Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.105275794A>G | CA162228 | TET2,TET2-AS1 | c.5284A>G (p.Ile1762Val) c.*1608A>G (n.*1608A>G) c.5347A>G (p.Ile1783Val) n.318+58592T>C c.4984A>G (p.Ile1662Val) c.1795A>G (p.Ile599Val) n.5186A>G n.5489A>G n.5221A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.105275794A>T | CA162231 | TET2,TET2-AS1 | c.5284A>T (p.Ile1762Leu) c.*1608A>T (n.*1608A>T) c.5347A>T (p.Ile1783Leu) n.318+58592T>A c.4984A>T (p.Ile1662Leu) c.1795A>T (p.Ile599Leu) n.5186A>T n.5489A>T n.5221A>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.105275794A>C | CA357815132 | TET2,TET2-AS1 | c.5284A>C (p.Ile1762Leu) c.*1608A>C (n.*1608A>C) c.5347A>C (p.Ile1783Leu) n.318+58592T>G c.4984A>C (p.Ile1662Leu) c.1795A>C (p.Ile599Leu) n.5186A>C n.5489A>C n.5221A>C | dbSNP |