTTTTCTTTTGTGCAAGTTCTTTATGTATTAAGGATATAAGCTTCTATCATATTTGCTTTGAATTTGTTTTTCTTTTTAATTTTAGTTAAAAAATTATGCCATTTTTCTCCTCTTCTGAAATTTTATTTTCTACTCACTTTTAAAAATAGTTTTCAATTAGTGAATATTCCAC... |
Task1_train_33875 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GCCATTATTCTAAGTGAAGTTACTCTGGAATGGAAAAATCAAATACCATATGTTCTTACTTATAAATGAGAGCTAAGCTATGGGCATGCAAAGGCATGCAGAGTGGTATAATGGATTTTGGAGACTCAGAAGGGGGAGGGTGGGAGGAGAGTGAGGGATATAAAAAACTACATATTGGGTACAATGTACACTACTCAGTTGACATGAGCACTAAAATCTCAGATTTCACCACTATACAACCCACCCATGTAACAAAAAAACATTTTACCCCAAAAGCTATTGAAATAAGAAAAATTAAAAAATATATAAAATTCCTTGCA... | GCCATTATTCTAAGTGAAGTTACTCTGGAATGGAAAAATCAAATACCATATGTTCTTACTTATAAATGAGAGCTAAGCTATGGGCATGCAAAGGCATGCAGAGTGGTATAATGGATTTTGGAGACTCAGAAGGGGGAGGGTGGGAGGAGAGTGAGGGATATAAAAAACTACATATTGGGTACAATGTACACTACTCAGTTGACATGAGCACTAAAATCTCAGATTTCACCACTATACAACCCACCCATGTAACAAAAAAACATTTTACCCCAAAAGCTATTGAAATAAGAAAAATTAAAAAATATATAAAATTCCTTGCA... |
Task1_train_33876 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AGCTAAGCTATGGGCATGCAAAGGCATGCAGAGTGGTATAATGGATTTTGGAGACTCAGAAGGGGGAGGGTGGGAGGAGAGTGAGGGATATAAAAAACTACATATTGGGTACAATGTACACTACTCAGTTGACATGAGCACTAAAATCTCAGATTTCACCACTATACAACCCACCCATGTAACAAAAAAACATTTTACCCCAAAAGCTATTGAAATAAGAAAAATTAAAAAATATATAAAATTCCTTGCATAGTATCAGCAGATTCTGGGCTTCTCAACAAGAATTGGAAGAGAGAAGAGAGAGGAAAAAGGAGCAAGAG... | AGCTAAGCTATGGGCATGCAAAGGCATGCAGAGTGGTATAATGGATTTTGGAGACTCAGAAGGGGGAGGGTGGGAGGAGAGTGAGGGATATAAAAAACTACATATTGGGTACAATGTACACTACTCAGTTGACATGAGCACTAAAATCTCAGATTTCACCACTATACAACCCACCCATGTAACAAAAAAACATTTTACCCCAAAAGCTATTGAAATAAGAAAAATTAAAAAATATATAAAATTCCTTGCATAGTATCAGCAGATTCTGGGCTTCTCAACAAGAATTGGAAGAGAGAAGAGAGAGGAAAAAGGAGCAAGAG... |
Task1_train_33877 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTTTAAGATATAAGGTACTTAAGCACAGGGAGATAATTATATCCTCTTGATTGTCCACATCCAAACACAGGGAGTAGGGCTTTCTCTTAAAGGAGTAAAACATTGGTACGCAAAGGGAAACTCACATCCTTTGTAAGAGCTGAGCTGAGCCCCCTGTGATGAGTGTGTTGGGGGCATGACCAAGCCCTAGGGATTGGAAGGGATGAGCTTCAAGCCTGGCAGCAACTAGCCTGTCATGTCTGAATTGAGTTTTCCCAAACATGAAGAGCTTGTGCTTGAATCTCTGGAGACGCTTGTATTATGTAAGTGATCTAAATTGC... | CTTTAAGATATAAGGTACTTAAGCACAGGGAGATAATTATATCCTCTTGATTGTCCACATCCAAACACAGGGAGTAGGGCTTTCTCTTAAAGGAGTAAAACATTGGTACGCAAAGGGAAACTCACATCCTTTGTAAGAGCTGAGCTGAGCCCCCTGTGATGAGTGTGTTGGGGGCATGACCAAGCCCTAGGGATTGGAAGGGATGAGCTTCAAGCCTGGCAGCAACTAGCCTGTCATGTCTGAATTGAGTTTTCCCAAACATGAAGAGCTTGTGCTTGAATCTCTGGAGACGCTTGTATTATGTAAGTGATCTAAATTGC... |
Task1_train_33878 | 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 | ATGGCTTCTCTCTTTCAGAGCGGAGAGCTGGTCTTCCACATGGTATTTATTTTACTTACCGTAGTGATTGACGCTGTTTATAAGCCGCACTCCCACTTGGGCATGGTTATTAGTCATCAGTACAATATCAAATAAGTCCTGTTCATCAGGATATAGATCACGGAGTCTAGCATTGACATACTGTAGTGCCTGCAGGTTACAAACATGAATGTGTGTAAAGAGGGGCAGGCAGGGTGGATCTGGGGAGGCCGGAGAGGAAGCATCTCATCAGAGTCAAATTCAAGCTCTGAAGAATCTTCACTGAGAGATTCTGGCTCCTT... | ATGGCTTCTCTCTTTCAGAGCGGAGAGCTGGTCTTCCACATGGTATTTATTTTACTTACCGTAGTGATTGACGCTGTTTATAAGCCGCACTCCCACTTGGGCATGGTTATTAGTCATCAGTACAATATCAAATAAGTCCTGTTCATCAGGATATAGATCACGGAGTCTAGCATTGACATACTGTAGTGCCTGCAGGTTACAAACATGAATGTGTGTAAAGAGGGGCAGGCAGGGTGGATCTGGGGAGGCCGGAGAGGAAGCATCTCATCAGAGTCAAATTCAAGCTCTGAAGAATCTTCACTGAGAGATTCTGGCTCCTT... |
Task1_train_33879 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CATCACTATAGAATTCCAGAAATATTCAAATAAAAGAATTTCTCTAAAAGTTTTCTTTTAATATCATGCCATTGGAATACAGATTCATGATGTATTAGGATTAGAGTGTGATGTGCATATGGTGATGATGTGAGCAGCAAATGGATGATGTCACCAATATGACAGAGGAAGGGTGGGGTGTCATGACAGTGCTTGCCATGGCCAAGCTGAAAGACCAGTAATGATTTAGTCATTCATATGCTTTGGCTTACAACATAATTATCATAATTACACTCTCTGGAGTTCATATATCTAAATTCTAGAATATTGTTATTGTTAAG... | CATCACTATAGAATTCCAGAAATATTCAAATAAAAGAATTTCTCTAAAAGTTTTCTTTTAATATCATGCCATTGGAATACAGATTCATGATGTATTAGGATTAGAGTGTGATGTGCATATGGTGATGATGTGAGCAGCAAATGGATGATGTCACCAATATGACAGAGGAAGGGTGGGGTGTCATGACAGTGCTTGCCATGGCCAAGCTGAAAGACCAGTAATGATTTAGTCATTCATATGCTTTGGCTTACAACATAATTATCATAATTACACTCTCTGGAGTTCATATATCTAAATTCTAGAATATTGTTATTGTTAAG... |
Task1_train_33880 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TAAACATTTTTCAAAATTGAGGGAAGTTACTTCTTATCTATATTTGTACAAATACAATCATTTCCAAAACTAACAAATTTGATTCCCTAAAAAAGGAGGAAAATCAGTAAGATGGAATATAAATATCACCTATTTAAGATAAATATTTTAAAACCTATCTTCTTTTCATTAGTACCTATTCGTATTTAGTTCTTTCCTTAGTATTTAGCCCTAGGAGTTGGAATTCAGATCACTCTTAGAAAATGAGAGGTGCTGTTAGATAACTAAATCAGAATAAAGAAAGTATTGATGAAATGCTGGTATTTTCCATAATACAGAGA... | TAAACATTTTTCAAAATTGAGGGAAGTTACTTCTTATCTATATTTGTACAAATACAATCATTTCCAAAACTAACAAATTTGATTCCCTAAAAAAGGAGGAAAATCAGTAAGATGGAATATAAATATCACCTATTTAAGATAAATATTTTAAAACCTATCTTCTTTTCATTAGTACCTATTCGTATTTAGTTCTTTCCTTAGTATTTAGCCCTAGGAGTTGGAATTCAGATCACTCTTAGAAAATGAGAGGTGCTGTTAGATAACTAAATCAGAATAAAGAAAGTATTGATGAAATGCTGGTATTTTCCATAATACAGAGA... |
Task1_train_33881 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GCAGGCATGCAATATCTATGATTGTTACTGGACGGATCTGCTGAATCAACACTAGTTGTATTAAATATAATATACTGATCTTGTTAGACTCTCACAGCCATATTCCTCATATTTATTTCTTTCAGCACAATTCATAATCATTCAGTTCCAAAACAAATACTTTACTCCATTTTCCAAACCTCCCAAGAATTGATTTCCCATCTTGTTCACTAATTTCAAAGAATACTCCAGTCACAGCTCATCAAAAGGGCAGAGCAGAAAAAGAAGTTTGTTTTTAAAAAAGCCTTCAATGTTAAACAAAATGAATGCACTTCTTAATG... | GCAGGCATGCAATATCTATGATTGTTACTGGACGGATCTGCTGAATCAACACTAGTTGTATTAAATATAATATACTGATCTTGTTAGACTCTCACAGCCATATTCCTCATATTTATTTCTTTCAGCACAATTCATAATCATTCAGTTCCAAAACAAATACTTTACTCCATTTTCCAAACCTCCCAAGAATTGATTTCCCATCTTGTTCACTAATTTCAAAGAATACTCCAGTCACAGCTCATCAAAAGGGCAGAGCAGAAAAAGAAGTTTGTTTTTAAAAAAGCCTTCAATGTTAAACAAAATGAATGCACTTCTTAATG... |
Task1_train_33882 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GACTCCTAGACATGCTCGGCCTGGCCCTGCTGCTCCGCAGGCAGACTCTAGTATTTCATTTCCCTGTGCCTCGGTTTCCCTCTAATAAAATAACAATCCTGGTTTCTTCCAGCCCGCTGGGATGTCAGGAGCGAGGACACAGGATGAGAGTGAACAGATGCCAGGGGCCTTGGGGACATGTAAATACCAGAAGCCGTCACGGTGACTCAGGCTTGGCGGGCACTTGCAGGGCTGTCTAATAGCCCGAGGCTGCTAATGAGGGGTACAGATGACAGCCTCCAGGGCCTGCATGCCTTGGTGTCACATAAGCCGTTCCTGGA... | GACTCCTAGACATGCTCGGCCTGGCCCTGCTGCTCCGCAGGCAGACTCTAGTATTTCATTTCCCTGTGCCTCGGTTTCCCTCTAATAAAATAACAATCCTGGTTTCTTCCAGCCCGCTGGGATGTCAGGAGCGAGGACACAGGATGAGAGTGAACAGATGCCAGGGGCCTTGGGGACATGTAAATACCAGAAGCCGTCACGGTGACTCAGGCTTGGCGGGCACTTGCAGGGCTGTCTAATAGCCCGAGGCTGCTAATGAGGGGTACAGATGACAGCCTCCAGGGCCTGCATGCCTTGGTGTCACATAAGCCGTTCCTGGA... |
Task1_train_33883 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | AAGAGGCTGATGCCAGTGCAGGCCTCCAGGGCTCCGTTTCTTGACCTGTGCCCACAGTGGATCCTGAAAGCAGTTTGGCGAGTCATGACCTTTCCAAACGTTGAAATAGAATAGAAAATATCCCAGTACAATACACTTAGTAAGGTTTTGTATGAGTTCTGGGAACTTTTGCTTCAGTTTTATGGGATGTTTATACATGTGTGTCCTGGGTCATGGCGTACCATATAGTTTTTACTATGGGTTGTAGCAAGTAGTTTCAGAAATGCTGTCTTACAGATATAATGAGATCATGCAAGCAAATGCTAACTTAGTTCCCAGCA... | AAGAGGCTGATGCCAGTGCAGGCCTCCAGGGCTCCGTTTCTTGACCTGTGCCCACAGTGGATCCTGAAAGCAGTTTGGCGAGTCATGACCTTTCCAAACGTTGAAATAGAATAGAAAATATCCCAGTACAATACACTTAGTAAGGTTTTGTATGAGTTCTGGGAACTTTTGCTTCAGTTTTATGGGATGTTTATACATGTGTGTCCTGGGTCATGGCGTACCATATAGTTTTTACTATGGGTTGTAGCAAGTAGTTTCAGAAATGCTGTCTTACAGATATAATGAGATCATGCAAGCAAATGCTAACTTAGTTCCCAGCA... |
Task1_train_33884 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GACAGGAGATAAATCCTTTCTGGGGAGCTCAGCTTGGCTGGCTGAGCCTGAGAGGCCTCCTCTCCCTCCTCCCTCTTGGGGGAAACAGAGTGGCAGGGCTGGTGAGCAGGGAGAGGCAGAGGATCTGCAGGGAATCTCAGAGAAAGTGCTCCTCGTGCAGCCCCAGTGTGCCTCTCCGGCCTCCCTCTCCACCCTGAGTCTCAACTTGGAACAGGGCTGCTTGAGGTCCCCAGAAGCCATTGATAGGGATAGAACCGGGACCTCAGGCATGAGGGCCTGACCTTCGTGGCTGGTGAGCAAATCCCCAGTGGTGGGGGGAT... | GACAGGAGATAAATCCTTTCTGGGGAGCTCAGCTTGGCTGGCTGAGCCTGAGAGGCCTCCTCTCCCTCCTCCCTCTTGGGGGAAACAGAGTGGCAGGGCTGGTGAGCAGGGAGAGGCAGAGGATCTGCAGGGAATCTCAGAGAAAGTGCTCCTCGTGCAGCCCCAGTGTGCCTCTCCGGCCTCCCTCTCCACCCTGAGTCTCAACTTGGAACAGGGCTGCTTGAGGTCCCCAGAAGCCATTGATAGGGATAGAACCGGGACCTCAGGCATGAGGGCCTGACCTTCGTGGCTGGTGAGCAAATCCCCAGTGGTGGGGGGAT... |
Task1_train_33885 | This variant is present on Chromosome 2. Is the change likely to result in a pathogenic outcome? | Benign | AAATGCTTTGCTTCCCGCATCTTTTCTAAATCGACTGTTAGAACATCCTGGGCTGTGTGCAGGGAGGCCTGAATGGGCTGAGGCCAGAAAGCTGAGCCAGGTGAGCAAGTGTTATCCCTGCGTAAGAGCCAAAATGCTGACTGCTAGAATCAAGTTACAAGCCTGGTGAAACAGTGCAGGGACTGAGATACCACAGGGTCCTCTGCTACACTAAAGAGAAGAGAAATGAAAGGAAAAAAGGAAAAACAAGTTTGCTATCCTCCTTTAGGTACCATTTTATAGAGAATCCACCATATGCCAGGCAACATACTAAATGCTAT... | AAATGCTTTGCTTCCCGCATCTTTTCTAAATCGACTGTTAGAACATCCTGGGCTGTGTGCAGGGAGGCCTGAATGGGCTGAGGCCAGAAAGCTGAGCCAGGTGAGCAAGTGTTATCCCTGCGTAAGAGCCAAAATGCTGACTGCTAGAATCAAGTTACAAGCCTGGTGAAACAGTGCAGGGACTGAGATACCACAGGGTCCTCTGCTACACTAAAGAGAAGAGAAATGAAAGGAAAAAAGGAAAAACAAGTTTGCTATCCTCCTTTAGGTACCATTTTATAGAGAATCCACCATATGCCAGGCAACATACTAAATGCTAT... |
Task1_train_33886 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCACCCCTCCTCTCCCAATCATACTTTCTTGGCCTTGAATGGATCCTGGCAGAGCTCCAGGGAGACATCTGGGGTCCGTATTGCCATGAAGCCCCTGGGGCTAGGACTCCCTAGCCATTCCTTCTCCACTCCTGGCAGGCTGAGTGAAATAAAGGACTTGTTATTTCATCTCGAGGCCTACCGGAGAGCCTTGCCTTGCAAAGGCAGACAGTCAGTGAGGAAGACTATGTGGCACATGAAGACACCAGAGGTGTTCCTCAGGATCAAAGTATGTACAAGCCTTTGTGAATATTTTTTCCTTCTCACTTGGCAAATACAAT... | CCACCCCTCCTCTCCCAATCATACTTTCTTGGCCTTGAATGGATCCTGGCAGAGCTCCAGGGAGACATCTGGGGTCCGTATTGCCATGAAGCCCCTGGGGCTAGGACTCCCTAGCCATTCCTTCTCCACTCCTGGCAGGCTGAGTGAAATAAAGGACTTGTTATTTCATCTCGAGGCCTACCGGAGAGCCTTGCCTTGCAAAGGCAGACAGTCAGTGAGGAAGACTATGTGGCACATGAAGACACCAGAGGTGTTCCTCAGGATCAAAGTATGTACAAGCCTTTGTGAATATTTTTTCCTTCTCACTTGGCAAATACAAT... |
Task1_train_33887 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CAGACAGTCAGTGAGGAAGACTATGTGGCACATGAAGACACCAGAGGTGTTCCTCAGGATCAAAGTATGTACAAGCCTTTGTGAATATTTTTTCCTTCTCACTTGGCAAATACAATTCCTGAGATCAATAACCTCGTCTTTTTAATTTTTTCCTCGTCTTTTTAACTATTTATAAAATATTGAATTATAAAATATGTAATTATAAATACTTTAATTATAAAATATGTAATTATAAATACTTTAATTATAAAATATGTAATTATAAATACTTTATAAAATATGTAATTATAAAATATGTAATTATAAACATTTTAATTATA... | CAGACAGTCAGTGAGGAAGACTATGTGGCACATGAAGACACCAGAGGTGTTCCTCAGGATCAAAGTATGTACAAGCCTTTGTGAATATTTTTTCCTTCTCACTTGGCAAATACAATTCCTGAGATCAATAACCTCGTCTTTTTAATTTTTTCCTCGTCTTTTTAACTATTTATAAAATATTGAATTATAAAATATGTAATTATAAATACTTTAATTATAAAATATGTAATTATAAATACTTTAATTATAAAATATGTAATTATAAATACTTTATAAAATATGTAATTATAAAATATGTAATTATAAACATTTTAATTATA... |
Task1_train_33888 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTTTATAAAATATGTAATTATAAAATATGTAATTATAAACATTTTAATTATAAAATATGTAATTATAAACATTTTAATTATAAAATATGTAATTATAAACATTTTAATTATAAAATATGTAATTATAAACATTTTAATTATAAAATATGTAATTATAAACATTTTAATTATAAAATATTTAATTATAAACATTTTAATTATAAAATATTTAATTATAAATATTTTAATTATAAAATATTTAATTATAAATATTTTAATTATAAAATATTTAATTATAAATATTTTAATTATAAAATATTTAATTATAAATACTTTAATTA... | CTTTATAAAATATGTAATTATAAAATATGTAATTATAAACATTTTAATTATAAAATATGTAATTATAAACATTTTAATTATAAAATATGTAATTATAAACATTTTAATTATAAAATATGTAATTATAAACATTTTAATTATAAAATATGTAATTATAAACATTTTAATTATAAAATATTTAATTATAAACATTTTAATTATAAAATATTTAATTATAAATATTTTAATTATAAAATATTTAATTATAAATATTTTAATTATAAAATATTTAATTATAAATATTTTAATTATAAAATATTTAATTATAAATACTTTAATTA... |
Task1_train_33889 | 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 | GTGGGGAAGAATTTTAAAGTTTTAAATACTACAGAAACCAGTCCTCTCTGAAAAATATACCCTGCCTATGGCTGAGCTTGCCTATGATTTAGATGATGAGGTATAACCCTCATCTTCCTGGATTTGCCCAGAATTAATAAATAATAGTGCTGATGGGATGTCATGTGTGCATCTAAACATTAAAATCAATCAAGGACTCATTGTAATACTTTCTAGAGAATATTTCCTCAGAGAAGAAGTTGCTTACCGCCTGTCTTTCACCTAGTTTGGGGAATCTCTGAATATTTGGTCCTGAATTAAATGTATCTGCCCCAATTCTC... | GTGGGGAAGAATTTTAAAGTTTTAAATACTACAGAAACCAGTCCTCTCTGAAAAATATACCCTGCCTATGGCTGAGCTTGCCTATGATTTAGATGATGAGGTATAACCCTCATCTTCCTGGATTTGCCCAGAATTAATAAATAATAGTGCTGATGGGATGTCATGTGTGCATCTAAACATTAAAATCAATCAAGGACTCATTGTAATACTTTCTAGAGAATATTTCCTCAGAGAAGAAGTTGCTTACCGCCTGTCTTTCACCTAGTTTGGGGAATCTCTGAATATTTGGTCCTGAATTAAATGTATCTGCCCCAATTCTC... |
Task1_train_33890 | 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 | GTTAATAATAATGAAAATATTAATTTAGAACTCGTAATAGTGTCTGCTTATTGAACAACCAATGCCAGCATCAGGCACTGTGCTTGGCATTTTAGATGCCTTATTTCATTGTCTTTAAATAACCTTGTGAGGTTTGGACTGTTATTAGTAGTCTGGGATACAGACAGAAACAGATACACATAATATCAACCAACTTCCCCAAGTGCGCACAGCTTCAAGACAGGGAAGTTAGAATTAAATCTATGCCCAGAGTTCATACTTTTTTTTTTTTTAAGATACAGTCTCACACTGTCACCCGGGCTGGAGTGTAACGGCGTGAT... | GTTAATAATAATGAAAATATTAATTTAGAACTCGTAATAGTGTCTGCTTATTGAACAACCAATGCCAGCATCAGGCACTGTGCTTGGCATTTTAGATGCCTTATTTCATTGTCTTTAAATAACCTTGTGAGGTTTGGACTGTTATTAGTAGTCTGGGATACAGACAGAAACAGATACACATAATATCAACCAACTTCCCCAAGTGCGCACAGCTTCAAGACAGGGAAGTTAGAATTAAATCTATGCCCAGAGTTCATACTTTTTTTTTTTTTAAGATACAGTCTCACACTGTCACCCGGGCTGGAGTGTAACGGCGTGAT... |
Task1_train_33891 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TCACACATTGCCCCATTTGATGGCATTTGCCCTCTCTCTTTCTGGATTTTTTTTAAACCACACAAACAATACCAAAACAAACATCCTTATGTGCCTATCTTCACACATTACTGCTTTTATTTTCATGGGCTAGAGTCCCAAAGACTAAAATATCTGTGTCAAAGGGTATTAAGTATTTTAAATTACAGTAGATATTGCCTGATGGCTCTCGTTTCCACCAGCAGCTCAGGACAGCACACTTTTCCTCACTGGCCTGCCAGCAACAGGTGCTATCACTGTTTTCCAGTTTTGCAGTATGATGGGTAAAAGCAGATAAATAT... | TCACACATTGCCCCATTTGATGGCATTTGCCCTCTCTCTTTCTGGATTTTTTTTAAACCACACAAACAATACCAAAACAAACATCCTTATGTGCCTATCTTCACACATTACTGCTTTTATTTTCATGGGCTAGAGTCCCAAAGACTAAAATATCTGTGTCAAAGGGTATTAAGTATTTTAAATTACAGTAGATATTGCCTGATGGCTCTCGTTTCCACCAGCAGCTCAGGACAGCACACTTTTCCTCACTGGCCTGCCAGCAACAGGTGCTATCACTGTTTTCCAGTTTTGCAGTATGATGGGTAAAAGCAGATAAATAT... |
Task1_train_33892 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GTGAAGATTTTCTTTCATTTCTTAGTCTGCCACCCTACCCCCATTCCCACCCCCACACCCGGGTTGGGGTGTAATGCCTCAGCAGTCTATTTCTGGATGTTACTGGCATTAAGTGAGAGCCATGTATAAACCAGATGTTTACCCCTTCTGATGTGGAATTCCCCAGGAGTCCATCTGTATTGTTTGAGGGAGAGATAGTGACGTGGAGGAGTAGGTTTTTGATAGTTTGAGTAACCTATTTAAAAAGTTCCTTGTGCCTTTGGGCTTGGTTGTCTTCTATGTACTGTATATACCACCTCTGTTTAATGAAGGAGATCTTC... | GTGAAGATTTTCTTTCATTTCTTAGTCTGCCACCCTACCCCCATTCCCACCCCCACACCCGGGTTGGGGTGTAATGCCTCAGCAGTCTATTTCTGGATGTTACTGGCATTAAGTGAGAGCCATGTATAAACCAGATGTTTACCCCTTCTGATGTGGAATTCCCCAGGAGTCCATCTGTATTGTTTGAGGGAGAGATAGTGACGTGGAGGAGTAGGTTTTTGATAGTTTGAGTAACCTATTTAAAAAGTTCCTTGTGCCTTTGGGCTTGGTTGTCTTCTATGTACTGTATATACCACCTCTGTTTAATGAAGGAGATCTTC... |
Task1_train_33893 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ATCTCCTCTTTTTGAAGGGCGCTAACCTCTAAATGTAGGATATGGTCACAGTGAAATTCTTTTTATCATGACTTTATCTGATTTCAAAAGAGATCCTACTTGTTTTGAAAAACCATCTGAAGTATGTTCAGATTCTATCCCAGAAAAGGCTTCTCTATTCTCAACTCTGCTGGTTACAGCCTAGTCCTAACCAGAGCCTTGCACAGGGCCTTTTTAAAATAAGGATCCTAAGTTTCTGGTAGGGATGTGTCCTTTGATGTTCACTTTCTTCCAGCTAAGCACCCAGCCAGCTACAAAGGCAAATTTGCTACATGTTTCTC... | ATCTCCTCTTTTTGAAGGGCGCTAACCTCTAAATGTAGGATATGGTCACAGTGAAATTCTTTTTATCATGACTTTATCTGATTTCAAAAGAGATCCTACTTGTTTTGAAAAACCATCTGAAGTATGTTCAGATTCTATCCCAGAAAAGGCTTCTCTATTCTCAACTCTGCTGGTTACAGCCTAGTCCTAACCAGAGCCTTGCACAGGGCCTTTTTAAAATAAGGATCCTAAGTTTCTGGTAGGGATGTGTCCTTTGATGTTCACTTTCTTCCAGCTAAGCACCCAGCCAGCTACAAAGGCAAATTTGCTACATGTTTCTC... |
Task1_train_33894 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTTCCCAAGTAGCTGGGATTACAGGCGCCCATCACCATGCCCAGCTAATTTTTATATTTTTGTTAGAGACAGGGTTTCACCACATTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACTTGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCATGGAGCCCAGCAACATAACCTTTTTTATAACTGGAGGAGTATCTCTATTATATAAGGAAAAGGTTGTCACAATGAAATAACATGATTTTTTTTCTAAATATAAATTGCCCGAATTAGTGCAGACATTTATTTTTCCACGTCATGCACCTGA... | TTTCCCAAGTAGCTGGGATTACAGGCGCCCATCACCATGCCCAGCTAATTTTTATATTTTTGTTAGAGACAGGGTTTCACCACATTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACTTGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCATGGAGCCCAGCAACATAACCTTTTTTATAACTGGAGGAGTATCTCTATTATATAAGGAAAAGGTTGTCACAATGAAATAACATGATTTTTTTTCTAAATATAAATTGCCCGAATTAGTGCAGACATTTATTTTTCCACGTCATGCACCTGA... |
Task1_train_33895 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACTTGTTTTATTCACTGCTGTATTCCCAATACGTAAGACTAGTGTCTGGCACATAGTAGCTATTCAATAAATATAATTGATGAATTATGTCCCACATGGCAAGCAGAATACATAGTAGGTGCTCAAAAAATATTGTTTTAATTAATGTGTTAATGAAGGATCCGAAAAGCACCATGATCTGAGGGGAATCCCAGGTCCTAGTTGTTGGTGAACCATTAAGTTAGTTGAGGACTCTTCTGAGATATCGACTTTAAGTCAAGGAGATAATCCTAACGCCAGGTCCTTAGGTGCGGGTCAAGCAAAGAGGCTATAGGGGTAAC... | ACTTGTTTTATTCACTGCTGTATTCCCAATACGTAAGACTAGTGTCTGGCACATAGTAGCTATTCAATAAATATAATTGATGAATTATGTCCCACATGGCAAGCAGAATACATAGTAGGTGCTCAAAAAATATTGTTTTAATTAATGTGTTAATGAAGGATCCGAAAAGCACCATGATCTGAGGGGAATCCCAGGTCCTAGTTGTTGGTGAACCATTAAGTTAGTTGAGGACTCTTCTGAGATATCGACTTTAAGTCAAGGAGATAATCCTAACGCCAGGTCCTTAGGTGCGGGTCAAGCAAAGAGGCTATAGGGGTAAC... |
Task1_train_33896 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GCCGCATGTTTCTATCTGAGTTTTAGCCACCTCCTTTACCTCAGACTAAGGCCCTTTCTCAGGCAAGTTAATAAAAAACTGGAAATTCATCTAGTGCTGTTTTTTTTTCTTGGTGTTGAATAGCATTCAGTAACTTCCTGCTTTTTGATCACTCTCCAGTGTCTTCAGGTTGTTGTTTTTTATATTTTTTATCTGGAATGTTAATTCACTACCCCCTATCTGAGTACAGACTTTCCAGGAAGGGCAACTCTATGAGGCAAAAATAACAAAGAAAACAAACTAGAGTAGACTCATTTGAGTTTTCTATGCTTCTAGTTGTT... | GCCGCATGTTTCTATCTGAGTTTTAGCCACCTCCTTTACCTCAGACTAAGGCCCTTTCTCAGGCAAGTTAATAAAAAACTGGAAATTCATCTAGTGCTGTTTTTTTTTCTTGGTGTTGAATAGCATTCAGTAACTTCCTGCTTTTTGATCACTCTCCAGTGTCTTCAGGTTGTTGTTTTTTATATTTTTTATCTGGAATGTTAATTCACTACCCCCTATCTGAGTACAGACTTTCCAGGAAGGGCAACTCTATGAGGCAAAAATAACAAAGAAAACAAACTAGAGTAGACTCATTTGAGTTTTCTATGCTTCTAGTTGTT... |
Task1_train_33897 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | ATTCCATATTCCTCATCCTCTTTAAATTATTCTACCCTGACAGTTATCTAGTCTCCCAACATCTCACCCCTAATCAATATATGGTTCTAAGTGAAACTAGATTTTCTTTCTTTCTTTCTTTTTTTTTTTTTTTGAAACAGGGTCTCGTTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGATCATGGCTCACTGCAGGCTGGACCTCCCAGGTTCAAGCAATTCTCCGCCTTTCAGCCTCCCGAGTAGCTACGACTACAGGTGTACGCCATCATGCCTGGCTAATTTTTTGTATTTTTTGTAGAGATGAGGTCTCACCATG... | ATTCCATATTCCTCATCCTCTTTAAATTATTCTACCCTGACAGTTATCTAGTCTCCCAACATCTCACCCCTAATCAATATATGGTTCTAAGTGAAACTAGATTTTCTTTCTTTCTTTCTTTTTTTTTTTTTTTGAAACAGGGTCTCGTTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGATCATGGCTCACTGCAGGCTGGACCTCCCAGGTTCAAGCAATTCTCCGCCTTTCAGCCTCCCGAGTAGCTACGACTACAGGTGTACGCCATCATGCCTGGCTAATTTTTTGTATTTTTTGTAGAGATGAGGTCTCACCATG... |
Task1_train_33898 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CCTAATGCTCTCCCTTCCCCCTCCCCACCCCTCCTTGATTCTTTTTCAAATAGGTTTTGGGAAATGCTGTCTGTACTCGGGGCCTGGAGAGTTTCTGTCCTCCATTGAGAAACCAAGCACATTGCTTGACTTGCCTCTTAGCGGGAGGGTGATGTTGAGAACAAGGTTAAATACCCACCTGTCAGGACATCAACCAGACCCAAAGACAAAAATCCACCAAAGATGCTAGAAGCACAGAGAAATCAGTCTCTACCTTGGTACTTAATATTGGTGACCTGGTACTTGAAATGCTCCCACAGAGGAAGGTAAGAGTTGGAGAT... | CCTAATGCTCTCCCTTCCCCCTCCCCACCCCTCCTTGATTCTTTTTCAAATAGGTTTTGGGAAATGCTGTCTGTACTCGGGGCCTGGAGAGTTTCTGTCCTCCATTGAGAAACCAAGCACATTGCTTGACTTGCCTCTTAGCGGGAGGGTGATGTTGAGAACAAGGTTAAATACCCACCTGTCAGGACATCAACCAGACCCAAAGACAAAAATCCACCAAAGATGCTAGAAGCACAGAGAAATCAGTCTCTACCTTGGTACTTAATATTGGTGACCTGGTACTTGAAATGCTCCCACAGAGGAAGGTAAGAGTTGGAGAT... |
Task1_train_33899 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | GGGGGAAACCTGAATAAAAAAACACATAAAGAGCTGCAACTATAGCAGCCAGGAAGCTGGTGGGAGGCCCAGGCAGGAGGGCAGGCTGCATGGGGGGGCCCGGCGGGAAGGAAGGTGGAGATGCAGGGGGCCGGCGGGGAGGAAGGTGGAGATGCAGCTGGCTCAGAGCACAGGCCCCCTGTGGGGTGGAGGCCACAGGCTGGCCTGGCACAGCTGGAGATGCAGCAGGGAGGTTGGGGCCTGGCATTCATGTGGAGGCTGGAGAAGAATGTGGGAGCTCTGGTCTGAAGGCCACGGTGGGGCAGGGTGGGGTGGGGGGT... | GGGGGAAACCTGAATAAAAAAACACATAAAGAGCTGCAACTATAGCAGCCAGGAAGCTGGTGGGAGGCCCAGGCAGGAGGGCAGGCTGCATGGGGGGGCCCGGCGGGAAGGAAGGTGGAGATGCAGGGGGCCGGCGGGGAGGAAGGTGGAGATGCAGCTGGCTCAGAGCACAGGCCCCCTGTGGGGTGGAGGCCACAGGCTGGCCTGGCACAGCTGGAGATGCAGCAGGGAGGTTGGGGCCTGGCATTCATGTGGAGGCTGGAGAAGAATGTGGGAGCTCTGGTCTGAAGGCCACGGTGGGGCAGGGTGGGGTGGGGGGT... |
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