Product Details

SNP ID

rs8102667

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:17234866 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGGTGAGACCCAGTCTCAAAAAAT[A/G]GAAATACAAATAAAAAAATAAAGTG

Phenotype

MIM: 132880

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

NR2F6 PubMed Links

Gene Details

Gene

NR2F6

Gene Name

nuclear receptor subfamily 2 group F member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005234.3		Intron			NP_005225.2

Gene

OCEL1

Gene Name

occludin/ELL domain containing 1

There are no transcripts associated with this gene.

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