| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.95544252G>A | CA13948293 | GLRX5 | c.*127G>A (n.*127G>A) n.607G>A c.1391G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.95544252G>T | CA710239574 | GLRX5 | c.*127G>T (n.*127G>T) n.607G>T c.1391G>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.95544252G= | CA2156509659 | GLRX5 | c.*127G= (n.*127G=) n.607G= c.1391G= | dbSNP |