FAF1
Fas associated factor 1
Summary
Interaction of Fas ligand (TNFSF6) with the FAS antigen (TNFRSF6) mediates programmed cell death, also called apoptosis, in a number of organ systems. The protein encoded by this gene binds to FAS antigen and can initiate apoptosis or enhance apoptosis initiated through FAS antigen. Initiation of apoptosis by the protein encoded by this gene requires a ubiquitin-like domain but not the FAS-binding domain. [provided by RefSeq, Jul 2008]
Known Variants91 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17106184 | 1:50,909,985 | G/A | intron variant | — |
| rs4926554 | 1:50,922,641 | A/G | upstream gene variant | — |
| rs4926555 | 1:50,933,830 | A/T | — | — |
| rs3827730 | 1:50,937,848 | T/G | — | — |
| rs2523116824 | 1:50,941,347 | A/G | — | uncertain significance |
| rs59743675 | 1:50,957,385 | A/C | — | benign |
| rs72898946 | 1:50,959,262 | A/C | intron variant | — |
| rs72898953 | 1:50,963,858 | T/C | downstream gene variant | — |
| rs113028610 | 1:50,964,446 | C/A | — | — |
| rs72898961 | 1:50,966,976 | G/A | upstream gene variant | — |
| rs116626164 | 1:50,975,227 | T/A | intron variant | — |
| rs12096443 | 1:50,984,962 | C/T | intron variant | — |
| rs56202902 | 1:50,991,452 | T/C | intron variant | — |
| rs10888692 | 1:50,991,473 | C/G | intron variant | — |
| rs11587148 | 1:50,994,712 | T/C | intron variant | — |
| rs3789579 | 1:50,996,923 | G/C | intron variant | — |
| rs370024425 | 1:51,005,335 | G/A | — | uncertain significance |
| rs373869477 | 1:51,005,348 | G/A | — | uncertain significance |
| rs57490213 | 1:51,005,792 | G/A | intron variant | — |
| rs147696085 | 1:51,021,867 | G/A | intron variant | — |
| rs750254606 | 1:51,032,761 | G/T | — | uncertain significance |
| rs2523436828 | 1:51,032,868 | T/G | — | uncertain significance |
| rs749975602 | 1:51,032,888 | T/C | — | uncertain significance |
| rs10218771 | 1:51,035,115 | T/C | intron variant | — |
| rs12121301 | 1:51,038,327 | T/A | intron variant | — |
| rs1262039388 | 1:51,048,294 | C/T | — | uncertain significance |
| rs2523487979 | 1:51,048,320 | A/T | — | uncertain significance |
| rs1268888531 | 1:51,050,360 | T/A | — | uncertain significance |
| rs1651142090 | 1:51,050,378 | C/A | — | uncertain significance |
| rs776272769 | 1:51,050,383 | G/A | — | uncertain significance |
| rs767641721 | 1:51,050,414 | C/G | — | uncertain significance |
| rs1651146827 | 1:51,050,472 | A/T | — | uncertain significance |
| rs72900903 | 1:51,053,585 | A/G | intron variant | — |
| rs369843554 | 1:51,061,814 | C/G | — | uncertain significance |
| rs2522443789 | 1:51,061,828 | A/G | — | uncertain significance |
| rs2522444564 | 1:51,061,878 | G/C | — | uncertain significance |
| rs3850873 | 1:51,062,976 | A/G | intron variant | — |
| rs12063643 | 1:51,066,887 | C/T | intron variant | — |
| rs12083078 | 1:51,066,950 | T/A | intron variant | — |
| rs74738164 | 1:51,078,223 | G/A | intron variant | — |
| rs11205751 | 1:51,115,173 | T/C | intron variant | — |
| rs112045565 | 1:51,116,118 | C/G | intron variant | — |
| rs113402151 | 1:51,120,672 | C/T | intron variant | — |
| rs114725961 | 1:51,137,703 | T/A | intron variant | — |
| rs114623137 | 1:51,141,894 | C/T | intron variant | — |
| rs12354253 | 1:51,148,711 | G/A | intron variant | — |
| rs932286944 | 1:51,171,511 | C/T | — | uncertain significance |
| rs6693790 | 1:51,181,099 | T/C | intron variant | — |
| rs11205766 | 1:51,191,935 | T/A | intron variant | — |
| rs1027095593 | 1:51,204,587 | G/C | — | uncertain significance |
| rs199634797 | 1:51,204,590 | T/C | — | uncertain significance |
| rs772853999 | 1:51,210,430 | G/C | — | uncertain significance |
| rs12565378 | 1:51,216,584 | C/T | downstream gene variant | — |
| rs12073283 | 1:51,219,188 | C/A | — | — |
| rs72690486 | 1:51,220,017 | T/G | downstream gene variant | — |
| rs115363550 | 1:51,220,036 | T/A | — | — |
| rs12063943 | 1:51,223,263 | T/A | — | — |
| rs12097606 | 1:51,227,064 | G/T | — | — |
| rs12569177 | 1:51,237,409 | G/C | intron variant | — |
| rs17384696 | 1:51,241,057 | C/A | upstream gene variant | — |
| rs201769100 | 1:51,253,675 | C/T | — | uncertain significance |
| rs2523294143 | 1:51,253,687 | C/G | — | uncertain significance |
| rs1661425542 | 1:51,253,701 | T/A | — | uncertain significance |
| rs143113861 | 1:51,253,746 | G/C | — | uncertain significance |
| rs201770728 | 1:51,253,825 | G/A | — | uncertain significance |
| rs1569949326 | 1:51,253,866 | C/A | — | uncertain significance |
| rs58795848 | 1:51,283,510 | A/G | intron variant | — |
| rs1972100 | 1:51,285,461 | A/T | — | — |
| rs17106373 | 1:51,312,220 | G/A | coding sequence variant | — |
| rs10888709 | 1:51,314,782 | A/C | downstream gene variant | — |
| rs1398868 | 1:51,319,346 | T/C | regulatory region variant | — |
| rs79948214 | 1:51,322,205 | A/G | intron variant | — |
| rs114540602 | 1:51,328,807 | T/A | intron variant | — |
| rs58235906 | 1:51,340,598 | T/C | intron variant | — |
| rs149288352 | 1:51,349,663 | G/A | intron variant | — |
| rs72904737 | 1:51,351,846 | G/A | intron variant | — |
| rs138422027 | 1:51,353,068 | C/A | intron variant | — |
| rs144432213 | 1:51,353,720 | C/T | — | — |
| rs150183244 | 1:51,356,091 | G/T | intron variant | — |
| rs553050641 | 1:51,361,898 | G/A | — | — |
| rs72904749 | 1:51,367,420 | C/G | — | — |
| rs184112992 | 1:51,371,609 | T/A | intron variant | — |
| rs12085666 | 1:51,391,569 | A/G | intron variant | — |
| rs12078434 | 1:51,393,645 | G/C | intron variant | — |
| rs61115731 | 1:51,398,101 | G/C | intron variant | — |
| rs112780433 | 1:51,401,419 | C/T | intron variant | — |
| rs76183105 | 1:51,413,964 | G/A | intron variant | — |
| rs56323917 | 1:51,417,052 | A/T | intron variant | — |
| rs185178768 | 1:51,418,378 | G/A | intron variant | — |
| rs143446041 | 1:51,419,038 | G/A | — | — |
| rs113836734 | 1:51,419,841 | A/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.