Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.25209907A>GCA384148531KRASc.116T>C (p.Val39Ala)
c.455T>C (p.Val152Ala)
c.*426T>C (n.*426T>C)
c.*153T>C (n.*153T>C)
n.929T>C
c.258T>C
c.*416T>C (n.*416T>C)
c.257T>C (p.Val86Ala)
c.380T>C (p.Val127Ala)
c.*9T>C (n.*9T>C)
dbSNP gnomAD v3 gnomAD v4
12g.25209907A>CCA256482KRASc.116T>G (p.Val39Gly)
c.455T>G (p.Val152Gly)
c.*426T>G (n.*426T>G)
c.*153T>G (n.*153T>G)
n.929T>G
c.258T>G
c.*416T>G (n.*416T>G)
c.257T>G (p.Val86Gly)
c.380T>G (p.Val127Gly)
c.*9T>G (n.*9T>G)
ClinVar dbSNP

Number of alleles fetched