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AATCTGTGTAAGCTCCATAAGATGA[C/G]GTTAGATGAGAAAAGGGCTCAGGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600285 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ETF1 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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ETF1 - eukaryotic translation termination factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256302.1 | Intron | NP_001243231.1 | ||||
NM_001282185.1 | Intron | NP_001269114.1 | ||||
NM_001291974.1 | Intron | NP_001278903.1 | ||||
NM_001291975.1 | Intron | NP_001278904.1 | ||||
NM_004730.3 | Intron | NP_004721.1 | ||||
XM_005271921.1 | Intron | XP_005271978.1 | ||||
XM_017009221.1 | Intron | XP_016864710.1 | ||||
XM_017009222.1 | Intron | XP_016864711.1 |