Product Details

SNP ID
rs16966242
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:9753632 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GACAACCATAGTATATACTTCCTCT[A/G]TCATAGAAAGGTGTTAAGCAAACAT
Phenotype
MIM: 138253
Polymorphism
A/G, Transition 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 13708 UTR 3 NP_000824.1
NM_001134407.2 13708 UTR 3 NP_001127879.1
NM_001134408.2 13708 UTR 3 NP_001127880.1
XM_011522458.2 13708 UTR 3 XP_011520760.1
XM_011522461.2 13708 UTR 3 XP_011520763.1
XM_017023172.1 13708 UTR 3 XP_016878661.1
XM_017023173.1 13708 UTR 3 XP_016878662.1

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