| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.2583535C>T | CA004897 | KCNQ1 | c.761C>T (p.Ala254Val) c.578C>T (p.Ala193Val) c.1022C>T (p.Ala341Val) c.641C>T (p.Ala214Val) c.224C>T (p.Ala75Val) | ClinVar dbSNP COSMIC |
| 11 | g.2583535C>A | CA004880 | KCNQ1 | c.761C>A (p.Ala254Glu) c.578C>A (p.Ala193Glu) c.1022C>A (p.Ala341Glu) c.641C>A (p.Ala214Glu) c.224C>A (p.Ala75Glu) | ClinVar dbSNP gnomAD v4 |
| 11 | g.2583535C>G | CA004889 | KCNQ1 | c.761C>G (p.Ala254Gly) c.578C>G (p.Ala193Gly) c.1022C>G (p.Ala341Gly) c.641C>G (p.Ala214Gly) c.224C>G (p.Ala75Gly) | ClinVar dbSNP |