Product Details

SNP ID
rs67664296
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:13537703 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCACCTGGGCAAGTTTTCAACCCC[C/T]AACCCCTCCAGCCACCCAGGACAAT
Phenotype
MIM: 138252
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
GRIN2B PubMed Links

Gene Details

Gene
GRIN2B
Gene Name
glutamate ionotropic receptor NMDA type subunit 2B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000834.3 30507 Intron NP_000825.2
XM_005253351.3 30507 UTR 3 XP_005253408.1
XM_011520628.2 30507 UTR 3 XP_011518930.1
XM_011520629.2 30507 UTR 3 XP_011518931.1
XM_017019219.1 30507 UTR 3 XP_016874708.1

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