Product Details

SNP ID
rs12436710
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.14:103125464 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATTGACTATAGGGACAGTTTAAGC[C/T]GAAATAACACCCTTCCAGATGAGAG
Phenotype
MIM: 603300
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
LINC00677 PubMed Links
Additional Information
For this assay, SNP(s) [rs8176360] are located under a probe and SNP(s) [rs115952674] 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
LINC00677
Gene Name
long intergenic non-protein coding RNA 677
There are no transcripts associated with this gene.

Gene
TNFAIP2
Gene Name
TNF alpha induced protein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006291.2 Intron NP_006282.2
XM_006720243.3 Intron XP_006720306.1
XM_011537112.2 Intron XP_011535414.1
XM_011537113.2 Intron XP_011535415.1
XM_011537114.2 Intron XP_011535416.1
XM_011537115.2 Intron XP_011535417.1
XM_017021616.1 Intron XP_016877105.1

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