Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.105275794A>GCA162228TET2,TET2-AS1c.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
4g.105275794A>TCA162231TET2,TET2-AS1c.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
4g.105275794A>CCA357815132TET2,TET2-AS1c.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

Number of alleles fetched