Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.25245350C>G | CA135567 | KRAS | c.35G>C (p.Gly12Ala) c.-88+5401G>C (n.-88+5401G>C) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
12 | g.25245350C>T | CA122538 | KRAS | c.35G>A (p.Gly12Asp) c.-88+5401G>A (n.-88+5401G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
12 | g.25245350C>A | CA122540 | KRAS | c.35G>T (p.Gly12Val) c.-88+5401G>T (n.-88+5401G>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |