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TATGCATATTTCTGTCCTCCTTTCT[C/G]CTGTTTTATGGGGACTGATTTTTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138247 | ||||||||||||||||||||
Literature Links: |
GRIA2 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 |
GRIA2 - glutamate ionotropic receptor AMPA type subunit 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000826.3 | 496 | Missense Mutation | CCT,GCT | P,A 13 | NP_000817.2 | |
NM_001083619.1 | 496 | Missense Mutation | CCT,GCT | P,A 13 | NP_001077088.1 | |
NM_001083620.1 | 496 | Intron | NP_001077089.1 | |||
XM_017008113.1 | 496 | Intron | XP_016863602.1 | |||
XM_017008114.1 | 496 | Intron | XP_016863603.1 | |||
XM_017008115.1 | 496 | Intron | XP_016863604.1 | |||
XM_017008116.1 | 496 | Intron | XP_016863605.1 | |||
XM_017008117.1 | 496 | Intron | XP_016863606.1 |