Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.18297801G>TCA409848870TMPRSS15c.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
21g.18297801G>ACA9984161TMPRSS15c.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
21g.18297801G=CA2379744571TMPRSS15c.2194C= (p.Pro732=)
c.2329C= (p.Pro777=)
c.2284C= (p.Pro762=)
c.2248C= (p.Pro750=)
c.2239C= (p.Pro747=)
ClinVar dbSNP

Number of alleles fetched