Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.113425552A>G | CA13509989 | DRD2 | c.-31-870T>C (n.-31-870T>C) n.35-870T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.113425552A>T | CA2001152098 | DRD2 | c.-31-870T>A (n.-31-870T>A) n.35-870T>A | dbSNP |