Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
---|---|---|---|---|---|---|---|
CG42633MI01058 |
| allele with one associated variant | insertion
| ||||
NT_033777.3:g.10782083T>A | variant | SNP
| |||||
NT_033777.3:g.10781233C>T | variant | SNP
| |||||
NT_033777.3:g.10781400T>A | variant | SNP
| |||||
NT_033777.3:g.10781145T>C | variant | SNP
| |||||
NT_033777.3:g.10781102A>G | variant | SNP
| |||||
NT_033777.3:g.10781539G>A | variant | SNP
| |||||
NT_033777.3:g.10781998T>C | variant | SNP
| |||||
NT_033777.3:g.10781836C>T | variant | SNP
| |||||
NT_033777.3:g.10782202C>A | variant | SNP
|