AA Mutation: p.C176F
Nucleotide Mutation: c.527G>T
dPCR wet-lab validated
Assay Name
dPCR Mutation Assay TP53 10645 Human
GeneGlobe Cat No (Assay ID)
DMH0000353
Species
Human (Homo sapiens)
Ensembl Gene ID
ENSG00000141510
Genomic Mutation ID (COSV by COSMIC)
COSV52661329
Legacy Mutation ID (COSM by COSMIC)
COSM10645
Amino Acid Change
p.C176F
Nucleotide Change
c.527G>T
Mutant description
Substitution - Missense
Control Sequence (wt)
CCCCAGCTGCTCACCATCGCTATCTGAGCAGCGCTCATGGTGGGGGCAGCGCCTCACAACCTCCGTCATGTGCTGTGACTGCTTGT
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
Primer Purification
Desalted
Reaction size
200rxns and 1000rxns