FLACC1
flagellum associated containing coiled-coil domains 1
Summary
Predicted to be located in cytoplasmic vesicle and outer dense fiber. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1035142 | 2:202,153,078 | T/A | — | — |
| rs700635 | 2:202,153,225 | C/A | downstream gene variant | — |
| rs779318488 | 2:202,153,391 | C/T | — | uncertain significance |
| rs2470542527 | 2:202,153,395 | T/C | — | uncertain significance |
| rs766488965 | 2:202,153,403 | C/T | — | uncertain significance |
| rs574880634 | 2:202,153,406 | T/G | — | uncertain significance |
| rs146230831 | 2:202,153,437 | C/G | — | uncertain significance |
| rs754875664 | 2:202,153,463 | C/T | — | likely benign |
| rs6714430 | 2:202,153,684 | C/T | downstream gene variant | — |
| rs17468277 | 2:202,154,200 | C/T | synonymous variant | benign |
| rs149980324 | 2:202,154,232 | C/T | — | uncertain significance |
| rs750680809 | 2:202,154,241 | C/T | — | uncertain significance |
| rs149151936 | 2:202,154,247 | A/G | — | likely benign |
| rs746144112 | 2:202,154,283 | T/C | — | uncertain significance |
| rs6715284 | 2:202,154,397 | C/G | downstream gene variant | — |
| rs1371919812 | 2:202,154,454 | T/C | — | uncertain significance |
| rs200570912 | 2:202,154,468 | T/C | — | uncertain significance |
| rs2470551773 | 2:202,154,490 | G/A | — | uncertain significance |
| rs1301018176 | 2:202,154,538 | C/G | — | uncertain significance |
| rs10180658 | 2:202,158,550 | C/A | — | — |
| rs75507031 | 2:202,160,762 | C/T | — | — |
| rs13016963 | 2:202,162,811 | A/T | — | — |
| rs2080303 | 2:202,165,206 | T/A | — | — |
| rs13002139 | 2:202,167,651 | G/T | intron variant | — |
| rs6712091 | 2:202,169,132 | T/C | intron variant | — |
| rs2470619720 | 2:202,172,246 | T/A | — | uncertain significance |
| rs777158451 | 2:202,172,250 | C/T | — | uncertain significance |
| rs199908248 | 2:202,172,256 | T/C | — | uncertain significance |
| rs7582362 | 2:202,176,294 | A/G | intron variant | — |
| rs6731171 | 2:202,179,011 | T/G | — | — |
| rs1830298 | 2:202,181,247 | C/G | — | — |
| rs2349073 | 2:202,186,986 | C/A | intron variant | — |
| rs147899975 | 2:202,195,200 | G/A | — | likely benign |
| rs200602814 | 2:202,195,493 | C/G | — | uncertain significance |
| rs370202023 | 2:202,195,529 | T/G | — | uncertain significance |
| rs6757783 | 2:202,199,824 | C/G | — | — |
| rs10201587 | 2:202,202,791 | A/T | — | — |
| rs764227368 | 2:202,211,288 | G/C | — | uncertain significance |
| rs555173620 | 2:202,211,297 | T/A | — | uncertain significance |
| rs373905313 | 2:202,211,337 | G/C | — | uncertain significance |
| rs149858712 | 2:202,211,355 | C/G | — | uncertain significance |
| rs774443454 | 2:202,211,361 | C/T | — | uncertain significance |
| rs1251151297 | 2:202,215,456 | T/C | — | uncertain significance |
| rs140281898 | 2:202,215,484 | A/G | — | likely benign |
| rs13014235 | 2:202,215,492 | C/T | missense variant | — |
| rs1346593859 | 2:202,216,031 | A/G | — | uncertain significance |
| rs147447278 | 2:202,216,039 | C/A | — | uncertain significance |
| rs746654168 | 2:202,216,056 | C/G | — | uncertain significance |
| rs775447073 | 2:202,216,088 | G/A | — | uncertain significance |
| rs11691602 | 2:202,227,699 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.