AA Mutation: p.G12V
Nucleotide Mutation: c.35G>T
dPCR wet-lab validated
Nucleotide Mutation: c.35G>T
dPCR wet-lab validated
Assay Name​
dPCR Mutation Assay NRAS 566 Human
GeneGlobe Cat No (Assay ID)​
DMH0000340
Species​
Human (Homo sapiens)
Gene Symbol​
NRAS
Gene aliases​
N-ras
Ensembl Gene ID​
ENSG00000213281
Entrez Gene ID​
4893
Genomic Mutation ID (COSV by COSMIC)​
COSV54736974
Legacy Mutation ID (COSM by COSMIC)​
COSM566
Amino Acid Change​
p.G12V
Nucleotide Change​
c.35G>T
Wildtype Allele​
C
Mutant Allele​
A
Mutation Strand​
-
Mutant description​
Substitution - Missense
Positive Control Sequence​
TCTGGATTAGCTGGATTGTCAGTGCGCTTTTCCCAACACCACCTGCTCCAACCACCACCAGTTTGTACTCAGTCATTTCACACCAGCAAGAACCTGTTGGAAACCAGTA
Amplicon length​
89
Recommended Restriction Enzyme​
HaeIII,EcoRI,XbaI,PvuII
Wet-lab validated​
dPCR wet-lab validated
Probe Fluorophore​
FAM/HEX, ATTO550/ROX or Cy5/ATTO700
Quencher​
Iowa Black
Primer Purification​
Desalted
Probe Purification​
HPLC
Reaction size​
200rxns and 1000rxns