Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.33744208C>T | CA16620687 | ASXL3 | c.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 |
18 | g.33744208C= | CA2294858043 | ASXL3 | c.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 |