Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.53339808G>A | CA8967136 | DCC | c.2260G>A (p.Val754Met) c.2061G>A c.2191G>A (p.Val731Met) c.1225G>A (p.Val409Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
18 | g.53339808G>C | CA402469432 | DCC | c.2260G>C (p.Val754Leu) c.2061G>C c.2191G>C (p.Val731Leu) c.1225G>C (p.Val409Leu) | dbSNP |