Product Details

SNP ID

rs6573951

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:70327283 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTAGCTATATAACCTTTGGAAAGT[A/G]ATTTAAGCCACCTGGGCATTAACTC

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

COX16 PubMed Links

Additional Information

For this assay, SNP(s) [rs143900105] 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

COX16

Gene Name

COX16, cytochrome c oxidase assembly homolog

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001204090.1		Intron			NP_001191019.1
NM_016468.6		Intron			NP_057552.1

Gene

SYNJ2BP-COX16

Gene Name

SYNJ2BP-COX16 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001202547.2		Intron			NP_001189476.1
NM_001202548.2		Intron			NP_001189477.1
NM_001202549.2		Intron			NP_001189478.1

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