Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.33743212C>TCA16620686ASXL3c.3367C>T (p.Gln1123Ter)
c.3364C>T (p.Gln1122Ter)
c.*2488C>T (n.*2488C>T)
c.*3023C>T (n.*3023C>T)
c.3576C>T (n.3576C>T)
c.3196C>T (p.Gln1066Ter)
c.3244C>T (p.Gln1082Ter)
c.3340C>T (p.Gln1114Ter)
c.3286C>T (p.Gln1096Ter)
c.3247C>T (p.Gln1083Ter)
c.328C>T (p.Gln110Ter)
ClinVar dbSNP
18g.33743212C=CA2294857605ASXL3c.3367C= (p.Gln1123=)
c.3364C= (p.Gln1122=)
c.*2488C= (n.*2488C=)
c.*3023C= (n.*3023C=)
c.3576C= (n.3576C=)
c.3196C= (p.Gln1066=)
c.3244C= (p.Gln1082=)
c.3340C= (p.Gln1114=)
c.3286C= (p.Gln1096=)
c.3247C= (p.Gln1083=)
c.328C= (p.Gln110=)
dbSNP

Number of alleles fetched