Product Details

SNP ID
rs148299142
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:236142704 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCGTGGGACCCAGCCCGCAACGAC[A/T]CGCTGCCGCCCACGCTGACCCCGGC
Phenotype
MIM: 604658
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
GPR137B PubMed Links

Gene Details

Gene
GPR137B
Gene Name
G protein-coupled receptor 137B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003272.3 173 Missense Mutation ACG,TCG T28S NP_003263.1
XM_017002209.1 173 Missense Mutation ACG,TCG T28S XP_016857698.1
XM_017002210.1 173 Missense Mutation ACG,TCG T28S XP_016857699.1

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