Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.25245328C>A | CA16602501 | KRAS | c.57G>T (p.Leu19Phe) c.-88+5423G>T (n.-88+5423G>T) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
12 | g.25245328C>T | CA478891900 | KRAS | c.57G>A (p.Leu19=) c.-88+5423G>A (n.-88+5423G>A) | dbSNP |
12 | g.25245328C>G | CA210356 | KRAS | c.57G>C (p.Leu19Phe) c.-88+5423G>C (n.-88+5423G>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |