Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.149378166C>ACA16042629TAB2n.666C>A
c.251C>A (p.Ser84Ter)
c.-96-506C>A (n.-96-506C>A)
c.29C>A (p.Ser10Ter)
c.155C>A (p.Ser52Ter)
ClinVar dbSNP
6g.149378166C>TCA365993159TAB2n.666C>T
c.251C>T (p.Ser84Leu)
c.-96-506C>T (n.-96-506C>T)
c.29C>T (p.Ser10Leu)
c.155C>T (p.Ser52Leu)
ClinVar dbSNP
6g.149378166C=CA1671914789TAB2n.666C=
c.251C= (p.Ser84=)
c.-96-506C= (n.-96-506C=)
c.29C= (p.Ser10=)
c.155C= (p.Ser52=)
dbSNP

Number of alleles fetched