Product Details

SNP ID
rs200443926
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:105051424 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCGATGGCCGAGTGCTTCACCTTG[C/G]CCTTCTGGGCAGCGCTTAAGCCCAT
Phenotype
MIM: 606167
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
GPR132 PubMed Links

Gene Details

Gene
GPR132
Gene Name
G protein-coupled receptor 132
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001278694.1 851 Missense Mutation GCC,GGC A238G NP_001265623.1
NM_001278695.1 851 Missense Mutation GCC,GGC A229G NP_001265624.1
NM_001278696.1 851 Missense Mutation GCC,GGC A50G NP_001265625.1
NM_013345.3 851 Missense Mutation GCC,GGC A238G NP_037477.1

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