Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.16148915T>C | CA338642677 | EPHA2 | c.286A>G (p.Ile96Val) n.338A>G c.124A>G (p.Ile42Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.16148915T>A | CA18343189 | EPHA2 | c.286A>T (p.Ile96Phe) n.338A>T c.124A>T (p.Ile42Phe) | dbSNP |