Product Details

SNP ID

rs200067411

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:152836291 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGCTCAAAAAGAAGAATGCGATCT[C/G]TATCAGCGTGCTGGTGTGGCTCATT

Phenotype

MIM: 601167

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

P2RY1 PubMed Links

Gene Details

Gene

P2RY1

Gene Name

purinergic receptor P2Y1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002563.4	1599	Missense Mutation	TCT,TGT	S170C	NP_002554.1

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