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CGAGGATGACAGCAATGCCAATGCT[T/G]GGGGGGCTCTTCTGAGAACGAGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138252 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GRIN2B 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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GRIN2B - glutamate ionotropic receptor NMDA type subunit 2B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000834.3 | 1071 | Silent Mutation | CCA,CCC | P,P 33 | NP_000825.2 | |
XM_005253351.3 | 1071 | Intron | XP_005253408.1 | |||
XM_011520628.2 | 1071 | Silent Mutation | CCA,CCC | P,P 33 | XP_011518930.1 | |
XM_011520629.2 | 1071 | Silent Mutation | CCA,CCC | P,P 33 | XP_011518931.1 | |
XM_017019219.1 | 1071 | Silent Mutation | CCA,CCC | P,P 33 | XP_016874708.1 |