Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.105275794A>G | CA162228 | TET2 | c.*1608A>G (p.=) c.5284A>G (p.Ile1762Val) c.5347A>G (p.Ile1783Val) c.4984A>G (p.Ile1662Val) c.1795A>G (p.Ile599Val) | ClinVar dbSNP ExAC gnomAD |
4 | g.105275794A>T | CA162231 | TET2 | c.*1608A>T (p.=) c.5284A>T (p.Ile1762Leu) c.5347A>T (p.Ile1783Leu) c.4984A>T (p.Ile1662Leu) c.1795A>T (p.Ile599Leu) | ClinVar dbSNP gnomAD |