Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
Y | g.12790481G>A | CA10573265 | USP9Y | c.3636G>A (p.Glu1212=) n.3648G>A c.3402G>A (p.Glu1134=) c.3651G>A (p.Glu1217=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
Y | g.12790481G= | CA2470558128 | USP9Y | c.3636G= (p.Glu1212=) n.3648G= c.3402G= (p.Glu1134=) c.3651G= (p.Glu1217=) | dbSNP |