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AAACAGCCAACAGGAACTCAAGCAG[C/T]CATAATTAGAGACAATTAAATGTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
13 submissions
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Phenotype: |
MIM: 606273 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EIF2B3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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EIF2B3 - eukaryotic translation initiation factor 2B subunit gamma | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166588.2 | Intron | NP_001160060.1 | ||||
NM_001261418.1 | Intron | NP_001248347.1 | ||||
NM_020365.4 | Intron | NP_065098.1 | ||||
XM_017002745.1 | Intron | XP_016858234.1 | ||||
XM_017002746.1 | Intron | XP_016858235.1 | ||||
XM_017002747.1 | Intron | XP_016858236.1 |