| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.80169007C>T | CA210332498 | ANXA11 | c.523G>A (p.Gly175Arg) c.424G>A (p.Gly142Arg) n.81G>A c.823G>A (p.Gly275Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.80169007C>A | CA5576260 | ANXA11 | c.523G>T (p.Gly175Trp) c.424G>T (p.Gly142Trp) n.81G>T c.823G>T (p.Gly275Trp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |