Product Details

SNP ID: rs148336004
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:175179059 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TATTTAGGGATAGAAATGATTACCT[C/G]GCATAACCAATGATAAGGCTGCCAA
Phenotype: MIM: 602736
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: ATP5G3 PubMed Links

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	492	Silent Mutation	GCC,GCG	A104A	NP_001002258.1
NM_001190329.1	492	Silent Mutation	GCC,GCG	A104A	NP_001177258.1
NM_001689.4	492	Silent Mutation	GCC,GCG	A104A	NP_001680.1