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GGATGAAAAGAGCTATGAAGATGAT[A/G]TAACAGTACGGTCCTAGTTACAATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606686 MIM: 601750 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EIF2B1 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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EIF2B1 - eukaryotic translation initiation factor 2B subunit alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001414.3 | Intron | NP_001405.1 |
GTF2H3 - general transcription factor IIH subunit 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271866.1 | Intron | NP_001258795.1 | ||||
NM_001271867.1 | Intron | NP_001258796.1 | ||||
NM_001271868.1 | Intron | NP_001258797.1 | ||||
NM_001516.4 | Intron | NP_001507.2 | ||||
XM_017019228.1 | Intron | XP_016874717.1 |