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)
Reaction size
200rxns and 1000rxns
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 or ATTO550/ROX
Quencher
Iowa Black
Primer Purification
Desalted
Probe Purification
HPLC