Product Details

SNP ID
rs2468339
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:104811299 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTATTGACACAGAATGGCTAAATTC[A/G]CTGTTAAGTCACACAATTGAACACT
Phenotype
MIM: 610802
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC41A2 PubMed Links
Additional Information
For this assay, SNP(s) [rs118023749] 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
SLC41A2
Gene Name
solute carrier family 41 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032148.3 Intron NP_115524.3
XM_005269176.1 Intron XP_005269233.1
XM_005269178.1 Intron XP_005269235.1
XM_005269179.1 Intron XP_005269236.1
XM_006719630.2 Intron XP_006719693.1
XM_011538807.2 Intron XP_011537109.1
XM_011538808.1 Intron XP_011537110.1
XM_011538809.1 Intron XP_011537111.1
XM_011538810.2 Intron XP_011537112.1
XM_011538811.2 Intron XP_011537113.1
XM_011538813.2 Intron XP_011537115.1
XM_017020013.1 Intron XP_016875502.1
XM_017020014.1 Intron XP_016875503.1
XM_017020015.1 Intron XP_016875504.1
XM_017020016.1 Intron XP_016875505.1
XM_017020017.1 Intron XP_016875506.1

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