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TGGCGGGGACGGGGGCGAGAGTGAA[A/C]GATTCAACCCGGGGGAGCTCAGGTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605409 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TCERG1 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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TCERG1 - transcription elongation regulator 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040006.1 | 263 | Silent Mutation | AGA,CGA | R,R 13 | NP_001035095.1 | |
NM_006706.3 | 263 | Silent Mutation | AGA,CGA | R,R 13 | NP_006697.2 | |
XM_005268365.2 | 263 | Silent Mutation | AGA,CGA | R,R 13 | XP_005268422.1 | |
XM_017008977.1 | 263 | Silent Mutation | AGA,CGA | R,R 13 | XP_016864466.1 | |
XM_017008978.1 | 263 | Silent Mutation | AGA,CGA | R,R 13 | XP_016864467.1 | |
XM_017008979.1 | 263 | Silent Mutation | AGA,CGA | R,R 13 | XP_016864468.1 | |
XM_017008980.1 | 263 | Silent Mutation | AGA,CGA | R,R 13 | XP_016864469.1 | |
XM_017008981.1 | 263 | Intron | XP_016864470.1 | |||
XM_017008982.1 | 263 | Intron | XP_016864471.1 | |||
XM_017008983.1 | 263 | Intron | XP_016864472.1 | |||
XM_017008984.1 | 263 | Silent Mutation | AGA,CGA | R,R 13 | XP_016864473.1 | |
XM_017008985.1 | 263 | Silent Mutation | AGA,CGA | R,R 13 | XP_016864474.1 |