Product Details

SNP ID
rs192006771
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:137139732 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCTCTGTCGGTGTGCGAGGACCT[C/T]ATCTCCAGCCAGGTGCCCTCCCCCA
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_000832.6 576 Silent Mutation CTC,CTT L82L NP_000823.4
NM_001185090.1 576 Silent Mutation CTC,CTT L82L NP_001172019.1
NM_001185091.1 576 Silent Mutation CTC,CTT L82L NP_001172020.1
NM_007327.3 576 Silent Mutation CTC,CTT L82L NP_015566.1
NM_021569.3 576 Silent Mutation CTC,CTT L82L NP_067544.1
XM_005266071.3 576 Silent Mutation CTC,CTT L82L XP_005266128.1
XM_005266072.3 576 Silent Mutation CTC,CTT L82L XP_005266129.1
XM_005266073.4 576 Silent Mutation CTC,CTT L82L XP_005266130.1
XM_011518583.2 576 Silent Mutation CTC,CTT L82L XP_011516885.1

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