Product Details

SNP ID
rs7036959
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:14085395 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCAATGGGACTGGGCGGTGAGGGAA[A/G]GGCAAAATAAAACCAGCCTCCATTC
Phenotype
MIM: 600728
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
NFIB PubMed Links
Additional Information
For this assay, SNP(s) [rs187346168] 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
NFIB
Gene Name
nuclear factor I B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001190737.1 6255 UTR 3 NP_001177666.1
NM_001190738.1 6255 UTR 3 NP_001177667.1
NM_001282787.1 6255 UTR 3 NP_001269716.1
NM_005596.3 6255 UTR 3 NP_005587.2
XM_005251467.2 6255 UTR 3 XP_005251524.1
XM_005251468.4 6255 UTR 3 XP_005251525.1
XM_005251469.2 6255 UTR 3 XP_005251526.1
XM_005251470.2 6255 UTR 3 XP_005251527.1
XM_005251471.3 6255 UTR 3 XP_005251528.1
XM_006716773.2 6255 UTR 3 XP_006716836.1
XM_006716774.2 6255 UTR 3 XP_006716837.1
XM_006716775.2 6255 UTR 3 XP_006716838.1
XM_017014739.1 6255 UTR 3 XP_016870228.1
XM_017014740.1 6255 UTR 3 XP_016870229.1
XM_017014741.1 6255 UTR 3 XP_016870230.1
XM_017014742.1 6255 UTR 3 XP_016870231.1

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