FILIP1L
filamin A interacting protein 1 like
Summary
Predicted to be involved in protein localization to actin cytoskeleton. Predicted to act upstream of or within several processes, including hindgut development; proteasomal protein catabolic process; and protein secretion. Predicted to be located in cytoplasm; membrane; and nucleus. Predicted to be active in actin cytoskeleton and centrosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants113 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs377049900 | 3:99,552,077 | G/A | — | likely benign |
| rs780442992 | 3:99,567,237 | A/G | — | likely benign |
| rs140594225 | 3:99,567,275 | C/T | — | uncertain significance |
| rs2472373680 | 3:99,567,309 | T/A | — | uncertain significance |
| rs374311994 | 3:99,567,383 | C/T | — | uncertain significance |
| rs371644128 | 3:99,567,396 | A/G | — | uncertain significance |
| rs2472374118 | 3:99,567,402 | A/C | — | uncertain significance |
| rs376775033 | 3:99,567,581 | G/C | — | uncertain significance |
| rs1442590252 | 3:99,567,599 | G/A | — | uncertain significance |
| rs371787329 | 3:99,567,606 | C/T | — | uncertain significance |
| rs200033744 | 3:99,567,611 | T/C | — | uncertain significance |
| rs776348364 | 3:99,567,620 | A/G | — | uncertain significance |
| rs745474780 | 3:99,567,621 | T/G | — | uncertain significance |
| rs1410491965 | 3:99,567,651 | C/A | — | uncertain significance |
| rs906777606 | 3:99,567,686 | C/T | — | uncertain significance |
| rs374858996 | 3:99,567,698 | G/A | — | uncertain significance |
| rs114299850 | 3:99,567,709 | C/G | — | likely benign |
| rs745635964 | 3:99,567,724 | A/G | — | likely benign |
| rs202229023 | 3:99,567,804 | C/A | — | uncertain significance |
| rs748911433 | 3:99,567,827 | G/C | — | uncertain significance |
| rs768236132 | 3:99,567,828 | G/A | — | uncertain significance |
| rs776867482 | 3:99,567,860 | A/G | — | uncertain significance |
| rs1434491375 | 3:99,567,918 | A/C | — | uncertain significance |
| rs753646644 | 3:99,567,954 | G/A | — | uncertain significance |
| rs200426741 | 3:99,568,008 | G/T | — | uncertain significance |
| rs1273023605 | 3:99,568,009 | G/A | — | likely benign |
| rs775766718 | 3:99,568,014 | C/T | — | uncertain significance |
| rs374898848 | 3:99,568,062 | G/A | — | uncertain significance |
| rs201518347 | 3:99,568,074 | T/C | — | uncertain significance |
| rs992235840 | 3:99,568,100 | T/C | — | uncertain significance |
| rs148447244 | 3:99,568,147 | G/A | — | benign |
| rs746318060 | 3:99,568,196 | C/A | — | uncertain significance |
| rs202066216 | 3:99,568,229 | A/G | — | uncertain significance |
| rs1943542032 | 3:99,568,230 | T/C | — | uncertain significance |
| rs1943542369 | 3:99,568,233 | C/G | — | uncertain significance |
| rs199518119 | 3:99,568,239 | C/G | — | uncertain significance |
| rs13353487 | 3:99,568,285 | G/A | — | benign |
| rs763793326 | 3:99,568,331 | A/C | — | uncertain significance |
| rs142569410 | 3:99,568,332 | T/A | — | uncertain significance |
| rs748343292 | 3:99,568,362 | C/T | — | uncertain significance |
| rs199915987 | 3:99,568,394 | T/G | — | uncertain significance |
| rs200062458 | 3:99,568,395 | C/T | — | uncertain significance |
| rs201896358 | 3:99,568,437 | T/C | — | uncertain significance |
| rs766923351 | 3:99,568,475 | A/G | — | uncertain significance |
| rs200619882 | 3:99,568,488 | C/G | — | uncertain significance |
| rs1943563570 | 3:99,568,557 | C/T | — | uncertain significance |
| rs547407141 | 3:99,568,565 | G/A | — | uncertain significance |
| rs776317854 | 3:99,568,652 | T/C | — | uncertain significance |
| rs2472381706 | 3:99,568,670 | G/A | — | uncertain significance |
| rs763379772 | 3:99,568,671 | C/G | — | uncertain significance |
| rs9843741 | 3:99,568,737 | A/G | — | benign |
| rs368624908 | 3:99,568,779 | G/A | — | uncertain significance |
| rs576553372 | 3:99,568,781 | T/A | — | uncertain significance |
| rs200756899 | 3:99,568,791 | T/G | — | uncertain significance |
| rs374712984 | 3:99,568,838 | G/A | — | uncertain significance |
| rs769449136 | 3:99,568,863 | C/T | — | uncertain significance |
| rs373504477 | 3:99,568,883 | G/A | — | uncertain significance |
| rs187341961 | 3:99,568,943 | T/C | — | uncertain significance |
| rs189755672 | 3:99,569,010 | G/A | — | uncertain significance |
| rs2472384296 | 3:99,569,019 | C/T | — | uncertain significance |
| rs2472384442 | 3:99,569,036 | G/A | — | uncertain significance |
| rs776850792 | 3:99,569,087 | C/T | — | uncertain significance |
| rs199705594 | 3:99,569,107 | C/A | — | uncertain significance |
| rs9828782 | 3:99,569,188 | C/T | — | benign |
| rs537419810 | 3:99,569,274 | C/G | — | uncertain significance |
| rs538097692 | 3:99,569,299 | C/T | — | likely benign |
| rs200354760 | 3:99,569,300 | G/A | — | uncertain significance |
| rs770746244 | 3:99,569,345 | A/G | — | uncertain significance |
| rs371654121 | 3:99,569,473 | C/T | — | likely benign |
| rs776377840 | 3:99,569,525 | C/T | — | uncertain significance |
| rs759335251 | 3:99,569,526 | G/A | — | uncertain significance |
| rs201606586 | 3:99,569,599 | G/T | — | likely benign |
| rs200063315 | 3:99,569,618 | T/A | — | uncertain significance |
| rs2472387831 | 3:99,569,667 | C/T | — | uncertain significance |
| rs36005744 | 3:99,569,770 | C/T | — | likely benign |
| rs199530891 | 3:99,569,847 | C/T | — | uncertain significance |
| rs141449044 | 3:99,569,880 | G/C | — | benign |
| rs193193058 | 3:99,570,589 | T/G | intron variant | — |
| rs7626245 | 3:99,570,761 | G/C | intron variant | — |
| rs793442 | 3:99,581,062 | A/G | — | — |
| rs3732444 | 3:99,581,439 | A/G | regulatory region variant | — |
| rs813218 | 3:99,592,596 | C/T | intron variant | — |
| rs751715182 | 3:99,643,078 | C/G | — | uncertain significance |
| rs200560124 | 3:99,643,132 | T/C | — | uncertain significance |
| rs372255083 | 3:99,643,134 | T/C | — | uncertain significance |
| rs201828035 | 3:99,643,175 | A/G | — | likely benign |
| rs793440 | 3:99,643,176 | C/T | — | benign |
| rs767721300 | 3:99,643,177 | G/T | — | uncertain significance |
| rs2472614651 | 3:99,643,186 | C/G | — | uncertain significance |
| rs191193772 | 3:99,643,257 | G/A | — | likely benign |
| rs563658045 | 3:99,648,749 | G/A | — | uncertain significance |
| rs932189098 | 3:99,648,767 | T/A | — | uncertain significance |
| rs2472628652 | 3:99,648,783 | C/T | — | uncertain significance |
| rs755586670 | 3:99,648,869 | C/T | — | uncertain significance |
| rs370095821 | 3:99,649,633 | T/C | — | uncertain significance |
| rs753925924 | 3:99,649,729 | C/A | — | uncertain significance |
| rs773891601 | 3:99,649,731 | T/C | — | uncertain significance |
| rs2472632266 | 3:99,649,775 | G/C | — | uncertain significance |
| rs769541275 | 3:99,649,801 | C/T | — | uncertain significance |
| rs202182798 | 3:99,649,815 | G/A | — | uncertain significance |
Showing 100 of 113 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.