Product Details

SNP ID

rs199844882

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:93585260 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCAGGGCCCGCCCGGTTCGGGCCA[C/G]AGCCAGCAGCACATCGAGTGCGTGG

Phenotype

MIM: 132890

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

NR2F1 PubMed Links

Additional Information

For this assay, SNP(s) [rs557800691] 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

NR2F1

Gene Name

nuclear receptor subfamily 2 group F member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005654.5	1924	Silent Mutation	CAC,CAG	H79Q	NP_005645.1
XM_017009797.1	1924	Intron			XP_016865286.1

Gene

NR2F1-AS1

Gene Name

NR2F1 antisense RNA 1

There are no transcripts associated with this gene.

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