TTF2
transcription termination factor 2
Summary
This gene encodes a member of the SWI2/SNF2 family of proteins, which play a critical role in altering protein-DNA interactions. The encoded protein has been shown to have dsDNA-dependent ATPase activity and RNA polymerase II termination activity. This protein interacts with cell division cycle 5-like, associates with human splicing complexes, and plays a role in pre-mRNA splicing. [provided by RefSeq, Jul 2008]
Known Variants83 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs751391686 | 1:117,602,991 | A/G | — | uncertain significance |
| rs138286826 | 1:117,603,131 | G/A | — | benign |
| rs917342290 | 1:117,603,146 | G/A | — | uncertain significance |
| rs199584993 | 1:117,605,027 | C/G | — | uncertain significance |
| rs538720192 | 1:117,612,106 | A/T | — | — |
| rs768847302 | 1:117,616,299 | A/G | — | uncertain significance |
| rs761825380 | 1:117,616,323 | C/T | — | uncertain significance |
| rs1041656326 | 1:117,617,596 | C/A | — | uncertain significance |
| rs73006031 | 1:117,617,598 | A/G | — | benign |
| rs147163097 | 1:117,617,682 | G/A | — | uncertain significance |
| rs192551233 | 1:117,617,684 | G/A | — | uncertain significance |
| rs35838803 | 1:117,617,687 | C/G | — | likely benign |
| rs1656881247 | 1:117,617,713 | G/C | — | uncertain significance |
| rs745804849 | 1:117,617,790 | A/G | — | uncertain significance |
| rs7535524 | 1:117,617,844 | A/G | — | benign |
| rs760088086 | 1:117,617,854 | T/G | — | likely benign |
| rs146902845 | 1:117,617,903 | T/C | — | uncertain significance |
| rs200709421 | 1:117,617,987 | C/A | — | uncertain significance |
| rs2527076902 | 1:117,617,998 | A/C | — | uncertain significance |
| rs17036832 | 1:117,618,024 | G/C | — | benign |
| rs766462506 | 1:117,618,041 | G/A | — | uncertain significance |
| rs778850536 | 1:117,618,057 | A/T | — | uncertain significance |
| rs144112278 | 1:117,618,063 | C/T | — | uncertain significance |
| rs1420061650 | 1:117,618,095 | G/A | — | uncertain significance |
| rs757979726 | 1:117,618,153 | G/A | — | likely benign |
| rs1656925689 | 1:117,618,179 | C/G | — | uncertain significance |
| rs777506049 | 1:117,618,203 | G/A | — | uncertain significance |
| rs142512730 | 1:117,618,235 | G/C | — | likely benign |
| rs146799971 | 1:117,618,263 | G/A | — | uncertain significance |
| rs199968118 | 1:117,618,311 | C/T | — | uncertain significance |
| rs759713972 | 1:117,618,327 | C/G | — | uncertain significance |
| rs753311484 | 1:117,618,364 | C/G | — | likely benign |
| rs2527082751 | 1:117,618,411 | C/A | — | uncertain significance |
| rs753261865 | 1:117,618,447 | G/A | — | uncertain significance |
| rs17036836 | 1:117,618,467 | C/T | — | benign |
| rs7549205 | 1:117,619,300 | G/A | — | benign |
| rs61737095 | 1:117,619,355 | C/T | — | benign |
| rs1354878352 | 1:117,619,359 | C/T | — | uncertain significance |
| rs139705346 | 1:117,619,362 | G/A | — | likely benign |
| rs137921158 | 1:117,620,607 | G/A | — | uncertain significance |
| rs374345000 | 1:117,620,657 | G/A | — | uncertain significance |
| rs1487729140 | 1:117,622,263 | G/T | — | uncertain significance |
| rs200744479 | 1:117,624,443 | T/A | — | likely benign |
| rs377417167 | 1:117,624,552 | C/T | — | uncertain significance |
| rs2527156598 | 1:117,626,684 | G/A | — | uncertain significance |
| rs147246961 | 1:117,626,751 | A/G | — | likely benign |
| rs144713709 | 1:117,626,760 | A/G | — | uncertain significance |
| rs773021123 | 1:117,626,766 | C/A | — | uncertain significance |
| rs764110430 | 1:117,626,774 | G/T | — | uncertain significance |
| rs968096857 | 1:117,629,094 | C/G | — | uncertain significance |
| rs1431706577 | 1:117,631,453 | T/A | — | uncertain significance |
| rs35565289 | 1:117,631,543 | C/T | — | uncertain significance |
| rs1343131724 | 1:117,631,595 | C/T | — | uncertain significance |
| rs145353452 | 1:117,632,685 | G/A | — | uncertain significance |
| rs1414178581 | 1:117,632,733 | A/G | — | uncertain significance |
| rs1204414647 | 1:117,632,797 | A/C | — | likely benign |
| rs762038460 | 1:117,632,803 | C/A | — | uncertain significance |
| rs765234615 | 1:117,633,226 | G/T | — | uncertain significance |
| rs1648563309 | 1:117,634,000 | C/G | — | uncertain significance |
| rs1648608313 | 1:117,634,453 | G/T | — | uncertain significance |
| rs201745403 | 1:117,634,472 | A/G | — | uncertain significance |
| rs748491105 | 1:117,634,493 | C/T | — | uncertain significance |
| rs150340120 | 1:117,634,500 | C/T | — | benign |
| rs34135400 | 1:117,634,507 | G/A | — | benign |
| rs199572074 | 1:117,634,538 | G/A | — | uncertain significance |
| rs752226907 | 1:117,635,365 | A/G | — | uncertain significance |
| rs888396411 | 1:117,635,386 | C/G | — | uncertain significance |
| rs61737102 | 1:117,635,400 | G/A | — | benign |
| rs41306197 | 1:117,635,401 | G/A | — | benign |
| rs546872594 | 1:117,635,438 | G/A | — | likely benign |
| rs139878101 | 1:117,635,449 | C/T | — | uncertain significance |
| rs2527240129 | 1:117,635,458 | A/G | — | uncertain significance |
| rs550488052 | 1:117,635,480 | T/C | — | uncertain significance |
| rs143131893 | 1:117,635,504 | G/A | — | likely benign |
| rs76420409 | 1:117,635,507 | T/C | — | benign |
| rs1649022835 | 1:117,637,972 | T/C | — | likely benign |
| rs148752375 | 1:117,638,841 | T/G | — | uncertain significance |
| rs144930443 | 1:117,638,882 | G/A | — | uncertain significance |
| rs747173677 | 1:117,638,913 | G/A | — | uncertain significance |
| rs1413798619 | 1:117,639,997 | G/A | — | uncertain significance |
| rs140571064 | 1:117,644,038 | A/T | — | conflicting classifications of pathogenicity |
| rs184925781 | 1:117,647,481 | G/A | 3 prime UTR variant | — |
| rs74446856 | 1:117,647,720 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.