Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.105275794A>GCA162228TET2c.*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
4g.105275794A>TCA162231TET2c.*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

Number of alleles fetched