| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.114716123C>T | CA123620 | NRAS | c.38G>A (p.Gly13Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 1 | g.114716123C>G | CA16602364 | NRAS | c.38G>C (p.Gly13Ala) | ClinVar dbSNP COSMIC |
| 1 | g.114716123C>A | CA16602363 | NRAS | c.38G>T (p.Gly13Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |