AA Mutation: p.A767_V769dup
Nucleotide Mutation: c.2309_2310delinsCCAGCGTGGAT
dPCR wet-lab validated
Nucleotide Mutation: c.2309_2310delinsCCAGCGTGGAT
dPCR wet-lab validated
Assay Name​
dPCR Mutation Assay EGFR 13558 Human
GeneGlobe Cat No (Assay ID)​
DMH0000273
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)​
COSV51775806
Legacy Mutation ID (COSM by COSMIC)​
COSM13558
Amino Acid Change​
p.A767_V769dup
Nucleotide Change​
c.2309_2310delinsCCAGCGTGGAT
Wildtype Allele​
GAC
Mutant Allele​
GCCAGCGTGGAT
Mutation Strand​
+
Mutant description​
Substitution - Missense
Positive Control Sequence​
TGCCTCTCCCTCCCTCCAGGAAGCCTACGTGATGGCCAGCGTGGACAACCCCCACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCACC
Amplicon length​
71
Recommended Restriction Enzyme​
CviQI,AluI,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