Product Details

SNP ID
rs151081297
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:73831262 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGGCCGTCCTGGGCTGGCTGGCC[A/G]TCATGCTGTGCTGCGCGCTGCCCAT
Phenotype
MIM: 602909 MIM: 612546
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CLDN4 PubMed Links
Additional Information
For this assay, SNP(s) [rs8629] are located under a primer 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
CLDN4
Gene Name
claudin 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001305.4 400 Missense Mutation ATC,GTC I21V NP_001296.1
Gene
WBSCR27
Gene Name
Williams Beuren syndrome chromosome region 27
There are no transcripts associated with this gene.

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