Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.45967788G>A | CA214980 | FYCO1 | c.1546C>T (p.Gln516Ter) n.1761C>T c.1426C>T (p.Gln476Ter) c.1402C>T (p.Gln468Ter) c.946C>T (p.Gln316Ter) | ClinVar dbSNP |
3 | g.45967788G= | CA1361904917 | FYCO1 | c.1546C= (p.Gln516=) n.1761C= c.1426C= (p.Gln476=) c.1402C= (p.Gln468=) c.946C= (p.Gln316=) | dbSNP |