Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.119670121T>C | CA282467 | BAG3 | c.451T>C (p.Cys151Arg) c.277T>C (p.Cys93Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.119670121T>G | CA378295122 | BAG3 | c.451T>G (p.Cys151Gly) c.277T>G (p.Cys93Gly) | dbSNP gnomAD v4 |
10 | g.119670121T= | CA1630848510 | BAG3 | c.451T= (p.Cys151=) c.277T= (p.Cys93=) | dbSNP |