AA Mutation: p.E746_P753delinsVS
Nucleotide Mutation: c.2237_2257delinsTCT
dPCR wet-lab validated
Nucleotide Mutation: c.2237_2257delinsTCT
dPCR wet-lab validated
Assay Name
dPCR Mutation Assay EGFR 18427 Human
GeneGlobe Cat No (Assay ID)
DMH0000274
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)
COSV51781339
Legacy Mutation ID (COSM by COSMIC)
COSM18427
Amino Acid Change
p.E746_P753delinsVS
Nucleotide Change
c.2237_2257delinsTCT
Wildtype Allele
GAATTAAGAGAAGCAACATCTC
Mutant Allele
GTCT
Mutation Strand
+
Mutant description
Substitution - Missense
Positive Control Sequence
CATAGGGACTCTGGATCCCAGAAGGTGAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAAGAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCTCGATGTGAGTTTCTGCTTTGCTGTGTG
Amplicon length
107
Recommended Restriction Enzyme
CviQI,AluI,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