Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.124398082A>GCA113987OATc.1180T>C (p.Cys394Arg)
n.690T>C
c.766T>C (p.Cys256Arg)
c.859T>C (p.Cys287Arg)
c.580T>C (p.Cys194Arg)
ClinVar dbSNP gnomAD v4 COSMIC
10g.124398082A=CA1942335692OATc.1180T= (p.Cys394=)
n.690T=
c.766T= (p.Cys256=)
c.859T= (p.Cys287=)
c.580T= (p.Cys194=)
dbSNP

Number of alleles fetched