AA Mutation: p.G13V
Nucleotide Mutation: c.38G>T
dPCR wet-lab validated
Nucleotide Mutation: c.38G>T
dPCR wet-lab validated
Assay Nameβ
dPCR Mutation Assay NRAS 574 Human
GeneGlobe Cat No (Assay ID)β
DMH0000344
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
COSV54736480
Legacy Mutation ID (COSM by COSMIC)β
COSM574
Amino Acid Changeβ
p.G13V
Nucleotide Changeβ
c.38G>T
Wildtype Alleleβ
C
Mutant Alleleβ
A
Mutation Strandβ
-
Mutant descriptionβ
Substitution - Missense
Positive Control Sequenceβ
TGGTTCTGGATTAGCTGGATTGTCAGTGCGCTTTTCCCAACACCACCTGCTCCAACCACCACCAGTTTGTACTCAGTCATTTCACAC
Amplicon lengthβ
67
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