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ATAGGTAAATTAGAAAGCAGACTGG[G/T]GGTAGTCAGACACTGAGGGTAGAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600788 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
TCEB1 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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TCEB1 - transcription elongation factor B subunit 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204857.1 | Intron | NP_001191786.1 | ||||
NM_001204858.1 | Intron | NP_001191787.1 | ||||
NM_001204859.1 | Intron | NP_001191788.1 | ||||
NM_001204860.1 | Intron | NP_001191789.1 | ||||
NM_001204861.1 | Intron | NP_001191790.1 | ||||
NM_001204862.1 | Intron | NP_001191791.1 | ||||
NM_001204863.1 | Intron | NP_001191792.1 | ||||
NM_001204864.1 | Intron | NP_001191793.1 | ||||
NM_005648.3 | Intron | NP_005639.1 | ||||
XM_011517580.2 | Intron | XP_011515882.1 | ||||
XM_011517581.2 | Intron | XP_011515883.1 |
Set Membership: |
HapMap |