Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.171114038G>A | CA343187460 | FMO3 | c.859G>A (p.Glu287Lys) c.670G>A (p.Glu224Lys) c.799G>A (p.Glu267Lys) c.112G>A (p.Glu38Lys) | dbSNP COSMIC |
1 | g.171114038G>T | CA16603456 | FMO3 | c.859G>T (p.Glu287Ter) c.670G>T (p.Glu224Ter) c.799G>T (p.Glu267Ter) c.112G>T (p.Glu38Ter) | ClinVar dbSNP gnomAD v4 |