Product Details

SNP ID

rs79533383

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:53670085 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTCCATCTTCACATGTACGTTAGA[A/G]TTTTGGATCATTCTTCCTTTTAGCA

Phenotype

MIM: 603193

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ATP5G2 PubMed Links

Additional Information

For this assay, SNP(s) [rs141952979] 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

ATP5G2

Gene Name

ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002031.2		Intron			NP_001002031.1
NM_005176.5		Intron			NP_005167.2
XM_017019460.1		Intron			XP_016874949.1
XM_017019461.1		Intron			XP_016874950.1
XM_017019462.1		Intron			XP_016874951.1

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