Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.170998308C>ACA355485898SLC2A2c.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
3g.170998308C>TCA019998SLC2A2c.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

Number of alleles fetched