Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.112088972A>GCA016709SDHDc.275A>G (p.Asp92Gly)
c.*347A>G (n.*347A>G)
c.158A>G (p.Asp53Gly)
n.280A>G
c.169+999A>G (n.169+999A>G)
c.265A>G
c.106A>G
n.359A>G
n.310A>G
ClinVar dbSNP
11g.112088972A>TCA16619272SDHDc.275A>T (p.Asp92Val)
c.*347A>T (n.*347A>T)
c.158A>T (p.Asp53Val)
n.280A>T
c.169+999A>T (n.169+999A>T)
c.265A>T
c.106A>T
n.359A>T
n.310A>T
ClinVar dbSNP

Number of alleles fetched