Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.92645436C>T | CA10654918 | KIF11 | c.2341C>T (p.Gln781Ter) c.*859C>T (n.*859C>T) c.2134C>T (p.Gln712Ter) c.*315C>T (n.*315C>T) | ClinVar dbSNP |
10 | g.92645436C= | CA1928269248 | KIF11 | c.2341C= (p.Gln781=) c.*859C= (n.*859C=) c.2134C= (p.Gln712=) c.*315C= (n.*315C=) | dbSNP |
10 | g.92645436C>G | CA377594009 | KIF11 | c.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 |