Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.74114349C>T | CA273293 | VCL | c.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 |
10 | g.74114349C= | CA1919906793 | VCL | c.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 |