Product Details

SNP ID

rs147773675

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:57235946 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCCTTGCCCATGTTGGGGCCGGG[C/T]CCCTGGCTGTGCCCCGAAGAGTAGC

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	1508	Silent Mutation	GGA,GGG	G353G	NP_005152.1

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