Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.92645436C>TCA10654918KIF11c.2341C>T (p.Gln781Ter)
c.*859C>T (n.*859C>T)
c.2134C>T (p.Gln712Ter)
c.*315C>T (n.*315C>T)
ClinVar dbSNP
10g.92645436C=CA1928269248KIF11c.2341C= (p.Gln781=)
c.*859C= (n.*859C=)
c.2134C= (p.Gln712=)
c.*315C= (n.*315C=)
dbSNP
10g.92645436C>GCA377594009KIF11c.2341C>G (p.Gln781Glu)
c.*859C>G (n.*859C>G)
c.2134C>G (p.Gln712Glu)
c.*315C>G (n.*315C>G)
ClinVar dbSNP gnomAD v4 COSMIC

Number of alleles fetched