Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.17219021G>A | CA224146 | FLCN | c.1060C>T (p.Gln354Ter) c.182C>T (p.Ala61Val) n.83C>T c.1114C>T (p.Gln372Ter) c.838C>T (p.Gln280Ter) n.2454C>T n.1618C>T | ClinVar dbSNP |
17 | g.17219021G= | CA2250418953 | FLCN | c.1060C= (p.Gln354=) c.182C= (p.Ala61=) n.83C= c.1114C= (p.Gln372=) c.838C= (p.Gln280=) n.2454C= n.1618C= | dbSNP |