| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.80663133G>A | CA4315238 | CD36 | c.573G>A (p.Pro191=) c.*85G>A (n.*85G>A) c.345G>A (p.Pro115=) c.430-1273G>A (n.430-1273G>A) n.752G>A c.471G>A (p.Pro157=) c.108G>A (p.Pro36=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.80663133G= | CA1720373049 | CD36 | c.573G= (p.Pro191=) c.*85G= (n.*85G=) c.345G= (p.Pro115=) c.430-1273G= (n.430-1273G=) n.752G= c.471G= (p.Pro157=) c.108G= (p.Pro36=) | dbSNP |