| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.49622053A>G | CA254037 | MGAT2 | c.785A>G (p.His262Arg) | ClinVar dbSNP |
| 14 | g.49622053A= | CA2135804791 | MGAT2 | c.785A= (p.His262=) | dbSNP |
| 14 | g.49622053A>C | CA389620447 | MGAT2 | c.785A>C (p.His262Pro) | dbSNP gnomAD v4 |