| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.49621979G>A | CA486349797 | MGAT2 | c.711G>A (p.Lys237=) | dbSNP gnomAD v4 |
| 14 | g.49621979G>C | CA249931 | MGAT2 | c.711G>C (p.Lys237Asn) | ClinVar dbSNP |
| 14 | g.49621979G= | CA2135804761 | MGAT2 | c.711G= (p.Lys237=) | dbSNP |