Product Details

SNP ID
rs4536441
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:44750657 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTTCTTCATCAGTCTACTTAATGG[C/T]TTCTAAATTTTGTGGATTTTCCCTC
Phenotype
MIM: 616017
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
TRIM69 PubMed Links
Additional Information
For this assay, SNP(s) [rs112110775] 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
TRIM69
Gene Name
tripartite motif containing 69
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001301144.1 Intron NP_001288073.1
NM_001301145.1 Intron NP_001288074.1
NM_001301146.1 Intron NP_001288075.1
NM_080745.4 Intron NP_542783.2
NM_182985.4 Intron NP_892030.3

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