Product Details

SNP ID
rs141515286
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:1465497 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCGGGACTCAGAACACACTCTCCTG[A/C]CTCTGGAGGCCGGGCCTGGTGGCTC
Phenotype
MIM: 300525
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
P2RY8 PubMed Links

Gene Details

Gene
P2RY8
Gene Name
purinergic receptor P2Y8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_178129.4 1427 Silent Mutation NP_835230.1
XM_005274429.3 1427 Missense Mutation XP_005274486.1
XM_006724443.3 1427 Silent Mutation XP_006724506.2
XM_011546178.2 1427 Missense Mutation XP_011544480.1
XM_011546179.2 1427 Missense Mutation XP_011544481.1

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