AA Mutation: p.C797S
Nucleotide Mutation: c.2389T>A
dPCR wet-lab validated
Nucleotide Mutation: c.2389T>A
dPCR wet-lab validated
Assay Name
dPCR Mutation Assay EGFR 6493937 Human
GeneGlobe Cat No (Assay ID)
DMH0000007
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)
COSV51766493
Legacy Mutation ID (COSM by COSMIC)
COSM6493937
Amino Acid Change
p.C797S
Nucleotide Change
c.2389T>A
Wildtype Allele
T
Mutant Allele
A
Mutation Strand
+
Mutant description
Substitution - Missense
Positive Control Sequence
GCCTCACCTCCACCGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCCTCCTGGACTATGTCCGGGAACACAAAGACAATATTG
Amplicon length
67
Recommended Restriction Enzyme
CviQI,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