Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.44406196G>ACA16043128HNF4Ac.188G>A (p.Arg63Gln)
c.254G>A (p.Arg85Gln)
c.228G>A
c.230G>A (p.Arg77Gln)
c.207G>A
n.230G>A
c.211G>A (p.Gly71Arg)
c.*21G>A (n.*21G>A)
c.179G>A (p.Arg60Gln)
c.233G>A (p.Arg78Gln)
c.371G>A (p.Arg124Gln)
c.302G>A (p.Arg101Gln)
ClinVar dbSNP COSMIC COSMIC COSMIC
20g.44406196G=CA2365758039HNF4Ac.188G= (p.Arg63=)
c.254G= (p.Arg85=)
c.228G=
c.230G= (p.Arg77=)
c.207G=
n.230G=
c.211G= (p.Gly71=)
c.*21G= (n.*21G=)
c.179G= (p.Arg60=)
c.233G= (p.Arg78=)
c.371G= (p.Arg124=)
c.302G= (p.Arg101=)
dbSNP

Number of alleles fetched