AA Mutation: p.L747_P753delinsQ
Nucleotide Mutation: c.2239_2258delinsCA
dPCR wet-lab validated
Nucleotide Mutation: c.2239_2258delinsCA
dPCR wet-lab validated
Assay Name
dPCR Mutation Assay EGFR 12387 Human
GeneGlobe Cat No (Assay ID)
DMH0000269
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)
COSV51785746
Legacy Mutation ID (COSM by COSMIC)
COSM12387
Amino Acid Change
p.L747_P753delinsQ
Nucleotide Change
c.2239_2258delinsCA
Wildtype Allele
ATTAAGAGAAGCAACATCTCC
Mutant Allele
ACA
Mutation Strand
+
Mutant description
Substitution - Missense
Positive Control Sequence
ATAGGGACTCTGGATCCCAGAAGGTGAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAAGAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCTCGATGTGAGTTTCTGCTTTGCTGTGTGGGGGTC
Amplicon length
112
Recommended Restriction Enzyme
CviQI,AluI,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