Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.122284922A>G | CA203219 | CASR | c.2737A>G (p.Arg913Gly) c.2998A>G (p.Arg1000Gly) c.2968A>G (p.Arg990Gly) c.2485A>G (p.Arg829Gly) c.2380A>G (p.Arg794Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122284922A= | CA1397873076 | CASR | c.2737A= (p.Arg913=) c.2998A= (p.Arg1000=) c.2968A= (p.Arg990=) c.2485A= (p.Arg829=) c.2380A= (p.Arg794=) | dbSNP |