Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.152328232C>ACA16602854FBXW7c.*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
4g.152328232C>TCA16602852FBXW7c.*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
4g.152328232C>GCA16602853FBXW7c.*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

Number of alleles fetched