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| Term | SNV | ID (Ontology) | SO:0001483 (Sequence Ontology) |
| Definition | SNVs are single nucleotide positions in genomic DNA at which different sequence alternatives exist. | ||
| Also Known As | "single nucleotide variant" | ||
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| SO.org | |||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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sequence_alteration__ biological_region____| substitution |__SNV 6814 rec. |__point_mutation 6814 rec. |__SNP |__transition | |__purine_transition(+) | |__pyrimidine_transition(+) |__transversion |__purine_to_pyrimidine_transversion(+) |__pyrimidine_to_purine_transversion(+) |
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| Is a | substitution | ||
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