Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
7 submissions
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Phenotype: |
MIM: 604128 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TCEA3 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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TCEA3 - transcription elongation factor A3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003196.2 | 1377 | Intron | NP_003187.1 | |||
XM_006710864.1 | 1377 | UTR 3 | XP_006710927.1 | |||
XM_011542053.2 | 1377 | Intron | XP_011540355.1 | |||
XM_017002200.1 | 1377 | Missense Mutation | TCT,TTT | S,F 429 | XP_016857689.1 | |
XM_017002201.1 | 1377 | Missense Mutation | TCT,TTT | S,F 408 | XP_016857690.1 | |
XM_017002202.1 | 1377 | Missense Mutation | TCT,TTT | S,F 408 | XP_016857691.1 | |
XM_017002203.1 | 1377 | Missense Mutation | TCT,TTT | S,F 392 | XP_016857692.1 | |
XM_017002204.1 | 1377 | Intron | XP_016857693.1 |