INTS4
integrator complex subunit 4
Summary
INTS4 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs188994465 | 11:77,590,036 | G/C | — | uncertain significance |
| rs367591609 | 11:77,590,065 | C/T | — | uncertain significance |
| rs1951690702 | 11:77,590,110 | C/T | — | uncertain significance |
| rs763501825 | 11:77,590,122 | C/A | — | uncertain significance |
| rs1457469965 | 11:77,590,162 | C/G | — | uncertain significance |
| rs745824061 | 11:77,594,919 | C/T | — | uncertain significance |
| rs2496237134 | 11:77,602,381 | T/A | — | uncertain significance |
| rs781385631 | 11:77,602,451 | G/A | — | uncertain significance |
| rs768496944 | 11:77,602,474 | G/A | — | uncertain significance |
| rs963215329 | 11:77,602,505 | G/A | — | uncertain significance |
| rs2496238548 | 11:77,602,508 | T/C | — | uncertain significance |
| rs762067165 | 11:77,602,785 | T/C | — | uncertain significance |
| rs148229876 | 11:77,602,810 | T/C | — | uncertain significance |
| rs368402326 | 11:77,602,818 | C/T | — | uncertain significance |
| rs777800218 | 11:77,602,821 | G/A | — | uncertain significance |
| rs746875147 | 11:77,602,822 | G/A | — | uncertain significance |
| rs767731234 | 11:77,602,837 | G/C | — | uncertain significance |
| rs963165394 | 11:77,602,876 | C/T | — | uncertain significance |
| rs202047343 | 11:77,605,346 | A/G | — | uncertain significance |
| rs1187542068 | 11:77,612,565 | C/T | — | uncertain significance |
| rs565544206 | 11:77,614,592 | C/T | — | likely benign |
| rs867570154 | 11:77,618,785 | C/T | — | uncertain significance |
| rs11534589 | 11:77,624,177 | G/C | regulatory region variant | — |
| rs770580492 | 11:77,629,924 | T/C | — | uncertain significance |
| rs373260073 | 11:77,632,403 | G/A | — | uncertain significance |
| rs149621926 | 11:77,633,432 | T/C | — | uncertain significance |
| rs2496380971 | 11:77,633,444 | G/A | — | uncertain significance |
| rs2496389950 | 11:77,635,800 | A/G | — | uncertain significance |
| rs2496389965 | 11:77,635,803 | T/C | — | uncertain significance |
| rs7119720 | 11:77,635,882 | A/C | — | likely benign |
| rs60143695 | 11:77,637,570 | T/C | intron variant | — |
| rs1469596535 | 11:77,639,407 | G/A | — | uncertain significance |
| rs577201312 | 11:77,639,435 | T/C | — | uncertain significance |
| rs748864691 | 11:77,649,703 | T/A | — | uncertain significance |
| rs2496447396 | 11:77,652,238 | C/T | — | uncertain significance |
| rs556128179 | 11:77,652,659 | G/A | — | — |
| rs769018750 | 11:77,667,038 | T/C | — | uncertain significance |
| rs756713835 | 11:77,667,091 | G/A | — | uncertain significance |
| rs191741859 | 11:77,669,843 | C/T | — | uncertain significance |
| rs547157454 | 11:77,669,870 | A/G | — | uncertain significance |
| rs146919684 | 11:77,671,396 | A/C | — | uncertain significance |
| rs368162001 | 11:77,671,427 | T/C | — | uncertain significance |
| rs2496521564 | 11:77,672,006 | T/A | — | uncertain significance |
| rs759046434 | 11:77,672,028 | G/C | — | uncertain significance |
| rs143806539 | 11:77,672,060 | A/G | — | uncertain significance |
| rs140056069 | 11:77,672,168 | G/A | — | uncertain significance |
| rs12420528 | 11:77,672,865 | A/G | intron variant | — |
| rs6592753 | 11:77,677,019 | A/G | intron variant | — |
| rs72941336 | 11:77,688,244 | C/T | intron variant | — |
| rs2496593317 | 11:77,690,142 | T/C | — | uncertain significance |
| rs144227709 | 11:77,702,195 | C/T | — | uncertain significance |
| rs7932496 | 11:77,707,577 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.