Product Details

SNP ID
rs201676598
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:1010683 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCGCTGCCACAGGCCCGGGACTCCC[C/G]CTGGCCCCAGGCGAGACGGGGCCCA
Phenotype
MIM: 606651 MIM: 611011
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
GRIN3B PubMed Links

Gene Details

Gene
GRIN3B
Gene Name
glutamate ionotropic receptor NMDA type subunit 3B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_138690.2 1775 Intron NP_619635.1
XM_017026243.1 1775 Intron XP_016881732.1
Gene
LOC105372235
Gene Name
uncharacterized LOC105372235
There are no transcripts associated with this gene.

Gene
TMEM259
Gene Name
transmembrane protein 259
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001033026.1 1775 Missense Mutation AGC,AGG S510R NP_001028198.1
NM_033420.3 1775 UTR 3 NP_219488.1
XM_005259675.2 1775 Missense Mutation AGC,AGG S551R XP_005259732.1
XM_005259676.2 1775 Missense Mutation AGC,AGG S545R XP_005259733.1
XM_005259677.2 1775 Missense Mutation AGC,AGG S534R XP_005259734.1
XM_005259678.2 1775 Missense Mutation AGC,AGG S516R XP_005259735.1
XM_017027457.1 1775 Missense Mutation AGC,AGG S499R XP_016882946.1

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