Product Details

SNP ID

rs78459819

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:100539433 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCTACCAGGCGCTGTACCAGAGGC[G/T]CCACACGGCGGGCATGCTGGCGCTG

Phenotype

MIM: 607468

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

GPR88 PubMed Links

Gene Details

Gene

GPR88

Gene Name

G protein-coupled receptor 88

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022049.2	871	Missense Mutation	CGC,CTC	R156L	NP_071332.2

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