Product Details

SNP ID
rs201262177
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:51861676 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATCTAAGGACAGGCCATGAGGGTT[C/T]GATTTTGTGTAAGAGACATGGCCAG
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
IQCF2 PubMed Links
Additional Information
For this assay, SNP(s) [rs114750576] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
IQCF2
Gene Name
IQ motif containing F2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_203424.1 48 Nonsense Mutation CGA,TGA R4* NP_982248.1

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