Product Details

SNP ID

rs10876478

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.12:53665955 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

AACACCGCTCTTCTAGAAGACAAGA[C/G]TAAGAGGGACAGATTATGTTCTCTC

Phenotype

MIM: 603193

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

ATP5G2 PubMed Links

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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