Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.119278256T>CCA128668CBLc.*638T>C (n.*638T>C)
c.1186T>C (p.Cys396Arg)
c.1180T>C (p.Cys394Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
11g.119278256T>ACA382912715CBLc.*638T>A (n.*638T>A)
c.1186T>A (p.Cys396Ser)
c.1180T>A (p.Cys394Ser)
dbSNP gnomAD v4
11g.119278256T>GCA382912721CBLc.*638T>G (n.*638T>G)
c.1186T>G (p.Cys396Gly)
c.1180T>G (p.Cys394Gly)
dbSNP gnomAD v4 COSMIC
11g.119278256T=CA2003905990CBLc.*638T= (n.*638T=)
c.1186T= (p.Cys396=)
c.1180T= (p.Cys394=)
dbSNP

Number of alleles fetched