Product Details

SNP ID
rs142582353
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:151213517 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATACCGCAAGATTTCTTTTGACTGG[A/C]AGCTGTAATGAGCTTCGGTCTGACT
Phenotype
MIM: 611318 MIM: 610116
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
GPR171 PubMed Links

Gene Details

Gene
GPR171
Gene Name
G protein-coupled receptor 171
There are no transcripts associated with this gene.

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 1088 Intron NP_443728.3
XM_006713487.3 1088 Intron XP_006713550.1
XM_011512390.2 1088 Intron XP_011510692.1
XM_011512394.2 1088 Intron XP_011510696.1
XM_011512399.2 1088 Intron XP_011510701.1
XM_017005676.1 1088 Intron XP_016861165.1
XM_017005677.1 1088 Intron XP_016861166.1
XM_017005678.1 1088 Intron XP_016861167.1
XM_017005679.1 1088 Intron XP_016861168.1
XM_017005680.1 1088 Intron XP_016861169.1
XM_017005681.1 1088 Intron XP_016861170.1
Gene
P2RY14
Gene Name
purinergic receptor P2Y14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001081455.1 1088 Missense Mutation TGC,TTC C267F NP_001074924.1
NM_014879.3 1088 Missense Mutation TGC,TTC C267F NP_055694.3
XM_005247922.3 1088 Missense Mutation TGC,TTC C267F XP_005247979.1
XM_005247923.3 1088 Missense Mutation TGC,TTC C267F XP_005247980.1
XM_011513340.2 1088 Missense Mutation TGC,TTC C267F XP_011511642.1
XM_017007583.1 1088 Missense Mutation TGC,TTC C267F XP_016863072.1

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