Product Details

SNP ID

rs35582

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:95028966 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTTCAAGCTTTGAGTATAACCAAT[C/G]TAGAAATGTTTAAAATTAAGTATTT

Phenotype

MIM: 601529

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

NR2C1 PubMed Links

Gene Details

Gene

NR2C1

Gene Name

nuclear receptor subfamily 2 group C member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001032287.2		Intron			NP_001027458.1
NM_001127362.1		Intron			NP_001120834.1
NM_003297.3		Intron			NP_003288.2
XM_005269133.2		Intron			XP_005269190.1
XM_006719584.2		Intron			XP_006719647.1
XM_006719585.2		Intron			XP_006719648.1
XM_011538716.2		Intron			XP_011537018.1
XM_011538717.2		Intron			XP_011537019.1

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