Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.25245347C>G | CA16602444 | KRAS | c.38G>C (p.Gly13Ala) c.-88+5404G>C (n.-88+5404G>C) | ClinVar dbSNP COSMIC COSMIC |
12 | g.25245347C>A | CA135573 | KRAS | c.38G>T (p.Gly13Val) c.-88+5404G>T (n.-88+5404G>T) | ClinVar dbSNP COSMIC COSMIC |
12 | g.25245347C>T | CA122534 | KRAS | c.38G>A (p.Gly13Asp) c.-88+5404G>A (n.-88+5404G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |