Product Details

SNP ID
rs117796776
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:20032364 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAAACACTTACAATGACTTTCCGGG[A/T]GCGGGCTGGGTATGAGACCGTGTGG
Phenotype
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
GPR139 PubMed Links

Gene Details

Gene
GPR139
Gene Name
G protein-coupled receptor 139
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001002911.3 595 Missense Mutation ACC,TCC T145S NP_001002911.1
NM_001318483.1 595 Missense Mutation ACC,TCC T52S NP_001305412.1

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