GTF3C5
general transcription factor IIIC subunit 5
Summary
Enables RNA polymerase III general transcription initiation factor activity. Predicted to be involved in 5S class rRNA transcription by RNA polymerase III and tRNA transcription by RNA polymerase III. Predicted to act upstream of or within skeletal muscle cell differentiation. Located in nucleoplasm. Part of transcription factor TFIIIC complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs140871186 | 9:135,905,702 | C/T | regulatory region variant | — |
| rs140936027 | 9:135,906,417 | G/T | — | uncertain significance |
| rs2539557705 | 9:135,906,418 | A/G | — | uncertain significance |
| rs757737273 | 9:135,906,438 | G/A | — | likely benign |
| rs773109105 | 9:135,906,456 | C/T | — | uncertain significance |
| rs1849717655 | 9:135,906,513 | A/G | — | uncertain significance |
| rs750479450 | 9:135,906,543 | G/A | — | uncertain significance |
| rs2539584954 | 9:135,917,495 | A/G | — | uncertain significance |
| rs138091600 | 9:135,917,552 | C/T | — | uncertain significance |
| rs144689336 | 9:135,917,579 | C/T | — | uncertain significance |
| rs147553955 | 9:135,917,580 | G/T | — | uncertain significance |
| rs781066927 | 9:135,917,610 | G/T | — | uncertain significance |
| rs8193016 | 9:135,917,744 | C/T | intron variant | — |
| rs756925114 | 9:135,919,159 | G/A | — | uncertain significance |
| rs139422900 | 9:135,919,199 | G/A | — | uncertain significance |
| rs763539610 | 9:135,919,204 | G/T | — | uncertain significance |
| rs368008906 | 9:135,919,235 | C/T | — | uncertain significance |
| rs2539589856 | 9:135,919,247 | C/T | — | uncertain significance |
| rs187715179 | 9:135,920,196 | C/T | intron variant | — |
| rs568334984 | 9:135,920,889 | C/T | — | — |
| rs372576423 | 9:135,926,196 | C/T | — | uncertain significance |
| rs143558287 | 9:135,926,241 | A/G | — | uncertain significance |
| rs1418633326 | 9:135,926,260 | T/G | — | uncertain significance |
| rs564242923 | 9:135,926,333 | G/A | — | uncertain significance |
| rs369895162 | 9:135,926,340 | G/A | — | likely benign |
| rs371028258 | 9:135,927,459 | C/T | — | uncertain significance |
| rs373298238 | 9:135,927,506 | C/G | — | uncertain significance |
| rs1345216877 | 9:135,929,288 | A/T | — | uncertain significance |
| rs778940831 | 9:135,929,795 | G/A | — | uncertain significance |
| rs374887172 | 9:135,929,800 | G/A | — | uncertain significance |
| rs369612433 | 9:135,929,816 | C/T | — | uncertain significance |
| rs369889499 | 9:135,929,846 | A/G | — | uncertain significance |
| rs199931911 | 9:135,929,851 | C/T | — | uncertain significance |
| rs375088854 | 9:135,930,147 | C/T | — | uncertain significance |
| rs1402158983 | 9:135,930,158 | G/A | — | likely benign |
| rs759593240 | 9:135,930,164 | C/T | — | uncertain significance |
| rs765264112 | 9:135,930,165 | G/A | — | uncertain significance |
| rs35181097 | 9:135,930,184 | G/C | — | uncertain significance |
| rs372612378 | 9:135,930,344 | C/T | — | uncertain significance |
| rs140832971 | 9:135,931,411 | A/C | — | uncertain significance |
| rs2539626999 | 9:135,932,153 | G/C | — | uncertain significance |
| rs144801827 | 9:135,932,181 | G/C | — | uncertain significance |
| rs1172130352 | 9:135,932,248 | A/G | — | uncertain significance |
| rs770781582 | 9:135,932,251 | C/T | — | uncertain significance |
| rs769796043 | 9:135,932,269 | G/A | — | uncertain significance |
| rs762614895 | 9:135,932,274 | A/G | — | uncertain significance |
| rs201440334 | 9:135,932,280 | C/T | — | uncertain significance |
| rs759989225 | 9:135,933,203 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.