Product Details

SNP ID

rs201004942

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:152836010 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAACAGCGTGGCCATCTGGATGTT[C/T]GTCTTCCACATGAAGCCCTGGAGCG

Phenotype

MIM: 601167

Polymorphism

C/T, Transition 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	1318	Silent Mutation	TTC,TTT	F76F	NP_002554.1

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