Product Details

SNP ID
rs199683188
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:1465486 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGCTGCGCCCCCGGGACTCAGAAC[A/G]CACTCTCCTGCCTCTGGAGGCCGGG
Phenotype
MIM: 300525
Polymorphism
A/G, 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 1438 Missense Mutation GCG,GTG A358V NP_835230.1
XM_005274429.3 1438 Missense Mutation GCG,GTG A358V XP_005274486.1
XM_006724443.3 1438 Missense Mutation GCG,GTG A547V XP_006724506.2
XM_011546178.2 1438 Missense Mutation GCG,GTG A358V XP_011544480.1
XM_011546179.2 1438 Missense Mutation GCG,GTG A358V XP_011544481.1

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