Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGTAACAACTGCTTTTGGGCTCAG[G/T]GATGAAGCTGTGCTCAGACAGCATG
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 |
---|---|---|
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 |
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 | 1915 | Missense Mutation | ACT,CCT | T,P 315 | NP_000825.2 | |
XM_005253351.3 | 1915 | Intron | XP_005253408.1 | |||
XM_011520628.2 | 1915 | Missense Mutation | ACT,CCT | T,P 315 | XP_011518930.1 | |
XM_011520629.2 | 1915 | Missense Mutation | ACT,CCT | T,P 315 | XP_011518931.1 | |
XM_017019219.1 | 1915 | Missense Mutation | ACT,CCT | T,P 315 | XP_016874708.1 |