| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.2717922C>G | CA149457 | KCNV2 | c.183C>G (p.Gly61=) n.684C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.2717922C>A | CA463853456 | KCNV2 | c.183C>A (p.Gly61=) n.684C>A | dbSNP |
| 9 | g.2717922C>T | CA187970526 | KCNV2 | c.183C>T (p.Gly61=) n.684C>T | ClinVar dbSNP gnomAD v4 |