FMN1

formin 1

Summary

This gene belongs to the formin homology family and encodes a protein that has a role in the formation of adherens junction and the polymerization of linear actin cables. The homologous gene in mouse is associated with limb deformity. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2015]

Known Variants362 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs57284764	15:33,057,566	C/A	regulatory region variant	—
rs16958710	15:33,066,327	G/A	—	benign
rs16958712	15:33,066,478	C/T	—	benign
rs114851360	15:33,066,510	C/T	—	likely benign
rs2056344395	15:33,066,525	C/T	—	uncertain significance
rs201674042	15:33,066,526	A/C	—	likely benign
rs767520219	15:33,066,542	C/T	—	uncertain significance
rs779059150	15:33,066,569	A/G	—	likely benign
rs28569405	15:33,066,582	T/A	—	benign
rs150830531	15:33,069,027	A/G	—	benign
rs2140870327	15:33,069,119	A/G	—	likely benign
rs80062147	15:33,069,304	G/A	—	benign
rs2123068	15:33,090,884	G/T	—	benign
rs368124119	15:33,091,014	G/C	—	uncertain significance
rs554779383	15:33,091,033	G/C	—	uncertain significance
rs763037303	15:33,091,076	C/T	—	uncertain significance
rs7162695	15:33,091,079	G/A	—	benign
rs76835557	15:33,091,084	C/T	—	conflicting classifications of pathogenicity
rs2057383957	15:33,091,135	A/G	—	uncertain significance
rs374934202	15:33,091,137	C/T	—	uncertain significance
rs1258806	15:33,091,281	C/A	—	benign
rs1020559	15:33,096,295	C/T	—	benign
rs147769257	15:33,096,488	T/C	—	conflicting classifications of pathogenicity
rs141073903	15:33,096,531	T/C	—	benign
rs146936281	15:33,096,543	A/G	—	benign
rs16959042	15:33,096,560	A/T	—	benign
rs12898436	15:33,096,663	G/C	—	benign
rs12900156	15:33,096,666	A/G	—	benign
rs16959063	15:33,105,730	G/A	intron variant	—
rs181884741	15:33,107,156	A/C	intron variant	—
rs12593365	15:33,107,990	T/C	intron variant	—
rs1258767	15:33,126,454	A/C	—	—
rs8034124	15:33,149,059	C/T	—	benign
rs8032931	15:33,149,087	G/A	—	benign
rs1451888	15:33,149,196	C/T	—	benign
rs766840354	15:33,149,204	A/C	—	likely benign
rs780093301	15:33,149,258	G/T	—	uncertain significance
rs2549008020	15:33,149,260	T/A	—	uncertain significance
rs116455579	15:33,149,262	C/T	—	benign
rs769997545	15:33,149,267	T/C	—	uncertain significance
rs2549008207	15:33,149,278	T/G	—	uncertain significance
rs371991451	15:33,149,283	C/T	—	likely benign
rs75076908	15:33,149,288	C/T	—	benign
rs12595237	15:33,180,232	G/A	—	benign
rs1165518398	15:33,180,357	G/A	—	likely benign
rs370021797	15:33,180,376	C/T	—	uncertain significance
rs1460570758	15:33,180,382	G/T	—	uncertain significance
rs370863163	15:33,180,445	A/C	—	uncertain significance
rs756145729	15:33,180,459	G/A	—	uncertain significance
rs1489857990	15:33,180,504	T/C	—	likely benign
rs769367320	15:33,180,507	T/C	—	likely benign
rs80005290	15:33,180,520	A/G	—	benign
rs769279423	15:33,191,017	C/T	—	likely benign
rs173224	15:33,191,023	G/A	—	benign
rs370853923	15:33,191,041	A/G	—	benign
rs200873951	15:33,191,049	G/A	—	uncertain significance
rs761915422	15:33,191,052	G/A	—	likely benign
rs535179017	15:33,191,067	C/T	—	uncertain significance
rs201891354	15:33,191,068	G/A	—	likely benign
rs1430367332	15:33,191,072	T/G	—	uncertain significance
rs78428401	15:33,191,187	G/A	—	benign
rs1466126	15:33,192,004	A/C	—	benign
rs374358070	15:33,192,230	C/T	—	uncertain significance
rs2141591066	15:33,192,240	C/T	—	likely benign
rs779699448	15:33,192,242	G/A	—	uncertain significance
rs369636169	15:33,192,306	G/A	—	uncertain significance
rs772402084	15:33,192,312	C/G	—	likely benign
rs764669683	15:33,192,315	G/A	—	likely benign
rs371178299	15:33,194,146	T/C	—	uncertain significance
rs781349125	15:33,194,152	G/C	—	uncertain significance
rs199507823	15:33,194,233	T/A	—	uncertain significance
rs201072930	15:33,200,725	C/T	—	uncertain significance
rs756376877	15:33,200,727	T/C	—	likely benign
rs66965190	15:33,200,867	A/G	—	benign
rs3812926	15:33,202,602	A/G	—	benign
rs139446870	15:33,202,692	C/T	—	conflicting classifications of pathogenicity
rs371197583	15:33,202,713	C/T	—	uncertain significance
rs43768	15:33,218,213	A/G	—	benign
rs897033964	15:33,218,437	C/T	—	uncertain significance
rs141556608	15:33,218,440	T/C	—	uncertain significance
rs200905611	15:33,218,472	G/T	—	uncertain significance
rs183633622	15:33,218,475	A/G	—	likely benign
rs76215711	15:33,218,487	G/T	—	benign
rs11855526	15:33,218,561	T/C	—	benign
rs12899881	15:33,228,334	T/A	intron variant	—
rs74014361	15:33,256,215	G/T	—	benign
rs12903110	15:33,256,219	C/T	—	benign
rs201484314	15:33,256,221	C/T	—	benign
rs11637012	15:33,256,251	C/T	—	benign
rs190832018	15:33,256,291	C/T	—	benign
rs2030937449	15:33,256,307	C/T	—	uncertain significance
rs199988791	15:33,256,336	G/A	—	uncertain significance
rs779344478	15:33,256,356	C/A	—	uncertain significance
rs373163646	15:33,256,359	C/A	—	uncertain significance
rs181700507	15:33,256,366	G/A	—	uncertain significance
rs753892267	15:33,256,408	C/T	—	uncertain significance
rs199592529	15:33,256,445	G/A	—	likely benign
rs77498561	15:33,256,476	C/T	—	likely benign
rs2956146	15:33,260,701	C/T	—	benign
rs2549373749	15:33,260,908	A/T	—	likely benign

Showing 100 of 362 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.