| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.215428331G>C | CA16617467 | FN1 | c.693C>G (p.Cys231Trp) | ClinVar dbSNP |
| 2 | g.215428331G= | CA1327370545 | FN1 | c.693C= (p.Cys231=) | dbSNP |
| 2 | g.215428331G>A | CA431157700 | FN1 | c.693C>T (p.Cys231=) | ClinVar dbSNP gnomAD v4 |