Search Thermo Fisher Scientific
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AAACCAGCAGTCACAGGAACATGCT[A/G]CTTTTAGATTTGCTTTGTCGCAACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138248 | ||||||||||||||||||||
Literature Links: |
GRIA1 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 |
GRIA1 - glutamate ionotropic receptor AMPA type subunit 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000827.3 | 75 | Missense Mutation | ACT,GCT | T,A 41 | NP_000818.2 | |
NM_001114183.1 | 75 | Missense Mutation | ACT,GCT | T,A 41 | NP_001107655.1 | |
NM_001258019.1 | 75 | Missense Mutation | ACT,GCT | T,A 41 | NP_001244948.1 | |
NM_001258020.1 | 75 | UTR 5 | NP_001244949.1 | |||
NM_001258021.1 | 75 | Missense Mutation | ACT,GCT | T,A 51 | NP_001244950.1 | |
NM_001258022.1 | 75 | Missense Mutation | ACT,GCT | T,A 51 | NP_001244951.1 | |
NM_001258023.1 | 75 | UTR 5 | NP_001244952.1 | |||
XM_011537635.2 | 75 | Missense Mutation | ACT,GCT | T,A 21 | XP_011535937.1 | |
XM_017009392.1 | 75 | Missense Mutation | ACT,GCT | T,A 51 | XP_016864881.1 | |
XM_017009393.1 | 75 | UTR 5 | XP_016864882.1 |