Product Details

SNP ID
rs148157935
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:1466445 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCACAGAGAGAAGAGGTTGCCCGG[C/G]ATGCTGACCGCCGCCACCAGCGAGT
Phenotype
MIM: 300525
Polymorphism
C/G, 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_178129.4 479 Missense Mutation ATC,ATG I38M NP_835230.1
XM_005274429.3 479 Missense Mutation ATC,ATG I38M XP_005274486.1
XM_006724443.3 479 Missense Mutation ATC,ATG I227M XP_006724506.2
XM_011546178.2 479 Missense Mutation ATC,ATG I38M XP_011544480.1
XM_011546179.2 479 Missense Mutation ATC,ATG I38M XP_011544481.1

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