INTS6
integrator complex subunit 6
Summary
DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. The protein encoded by this gene is a DEAD box protein that is part of a complex that interacts with the C-terminus of RNA polymerase II and is involved in 3' end processing of snRNAs. In addition, this gene is a candidate tumor suppressor and is located in the critical region of loss of heterozygosity (LOH). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2015]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9563043 | 13:51,908,316 | A/C | upstream gene variant | — |
| rs9535646 | 13:51,913,708 | C/T | upstream gene variant | — |
| rs968997787 | 13:51,939,895 | C/T | — | uncertain significance |
| rs61749884 | 13:51,941,943 | T/C | — | benign |
| rs149924575 | 13:51,941,976 | T/C | — | likely benign |
| rs1955723259 | 13:51,942,004 | T/C | — | uncertain significance |
| rs144985389 | 13:51,942,005 | G/A | — | uncertain significance |
| rs369330400 | 13:51,943,129 | C/G | — | uncertain significance |
| rs2541609176 | 13:51,943,141 | T/G | — | uncertain significance |
| rs1346522851 | 13:51,943,161 | T/C | — | uncertain significance |
| rs1452725204 | 13:51,943,192 | T/C | — | uncertain significance |
| rs2541609556 | 13:51,943,224 | T/G | — | uncertain significance |
| rs1566204390 | 13:51,943,302 | T/C | — | uncertain significance |
| rs149115928 | 13:51,943,306 | T/C | — | benign |
| rs745881357 | 13:51,943,312 | G/A | — | uncertain significance |
| rs199886113 | 13:51,943,338 | G/C | — | likely benign |
| rs772715089 | 13:51,943,350 | G/A | — | uncertain significance |
| rs940701927 | 13:51,943,434 | G/C | — | uncertain significance |
| rs1350015254 | 13:51,943,437 | G/A | — | uncertain significance |
| rs1197289460 | 13:51,948,373 | T/A | — | uncertain significance |
| rs369348837 | 13:51,948,491 | T/C | — | uncertain significance |
| rs2541624764 | 13:51,948,851 | A/G | — | uncertain significance |
| rs577704602 | 13:51,950,265 | G/A | — | uncertain significance |
| rs2137893338 | 13:51,950,306 | A/T | — | uncertain significance |
| rs140156322 | 13:51,952,423 | G/A | — | likely benign |
| rs1429931122 | 13:51,952,494 | T/C | — | uncertain significance |
| rs139832932 | 13:51,952,535 | T/C | — | uncertain significance |
| rs1167813565 | 13:51,952,583 | A/C | — | uncertain significance |
| rs757102632 | 13:51,953,647 | T/C | — | uncertain significance |
| rs61749885 | 13:51,956,225 | T/G | — | benign |
| rs2541651214 | 13:51,957,503 | A/C | — | uncertain significance |
| rs2541652208 | 13:51,957,796 | T/A | — | uncertain significance |
| rs138030207 | 13:51,961,679 | A/G | — | benign |
| rs2541682258 | 13:51,969,434 | A/G | — | uncertain significance |
| rs200603697 | 13:51,969,476 | T/A | — | uncertain significance |
| rs757017771 | 13:51,969,494 | C/G | — | uncertain significance |
| rs780323468 | 13:51,969,513 | A/G | — | uncertain significance |
| rs141573619 | 13:52,004,522 | A/G | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.