Product Details

SNP ID: rs567969
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.5:173008013 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: GGCTACAAGATCAAAGAGGTACCAC[A/G]TTCTGGCCTCGAGCCATAGTAGGCT
Phenotype: MIM: 603931
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: ATP6V0E1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003945.3		Intron			NP_003936.1