Product Details

SNP ID: rs199759060
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:172983918 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGTGATGAGCGTGTTCTGGGGCTTC[G/T]TCGGCTTCTTGGTGCCTTGGTTCAT
Phenotype: MIM: 603931
Polymorphism: G/T, Transversion 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