| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.80671133T>G | CA4315506 | CD36 | c.975T>G (p.Tyr325Ter) c.858T>G (p.Tyr286Ter) n.1757T>G c.747T>G (p.Tyr249Ter) c.795T>G (p.Tyr265Ter) c.819-789T>G (n.819-789T>G) n.998-789T>G c.873T>G (p.Tyr291Ter) c.510T>G (p.Tyr170Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.80671133T= | CA1720370787 | CD36 | c.975T= (p.Tyr325=) c.858T= (p.Tyr286=) n.1757T= c.747T= (p.Tyr249=) c.795T= (p.Tyr265=) c.819-789T= (n.819-789T=) n.998-789T= c.873T= (p.Tyr291=) c.510T= (p.Tyr170=) | dbSNP |