| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.2583545G>T | CA472038461 | KCNQ1 | c.771G>T (p.Ala257=) c.588G>T (p.Ala196=) c.1032G>T (p.Ala344=) c.651G>T (p.Ala217=) c.234G>T (p.Ala78=) | ClinVar dbSNP |
| 11 | g.2583545G>C | CA005015 | KCNQ1 | c.771G>C (p.Ala257=) c.588G>C (p.Ala196=) c.1032G>C (p.Ala344=) c.651G>C (p.Ala217=) c.234G>C (p.Ala78=) | ClinVar dbSNP |
| 11 | g.2583545G>A | CA005005 | KCNQ1 | c.771G>A (p.Ala257=) c.588G>A (p.Ala196=) c.1032G>A (p.Ala344=) c.651G>A (p.Ala217=) c.234G>A (p.Ala78=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |