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CGCCTGAAGCAGCATCTCCTGGATG[C/T]GGACCTGCTGCAGGATGGCAGGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606651 MIM: 611011 | ||||||||||||||||||||
Literature Links: |
GRIN3B 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 |
GRIN3B - glutamate ionotropic receptor NMDA type subunit 3B | ||||||
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There are no transcripts associated with this gene. |
LOC105372235 - uncharacterized LOC105372235 | ||||||
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There are no transcripts associated with this gene. |
TMEM259 - transmembrane protein 259 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033026.1 | 1621 | Missense Mutation | CAC,CGC | H,R 459 | NP_001028198.1 | |
NM_033420.3 | 1621 | UTR 3 | NP_219488.1 | |||
XM_005259675.2 | 1621 | Missense Mutation | CAC,CGC | H,R 500 | XP_005259732.1 | |
XM_005259676.2 | 1621 | Missense Mutation | CAC,CGC | H,R 494 | XP_005259733.1 | |
XM_005259677.2 | 1621 | Missense Mutation | CAC,CGC | H,R 483 | XP_005259734.1 | |
XM_005259678.2 | 1621 | Missense Mutation | CAC,CGC | H,R 465 | XP_005259735.1 | |
XM_017027457.1 | 1621 | Missense Mutation | CAC,CGC | H,R 448 | XP_016882946.1 |