FRY

FRY microtubule binding protein

Summary

Predicted to enable enzyme inhibitor activity. Predicted to be involved in cell morphogenesis and neuron projection development. Predicted to be located in centrosome; cytoplasm; and spindle pole. Predicted to be active in cell cortex and site of polarized growth. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants152 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs184309723	13:32,652,978	C/T	—	likely benign
rs35417728	13:32,652,979	G/A	—	conflicting classifications of pathogenicity
rs763116067	13:32,653,004	C/T	—	uncertain significance
rs764328203	13:32,653,005	G/A	—	likely benign
rs777808672	13:32,653,064	A/G	—	likely benign
rs972665662	13:32,653,066	G/T	—	uncertain significance
rs376716820	13:32,653,145	T/C	—	uncertain significance
rs407004	13:32,657,434	G/C	intron variant	—
rs2500515424	13:32,676,111	G/A	—	likely benign
rs760404697	13:32,676,113	C/T	—	uncertain significance
rs776423516	13:32,691,523	G/A	—	uncertain significance
rs755977980	13:32,698,748	C/T	—	uncertain significance
rs771595227	13:32,698,790	G/A	—	uncertain significance
rs754793180	13:32,698,946	A/G	—	uncertain significance
rs753435154	13:32,705,816	G/C	—	uncertain significance
rs200632433	13:32,709,236	A/G	—	likely benign
rs7331540	13:32,710,520	G/C	intron variant	—
rs1593667198	13:32,721,472	T/C	—	likely benign
rs116121141	13:32,729,705	G/A	—	benign
rs114839670	13:32,735,290	A/G	—	benign
rs1036061175	13:32,735,355	T/C	—	uncertain significance
rs777478179	13:32,745,159	C/A	—	uncertain significance
rs746694603	13:32,745,167	T/C	—	likely benign
rs116459776	13:32,745,177	C/A	—	benign
rs200809158	13:32,745,223	C/T	—	uncertain significance
rs190949758	13:32,745,296	A/T	—	benign
rs150360445	13:32,745,396	A/G	—	likely benign
rs116019557	13:32,747,569	C/T	—	benign
rs114461962	13:32,747,593	T/C	—	benign
rs773034236	13:32,749,697	G/A	—	likely benign
rs372753231	13:32,749,731	A/G	—	uncertain significance
rs200312076	13:32,749,758	G/A	—	uncertain significance
rs703219	13:32,750,753	C/T	intron variant	—
rs376360067	13:32,752,346	G/T	—	likely benign
rs1170004807	13:32,752,531	C/T	—	uncertain significance
rs756822384	13:32,753,007	G/T	—	uncertain significance
rs896212372	13:32,753,071	A/C	—	likely benign
rs1231229532	13:32,753,089	T/C	—	likely benign
rs2500802703	13:32,753,148	G/A	—	uncertain significance
rs1332945507	13:32,757,139	T/C	—	likely benign
rs28673560	13:32,758,739	C/T	—	benign
rs798971	13:32,758,834	G/A	—	benign
rs766612663	13:32,759,117	A/C	—	uncertain significance
rs768173822	13:32,759,186	A/G	—	uncertain significance
rs773824706	13:32,759,192	C/T	—	likely benign
rs200244322	13:32,759,240	G/A	—	uncertain significance
rs1593712154	13:32,760,404	C/T	—	likely benign
rs2500823481	13:32,760,444	C/A	—	uncertain significance
rs140270659	13:32,761,675	A/G	—	benign
rs1237938851	13:32,761,752	T/C	—	uncertain significance
rs200876478	13:32,768,348	T/C	—	likely benign
rs35912297	13:32,768,423	G/A	—	benign
rs41292163	13:32,768,428	G/A	—	likely benign
rs200315543	13:32,776,571	G/C	—	uncertain significance
rs757108918	13:32,776,575	C/T	—	uncertain significance
rs117167401	13:32,776,576	G/A	—	likely benign
rs138780336	13:32,776,604	G/A	—	likely benign
rs182574298	13:32,782,997	C/T	—	benign
rs200785375	13:32,783,027	G/A	—	likely benign
rs775723459	13:32,783,039	G/T	—	uncertain significance
rs146669548	13:32,783,048	C/T	—	likely benign
rs114097884	13:32,783,168	C/T	—	benign
rs756765597	13:32,783,169	G/A	—	uncertain significance
rs953732762	13:32,783,792	G/A	—	uncertain significance
rs1472969045	13:32,785,090	G/A	—	uncertain significance
rs188033309	13:32,785,101	C/T	—	likely benign
rs201639194	13:32,785,102	G/A	—	benign
rs111657385	13:32,785,131	C/T	—	benign
rs2500905873	13:32,785,148	G/A	—	uncertain significance
rs771176469	13:32,786,433	C/A	—	likely benign
rs2500976354	13:32,792,887	T/C	—	uncertain significance
rs368924097	13:32,798,442	G/A	—	likely benign
rs371353662	13:32,798,472	C/G	—	likely benign
rs2501027334	13:32,798,479	G/T	—	uncertain significance
rs372599052	13:32,799,081	C/T	—	uncertain significance
rs749003208	13:32,799,107	G/A	—	uncertain significance
rs1046467083	13:32,799,158	C/T	—	uncertain significance
rs1370582529	13:32,799,164	G/A	—	uncertain significance
rs761819716	13:32,800,030	G/A	—	uncertain significance
rs61946739	13:32,800,075	G/A	—	likely benign
rs773502277	13:32,802,629	C/T	—	uncertain significance
rs770996200	13:32,802,632	T/C	—	uncertain significance
rs191219337	13:32,802,729	T/C	—	benign
rs543680542	13:32,805,317	G/A	—	uncertain significance
rs780097534	13:32,805,382	A/G	—	likely benign
rs55673178	13:32,805,419	T/C	—	likely benign
rs201934314	13:32,805,429	C/A	—	uncertain significance
rs1445528075	13:32,810,231	C/T	—	uncertain significance
rs754593854	13:32,810,262	C/G	—	uncertain significance
rs766442520	13:32,811,598	A/G	—	likely benign
rs138935146	13:32,811,642	A/G	—	likely benign
rs746991816	13:32,811,829	G/A	—	uncertain significance
rs368340587	13:32,811,999	C/T	—	likely benign
rs1384752345	13:32,812,068	C/A	—	uncertain significance
rs772967229	13:32,812,099	A/G	—	uncertain significance
rs74044948	13:32,813,444	T/C	—	likely benign
rs74044949	13:32,813,453	G/A	—	benign
rs193120945	13:32,813,873	A/G	—	likely benign
rs370933276	13:32,813,940	G/A	—	likely benign
rs773344773	13:32,818,248	A/G	—	uncertain significance

Showing 100 of 152 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.