Product Details

SNP ID
rs1063138
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:75874279 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCCCAGCTGTAGCTCTGTCTCCCA[A/G]AAGTGAGGTCTGCAGGGGAACAGGG
Phenotype
MIM: 611041
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
TRIM47 PubMed Links
Additional Information
For this assay, SNP(s) [rs75830455,rs77043448] 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
TRIM47
Gene Name
tripartite motif containing 47
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_033452.2 2148 UTR 3 NP_258411.2
XM_005257787.4 2148 UTR 3 XP_005257844.1
XM_005257788.4 2148 UTR 3 XP_005257845.1
Gene
TRIM65
Gene Name
tripartite motif containing 65
There are no transcripts associated with this gene.

View Full Product Details