Product Details

SNP ID

rs142180569

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:1465637 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTCTGGGCACCCGGCGGCAGCCCA[A/G]ATATTCCCGCAGGCGCAGCTGGAAT

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	1287	Silent Mutation	CTG,TTG	L308L	NP_835230.1
XM_005274429.3	1287	Silent Mutation	CTG,TTG	L308L	XP_005274486.1
XM_006724443.3	1287	Silent Mutation	CTG,TTG	L497L	XP_006724506.2
XM_011546178.2	1287	Silent Mutation	CTG,TTG	L308L	XP_011544480.1
XM_011546179.2	1287	Silent Mutation	CTG,TTG	L308L	XP_011544481.1

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