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_34900 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CTGTGCCCAGAGCAAGTTTGCCCAGGGATACGGTGCGCTCCGCGAGCATCTGCTGGGCTTGCACAGGGGACGGGGAGGGACCTCTGGTTTCATTTCTCTGCCGACAATCCCCTCACACACATCTTACCCCGCCCCCTCCAGTCCCTCCCCTCTGAGGCCTCACTCTTAAGCTGGGGATGAGGGGGTGGGGTGCTGTCCGTGGCCCCCACTGTCCCTCCTCTCAGGGCGCCCTGTTAGCGTGCCCTGGGCGGAGCCAACCCCCCACGTCCTCTCGGATCTTCCCTCCACTCAGGGCCTGGGTCCCCTTCGGGCCTGTGTGA... | CTGTGCCCAGAGCAAGTTTGCCCAGGGATACGGTGCGCTCCGCGAGCATCTGCTGGGCTTGCACAGGGGACGGGGAGGGACCTCTGGTTTCATTTCTCTGCCGACAATCCCCTCACACACATCTTACCCCGCCCCCTCCAGTCCCTCCCCTCTGAGGCCTCACTCTTAAGCTGGGGATGAGGGGGTGGGGTGCTGTCCGTGGCCCCCACTGTCCCTCCTCTCAGGGCGCCCTGTTAGCGTGCCCTGGGCGGAGCCAACCCCCCACGTCCTCTCGGATCTTCCCTCCACTCAGGGCCTGGGTCCCCTTCGGGCCTGTGTGA... |
Task1_train_34901 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | TTTTCCAGGTAGGTGGAAGTGGAAGTCAGGGCGCCCGAAGCCCAGAACTGAATCCAAGACCCAGGGGCCCCTCTCCTCTGTGGCCTCAGCTGCTGCTTCCGCCGGAGGATGAAGTGAACCTGACCAGAGGACTCTGAGCAGAGCCCCTTCACCTGCTCTGGAGGCATGGGTCCCACGTATCCTTCCACTTGGCGGATTTGTGGCACATGCCTGCCTGTGCCAAGCGTTGTTCTAGGCCTTCCTGGGCGCAGCGTCTAGCAGGGAAGACGGTGGCCCATGGGCAGGTGCCGGCAGGTGTGTGGGGTGCGATTCCCACTGCT... | TTTTCCAGGTAGGTGGAAGTGGAAGTCAGGGCGCCCGAAGCCCAGAACTGAATCCAAGACCCAGGGGCCCCTCTCCTCTGTGGCCTCAGCTGCTGCTTCCGCCGGAGGATGAAGTGAACCTGACCAGAGGACTCTGAGCAGAGCCCCTTCACCTGCTCTGGAGGCATGGGTCCCACGTATCCTTCCACTTGGCGGATTTGTGGCACATGCCTGCCTGTGCCAAGCGTTGTTCTAGGCCTTCCTGGGCGCAGCGTCTAGCAGGGAAGACGGTGGCCCATGGGCAGGTGCCGGCAGGTGTGTGGGGTGCGATTCCCACTGCT... |
Task1_train_34902 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ACATGCCTGCCTGTGCCAAGCGTTGTTCTAGGCCTTCCTGGGCGCAGCGTCTAGCAGGGAAGACGGTGGCCCATGGGCAGGTGCCGGCAGGTGTGTGGGGTGCGATTCCCACTGCTGTGGAGAAAGCAAAGCAGTTGGGGGACTATGATATATGGGTGCTTAGGGGGCCCCCTCTGGGGACGTGGCCTTGAGCAGGGGCCAGAGGGAAGAGAGGGGGAGCCCTGTGGGAATTTGGGGCAAGCACCTCCTAGGCAGAGGGAACAGCCAGTGCAAGGGTCCTGAGGCCGGGCTGGCCGGGGGAGGAGCAGGAGGAGGCGCCC... | ACATGCCTGCCTGTGCCAAGCGTTGTTCTAGGCCTTCCTGGGCGCAGCGTCTAGCAGGGAAGACGGTGGCCCATGGGCAGGTGCCGGCAGGTGTGTGGGGTGCGATTCCCACTGCTGTGGAGAAAGCAAAGCAGTTGGGGGACTATGATATATGGGTGCTTAGGGGGCCCCCTCTGGGGACGTGGCCTTGAGCAGGGGCCAGAGGGAAGAGAGGGGGAGCCCTGTGGGAATTTGGGGCAAGCACCTCCTAGGCAGAGGGAACAGCCAGTGCAAGGGTCCTGAGGCCGGGCTGGCCGGGGGAGGAGCAGGAGGAGGCGCCC... |
Task1_train_34903 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TGTGAGGCCGTGGGGAGCCACTGAGAATCTGAGCAGAGAAGGGCTGTGATGTGCCTTGGATTTTAACAGGCTCCCCGGGCTGCTGTGCAGACAGGAGTTCAGGAATTATGTCCTCAGAGTCCTATGATTTTGTCAAGATGATTGAGTTCTGTGCCCCCGGCCCAGCGCTGTGTCCAGCGCAATCCTGCCAGCCACATGCAGCCACTGAAATTCATTACAATTTAAGGAAAGTAAAAGTCCTGCCCCTCCGTCGCACCAGCCACCTGTCGTTTCTGTAGCCACAGGTGGCTCCTGGCTGCTGGAATACAGCCTGTCTCCAT... | TGTGAGGCCGTGGGGAGCCACTGAGAATCTGAGCAGAGAAGGGCTGTGATGTGCCTTGGATTTTAACAGGCTCCCCGGGCTGCTGTGCAGACAGGAGTTCAGGAATTATGTCCTCAGAGTCCTATGATTTTGTCAAGATGATTGAGTTCTGTGCCCCCGGCCCAGCGCTGTGTCCAGCGCAATCCTGCCAGCCACATGCAGCCACTGAAATTCATTACAATTTAAGGAAAGTAAAAGTCCTGCCCCTCCGTCGCACCAGCCACCTGTCGTTTCTGTAGCCACAGGTGGCTCCTGGCTGCTGGAATACAGCCTGTCTCCAT... |
Task1_train_34904 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AGGACCAGAGGCTCTGCAGAGATACTGAGAACTCAGGGACTTGGAAGCTAGGTGGGCTGATGGTGGGTGGGTGGGCTCACCCTGCTCACCCTGCCCTTCCTGTGCCCAGGACAATGGTGGGAGCTCAGGCCCCACGGAGCAGGCGGCCTGGAGGTACTCACAGACTCATCAGGCCATCCTGGGGCCCTTTGGGGAGCTGCTGACAGAGGATGACCTGGTCTACCTGGAGAAGCAGATTGCAGACCTGCAGCTTCGGCGCCGCTGTCAGGAGTATGAGAGTGAGCTGGGCCGGTTGGCGGCTGAGCTGCAGGCCCTGCTGC... | AGGACCAGAGGCTCTGCAGAGATACTGAGAACTCAGGGACTTGGAAGCTAGGTGGGCTGATGGTGGGTGGGTGGGCTCACCCTGCTCACCCTGCCCTTCCTGTGCCCAGGACAATGGTGGGAGCTCAGGCCCCACGGAGCAGGCGGCCTGGAGGTACTCACAGACTCATCAGGCCATCCTGGGGCCCTTTGGGGAGCTGCTGACAGAGGATGACCTGGTCTACCTGGAGAAGCAGATTGCAGACCTGCAGCTTCGGCGCCGCTGTCAGGAGTATGAGAGTGAGCTGGGCCGGTTGGCGGCTGAGCTGCAGGCCCTGCTGC... |
Task1_train_34905 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GCCAGGGATCACAGCAGGGTGCTTTGGAGACGCCCCCTGGCCCTTGCCAGCGGCCAAGCCAGGCTCCTCAGGGTGGGGGCTCAGGAGACAGGTTTCCCTCCATGTCCCAGCCGGAGAGGTGGGAGGGGGAGGCTGGGCCACCCCTCAGATGGCAGCCAGGGCCACTCAGCCACAGTCGCCAGCCTGGCTGGGCTCAGGCCTTTTGTTGTCCTGCCCACTCGGCTTCCTCACTCCGGGCCTGGGCAGGCACTGGGGTGAGGCTCTGAGACCCTCAGGAAGCCCCGACCCATGCAGGGACTGCAGGGTGACAGGTGTCAGCA... | GCCAGGGATCACAGCAGGGTGCTTTGGAGACGCCCCCTGGCCCTTGCCAGCGGCCAAGCCAGGCTCCTCAGGGTGGGGGCTCAGGAGACAGGTTTCCCTCCATGTCCCAGCCGGAGAGGTGGGAGGGGGAGGCTGGGCCACCCCTCAGATGGCAGCCAGGGCCACTCAGCCACAGTCGCCAGCCTGGCTGGGCTCAGGCCTTTTGTTGTCCTGCCCACTCGGCTTCCTCACTCCGGGCCTGGGCAGGCACTGGGGTGAGGCTCTGAGACCCTCAGGAAGCCCCGACCCATGCAGGGACTGCAGGGTGACAGGTGTCAGCA... |
Task1_train_34906 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GAGGGCAGAGCCGCCTTCACCGGGGCCAGCGCCTCCTGGGGAGGGGCCAGGCAGGAACCCCATGCATGCAGTGTTGGGTGGGTACTTCGTGTACCGGCCGGGATGCTGGGGTGTGGGGCCCCGGCCACGTGAGCTGCCCTGTGCGCGAGCCCGGGTTGGTCCGCGAGGCCCTGTGGGCTCCCAGGTGCTTCCCCGCTCTGGGGTCAAGAGGTGGCACCGGGGTCGGGAAGTCGGGGAGCCCTAGCTCCCATCGCCTGCACCTGTACCTGCACCGTGGCTGCCCGGGCCAGATTCTTGGCCTCCTGGTTCTCCAGCTGAGC... | GAGGGCAGAGCCGCCTTCACCGGGGCCAGCGCCTCCTGGGGAGGGGCCAGGCAGGAACCCCATGCATGCAGTGTTGGGTGGGTACTTCGTGTACCGGCCGGGATGCTGGGGTGTGGGGCCCCGGCCACGTGAGCTGCCCTGTGCGCGAGCCCGGGTTGGTCCGCGAGGCCCTGTGGGCTCCCAGGTGCTTCCCCGCTCTGGGGTCAAGAGGTGGCACCGGGGTCGGGAAGTCGGGGAGCCCTAGCTCCCATCGCCTGCACCTGTACCTGCACCGTGGCTGCCCGGGCCAGATTCTTGGCCTCCTGGTTCTCCAGCTGAGC... |
Task1_train_34907 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | GTCAACTGCTTGGCACGCGCTGAAGCTACAGTTAACAATCAGTGAGCACATATTAAATGATAAAATAATGCTGATGGTAAACATTCATAACAGCAGAGTAAGATTTTGGCAGTTTTGTGTTTCGGTAACATAACTGTAACCTTAGATGAACACCTATCCCTTCATGATCTGACTTTAGAGGCAAGGAGTTTGTAACATCTAATGGCCATAAGAATGCAGACTGCTACCTTATCATAGGCATAGGCAGCTGATGTTACTTTGTAAATTAACGAAAAATTAAAGTGTTCTTGTGTTTATGAAGAATAGGTTTAATAGTCAGG... | GTCAACTGCTTGGCACGCGCTGAAGCTACAGTTAACAATCAGTGAGCACATATTAAATGATAAAATAATGCTGATGGTAAACATTCATAACAGCAGAGTAAGATTTTGGCAGTTTTGTGTTTCGGTAACATAACTGTAACCTTAGATGAACACCTATCCCTTCATGATCTGACTTTAGAGGCAAGGAGTTTGTAACATCTAATGGCCATAAGAATGCAGACTGCTACCTTATCATAGGCATAGGCAGCTGATGTTACTTTGTAAATTAACGAAAAATTAAAGTGTTCTTGTGTTTATGAAGAATAGGTTTAATAGTCAGG... |
Task1_train_34908 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTCCTAGAGACCTGCTGCTACTTCTCTCCCTTCAGATCCTTCTCTCGTTTCCCATATCTGAGCCCTCCATTCCAGTCGCCACGCACCCCTGCATTCGGCCCTGGCCGGCTGTCTCCCGTCGGCCTCTTGCCCTGGTGCCTGCTGGCTTCTTGGTACCTGAGCTGCCTTCCTCCTCCAGCCTCACCCAGCAACAATGTGGCGTCTGTGAGTGCTTCCTTGAGCCTGGGCCTCTCCTCCCTCCCAGGCTGACTTAGGTGCCCCTGTAGGCTTCCTATAGGCTGTTGTTTAATTGTTGTGTTTATCTGTGTCCCCAGTACACG... | CTCCTAGAGACCTGCTGCTACTTCTCTCCCTTCAGATCCTTCTCTCGTTTCCCATATCTGAGCCCTCCATTCCAGTCGCCACGCACCCCTGCATTCGGCCCTGGCCGGCTGTCTCCCGTCGGCCTCTTGCCCTGGTGCCTGCTGGCTTCTTGGTACCTGAGCTGCCTTCCTCCTCCAGCCTCACCCAGCAACAATGTGGCGTCTGTGAGTGCTTCCTTGAGCCTGGGCCTCTCCTCCCTCCCAGGCTGACTTAGGTGCCCCTGTAGGCTTCCTATAGGCTGTTGTTTAATTGTTGTGTTTATCTGTGTCCCCAGTACACG... |
Task1_train_34909 | 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 | ATAATTAGTAATGCGTTTGTGACCAGCTTAGTGCCAGAAGCCTTTGCTGTCTTTTGGTTGACCGCTGTGGGGTAGGTTTCCAGAAGCGCAGTGGCTGGCACAAAGGGTGTGGCATTATGGCTACTGCGTGCCCTTAATGACCCTTCACCCCACACCTTCTCCAGTGTTGTTAAGGCATGCTGATTTTGATGGACGAAAAACAAAAACGTTGATGACCAGTGAAATGGTCCTTGTCATCGCGTGTGAGTGTTTTGGGCGTCTCTGACCTGCCTGTTCTTTGGTTTCTCTGGGTTCTTACTGATTTGCTTGCACGTGCTGTA... | ATAATTAGTAATGCGTTTGTGACCAGCTTAGTGCCAGAAGCCTTTGCTGTCTTTTGGTTGACCGCTGTGGGGTAGGTTTCCAGAAGCGCAGTGGCTGGCACAAAGGGTGTGGCATTATGGCTACTGCGTGCCCTTAATGACCCTTCACCCCACACCTTCTCCAGTGTTGTTAAGGCATGCTGATTTTGATGGACGAAAAACAAAAACGTTGATGACCAGTGAAATGGTCCTTGTCATCGCGTGTGAGTGTTTTGGGCGTCTCTGACCTGCCTGTTCTTTGGTTTCTCTGGGTTCTTACTGATTTGCTTGCACGTGCTGTA... |
Task1_train_34910 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GATAATGCATTTATAATTTGCTTACTGTGATGGTGAATATGGTAGAGTATGGAAAACATTTGACACTTTGAAATCAAGTACACAACTTAAAATTATTAGAGTGTTTTCTTCTAAAGTTGAGCATCTACAACCGCCAAACTTATGTTTATTTTTAGATTTTTTTTTGTTAAGAACTTAATATTTCATGTTTATTCTCTGGTTACCCTGAGTAAAATATAAATAACTGTTTGAATCAGACTATTTAAGTCAGTATCATTTTCACAGATTGATAAAAATGTCTTTGCAAAATTATGTGTCATCTATTTTATGTAGTTCTATTA... | GATAATGCATTTATAATTTGCTTACTGTGATGGTGAATATGGTAGAGTATGGAAAACATTTGACACTTTGAAATCAAGTACACAACTTAAAATTATTAGAGTGTTTTCTTCTAAAGTTGAGCATCTACAACCGCCAAACTTATGTTTATTTTTAGATTTTTTTTTGTTAAGAACTTAATATTTCATGTTTATTCTCTGGTTACCCTGAGTAAAATATAAATAACTGTTTGAATCAGACTATTTAAGTCAGTATCATTTTCACAGATTGATAAAAATGTCTTTGCAAAATTATGTGTCATCTATTTTATGTAGTTCTATTA... |
Task1_train_34911 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | GGGTACTAGGGCCCTGAAGGTCTGTGTGAAGCTGAGCCCCACAGTCGCTGTGCAGATGAAGACCTTGATGTTGGGAGGAATGTGTTCCAGTTTTAGAGGACGGGGATAAAGGAGACTGAGGCAGCATGGTCAGAGTTGTAGGAGACAGCCAGACAGTGTGGGCAGGGAGACCTGAGTTCAGGTCCTGCTCTGCCATTAACCTTAGTGTTTTCTGGCAACTTCTGGCCTTCTGTGGGCCTCAGCCTCCTGATGTCACTCCTGAAGGTACCACTGTTTCCCTCTTCAGTGGCGGCCCTGCCCCATCTTGGGTTTCTCGTGGC... | GGGTACTAGGGCCCTGAAGGTCTGTGTGAAGCTGAGCCCCACAGTCGCTGTGCAGATGAAGACCTTGATGTTGGGAGGAATGTGTTCCAGTTTTAGAGGACGGGGATAAAGGAGACTGAGGCAGCATGGTCAGAGTTGTAGGAGACAGCCAGACAGTGTGGGCAGGGAGACCTGAGTTCAGGTCCTGCTCTGCCATTAACCTTAGTGTTTTCTGGCAACTTCTGGCCTTCTGTGGGCCTCAGCCTCCTGATGTCACTCCTGAAGGTACCACTGTTTCCCTCTTCAGTGGCGGCCCTGCCCCATCTTGGGTTTCTCGTGGC... |
Task1_train_34912 | 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 | GTGGCCATGAGCTGCCCTGGAGGGACATGAACTCCCAGGGACTTCAGCTGGGAAAAGTAGCTCTGGTGGTCCAAGGTCAGTGGTGTGGGGTATTCTCAGCAAAAGCACAGGGAAGTTGGGGAAGGGGCTCAGAACCCCTCACAGGGACCTGGGGGCTCTGGGCAGAGCACTGATGGCTTCTGCTACGGGGTAATCACACTCGATACAAATGGATCAGACAATTGTCCTGCCCCTTGTGTCTCATGATCACAAGCAGGAAGGGTGAACCCGGTGTCTCCGTGCTTCCGGGAAAGTTGGTGAAGGAAAATACAAACTCAAGA... | GTGGCCATGAGCTGCCCTGGAGGGACATGAACTCCCAGGGACTTCAGCTGGGAAAAGTAGCTCTGGTGGTCCAAGGTCAGTGGTGTGGGGTATTCTCAGCAAAAGCACAGGGAAGTTGGGGAAGGGGCTCAGAACCCCTCACAGGGACCTGGGGGCTCTGGGCAGAGCACTGATGGCTTCTGCTACGGGGTAATCACACTCGATACAAATGGATCAGACAATTGTCCTGCCCCTTGTGTCTCATGATCACAAGCAGGAAGGGTGAACCCGGTGTCTCCGTGCTTCCGGGAAAGTTGGTGAAGGAAAATACAAACTCAAGA... |
Task1_train_34913 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | ACAGGAAAAATTCCAATTTAAACAGAGAACCCCATTTTAGAAATTTAAATGAAATAACTTTTTTTTGAGACAGGGTCCGGCTCTATCATCCAGGCTGGAAAGTAGTGGCACAATCACAGCACACTGCAGCCTTGGCCTGCTGGGCTCAAGCAATCCTCCCACCTCAGCACCTCAGCCTCCCGAGTTGCTGGGACTACAGGCATATGCCACCACACCTGGCTGATGTTTGTATTTTTAGTAGAGATGGGGTCTCACCACGTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGCGATCCTCCTGCCTCAGCCTCCCAAAG... | ACAGGAAAAATTCCAATTTAAACAGAGAACCCCATTTTAGAAATTTAAATGAAATAACTTTTTTTTGAGACAGGGTCCGGCTCTATCATCCAGGCTGGAAAGTAGTGGCACAATCACAGCACACTGCAGCCTTGGCCTGCTGGGCTCAAGCAATCCTCCCACCTCAGCACCTCAGCCTCCCGAGTTGCTGGGACTACAGGCATATGCCACCACACCTGGCTGATGTTTGTATTTTTAGTAGAGATGGGGTCTCACCACGTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGCGATCCTCCTGCCTCAGCCTCCCAAAG... |
Task1_train_34914 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CCCTCTGCAGCTTTTCACGTGTGGAACCTTCCAGAAGTGACAGATGGCCATGCTAGGGTCCACAGAAAGACAACTATTTTGCTTTAAAGGAAATGGGCTGGGCACAGTGGCTCACGCCTGTCATCCTGGCACTTTGGGAGGCCGAGGTGGGCGCAGATCACTGGAGCCCAGGAGTTCAGGACCAGCCTGAGCAGCATGGTGAAATCCCATGTCTACCAAAAATACAAACATTAGCCAGTCTCCTAACCTAGTCTCAAAATAAATAAATAAAAATTTTAAAAATTAAATTAAAAAAAAAAGTTCCAGTGAGCATTCCTAGT... | CCCTCTGCAGCTTTTCACGTGTGGAACCTTCCAGAAGTGACAGATGGCCATGCTAGGGTCCACAGAAAGACAACTATTTTGCTTTAAAGGAAATGGGCTGGGCACAGTGGCTCACGCCTGTCATCCTGGCACTTTGGGAGGCCGAGGTGGGCGCAGATCACTGGAGCCCAGGAGTTCAGGACCAGCCTGAGCAGCATGGTGAAATCCCATGTCTACCAAAAATACAAACATTAGCCAGTCTCCTAACCTAGTCTCAAAATAAATAAATAAAAATTTTAAAAATTAAATTAAAAAAAAAAGTTCCAGTGAGCATTCCTAGT... |
Task1_train_34915 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | ACAGAACAATAAGAAAACAAAGAATAAAAACACACAGCTTATTTTAAAATTATAAAATATAGCCAAAAACCACATGAAAAAGTGGTCAACCTTGCTACAAAAAAACAAAAGACTATTAACAAGGAAACATTAGTTTTTCATGTGTCAAAATGAGAAATAATTTAAAAAATGATTACAGAGTTAGGACAAGACAATGAGTACCATCCTAAACTGCTAATGGTAATGAAACCTAGAGGACGCTGGGTCTACAGCATTAGGAATCCATTCAAAGAGTATATACATAAGATTGACCTATAAGGATGCTCAATGAAGTATGATGT... | ACAGAACAATAAGAAAACAAAGAATAAAAACACACAGCTTATTTTAAAATTATAAAATATAGCCAAAAACCACATGAAAAAGTGGTCAACCTTGCTACAAAAAAACAAAAGACTATTAACAAGGAAACATTAGTTTTTCATGTGTCAAAATGAGAAATAATTTAAAAAATGATTACAGAGTTAGGACAAGACAATGAGTACCATCCTAAACTGCTAATGGTAATGAAACCTAGAGGACGCTGGGTCTACAGCATTAGGAATCCATTCAAAGAGTATATACATAAGATTGACCTATAAGGATGCTCAATGAAGTATGATGT... |
Task1_train_34916 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCAAATAAGGACTAAAGGGGAGCTGCTTCAGCTTGATAAAGCACATGCGTGAAAACTCTGCATCATTGTACTTAATCATGAAAGACTGAATGCTTGCCTTCTAAGGAGGAAACAAGGCAAGGATATCTGCTCTGCCCACTCTTATTCAACAGAGCACTGGAAGTTCTAGTAATAGGCCATGCAGTATGGCAAAAAATAAAAAATGAAATTCATACAGATCAGAAAGGAAGAAATAAAACTGTCTATTTTTAGTTGACATGACTGTTCACATAGAAAACCCAAAGGAATCTACAAAAACCTCCTGGAACTAATGAGTGAGC... | GCAAATAAGGACTAAAGGGGAGCTGCTTCAGCTTGATAAAGCACATGCGTGAAAACTCTGCATCATTGTACTTAATCATGAAAGACTGAATGCTTGCCTTCTAAGGAGGAAACAAGGCAAGGATATCTGCTCTGCCCACTCTTATTCAACAGAGCACTGGAAGTTCTAGTAATAGGCCATGCAGTATGGCAAAAAATAAAAAATGAAATTCATACAGATCAGAAAGGAAGAAATAAAACTGTCTATTTTTAGTTGACATGACTGTTCACATAGAAAACCCAAAGGAATCTACAAAAACCTCCTGGAACTAATGAGTGAGC... |
Task1_train_34917 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCTTCACTCATCTGCACATCCTCCTTCAGCTCTGGCGTCTACTCGGTCCCTAACAGGTATCTGGATGCATTCCTCAGTTCCTTCCTATTCCCACTCTAACCCCAAATGCTGATTTGAACACTTACATAGCTCTCAAATGGGCCCGGCCACTGCATCCAAATCCTGCATCCACTGCTCAACCCAGGGTAGTGCTCATCCCTCACGTGCACAATCCCAGCAGCCTCCCTCACAGCCTCCTTGCCTCCCACGGGGTCCCCTCTCCATCTGTCACACACCTGCCAAATAGACGGTCCAAGGCAGGAAACTGAACGTACCTCTAC... | CCTTCACTCATCTGCACATCCTCCTTCAGCTCTGGCGTCTACTCGGTCCCTAACAGGTATCTGGATGCATTCCTCAGTTCCTTCCTATTCCCACTCTAACCCCAAATGCTGATTTGAACACTTACATAGCTCTCAAATGGGCCCGGCCACTGCATCCAAATCCTGCATCCACTGCTCAACCCAGGGTAGTGCTCATCCCTCACGTGCACAATCCCAGCAGCCTCCCTCACAGCCTCCTTGCCTCCCACGGGGTCCCCTCTCCATCTGTCACACACCTGCCAAATAGACGGTCCAAGGCAGGAAACTGAACGTACCTCTAC... |
Task1_train_34918 | 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 | GTACCTCTACCCCCACCTTAATTGCCAGACGAGTCCATGCTGCCTGCCACACCTGTGAGCCCTCGGGTCCTGATCTGCCTGCCACGCCTGGGAGCTCTCGGGTCCTGACCTGCCCGCCACGCCTGGGAGCTCTCGGGTCCTGATCTGCCCGCCACACCTGTTAGCTCTGGGGGTCCTGATCCGCCTGCCATGCAGGAAGCTCTCGGGGCTCTGATCTGCCTGCCACGCCTGGGAGCTCTGGGGGTCCTGATCTGCCCACCATGCCTGGGAGCTCTCGGGTCCTGATCTGCCCGCCACACCTGGGAGCTCTCGGGGCTCTG... | GTACCTCTACCCCCACCTTAATTGCCAGACGAGTCCATGCTGCCTGCCACACCTGTGAGCCCTCGGGTCCTGATCTGCCTGCCACGCCTGGGAGCTCTCGGGTCCTGACCTGCCCGCCACGCCTGGGAGCTCTCGGGTCCTGATCTGCCCGCCACACCTGTTAGCTCTGGGGGTCCTGATCCGCCTGCCATGCAGGAAGCTCTCGGGGCTCTGATCTGCCTGCCACGCCTGGGAGCTCTGGGGGTCCTGATCTGCCCACCATGCCTGGGAGCTCTCGGGTCCTGATCTGCCCGCCACACCTGGGAGCTCTCGGGGCTCTG... |
Task1_train_34919 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GATCTGCCCACCATGCCTGGGAGCTCTCGGGTCCTGATCTGCCCGCCACACCTGGGAGCTCTCGGGGCTCTGATGTTACCCACCATACATGTGAGCTCTTGGGGCTCTGTCCTCTTTTTGTCTCAAGTCTCCCCTTTGGTGAACACCAGGCTCCTATGAGGCTGCGTCTTTGAGCTCTGCACAGCTCCATGCTGCTTCCTGCCTCTGAGGCTTTGCTATCATTGAAATTGCCTGGAACACCCTTCCTTTTCCACCCTTTAAATTGAATAACCTCTATTCCTGTTTTAAGGTGTAGATATCATGCCATCCAGGTGGCCCTC... | GATCTGCCCACCATGCCTGGGAGCTCTCGGGTCCTGATCTGCCCGCCACACCTGGGAGCTCTCGGGGCTCTGATGTTACCCACCATACATGTGAGCTCTTGGGGCTCTGTCCTCTTTTTGTCTCAAGTCTCCCCTTTGGTGAACACCAGGCTCCTATGAGGCTGCGTCTTTGAGCTCTGCACAGCTCCATGCTGCTTCCTGCCTCTGAGGCTTTGCTATCATTGAAATTGCCTGGAACACCCTTCCTTTTCCACCCTTTAAATTGAATAACCTCTATTCCTGTTTTAAGGTGTAGATATCATGCCATCCAGGTGGCCCTC... |
Task1_train_34920 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ATGCATCTGTGCCAACACGTGCTAGCATGTGCTGACACGGGGCCAACAGGTGTGTGCTAACGTGATGGGAGCTGACAAAATGCATGAGCTTTACTTGTACATGTGCTCACCGTGCACGCAACACACACATGAACTAAGGTGTACATGGGGGGGGCATGAGGTAAGCCAGCATGCATACACACCAGCTCACACGGGCTCATGTGCACACAAGCTGGACCAAGGTGAGCCAGCGTATGTACATGTCAACACCTGCATGAGCCAGCGTGGACATACGAGACACGGCAGGCCAGCAAGCATGCAGAATGGCCTCTGTGTATGTG... | ATGCATCTGTGCCAACACGTGCTAGCATGTGCTGACACGGGGCCAACAGGTGTGTGCTAACGTGATGGGAGCTGACAAAATGCATGAGCTTTACTTGTACATGTGCTCACCGTGCACGCAACACACACATGAACTAAGGTGTACATGGGGGGGGCATGAGGTAAGCCAGCATGCATACACACCAGCTCACACGGGCTCATGTGCACACAAGCTGGACCAAGGTGAGCCAGCGTATGTACATGTCAACACCTGCATGAGCCAGCGTGGACATACGAGACACGGCAGGCCAGCAAGCATGCAGAATGGCCTCTGTGTATGTG... |
Task1_train_34921 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCTGAGGAGTCTGAGGACTGTCCTCCCACAGACCTGCAGTGAGGGGCCCTCCATGCGCAGATGAGGGGCCACTGACCCACCTGCGCTTCTGCTGGAGGAGGGGAAGCTGGGCCCAAAGGCCCAGGGAGGCAGCGTGGGCTCTGCCAATGTGGGCTGCCCCTCGCACACAGGGCTCACAGGGCAGGCCTTGCTGGGGTCCAGGGCTGTTGGAGGACCCCGAGGGCTGAGGAGCAGCCAGGACCCGCCTGCTCCCATCCTCACCCAGATCAGGAACCAGGGCCTCCCTGTTCACGGTGACACAGGTCAGGGCTCAGAGTGAC... | GCTGAGGAGTCTGAGGACTGTCCTCCCACAGACCTGCAGTGAGGGGCCCTCCATGCGCAGATGAGGGGCCACTGACCCACCTGCGCTTCTGCTGGAGGAGGGGAAGCTGGGCCCAAAGGCCCAGGGAGGCAGCGTGGGCTCTGCCAATGTGGGCTGCCCCTCGCACACAGGGCTCACAGGGCAGGCCTTGCTGGGGTCCAGGGCTGTTGGAGGACCCCGAGGGCTGAGGAGCAGCCAGGACCCGCCTGCTCCCATCCTCACCCAGATCAGGAACCAGGGCCTCCCTGTTCACGGTGACACAGGTCAGGGCTCAGAGTGAC... |
Task1_train_34922 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGAGGGGCCACTGACCCACCTGCGCTTCTGCTGGAGGAGGGGAAGCTGGGCCCAAAGGCCCAGGGAGGCAGCGTGGGCTCTGCCAATGTGGGCTGCCCCTCGCACACAGGGCTCACAGGGCAGGCCTTGCTGGGGTCCAGGGCTGTTGGAGGACCCCGAGGGCTGAGGAGCAGCCAGGACCCGCCTGCTCCCATCCTCACCCAGATCAGGAACCAGGGCCTCCCTGTTCACGGTGACACAGGTCAGGGCTCAGAGTGACCCTCAGCTGTCACCTGCTCACAGGGATGCTGGTGGCTGGTGAGACCCCGCACTGCAGACGG... | TGAGGGGCCACTGACCCACCTGCGCTTCTGCTGGAGGAGGGGAAGCTGGGCCCAAAGGCCCAGGGAGGCAGCGTGGGCTCTGCCAATGTGGGCTGCCCCTCGCACACAGGGCTCACAGGGCAGGCCTTGCTGGGGTCCAGGGCTGTTGGAGGACCCCGAGGGCTGAGGAGCAGCCAGGACCCGCCTGCTCCCATCCTCACCCAGATCAGGAACCAGGGCCTCCCTGTTCACGGTGACACAGGTCAGGGCTCAGAGTGACCCTCAGCTGTCACCTGCTCACAGGGATGCTGGTGGCTGGTGAGACCCCGCACTGCAGACGG... |
Task1_train_34923 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | GCTGGTGGAGCACTCTCTGCACCAGGAGGGCAGCCCCGTCCATGCCTCCCTGCCCTCCTCCCCCATCCATGCCCTCCCTGCCTCCCTGACTCCTCCCCTGTCCCTGCCCTTTGTGCCTCCCTGTCCTCCTCCCCCGTCCCTGTCCTCCCTTCCTATCTCCCTGCTCTCCTTCCCCATTCTTGCCCTCCCTGCCTCCCTGCCCCCCTGCTTCCCTGCCTCCTTGCCCTTGTCTTCCCATCCTTGCCCTCCCTGCCCTCCTCCCCAATCCGTGCCCTCCCTGCCCTCCTCCCCCAGTCCTTGCCCTCCCTGCCCTCCTCCCT... | GCTGGTGGAGCACTCTCTGCACCAGGAGGGCAGCCCCGTCCATGCCTCCCTGCCCTCCTCCCCCATCCATGCCCTCCCTGCCTCCCTGACTCCTCCCCTGTCCCTGCCCTTTGTGCCTCCCTGTCCTCCTCCCCCGTCCCTGTCCTCCCTTCCTATCTCCCTGCTCTCCTTCCCCATTCTTGCCCTCCCTGCCTCCCTGCCCCCCTGCTTCCCTGCCTCCTTGCCCTTGTCTTCCCATCCTTGCCCTCCCTGCCCTCCTCCCCAATCCGTGCCCTCCCTGCCCTCCTCCCCCAGTCCTTGCCCTCCCTGCCCTCCTCCCT... |
Task1_train_34924 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | ACGCTGATTGGTCAATTTTACAGAGTGCTGATTGGTGCATTTACAATCCTTTAGCTAGACACTGAGCATTGATTGGTGCATTTACAATCCTTTAGCTAGACACAAAAGTTCTCCAAGTCCCCACCCAACCCAGAAGCTCAGCTGGCTTCACCTCTCAATAATGCTCACCAACTTGTTAACCATAACAAACCCACTGCATGTTACTAATAAGTAACACTGTCACAAAAAGTTATTTTACAAAACAAAACCAGTTGGGGAGAAGGATGGCACTGTTTTCCACCTTTGCTGGATTCCCCTATCTGCTCTGCACAGCCTTGGTG... | ACGCTGATTGGTCAATTTTACAGAGTGCTGATTGGTGCATTTACAATCCTTTAGCTAGACACTGAGCATTGATTGGTGCATTTACAATCCTTTAGCTAGACACAAAAGTTCTCCAAGTCCCCACCCAACCCAGAAGCTCAGCTGGCTTCACCTCTCAATAATGCTCACCAACTTGTTAACCATAACAAACCCACTGCATGTTACTAATAAGTAACACTGTCACAAAAAGTTATTTTACAAAACAAAACCAGTTGGGGAGAAGGATGGCACTGTTTTCCACCTTTGCTGGATTCCCCTATCTGCTCTGCACAGCCTTGGTG... |
Task1_train_34925 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TGGCACAGGGAAGAGACGTGGGTCTGCTGAGCATAGGATTCAGCCCTGATGGTGGCCCTCCACCCCCACCAGCTGGTGCCAGGACCTACTCGATCATGGACAGCGCCATCCTCCGCATGGTCCCTTTGTCGAAGCTGCTGGTGCACGGTGAGGGCGAGGCCATCTTCAGCAAGCTGTGGGACTGGGCGCTTCTCTCCAGCATGGCCTGCGAGAGCTCGATGGAGAAGTCGCACACACACACGTTGGACTCAAATTTCGTCTCAGCACTGCACAGACTGCCCCGGTCTGTGTTTCCCAACACGTCCTCAAGCCCGCTTTCC... | TGGCACAGGGAAGAGACGTGGGTCTGCTGAGCATAGGATTCAGCCCTGATGGTGGCCCTCCACCCCCACCAGCTGGTGCCAGGACCTACTCGATCATGGACAGCGCCATCCTCCGCATGGTCCCTTTGTCGAAGCTGCTGGTGCACGGTGAGGGCGAGGCCATCTTCAGCAAGCTGTGGGACTGGGCGCTTCTCTCCAGCATGGCCTGCGAGAGCTCGATGGAGAAGTCGCACACACACACGTTGGACTCAAATTTCGTCTCAGCACTGCACAGACTGCCCCGGTCTGTGTTTCCCAACACGTCCTCAAGCCCGCTTTCC... |
Task1_train_34926 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CGTCAACAGTGTGACCTCATTCAGAGTTTCACTCATGTCCCAGGCCCCATGGTAAGCGTGTCACAGTCACTGGCTTTCAGACACATGGTCTTACCAGCTTTGACTTTTTTTTTAAACGAGAGTGCTAAAATCACTGCCATTGTGTTTCTGGCCGTAAAGTGGCAGAGCCAGGACCGCACCAGGTGCCTGGTGCCCAGCCTGCACTCCCCCGATGCTGGGTCAGAATGCTTACCCCTGAAGGAGCCCTGCGGTGGACGCTGTGGGTGCAAGCAGCTGGCCCAGTGTCGGGGCGCCAGGCTCCCAGCAGCAGGAGGGGCTGC... | CGTCAACAGTGTGACCTCATTCAGAGTTTCACTCATGTCCCAGGCCCCATGGTAAGCGTGTCACAGTCACTGGCTTTCAGACACATGGTCTTACCAGCTTTGACTTTTTTTTTAAACGAGAGTGCTAAAATCACTGCCATTGTGTTTCTGGCCGTAAAGTGGCAGAGCCAGGACCGCACCAGGTGCCTGGTGCCCAGCCTGCACTCCCCCGATGCTGGGTCAGAATGCTTACCCCTGAAGGAGCCCTGCGGTGGACGCTGTGGGTGCAAGCAGCTGGCCCAGTGTCGGGGCGCCAGGCTCCCAGCAGCAGGAGGGGCTGC... |
Task1_train_34927 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GTCCTCAGGCCAGCTGCCCATTGGGAATGAAACTCTACCAACAGCCACCTGGGGGAGCTGGAAGTGAATCTCATCTTAGCTGAGCCTTCTGATGAGACTGCAGCCCCAGCTGACACCTGGATTGCAGACTCATGAAAGACCTGAAACTCTACCAACAGCCACCTGGGGGAGCTGGAAGTGAATCTCCTCGTAGCTGAGCCTTCTGATGAGACTGCAGCCCCGGCTGACACCTGGATTGCAGACTCATGAAAGACCTGAAACTCTACCAACAGCCACCTGGGGGAGCTGGAAGTGAATCTCCTCGTAGCTGAGCCTTCTGA... | GTCCTCAGGCCAGCTGCCCATTGGGAATGAAACTCTACCAACAGCCACCTGGGGGAGCTGGAAGTGAATCTCATCTTAGCTGAGCCTTCTGATGAGACTGCAGCCCCAGCTGACACCTGGATTGCAGACTCATGAAAGACCTGAAACTCTACCAACAGCCACCTGGGGGAGCTGGAAGTGAATCTCCTCGTAGCTGAGCCTTCTGATGAGACTGCAGCCCCGGCTGACACCTGGATTGCAGACTCATGAAAGACCTGAAACTCTACCAACAGCCACCTGGGGGAGCTGGAAGTGAATCTCCTCGTAGCTGAGCCTTCTGA... |
Task1_train_34928 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TTTGGGGGACCTTTTGTGCTCCTCTGGGCAGAGGGAGGAGGCAGAGGGAGGAGGAAGGCCCTTCGCTGTGGGCTGAGTCCTTCCCACCTTCCATACCAGCCCAGCAGGAAGCCACTGCAGGATGCCCCAGAGGACAGCCTGATGGTTGGGGGAGAGGCTTCTCCCGCCCTCACCCCTCCGGGTTCTTCCTGGACCCACTGAGTAACCCAGGTGGTGGGACGTGTGGCTGTGAGTCCTGGACTCTGGGCGCTCACCAGCAGCTCCGTCTCACACCTGCCTGCGTGTGACACCAGCACCCCTTATGATGAGGAAACAAGTTT... | TTTGGGGGACCTTTTGTGCTCCTCTGGGCAGAGGGAGGAGGCAGAGGGAGGAGGAAGGCCCTTCGCTGTGGGCTGAGTCCTTCCCACCTTCCATACCAGCCCAGCAGGAAGCCACTGCAGGATGCCCCAGAGGACAGCCTGATGGTTGGGGGAGAGGCTTCTCCCGCCCTCACCCCTCCGGGTTCTTCCTGGACCCACTGAGTAACCCAGGTGGTGGGACGTGTGGCTGTGAGTCCTGGACTCTGGGCGCTCACCAGCAGCTCCGTCTCACACCTGCCTGCGTGTGACACCAGCACCCCTTATGATGAGGAAACAAGTTT... |
Task1_train_34929 | 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 | TCCCGAGCAGGCAAAGGTCACAGAGGCGGCCAGGGCAGGGTTGAAGAAGGCAGACGTGAAGGGCCCGGCTGTGGGCAGAGCACAGACAGCCCTGGTCCCCAGCCCTGCCTGACGCCCCTCTGCAGGCCAGGACCTGATCCCCGCCACCGAATCCACACCGAGAGCCCCACTGTGTGCAGGCCTGGGAGCTGCTCTCGGCTCCTGAAGCCCCGCCTGGTCCCCCGCACCGATGGACACACGATGCAGCAAGGCCGGGTCAGCCAAGGTCTGGGTCAGGGGCAGCAGCTTGGGGGCCCCCCAGGGCCGTCCAACACCCTCGC... | TCCCGAGCAGGCAAAGGTCACAGAGGCGGCCAGGGCAGGGTTGAAGAAGGCAGACGTGAAGGGCCCGGCTGTGGGCAGAGCACAGACAGCCCTGGTCCCCAGCCCTGCCTGACGCCCCTCTGCAGGCCAGGACCTGATCCCCGCCACCGAATCCACACCGAGAGCCCCACTGTGTGCAGGCCTGGGAGCTGCTCTCGGCTCCTGAAGCCCCGCCTGGTCCCCCGCACCGATGGACACACGATGCAGCAAGGCCGGGTCAGCCAAGGTCTGGGTCAGGGGCAGCAGCTTGGGGGCCCCCCAGGGCCGTCCAACACCCTCGC... |
Task1_train_34930 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ACTGTGTGCAGGCCTGGGAGCTGCTCTCGGCTCCTGAAGCCCCGCCTGGTCCCCCGCACCGATGGACACACGATGCAGCAAGGCCGGGTCAGCCAAGGTCTGGGTCAGGGGCAGCAGCTTGGGGGCCCCCCAGGGCCGTCCAACACCCTCGCGACATCTCACCGGGATCCCGTGCCCCGCCCATGCTGCCCTCCAGCACCCCACCCTGTGGGATGTGGCCTTCGAGAAAGACGGACAGAGAGAGATGGAGAGAGACACTAAGAGAGACAGATAGTGAGAGAGAGACAAAAAGACACAGAGAGAGACAGGGAGACAGAGAG... | ACTGTGTGCAGGCCTGGGAGCTGCTCTCGGCTCCTGAAGCCCCGCCTGGTCCCCCGCACCGATGGACACACGATGCAGCAAGGCCGGGTCAGCCAAGGTCTGGGTCAGGGGCAGCAGCTTGGGGGCCCCCCAGGGCCGTCCAACACCCTCGCGACATCTCACCGGGATCCCGTGCCCCGCCCATGCTGCCCTCCAGCACCCCACCCTGTGGGATGTGGCCTTCGAGAAAGACGGACAGAGAGAGATGGAGAGAGACACTAAGAGAGACAGATAGTGAGAGAGAGACAAAAAGACACAGAGAGAGACAGGGAGACAGAGAG... |
Task1_train_34931 | This genomic variant is located on Chromosome 2. Can you determine its pathogenicity and name any linked disease? | Benign | ACATCTCACCGGGATCCCGTGCCCCGCCCATGCTGCCCTCCAGCACCCCACCCTGTGGGATGTGGCCTTCGAGAAAGACGGACAGAGAGAGATGGAGAGAGACACTAAGAGAGACAGATAGTGAGAGAGAGACAAAAAGACACAGAGAGAGACAGGGAGACAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGATCTCAGAAATAAAGGAGCAGCAGCAGAGGAGAGAAGACGACATGGCTGTGCGATGTGAGACAAGGGAAGGCGGCGG... | ACATCTCACCGGGATCCCGTGCCCCGCCCATGCTGCCCTCCAGCACCCCACCCTGTGGGATGTGGCCTTCGAGAAAGACGGACAGAGAGAGATGGAGAGAGACACTAAGAGAGACAGATAGTGAGAGAGAGACAAAAAGACACAGAGAGAGACAGGGAGACAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGATCTCAGAAATAAAGGAGCAGCAGCAGAGGAGAGAAGACGACATGGCTGTGCGATGTGAGACAAGGGAAGGCGGCGG... |
Task1_train_34932 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCCGCCCATGCTGCCCTCCAGCACCCCACCCTGTGGGATGTGGCCTTCGAGAAAGACGGACAGAGAGAGATGGAGAGAGACACTAAGAGAGACAGATAGTGAGAGAGAGACAAAAAGACACAGAGAGAGACAGGGAGACAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGATCTCAGAAATAAAGGAGCAGCAGCAGAGGAGAGAAGACGACATGGCTGTGCGATGTGAGACAAGGGAAGGCGGCGGCAGCCGGGCCGCTGTCCTGCAG... | CCCGCCCATGCTGCCCTCCAGCACCCCACCCTGTGGGATGTGGCCTTCGAGAAAGACGGACAGAGAGAGATGGAGAGAGACACTAAGAGAGACAGATAGTGAGAGAGAGACAAAAAGACACAGAGAGAGACAGGGAGACAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGAGAGGAGAGACAGAGAGAGATCTCAGAAATAAAGGAGCAGCAGCAGAGGAGAGAAGACGACATGGCTGTGCGATGTGAGACAAGGGAAGGCGGCGGCAGCCGGGCCGCTGTCCTGCAG... |
Task1_train_34933 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | AGGAGTCAAGGTCTCCAGTGGTGTCGGATTAGAATATGAGGAATCCGTCTGAGCTCATTCTCCACAGGATCCCACGAGGGAAAGCCTGGCTTTTCCCTGTGCAGATGCCAGGCCTCTACAGGTTCCAGAAGGTTCCTCTGCTCCTCTGAGAGGGCAGGGCACTTGCACAGGGAACAGGCAGCCGAAGGCAGCCACAGCCCTACTGGAACCAGGGTTTCTCTGCCTCCTGGGAAGAGGTCAGTGGATGGGTTGGGGAGGGGGACAGGCGGCCTTCCTGTGGGAGTCGAAGAGCCTGGGGCCTCCCCTCCTTGGAGGCGACC... | AGGAGTCAAGGTCTCCAGTGGTGTCGGATTAGAATATGAGGAATCCGTCTGAGCTCATTCTCCACAGGATCCCACGAGGGAAAGCCTGGCTTTTCCCTGTGCAGATGCCAGGCCTCTACAGGTTCCAGAAGGTTCCTCTGCTCCTCTGAGAGGGCAGGGCACTTGCACAGGGAACAGGCAGCCGAAGGCAGCCACAGCCCTACTGGAACCAGGGTTTCTCTGCCTCCTGGGAAGAGGTCAGTGGATGGGTTGGGGAGGGGGACAGGCGGCCTTCCTGTGGGAGTCGAAGAGCCTGGGGCCTCCCCTCCTTGGAGGCGACC... |
Task1_train_34934 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTGGGGTGCTGGTGCCCGGGACCACACTCCCTCCTTCAGGAGGGTTTCTGGGCTATGAGAGACTCGGCCACACCTGCTGGGCCTCAGTCTGGCTGTCTTCAGCTCTCCCCCGACCATGTCCCTGGGTTTTGGTCTTGCAGGAAATAAACTCCACTCTTTTAACTAAAAGCCAGTGGATCTCAAGTGCTATTCCATGACCCACCTGTTCCCACAGGCAGAGGCTCCAGGCTCCAGGCAAAAGCTCTGACAAATACTTCTCCCCGACTGACCCCACACTCTCGCTCCCACCTCCAGCCTCAGACCCCCGTGAAGGAGCGTCC... | CTGGGGTGCTGGTGCCCGGGACCACACTCCCTCCTTCAGGAGGGTTTCTGGGCTATGAGAGACTCGGCCACACCTGCTGGGCCTCAGTCTGGCTGTCTTCAGCTCTCCCCCGACCATGTCCCTGGGTTTTGGTCTTGCAGGAAATAAACTCCACTCTTTTAACTAAAAGCCAGTGGATCTCAAGTGCTATTCCATGACCCACCTGTTCCCACAGGCAGAGGCTCCAGGCTCCAGGCAAAAGCTCTGACAAATACTTCTCCCCGACTGACCCCACACTCTCGCTCCCACCTCCAGCCTCAGACCCCCGTGAAGGAGCGTCC... |
Task1_train_34935 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | TTGTCGAGGGCGCGGCCTGCAGAGAAGGAACCATCCCTGGTGCACAGAGAAAAGGGAGCCTGCCAGAGAGAGGCCCTCAGTGGGGGTGGGGGAGAGAGGACAGGGCCCCGGGTACACTGGCTGCGGGCAGGGCCAGGGGGATACAGCCCCAGGGACAGATGCAGCAATGGGGCAGGTGTGGATGCTCCCAACCCTTCCATTGCTGTGTGAAGCAGTAAGTGAGGCCCAGTGAGTGGGTGGGCTGGGAGAAGGGGAGGCCGAAGGGGCCAGAGATGTGCCCACAGATAGGTGGGCGTGGATGTAAAGTGAGGGTTGGCAGT... | TTGTCGAGGGCGCGGCCTGCAGAGAAGGAACCATCCCTGGTGCACAGAGAAAAGGGAGCCTGCCAGAGAGAGGCCCTCAGTGGGGGTGGGGGAGAGAGGACAGGGCCCCGGGTACACTGGCTGCGGGCAGGGCCAGGGGGATACAGCCCCAGGGACAGATGCAGCAATGGGGCAGGTGTGGATGCTCCCAACCCTTCCATTGCTGTGTGAAGCAGTAAGTGAGGCCCAGTGAGTGGGTGGGCTGGGAGAAGGGGAGGCCGAAGGGGCCAGAGATGTGCCCACAGATAGGTGGGCGTGGATGTAAAGTGAGGGTTGGCAGT... |
Task1_train_34936 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | AGCCGCCTCTAGTGGCCACACACCTCATCTGCCGTGGGCCACGCACGCTCACTGCCCGTGACCTGGCAGCTTGGAAGGCAGCTGCAACTGCACCAGCCCGGCCACAGGCCACAGCCCCGGGCTGGTCTCACCGGTTCCCAGGGTGGGGGCAGCCTGACCCCTGTCACCTAGGCTGCCACTTCCCCTTTAAGGTGAGTGTCAGGAAACGATGCCTGGAATCTCCCTGCATGCCCAGCCCAGCGCAGCTTCAGGGGCTGTGGGCGCGGCCTGCAGTATCGAGTCTGCTTTCTCAGGAGGCACTCTGGGGGCGTGAGGAGCCT... | AGCCGCCTCTAGTGGCCACACACCTCATCTGCCGTGGGCCACGCACGCTCACTGCCCGTGACCTGGCAGCTTGGAAGGCAGCTGCAACTGCACCAGCCCGGCCACAGGCCACAGCCCCGGGCTGGTCTCACCGGTTCCCAGGGTGGGGGCAGCCTGACCCCTGTCACCTAGGCTGCCACTTCCCCTTTAAGGTGAGTGTCAGGAAACGATGCCTGGAATCTCCCTGCATGCCCAGCCCAGCGCAGCTTCAGGGGCTGTGGGCGCGGCCTGCAGTATCGAGTCTGCTTTCTCAGGAGGCACTCTGGGGGCGTGAGGAGCCT... |
Task1_train_34937 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GGCGCCCAGGGCCAGCAAGCTTGCACAGGGAGGGCCCGGGGGGTCGGGGCCCATCCAGCGTGCCGAGCAGCTGTGGATCCCAGATGTGGTCACACCGTTCCAGGGCAGGTGGGGCCCTGATGTCACTGGTGGTGCACACTCTTCAGAGTCACCATCCCAGTGGCTGCAGGGCACTCCCCTAATGCCCAGGAGGCAGACACTGGGGTCTCCTACAGTGAGGGTTTCAGGGAGCACGGCAGGGAACTCACTGGGACTGCGTCCTGGGGGTCAGCACCCAGAACTGGAGTTTTCAGGCTTAAAGCAGGAACATTCTTCTAGGG... | GGCGCCCAGGGCCAGCAAGCTTGCACAGGGAGGGCCCGGGGGGTCGGGGCCCATCCAGCGTGCCGAGCAGCTGTGGATCCCAGATGTGGTCACACCGTTCCAGGGCAGGTGGGGCCCTGATGTCACTGGTGGTGCACACTCTTCAGAGTCACCATCCCAGTGGCTGCAGGGCACTCCCCTAATGCCCAGGAGGCAGACACTGGGGTCTCCTACAGTGAGGGTTTCAGGGAGCACGGCAGGGAACTCACTGGGACTGCGTCCTGGGGGTCAGCACCCAGAACTGGAGTTTTCAGGCTTAAAGCAGGAACATTCTTCTAGGG... |
Task1_train_34938 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | TACCTGACTGGCGTTGAATGTATGGTTCAGTGTGCAGTGAACAGAACACAGGCCATGGTGCCAGGCGCGGGAGGCAGCCCCCTTCTCTGCCCATTCTGAACGGGAGCCCTTCTCACTGACTGCACAGAGGCACGCGCAGGCCGCCTGCTGGGGGGCCGGGGCGTCCAGGCAGCGGGGCCTTGGGGGACGCTCGGTGACTCGGAGCCGGGATGGAGGGCTTGTGCCCCATCCCCAGGGCACTGCGCAGCGGGAGAGGGCGCTGCAATGAGGAGGCGGCTGCTGGAGTGTCGCTTCACCTCCTCCTGCCTGATGCCACAACC... | TACCTGACTGGCGTTGAATGTATGGTTCAGTGTGCAGTGAACAGAACACAGGCCATGGTGCCAGGCGCGGGAGGCAGCCCCCTTCTCTGCCCATTCTGAACGGGAGCCCTTCTCACTGACTGCACAGAGGCACGCGCAGGCCGCCTGCTGGGGGGCCGGGGCGTCCAGGCAGCGGGGCCTTGGGGGACGCTCGGTGACTCGGAGCCGGGATGGAGGGCTTGTGCCCCATCCCCAGGGCACTGCGCAGCGGGAGAGGGCGCTGCAATGAGGAGGCGGCTGCTGGAGTGTCGCTTCACCTCCTCCTGCCTGATGCCACAACC... |
Task1_train_34939 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | TGACAGGGAACCCTGCAGAGGCTGAGTTTGAGGACACTGTGCAGAGTCAAGACTGGGGCCAGTGCCTCACTAGGGGAGGCAGAGACCTGCTGGGCAGCTGTGCTGGCCCCACCAGGAGGTGCGGGGGCCCCAGCCTGTGGCACCCTCGTCAGTTTTAAGCGGTCCAAGGAGGAGAAGGAGCAGAAGCTGCTCATCCTGGAGGAGGCCCAGGCGGCGTTGCAGCAGGAGGCCAGTGCACTGCGGGCCCACCTGTGGGAGCTGGAGCAGGCAGGGGGGGACGCCCGTCAGGAGCTCCGGGAACTCCACAGACAGGTAGGGCG... | TGACAGGGAACCCTGCAGAGGCTGAGTTTGAGGACACTGTGCAGAGTCAAGACTGGGGCCAGTGCCTCACTAGGGGAGGCAGAGACCTGCTGGGCAGCTGTGCTGGCCCCACCAGGAGGTGCGGGGGCCCCAGCCTGTGGCACCCTCGTCAGTTTTAAGCGGTCCAAGGAGGAGAAGGAGCAGAAGCTGCTCATCCTGGAGGAGGCCCAGGCGGCGTTGCAGCAGGAGGCCAGTGCACTGCGGGCCCACCTGTGGGAGCTGGAGCAGGCAGGGGGGGACGCCCGTCAGGAGCTCCGGGAACTCCACAGACAGGTAGGGCG... |
Task1_train_34940 | 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 | GGCTCTGGGGTAGGAGCCTCAGGATCCCAGACTCATCCCTGCTCAGTCTCTGGGGTAGGAGCCTCAGGAGCCCAGGCTCATCCCTGCTCAGTCTCTGGGTCAGGAGCCTCAGGATCCCAGGCTCATCCCTGCTCAGTCTCTGGGGTAGGAGCCTCAGGATCCCAGGCTCATCCCTGCTCAGTCTCTGGGGTAGGAGCCTCTGGAGCCCAGGCTCATCCCTGCTCAGTCTCTGGGGTAGGAGCCTCAGGAGCCCAGGCTCATCCCTGCTCAGTCTCTGGGGTAGGAGCCTCTGGAGCCCAGGCTCATCCCTGCTCAGGCTC... | GGCTCTGGGGTAGGAGCCTCAGGATCCCAGACTCATCCCTGCTCAGTCTCTGGGGTAGGAGCCTCAGGAGCCCAGGCTCATCCCTGCTCAGTCTCTGGGTCAGGAGCCTCAGGATCCCAGGCTCATCCCTGCTCAGTCTCTGGGGTAGGAGCCTCAGGATCCCAGGCTCATCCCTGCTCAGTCTCTGGGGTAGGAGCCTCTGGAGCCCAGGCTCATCCCTGCTCAGTCTCTGGGGTAGGAGCCTCAGGAGCCCAGGCTCATCCCTGCTCAGTCTCTGGGGTAGGAGCCTCTGGAGCCCAGGCTCATCCCTGCTCAGGCTC... |
Task1_train_34941 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | GTTGCCAGCTCAGCAGTAGCCTGACTCAGGCAGGCCATGAGGCACCTTGCCAGGTGCTGGATTTAAGGGGCAAAGAACATTCGTTGTTCACTCAGCCCCCTGCACGTCCCGGGGTCTAAGGTGGTCCCTGGTCAGGAGCCGGGACTGGCGTTCTCTCTCTTCAGCCAGGAAGCCAGAATGCACATCCCAGGAACTTTCACTCACCTTTCCCCAGTTTGTCCCCAACTCACACCCAGACCTGTCACAGGGCGGTGCAGGCACAAGGCCAGCAGGAGCACCCGTGTGAGAGCCACAGAGACGCCCTGCTCCCAGGCTGGCAC... | GTTGCCAGCTCAGCAGTAGCCTGACTCAGGCAGGCCATGAGGCACCTTGCCAGGTGCTGGATTTAAGGGGCAAAGAACATTCGTTGTTCACTCAGCCCCCTGCACGTCCCGGGGTCTAAGGTGGTCCCTGGTCAGGAGCCGGGACTGGCGTTCTCTCTCTTCAGCCAGGAAGCCAGAATGCACATCCCAGGAACTTTCACTCACCTTTCCCCAGTTTGTCCCCAACTCACACCCAGACCTGTCACAGGGCGGTGCAGGCACAAGGCCAGCAGGAGCACCCGTGTGAGAGCCACAGAGACGCCCTGCTCCCAGGCTGGCAC... |
Task1_train_34942 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | TCATATAATGCTGAGAGAAGACAATATATATCATGATGTACTATGAATAAAGTTCATAAACAACAAAAACATTCACTATTGTTTAGGCAATTTATAAAATTTTTAAGCTAATTTTAATTACATATTTTACTGCCAGAAAACCTAGTTTTTAAAGACAAGGAAATTATAAACCCAGAGATTCTTATCGCAAGGGAAGAGAAGGGTACACGGTCGGATGAGCCCATTCAGCATTCTGGCTGCCGGGGTGGCTGCTAGTCCCAGATGTCACTAAGTCATTACCATTTATTTACTTTTTAAGCATGAAATTAAACTTTAAAAAA... | TCATATAATGCTGAGAGAAGACAATATATATCATGATGTACTATGAATAAAGTTCATAAACAACAAAAACATTCACTATTGTTTAGGCAATTTATAAAATTTTTAAGCTAATTTTAATTACATATTTTACTGCCAGAAAACCTAGTTTTTAAAGACAAGGAAATTATAAACCCAGAGATTCTTATCGCAAGGGAAGAGAAGGGTACACGGTCGGATGAGCCCATTCAGCATTCTGGCTGCCGGGGTGGCTGCTAGTCCCAGATGTCACTAAGTCATTACCATTTATTTACTTTTTAAGCATGAAATTAAACTTTAAAAAA... |
Task1_train_34943 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | ATCTCAAAATAAATAAATAAAATCTTGTTTGTCTTTTGATTCTGTTAATTTGAAATGGAAATATTAGTATGAACTCATAATGTGTTTATTTTTTAAAGAAGCCTAATTTTCTAGTTCTGTTCATTGAAAGGCCTGAAGCTGTGACATCCCATAATAGGGAGCGGTGTGAGTGCCAGGCTGTGGGCTCTAGATCTCGTTCTCACCAAGAAGCCAGTGATCTTTGGAGAAATGGGTGATTCCAAGACTGAAGCAGGATGTGGACAAAATAAGCCCAGGACATGTTGTGTAAAAAGCAAGCAAGCTTTCAAAACAGCAGACCA... | ATCTCAAAATAAATAAATAAAATCTTGTTTGTCTTTTGATTCTGTTAATTTGAAATGGAAATATTAGTATGAACTCATAATGTGTTTATTTTTTAAAGAAGCCTAATTTTCTAGTTCTGTTCATTGAAAGGCCTGAAGCTGTGACATCCCATAATAGGGAGCGGTGTGAGTGCCAGGCTGTGGGCTCTAGATCTCGTTCTCACCAAGAAGCCAGTGATCTTTGGAGAAATGGGTGATTCCAAGACTGAAGCAGGATGTGGACAAAATAAGCCCAGGACATGTTGTGTAAAAAGCAAGCAAGCTTTCAAAACAGCAGACCA... |
Task1_train_34944 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AGACCAATGAGTAGCCACACGTACTTGTTTGGCATTACCAAGTGTCCGGGCAAGGCCGCAGCCTGCAGCTCACCAGCCGTGCTGCTCGGCCTGTGCACGTCACCGGCTCTTCCCTAGGGTAGCTTTTGCTTGCTTTCTCCCACGTCCATCCTCTCTCTCTCTGACTCACAGCCAGCCAGGTTTCTAGCCTTGTCATTCCTAAACTACTGCCTCAAGCCAGGCGGGCGCACACAAACTAAAATGCTAATCTCCACAGCGGTGTCTGGACTAATGGTGTCCCCCACCGTGGAATGTATGTGAGCTAAAGACAGGATCTCAGC... | AGACCAATGAGTAGCCACACGTACTTGTTTGGCATTACCAAGTGTCCGGGCAAGGCCGCAGCCTGCAGCTCACCAGCCGTGCTGCTCGGCCTGTGCACGTCACCGGCTCTTCCCTAGGGTAGCTTTTGCTTGCTTTCTCCCACGTCCATCCTCTCTCTCTCTGACTCACAGCCAGCCAGGTTTCTAGCCTTGTCATTCCTAAACTACTGCCTCAAGCCAGGCGGGCGCACACAAACTAAAATGCTAATCTCCACAGCGGTGTCTGGACTAATGGTGTCCCCCACCGTGGAATGTATGTGAGCTAAAGACAGGATCTCAGC... |
Task1_train_34945 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | CAGACGGTAAACGTTTTCAGCTTTGCAGACCAGAGGTCCCTGTGGCTACAGTAGCGCAGACACAGCCACAGGCATGTCATTGAATGGCTGCGGCTATGTTCCAATAAAAACTTATTTACAATAACAGGTGGTGGCCAAATTGGCCCATGGGCCTTATTTGGTGAACCCTGTTCTATGAGATCACCTAGGCTTCAGCCTTAAACAGTGGAAGCCATCCCCTGAATGACAAGTCACAAGGGTATCAAAGAAAGACCCCTGAATTTTCATGGAAAAAGCTATTCAGACCCCTGCTTGGAAAGCTAAGGCACACTGCCACGAAG... | CAGACGGTAAACGTTTTCAGCTTTGCAGACCAGAGGTCCCTGTGGCTACAGTAGCGCAGACACAGCCACAGGCATGTCATTGAATGGCTGCGGCTATGTTCCAATAAAAACTTATTTACAATAACAGGTGGTGGCCAAATTGGCCCATGGGCCTTATTTGGTGAACCCTGTTCTATGAGATCACCTAGGCTTCAGCCTTAAACAGTGGAAGCCATCCCCTGAATGACAAGTCACAAGGGTATCAAAGAAAGACCCCTGAATTTTCATGGAAAAAGCTATTCAGACCCCTGCTTGGAAAGCTAAGGCACACTGCCACGAAG... |
Task1_train_34946 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AATGAAAACACTGGCACAGTGAAATGTCTCATTTCCAAACAGTTTTGCCTATGGCCAAGCAAGGCAATAAAGACAAACTCTCCCTTTTCCCCATTGCGTGTGGGCTGCCAGGTACAAGTAAGGGAATCTTTGCTGTGCCCACTGTCCTCCAGTAGAGAACCCAACAGGCAAGGGCCCCACTCAGGTATCAGCTCACCTCCTGCACCTCCCCTTAGCAGGAACTCCTTCCACTGGCAAAGGACTGCCACTGCCATCTGACTCAACTGTGGCGATGTGGACGGAGTCACCGAGCTGCTTTTCTTTTGCAAAACAAAAGTCTT... | AATGAAAACACTGGCACAGTGAAATGTCTCATTTCCAAACAGTTTTGCCTATGGCCAAGCAAGGCAATAAAGACAAACTCTCCCTTTTCCCCATTGCGTGTGGGCTGCCAGGTACAAGTAAGGGAATCTTTGCTGTGCCCACTGTCCTCCAGTAGAGAACCCAACAGGCAAGGGCCCCACTCAGGTATCAGCTCACCTCCTGCACCTCCCCTTAGCAGGAACTCCTTCCACTGGCAAAGGACTGCCACTGCCATCTGACTCAACTGTGGCGATGTGGACGGAGTCACCGAGCTGCTTTTCTTTTGCAAAACAAAAGTCTT... |
Task1_train_34947 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | TTCCCCAAACAGGAAGGGCCTGTTCTTCACAAAGATAAAGAAAACTGCCAGCATTTTGCTGGCCTTAAGAAGCCATGCAAAATTAACCAGTACATCATGAATTAACTTCTTTTACTCTGCTGTGCACTGAATACCATTATGAAGCAATATACTTTTGGATTAAAAATAAGCATTTTTGTGGAAAATCTGCTACATGTTTTCATAAAATAAAGTGCTATGATGTACTAAAACCTCACATTGCCTTCTCGTAATTTTATTTTTATCACAAGAAGGAAATACATAGTGATTCCTGAACCGGAAGAATGAACCCCATCTTCCAA... | TTCCCCAAACAGGAAGGGCCTGTTCTTCACAAAGATAAAGAAAACTGCCAGCATTTTGCTGGCCTTAAGAAGCCATGCAAAATTAACCAGTACATCATGAATTAACTTCTTTTACTCTGCTGTGCACTGAATACCATTATGAAGCAATATACTTTTGGATTAAAAATAAGCATTTTTGTGGAAAATCTGCTACATGTTTTCATAAAATAAAGTGCTATGATGTACTAAAACCTCACATTGCCTTCTCGTAATTTTATTTTTATCACAAGAAGGAAATACATAGTGATTCCTGAACCGGAAGAATGAACCCCATCTTCCAA... |
Task1_train_34948 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGAATTTCCCAGGCATTTACTGGAAAGATCAGAGAGTAATATGGGAGAGTAGTTTCCTCCATATTGCTGGTTTGGGTTGATGTTTCCTTCTATAATAAAATAGTCATTGAAGCATTCACAACTAACATTCTCAAGCTGAACTCAATGAAAAGGAGTTCCATCACCATCGTCATCATAACAGTAATAACAATAATAGTAATCATGAGGACACACAACACCAATGCTGACGTCCTGGTTACCAGGGTCACCATATATCTTCTCCAAGCCAGGGCACCTTGAGTGAAAGAGGCCCTATTAAAACCGCACTAACTGGTGTAAAC... | AGAATTTCCCAGGCATTTACTGGAAAGATCAGAGAGTAATATGGGAGAGTAGTTTCCTCCATATTGCTGGTTTGGGTTGATGTTTCCTTCTATAATAAAATAGTCATTGAAGCATTCACAACTAACATTCTCAAGCTGAACTCAATGAAAAGGAGTTCCATCACCATCGTCATCATAACAGTAATAACAATAATAGTAATCATGAGGACACACAACACCAATGCTGACGTCCTGGTTACCAGGGTCACCATATATCTTCTCCAAGCCAGGGCACCTTGAGTGAAAGAGGCCCTATTAAAACCGCACTAACTGGTGTAAAC... |
Task1_train_34949 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TGATATTCTAGAAAACAAAGCAGGGACATTTCAGAACCTGGAGGATCCACGCTGACCCACTGGACCGTCCCCCTGGGGGAGGAATGAACACAAGGAGAGCCAGTCCCTGAGGGTTCACCCTTAAGGTCAGGAAAGGCCTCGGGCCAAATGCCCTTCGACGCACCTGAAGCCCCTCAGATGCTCAACATGTGATCTGTGATTTTCCCCTTAAGAAAAAGGTAAAAACATACTCTGCGGCAAGTTACAGTGACATCGACACATCTTTGGAGCAGACATCTGGCCTTTGGCCCCATGTTTAGATGGATCTGGGAGCCTGTGTT... | TGATATTCTAGAAAACAAAGCAGGGACATTTCAGAACCTGGAGGATCCACGCTGACCCACTGGACCGTCCCCCTGGGGGAGGAATGAACACAAGGAGAGCCAGTCCCTGAGGGTTCACCCTTAAGGTCAGGAAAGGCCTCGGGCCAAATGCCCTTCGACGCACCTGAAGCCCCTCAGATGCTCAACATGTGATCTGTGATTTTCCCCTTAAGAAAAAGGTAAAAACATACTCTGCGGCAAGTTACAGTGACATCGACACATCTTTGGAGCAGACATCTGGCCTTTGGCCCCATGTTTAGATGGATCTGGGAGCCTGTGTT... |
Task1_train_34950 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | GGGAGGGAGGGAGGACTGTGGGGCTCAGGCTCGGGGCTCAGCCACGCCACTGGCAACTGTGCCATCCTTGATCTGGCACCAGGATACTGGCCCCACAGGCAGCACTACACCAGCTGCGCAGCTGTGGATGTTACCTCCCACCCCTCAGCCTTGGGCAGCGTCCCAGCATCCACCTCTGTGGGTGGCCCAGCTCCTGGGAGAAGACTCAGGGGACAAGAGTGGTCAGCTGGGAGACCACATAGGCTCCGGCCCTTGGTCAAGGCCTCAGCGCACAGGAAGCTCAAAACTGAGCATGTCCCACCCCTAAGGCCACCCTTGCC... | GGGAGGGAGGGAGGACTGTGGGGCTCAGGCTCGGGGCTCAGCCACGCCACTGGCAACTGTGCCATCCTTGATCTGGCACCAGGATACTGGCCCCACAGGCAGCACTACACCAGCTGCGCAGCTGTGGATGTTACCTCCCACCCCTCAGCCTTGGGCAGCGTCCCAGCATCCACCTCTGTGGGTGGCCCAGCTCCTGGGAGAAGACTCAGGGGACAAGAGTGGTCAGCTGGGAGACCACATAGGCTCCGGCCCTTGGTCAAGGCCTCAGCGCACAGGAAGCTCAAAACTGAGCATGTCCCACCCCTAAGGCCACCCTTGCC... |
Task1_train_34951 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGAGTCCACCTTCTGAAACAGGCAAAGCACACAGCCCTTGCCCTCAACTCCTGCAAAAAGATCTAAGGATTAAGTCAGTCTGCACAGCTAACACACACTCTCACTGCGTGTCTGAACATGGTCCCCAGAATCCACTTAGGCAACCACCAGGTCCACTCGGAAGCACAAACAGCATAAGATCAACACTTCTGTGTCTAAATTACACTCAAAGCCAGGCGTGCCTATAATCCCAGTTCTTTGGAAGGCTGAGGCAGGAAGGTTGCTTGAGTTCAGGAGTTCAAGACCAGCCTGGACAACACAGCGAGACCCTGTCCCTACTA... | AGAGTCCACCTTCTGAAACAGGCAAAGCACACAGCCCTTGCCCTCAACTCCTGCAAAAAGATCTAAGGATTAAGTCAGTCTGCACAGCTAACACACACTCTCACTGCGTGTCTGAACATGGTCCCCAGAATCCACTTAGGCAACCACCAGGTCCACTCGGAAGCACAAACAGCATAAGATCAACACTTCTGTGTCTAAATTACACTCAAAGCCAGGCGTGCCTATAATCCCAGTTCTTTGGAAGGCTGAGGCAGGAAGGTTGCTTGAGTTCAGGAGTTCAAGACCAGCCTGGACAACACAGCGAGACCCTGTCCCTACTA... |
Task1_train_34952 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AAATATGAAACAACTCTATTCAGGCAGTGGACAGCAGGCAGCACGCACCTGCAGGCTCTGAGGAGGGAGTTCCAGCGCGAGCCCCGTGATCACCCCACTCCTTACCTGGGATGTTTCCCAAGCAGAACACAGTACTTCTGAGTGGAAGAGGCAGAGATCAACATCTCTGGCAGCTAGAGTGTGCCAGACAGGGCCCCAGAGAGAAGGGGAGCTGTGCAGAGCAGAGGTCCAGAAGTCCATGCAGGGACCCCCCAGTCGGACCACAGCTGTGGGCAGGGCAGTGGGCAGTGTGGGCCCCAGAGTAGAACGCCCCTGCTTGC... | AAATATGAAACAACTCTATTCAGGCAGTGGACAGCAGGCAGCACGCACCTGCAGGCTCTGAGGAGGGAGTTCCAGCGCGAGCCCCGTGATCACCCCACTCCTTACCTGGGATGTTTCCCAAGCAGAACACAGTACTTCTGAGTGGAAGAGGCAGAGATCAACATCTCTGGCAGCTAGAGTGTGCCAGACAGGGCCCCAGAGAGAAGGGGAGCTGTGCAGAGCAGAGGTCCAGAAGTCCATGCAGGGACCCCCCAGTCGGACCACAGCTGTGGGCAGGGCAGTGGGCAGTGTGGGCCCCAGAGTAGAACGCCCCTGCTTGC... |
Task1_train_34953 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGCGGAAAGGATGGGAGGAAGGCTAGGACCCCTCCTGTCCTTTTGCAGATGGGGCCCTGAGCATGGGATGTGCCTGAGGTCACCCCTCAGGCATTAGCAGAGCCAGCAGTGTGATCTGGGTCTCCCAATCTCCCCAGCCCCCGGGTGAAACCCTGGCCCACCACTCAGCACATGCTACGTAACCTCAAGGAGCCTCAGTTTCCCCCCACATAAACAGAGCTTACGAGGTCTGCCTGGCAAGGCTTCCAGCAGAGGTGGCACTTGTGGCTGTTCCTGTGGAATCCCACCTCCTCGAGACCCTCCAAGGCAGCAACTATGAC... | GGCGGAAAGGATGGGAGGAAGGCTAGGACCCCTCCTGTCCTTTTGCAGATGGGGCCCTGAGCATGGGATGTGCCTGAGGTCACCCCTCAGGCATTAGCAGAGCCAGCAGTGTGATCTGGGTCTCCCAATCTCCCCAGCCCCCGGGTGAAACCCTGGCCCACCACTCAGCACATGCTACGTAACCTCAAGGAGCCTCAGTTTCCCCCCACATAAACAGAGCTTACGAGGTCTGCCTGGCAAGGCTTCCAGCAGAGGTGGCACTTGTGGCTGTTCCTGTGGAATCCCACCTCCTCGAGACCCTCCAAGGCAGCAACTATGAC... |
Task1_train_34954 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCCACCCCTCCGCTCCATGCCTTGCAGGCAGGAACTGTGTGGCAGCAAGGACAGCTTCGAGATGTGCCCACTTTGCCTCGACTGCCCTTTCTGGCTGCTCTCCAGCGCCTGTGCCCTGGCCCAGGTACGAGAAGAGGTGGGTGGGGTAAGGGATTTGAGAGTCGGGGATGAGGAGGGCAGCTCCCCTTGTCCTGGTCCTGACTCTGCCTGCACCAGCCCCTGTCCTGCTTGTCACCAGCTAAAGGCAGAACGCTCCATGAGCTCCTTAACCTTTGTTCTCTTGCCTGGAACTGGGGTTACACCCGGCACACACCTCCCAG... | CCCACCCCTCCGCTCCATGCCTTGCAGGCAGGAACTGTGTGGCAGCAAGGACAGCTTCGAGATGTGCCCACTTTGCCTCGACTGCCCTTTCTGGCTGCTCTCCAGCGCCTGTGCCCTGGCCCAGGTACGAGAAGAGGTGGGTGGGGTAAGGGATTTGAGAGTCGGGGATGAGGAGGGCAGCTCCCCTTGTCCTGGTCCTGACTCTGCCTGCACCAGCCCCTGTCCTGCTTGTCACCAGCTAAAGGCAGAACGCTCCATGAGCTCCTTAACCTTTGTTCTCTTGCCTGGAACTGGGGTTACACCCGGCACACACCTCCCAG... |
Task1_train_34955 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | CAGAGCTCTTGGCACTGCTTTGCAATTCCGGGAGGAGCCCATTACCCCTAAAGCCTTAAGGAACAATGCGGGGGGCTGGGCGGGTGGACTGCCCTCCCACATCTGACCAACAGACACAGACGCTTTCACTGAGTCCGATCTGCAAAGCTGTTGGCTCTCACTGCGTCCACCCCTCAGCCCCAGACCCCATCCCTCCCTGCTGCCCTTCAATTGCAAAGCAACAGGCTTGTCCCGGCCACATCTCCCCCAAGGACTATAGCAGCCACTGAGACCCATGTTGGATCAAAGGCCATTTTCCTGTATTCCCGTCCCCAGGAAGC... | CAGAGCTCTTGGCACTGCTTTGCAATTCCGGGAGGAGCCCATTACCCCTAAAGCCTTAAGGAACAATGCGGGGGGCTGGGCGGGTGGACTGCCCTCCCACATCTGACCAACAGACACAGACGCTTTCACTGAGTCCGATCTGCAAAGCTGTTGGCTCTCACTGCGTCCACCCCTCAGCCCCAGACCCCATCCCTCCCTGCTGCCCTTCAATTGCAAAGCAACAGGCTTGTCCCGGCCACATCTCCCCCAAGGACTATAGCAGCCACTGAGACCCATGTTGGATCAAAGGCCATTTTCCTGTATTCCCGTCCCCAGGAAGC... |
Task1_train_34956 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | TTTCACCATGTGGGCAAAGCTGGTCTTGAACTCCTGACCTCAGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCCTGAGCCACCTTTCACGCCCGTCCTATTCTCTTTTTTCTTTGGGACAGAGTCTTGCTCTGTCACCCAGGCTGGAGTACAGTGGTGTGATCTGGGCTCACTGCAACCCCCGCCTCCTGGGTTCTTGTGCATCAGCCTGCCAAGTAGCTGGGATTACAGGCGTGCGCTACCACACCCAGATGATTTTTTTTTTTTTGTATTTTTAGTAGAGACAAAGGTTTCACCATGTTGGCCA... | TTTCACCATGTGGGCAAAGCTGGTCTTGAACTCCTGACCTCAGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCCTGAGCCACCTTTCACGCCCGTCCTATTCTCTTTTTTCTTTGGGACAGAGTCTTGCTCTGTCACCCAGGCTGGAGTACAGTGGTGTGATCTGGGCTCACTGCAACCCCCGCCTCCTGGGTTCTTGTGCATCAGCCTGCCAAGTAGCTGGGATTACAGGCGTGCGCTACCACACCCAGATGATTTTTTTTTTTTTGTATTTTTAGTAGAGACAAAGGTTTCACCATGTTGGCCA... |
Task1_train_34957 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | CCTCTCTAGAAAGGGAAACACAGACTTCACAGGGAAGCTGGCTCCAGGAGGAGGATCCCAGGCCCCCAGAACAAAGCAGCTTCTCGGGTTCCAACACCTGACACAGCAGCCACCAGAAATGAGCTTCTGAAATGTGGCTAGTGTGACTAAGGAAAAGTTAATTTTATATTTTAATTAATTTTAAGAACTAATACTCAATTTAGTTATTGGAAAACTTTTAAGTGTGTTTCGAACAACCTGGAGTAGAACAATCTGCTCTTTCAAATGAAGATTTTATAACATCTAAACACAGATCAAGGATTTTGGATGAAAATCTGGCA... | CCTCTCTAGAAAGGGAAACACAGACTTCACAGGGAAGCTGGCTCCAGGAGGAGGATCCCAGGCCCCCAGAACAAAGCAGCTTCTCGGGTTCCAACACCTGACACAGCAGCCACCAGAAATGAGCTTCTGAAATGTGGCTAGTGTGACTAAGGAAAAGTTAATTTTATATTTTAATTAATTTTAAGAACTAATACTCAATTTAGTTATTGGAAAACTTTTAAGTGTGTTTCGAACAACCTGGAGTAGAACAATCTGCTCTTTCAAATGAAGATTTTATAACATCTAAACACAGATCAAGGATTTTGGATGAAAATCTGGCA... |
Task1_train_34958 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GGTCTTGAATTCTTAGCCTCAAGTGATCCTCCAGCCTTGGTCTGCTAAAGTGCTGGGATTATAGGTGTGAGCCACTATGCCCAGCCAGAAATAATTTTTCAAAAGAGATGTGTACTCCTTCCTCATGCTTTGCAGAACTTAACAGAGGGTGGTTTAGGGTACCCAGAGGACAGTCCAGCACCAGTAGTACCAAGATCAGAAGCAGTTCTCCATGCAGAATTGAGACCTAGATGATCATCTGCAATGAAGCAGTGGGATTTGTGCTTCCTTCAAATGTAAAATTTAATTTTTGGTATTTTGCATCTTTTTTGAAGTTAAAT... | GGTCTTGAATTCTTAGCCTCAAGTGATCCTCCAGCCTTGGTCTGCTAAAGTGCTGGGATTATAGGTGTGAGCCACTATGCCCAGCCAGAAATAATTTTTCAAAAGAGATGTGTACTCCTTCCTCATGCTTTGCAGAACTTAACAGAGGGTGGTTTAGGGTACCCAGAGGACAGTCCAGCACCAGTAGTACCAAGATCAGAAGCAGTTCTCCATGCAGAATTGAGACCTAGATGATCATCTGCAATGAAGCAGTGGGATTTGTGCTTCCTTCAAATGTAAAATTTAATTTTTGGTATTTTGCATCTTTTTTGAAGTTAAAT... |
Task1_train_34959 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCAACAGAGGCTGAAGCAGGAGGATCACTTGAGGCCAGGTGTTTGAGACCAGCCTGGGCAACATAGCAAGACCCCATCTCTACAAAAGGTCCTGCTGGCCTTTACCTGAGATGCCCATCTGCCTTTAACTCGTTAAACAAGAAAAAATTAAAAATAGAAAATTAGCCAGGATTGGTATCAGGTGCCTGTATTCCCAGCTGCTCCAGAGGCTGAGACAGGATGATTGCTTAAGCCCAGGAGTTTGAGACTCCTTATCTCTTAAGGAAAGAAAGGTTACTTTTTGTCCTTTGTTACTAAGTATTTTGTGGAGCGATACTTTG... | CCAACAGAGGCTGAAGCAGGAGGATCACTTGAGGCCAGGTGTTTGAGACCAGCCTGGGCAACATAGCAAGACCCCATCTCTACAAAAGGTCCTGCTGGCCTTTACCTGAGATGCCCATCTGCCTTTAACTCGTTAAACAAGAAAAAATTAAAAATAGAAAATTAGCCAGGATTGGTATCAGGTGCCTGTATTCCCAGCTGCTCCAGAGGCTGAGACAGGATGATTGCTTAAGCCCAGGAGTTTGAGACTCCTTATCTCTTAAGGAAAGAAAGGTTACTTTTTGTCCTTTGTTACTAAGTATTTTGTGGAGCGATACTTTG... |
Task1_train_34960 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | TCAGAGATGATAGGAATAAGGGCACAAACTGAGAGTCTGCAGGGAGAAAGTGACCGAGCAGAGAAGCTCACTGCTGGCAGGCACAGGGCAACCAGGGGCAGGGATGCTGTGGCCTCAGGGTGGCCTCCACTCTCCTAGCCCAGGGGAGTCTGCCTACAGCTACGGTTTTGCAGATGGACCCTAAAAGAAAAGACTCAGGGTCCAGGGAGTTTGTAGACTATATTGGGCCTGGAGTCCACAGAGAAGGGAGACATGGGGTCCCTGAGTGGCAGCTGGATGGGAAGAGGCCATGGGGCCTCTAGGAGGGAGGGAGTCAGTGC... | TCAGAGATGATAGGAATAAGGGCACAAACTGAGAGTCTGCAGGGAGAAAGTGACCGAGCAGAGAAGCTCACTGCTGGCAGGCACAGGGCAACCAGGGGCAGGGATGCTGTGGCCTCAGGGTGGCCTCCACTCTCCTAGCCCAGGGGAGTCTGCCTACAGCTACGGTTTTGCAGATGGACCCTAAAAGAAAAGACTCAGGGTCCAGGGAGTTTGTAGACTATATTGGGCCTGGAGTCCACAGAGAAGGGAGACATGGGGTCCCTGAGTGGCAGCTGGATGGGAAGAGGCCATGGGGCCTCTAGGAGGGAGGGAGTCAGTGC... |
Task1_train_34961 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACAAAACCAAATCTGGGTGTCAGAGGCCAAGACCCCAGGTTGGGATCAGGGACCACCCCCTCACGGGGCATAAGGTCAGTTTTCCCCCAGAGCCCGGGCCCCTGTCCCCCTACAGTGCAAGTGTGGTCCCTGGAGCCCCGGTGTGGAGTGGTGAGTCCCGGAGTAGTGCTTGTCTTGGAAAGAGGGGCCCTTGGCCAGCCACCCCTCAGCGACACTATACAACTCCTGGAGCGCCTGCCAGGATTGAAGCCATGACCAGGTGCAGGTGGGTGCCAGGCCCGCTGTGGGTGGGCACTGGTCCTCAGCACCACTCACCACTG... | ACAAAACCAAATCTGGGTGTCAGAGGCCAAGACCCCAGGTTGGGATCAGGGACCACCCCCTCACGGGGCATAAGGTCAGTTTTCCCCCAGAGCCCGGGCCCCTGTCCCCCTACAGTGCAAGTGTGGTCCCTGGAGCCCCGGTGTGGAGTGGTGAGTCCCGGAGTAGTGCTTGTCTTGGAAAGAGGGGCCCTTGGCCAGCCACCCCTCAGCGACACTATACAACTCCTGGAGCGCCTGCCAGGATTGAAGCCATGACCAGGTGCAGGTGGGTGCCAGGCCCGCTGTGGGTGGGCACTGGTCCTCAGCACCACTCACCACTG... |
Task1_train_34962 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | AGCTACTGTGCCTGGCTTACACACCAAATTTTTAATAACAACAAGGAATAGAACTTGGGAGGTGGATGACAAACAATAATTTTTTTACCACTTCTTAGTCTATTTCTGCAGTTTTAATTTTTGCAACAGAGAATGTATTGTATTTCTTTTTTTTTTTTTTTCTCTTTTGAGACAGAGTTGTGCTCTTTGTCACGCAGGCTGACAAAGAGTAGTGCAGTGGTGCCATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGCATTACAGGAGTGTGCCACCATGCC... | AGCTACTGTGCCTGGCTTACACACCAAATTTTTAATAACAACAAGGAATAGAACTTGGGAGGTGGATGACAAACAATAATTTTTTTACCACTTCTTAGTCTATTTCTGCAGTTTTAATTTTTGCAACAGAGAATGTATTGTATTTCTTTTTTTTTTTTTTTCTCTTTTGAGACAGAGTTGTGCTCTTTGTCACGCAGGCTGACAAAGAGTAGTGCAGTGGTGCCATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGCATTACAGGAGTGTGCCACCATGCC... |
Task1_train_34963 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACAGGCATTTGGTGCTGAATGCTGTTTGGGAATGACGAGGAAAACTTTCGGATTTTTGCGTTTTTTTTTTCAGCATGTTGGGATAAGTACTGTGTTCACGTGGTTGGGAATCTGAAGGGTATAAGAGCCGGAACTGTGTCCTTGCACCCTCACGTCCCTCCCCCAGGCACCACCTCCTGTGCAGCCTTCATGGCCTTCGAGTGGCCCAGAGAGCGTGTGTCTGGATGTGAGCGTGTGTGGGCGCGTGCTGAGTGTGCATGGATGAGTGTGAGCCATGGTGAGTGTGTCCCCCTCACACCTACATTTAAACACACGGGCGG... | ACAGGCATTTGGTGCTGAATGCTGTTTGGGAATGACGAGGAAAACTTTCGGATTTTTGCGTTTTTTTTTTCAGCATGTTGGGATAAGTACTGTGTTCACGTGGTTGGGAATCTGAAGGGTATAAGAGCCGGAACTGTGTCCTTGCACCCTCACGTCCCTCCCCCAGGCACCACCTCCTGTGCAGCCTTCATGGCCTTCGAGTGGCCCAGAGAGCGTGTGTCTGGATGTGAGCGTGTGTGGGCGCGTGCTGAGTGTGCATGGATGAGTGTGAGCCATGGTGAGTGTGTCCCCCTCACACCTACATTTAAACACACGGGCGG... |
Task1_train_34964 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | GGAAGCAGTTAACCGAATCGGGGGCTCTGTTGTGGATGCTCCGCCCCATTTAGGAGGAAGAAGGCAGATCTGGGCCTGAAATGGGACGGTCTCTGAGCTGTGGCGCAGCCCCAGAGTGCACACCACGCTCCATGCACCTCCTGGGCAGGGTGGCAGTAGTGGGGAACATGGGCTGGAGCTCTGTGGCTCACACTTTTTGTTTGTTTGTTTGTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCT... | GGAAGCAGTTAACCGAATCGGGGGCTCTGTTGTGGATGCTCCGCCCCATTTAGGAGGAAGAAGGCAGATCTGGGCCTGAAATGGGACGGTCTCTGAGCTGTGGCGCAGCCCCAGAGTGCACACCACGCTCCATGCACCTCCTGGGCAGGGTGGCAGTAGTGGGGAACATGGGCTGGAGCTCTGTGGCTCACACTTTTTGTTTGTTTGTTTGTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCT... |
Task1_train_34965 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ACTGGTAAAGTTCAATGTTCCAGAAACACGGCAGGGGAAAGGAGATGCACTGTCAGCTGTCTTGGTCAGAGAGGCCAGCTCTACCCTGTCGAGGAAGAAGAAAGCACAGGCAAAGAAGAGAGCAGAGGATGGTGGCGGGGGAAGCGTGGGCACAGCCAGCAGGTGACTCATCCATGCTCATGACCCCTAGCCTGGACTGCAAGGATGTTCTCAGCCAAATACCACAAGTCCACCATCATCCCTACAGCTGCCAAGATCACAGATGTACAAAGACACGGGGCCTGACACTAGTGAGAAGCACTGCTCAAGACAGAGAAAGA... | ACTGGTAAAGTTCAATGTTCCAGAAACACGGCAGGGGAAAGGAGATGCACTGTCAGCTGTCTTGGTCAGAGAGGCCAGCTCTACCCTGTCGAGGAAGAAGAAAGCACAGGCAAAGAAGAGAGCAGAGGATGGTGGCGGGGGAAGCGTGGGCACAGCCAGCAGGTGACTCATCCATGCTCATGACCCCTAGCCTGGACTGCAAGGATGTTCTCAGCCAAATACCACAAGTCCACCATCATCCCTACAGCTGCCAAGATCACAGATGTACAAAGACACGGGGCCTGACACTAGTGAGAAGCACTGCTCAAGACAGAGAAAGA... |
Task1_train_34966 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTACCAGTTATGCCCTTTCTTCCTTTTTAATTTACTTTTATTGCTTTTATTTTATTTGAGACGGAGTCCTGCTCTGTCCCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCACCCTCCACCTCCCGGGTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCCCACCACCACGCCCGGCTAATTTTTGTATTTTTATTTTATTTTTTTGAGATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAAGCTCCACCTCCCGAGTTCATCCCAT... | TTACCAGTTATGCCCTTTCTTCCTTTTTAATTTACTTTTATTGCTTTTATTTTATTTGAGACGGAGTCCTGCTCTGTCCCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCACCCTCCACCTCCCGGGTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCCCACCACCACGCCCGGCTAATTTTTGTATTTTTATTTTATTTTTTTGAGATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAAGCTCCACCTCCCGAGTTCATCCCAT... |
Task1_train_34967 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AGTTACCCTTGACAATGGGCAAACTCCCACACTCATCTGCAGAGCAAGGGCCAGCCAGGTAGGAAGGGCCAGGTGGATGTCTCCTTTCCAGGGTTGTATGAATGATTCACCTGGGAAGAAGGTGAGTGGCCTCTGGGGATGTGGTTAAGGAGGACAGGAATGACTCCTTGCAACTGCTGCTCCAGAGCCTCATCACCAGGACAAATCCAGCTCGCCGGTTTTCTGTGTGACTACCAGGACCCATCTGCTGTCACGGGCGTAGCCTCCACCTCTTGCACAGCTCCGCAGTCCTGCCTCGGGCCAAGTGTGGTCTCCTGCTC... | AGTTACCCTTGACAATGGGCAAACTCCCACACTCATCTGCAGAGCAAGGGCCAGCCAGGTAGGAAGGGCCAGGTGGATGTCTCCTTTCCAGGGTTGTATGAATGATTCACCTGGGAAGAAGGTGAGTGGCCTCTGGGGATGTGGTTAAGGAGGACAGGAATGACTCCTTGCAACTGCTGCTCCAGAGCCTCATCACCAGGACAAATCCAGCTCGCCGGTTTTCTGTGTGACTACCAGGACCCATCTGCTGTCACGGGCGTAGCCTCCACCTCTTGCACAGCTCCGCAGTCCTGCCTCGGGCCAAGTGTGGTCTCCTGCTC... |
Task1_train_34968 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GCGTCCTGGAGGAGCTGAGCCGGTATGTGGAGGAACGGGACTTCATCATGCCGCTGGACTTAGGAGCCAAGGGCAGCTGCCACATCGGGGGAAACGTGGCAACCAACGCTGGAGGCCTGCGGTTTCTTCGATATGGCTCACTGCATGGGACTGTCCTGGGCCTGGAAGTGGTGAGCTGGGGCAGCTGCTTGGTGCAGAGGTCGCCACGGGGTGTCCTCTCACGGCTCTCATGGGCCCACGTGGTGGCACAGGTGCATGGGGCCCCTCGGGGTGGGAGGTCTTGGTTCCTGGCCCTGGGCCCCTCAAGGATGTGTGGGCTA... | GCGTCCTGGAGGAGCTGAGCCGGTATGTGGAGGAACGGGACTTCATCATGCCGCTGGACTTAGGAGCCAAGGGCAGCTGCCACATCGGGGGAAACGTGGCAACCAACGCTGGAGGCCTGCGGTTTCTTCGATATGGCTCACTGCATGGGACTGTCCTGGGCCTGGAAGTGGTGAGCTGGGGCAGCTGCTTGGTGCAGAGGTCGCCACGGGGTGTCCTCTCACGGCTCTCATGGGCCCACGTGGTGGCACAGGTGCATGGGGCCCCTCGGGGTGGGAGGTCTTGGTTCCTGGCCCTGGGCCCCTCAAGGATGTGTGGGCTA... |
Task1_train_34969 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGTGGGCTGAGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAAACTTTGAATAATTTTTTGTGATGTTTTATAATCAGGCAATTCCATTTTTTCAAGTCTGTGTAGTCTGTGAAAGTTTTTTTTAGAGACAAGGTCTCACTCTGTTGCCCAAGCTGAAGTGCAGTGGTGTGATCATAGCCCCTGGGTTCAAGCCATCCTCTTGAGTAGCTGGGATTACAGGTGCACACCACCATGCCTAGGTAATTAAAAAAAATTTTGTATGTAGAAACAGGGTCTCATGTAACTCC... | AGTGGGCTGAGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAAACTTTGAATAATTTTTTGTGATGTTTTATAATCAGGCAATTCCATTTTTTCAAGTCTGTGTAGTCTGTGAAAGTTTTTTTTAGAGACAAGGTCTCACTCTGTTGCCCAAGCTGAAGTGCAGTGGTGTGATCATAGCCCCTGGGTTCAAGCCATCCTCTTGAGTAGCTGGGATTACAGGTGCACACCACCATGCCTAGGTAATTAAAAAAAATTTTGTATGTAGAAACAGGGTCTCATGTAACTCC... |
Task1_train_34970 | 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 | TGAAAGTTTTTTTTAGAGACAAGGTCTCACTCTGTTGCCCAAGCTGAAGTGCAGTGGTGTGATCATAGCCCCTGGGTTCAAGCCATCCTCTTGAGTAGCTGGGATTACAGGTGCACACCACCATGCCTAGGTAATTAAAAAAAATTTTGTATGTAGAAACAGGGTCTCATGTAACTCCTGGGCTAAACGATCCTCCCACTGTGGCCTCCTAAAGTGCGGGGGTTATAGGTGTGAGCCTGAGCCGCTGCACCCAGCCTGTGTGGTCTGTTTTTAGTGTCTGTTGTTTCTGCTGGTTCATGCTCCTGGCTCCTTAGTTTCTT... | TGAAAGTTTTTTTTAGAGACAAGGTCTCACTCTGTTGCCCAAGCTGAAGTGCAGTGGTGTGATCATAGCCCCTGGGTTCAAGCCATCCTCTTGAGTAGCTGGGATTACAGGTGCACACCACCATGCCTAGGTAATTAAAAAAAATTTTGTATGTAGAAACAGGGTCTCATGTAACTCCTGGGCTAAACGATCCTCCCACTGTGGCCTCCTAAAGTGCGGGGGTTATAGGTGTGAGCCTGAGCCGCTGCACCCAGCCTGTGTGGTCTGTTTTTAGTGTCTGTTGTTTCTGCTGGTTCATGCTCCTGGCTCCTTAGTTTCTT... |
Task1_train_34971 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TGCTTTTGCTAGGTGTCTTTGGGTCTGTTCAGCCTGAGAGTGACCAAGTTCACAGGATGAAATTCTGTGAAACTCCCAGGTAGCAAGTCAGTGTAGGGCTGTGTCGGGCTGATCCATGGTCATGATTTATCAGGAGAGTGTTTTTTTTTTTTTTTACATTATTCTTCTGTATTTTTTTGAGAGACAAGGTCTCACTCTGTCATCCAGGCTGGAGTGCAGTGGTGCAATCGTGGCTCACTGCAGCCTTGAACTCCTGCACTGAAGGGATCCTCCTGCCTCCCTAGTAGCTGGGACCAGGTGTGTACCACCATACCTGGCTA... | TGCTTTTGCTAGGTGTCTTTGGGTCTGTTCAGCCTGAGAGTGACCAAGTTCACAGGATGAAATTCTGTGAAACTCCCAGGTAGCAAGTCAGTGTAGGGCTGTGTCGGGCTGATCCATGGTCATGATTTATCAGGAGAGTGTTTTTTTTTTTTTTTACATTATTCTTCTGTATTTTTTTGAGAGACAAGGTCTCACTCTGTCATCCAGGCTGGAGTGCAGTGGTGCAATCGTGGCTCACTGCAGCCTTGAACTCCTGCACTGAAGGGATCCTCCTGCCTCCCTAGTAGCTGGGACCAGGTGTGTACCACCATACCTGGCTA... |
Task1_train_34972 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | CTCCTGGATCTGCCCCAATCAGGCCTTGCCCGCTTCACTGGTGCCCCTCCCACCATGGCTGCCACTGTCCTCCCACAGCCAACCCAGCCATCAGTTCTCATTGCCCCTCTCGCCCATTGCCTCCGGCACAAGCCTGGCCTGTGATGCTGCCCCCACACCGCCTCCTCCCCGCCCTCCACCTTCAGCCCCTGGTGGGGCTCCTCACCACCTGACCCCGGAACGGCTGGGGCAGCCTTGACTGCTTCTGCCGACTTACTCTCTGGGCGGCAGTGCCATCTGGATCGGTGGTTCCTCTTCATCCAGGTTTTCTGTGTTCTGCT... | CTCCTGGATCTGCCCCAATCAGGCCTTGCCCGCTTCACTGGTGCCCCTCCCACCATGGCTGCCACTGTCCTCCCACAGCCAACCCAGCCATCAGTTCTCATTGCCCCTCTCGCCCATTGCCTCCGGCACAAGCCTGGCCTGTGATGCTGCCCCCACACCGCCTCCTCCCCGCCCTCCACCTTCAGCCCCTGGTGGGGCTCCTCACCACCTGACCCCGGAACGGCTGGGGCAGCCTTGACTGCTTCTGCCGACTTACTCTCTGGGCGGCAGTGCCATCTGGATCGGTGGTTCCTCTTCATCCAGGTTTTCTGTGTTCTGCT... |
Task1_train_34973 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ACCCCAGCCCTCTACGCGTCTGCAGCCACACCCCGACATGGTGCTCGGGTCACAGGCCTTGAGGTGCTCCTGTGTCACCCAGTGCAGGTGTCTGCCCCCAGCCTCTGCGCCTGTGAGACCTTCTCTCTGGAAAATTCTTCTCTGATATCCACATGCCTTTGCATTGCCTCCCTGTCTCGCCCTGAAAGGTGGGCACGGGCCCCCTCCTGCTGCAGCGTCTCTGGGGCTGCCCGCCTGCAGACATCTCCACTCAGTTCCTTTCCATCTTTGCACTTGAGGGTCGGCTTCCCCAGGGCAGCGGCCTCACTGGTAGCCCCCAC... | ACCCCAGCCCTCTACGCGTCTGCAGCCACACCCCGACATGGTGCTCGGGTCACAGGCCTTGAGGTGCTCCTGTGTCACCCAGTGCAGGTGTCTGCCCCCAGCCTCTGCGCCTGTGAGACCTTCTCTCTGGAAAATTCTTCTCTGATATCCACATGCCTTTGCATTGCCTCCCTGTCTCGCCCTGAAAGGTGGGCACGGGCCCCCTCCTGCTGCAGCGTCTCTGGGGCTGCCCGCCTGCAGACATCTCCACTCAGTTCCTTTCCATCTTTGCACTTGAGGGTCGGCTTCCCCAGGGCAGCGGCCTCACTGGTAGCCCCCAC... |
Task1_train_34974 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGTGTCACCCAGTGCAGGTGTCTGCCCCCAGCCTCTGCGCCTGTGAGACCTTCTCTCTGGAAAATTCTTCTCTGATATCCACATGCCTTTGCATTGCCTCCCTGTCTCGCCCTGAAAGGTGGGCACGGGCCCCCTCCTGCTGCAGCGTCTCTGGGGCTGCCCGCCTGCAGACATCTCCACTCAGTTCCTTTCCATCTTTGCACTTGAGGGTCGGCTTCCCCAGGGCAGCGGCCTCACTGGTAGCCCCCACCAACCCTGGAGCACTAACACGCCTGTTGGATGAGGTCCTGAGTGCAGGGAAGACCTGAGTGCTGATTGTG... | TGTGTCACCCAGTGCAGGTGTCTGCCCCCAGCCTCTGCGCCTGTGAGACCTTCTCTCTGGAAAATTCTTCTCTGATATCCACATGCCTTTGCATTGCCTCCCTGTCTCGCCCTGAAAGGTGGGCACGGGCCCCCTCCTGCTGCAGCGTCTCTGGGGCTGCCCGCCTGCAGACATCTCCACTCAGTTCCTTTCCATCTTTGCACTTGAGGGTCGGCTTCCCCAGGGCAGCGGCCTCACTGGTAGCCCCCACCAACCCTGGAGCACTAACACGCCTGTTGGATGAGGTCCTGAGTGCAGGGAAGACCTGAGTGCTGATTGTG... |
Task1_train_34975 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CTGTTTTCCCAGCAGAAAGAGCAGGACAGCCGCCGGGGATTCTCTCAGCTTCTGCTTGAGATGGGGCGGGAACGTGAGCCCAACTGCCCTTGGTGGTGCGGGTGGGGACCCTCATCCCGCACTGGCTGCTTTGCTGGAGTGGCAGTCAGTCATGCAGCCCCCACACCACCCCCAGGAGGGCGACCCTGGCACCCCAGCCTCCACACATCAGCCCCCATGCCCCCACAAAGGAAGGCTGCCCCCAACACCCCCAACCTCTCTACCAGCCCCCATGCCACCCCCAGGGCGGGCCGTCCTCCATGCCCCCAGCCTCTGCACAT... | CTGTTTTCCCAGCAGAAAGAGCAGGACAGCCGCCGGGGATTCTCTCAGCTTCTGCTTGAGATGGGGCGGGAACGTGAGCCCAACTGCCCTTGGTGGTGCGGGTGGGGACCCTCATCCCGCACTGGCTGCTTTGCTGGAGTGGCAGTCAGTCATGCAGCCCCCACACCACCCCCAGGAGGGCGACCCTGGCACCCCAGCCTCCACACATCAGCCCCCATGCCCCCACAAAGGAAGGCTGCCCCCAACACCCCCAACCTCTCTACCAGCCCCCATGCCACCCCCAGGGCGGGCCGTCCTCCATGCCCCCAGCCTCTGCACAT... |
Task1_train_34976 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AGGGGTTAGGGCTCTGCCATGGGGGCGTGGGCATCTGCTCTGACAAACAACGTGTGCATTTGATTGGTGTTCCTGAGTCACCGTGGACCAGGCAGGCTGCCAGAGCGGCTGATTCTTAGCGGGGAGCTGGGGCCGGGCAGACACCCTGACTCCCTGGGGCTCCCAGCAGGGCCCCACTGGCAACAGGCAGCCTCCTCCCTCTGGCCGCCGGGCCTCCGTCCCTTTCCCAGCCTGGGGCTGGGACCACCGCTCCACACCACACTGCACTGCCCTTGTCTGCCCCAGCAGGGGGTGAAGGTGGCTGGTGGCTGAGGACCCCC... | AGGGGTTAGGGCTCTGCCATGGGGGCGTGGGCATCTGCTCTGACAAACAACGTGTGCATTTGATTGGTGTTCCTGAGTCACCGTGGACCAGGCAGGCTGCCAGAGCGGCTGATTCTTAGCGGGGAGCTGGGGCCGGGCAGACACCCTGACTCCCTGGGGCTCCCAGCAGGGCCCCACTGGCAACAGGCAGCCTCCTCCCTCTGGCCGCCGGGCCTCCGTCCCTTTCCCAGCCTGGGGCTGGGACCACCGCTCCACACCACACTGCACTGCCCTTGTCTGCCCCAGCAGGGGGTGAAGGTGGCTGGTGGCTGAGGACCCCC... |
Task1_train_34977 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CTGGGGACACTGAGCTCCTCCTTGCTCGAGGTTTTGGGTCCTCATTGTCCACATGACCTCCTGCTGGGCGAATTCTGGGATGACCCTGTGTCCTGGGCACATGGCTGGCAGGGTCCCGGGGGCTCTCTGGCCAGCCTCCCCTGCACCCTGGCACCAACCAGCCTGGCCGAGGGTCAGCTCCCAGAGCCGTGTTGAGAGGGGAAGGGGCTGATTCCACAGACATTTGGGGTGGAGTGGGTGCGAGGGAGGGTGGGGGAGGGGCTGCTCCAGATCTGGGGTGAGGGAGTCAGAAACAGGGCTGACCCCAAGGTGGGTACAGG... | CTGGGGACACTGAGCTCCTCCTTGCTCGAGGTTTTGGGTCCTCATTGTCCACATGACCTCCTGCTGGGCGAATTCTGGGATGACCCTGTGTCCTGGGCACATGGCTGGCAGGGTCCCGGGGGCTCTCTGGCCAGCCTCCCCTGCACCCTGGCACCAACCAGCCTGGCCGAGGGTCAGCTCCCAGAGCCGTGTTGAGAGGGGAAGGGGCTGATTCCACAGACATTTGGGGTGGAGTGGGTGCGAGGGAGGGTGGGGGAGGGGCTGCTCCAGATCTGGGGTGAGGGAGTCAGAAACAGGGCTGACCCCAAGGTGGGTACAGG... |
Task1_train_34978 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TGTCTTGCTGACCTGTGGCCCTGTACTGACCAGCAGAGCATGGGGGTCCCTCGTACCCCTTCACGGACAGTGCTCTTCGAGCGGGAGAGGACGGGCCTGACCTACCGCGTGCCCTCGCTGCTCCCCGTGCCCCCCGGGCCCACCCTGCTGGCCTTTGTGGAGCAGCGGCTCAGCCCTGACGACTCCCACGCCCACCGCCTGGTGCTGAGGAGGGGCACGCTGGCCGGGGGCTCCGTGCGGGTGAGTGAGTGGCCGGGGGCTCTGTGTGGGTGTAGTGGCCGGATCTGCTGGGGCTGCACACCCCGGGATGGGGCGGGGGT... | TGTCTTGCTGACCTGTGGCCCTGTACTGACCAGCAGAGCATGGGGGTCCCTCGTACCCCTTCACGGACAGTGCTCTTCGAGCGGGAGAGGACGGGCCTGACCTACCGCGTGCCCTCGCTGCTCCCCGTGCCCCCCGGGCCCACCCTGCTGGCCTTTGTGGAGCAGCGGCTCAGCCCTGACGACTCCCACGCCCACCGCCTGGTGCTGAGGAGGGGCACGCTGGCCGGGGGCTCCGTGCGGGTGAGTGAGTGGCCGGGGGCTCTGTGTGGGTGTAGTGGCCGGATCTGCTGGGGCTGCACACCCCGGGATGGGGCGGGGGT... |
Task1_train_34979 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | CCGAGAGGAAGCCCCAGGACGTCTGGGTTCTGCTACCTGAGCACAGCCTGGTCCCGGGATGCCTGGACGGCGGTGGTGTCCAGTACCTGCTGGTGGGGCTCTCGAGGTGCGGCCAGAGGTTGGGGACCCTGGGAGAGGCAGGGGGCTGAAGGTGCTTTTCCACGGGACCTTGGGTGGTCCCAGAGGCTGGGTGGGGCTGTTGGGCCTCGTCTTGTCCCCGAGACGGGAGGGTGGGGCTGGGTGCTCCTTCTCCCGCCGGAGCCCCTGCCTCGCCATGCTGGGCACACGGCTGCTGACGCAGGGGTCCCGGGGAAGACATG... | CCGAGAGGAAGCCCCAGGACGTCTGGGTTCTGCTACCTGAGCACAGCCTGGTCCCGGGATGCCTGGACGGCGGTGGTGTCCAGTACCTGCTGGTGGGGCTCTCGAGGTGCGGCCAGAGGTTGGGGACCCTGGGAGAGGCAGGGGGCTGAAGGTGCTTTTCCACGGGACCTTGGGTGGTCCCAGAGGCTGGGTGGGGCTGTTGGGCCTCGTCTTGTCCCCGAGACGGGAGGGTGGGGCTGGGTGCTCCTTCTCCCGCCGGAGCCCCTGCCTCGCCATGCTGGGCACACGGCTGCTGACGCAGGGGTCCCGGGGAAGACATG... |
Task1_train_34980 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ACGTCTGGGTTCTGCTACCTGAGCACAGCCTGGTCCCGGGATGCCTGGACGGCGGTGGTGTCCAGTACCTGCTGGTGGGGCTCTCGAGGTGCGGCCAGAGGTTGGGGACCCTGGGAGAGGCAGGGGGCTGAAGGTGCTTTTCCACGGGACCTTGGGTGGTCCCAGAGGCTGGGTGGGGCTGTTGGGCCTCGTCTTGTCCCCGAGACGGGAGGGTGGGGCTGGGTGCTCCTTCTCCCGCCGGAGCCCCTGCCTCGCCATGCTGGGCACACGGCTGCTGACGCAGGGGTCCCGGGGAAGACATGGCGGGTGCCTCATGGAGA... | ACGTCTGGGTTCTGCTACCTGAGCACAGCCTGGTCCCGGGATGCCTGGACGGCGGTGGTGTCCAGTACCTGCTGGTGGGGCTCTCGAGGTGCGGCCAGAGGTTGGGGACCCTGGGAGAGGCAGGGGGCTGAAGGTGCTTTTCCACGGGACCTTGGGTGGTCCCAGAGGCTGGGTGGGGCTGTTGGGCCTCGTCTTGTCCCCGAGACGGGAGGGTGGGGCTGGGTGCTCCTTCTCCCGCCGGAGCCCCTGCCTCGCCATGCTGGGCACACGGCTGCTGACGCAGGGGTCCCGGGGAAGACATGGCGGGTGCCTCATGGAGA... |
Task1_train_34981 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CACTCGGCTCCTTGGGCCAGCGCTGCCCTTGGACACAGGCTCATCTCCTGCTTCCATGGCACTGCCGTGGTCTCGCAGCCATCAGTGCTGACAGGTGGGCCCTGGGGCGTGCCGGAGCCTGTGGTCACCATCCGGCCCTGTGTTGCACACAGCGGGGTGCTCGGCCCTGATCGGGGGCCCGGGGTGGCTGTGGGTCACAAGTGAGCCTCACAGGCCGTCATCACGGTTGTGGTGCCGTCAGCGCAGCAGGGCGGGCGCCATGCGCTTCTCCAACTGGCAAGGCATCCACAGCTCGGCCGGGTGCCAGCTGGGAGGGGCGC... | CACTCGGCTCCTTGGGCCAGCGCTGCCCTTGGACACAGGCTCATCTCCTGCTTCCATGGCACTGCCGTGGTCTCGCAGCCATCAGTGCTGACAGGTGGGCCCTGGGGCGTGCCGGAGCCTGTGGTCACCATCCGGCCCTGTGTTGCACACAGCGGGGTGCTCGGCCCTGATCGGGGGCCCGGGGTGGCTGTGGGTCACAAGTGAGCCTCACAGGCCGTCATCACGGTTGTGGTGCCGTCAGCGCAGCAGGGCGGGCGCCATGCGCTTCTCCAACTGGCAAGGCATCCACAGCTCGGCCGGGTGCCAGCTGGGAGGGGCGC... |
Task1_train_34982 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AGGCATCCACAGCTCGGCCGGGTGCCAGCTGGGAGGGGCGCGGGGCAGCTCCACATCCTCGCAGATGCCCGGCCTGACAGGCCCCCAGGCTGCTGGCTGGTCCGTCCCTCTGTGGAGACACCCTGGGCAAAGGGGGAGTCGTCCTGCCCTTTGACACAGCTCCTCAGTGCCTGAGACCCCTGGGGCCAGGTGTGTGCAGAATCCCAGCTTTTTCAGAAGCTGGGAAAGTAATAACCCGTGTTGGGGTCTGAGAAGTGCTGGGAAGCACATCACTGTTCCCACAGCCAGGTGGAGATGGCTCTGAGCGGCTCCCAGCTGGC... | AGGCATCCACAGCTCGGCCGGGTGCCAGCTGGGAGGGGCGCGGGGCAGCTCCACATCCTCGCAGATGCCCGGCCTGACAGGCCCCCAGGCTGCTGGCTGGTCCGTCCCTCTGTGGAGACACCCTGGGCAAAGGGGGAGTCGTCCTGCCCTTTGACACAGCTCCTCAGTGCCTGAGACCCCTGGGGCCAGGTGTGTGCAGAATCCCAGCTTTTTCAGAAGCTGGGAAAGTAATAACCCGTGTTGGGGTCTGAGAAGTGCTGGGAAGCACATCACTGTTCCCACAGCCAGGTGGAGATGGCTCTGAGCGGCTCCCAGCTGGC... |
Task1_train_34983 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GCACGAACGTGTCCACGGGCTCTGTGGCCAGTGTGGTTGGAGGCTGCAGGCAGGGCAGTGTGGCTATAGAACATTCTGTCATCCAGAAACTTCCACTGCCTGGAACTGAATCATAGCCTCTCACTCATGCAGGGTTCCCTGAAGCTCACAGCTGCTTGTGTGGCTAGCAAATGGTCACCGGTCTGATGACCGCCATGGACAAGCCAATCCCTCCCAGTGCTCTCCCCAAACCTCTCCTCGCCTGGTGACGCCCAGCAGGGCTGCCCGGGCCATGACCGCAGGCCTCCGTGACATCCTTCCCCTCAGCTGGCAGGCGACCT... | GCACGAACGTGTCCACGGGCTCTGTGGCCAGTGTGGTTGGAGGCTGCAGGCAGGGCAGTGTGGCTATAGAACATTCTGTCATCCAGAAACTTCCACTGCCTGGAACTGAATCATAGCCTCTCACTCATGCAGGGTTCCCTGAAGCTCACAGCTGCTTGTGTGGCTAGCAAATGGTCACCGGTCTGATGACCGCCATGGACAAGCCAATCCCTCCCAGTGCTCTCCCCAAACCTCTCCTCGCCTGGTGACGCCCAGCAGGGCTGCCCGGGCCATGACCGCAGGCCTCCGTGACATCCTTCCCCTCAGCTGGCAGGCGACCT... |
Task1_train_34984 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TGGGCCCCACGGTGATGGTCCCCGAGCAACAGCTATGTTCACCCTTGCCAGGCCATGGCTGCTGACTGGTGGGGCCCAGGGCAGCTCCATGCATGAGAGGGTCAGCTGGGCAGGATGTCAGCAGCTGCCACGGTCCCACAGACTTGGCGCCTCCGGGCCTGGAGTCCTCGGCCCTCACAGCCGGCCGCCCATCCCAGAGAGGCTGCCAGGACAGCCAGCCCCATGGTGGTGGAAGCAGCGGCCCCTGTCCCTTTACAGGGGACCGTGGGGTCCCGAGCCAGGGGCTGCGAATGGCCGGTCTCCCACATGGGCCAGCTCCT... | TGGGCCCCACGGTGATGGTCCCCGAGCAACAGCTATGTTCACCCTTGCCAGGCCATGGCTGCTGACTGGTGGGGCCCAGGGCAGCTCCATGCATGAGAGGGTCAGCTGGGCAGGATGTCAGCAGCTGCCACGGTCCCACAGACTTGGCGCCTCCGGGCCTGGAGTCCTCGGCCCTCACAGCCGGCCGCCCATCCCAGAGAGGCTGCCAGGACAGCCAGCCCCATGGTGGTGGAAGCAGCGGCCCCTGTCCCTTTACAGGGGACCGTGGGGTCCCGAGCCAGGGGCTGCGAATGGCCGGTCTCCCACATGGGCCAGCTCCT... |
Task1_train_34985 | Here’s a variant located on Chromosome 3. What is the predicted biological effect — harmless or disease-causing? | Benign | ACTCACCTTTTGTAGTTAAGGCAGTATTTTGCTTTTTATAATGAAAGCATTTTTCCATGTTTTATTTCATTGATTAGGATAACTCATTTCATCAGAAGAGTAGTGTCAATTAACATAGTGACACATTGAACATATATGTTAAATTTACCAGTAGAAGTTAAATTACAAGTATAAGTTATTTGTCATTAGAAAATATTCTGAAGCATACATGAGTCATTTTTTCCAATTCCCATTTTAAGATGGGTCAGTTGAGGTCAGCCAGAGTAGAATAATGCCATTACTCTAATTCAGGACAAAGATTCACAACTTTTTTGGAGGTG... | ACTCACCTTTTGTAGTTAAGGCAGTATTTTGCTTTTTATAATGAAAGCATTTTTCCATGTTTTATTTCATTGATTAGGATAACTCATTTCATCAGAAGAGTAGTGTCAATTAACATAGTGACACATTGAACATATATGTTAAATTTACCAGTAGAAGTTAAATTACAAGTATAAGTTATTTGTCATTAGAAAATATTCTGAAGCATACATGAGTCATTTTTTCCAATTCCCATTTTAAGATGGGTCAGTTGAGGTCAGCCAGAGTAGAATAATGCCATTACTCTAATTCAGGACAAAGATTCACAACTTTTTTGGAGGTG... |
Task1_train_34986 | Chromosome 3 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGTAAATGTTATTTAAATTTAAAAAAAGGCAGGAGGTATAAAAAAATTGGCAAGAATAGAGCTGAAAATTTTTGCCATGGTATAGACCTATCCTGAGATTAAATTATATCTCATTTTCACATAATACTTTAGATCATTATTTTACTTTATTCTTTCAAGTAAATGGTATTAGAAAATTAGACTAGTTTTCAAAGACCCAAAGACTAGGGAGTCCGGGAGATCTTGCTGAAAGTGAGTTACTTGCTCTAATAAAGGATGGACTCTTGAAAAAATCCTGTTTTAGGGGAAGTGAGTTCCAGAGCAGCCTATAACTTGGCAAA... | AGTAAATGTTATTTAAATTTAAAAAAAGGCAGGAGGTATAAAAAAATTGGCAAGAATAGAGCTGAAAATTTTTGCCATGGTATAGACCTATCCTGAGATTAAATTATATCTCATTTTCACATAATACTTTAGATCATTATTTTACTTTATTCTTTCAAGTAAATGGTATTAGAAAATTAGACTAGTTTTCAAAGACCCAAAGACTAGGGAGTCCGGGAGATCTTGCTGAAAGTGAGTTACTTGCTCTAATAAAGGATGGACTCTTGAAAAAATCCTGTTTTAGGGGAAGTGAGTTCCAGAGCAGCCTATAACTTGGCAAA... |
Task1_train_34987 | This sequence change occurs on Chromosome 3. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCGAGATCGCGCCACTGCACTCCAACCTGGGTGACAGAGCAAGAAATCTGTCTCAAAAAAAAAAAAAGAAGAAGAAGAAGAAGAAGAGTGGATTGGGCTAAATTTGTCTTTACTTAGGACTCTAATGTCCTTTCCCTTGAGATCTCACTTGATTGTCTTATGGTCCGGTGAGGTGAGGGGAAATGAATTCTTAATGAGTGTCCTTGTCTTAGGTAATATGACTTAGATCTCACAATTAATAGGGAAAAGCTAGGAGTGGGATCCACTGGCTTCAGAGCCTCCTATACCCTATGAAGAAAATTCTTAACCAAGAAAGTACT... | CCGAGATCGCGCCACTGCACTCCAACCTGGGTGACAGAGCAAGAAATCTGTCTCAAAAAAAAAAAAAGAAGAAGAAGAAGAAGAAGAGTGGATTGGGCTAAATTTGTCTTTACTTAGGACTCTAATGTCCTTTCCCTTGAGATCTCACTTGATTGTCTTATGGTCCGGTGAGGTGAGGGGAAATGAATTCTTAATGAGTGTCCTTGTCTTAGGTAATATGACTTAGATCTCACAATTAATAGGGAAAAGCTAGGAGTGGGATCCACTGGCTTCAGAGCCTCCTATACCCTATGAAGAAAATTCTTAACCAAGAAAGTACT... |
Task1_train_34988 | A mutation located on Chromosome 3 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CATGTTTACTTTTTATGTTACCTCTCCATTTCTAAAAAGACCTTTGTATGCTACGGGTATTTACTTTTCAGTTTTTACTATCCCAGTTTTAAGATGTGTTACGTATTGACTTTCCATAAGGGAAGATGATTTAGCTTTCTTACCACACCCTTCTCAACAACAAGCACGTATAATTCTCCTTCTTCTGTCTTCCTAGTATATTTATATCATAATTTTTGGTTAAGTCAATATTCAGGGTTCACGTTTATGACTCTGTATTGTTTACAGCCAGATTGTGGAGTATATTGTGATGACATTTCTTCTATTGGCATGTTTTTAAA... | CATGTTTACTTTTTATGTTACCTCTCCATTTCTAAAAAGACCTTTGTATGCTACGGGTATTTACTTTTCAGTTTTTACTATCCCAGTTTTAAGATGTGTTACGTATTGACTTTCCATAAGGGAAGATGATTTAGCTTTCTTACCACACCCTTCTCAACAACAAGCACGTATAATTCTCCTTCTTCTGTCTTCCTAGTATATTTATATCATAATTTTTGGTTAAGTCAATATTCAGGGTTCACGTTTATGACTCTGTATTGTTTACAGCCAGATTGTGGAGTATATTGTGATGACATTTCTTCTATTGGCATGTTTTTAAA... |
Task1_train_34989 | A change on Chromosome 3 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ATATAAAAAATTAGCCGGGCGTGGTGGCGGCTGCCTGTAGTCCCAGCTGTTAGGCAGGAGAATGGTGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCTGAGATTGTGCCACTGCACTCCAGTCTGGGCAACAGAGCGAGACTCCATCTCAAAAAAAAAGAATAGACTCTGGAGCCAAAATCCCTGGGTTCAAATTCTGACTCCGTCACTCACTAGCCACAAAACAAAAACGTTAATTAATATTGGCTTCCTTTGTACCGCTGTTGTGAGGTTTAAGAGAGTTAATTGTAAATGCTTAGAACAGTGCCTGACACATGTACA... | ATATAAAAAATTAGCCGGGCGTGGTGGCGGCTGCCTGTAGTCCCAGCTGTTAGGCAGGAGAATGGTGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCTGAGATTGTGCCACTGCACTCCAGTCTGGGCAACAGAGCGAGACTCCATCTCAAAAAAAAAGAATAGACTCTGGAGCCAAAATCCCTGGGTTCAAATTCTGACTCCGTCACTCACTAGCCACAAAACAAAAACGTTAATTAATATTGGCTTCCTTTGTACCGCTGTTGTGAGGTTTAAGAGAGTTAATTGTAAATGCTTAGAACAGTGCCTGACACATGTACA... |
Task1_train_34990 | A variant was discovered on Chromosome 3. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ACTCTACTAATTAATACTTGAGGTTTTATGTACATATATATAAAATTAGTTTTATGTCACTTTTTTCATTCAACATATGAGAACATTTGTTTATTACCATTTTTGTGAATGGCTAATAGATTAACATGGTTCAAAATTCACAAAGTTTTAAAGGCTCTACAGTGAAGTCTCCTGATCTGTAATGAACAGGACTGCCCATTTAACCACACCCTTGCTAACACTGTTATCAAGTGTTTGCATCGTTGCCGATCTGAAAGACGCTATCTTGGAAATGGGTATTTACTGGCCGGGCATGGTGGCTTATGCCTGTAACCCTAGCA... | ACTCTACTAATTAATACTTGAGGTTTTATGTACATATATATAAAATTAGTTTTATGTCACTTTTTTCATTCAACATATGAGAACATTTGTTTATTACCATTTTTGTGAATGGCTAATAGATTAACATGGTTCAAAATTCACAAAGTTTTAAAGGCTCTACAGTGAAGTCTCCTGATCTGTAATGAACAGGACTGCCCATTTAACCACACCCTTGCTAACACTGTTATCAAGTGTTTGCATCGTTGCCGATCTGAAAGACGCTATCTTGGAAATGGGTATTTACTGGCCGGGCATGGTGGCTTATGCCTGTAACCCTAGCA... |
Task1_train_34991 | Given a variant located on Chromosome 3, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGATCTACTGCTTCTGCCTCCCTTCCTGCTCCATTGTCTAAACACAATTGGAACCAGAGCACAAGGGATCCCACTGACGAAACCCAACAGAATGAGCCTCCTGGGGCATAAAGCAGGGTAGGGAAGGGTGAAAAGTGGATCTGGAAGGGAAACAGAAGACATTCAGCACAGTCCATCCCTCCCCCAGCAACACTCCCCCAGGAACCCTCCCCCATCATTTACTGTTATTTTTAATTCAAAAATTGCAAAAATGCCAAAACAGGATGAAATGATATCAGTTCAGTCAACTTCCCAACAGAAACCCAAAACATGAGCAACCA... | TGATCTACTGCTTCTGCCTCCCTTCCTGCTCCATTGTCTAAACACAATTGGAACCAGAGCACAAGGGATCCCACTGACGAAACCCAACAGAATGAGCCTCCTGGGGCATAAAGCAGGGTAGGGAAGGGTGAAAAGTGGATCTGGAAGGGAAACAGAAGACATTCAGCACAGTCCATCCCTCCCCCAGCAACACTCCCCCAGGAACCCTCCCCCATCATTTACTGTTATTTTTAATTCAAAAATTGCAAAAATGCCAAAACAGGATGAAATGATATCAGTTCAGTCAACTTCCCAACAGAAACCCAAAACATGAGCAACCA... |
Task1_train_34992 | A mutation has occurred on Chromosome 3. What is the medical relevance of this mutation? | Benign | CATTGTCTAAACACAATTGGAACCAGAGCACAAGGGATCCCACTGACGAAACCCAACAGAATGAGCCTCCTGGGGCATAAAGCAGGGTAGGGAAGGGTGAAAAGTGGATCTGGAAGGGAAACAGAAGACATTCAGCACAGTCCATCCCTCCCCCAGCAACACTCCCCCAGGAACCCTCCCCCATCATTTACTGTTATTTTTAATTCAAAAATTGCAAAAATGCCAAAACAGGATGAAATGATATCAGTTCAGTCAACTTCCCAACAGAAACCCAAAACATGAGCAACCACCAAAAGATGGTTTTCATAAAACGATCTTTT... | CATTGTCTAAACACAATTGGAACCAGAGCACAAGGGATCCCACTGACGAAACCCAACAGAATGAGCCTCCTGGGGCATAAAGCAGGGTAGGGAAGGGTGAAAAGTGGATCTGGAAGGGAAACAGAAGACATTCAGCACAGTCCATCCCTCCCCCAGCAACACTCCCCCAGGAACCCTCCCCCATCATTTACTGTTATTTTTAATTCAAAAATTGCAAAAATGCCAAAACAGGATGAAATGATATCAGTTCAGTCAACTTCCCAACAGAAACCCAAAACATGAGCAACCACCAAAAGATGGTTTTCATAAAACGATCTTTT... |
Task1_train_34993 | A variant was discovered on Chromosome 3. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CTCCTTACTTGTTCATTTATCTTACCTGTTTATAAGTCTCATTAAATCCTTTTAGGAATAAAGCAGGTATAAAATGGTTTGAGTTCTATGTAAGCAAGAATTACTATATACATAAAAAAATCTGCTGGGTTCATGAGAGATACTTTAATCTGAAATCAGTTTGAAAATATGCTTCACGATGCTAATGAGGATCTAACCAGAGATCAGGCTTCACATAGAGTTTAGATTGAGGATTGTCTTCTTTTTATATAACATTTTACAAATGTAATGTTTTGAAAATACAGGTACATTTAAATGACAGATTTTTTTCATATTCCTTT... | CTCCTTACTTGTTCATTTATCTTACCTGTTTATAAGTCTCATTAAATCCTTTTAGGAATAAAGCAGGTATAAAATGGTTTGAGTTCTATGTAAGCAAGAATTACTATATACATAAAAAAATCTGCTGGGTTCATGAGAGATACTTTAATCTGAAATCAGTTTGAAAATATGCTTCACGATGCTAATGAGGATCTAACCAGAGATCAGGCTTCACATAGAGTTTAGATTGAGGATTGTCTTCTTTTTATATAACATTTTACAAATGTAATGTTTTGAAAATACAGGTACATTTAAATGACAGATTTTTTTCATATTCCTTT... |
Task1_train_34994 | A mutation on Chromosome 3 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CCACATCCCATTCTGGAACCCAGAGGAAAATAGAATGTTTAAAAATGAAAAATGTTCAATGCTTGCCAGAGGAATCTAGATAAAATTTTGAGACAGACCAATGTATATATGCAAATGAGATGGCTGCCCTATTAAAAAATAGATAAACAGATGTAAGGATTTCTCCTTAGAAAGAGGGACAGACTGGCTTGGCGCGGTGGCTCACGTTTGTAATCCCAGCACGCTGGGAGGCCAAGGCAAGCGGATCACAAGGTCAGGAGATTGAGACCATCCGGGCCAACATGGTGAAACCCCATCTCTATTAAAAATACAAAAATTAG... | CCACATCCCATTCTGGAACCCAGAGGAAAATAGAATGTTTAAAAATGAAAAATGTTCAATGCTTGCCAGAGGAATCTAGATAAAATTTTGAGACAGACCAATGTATATATGCAAATGAGATGGCTGCCCTATTAAAAAATAGATAAACAGATGTAAGGATTTCTCCTTAGAAAGAGGGACAGACTGGCTTGGCGCGGTGGCTCACGTTTGTAATCCCAGCACGCTGGGAGGCCAAGGCAAGCGGATCACAAGGTCAGGAGATTGAGACCATCCGGGCCAACATGGTGAAACCCCATCTCTATTAAAAATACAAAAATTAG... |
Task1_train_34995 | Chromosome 3 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGGGAGGAGGGATAAATAGGTGGAGCACTGAGGATTTTTAGGGCAATGAAACTACTCTGTATAATACTACAGCAGTGAATTTATGTAATTATACATTTGTCCAAACTCATAGAATGTACAACGCCAAGGGTGAACCCTAGTATAAACTACGGACTCTGGTGATAATGATGTTATCAACGTAGGTTTATTAATTATAACAAAGGCACCACTCTGGGCAGGGTGGTGTTGATAGTGGGGGAGGGTATGCAAGTGTAGTGGCAGAGGATATACAGGAAATCTCTGTACCTTTATCTCAATTTTACTCTGAACCTAAAATTGCT... | GGGGAGGAGGGATAAATAGGTGGAGCACTGAGGATTTTTAGGGCAATGAAACTACTCTGTATAATACTACAGCAGTGAATTTATGTAATTATACATTTGTCCAAACTCATAGAATGTACAACGCCAAGGGTGAACCCTAGTATAAACTACGGACTCTGGTGATAATGATGTTATCAACGTAGGTTTATTAATTATAACAAAGGCACCACTCTGGGCAGGGTGGTGTTGATAGTGGGGGAGGGTATGCAAGTGTAGTGGCAGAGGATATACAGGAAATCTCTGTACCTTTATCTCAATTTTACTCTGAACCTAAAATTGCT... |
Task1_train_34996 | Assess the clinical impact of this variant found on Chromosome 3. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GAAATAGCTGCATAAATTCATGATAAATTTTATCTTTAAAAAAAAATCCTATACTATATACACTGAAAAACCCTAGATCCCGTGACAGGCAGTGAGCATAAAGTTGATTTGGTATTTAAATGAGATACATATAAAACACAACTCTCTGGCATATGAGATATTAATGGTGCTCTGAAATGGAAAAATACAAATTCAAGTAAATTTGGGAAATTCTGAATTTCCCTCTTGGAGGTTACATTTTATGTTATATGTTAAATGTTCTGGAAAAGTCAGTGAAGCAACCTAAAACATTTTAGCACAGTGGCTGTCCGGAACCCTTT... | GAAATAGCTGCATAAATTCATGATAAATTTTATCTTTAAAAAAAAATCCTATACTATATACACTGAAAAACCCTAGATCCCGTGACAGGCAGTGAGCATAAAGTTGATTTGGTATTTAAATGAGATACATATAAAACACAACTCTCTGGCATATGAGATATTAATGGTGCTCTGAAATGGAAAAATACAAATTCAAGTAAATTTGGGAAATTCTGAATTTCCCTCTTGGAGGTTACATTTTATGTTATATGTTAAATGTTCTGGAAAAGTCAGTGAAGCAACCTAAAACATTTTAGCACAGTGGCTGTCCGGAACCCTTT... |
Task1_train_34997 | This mutation on Chromosome 3 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CAGAAAGACTTTTAAAAACTGTGTTGTGTAGAATCACTTCCCCATAAACACAAGATGAGCTGGGCAGCTAGTTGCTGTCAGAATACCACTGAGGAACACTCACACCTCCTGAAGATGTCTAATTTTTTTAACTCCTCTGATTATTGGAAAGCTCTTTGTTATTTTGAGCTAAAATTTCTCTGTATGTAACTTCTCCTTATTGGTTTTCTTTATTTCCTTGGCAGATTCAAGGAGGTAATGGCCATTTTTTTCTGAAGTCCCAGTCCCAGTTAACCTACTAAGTCCTACATATTGGTCAGGATGAAGGTCAGAGCATCTAT... | CAGAAAGACTTTTAAAAACTGTGTTGTGTAGAATCACTTCCCCATAAACACAAGATGAGCTGGGCAGCTAGTTGCTGTCAGAATACCACTGAGGAACACTCACACCTCCTGAAGATGTCTAATTTTTTTAACTCCTCTGATTATTGGAAAGCTCTTTGTTATTTTGAGCTAAAATTTCTCTGTATGTAACTTCTCCTTATTGGTTTTCTTTATTTCCTTGGCAGATTCAAGGAGGTAATGGCCATTTTTTTCTGAAGTCCCAGTCCCAGTTAACCTACTAAGTCCTACATATTGGTCAGGATGAAGGTCAGAGCATCTAT... |
Task1_train_34998 | Chromosome 3 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AAAGCAAATGCTTGGCTTTTTCAGGACCTCCTGCTTCCTGGGCAGGAAGCATTTCCTAAGATAAGCACTGGAAAGTCTCTGAGATGAAAGTCCATCCTCTCATTTTGCAGGGGGTAAGGAAGCCAAGGCTCCAAGCAGAAGACCATCTTATTTGAGATGAGTGCCTGAGCCAAGTCCTGATATTTTCCACCAGCACCCTGACTTATTTGCCCCCAGTTAAACTAATTTCAGACAATTCACTTACTAGTAAAGGGTTGAAATGTCCACTCGCTTATCCTGGATTCACTAAAGGTCTCCAGACGGTACTAAAAGGAAAAAAA... | AAAGCAAATGCTTGGCTTTTTCAGGACCTCCTGCTTCCTGGGCAGGAAGCATTTCCTAAGATAAGCACTGGAAAGTCTCTGAGATGAAAGTCCATCCTCTCATTTTGCAGGGGGTAAGGAAGCCAAGGCTCCAAGCAGAAGACCATCTTATTTGAGATGAGTGCCTGAGCCAAGTCCTGATATTTTCCACCAGCACCCTGACTTATTTGCCCCCAGTTAAACTAATTTCAGACAATTCACTTACTAGTAAAGGGTTGAAATGTCCACTCGCTTATCCTGGATTCACTAAAGGTCTCCAGACGGTACTAAAAGGAAAAAAA... |
Task1_train_34999 | Given a variant located on Chromosome 3, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCTCCCTGATATCAAGATCTTCCTTCTTGATCTTCATCCATAGGGTGACAGAATGGGAAGAGGTCTTGGACATCACTTGCCCTCTCCTTTTACATGTGAGGAAATGGAGGCTCAGAGAGGTCAGCTGACTTGCCCAAGGTCACACAGCCACACAGTGGCCTCTTCTTTCAGATTCCTGCTCTAACCACTGCCTGCAAGTGATTATGTGCTCCTCAGAGGGTGGCTGGATGAGCAGCACTAGAAAATGTGACTGTAAAAGCTGCTCCTCTGCTCTGTCAATACAGGAGACAGAAGTGCCTGTCAGAGGCAGGACTTCCCTG... | TCTCCCTGATATCAAGATCTTCCTTCTTGATCTTCATCCATAGGGTGACAGAATGGGAAGAGGTCTTGGACATCACTTGCCCTCTCCTTTTACATGTGAGGAAATGGAGGCTCAGAGAGGTCAGCTGACTTGCCCAAGGTCACACAGCCACACAGTGGCCTCTTCTTTCAGATTCCTGCTCTAACCACTGCCTGCAAGTGATTATGTGCTCCTCAGAGGGTGGCTGGATGAGCAGCACTAGAAAATGTGACTGTAAAAGCTGCTCCTCTGCTCTGTCAATACAGGAGACAGAAGTGCCTGTCAGAGGCAGGACTTCCCTG... |
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