Product Details

SNP ID
rs148446487
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:13541253 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCTACTCTGAAGTATTAATGCTGG[A/G]ATAGTCACTGGGTAACAAAGCTCCC
Phenotype
MIM: 138252
Polymorphism
A/G, 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 26957 Intron NP_000825.2
XM_005253351.3 26957 UTR 3 XP_005253408.1
XM_011520628.2 26957 UTR 3 XP_011518930.1
XM_011520629.2 26957 UTR 3 XP_011518931.1
XM_017019219.1 26957 UTR 3 XP_016874708.1

View Full Product Details