SCML4
Scm polycomb group protein like 4
Summary
Predicted to enable chromatin binding activity and histone binding activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs922886500 | 6:108,026,454 | C/T | — | uncertain significance |
| rs1433013404 | 6:108,026,478 | A/G | — | uncertain significance |
| rs2483298494 | 6:108,026,493 | C/A | — | uncertain significance |
| rs772296500 | 6:108,026,525 | A/G | — | uncertain significance |
| rs61742583 | 6:108,029,133 | C/T | — | benign |
| rs767298871 | 6:108,029,179 | C/T | — | uncertain significance |
| rs200680801 | 6:108,029,194 | G/A | — | benign |
| rs1728120 | 6:108,031,065 | C/G | — | — |
| rs1739857 | 6:108,036,437 | T/G | — | — |
| rs28360512 | 6:108,037,863 | A/G | regulatory region variant | — |
| rs147577936 | 6:108,039,361 | C/G | intron variant | — |
| rs146474518 | 6:108,041,933 | G/A | — | uncertain significance |
| rs773253589 | 6:108,042,009 | G/A | — | uncertain significance |
| rs749158523 | 6:108,042,101 | G/A | — | uncertain significance |
| rs369480751 | 6:108,053,514 | T/C | — | — |
| rs1237861901 | 6:108,066,180 | C/T | — | uncertain significance |
| rs140445627 | 6:108,066,288 | C/T | — | uncertain significance |
| rs536132560 | 6:108,067,917 | C/T | — | uncertain significance |
| rs201217173 | 6:108,067,928 | A/T | — | uncertain significance |
| rs372377654 | 6:108,067,953 | G/A | — | uncertain significance |
| rs755393210 | 6:108,068,015 | A/C | — | uncertain significance |
| rs1778451517 | 6:108,070,951 | G/C | — | uncertain significance |
| rs145577601 | 6:108,070,965 | G/A | — | uncertain significance |
| rs762313147 | 6:108,071,015 | G/C | — | uncertain significance |
| rs765505347 | 6:108,093,476 | G/A | — | uncertain significance |
| rs184505614 | 6:108,093,512 | G/A | — | uncertain significance |
| rs72933176 | 6:108,095,328 | A/G | intron variant | — |
| rs112538772 | 6:108,112,220 | G/A | intron variant | — |
| rs11966931 | 6:108,131,298 | G/A | intron variant | — |
| rs78541469 | 6:108,154,944 | A/T | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.