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CAAAATGCTTTGTGAGCTTGATCAG[C/T]TGGCACTTCTGAATCAGAGAAAGAT
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) - 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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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 |