Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.114716127C>A | CA297020 | NRAS | c.34G>T (p.Gly12Cys) | ClinVar dbSNP COSMIC |
1 | g.114716127C>G | CA297030 | NRAS | c.34G>C (p.Gly12Arg) | ClinVar dbSNP COSMIC |
1 | g.114716127C>T | CA180753 | NRAS | c.34G>A (p.Gly12Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
1 | g.114716127C= | CA1141580994 | NRAS | c.34G= (p.Gly12=) | dbSNP |