AA Mutation: p.G13C
Nucleotide Mutation: c.37G>T
dPCR wet-lab validated
Nucleotide Mutation: c.37G>T
dPCR wet-lab validated
Assay Nameβ
dPCR Mutation Assay NRAS 570 Human
GeneGlobe Cat No (Assay ID)β
DMH0000342
Speciesβ
Human (Homo sapiens)
Gene Symbolβ
NRAS
Gene aliasesβ
N-ras
Ensembl Gene IDβ
ENSG00000213281
Entrez Gene IDβ
4893
Genomic Mutation ID (COSV by COSMIC)β
COSV54736386
Legacy Mutation ID (COSM by COSMIC)β
COSM570
Amino Acid Changeβ
p.G13C
Nucleotide Changeβ
c.37G>T
Wildtype Alleleβ
C
Mutant Alleleβ
A
Mutation Strandβ
-
Mutant descriptionβ
Substitution - Missense
Positive Control Sequenceβ
GGGATCATATTCATCTACAAAGTGGTTCTGGATTAGCTGGATTGTCAGTGCGCTTTTCCCAACACCACCTGCTCCAACCACCACCAGTTTGTACTCAGTCATTTCACAC
Amplicon lengthβ
89
Recommended Restriction Enzymeβ
HaeIII,EcoRI,XbaI,PvuII
Wet-lab validatedβ
dPCR wet-lab validated
Probe Fluorophoreβ
FAM/HEX, ATTO550/ROX or Cy5/ATTO700
Quencherβ
Iowa Black
Primer Purificationβ
Desalted
Probe Purificationβ
HPLC
Reaction sizeβ
200rxns and 1000rxns