| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 21 | g.42388436G>T | CA261815 | TMPRSS3 | c.413C>A (p.Ala138Glu) c.407C>A (p.Ala136Glu) n.281C>A n.700C>A c.32C>A (p.Ala11Glu) n.1369C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 21 | g.42388436G>A | CA410375346 | TMPRSS3 | c.413C>T (p.Ala138Val) c.407C>T (p.Ala136Val) n.281C>T n.700C>T c.32C>T (p.Ala11Val) n.1369C>T | dbSNP gnomAD v3 gnomAD v4 |