Product Details

SNP ID
rs2425902
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.20:46721941 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCCAGGCAGACAGAAGAAGTAACAA[A/G]TGTTTACTACACCCAGAGGCTTGTA
Phenotype
MIM: 606145
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC2A10 PubMed Links
Additional Information
For this assay, SNP(s) [rs77000636] 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
SLC2A10
Gene Name
solute carrier family 2 member 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_030777.3 Intron NP_110404.1
XM_011529060.2 Intron XP_011527362.1
XM_011529061.2 Intron XP_011527363.1
XM_011529062.2 Intron XP_011527364.1
XM_011529063.2 Intron XP_011527365.1
XM_011529064.2 Intron XP_011527366.1
XM_011529065.2 Intron XP_011527367.1
XM_017028087.1 Intron XP_016883576.1

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