Product Details

SNP ID

rs1062647

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:175178213 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTCCCATGACACCAATACTACAGT[C/T]TTCGGAGTCACAGTAAGATACACAG

Phenotype

MIM: 602736

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ATP5G3 PubMed Links

Additional Information

For this assay, SNP(s) [rs189393963] 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

ATP5G3

Gene Name

ATP synthase, H+ transporting, mitochondrial Fo complex subunit C3 (subunit 9)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002258.4	1338	UTR 3			NP_001002258.1
NM_001190329.1	1338	UTR 3			NP_001177258.1
NM_001689.4	1338	UTR 3			NP_001680.1

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