Product Details

SNP ID
rs200926939
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:120167042 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCTCTGTTGCTTTTCACACCAGC[A/G]TGGGTTTCAAGTCATCTTTGAAGTT
Phenotype
MIM: 610464
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
GPR156 PubMed Links

Gene Details

Gene
GPR156
Gene Name
G protein-coupled receptor 156
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001168271.1 2897 Missense Mutation ACG,ATG T808M NP_001161743.1
NM_153002.2 2897 Missense Mutation ACG,ATG T812M NP_694547.2
XM_005247165.2 2897 Missense Mutation ACG,ATG T812M XP_005247222.1
XM_011512484.2 2897 Missense Mutation ACG,ATG T731M XP_011510786.1
XM_011512487.1 2897 Missense Mutation ACG,ATG T731M XP_011510789.1
XM_011512488.2 2897 Missense Mutation ACG,ATG T426M XP_011510790.1
XM_017005795.1 2897 Missense Mutation ACG,ATG T812M XP_016861284.1
XM_017005796.1 2897 Missense Mutation ACG,ATG T812M XP_016861285.1
XM_017005797.1 2897 Missense Mutation ACG,ATG T808M XP_016861286.1

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