Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.96235528C>TCA5140237HSD17B3c.865G>A (p.Gly289Ser)
c.505G>A (p.Gly169Ser)
c.757G>A (p.Gly253Ser)
c.829G>A (p.Gly277Ser)
c.703G>A (p.Gly235Ser)
n.3337G>A
c.715G>A (p.Gly239Ser)
n.718G>A
n.125G>A
n.424G>A
ClinVar dbSNP ExAC gnomAD COSMIC
9g.96235528C>GCA196609213HSD17B3c.865G>C (p.Gly289Arg)
c.505G>C (p.Gly169Arg)
c.757G>C (p.Gly253Arg)
c.829G>C (p.Gly277Arg)
c.703G>C (p.Gly235Arg)
n.3337G>C
c.715G>C (p.Gly239Arg)
n.718G>C
n.125G>C
n.424G>C
dbSNP
9g.96235528C>ACA196609212HSD17B3c.865G>T (p.Gly289Cys)
c.505G>T (p.Gly169Cys)
c.757G>T (p.Gly253Cys)
c.829G>T (p.Gly277Cys)
c.703G>T (p.Gly235Cys)
n.3337G>T
c.715G>T (p.Gly239Cys)
n.718G>T
n.125G>T
n.424G>T
dbSNP

Number of alleles fetched