| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.6645324C>T | CA372886699 | GLDC | c.176G>A (p.Arg59Lys) c.335C>T (p.Ser112Phe) | ClinVar dbSNP |
| 9 | g.6645324C>G | CA263308 | GLDC | c.176G>C (p.Arg59Thr) c.335C>G (p.Ser112Cys) | ClinVar dbSNP gnomAD v4 |
| 9 | g.6645324C= | CA1830571142 | GLDC | c.176G= (p.Arg59=) c.335C= (p.Ser112=) | dbSNP |