Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.33743212C>T | CA16620686 | ASXL3 | c.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 |
18 | g.33743212C= | CA2294857605 | ASXL3 | c.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 |