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AGGCGGCCGATTTGGGGCTGGGGGC[C/T]GCCGTCCCCGTGGAGCTGAGGCGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604890 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GTF3C5 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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GTF3C5 - general transcription factor IIIC subunit 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122823.1 | 373 | Silent Mutation | GCC,GCT | A,A 12 | NP_001116295.1 | |
NM_001286709.1 | 373 | UTR 5 | NP_001273638.1 | |||
NM_012087.3 | 373 | Silent Mutation | GCC,GCT | A,A 12 | NP_036219.2 | |
XM_005272234.3 | 373 | Silent Mutation | GCC,GCT | A,A 12 | XP_005272291.1 | |
XM_011519201.1 | 373 | Intron | XP_011517503.1 | |||
XM_017015315.1 | 373 | Intron | XP_016870804.1 | |||
XM_017015316.1 | 373 | Intron | XP_016870805.1 |
LOC105376306 - uncharacterized LOC105376306 | ||||||
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There are no transcripts associated with this gene. |