Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94962487G>A | CA211713591 | CYP2C9 | c.820-9617G>A (n.820-9617G>A) c.819+13203G>A (n.819+13203G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94962487G>C | CA1929321892 | CYP2C9 | c.820-9617G>C (n.820-9617G>C) c.819+13203G>C (n.819+13203G>C) | dbSNP |