| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.49524145C>T | CA9903505 | PTGIS | c.768G>A (p.Leu256=) n.589G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49524145C>A | CA315139771 | PTGIS | c.768G>T (p.Leu256=) n.589G>T | dbSNP |
| 20 | g.49524145C>G | CA315139772 | PTGIS | c.768G>C (p.Leu256=) n.589G>C | dbSNP |
| 20 | g.49524145C= | CA2368105290 | PTGIS | c.768G= (p.Leu256=) n.589G= | dbSNP |