TENT5C
terminal nucleotidyltransferase 5C
Summary
Enables poly(A) RNA polymerase activity. Involved in mRNA stabilization and negative regulation of cell differentiation. Located in centrosome; cytoplasm; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1992117 | 1:118,147,142 | C/G | upstream gene variant | — |
| rs34754277 | 1:118,147,892 | T/C | regulatory region variant | — |
| rs11587735 | 1:118,153,011 | A/C | upstream gene variant | — |
| rs35602316 | 1:118,154,775 | G/A | regulatory region variant | — |
| rs3767810 | 1:118,154,938 | A/C | — | — |
| rs34039852 | 1:118,155,103 | T/C | regulatory region variant | — |
| rs199858224 | 1:118,155,152 | A/T | — | — |
| rs1370297 | 1:118,156,053 | G/A | regulatory region variant | — |
| rs3767814 | 1:118,156,539 | G/A | intron variant | — |
| rs1657820 | 1:118,158,607 | A/G | intron variant | — |
| rs11580646 | 1:118,162,419 | C/A | — | — |
| rs10923357 | 1:118,164,771 | C/A | — | — |
| rs34495780 | 1:118,165,536 | G/A | — | not provided |
| rs587778307 | 1:118,165,579 | C/G | — | uncertain significance |
| rs779398843 | 1:118,165,599 | G/A | — | uncertain significance |
| rs148397151 | 1:118,165,603 | G/A | — | uncertain significance |
| rs1653931101 | 1:118,165,630 | C/T | — | uncertain significance |
| rs2525195544 | 1:118,165,641 | A/G | — | uncertain significance |
| rs756798728 | 1:118,165,656 | C/T | — | uncertain significance |
| rs776281952 | 1:118,165,663 | G/A | — | likely benign |
| rs1630312 | 1:118,165,691 | C/G | — | not provided |
| rs745917069 | 1:118,165,695 | G/A | — | uncertain significance |
| rs781549053 | 1:118,165,930 | C/T | — | uncertain significance |
| rs145001981 | 1:118,165,936 | C/T | — | uncertain significance |
| rs749332682 | 1:118,165,942 | G/A | — | uncertain significance |
| rs2525196462 | 1:118,166,071 | T/C | — | uncertain significance |
| rs373419973 | 1:118,166,074 | A/G | — | uncertain significance |
| rs587778306 | 1:118,166,263 | C/T | — | not provided |
| rs587778308 | 1:118,166,265 | G/T | — | not provided |
| rs761103312 | 1:118,166,292 | C/T | — | uncertain significance |
| rs77871185 | 1:118,166,331 | A/G | — | not provided |
| rs149654076 | 1:118,166,379 | G/A | — | not provided |
| rs145471785 | 1:118,166,385 | A/G | — | not provided |
| rs775789017 | 1:118,166,421 | C/T | — | uncertain significance |
| rs764287568 | 1:118,166,436 | G/A | — | uncertain significance |
| rs930666933 | 1:118,166,526 | A/G | — | uncertain significance |
| rs757856198 | 1:118,166,545 | A/G | — | uncertain significance |
| rs1354785362 | 1:118,166,572 | C/G | — | uncertain significance |
| rs752308622 | 1:118,166,607 | G/A | — | uncertain significance |
| rs1185278454 | 1:118,166,631 | A/G | — | uncertain significance |
| rs749590706 | 1:118,166,641 | A/G | — | uncertain significance |
| rs61807822 | 1:118,171,453 | G/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.