Product Details

SNP ID
rs201816843
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:137139534 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCTCGCCCTGCTGTTCTCCTGCTC[C/T]GTCGCCCGTGCCGCGTGCGACCCCA
Phenotype
MIM: 138249
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
GRIN1 PubMed Links

Gene Details

Gene
GRIN1
Gene Name
glutamate ionotropic receptor NMDA type subunit 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000832.6 378 Silent Mutation TCC,TCT S16S NP_000823.4
NM_001185090.1 378 Silent Mutation TCC,TCT S16S NP_001172019.1
NM_001185091.1 378 Silent Mutation TCC,TCT S16S NP_001172020.1
NM_007327.3 378 Silent Mutation TCC,TCT S16S NP_015566.1
NM_021569.3 378 Silent Mutation TCC,TCT S16S NP_067544.1
XM_005266071.3 378 Silent Mutation TCC,TCT S16S XP_005266128.1
XM_005266072.3 378 Silent Mutation TCC,TCT S16S XP_005266129.1
XM_005266073.4 378 Silent Mutation TCC,TCT S16S XP_005266130.1
XM_011518583.2 378 Silent Mutation TCC,TCT S16S XP_011516885.1

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