| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.6645498A>T | CA372887715 | GLDC | c.2T>A (p.Met1Lys) c.509A>T (p.His170Leu) | ClinVar dbSNP |
| 9 | g.6645498A>G | CA256167 | GLDC | c.2T>C (p.Met1Thr) c.509A>G (p.His170Arg) | ClinVar dbSNP gnomAD v4 |
| 9 | g.6645498A= | CA1830571504 | GLDC | c.2T= (p.Met1=) c.509A= (p.His170=) | dbSNP |