Product Details

SNP ID
rs150296778
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:151199210 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTAATGCCAGAGTAAGCAGGAAATC[A/G]GCTGTAAGCAAATTAATTAAGTAGA
Phenotype
MIM: 611318
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
GPR171 PubMed Links

Gene Details

Gene
GPR171
Gene Name
G protein-coupled receptor 171
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_013308.3 417 Silent Mutation GCC,GCT A59A NP_037440.3
XM_005247402.3 417 Silent Mutation GCC,GCT A59A XP_005247459.1
XM_005247403.3 417 Silent Mutation GCC,GCT A59A XP_005247460.1
XM_017006274.1 417 Silent Mutation GCC,GCT A59A XP_016861763.1
Gene
MED12L
Gene Name
mediator complex subunit 12 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_053002.5 417 Intron NP_443728.3
XM_006713487.3 417 Intron XP_006713550.1
XM_011512390.2 417 Intron XP_011510692.1
XM_011512394.2 417 Intron XP_011510696.1
XM_011512399.2 417 Intron XP_011510701.1
XM_017005676.1 417 Intron XP_016861165.1
XM_017005677.1 417 Intron XP_016861166.1
XM_017005678.1 417 Intron XP_016861167.1
XM_017005679.1 417 Intron XP_016861168.1
XM_017005680.1 417 Intron XP_016861169.1
XM_017005681.1 417 Intron XP_016861170.1

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