Product Details

SNP ID
rs145915972
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:39801246 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAGCTCTTCTGGGGTGTTGCCCAA[C/G]GGGGGAAGCAGCCGCTTCTTGCTGT
Phenotype
MIM: 612183
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
GPR176 PubMed Links

Gene Details

Gene
GPR176
Gene Name
G protein-coupled receptor 176
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001271854.1 2623 Silent Mutation CCC,CCG P477P NP_001258783.1
NM_001271855.1 2623 Silent Mutation CCC,CCG P433P NP_001258784.1
NM_007223.2 2623 Silent Mutation CCC,CCG P478P NP_009154.1
XM_011521167.2 2623 Silent Mutation CCC,CCG P446P XP_011519469.1
XM_011521168.2 2623 Silent Mutation CCC,CCG P446P XP_011519470.1
XM_017021873.1 2623 Silent Mutation CCC,CCG P446P XP_016877362.1
XM_017021874.1 2623 Silent Mutation CCC,CCG P315P XP_016877363.1
XM_017021875.1 2623 Silent Mutation CCC,CCG P315P XP_016877364.1
XM_017021876.1 2623 Silent Mutation CCC,CCG P315P XP_016877365.1
XM_017021877.1 2623 Silent Mutation CCC,CCG P315P XP_016877366.1
XM_017021878.1 2623 Silent Mutation CCC,CCG P315P XP_016877367.1

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