Product Details

SNP ID
rs5992749
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.22:17593757 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CATATCTAGGTCAGGGAATAACTAG[A/G]TTGGCAGCCACAGCAATAGACTCCC
Phenotype
MIM: 108746 MIM: 609303
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
ATP6V1E1 PubMed Links
Additional Information
For this assay, SNP(s) [rs77745907] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
ATP6V1E1
Gene Name
ATPase H+ transporting V1 subunit E1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039366.1 Intron NP_001034455.1
NM_001039367.1 Intron NP_001034456.1
NM_001696.3 Intron NP_001687.1
Gene
LOC101929372
Gene Name
uncharacterized LOC101929372
There are no transcripts associated with this gene.

Gene
SLC25A18
Gene Name
solute carrier family 25 member 18
There are no transcripts associated with this gene.

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