| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.7325356T>A | CA121120 | STS | c.1099T>A (p.Trp367Arg) n.1339T>A c.961T>A (p.Trp321Arg) c.1114T>A (p.Trp372Arg) c.1135T>A (p.Trp379Arg) | ClinVar dbSNP |
| X | g.7325356T= | CA2414189592 | STS | c.1099T= (p.Trp367=) n.1339T= c.961T= (p.Trp321=) c.1114T= (p.Trp372=) c.1135T= (p.Trp379=) | dbSNP |