Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.25245348C>G | CA122542 | KRAS | c.37G>C (p.Gly13Arg) c.-88+5403G>C (n.-88+5403G>C) | ClinVar dbSNP COSMIC COSMIC |
12 | g.25245348C>A | CA135570 | KRAS | c.37G>T (p.Gly13Cys) c.-88+5403G>T (n.-88+5403G>T) | ClinVar dbSNP gnomAD v2 COSMIC COSMIC |
12 | g.25245348C>T | CA16602445 | KRAS | c.37G>A (p.Gly13Ser) c.-88+5403G>A (n.-88+5403G>A) | ClinVar dbSNP COSMIC |