| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.186539566C>A | CA126996 | CRYGS | c.53G>T (p.Gly18Val) n.955G>T | ClinVar dbSNP |
| 3 | g.186539566C= | CA1426983570 | CRYGS | c.53G= (p.Gly18=) n.955G= | dbSNP |
| 3 | g.186539566C>T | CA355704934 | CRYGS | c.53G>A (p.Gly18Asp) n.955G>A | ClinVar dbSNP |