Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.33744208C>TCA16620687ASXL3c.4363C>T (p.Gln1455Ter)
c.4360C>T (p.Gln1454Ter)
c.4240C>T (p.Gln1414Ter)
c.4336C>T (p.Gln1446Ter)
c.4282C>T (p.Gln1428Ter)
c.4243C>T (p.Gln1415Ter)
c.4192C>T (p.Gln1398Ter)
c.1324C>T (p.Gln442Ter)
ClinVar dbSNP
18g.33744208C=CA2294858043ASXL3c.4363C= (p.Gln1455=)
c.4360C= (p.Gln1454=)
c.4240C= (p.Gln1414=)
c.4336C= (p.Gln1446=)
c.4282C= (p.Gln1428=)
c.4243C= (p.Gln1415=)
c.4192C= (p.Gln1398=)
c.1324C= (p.Gln442=)
dbSNP

Number of alleles fetched