| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.114716126C>G | CA280928 | NRAS | c.35G>C (p.Gly12Ala) | ClinVar dbSNP gnomAD v4 COSMIC |
| 1 | g.114716126C>A | CA261525 | NRAS | c.35G>T (p.Gly12Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 1 | g.114716126C>T | CA130425 | NRAS | c.35G>A (p.Gly12Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |