Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.74114349C>TCA273293VCLc.3115C>T (p.Gln1039Ter)
c.2911C>T (p.Gln971Ter)
c.2131C>T (p.Gln711Ter)
n.5714C>T
c.*2870C>T (n.*2870C>T)
c.3118C>T (p.Gln1040Ter)
c.2914C>T (p.Gln972Ter)
ClinVar dbSNP
10g.74114349C=CA1919906793VCLc.3115C= (p.Gln1039=)
c.2911C= (p.Gln971=)
c.2131C= (p.Gln711=)
n.5714C=
c.*2870C= (n.*2870C=)
c.3118C= (p.Gln1040=)
c.2914C= (p.Gln972=)
dbSNP

Number of alleles fetched