Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.114716124C>G | CA151261 | NRAS | c.37G>C (p.Gly13Arg) | ClinVar dbSNP gnomAD v4 COSMIC |
1 | g.114716124C>A | CA16602248 | NRAS | c.37G>T (p.Gly13Cys) | ClinVar dbSNP gnomAD v4 COSMIC |
1 | g.114716124C>T | CA16602674 | NRAS | c.37G>A (p.Gly13Ser) | ClinVar dbSNP COSMIC |
1 | g.114716124C= | CA1141580992 | NRAS | c.37G= (p.Gly13=) | dbSNP |