IWS1
interacts with SUPT6H, CTD assembly factor 1
Summary
Involved in regulation of mRNA export from nucleus; regulation of mRNA processing; and transcription elongation-coupled chromatin remodeling. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs749577368 | 2:128,238,744 | G/A | — | uncertain significance |
| rs183827949 | 2:128,240,242 | C/T | intron variant | — |
| rs74492489 | 2:128,247,169 | A/T | coding sequence variant | — |
| rs765053803 | 2:128,247,420 | C/T | — | uncertain significance |
| rs1690253894 | 2:128,249,600 | T/C | — | uncertain significance |
| rs778049511 | 2:128,250,880 | C/T | — | uncertain significance |
| rs748113727 | 2:128,252,483 | T/G | — | uncertain significance |
| rs2468110392 | 2:128,260,408 | C/T | — | uncertain significance |
| rs533950933 | 2:128,260,446 | T/G | — | uncertain significance |
| rs1238066450 | 2:128,261,015 | T/C | — | uncertain significance |
| rs1332859879 | 2:128,261,047 | T/C | — | uncertain significance |
| rs34912560 | 2:128,261,094 | T/C | — | benign |
| rs371954871 | 2:128,261,119 | T/C | — | uncertain significance |
| rs767766594 | 2:128,261,137 | C/T | — | uncertain significance |
| rs139425745 | 2:128,262,348 | A/C | — | uncertain significance |
| rs747054879 | 2:128,262,440 | C/T | — | uncertain significance |
| rs146708771 | 2:128,262,475 | C/T | — | uncertain significance |
| rs73953629 | 2:128,262,612 | C/T | — | benign |
| rs781402221 | 2:128,262,652 | G/A | — | uncertain significance |
| rs1691050791 | 2:128,262,660 | G/C | — | uncertain significance |
| rs749359752 | 2:128,262,782 | G/C | — | uncertain significance |
| rs879239193 | 2:128,262,819 | C/G | — | uncertain significance |
| rs374766966 | 2:128,262,841 | C/T | — | uncertain significance |
| rs2104704050 | 2:128,262,863 | G/C | — | uncertain significance |
| rs769622832 | 2:128,262,883 | T/G | — | uncertain significance |
| rs748823842 | 2:128,262,907 | G/A | — | uncertain significance |
| rs570035590 | 2:128,263,088 | T/C | — | uncertain significance |
| rs766986149 | 2:128,263,124 | C/T | — | uncertain significance |
| rs111686968 | 2:128,263,138 | T/A | — | uncertain significance |
| rs746988296 | 2:128,263,180 | C/T | — | likely benign |
| rs2468126369 | 2:128,263,255 | A/G | — | likely benign |
| rs1182332757 | 2:128,263,261 | T/C | — | uncertain significance |
| rs373684123 | 2:128,281,287 | C/G | — | uncertain significance |
| rs368146784 | 2:128,281,335 | G/A | — | uncertain significance |
| rs375620020 | 2:128,283,779 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.