Product Details

SNP ID
rs9940680
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:9757000 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTCCCTGATACATTCATACCCTGGT[C/G]TATCAGAAGGGTTCTTCAAATGTCA
Phenotype
MIM: 138253
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
GRIN2A PubMed Links

Gene Details

Gene
GRIN2A
Gene Name
glutamate ionotropic receptor NMDA type subunit 2A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000833.4 10340 UTR 3 NP_000824.1
NM_001134407.2 10340 UTR 3 NP_001127879.1
NM_001134408.2 10340 UTR 3 NP_001127880.1
XM_011522458.2 10340 UTR 3 XP_011520760.1
XM_011522461.2 10340 UTR 3 XP_011520763.1
XM_017023172.1 10340 UTR 3 XP_016878661.1
XM_017023173.1 10340 UTR 3 XP_016878662.1

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