Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.142875713G>TCA213652CYP11B1,GMLc.1120C>A (p.Arg374=)
c.1198C>A (p.Arg400=)
c.937C>A (p.Arg313=)
c.214+34488G>T (p.=)
n.1515C>A
c.1333C>A (p.Arg445=)
n.85C>A (p.Arg29=)
c.181+34488G>T (p.=)
ClinVar dbSNP ExAC gnomAD
8g.142875713G>ACA213654CYP11B1,GMLc.1120C>T (p.Arg374Trp)
c.1198C>T (p.Arg400Trp)
c.937C>T (p.Arg313Trp)
c.214+34488G>A (p.=)
n.1515C>T
c.1333C>T (p.Arg445Trp)
n.85C>T (p.Arg29Trp)
c.181+34488G>A (p.=)
ClinVar dbSNP ExAC gnomAD COSMIC

Number of alleles fetched