Product Details

SNP ID
rs200854787
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:57236055 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAGAGCATGGAGGTGCAGGCCTGG[C/T]GGAAGCGGGGGTCGAAAAAGGCATA
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 1399 Missense Mutation CAC,CGC H317R NP_005152.1

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