Product Details

SNP ID
rs2282624
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:57234437 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGAGCAGGAACCCAGCTCAGTAGGA[C/T]GCCCCCAAGCCTTGGCGCCAGCTGC
Phenotype
MIM: 600052
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
APLNR PubMed Links

Gene Details

Gene
APLNR
Gene Name
apelin receptor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005161.4 3017 UTR 3 NP_005152.1

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