| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.68839723C>T | CA16043924 | EFNB1 | c.466C>T (p.Arg156Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| X | g.68839723C>G | CA413438015 | EFNB1 | c.466C>G (p.Arg156Gly) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.68839723C= | CA2435564170 | EFNB1 | c.466C= (p.Arg156=) | dbSNP |