Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.18359856G>ACA116670TMPRSS15c.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
21g.18359856G>CCA409852110TMPRSS15c.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
21g.18359856G>TCA409852111TMPRSS15c.781C>A (p.Gln261Lys)
c.916C>A (p.Gln306Lys)
c.871C>A (p.Gln291Lys)
c.835C>A (p.Gln279Lys)
c.826C>A (p.Gln276Lys)
dbSNP gnomAD v4
21g.18359856G=CA2379773825TMPRSS15c.781C= (p.Gln261=)
c.916C= (p.Gln306=)
c.871C= (p.Gln291=)
c.835C= (p.Gln279=)
c.826C= (p.Gln276=)
dbSNP

Number of alleles fetched