Product Details

SNP ID

rs9467360

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:10722960 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGGGAAGCACAGAGATTCCCCGCC[C/G]CGTTCCCTGGACTCAGGAGCTCGCC

Phenotype

MIM: 615318

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

TMEM14C PubMed Links

Additional Information

For this assay, SNP(s) [rs111553244,rs112097099] 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

TMEM14C

Gene Name

transmembrane protein 14C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001165258.1	46	UTR 5			NP_001158730.1
NM_016462.3	46	UTR 5			NP_057546.1

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