AA Mutation: p.D770_N771insG
Nucleotide Mutation: c.2310_2311insGGT
dPCR wet-lab validated
Nucleotide Mutation: c.2310_2311insGGT
dPCR wet-lab validated
Assay Name
dPCR Mutation Assay EGFR 12378 Human
GeneGlobe Cat No (Assay ID)
DMH0000248
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)
COSV51769298
Legacy Mutation ID (COSM by COSMIC)
COSM12378
Amino Acid Change
p.D770_N771insG
Nucleotide Change
c.2310_2311insGGT
Wildtype Allele
C
Mutant Allele
CGGT
Mutation Strand
+
Mutant description
Substitution - Missense
Positive Control Sequence
TCTCCCTCCCTCCAGGAAGCCTACGTGATGGCCAGCGTGGACAACCCCCACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCACCGT
Amplicon length
69
Recommended Restriction Enzyme
CviQI,AluI,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