FMNL1
formin like 1
Summary
This gene encodes a formin-related protein. Formin-related proteins have been implicated in morphogenesis, cytokinesis, and cell polarity. An alternative splice variant has been described but its full length sequence has not been determined. [provided by RefSeq, Jul 2008]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1001732920 | 17:43,299,543 | C/T | — | likely benign |
| rs202024994 | 17:43,308,023 | A/G | — | uncertain significance |
| rs2043459216 | 17:43,309,840 | A/C | — | uncertain significance |
| rs749568309 | 17:43,309,841 | C/G | — | uncertain significance |
| rs2508776298 | 17:43,309,846 | G/T | — | uncertain significance |
| rs2508785881 | 17:43,311,083 | C/G | — | uncertain significance |
| rs1228289595 | 17:43,311,486 | A/T | — | uncertain significance |
| rs1446949290 | 17:43,311,542 | C/T | — | uncertain significance |
| rs201153167 | 17:43,313,597 | A/G | — | uncertain significance |
| rs199710165 | 17:43,315,928 | C/T | — | benign |
| rs769920910 | 17:43,315,938 | G/C | — | uncertain significance |
| rs2508820845 | 17:43,315,944 | A/C | — | uncertain significance |
| rs771585864 | 17:43,315,976 | C/T | — | uncertain significance |
| rs1243523167 | 17:43,316,001 | T/A | — | uncertain significance |
| rs2508825441 | 17:43,316,419 | A/G | — | uncertain significance |
| rs146321570 | 17:43,317,988 | C/T | — | uncertain significance |
| rs556541257 | 17:43,318,175 | C/T | — | — |
| rs777882396 | 17:43,318,774 | T/C | — | uncertain significance |
| rs1473840101 | 17:43,318,903 | G/T | — | uncertain significance |
| rs781102841 | 17:43,318,950 | A/G | — | uncertain significance |
| rs1390541195 | 17:43,318,972 | C/T | — | uncertain significance |
| rs773918631 | 17:43,318,983 | A/C | — | uncertain significance |
| rs183400333 | 17:43,318,984 | C/T | — | uncertain significance |
| rs983483815 | 17:43,318,992 | C/T | — | uncertain significance |
| rs1230236354 | 17:43,319,268 | C/A | — | uncertain significance |
| rs1226460594 | 17:43,319,276 | G/T | — | uncertain significance |
| rs540975102 | 17:43,319,283 | C/T | — | uncertain significance |
| rs2043709652 | 17:43,319,328 | C/T | — | uncertain significance |
| rs1308902731 | 17:43,319,352 | C/G | — | uncertain significance |
| rs1187518930 | 17:43,319,396 | C/T | — | uncertain significance |
| rs763054769 | 17:43,319,423 | G/A | — | uncertain significance |
| rs1019213170 | 17:43,319,433 | C/T | — | uncertain significance |
| rs2508853190 | 17:43,319,486 | G/C | — | uncertain significance |
| rs376978325 | 17:43,319,716 | G/A | — | uncertain significance |
| rs946321398 | 17:43,319,742 | C/T | — | likely benign |
| rs530324471 | 17:43,320,519 | A/G | — | uncertain significance |
| rs147957951 | 17:43,320,548 | C/T | — | uncertain significance |
| rs2508863025 | 17:43,320,581 | G/C | — | uncertain significance |
| rs201901138 | 17:43,321,172 | C/T | — | uncertain significance |
| rs150127230 | 17:43,321,244 | G/A | — | uncertain significance |
| rs774732222 | 17:43,321,252 | C/T | — | uncertain significance |
| rs371426654 | 17:43,321,261 | C/T | — | uncertain significance |
| rs545973902 | 17:43,321,292 | G/T | — | uncertain significance |
| rs138140582 | 17:43,321,333 | C/T | — | uncertain significance |
| rs200065435 | 17:43,321,367 | C/T | — | uncertain significance |
| rs1187333085 | 17:43,321,543 | C/G | — | uncertain significance |
| rs2508870634 | 17:43,321,598 | G/A | — | uncertain significance |
| rs1278665149 | 17:43,322,373 | A/G | — | uncertain significance |
| rs929657813 | 17:43,322,417 | G/C | — | uncertain significance |
| rs141887433 | 17:43,322,628 | G/A | — | uncertain significance |
| rs150643495 | 17:43,322,641 | C/T | — | uncertain significance |
| rs377725425 | 17:43,322,694 | C/T | — | uncertain significance |
| rs2508878269 | 17:43,322,746 | C/T | — | uncertain significance |
| rs761626118 | 17:43,322,773 | A/T | — | uncertain significance |
| rs145693762 | 17:43,323,081 | G/A | — | uncertain significance |
| rs151174346 | 17:43,323,312 | C/T | — | likely benign |
| rs2508883504 | 17:43,323,326 | C/T | — | uncertain significance |
| rs2508887173 | 17:43,323,584 | C/T | — | uncertain significance |
| rs768445927 | 17:43,323,893 | C/G | — | uncertain significance |
| rs761421986 | 17:43,323,899 | G/C | — | uncertain significance |
| rs1467307071 | 17:43,323,919 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.