Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.67811606C>TCA209166007DNAJC12c.215G>A (p.Arg72Gln)
c.*234G>A (n.*234G>A)
c.*135G>A (n.*135G>A)
c.305G>A (p.Arg102Gln)
c.245G>A (p.Arg82Gln)
c.-32G>A (n.-32G>A)
dbSNP gnomAD v4
10g.67811606C>GCA16609234DNAJC12c.215G>C (p.Arg72Pro)
c.*234G>C (n.*234G>C)
c.*135G>C (n.*135G>C)
c.305G>C (p.Arg102Pro)
c.245G>C (p.Arg82Pro)
c.-32G>C (n.-32G>C)
ClinVar dbSNP COSMIC COSMIC
10g.67811606C>ACA377098709DNAJC12c.215G>T (p.Arg72Leu)
c.*234G>T (n.*234G>T)
c.*135G>T (n.*135G>T)
c.305G>T (p.Arg102Leu)
c.245G>T (p.Arg82Leu)
c.-32G>T (n.-32G>T)
dbSNP gnomAD v4
10g.67811606C=CA1917049497DNAJC12c.215G= (p.Arg72=)
c.*234G= (n.*234G=)
c.*135G= (n.*135G=)
c.305G= (p.Arg102=)
c.245G= (p.Arg82=)
c.-32G= (n.-32G=)
dbSNP

Number of alleles fetched