Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.152328232C>A | CA16602854 | FBXW7 | c.*87G>T (n.*87G>T) c.893G>T (p.Arg298Leu) c.1394G>T (p.Arg465Leu) c.*1041G>T (n.*1041G>T) c.*370G>T (n.*370G>T) c.1040G>T (p.Arg347Leu) c.1154G>T (p.Arg385Leu) n.943G>T c.866G>T (p.Arg289Leu) n.842G>T n.581G>T c.1310G>T (p.Arg437Leu) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
4 | g.152328232C>T | CA16602852 | FBXW7 | c.*87G>A (n.*87G>A) c.893G>A (p.Arg298His) c.1394G>A (p.Arg465His) c.*1041G>A (n.*1041G>A) c.*370G>A (n.*370G>A) c.1040G>A (p.Arg347His) c.1154G>A (p.Arg385His) n.943G>A c.866G>A (p.Arg289His) n.842G>A n.581G>A c.1310G>A (p.Arg437His) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
4 | g.152328232C>G | CA16602853 | FBXW7 | c.*87G>C (n.*87G>C) c.893G>C (p.Arg298Pro) c.1394G>C (p.Arg465Pro) c.*1041G>C (n.*1041G>C) c.*370G>C (n.*370G>C) c.1040G>C (p.Arg347Pro) c.1154G>C (p.Arg385Pro) n.943G>C c.866G>C (p.Arg289Pro) n.842G>C n.581G>C c.1310G>C (p.Arg437Pro) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |