AA Mutation: p.G719C
Nucleotide Mutation: c.2155G>T
dPCR wet-lab validated
Nucleotide Mutation: c.2155G>T
dPCR wet-lab validated
Assay Name​
dPCR Mutation Assay EGFR 6253 Human
GeneGlobe Cat No (Assay ID)​
DMH0000280
Species​
Human (Homo sapiens)
Gene Symbol​
EGFR
Gene aliases​
ERBB1;ERRP;ERBB
Ensembl Gene ID​
ENSG00000146648
Entrez Gene ID​
1956
Genomic Mutation ID (COSV by COSMIC)​
COSV51766606
Legacy Mutation ID (COSM by COSMIC)​
COSM6253
Amino Acid Change​
p.G719C
Nucleotide Change​
c.2155G>T
Wildtype Allele​
G
Mutant Allele​
T
Mutation Strand​
+
Mutant description​
Substitution - Missense
Positive Control Sequence​
GAGAAGCTCCCAACCAAGCTCTCTTGAGGATCTTGAAGGAAACTGAATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTTCGGCACGGTGTATAAGGTAAGGTCCCTGGCACAG
Amplicon length​
96
Recommended Restriction Enzyme​
CviQI,HaeIII,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