Product Details

SNP ID
rs9568732
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.13:52419277 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAGGAGGAAGAACAGCTGAAGAATA[G/A]CCACTGCTGATACCCAGCCAAAGGG
Phenotype
MIM: 610903
Polymorphism
G/A, Transition Substitution
Allele Nomenclature
Literature Links
VPS36 PubMed Links
Additional Information
For this assay, SNP(s) [rs141607730] 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
VPS36
Gene Name
vacuolar protein sorting 36 homolog
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282168.1 Intron NP_001269097.1
NM_001282169.1 Intron NP_001269098.1
NM_016075.3 Intron NP_057159.2

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