| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.111776247C>T | CA052108 | KCND3 | c.1798G>A (p.Gly600Arg) c.1741G>A (p.Gly581Arg) c.*17G>A (n.*17G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 1 | g.111776247C>A | CA341655689 | KCND3 | c.1798G>T (p.Gly600Ter) c.1741G>T (p.Gly581Ter) c.*17G>T (n.*17G>T) | dbSNP |