Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.116830819T>A | CA477048259 | APOC3 | c.102T>A (p.Gly34=) c.156T>A (p.Gly52=) n.134T>A | dbSNP gnomAD v4 |
11 | g.116830819T>C | CA6289656 | APOC3 | c.102T>C (p.Gly34=) c.156T>C (p.Gly52=) n.134T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.116830819T= | CA1630855356 | APOC3 | c.102T= (p.Gly34=) c.156T= (p.Gly52=) n.134T= | dbSNP |