Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.170998308C>A | CA355485898 | SLC2A2 | c.1259G>T (p.Trp420Leu) c.*726G>T (n.*726G>T) c.902G>T (p.Trp301Leu) c.740G>T (p.Trp247Leu) c.1214G>T (p.Trp405Leu) c.1040G>T (p.Trp347Leu) | dbSNP |
3 | g.170998308C>T | CA019998 | SLC2A2 | c.1259G>A (p.Trp420Ter) c.*726G>A (n.*726G>A) c.902G>A (p.Trp301Ter) c.740G>A (p.Trp247Ter) c.1214G>A (p.Trp405Ter) c.1040G>A (p.Trp347Ter) | ClinVar dbSNP |