Product Details

SNP ID

rs6767905

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:14958687 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAATAGGATTTTTTTGTTGTTGTTG[A/T]TCCAGATTGGTTGGGTGCTGCGGCT

Phenotype

MIM: 601426

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

NR2C2 PubMed Links

Additional Information

For this assay, SNP(s) [rs116130753] 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

NR2C2

Gene Name

nuclear receptor subfamily 2 group C member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001291694.1		Intron			NP_001278623.1
NM_003298.4		Intron			NP_003289.2
XM_011534058.2		Intron			XP_011532360.1
XM_011534059.2		Intron			XP_011532361.1
XM_011534061.2		Intron			XP_011532363.1
XM_011534063.2		Intron			XP_011532365.1
XM_011534064.2		Intron			XP_011532366.1
XM_011534065.2		Intron			XP_011532367.1
XM_011534066.2		Intron			XP_011532368.1
XM_017007118.1		Intron			XP_016862607.1
XM_017007119.1		Intron			XP_016862608.1
XM_017007120.1		Intron			XP_016862609.1

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