Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.34370557C>T | CA117924 | KCNE2 | c.79C>T (p.Arg27Cys) n.764G>A n.885G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.34370557C>A | CA410196238 | KCNE2 | c.79C>A (p.Arg27Ser) n.764G>T n.885G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
21 | g.34370557C= | CA2387099295 | KCNE2 | c.79C= (p.Arg27=) n.764G= n.885G= | dbSNP |