AA Mutation: p.T790M
Nucleotide Mutation: c.2369C>T
dPCR wet-lab validated
Nucleotide Mutation: c.2369C>T
dPCR wet-lab validated
Assay Name​
dPCR Mutation Assay EGFR 6240 Human
GeneGlobe Cat No (Assay ID)​
DMH0000085
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)​
COSV51765492
Legacy Mutation ID (COSM by COSMIC)​
COSM6240
Amino Acid Change​
p.T790M
Nucleotide Change​
c.2369C>T
Wildtype Allele​
C
Mutant Allele​
T
Mutation Strand​
+
Mutant description​
Substitution - Missense
Positive Control Sequence​
CACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCACCGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCCTCCTGGACTATGTCCGGGAACACAAAGACAATATTGGCTCCCAGTACCTGCTCAACTGGTGTGTGCAGATCGCAAAGGTAATCAGGGAAGGGAGATAC
Amplicon length​
154
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