Product Details

SNP ID: rs6488898
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:123719285 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CAGGGCCACTTCTTTTATCTCTAAA[A/G]TCTTTACCATCTTAGTCTGGTACTA
Phenotype: MIM: 611716
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: ATP6V0A2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012463.3		Intron			NP_036595.2