Product Details

SNP ID
rs142901780
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:151294206 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTAATCATAATATATGCGAACTTCC[G/T]ATCTTCTCACACTTTGCAGTGATCT
Phenotype
MIM: 606379 MIM: 611318
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
GPR87 PubMed Links

Gene Details

Gene
GPR87
Gene Name
G protein-coupled receptor 87
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_023915.3 1401 Missense Mutation TGG,TTG W347L NP_076404.3
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 1401 Intron NP_443728.3
XM_006713487.3 1401 Intron XP_006713550.1
XM_011512390.2 1401 Intron XP_011510692.1
XM_011512394.2 1401 Intron XP_011510696.1
XM_011512399.2 1401 Intron XP_011510701.1
XM_017005676.1 1401 Intron XP_016861165.1
XM_017005677.1 1401 Intron XP_016861166.1
XM_017005678.1 1401 Intron XP_016861167.1
XM_017005679.1 1401 Intron XP_016861168.1
XM_017005680.1 1401 Intron XP_016861169.1
XM_017005681.1 1401 Intron XP_016861170.1

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