| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.152328233G>C | CA16602855 | FBXW7 | c.*86C>G (n.*86C>G) c.892C>G (p.Arg298Gly) c.1393C>G (p.Arg465Gly) c.*1040C>G (n.*1040C>G) c.*369C>G (n.*369C>G) c.1039C>G (p.Arg347Gly) c.1153C>G (p.Arg385Gly) n.942C>G c.865C>G (p.Arg289Gly) n.841C>G n.580C>G c.1309C>G (p.Arg437Gly) | ClinVar dbSNP |
| 4 | g.152328233G>A | CA16602851 | FBXW7 | c.*86C>T (n.*86C>T) c.892C>T (p.Arg298Cys) c.1393C>T (p.Arg465Cys) c.*1040C>T (n.*1040C>T) c.*369C>T (n.*369C>T) c.1039C>T (p.Arg347Cys) c.1153C>T (p.Arg385Cys) n.942C>T c.865C>T (p.Arg289Cys) n.841C>T n.580C>T c.1309C>T (p.Arg437Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
| 4 | g.152328233G>T | CA358618757 | FBXW7 | c.*86C>A (n.*86C>A) c.892C>A (p.Arg298Ser) c.1393C>A (p.Arg465Ser) c.*1040C>A (n.*1040C>A) c.*369C>A (n.*369C>A) c.1039C>A (p.Arg347Ser) c.1153C>A (p.Arg385Ser) n.942C>A c.865C>A (p.Arg289Ser) n.841C>A n.580C>A c.1309C>A (p.Arg437Ser) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |