Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.18297801G>T | CA409848870 | TMPRSS15 | c.2194C>A (p.Pro732Thr) c.2329C>A (p.Pro777Thr) c.2284C>A (p.Pro762Thr) c.2248C>A (p.Pro750Thr) c.2239C>A (p.Pro747Thr) | dbSNP |
21 | g.18297801G>A | CA9984161 | TMPRSS15 | c.2194C>T (p.Pro732Ser) c.2329C>T (p.Pro777Ser) c.2284C>T (p.Pro762Ser) c.2248C>T (p.Pro750Ser) c.2239C>T (p.Pro747Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |