Product Details

SNP ID
rs656612
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:121138849 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CATGCTTCTTGGCCCATGGAGGTTG[A/C]CAGCTCACCTTGGTACTTTACTACT
Phenotype
MIM: 602566
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
P2RX7 PubMed Links

Gene Details

Gene
P2RX7
Gene Name
purinergic receptor P2X 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002562.5 Intron NP_002553.3
XM_011538419.2 Intron XP_011536721.1
XM_011538420.2 Intron XP_011536722.1
XM_017019364.1 Intron XP_016874853.1
XM_017019365.1 Intron XP_016874854.1
XM_017019366.1 Intron XP_016874855.1
XM_017019367.1 Intron XP_016874856.1

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