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CCAAGCACCTCTGGGTGCAGGCTGG[A/G]AGCAAGAGCTGGGGGAGGGAGAACC
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | Intron | NP_000823.4 | ||||
NM_001185090.1 | Intron | NP_001172019.1 | ||||
NM_001185091.1 | Intron | NP_001172020.1 | ||||
NM_007327.3 | Intron | NP_015566.1 | ||||
NM_021569.3 | Intron | NP_067544.1 | ||||
XM_005266071.3 | Intron | XP_005266128.1 | ||||
XM_005266072.3 | Intron | XP_005266129.1 | ||||
XM_005266073.4 | Intron | XP_005266130.1 | ||||
XM_011518583.2 | Intron | XP_011516885.1 |