Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.119676479C>T | CA10576779 | BAG3 | c.925C>T (p.Arg309Ter) c.748C>T (p.Arg250Ter) c.922C>T (p.Arg308Ter) | ClinVar dbSNP gnomAD v4 |
10 | g.119676479C>G | CA378296277 | BAG3 | c.925C>G (p.Arg309Gly) c.748C>G (p.Arg250Gly) c.922C>G (p.Arg308Gly) | ClinVar dbSNP |
10 | g.119676479C>A | CA471634776 | BAG3 | c.925C>A (p.Arg309=) c.748C>A (p.Arg250=) c.922C>A (p.Arg308=) | dbSNP gnomAD v4 |