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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