Product Details

SNP ID

rs7605667

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:68046795 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TATAAGAAGCAGGCTTAGGCAATAC[C/G]AAAGACAGAAGAAACATAATGAGAT

Phenotype

MIM: 606997

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

C1D PubMed Links

Additional Information

For this assay, SNP(s) [rs113178313] 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

C1D

Gene Name

C1D nuclear receptor corepressor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001190263.1		Intron			NP_001177192.1
NM_001190265.1		Intron			NP_001177194.1
NM_006333.3		Intron			NP_006324.1
NM_173177.2		Intron			NP_775269.1

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