Product Details

SNP ID
rs884218
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:136953118 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGTGGCTCAGGTGCGCCATGGGCCC[T/C]GTCCCAGCACAGGCAGCTTCATGAC
Phenotype
MIM: 120930 MIM: 609072 MIM: 612905
Polymorphism
T/C, Transition Substitution
Allele Nomenclature
Literature Links
C8G PubMed Links
Additional Information
For this assay, SNP(s) [rs115757662] 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
C8G
Gene Name
complement component 8, gamma polypeptide
There are no transcripts associated with this gene.

Gene
FBXW5
Gene Name
F-box and WD repeat domain containing 5
There are no transcripts associated with this gene.

Gene
LCN12
Gene Name
lipocalin 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_178536.3 Intron NP_848631.2
XM_006717065.3 Intron XP_006717128.1
XM_011518560.2 Intron XP_011516862.1
XM_011518561.2 Intron XP_011516863.2
XM_011518562.2 Intron XP_011516864.1
XM_017014631.1 Intron XP_016870120.1
XM_017014632.1 Intron XP_016870121.1

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