Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCATCCAGATGGCTCTGTCGGTGTG[C/T]GAGGACCTCATCTCCAGCCAGGTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138249 | ||||||||||||||||||||
Literature Links: |
GRIN1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
GRIN1 - glutamate ionotropic receptor NMDA type subunit 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000832.6 | 567 | Silent Mutation | TGC,TGT | C,C 79 | NP_000823.4 | |
NM_001185090.1 | 567 | Silent Mutation | TGC,TGT | C,C 79 | NP_001172019.1 | |
NM_001185091.1 | 567 | Silent Mutation | TGC,TGT | C,C 79 | NP_001172020.1 | |
NM_007327.3 | 567 | Silent Mutation | TGC,TGT | C,C 79 | NP_015566.1 | |
NM_021569.3 | 567 | Silent Mutation | TGC,TGT | C,C 79 | NP_067544.1 | |
XM_005266071.3 | 567 | Silent Mutation | TGC,TGT | C,C 79 | XP_005266128.1 | |
XM_005266072.3 | 567 | Silent Mutation | TGC,TGT | C,C 79 | XP_005266129.1 | |
XM_005266073.4 | 567 | Silent Mutation | TGC,TGT | C,C 79 | XP_005266130.1 | |
XM_011518583.2 | 567 | Silent Mutation | TGC,TGT | C,C 79 | XP_011516885.1 |