Product Details

SNP ID
rs7406077
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:75453934 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCTTCCAACATGGCCCAGGGAAGCC[A/T]AAAGATTGAACACTCCTGAGCTAAG
Phenotype
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
TMEM94 PubMed Links
Additional Information
For this assay, SNP(s) [rs115392897] 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
TMEM94
Gene Name
transmembrane protein 94
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321148.1 Intron NP_001308077.1
NM_001321149.1 Intron NP_001308078.1
NM_014738.5 Intron NP_055553.3
XM_005257864.2 Intron XP_005257921.1
XM_011525514.1 Intron XP_011523816.1
XM_011525515.1 Intron XP_011523817.1
XM_011525516.1 Intron XP_011523818.1
XM_011525517.1 Intron XP_011523819.1
XM_011525519.1 Intron XP_011523821.1
XM_011525520.2 Intron XP_011523822.1
XM_011525521.1 Intron XP_011523823.1
XM_017025433.1 Intron XP_016880922.1
XM_017025434.1 Intron XP_016880923.1
XM_017025435.1 Intron XP_016880924.1
XM_017025436.1 Intron XP_016880925.1
XM_017025437.1 Intron XP_016880926.1
XM_017025438.1 Intron XP_016880927.1
XM_017025439.1 Intron XP_016880928.1
XM_017025440.1 Intron XP_016880929.1
XM_017025441.1 Intron XP_016880930.1
XM_017025442.1 Intron XP_016880931.1
XM_017025443.1 Intron XP_016880932.1
XM_017025444.1 Intron XP_016880933.1
XM_017025445.1 Intron XP_016880934.1
XM_017025446.1 Intron XP_016880935.1
XM_017025447.1 Intron XP_016880936.1
XM_017025448.1 Intron XP_016880937.1
XM_017025449.1 Intron XP_016880938.1
XM_017025450.1 Intron XP_016880939.1

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