Product Details

SNP ID

rs6829969

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:83140604 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTCTTTTATGCTCCTTTATCCTCT[A/G]TTTTACCCCCAATCTGCTGTCTTTC

Phenotype

MIM: 609825

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

COQ2 PubMed Links

Additional Information

For this assay, SNP(s) [rs112230286] 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

COQ2

Gene Name

coenzyme Q2, polyprenyltransferase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015697.7		Intron			NP_056512.5
XM_011531855.2		Intron			XP_011530157.1
XM_011531857.2		Intron			XP_011530159.1
XM_011531859.2		Intron			XP_011530161.1
XM_011531860.2		Intron			XP_011530162.1
XM_011531862.2		Intron			XP_011530164.1
XM_011531863.2		Intron			XP_011530165.1
XM_011531866.2		Intron			XP_011530168.1
XM_011531867.2		Intron			XP_011530169.1
XM_017008031.1		Intron			XP_016863520.1
XM_017008032.1		Intron			XP_016863521.1

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