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TTTCCAGACAGATTGTCTTGTTATT[G/T]TCTGGATTTTGGGGACTCGCCATGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138246 | ||||||||||||||||||||
Literature Links: |
GRIA4 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 |
GRIA4 - glutamate ionotropic receptor AMPA type subunit 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000829.3 | 526 | Missense Mutation | TTG,TTT | L,F 12 | NP_000820.3 | |
NM_001077243.2 | 526 | Missense Mutation | TTG,TTT | L,F 12 | NP_001070711.2 | |
NM_001077244.1 | 526 | Missense Mutation | TTG,TTT | L,F 12 | NP_001070712.1 | |
NM_001112812.1 | 526 | Missense Mutation | TTG,TTT | L,F 12 | NP_001106283.1 | |
XM_005271518.3 | 526 | Missense Mutation | TTG,TTT | L,F 12 | XP_005271575.1 | |
XM_006718823.1 | 526 | Missense Mutation | TTG,TTT | L,F 12 | XP_006718886.1 | |
XM_011542775.2 | 526 | Missense Mutation | TTG,TTT | L,F 12 | XP_011541077.1 | |
XM_011542776.2 | 526 | Intron | XP_011541078.1 | |||
XM_011542777.2 | 526 | Intron | XP_011541079.1 | |||
XM_017017609.1 | 526 | Missense Mutation | TTG,TTT | L,F 12 | XP_016873098.1 | |
XM_017017610.1 | 526 | Missense Mutation | TTG,TTT | L,F 12 | XP_016873099.1 | |
XM_017017611.1 | 526 | Intron | XP_016873100.1 |