Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.18359856G>A | CA116670 | TMPRSS15 | c.781C>T (p.Gln261Ter) c.916C>T (p.Gln306Ter) c.871C>T (p.Gln291Ter) c.835C>T (p.Gln279Ter) c.826C>T (p.Gln276Ter) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
21 | g.18359856G>C | CA409852110 | TMPRSS15 | c.781C>G (p.Gln261Glu) c.916C>G (p.Gln306Glu) c.871C>G (p.Gln291Glu) c.835C>G (p.Gln279Glu) c.826C>G (p.Gln276Glu) | dbSNP gnomAD v3 gnomAD v4 |