AA Mutation: p.A382Vfs*4
Nucleotide Mutation: c.1141_1144dup
dPCR wet-lab validated
Nucleotide Mutation: c.1141_1144dup
dPCR wet-lab validated
Assay Name​
dPCR Mutation Assay WT1 21392 Human
GeneGlobe Cat No (Assay ID)​
DMH0000575
Species​
Human (Homo sapiens)
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)​
COSV60065589
Legacy Mutation ID (COSM by COSMIC)​
COSM21392
Amino Acid Change​
p.A382Vfs*4
Nucleotide Change​
c.1141_1144dup
Wildtype Allele​
A
Mutant Allele​
AACCG
Mutation Strand​
-
Mutant description​
Substitution - Missense
Positive Control Sequence​
TTATTGCAGCCTGGGTAAGCACACATGAAGGGGCGTTTCTCACTGGTCTCAGATGCCGACCGTACAAGAGTCGGGGCTACTCCAGGCACACGTCGCACATCCTGCAGGCAGAG
Amplicon length​
93
Recommended Restriction Enzyme​
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
Reaction size​
200rxns and 1000rxns