FAM47E
family with sequence similarity 47 member E
Summary
Enables enzyme activator activity. Involved in protein localization to chromatin and transcription initiation-coupled chromatin remodeling. Located in chromatin; cytoplasm; and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61216514 | 4:77,163,722 | G/A | intron variant | — |
| rs774937852 | 4:77,172,925 | G/A | — | likely benign |
| rs866894892 | 4:77,172,951 | G/C | — | uncertain significance |
| rs1734183130 | 4:77,177,345 | A/T | — | uncertain significance |
| rs946201510 | 4:77,177,407 | G/A | — | likely benign |
| rs2476398064 | 4:77,177,413 | G/C | — | uncertain significance |
| rs774362095 | 4:77,177,508 | A/C | — | uncertain significance |
| rs1267731930 | 4:77,177,570 | C/T | — | uncertain significance |
| rs764019899 | 4:77,177,638 | G/A | — | uncertain significance |
| rs1005224775 | 4:77,177,671 | A/G | — | likely benign |
| rs7695720 | 4:77,183,300 | A/C | intron variant | — |
| rs1183541859 | 4:77,184,913 | G/T | — | uncertain significance |
| rs982121618 | 4:77,184,954 | C/T | — | uncertain significance |
| rs62300803 | 4:77,189,418 | C/T | intron variant | — |
| rs182113748 | 4:77,189,667 | A/G | intron variant | — |
| rs2476431084 | 4:77,189,827 | C/T | — | uncertain significance |
| rs187818578 | 4:77,189,868 | C/T | — | uncertain significance |
| rs2476431238 | 4:77,189,890 | A/G | — | uncertain significance |
| rs1734750341 | 4:77,189,904 | C/T | — | uncertain significance |
| rs2476438858 | 4:77,192,755 | A/G | — | uncertain significance |
| rs772084828 | 4:77,192,772 | T/C | — | uncertain significance |
| rs375151279 | 4:77,192,790 | C/A | — | uncertain significance |
| rs867217004 | 4:77,192,806 | C/T | — | likely benign |
| rs960123621 | 4:77,192,836 | T/C | — | uncertain significance |
| rs1471009178 | 4:77,192,872 | C/T | — | uncertain significance |
| rs534203291 | 4:77,192,917 | C/T | — | uncertain significance |
| rs1837870 | 4:77,197,223 | C/A | intron variant | — |
| rs28636815 | 4:77,197,397 | A/G | intron variant | — |
| rs116809741 | 4:77,197,521 | G/T | — | — |
| rs28507491 | 4:77,197,651 | G/A | intron variant | — |
| rs6810903 | 4:77,198,363 | C/T | intron variant | — |
| rs6858344 | 4:77,198,566 | G/T | — | — |
| rs6812193 | 4:77,198,986 | C/T | intron variant | — |
| rs772174756 | 4:77,199,254 | G/T | — | uncertain significance |
| rs1735203947 | 4:77,199,262 | C/T | — | uncertain significance |
| rs775026509 | 4:77,199,321 | C/T | — | uncertain significance |
| rs758671265 | 4:77,201,440 | C/A | — | uncertain significance |
| rs777959224 | 4:77,201,441 | G/A | — | uncertain significance |
| rs375654215 | 4:77,204,598 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.