Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.32807793G>A | CA118461 | DNMT3B | c.*1403G>A (n.*1403G>A) c.2263G>A (p.Val755Met) c.*1006G>A (n.*1006G>A) c.*1195G>A (n.*1195G>A) c.2233G>A (p.Val745Met) n.477G>A c.2428G>A (p.Val810Met) c.2452G>A (p.Val818Met) c.2203G>A (p.Val735Met) c.2392G>A (p.Val798Met) c.2077G>A (p.Val693Met) c.1975G>A (p.Val659Met) c.2239G>A (p.Val747Met) c.2113G>A (p.Val705Met) n.2230G>A n.2241G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
20 | g.32807793G>T | CA9810922 | DNMT3B | c.*1403G>T (n.*1403G>T) c.2263G>T (p.Val755Leu) c.*1006G>T (n.*1006G>T) c.*1195G>T (n.*1195G>T) c.2233G>T (p.Val745Leu) n.477G>T c.2428G>T (p.Val810Leu) c.2452G>T (p.Val818Leu) c.2203G>T (p.Val735Leu) c.2392G>T (p.Val798Leu) c.2077G>T (p.Val693Leu) c.1975G>T (p.Val659Leu) c.2239G>T (p.Val747Leu) c.2113G>T (p.Val705Leu) n.2230G>T n.2241G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |