Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.136677537G>C | CA375584110 | AGPAT2 | c.202C>G (p.Arg68Gly) n.210C>G | dbSNP gnomAD v4 |
9 | g.136677537G>T | CA467741035 | AGPAT2 | c.202C>A (p.Arg68=) n.210C>A | dbSNP |
9 | g.136677537G>A | CA277942 | AGPAT2 | c.202C>T (p.Arg68Ter) n.210C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |