Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.119672373C>T | CA308228 | BAG3 | c.626C>T (p.Pro209Leu) c.452C>T (p.Pro151Leu) | ClinVar dbSNP COSMIC |
10 | g.119672373C>A | CA170913 | BAG3 | c.626C>A (p.Pro209Gln) c.452C>A (p.Pro151Gln) | ClinVar dbSNP |
10 | g.119672373C= | CA1940193308 | BAG3 | c.626C= (p.Pro209=) c.452C= (p.Pro151=) | dbSNP |