Cyfip1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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145 records found for search term Cyfip1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15185505	CV778130	deletion	NM_014608.6(CYFIP1):c.666+7del	not provided [RCV000953004]	benign	15	22939404	22939404	Human		name
15165829	CV779762	single nucleotide variant	NM_014608.6(CYFIP1):c.993-7T>C	not provided [RCV000971036]	benign	15	22932347	22932347	Human		name
405271586	CV3209496	single nucleotide variant	NM_014608.6(CYFIP1):c.3210+6G>A	CYFIP1-related disorder [RCV003949809]	likely benign	15	22874544	22874544	Human		name , trait , alternate_id
15166912	CV778126	single nucleotide variant	NM_014608.6(CYFIP1):c.1233+9C>G	not provided [RCV000948943]	benign	15	22927897	22927897	Human		name
15182222	CV779662	single nucleotide variant	NM_014608.6(CYFIP1):c.3043-4C>G	not provided [RCV000974580]	benign	15	22875275	22875275	Human		name
401904598	CV2817186	single nucleotide variant	NM_001324120.2(CYFIP1):c.-238G>A	not provided [RCV003426451]	likely benign	15	22980799	22980799	Human		name
401911346	CV2817191	single nucleotide variant	NM_014608.6(CYFIP1):c.1675-307G>A	not provided [RCV003426456]	likely benign	15	22916937	22916937	Human		name
405274542	CV3208863	single nucleotide variant	NM_014608.6(CYFIP1):c.1675-209C>T	CYFIP1-related disorder [RCV003951661]	likely benign	15	22916839	22916839	Human		name , trait , alternate_id
15166902	CV778225	duplication	NM_014608.6(CYFIP1):c.666+3_666+6dup	not provided [RCV000948941]	benign	15	22939404	22939405	Human		name
8584204	CV118776	single nucleotide variant	NM_001287810.1(CYFIP1):c.-125-6223G>C	Lung cancer [RCV000099296]	uncertain significance	15	22954252	22954252	Human		name
15150092	CV739466	single nucleotide variant	NM_014608.6(CYFIP1):c.87C>T (p.Ile29=)	not provided [RCV000901076]	benign	15	22947199	22947199	Human		name
15159196	CV739467	single nucleotide variant	NM_014608.6(CYFIP1):c.81C>A (p.Pro27=)	not provided [RCV000902886]	likely benign	15	22947205	22947205	Human		name
15125389	CV739465	single nucleotide variant	NM_014608.6(CYFIP1):c.153A>G (p.Ala51=)	not provided [RCV000896753]	likely benign	15	22947057	22947057	Human		name
156354927	CV2324378	single nucleotide variant	NM_014608.6(CYFIP1):c.70G>A (p.Asp24Asn)	not specified [RCV004178878]	uncertain significance	15	22947216	22947216	Human		name
401911342	CV2817188	single nucleotide variant	NM_014608.6(CYFIP1):c.975C>T (p.Tyr325=)	not provided [RCV003426453]	likely benign	15	22933819	22933819	Human		name
15192152	CV703085	single nucleotide variant	NM_014608.6(CYFIP1):c.912G>A (p.Val304=)	not provided [RCV000954984]	benign\|likely benign	15	22933882	22933882	Human		name
15165711	CV754294	single nucleotide variant	NM_014608.6(CYFIP1):c.963C>G (p.Thr321=)	not provided [RCV000926693]	likely benign	15	22933831	22933831	Human		name
15176453	CV770038	single nucleotide variant	NM_014608.6(CYFIP1):c.472C>T (p.Leu158=)	not provided [RCV000928921]	benign	15	22943270	22943270	Human		name
155965077	CV2308458	single nucleotide variant	NM_014608.6(CYFIP1):c.245T>C (p.Met82Thr)	not specified [RCV004166750]	uncertain significance	15	22944902	22944902	Human		name
401911343	CV2817189	single nucleotide variant	NM_014608.6(CYFIP1):c.1287C>G (p.Pro429=)	not provided [RCV003426454]	likely benign	15	22926054	22926054	Human		name
597656333	CV3658038	single nucleotide variant	NM_014608.6(CYFIP1):c.101C>A (p.Ser34Tyr)	not specified [RCV004911156]	uncertain significance	15	22947185	22947185	Human		name
598237090	CV3956280	single nucleotide variant	NM_014608.6(CYFIP1):c.269C>T (p.Ser90Phe)	not specified [RCV005320573]	uncertain significance	15	22944878	22944878	Human		name
15166907	CV703084	single nucleotide variant	NM_014608.6(CYFIP1):c.1041G>A (p.Glu347=)	not provided [RCV000948942]	benign	15	22932292	22932292	Human		name
15179883	CV714326	single nucleotide variant	NM_014608.6(CYFIP1):c.2508C>T (p.Tyr836=)	not provided [RCV000974017]	benign	15	22903786	22903786	Human		name
15147447	CV714327	single nucleotide variant	NM_014608.6(CYFIP1):c.2274C>T (p.Leu758=)	not provided [RCV000967341]	benign	15	22909308	22909308	Human		name
15180318	CV714328	single nucleotide variant	NM_014608.6(CYFIP1):c.2238C>T (p.Tyr746=)	not provided [RCV000974122]	benign	15	22910550	22910550	Human		name
15159130	CV714329	single nucleotide variant	NM_014608.6(CYFIP1):c.1977G>C (p.Ser659=)	not provided [RCV000969652]	benign	15	22914734	22914734	Human		name
15120371	CV739461	single nucleotide variant	NM_014608.6(CYFIP1):c.2895C>T (p.His965=)	not provided [RCV000895882]	likely benign	15	22881862	22881862	Human		name
15159968	CV739462	single nucleotide variant	NM_014608.6(CYFIP1):c.2526C>T (p.His842=)	not provided [RCV000903049]	likely benign	15	22903768	22903768	Human		name
15160133	CV739463	single nucleotide variant	NM_014608.6(CYFIP1):c.1650C>T (p.Arg550=)	not provided [RCV000903083]	likely benign	15	22917812	22917812	Human		name
15149233	CV739464	single nucleotide variant	NM_014608.6(CYFIP1):c.1383G>A (p.Leu461=)	not provided [RCV000900891]	benign	15	22918835	22918835	Human		name
15167890	CV754293	single nucleotide variant	NM_014608.6(CYFIP1):c.1356G>A (p.Val452=)	not provided [RCV000927181]	likely benign	15	22925985	22925985	Human		name
15177568	CV770036	single nucleotide variant	NM_014608.6(CYFIP1):c.2451G>A (p.Thr817=)	not provided [RCV000929189]	likely benign	15	22903843	22903843	Human		name
15181101	CV770037	single nucleotide variant	NM_014608.6(CYFIP1):c.1575T>C (p.His525=)	not provided [RCV000930045]	likely benign	15	22917887	22917887	Human		name
156101027	CV2291319	single nucleotide variant	NM_014608.6(CYFIP1):c.418G>T (p.Val140Leu)	not specified [RCV004162011]	uncertain significance	15	22943324	22943324	Human		name
156044584	CV2381644	single nucleotide variant	NM_014608.6(CYFIP1):c.658A>G (p.Ile220Val)	not specified [RCV004232115]	uncertain significance	15	22939419	22939419	Human		name
156141837	CV2383727	single nucleotide variant	NM_014608.6(CYFIP1):c.790C>G (p.Leu264Val)	not specified [RCV004231609]	uncertain significance	15	22939197	22939197	Human		name
401911341	CV2817187	single nucleotide variant	NM_014608.6(CYFIP1):c.910G>A (p.Val304Met)	not provided [RCV003426452]	uncertain significance	15	22933884	22933884	Human		name
401911347	CV2817192	single nucleotide variant	NM_014608.6(CYFIP1):c.3057G>A (p.Val1019=)	not provided [RCV003426457]	likely benign	15	22875257	22875257	Human		name
405666299	CV3239472	single nucleotide variant	NM_014608.6(CYFIP1):c.404G>A (p.Arg135His)	not specified [RCV004367716]	uncertain significance	15	22943338	22943338	Human		name
405666304	CV3239473	single nucleotide variant	NM_014608.6(CYFIP1):c.457G>A (p.Val153Met)	not specified [RCV004367717]	uncertain significance	15	22943285	22943285	Human		name
405666307	CV3239474	single nucleotide variant	NM_014608.6(CYFIP1):c.845A>G (p.Tyr282Cys)	not specified [RCV004367718]	uncertain significance	15	22937159	22937159	Human		name
407452220	CV3420037	single nucleotide variant	NM_014608.6(CYFIP1):c.508G>C (p.Val170Leu)	not specified [RCV004608386]	uncertain significance	15	22943234	22943234	Human		name
407452224	CV3420039	single nucleotide variant	NM_014608.6(CYFIP1):c.769C>T (p.Pro257Ser)	not specified [RCV004608388]	uncertain significance	15	22939218	22939218	Human		name
597656281	CV3658030	single nucleotide variant	NM_014608.6(CYFIP1):c.877T>C (p.Ser293Pro)	not specified [RCV004911149]	uncertain significance	15	22937127	22937127	Human		name
597656303	CV3658033	single nucleotide variant	NM_014608.6(CYFIP1):c.722T>C (p.Ile241Thr)	not specified [RCV004911152]	uncertain significance	15	22939265	22939265	Human		name
597656349	CV3658040	single nucleotide variant	NM_014608.6(CYFIP1):c.368T>C (p.Met123Thr)	not specified [RCV004911158]	uncertain significance	15	22944577	22944577	Human		name
597656359	CV3658041	single nucleotide variant	NM_014608.6(CYFIP1):c.433C>T (p.His145Tyr)	not specified [RCV004911159]	uncertain significance	15	22943309	22943309	Human		name
15121976	CV714324	single nucleotide variant	NM_014608.6(CYFIP1):c.3603G>A (p.Leu1201=)	not provided [RCV000962992]	benign	15	22870187	22870187	Human		name
15131013	CV714325	single nucleotide variant	NM_014608.6(CYFIP1):c.3162C>T (p.Tyr1054=)	not provided [RCV000964532]	benign\|likely benign	15	22874598	22874598	Human		name
15195478	CV725916	single nucleotide variant	NM_014608.6(CYFIP1):c.3099G>T (p.Pro1033=)	not provided [RCV000889515]	benign	15	22875215	22875215	Human		name
15160942	CV739459	single nucleotide variant	NM_014608.6(CYFIP1):c.3336T>C (p.Pro1112=)	not provided [RCV000903247]	likely benign	15	22873604	22873604	Human		name
15173358	CV739460	single nucleotide variant	NM_014608.6(CYFIP1):c.3330C>T (p.Arg1110=)	not provided [RCV000905844]	likely benign	15	22873610	22873610	Human		name
15167673	CV754290	single nucleotide variant	NM_014608.6(CYFIP1):c.3366C>T (p.Asp1122=)	not provided [RCV000927135]	likely benign	15	22873574	22873574	Human		name
15138650	CV754291	single nucleotide variant	NM_014608.6(CYFIP1):c.3165C>T (p.Ala1055=)	not provided [RCV000921372]	likely benign	15	22874595	22874595	Human		name
15139870	CV754292	single nucleotide variant	NM_014608.6(CYFIP1):c.3135C>T (p.Ala1045=)	not provided [RCV000921584]	likely benign	15	22874625	22874625	Human		name
15199777	CV770035	single nucleotide variant	NM_014608.6(CYFIP1):c.3036G>A (p.Gln1012=)	not provided [RCV000935198]	likely benign	15	22879919	22879919	Human		name
8627615	CV82759	single nucleotide variant	NM_014608.3(CYFIP1):c.886G>A (p.Asp296Asn)	Malignant melanoma [RCV000062839]	not provided	15	22937118	22937118	Human		name
156173200	CV2194334	single nucleotide variant	NM_014608.6(CYFIP1):c.2450C>T (p.Thr817Met)	not specified [RCV004079446]	uncertain significance	15	22903844	22903844	Human		name
156400537	CV2199248	single nucleotide variant	NM_014608.6(CYFIP1):c.2023G>A (p.Ala675Thr)	not specified [RCV004082608]	uncertain significance	15	22912238	22912238	Human		name
156149828	CV2213023	single nucleotide variant	NM_014608.6(CYFIP1):c.2419A>G (p.Met807Val)	not specified [RCV004091614]	uncertain significance	15	22903875	22903875	Human		name
155969428	CV2213334	single nucleotide variant	NM_014608.6(CYFIP1):c.2826A>T (p.Gln942His)	not specified [RCV004085539]	uncertain significance	15	22881931	22881931	Human		name
156326924	CV2219723	single nucleotide variant	NM_014608.6(CYFIP1):c.1154C>T (p.Ala385Val)	not specified [RCV004095427]	uncertain significance	15	22927985	22927985	Human		name
155928789	CV2224436	single nucleotide variant	NM_014608.6(CYFIP1):c.2314G>A (p.Val772Ile)	not specified [RCV004098039]	uncertain significance	15	22909268	22909268	Human		name
156097228	CV2253169	single nucleotide variant	NM_014608.6(CYFIP1):c.2972C>T (p.Thr991Met)	not specified [RCV004120937]	uncertain significance	15	22879983	22879983	Human		name
156236785	CV2268856	single nucleotide variant	NM_014608.6(CYFIP1):c.2779G>A (p.Ala927Thr)	not specified [RCV004126142]	uncertain significance	15	22882909	22882909	Human		name
155918878	CV2279308	single nucleotide variant	NM_014608.6(CYFIP1):c.1613A>T (p.Asp538Val)	not specified [RCV004139825]	uncertain significance	15	22917849	22917849	Human		name
155918888	CV2279309	single nucleotide variant	NM_014608.6(CYFIP1):c.1614C>A (p.Asp538Glu)	not specified [RCV004139826]	uncertain significance	15	22917848	22917848	Human		name
155903910	CV2282314	single nucleotide variant	NM_014608.6(CYFIP1):c.2932C>T (p.His978Tyr)	not specified [RCV004133141]	uncertain significance	15	22880023	22880023	Human		name
156017355	CV2295586	single nucleotide variant	NM_014608.6(CYFIP1):c.2467G>A (p.Ala823Thr)	not specified [RCV004160674]	uncertain significance	15	22903827	22903827	Human		name
156303169	CV2308219	single nucleotide variant	NM_014608.6(CYFIP1):c.2312G>A (p.Arg771His)	not specified [RCV004164720]	uncertain significance	15	22909270	22909270	Human		name
156059305	CV2316968	single nucleotide variant	NM_014608.6(CYFIP1):c.1294G>A (p.Ala432Thr)	not specified [RCV004174469]	uncertain significance	15	22926047	22926047	Human		name
155986691	CV2363698	single nucleotide variant	NM_014608.6(CYFIP1):c.1091C>T (p.Ala364Val)	not specified [RCV004216643]	uncertain significance	15	22932242	22932242	Human		name
156402412	CV2363985	single nucleotide variant	NM_014608.6(CYFIP1):c.2575G>A (p.Gly859Ser)	not specified [RCV004218951]	uncertain significance	15	22903719	22903719	Human		name
329392511	CV2439036	single nucleotide variant	NM_014608.6(CYFIP1):c.2659T>C (p.Tyr887His)	not specified [RCV004264539]	uncertain significance	15	22892907	22892907	Human		name
329387029	CV2452798	single nucleotide variant	NM_014608.6(CYFIP1):c.1804T>C (p.Tyr602His)	not specified [RCV004275333]	uncertain significance	15	22916501	22916501	Human		name
329393590	CV2453452	single nucleotide variant	NM_014608.6(CYFIP1):c.1976C>T (p.Ser659Leu)	not specified [RCV004267055]	uncertain significance	15	22914735	22914735	Human		name
329397202	CV2460014	single nucleotide variant	NM_014608.6(CYFIP1):c.1127G>A (p.Gly376Asp)	not specified [RCV004279486]	uncertain significance	15	22928012	22928012	Human		name
401769849	CV2693076	single nucleotide variant	NM_014608.6(CYFIP1):c.2176C>T (p.Arg726Trp)	not specified [RCV004308618]	uncertain significance	15	22910612	22910612	Human		name
401747518	CV2696721	single nucleotide variant	NM_014608.6(CYFIP1):c.1573C>T (p.His525Tyr)	not specified [RCV004290696]	uncertain significance	15	22917889	22917889	Human		name
401761696	CV2699385	single nucleotide variant	NM_014608.6(CYFIP1):c.2743C>G (p.Gln915Glu)	not specified [RCV004305967]	uncertain significance	15	22882945	22882945	Human		name
401731436	CV2701362	single nucleotide variant	NM_014608.6(CYFIP1):c.1613A>G (p.Asp538Gly)	not specified [RCV004311733]	uncertain significance	15	22917849	22917849	Human		name
401771993	CV2723015	single nucleotide variant	NM_014608.6(CYFIP1):c.1438G>A (p.Val480Ile)	not specified [RCV004327185]	uncertain significance	15	22918780	22918780	Human		name
401731677	CV2736579	single nucleotide variant	NM_014608.6(CYFIP1):c.1798T>C (p.Phe600Leu)	Autism [RCV003313341]\|not specified [RCV004333262]	pathogenic\|uncertain significance	15	22916507	22916507	Human	2	name
401731691	CV2736584	single nucleotide variant	NM_014608.6(CYFIP1):c.1348G>T (p.Ala450Ser)	Autism [RCV003313346]	uncertain significance	15	22925993	22925993	Human	2	name
401874766	CV2781224	single nucleotide variant	NM_014608.6(CYFIP1):c.1126G>A (p.Gly376Ser)	not specified [RCV004352261]	uncertain significance	15	22928013	22928013	Human		name
401870268	CV2792325	single nucleotide variant	NM_014608.6(CYFIP1):c.2210C>T (p.Thr737Met)	not specified [RCV004361503]	uncertain significance	15	22910578	22910578	Human		name
401911345	CV2817190	single nucleotide variant	NM_014608.6(CYFIP1):c.1424C>G (p.Ala475Gly)	not provided [RCV003426455]	uncertain significance	15	22918794	22918794	Human		name
405666217	CV3239456	single nucleotide variant	NM_014608.6(CYFIP1):c.1050C>G (p.Ile350Met)	not specified [RCV004367700]	uncertain significance	15	22932283	22932283	Human		name
405666227	CV3239458	single nucleotide variant	NM_014608.6(CYFIP1):c.1226T>C (p.Met409Thr)	not specified [RCV004367702]	uncertain significance	15	22927913	22927913	Human		name
405666233	CV3239459	single nucleotide variant	NM_014608.6(CYFIP1):c.1856C>T (p.Ser619Leu)	not specified [RCV004367703]	uncertain significance	15	22914855	22914855	Human		name
405666240	CV3239460	single nucleotide variant	NM_014608.6(CYFIP1):c.2164C>T (p.Leu722Phe)	not specified [RCV004367704]	uncertain significance	15	22910624	22910624	Human		name
405666245	CV3239461	single nucleotide variant	NM_014608.6(CYFIP1):c.2417G>A (p.Arg806His)	not specified [RCV004367705]	uncertain significance	15	22903877	22903877	Human		name
405666250	CV3239462	single nucleotide variant	NM_014608.6(CYFIP1):c.2443T>G (p.Tyr815Asp)	not specified [RCV004367706]	uncertain significance	15	22903851	22903851	Human		name
405666256	CV3239463	single nucleotide variant	NM_014608.6(CYFIP1):c.2579C>G (p.Ser860Cys)	not specified [RCV004367707]	uncertain significance	15	22903715	22903715	Human		name
405666260	CV3239464	single nucleotide variant	NM_014608.6(CYFIP1):c.2772G>C (p.Gln924His)	not specified [RCV004367708]	uncertain significance	15	22882916	22882916	Human		name
407452209	CV3420032	single nucleotide variant	NM_014608.6(CYFIP1):c.1514A>C (p.Asn505Thr)	not specified [RCV004608381]	uncertain significance	15	22918704	22918704	Human		name
407452211	CV3420033	single nucleotide variant	NM_014608.6(CYFIP1):c.2782G>A (p.Val928Met)	not specified [RCV004608382]	uncertain significance	15	22882906	22882906	Human		name
407452216	CV3420035	single nucleotide variant	NM_014608.6(CYFIP1):c.1003A>G (p.Thr335Ala)	not specified [RCV004608384]	uncertain significance	15	22932330	22932330	Human		name
407452218	CV3420036	single nucleotide variant	NM_014608.6(CYFIP1):c.2183G>A (p.Arg728Gln)	not specified [RCV004608385]	uncertain significance	15	22910605	22910605	Human		name
407452222	CV3420038	single nucleotide variant	NM_014608.6(CYFIP1):c.2127G>C (p.Gln709His)	not specified [RCV004608387]	uncertain significance	15	22910769	22910769	Human		name
597656288	CV3658031	single nucleotide variant	NM_014608.6(CYFIP1):c.2527G>A (p.Val843Ile)	not specified [RCV004911150]	uncertain significance	15	22903767	22903767	Human		name
597656295	CV3658032	single nucleotide variant	NM_014608.6(CYFIP1):c.2243C>T (p.Thr748Met)	not specified [RCV004911151]	uncertain significance	15	22910545	22910545	Human		name
597656311	CV3658034	single nucleotide variant	NM_014608.6(CYFIP1):c.1954A>G (p.Ile652Val)	not specified [RCV004911153]	uncertain significance	15	22914757	22914757	Human		name
597656319	CV3658035	single nucleotide variant	NM_014608.6(CYFIP1):c.1946C>T (p.Thr649Met)	not specified [RCV004911154]	uncertain significance	15	22914765	22914765	Human		name
597656366	CV3658042	single nucleotide variant	NM_014608.6(CYFIP1):c.2597G>A (p.Arg866Gln)	not specified [RCV004911160]	uncertain significance	15	22892969	22892969	Human		name
597656375	CV3658043	single nucleotide variant	NM_014608.6(CYFIP1):c.1723G>A (p.Gly575Ser)	not specified [RCV004911161]	uncertain significance	15	22916582	22916582	Human		name
598237053	CV3956272	single nucleotide variant	NM_014608.6(CYFIP1):c.2470A>G (p.Met824Val)	not specified [RCV005320566]	uncertain significance	15	22903824	22903824	Human		name
598237058	CV3956273	single nucleotide variant	NM_014608.6(CYFIP1):c.2225C>T (p.Pro742Leu)	not specified [RCV005320567]	uncertain significance	15	22910563	22910563	Human		name
598237064	CV3956274	single nucleotide variant	NM_014608.6(CYFIP1):c.1709T>C (p.Ile570Thr)	not specified [RCV005320568]	uncertain significance	15	22916596	22916596	Human		name
598237068	CV3956275	single nucleotide variant	NM_014608.6(CYFIP1):c.1093C>T (p.Arg365Cys)	not specified [RCV005320569]	uncertain significance	15	22932240	22932240	Human		name
598160413	CV3956276	single nucleotide variant	NM_014608.6(CYFIP1):c.1586A>G (p.Asn529Ser)	not specified [RCV005328767]	uncertain significance	15	22917876	22917876	Human		name
598237073	CV3956277	single nucleotide variant	NM_014608.6(CYFIP1):c.2327T>C (p.Met776Thr)	not specified [RCV005320570]	uncertain significance	15	22909255	22909255	Human		name
598237078	CV3956278	single nucleotide variant	NM_014608.6(CYFIP1):c.2846T>G (p.Val949Gly)	not specified [RCV005320571]	uncertain significance	15	22881911	22881911	Human		name
598237094	CV3956281	single nucleotide variant	NM_014608.6(CYFIP1):c.1681A>G (p.Met561Val)	not specified [RCV005320574]	uncertain significance	15	22916624	22916624	Human		name
598237107	CV3956283	single nucleotide variant	NM_014608.6(CYFIP1):c.1820A>C (p.Asn607Thr)	not specified [RCV005320576]	uncertain significance	15	22916485	22916485	Human		name
15202425	CV703081	single nucleotide variant	NM_014608.6(CYFIP1):c.2707G>A (p.Gly903Ser)	not provided [RCV000957911]	benign	15	22882981	22882981	Human		name
15202421	CV703082	single nucleotide variant	NM_014608.6(CYFIP1):c.2383A>G (p.Ile795Val)	not provided [RCV000957910]	benign	15	22909199	22909199	Human		name
15161046	CV703083	single nucleotide variant	NM_014608.6(CYFIP1):c.1153G>A (p.Ala385Thr)	not provided [RCV000947601]	benign	15	22927986	22927986	Human		name
15167245	CV725917	single nucleotide variant	NM_014608.6(CYFIP1):c.2459G>A (p.Gly820Asp)	not provided [RCV000882807]	likely benign	15	22903835	22903835	Human		name
156290415	CV2299504	single nucleotide variant	NM_014608.6(CYFIP1):c.3692G>A (p.Gly1231Glu)	not specified [RCV004154572]	uncertain significance	15	22870098	22870098	Human		name
156060557	CV2305415	single nucleotide variant	NM_014608.6(CYFIP1):c.3518G>A (p.Arg1173His)	not specified [RCV004165141]	uncertain significance	15	22872904	22872904	Human		name
155975139	CV2342633	single nucleotide variant	NM_014608.6(CYFIP1):c.3452A>T (p.Gln1151Leu)	not specified [RCV004196719]	uncertain significance	15	22872970	22872970	Human		name
155929160	CV2363455	single nucleotide variant	NM_014608.6(CYFIP1):c.3275T>C (p.Met1092Thr)	not specified [RCV004216030]	uncertain significance	15	22873665	22873665	Human		name
156130183	CV2364864	single nucleotide variant	NM_014608.6(CYFIP1):c.3656T>C (p.Ile1219Thr)	not specified [RCV004219724]	uncertain significance	15	22870134	22870134	Human		name
155934263	CV2372426	single nucleotide variant	NM_014608.6(CYFIP1):c.3733C>T (p.Pro1245Ser)	not specified [RCV004219233]	uncertain significance	15	22870057	22870057	Human		name
156216517	CV2386073	single nucleotide variant	NM_014608.6(CYFIP1):c.3295C>T (p.Arg1099Trp)	not specified [RCV004229131]	uncertain significance	15	22873645	22873645	Human		name
329389851	CV2441372	single nucleotide variant	NM_014608.6(CYFIP1):c.3036G>C (p.Gln1012His)	not specified [RCV004257177]	uncertain significance	15	22879919	22879919	Human		name
329392991	CV2449424	single nucleotide variant	NM_014608.6(CYFIP1):c.3659C>T (p.Thr1220Ile)	not specified [RCV004266584]	uncertain significance	15	22870131	22870131	Human		name
401724939	CV2715035	single nucleotide variant	NM_014608.6(CYFIP1):c.3074C>T (p.Ala1025Val)	not specified [RCV004322347]	uncertain significance	15	22875240	22875240	Human		name
401878872	CV2754860	single nucleotide variant	NM_014608.6(CYFIP1):c.3167C>T (p.Pro1056Leu)	not specified [RCV004341335]	uncertain significance	15	22874593	22874593	Human		name
401886009	CV2771562	single nucleotide variant	NM_014608.6(CYFIP1):c.3302G>T (p.Arg1101Leu)	not specified [RCV004348586]	uncertain significance	15	22873638	22873638	Human		name
401878842	CV2777925	single nucleotide variant	NM_014608.6(CYFIP1):c.3697G>A (p.Gly1233Ser)	not specified [RCV004347892]	likely benign	15	22870093	22870093	Human		name
401920050	CV2796492	single nucleotide variant	NM_014608.6(CYFIP1):c.3220A>G (p.Ile1074Val)	CYFIP1-related disorder [RCV003402528]	uncertain significance	15	22873720	22873720	Human		name , trait , alternate_id
405666268	CV3239466	single nucleotide variant	NM_014608.6(CYFIP1):c.3007G>A (p.Ala1003Thr)	not specified [RCV004367710]	uncertain significance	15	22879948	22879948	Human		name
405666274	CV3239467	single nucleotide variant	NM_014608.6(CYFIP1):c.3355A>G (p.Met1119Val)	not specified [RCV004367711]	uncertain significance	15	22873585	22873585	Human		name
405666280	CV3239468	single nucleotide variant	NM_014608.6(CYFIP1):c.3367G>A (p.Glu1123Lys)	not specified [RCV004367712]	uncertain significance	15	22873573	22873573	Human		name
405666284	CV3239469	single nucleotide variant	NM_014608.6(CYFIP1):c.3370T>C (p.Cys1124Arg)	not specified [RCV004367713]	uncertain significance	15	22873570	22873570	Human		name
405666289	CV3239470	single nucleotide variant	NM_014608.6(CYFIP1):c.3400A>T (p.Met1134Leu)	not specified [RCV004367714]	uncertain significance	15	22873540	22873540	Human		name
405666294	CV3239471	single nucleotide variant	NM_014608.6(CYFIP1):c.3670A>G (p.Lys1224Glu)	not specified [RCV004367715]	uncertain significance	15	22870120	22870120	Human		name
407452213	CV3420034	single nucleotide variant	NM_014608.6(CYFIP1):c.3712C>G (p.His1238Asp)	not specified [RCV004608383]	uncertain significance	15	22870078	22870078	Human		name
597656342	CV3658039	single nucleotide variant	NM_014608.6(CYFIP1):c.3274A>G (p.Met1092Val)	not specified [RCV004911157]	uncertain significance	15	22873666	22873666	Human		name
598237083	CV3956279	single nucleotide variant	NM_014608.6(CYFIP1):c.3365A>G (p.Asp1122Gly)	not specified [RCV005320572]	uncertain significance	15	22873575	22873575	Human		name
598237099	CV3956282	single nucleotide variant	NM_014608.6(CYFIP1):c.3704C>T (p.Pro1235Leu)	not specified [RCV005320575]	uncertain significance	15	22870086	22870086	Human		name
15187277	CV703080	single nucleotide variant	NM_014608.6(CYFIP1):c.3008C>T (p.Ala1003Val)	not provided [RCV000953539]	benign	15	22879947	22879947	Human		name

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