Product Details

SNP ID
rs9891306
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:34576507 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTGAGACAGAGTCGGATTCCAGGAT[A/G]ATCCCAGGAACATGTCTTCATGATG
Phenotype
MIM: 616178
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
C17orf102 PubMed Links
Additional Information
For this assay, SNP(s) [rs79703349] 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
C17orf102
Gene Name
chromosome 17 open reading frame 102
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_207454.2 1613 UTR 3 NP_997337.2
Gene
TMEM132E
Gene Name
transmembrane protein 132E
There are no transcripts associated with this gene.

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