Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCACCAGGAATGCCTCCTGTGACTG[C/G]TCCTGGTACTCCAGCACTACCTCCT
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 597 | Missense Mutation | GCT,GGT | A,G 124 | NP_001035095.1 | |
NM_006706.3 | 597 | Missense Mutation | GCT,GGT | A,G 124 | NP_006697.2 | |
XM_005268365.2 | 597 | Missense Mutation | GCT,GGT | A,G 124 | XP_005268422.1 | |
XM_017008977.1 | 597 | Missense Mutation | GCT,GGT | A,G 124 | XP_016864466.1 | |
XM_017008978.1 | 597 | Missense Mutation | GCT,GGT | A,G 124 | XP_016864467.1 | |
XM_017008979.1 | 597 | Missense Mutation | GCT,GGT | A,G 124 | XP_016864468.1 | |
XM_017008980.1 | 597 | Missense Mutation | GCT,GGT | A,G 124 | XP_016864469.1 | |
XM_017008981.1 | 597 | Intron | XP_016864470.1 | |||
XM_017008982.1 | 597 | UTR 5 | XP_016864471.1 | |||
XM_017008983.1 | 597 | UTR 5 | XP_016864472.1 | |||
XM_017008984.1 | 597 | Missense Mutation | GCT,GGT | A,G 124 | XP_016864473.1 | |
XM_017008985.1 | 597 | Missense Mutation | GCT,GGT | A,G 124 | XP_016864474.1 |