Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.112775676G>CCA16022349APCc.470G>C (p.Trp157Ser)
n.526G>C
c.*476G>C (n.*476G>C)
c.500G>C (p.Trp167Ser)
c.395G>C (p.Trp132Ser)
c.293G>C (p.Trp98Ser)
c.-566G>C (n.-566G>C)
dbSNP
5g.112775676G>ACA009701APCc.470G>A (p.Trp157Ter)
n.526G>A
c.*476G>A (n.*476G>A)
c.500G>A (p.Trp167Ter)
c.395G>A (p.Trp132Ter)
c.293G>A (p.Trp98Ter)
c.-566G>A (n.-566G>A)
ClinVar dbSNP

Number of alleles fetched