AA Mutation: p.C176F
Nucleotide Mutation: c.527G>T
dPCR wet-lab validated
Nucleotide Mutation: c.527G>T
dPCR wet-lab validated
Assay Nameβ
dPCR Mutation Assay TP53 10645 Human
GeneGlobe Cat No (Assay ID)β
DMH0000353
Speciesβ
Human (Homo sapiens)
Gene Symbolβ
TP53
Gene aliasesβ
p53;LFS1
Ensembl Gene IDβ
ENSG00000141510
Entrez Gene IDβ
7157
Genomic Mutation ID (COSV by COSMIC)β
COSV52661329
Legacy Mutation ID (COSM by COSMIC)β
COSM10645
Amino Acid Changeβ
p.C176F
Nucleotide Changeβ
c.527G>T
Wildtype Alleleβ
C
Mutant Alleleβ
A
Mutation Strandβ
-
Mutant descriptionβ
Substitution - Missense
Positive Control Sequenceβ
CCCCAGCTGCTCACCATCGCTATCTGAGCAGCGCTCATGGTGGGGGCAGCGCCTCACAACCTCCGTCATGTGCTGTGACTGCTTGT
Amplicon lengthβ
66
Recommended Restriction Enzymeβ
CviQI,AluI,HaeIII,EcoRI,XbaI,PvuII
Wet-lab validatedβ
dPCR wet-lab validated
Probe Fluorophoreβ
FAM/HEX, ATTO550/ROX or Cy5/ATTO700
Quencherβ
Iowa Black
Primer Purificationβ
Desalted
Probe Purificationβ
HPLC
Reaction sizeβ
200rxns and 1000rxns