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SNP ID: rs16863317
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:151326671 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAGTATAAAGTTCAAGAGATGGATA[A/G]GTAGCTAGGAGGTAAGGCCAGAAAG
Phenotype: MIM: 606379 MIM: 611318 MIM: 606380
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: GPR87 PubMed Links

Gene Details

Gene: GPR87
Gene Name: G protein-coupled receptor 87

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	2406	Intron			NP_443728.3
XM_006713487.3	2406	Intron			XP_006713550.1
XM_011512390.2	2406	Intron			XP_011510692.1
XM_011512394.2	2406	Intron			XP_011510696.1
XM_011512399.2	2406	Intron			XP_011510701.1
XM_017005676.1	2406	Intron			XP_016861165.1
XM_017005677.1	2406	Intron			XP_016861166.1
XM_017005678.1	2406	Intron			XP_016861167.1
XM_017005679.1	2406	Intron			XP_016861168.1
XM_017005680.1	2406	Intron			XP_016861169.1
XM_017005681.1	2406	Intron			XP_016861170.1

Gene: P2RY13
Gene Name: purinergic receptor P2Y13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_176894.2	2406	UTR 3			NP_795713.2
XM_006713664.1	2406	UTR 3			XP_006713727.1

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