Product Details

SNP ID
rs17776046
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.10:59652443 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
GCCTTGCAGTGGATTAAATGGAGTC[A/G]GCAGAGAAATTATACTTCTTTACAC
Phenotype
MIM: 614242
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC16A9 PubMed Links
Additional Information
For this assay, SNP(s) [rs79262114] 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
SLC16A9
Gene Name
solute carrier family 16 member 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001323977.1 2261 UTR 3 NP_001310906.1
NM_001323978.1 2261 UTR 3 NP_001310907.1
NM_001323979.1 2261 UTR 3 NP_001310908.1
NM_001323980.1 2261 UTR 3 NP_001310909.1
NM_001323981.1 2261 UTR 3 NP_001310910.1
NM_194298.2 2261 UTR 3 NP_919274.1
XM_017015883.1 2261 UTR 3 XP_016871372.1
XM_017015884.1 2261 UTR 3 XP_016871373.1

View Full Product Details