Product Details

SNP ID

rs11063205

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:4488579 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTTACCTGGACAAACCTTTCCCTC[A/G]AGTAGAAAATTAAGACACATTCTGT

Phenotype

MIM: 616082

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C12orf4 PubMed Links

Additional Information

For this assay, SNP(s) [rs114520620] 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

C12orf4

Gene Name

chromosome 12 open reading frame 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001304811.1	2883	UTR 3			NP_001291740.1
NM_020374.3	2883	UTR 3			NP_065107.1
XM_005253716.1	2883	UTR 3			XP_005253773.1
XM_006718992.3	2883	Intron			XP_006719055.1

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