| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.172665636A>G | CA341738 | FASLG | c.466A>G (p.Arg156Gly) c.*36A>G (n.*36A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.172665636A>T | CA343805913 | FASLG | c.466A>T (p.Arg156Trp) c.*36A>T (n.*36A>T) | dbSNP gnomAD v4 |
| 1 | g.172665636A= | CA1141189172 | FASLG | c.466A= (p.Arg156=) c.*36A= (n.*36A=) | dbSNP |