SCFD1
sec1 family domain containing 1
Summary
Predicted to enable syntaxin binding activity. Involved in negative regulation of autophagosome assembly; regulation of protein transport; and response to toxic substance. Located in cis-Golgi network. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61754480 | 14:31,099,759 | T/C | — | uncertain significance |
| rs1400474401 | 14:31,103,190 | C/T | — | uncertain significance |
| rs751290560 | 14:31,107,373 | A/G | — | uncertain significance |
| rs754825986 | 14:31,107,382 | A/G | — | uncertain significance |
| rs35121540 | 14:31,112,596 | T/C | — | uncertain significance |
| rs146685783 | 14:31,118,745 | A/G | — | uncertain significance |
| rs751020811 | 14:31,118,778 | A/G | — | uncertain significance |
| rs2502104499 | 14:31,119,834 | A/G | — | uncertain significance |
| rs143379048 | 14:31,119,863 | C/T | — | benign |
| rs367994059 | 14:31,122,766 | C/T | — | uncertain significance |
| rs915070977 | 14:31,139,523 | G/A | — | uncertain significance |
| rs138143410 | 14:31,143,140 | G/A | — | uncertain significance |
| rs10139154 | 14:31,147,498 | C/T | downstream gene variant | — |
| rs1890579255 | 14:31,164,000 | T/G | — | uncertain significance |
| rs61754285 | 14:31,164,033 | G/A | — | conflicting classifications of pathogenicity |
| rs183277492 | 14:31,165,864 | G/A | intron variant | — |
| rs575907749 | 14:31,169,430 | T/C | — | uncertain significance |
| rs1891136381 | 14:31,171,536 | A/G | — | uncertain significance |
| rs1390389186 | 14:31,171,547 | A/C | — | uncertain significance |
| rs776141632 | 14:31,175,030 | G/A | — | uncertain significance |
| rs375686488 | 14:31,175,045 | G/A | — | uncertain significance |
| rs2502443697 | 14:31,175,049 | C/T | — | uncertain significance |
| rs2502522187 | 14:31,191,112 | C/T | — | uncertain significance |
| rs1237071803 | 14:31,191,758 | A/G | — | uncertain significance |
| rs534756177 | 14:31,194,007 | G/A | — | — |
| rs1893721685 | 14:31,204,006 | G/A | — | uncertain significance |
| rs139769371 | 14:31,204,014 | A/C | — | uncertain significance |
| rs368373461 | 14:31,204,062 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.