Product Details

SNP ID
rs4833772
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:121766336 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CAGCTTCAGAAGTCACGTGCCATCA[C/G]ATCTGTAATATCCTACTGGTCACAC
Phenotype
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
PP12613 PubMed Links
Additional Information
For this assay, SNP(s) [rs77005784] are located under a probe 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
PP12613
Gene Name
uncharacterized LOC100192379
There are no transcripts associated with this gene.

Gene
TMEM155
Gene Name
transmembrane protein 155
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001317837.1 Intron NP_001304766.1
NM_001317838.1 Intron NP_001304767.1
NM_001317839.1 Intron NP_001304768.1
NM_001317841.1 Intron NP_001304770.1
NM_001317842.1 Intron NP_001304771.1
NM_152399.3 Intron NP_689612.3
XM_005262737.2 Intron XP_005262794.1
XM_017007725.1 Intron XP_016863214.1
XM_017007726.1 Intron XP_016863215.1

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