TCERG1L
transcription elongation regulator 1 like
Summary
Predicted to enable RNA polymerase binding activity and transcription coregulator activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200682392 | 10:132,891,438 | C/T | — | uncertain significance |
| rs139123582 | 10:132,891,465 | C/T | — | likely benign |
| rs147204742 | 10:132,891,531 | C/T | — | uncertain significance |
| rs769421483 | 10:132,891,539 | C/G | — | uncertain significance |
| rs201034812 | 10:132,891,546 | C/T | — | uncertain significance |
| rs751858553 | 10:132,896,594 | G/C | — | uncertain significance |
| rs2493509406 | 10:132,896,648 | A/G | — | uncertain significance |
| rs762126091 | 10:132,902,592 | T/C | — | uncertain significance |
| rs1402069579 | 10:132,902,606 | A/T | — | uncertain significance |
| rs759083298 | 10:132,915,100 | G/A | — | uncertain significance |
| rs894288962 | 10:132,915,101 | C/G | — | uncertain significance |
| rs199911619 | 10:132,915,126 | G/A | — | uncertain significance |
| rs150958404 | 10:132,915,135 | G/A | — | uncertain significance |
| rs760903688 | 10:132,915,152 | C/T | — | likely benign |
| rs145788961 | 10:132,915,193 | C/T | — | uncertain significance |
| rs74445317 | 10:132,917,130 | T/C | — | — |
| rs2493551224 | 10:132,932,648 | C/T | — | uncertain significance |
| rs1314319228 | 10:132,944,819 | T/C | — | uncertain significance |
| rs145173247 | 10:132,944,897 | C/T | — | uncertain significance |
| rs10741243 | 10:132,947,962 | C/G | intron variant | — |
| rs11017771 | 10:132,954,191 | G/C | intron variant | — |
| rs7081254 | 10:132,955,696 | T/C | intron variant | — |
| rs201354515 | 10:132,961,463 | G/A | — | uncertain significance |
| rs565261722 | 10:132,965,089 | T/G | — | uncertain significance |
| rs766040739 | 10:132,965,104 | T/A | — | uncertain significance |
| rs753532844 | 10:132,965,110 | C/G | — | uncertain significance |
| rs147188443 | 10:132,965,118 | C/T | — | uncertain significance |
| rs558850072 | 10:133,006,772 | G/A | — | — |
| rs757070952 | 10:133,058,513 | C/T | — | likely benign |
| rs367822256 | 10:133,058,528 | C/T | — | uncertain significance |
| rs762386085 | 10:133,058,575 | T/G | — | uncertain significance |
| rs761569207 | 10:133,058,579 | G/A | — | likely benign |
| rs1443021211 | 10:133,058,590 | C/G | — | uncertain significance |
| rs372812956 | 10:133,058,603 | G/A | — | uncertain significance |
| rs768095460 | 10:133,058,612 | G/A | — | uncertain significance |
| rs943807432 | 10:133,058,636 | T/C | — | uncertain significance |
| rs750754103 | 10:133,058,648 | C/T | — | uncertain significance |
| rs149055623 | 10:133,058,649 | G/A | — | likely benign |
| rs768205119 | 10:133,058,657 | C/T | — | uncertain significance |
| rs4751360 | 10:133,097,784 | C/G | — | — |
| rs41282900 | 10:133,106,536 | G/C | — | likely benign |
| rs2493754817 | 10:133,106,616 | C/A | — | uncertain significance |
| rs1846838204 | 10:133,106,635 | A/G | — | uncertain significance |
| rs2493756219 | 10:133,107,423 | T/A | — | uncertain significance |
| rs576330871 | 10:133,107,457 | T/C | — | likely benign |
| rs745908436 | 10:133,107,540 | G/A | — | uncertain significance |
| rs1032169405 | 10:133,109,576 | A/G | — | uncertain significance |
| rs540582305 | 10:133,109,652 | G/C | — | uncertain significance |
| rs1800227124 | 10:133,109,676 | G/A | — | uncertain significance |
| rs1846897854 | 10:133,109,700 | G/C | — | uncertain significance |
| rs891881206 | 10:133,109,818 | C/G | — | uncertain significance |
| rs2493761859 | 10:133,109,862 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.