Product Details

SNP ID

rs10854865

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:49419583 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATATACATTTATGTGTAAGATAAAC[A/G]CAGAAGCAGAAGTTGGCCAAAACCA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C22orf34 PubMed Links

Additional Information

For this assay, SNP(s) [rs114958194] 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

C22orf34

Gene Name

chromosome 22 open reading frame 34

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001289922.2		Intron			NP_001276851.1
XM_011530167.2		Intron			XP_011528469.1
XM_017028796.1		Intron			XP_016884285.1

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