Product Details

SNP ID

rs137997556

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:57236062 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGGAGGTGCAGGCCTGGCGGAAGC[C/G]GGGGTCGAAAAAGGCATAGAGGAAG

Phenotype

MIM: 600052

Polymorphism

C/G, Transversion 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	1392	Missense Mutation	CGC,GGC	R315G	NP_005152.1

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