Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.124500689C>TCA122717NR5A1c.271G>A (p.Gly91Ser)
c.39+259G>A (n.39+259G>A)
c.10G>A (p.Gly4Ser)
 ClinVar dbSNP
9g.124500689C=CA1878469631NR5A1c.271G= (p.Gly91=)
c.39+259G= (n.39+259G=)
c.10G= (p.Gly4=)
 dbSNP

Number of alleles fetched