AA Mutation: p.R458*
Nucleotide Mutation: c.1372C>T
dPCR wet-lab validated
Nucleotide Mutation: c.1372C>T
dPCR wet-lab validated
Assay Name
dPCR Mutation Assay WT1 21397 Human
GeneGlobe Cat No (Assay ID)
DMH0000059
Species
Human (Homo sapiens)
Reaction size
200rxns and 1000rxns
Gene Symbol
WT1
Gene aliases
WAGR;WIT-2;AWT1;NPHS4;WT-1;GUD
Ensembl Gene ID
ENSG00000184937
Entrez Gene ID
7490
Genomic Mutation ID (COSV by COSMIC)
COSV60066326
Legacy Mutation ID (COSM by COSMIC)
COSM21397
Amino Acid Change
p.R458*
Nucleotide Change
c.1372C>T
Wildtype Allele
G
Mutant Allele
A
Mutation Strand
-
Mutant description
Substitution - Missense
Positive Control Sequence
GTCCTGGTGTGGGTCTTCAGGTGGTCGGACCGGGAGAACTTTCGCTGACAAGTTTTACACTGGAATGGTTTCACACCTAAATGGACAGAG
Amplicon length
70
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