Product Details

SNP ID
rs11613296
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:125191772 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAGTGATTAGATGGCTATGTTGAA[C/G]GGCAAGACTTTGGCAGGCCGAATTT
Phenotype
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
TMEM132B PubMed Links
Additional Information
For this assay, SNP(s) [rs79703590] 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
TMEM132B
Gene Name
transmembrane protein 132B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286219.1 Intron NP_001273148.1
NM_052907.3 Intron NP_443139.2
XM_011537852.2 Intron XP_011536154.1
XM_011537854.2 Intron XP_011536156.1
XM_017018767.1 Intron XP_016874256.1

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