Product Details

SNP ID
rs201740586
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:1466449 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGAGAGAAGAGGTTGCCCGGGATG[C/T]TGACCGCCGCCACCAGCGAGTACAC
Phenotype
MIM: 300525
Polymorphism
C/T, Transition 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_178129.4 475 Missense Mutation AAC,AGC N37S NP_835230.1
XM_005274429.3 475 Missense Mutation AAC,AGC N37S XP_005274486.1
XM_006724443.3 475 Missense Mutation AAC,AGC N226S XP_006724506.2
XM_011546178.2 475 Missense Mutation AAC,AGC N37S XP_011544480.1
XM_011546179.2 475 Missense Mutation AAC,AGC N37S XP_011544481.1

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