Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
Y | g.12778040C>T | CA10573193 | USP9Y | c.2661C>T (p.Leu887=) n.2673C>T c.2427C>T (p.Leu809=) c.2676C>T (p.Leu892=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
Y | g.12778040C= | CA2470557526 | USP9Y | c.2661C= (p.Leu887=) n.2673C= c.2427C= (p.Leu809=) c.2676C= (p.Leu892=) | dbSNP |