AA Mutation: p.V600D
Nucleotide Mutation: c.1799_1800delinsAT
dPCR wet-lab validated
Nucleotide Mutation: c.1799_1800delinsAT
dPCR wet-lab validated
Assay Name
dPCR Mutation Assay BRAF 477 Human
GeneGlobe Cat No (Assay ID)
DMH0000039
Species
Human (Homo sapiens)
Reaction size
200rxns and 1000rxns
Gene Symbol
BRAF
Gene aliases
BRAF1;BRAF-1
Ensembl Gene ID
ENSG00000157764
Entrez Gene ID
673
Genomic Mutation ID (COSV by COSMIC)
COSV56059623
Legacy Mutation ID (COSM by COSMIC)
COSM477
Amino Acid Change
p.V600D
Nucleotide Change
c.1799_1800delinsAT
Wildtype Allele
TCA
Mutant Allele
TAT
Mutation Strand
-
Mutant description
Substitution - Missense
Positive Control Sequence
GAAAAATAGCCTCAATTCTTACCATCCACAAAATGGATCCAGACAACTGTTCAAACTGATGGGACCCACTCCATCGAGATTTCACTGTAGCTAGACCAAAATCACCTATTTTTACTGTGAGGTCTTCAT
Amplicon length
109
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