Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.133951305C>T | CA129009 | SLCO2A1 | c.764G>A (p.Gly255Glu) n.521-2605G>A n.1026G>A c.536G>A (p.Gly179Glu) c.260G>A (p.Gly87Glu) | ClinVar dbSNP gnomAD v4 |
3 | g.133951305C= | CA1403200187 | SLCO2A1 | c.764G= (p.Gly255=) n.521-2605G= n.1026G= c.536G= (p.Gly179=) c.260G= (p.Gly87=) | dbSNP |