Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.25245346G>TCA176496KRASc.39C>A (p.Gly13=)
c.-88+5405C>A (n.-88+5405C>A)
ClinVar dbSNP COSMIC
12g.25245346G>ACA135576KRASc.39C>T (p.Gly13=)
c.-88+5405C>T (n.-88+5405C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC

Number of alleles fetched