Product Details

SNP ID

rs140553172

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:151213494 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTAGCAGAGTGAATTCTTTCATAT[A/G]CCGCAAGATTTCTTTTGACTGGCAG

Phenotype

MIM: 611318 MIM: 610116

Polymorphism

A/G, Transition 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	1111	Intron			NP_443728.3
XM_006713487.3	1111	Intron			XP_006713550.1
XM_011512390.2	1111	Intron			XP_011510692.1
XM_011512394.2	1111	Intron			XP_011510696.1
XM_011512399.2	1111	Intron			XP_011510701.1
XM_017005676.1	1111	Intron			XP_016861165.1
XM_017005677.1	1111	Intron			XP_016861166.1
XM_017005678.1	1111	Intron			XP_016861167.1
XM_017005679.1	1111	Intron			XP_016861168.1
XM_017005680.1	1111	Intron			XP_016861169.1
XM_017005681.1	1111	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	1111	Missense Mutation	CAT,TAT	H275Y	NP_001074924.1
NM_014879.3	1111	Missense Mutation	CAT,TAT	H275Y	NP_055694.3
XM_005247922.3	1111	Missense Mutation	CAT,TAT	H275Y	XP_005247979.1
XM_005247923.3	1111	Missense Mutation	CAT,TAT	H275Y	XP_005247980.1
XM_011513340.2	1111	Missense Mutation	CAT,TAT	H275Y	XP_011511642.1
XM_017007583.1	1111	Missense Mutation	CAT,TAT	H275Y	XP_016863072.1

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