Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.25245345C>G | CA384157453 | KRAS | c.40G>C (p.Val14Leu) c.-88+5406G>C (n.-88+5406G>C) | dbSNP |
12 | g.25245345C>T | CA156358 | KRAS | c.40G>A (p.Val14Ile) c.-88+5406G>A (n.-88+5406G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
12 | g.25245345C= | CA2022898326 | KRAS | c.40G= (p.Val14=) c.-88+5406G= (n.-88+5406G=) | dbSNP |