Product Details

SNP ID

rs4432059

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:111248453 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATCTCCCTGACAGGCAGAGAATGGA[C/T]CAAATATAGATCCATCCACCAATGA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C11orf53 PubMed Links

Additional Information

For this assay, SNP(s) [rs78529703] 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

C11orf53

Gene Name

chromosome 11 open reading frame 53

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198498.2		Intron			NP_940900.1
XM_011542803.2		Intron			XP_011541105.1
XM_011542804.2		Intron			XP_011541106.1

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