SCMH1
Scm polycomb group protein homolog 1
Summary
Predicted to enable chromatin binding activity and histone binding activity. Predicted to be involved in heterochromatin formation and negative regulation of DNA-templated transcription. Predicted to act upstream of or within anterior/posterior pattern specification; chromatin remodeling; and spermatogenesis. Predicted to be located in nucleoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1140227 | 1:41,493,811 | C/G | — | — |
| rs143523539 | 1:41,493,888 | C/T | — | uncertain significance |
| rs780713552 | 1:41,493,990 | T/C | — | uncertain significance |
| rs747407979 | 1:41,494,374 | C/A | — | uncertain significance |
| rs1644080676 | 1:41,494,379 | C/A | — | uncertain significance |
| rs369637138 | 1:41,494,392 | T/C | — | uncertain significance |
| rs2281509 | 1:41,500,009 | T/C | intron variant | — |
| rs148897535 | 1:41,503,044 | T/C | — | likely benign |
| rs1380677081 | 1:41,503,069 | C/T | — | uncertain significance |
| rs2524817303 | 1:41,503,084 | C/T | — | uncertain significance |
| rs780097526 | 1:41,503,099 | G/A | — | uncertain significance |
| rs561244725 | 1:41,503,154 | T/C | — | uncertain significance |
| rs564084016 | 1:41,503,181 | G/A | — | uncertain significance |
| rs755215679 | 1:41,503,213 | C/A | — | uncertain significance |
| rs12729448 | 1:41,509,834 | G/A | intron variant | — |
| rs375356330 | 1:41,512,094 | C/T | — | uncertain significance |
| rs141951539 | 1:41,512,115 | T/C | — | uncertain significance |
| rs191253318 | 1:41,512,133 | G/A | — | uncertain significance |
| rs2525188362 | 1:41,512,164 | A/T | — | uncertain significance |
| rs753695456 | 1:41,512,211 | C/T | — | uncertain significance |
| rs2525258345 | 1:41,514,392 | T/G | — | uncertain significance |
| rs148739697 | 1:41,514,407 | C/T | — | uncertain significance |
| rs376970948 | 1:41,514,472 | C/T | — | uncertain significance |
| rs6686842 | 1:41,530,871 | T/G | — | — |
| rs755833243 | 1:41,536,360 | C/T | — | likely benign |
| rs760590161 | 1:41,536,369 | G/C | — | uncertain significance |
| rs1740615 | 1:41,538,516 | C/A | — | — |
| rs143365597 | 1:41,540,902 | G/A | missense variant | — |
| rs142101369 | 1:41,540,922 | G/C | — | uncertain significance |
| rs1657945029 | 1:41,541,007 | C/T | — | uncertain significance |
| rs759220732 | 1:41,541,121 | C/A | — | uncertain significance |
| rs140590267 | 1:41,541,123 | A/G | — | uncertain significance |
| rs11209489 | 1:41,550,202 | T/A | — | — |
| rs6600365 | 1:41,556,253 | C/T | intron variant | — |
| rs373257448 | 1:41,579,032 | C/T | — | uncertain significance |
| rs771472375 | 1:41,582,621 | C/A | — | uncertain significance |
| rs775677371 | 1:41,582,637 | G/T | — | uncertain significance |
| rs140656390 | 1:41,582,667 | G/A | — | uncertain significance |
| rs2527950859 | 1:41,608,589 | T/C | — | uncertain significance |
| rs114233776 | 1:41,618,297 | G/A | missense variant | — |
| rs545395137 | 1:41,618,304 | C/G | — | uncertain significance |
| rs114198068 | 1:41,624,749 | T/C | intron variant | — |
| rs113987575 | 1:41,639,437 | T/C | intron variant | — |
| rs144558165 | 1:41,653,498 | A/T | intron variant | — |
| rs61774685 | 1:41,674,613 | A/G | — | — |
| rs17358038 | 1:41,678,044 | G/A | intron variant | — |
| rs11209718 | 1:41,688,938 | C/A | — | — |
| rs528435438 | 1:41,695,286 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.