| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.7325357G>C | CA121123 | STS | c.1100G>C (p.Trp367Ser) n.1340G>C c.962G>C (p.Trp321Ser) c.1115G>C (p.Trp372Ser) c.1136G>C (p.Trp379Ser) | ClinVar dbSNP gnomAD v4 |
| X | g.7325357G>A | CA412022355 | STS | c.1100G>A (p.Trp367Ter) n.1340G>A c.962G>A (p.Trp321Ter) c.1115G>A (p.Trp372Ter) c.1136G>A (p.Trp379Ter) | dbSNP gnomAD v4 |
| X | g.7325357G>T | CA412022356 | STS | c.1100G>T (p.Trp367Leu) n.1340G>T c.962G>T (p.Trp321Leu) c.1115G>T (p.Trp372Leu) c.1136G>T (p.Trp379Leu) | dbSNP gnomAD v4 |
| X | g.7325357G= | CA2414189593 | STS | c.1100G= (p.Trp367=) n.1340G= c.962G= (p.Trp321=) c.1115G= (p.Trp372=) c.1136G= (p.Trp379=) | dbSNP |