Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.152328233G>CCA16602855FBXW7c.*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
4g.152328233G>ACA16602851FBXW7c.*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
4g.152328233G>TCA358618757FBXW7c.*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
4g.152328233G=CA2837997375FBXW7c.*86C= (n.*86C=)
c.892C= (p.Arg298=)
c.1393C= (p.Arg465=)
c.*1040C= (n.*1040C=)
c.*369C= (n.*369C=)
c.1039C= (p.Arg347=)
c.1153C= (p.Arg385=)
n.942C=
c.865C= (p.Arg289=)
n.841C=
n.580C=
c.1309C= (p.Arg437=)
dbSNP dbSNP

Number of alleles fetched