Product Details

SNP ID
rs187192
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:88194409 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAATCAACCACTGATGGCCACTTA[G/T]GTTGACCCCATGACTTTGCCACTGT
Phenotype
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
TMEM161B PubMed Links
Additional Information
For this assay, SNP(s) [rs75762615] 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
TMEM161B
Gene Name
transmembrane protein 161B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001289007.1 3209 Intron NP_001275936.1
NM_001289008.1 3209 Intron NP_001275937.1
NM_153354.4 3209 Intron NP_699185.1
XM_006714553.1 3209 Intron XP_006714616.1
XM_006714554.3 3209 Intron XP_006714617.1
XM_006714555.3 3209 Intron XP_006714618.1
XM_006714556.3 3209 Intron XP_006714619.2
XM_011543201.2 3209 Intron XP_011541503.1
XM_011543202.2 3209 Intron XP_011541504.2
XM_011543203.2 3209 Intron XP_011541505.2
XM_011543204.2 3209 Intron XP_011541506.2
XM_017009093.1 3209 Intron XP_016864582.1
XM_017009094.1 3209 Intron XP_016864583.1
XM_017009095.1 3209 Intron XP_016864584.1
XM_017009096.1 3209 Intron XP_016864585.1
XM_017009097.1 3209 Intron XP_016864586.1
XM_017009098.1 3209 Intron XP_016864587.1
XM_017009099.1 3209 Intron XP_016864588.1
XM_017009100.1 3209 Intron XP_016864589.1
XM_017009101.1 3209 Intron XP_016864590.1
XM_017009102.1 3209 Intron XP_016864591.1
XM_017009103.1 3209 Intron XP_016864592.1
XM_017009104.1 3209 Intron XP_016864593.1
XM_017009105.1 3209 Intron XP_016864594.1
XM_017009106.1 3209 Intron XP_016864595.1
XM_017009107.1 3209 Intron XP_016864596.1
XM_017009108.1 3209 Intron XP_016864597.1
XM_017009109.1 3209 UTR 3 XP_016864598.1
XM_017009110.1 3209 UTR 3 XP_016864599.1

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