Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.74074790dup | CA10576823 | VCL | c.670dup (p.Glu224GlyfsTer17) n.332-26264dup n.628dup c.*425dup (n.*425dup) | ClinVar dbSNP |
10 | g.74074790G= | CA3174152787 | VCL | c.670G= (p.Glu224=) n.332-26264G= n.628G= c.*425G= (n.*425G=) | dbSNP |