Ift88 Variant Search Result - Rat Genome Database

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486 records found for search term Ift88

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8582698	CV117252	single nucleotide variant	NM_006531.3(IFT88):c.-1332T>C	Lung cancer [RCV000097773]	uncertain significance	13	20565931	20565931	Human		name
151808830	CV1362832	single nucleotide variant	NM_006531.5(IFT88):c.265-9T>C	not provided [RCV001991626]	likely benign	13	20591609	20591609	Human		name
152057315	CV1618916	single nucleotide variant	NM_006531.5(IFT88):c.264+9A>G	IFT88-related disorder [RCV003958850]\|not provided [RCV002127938]	likely benign	13	20591029	20591029	Human		name , trait , alternate_id
152150159	CV1625694	single nucleotide variant	NM_006531.5(IFT88):c.698-7A>T	IFT88-related disorder [RCV003933485]\|not provided [RCV002139395]	benign\|likely benign	13	20599444	20599444	Human		name , trait , alternate_id
152027460	CV1628722	single nucleotide variant	NM_006531.5(IFT88):c.154-9C>T	not provided [RCV002104900]	likely benign	13	20589802	20589802	Human		name
156058973	CV1930877	single nucleotide variant	NM_006531.5(IFT88):c.211-5A>G	not provided [RCV002638215]	likely benign	13	20590962	20590962	Human		name
156227614	CV1955856	single nucleotide variant	NM_006531.5(IFT88):c.91-14C>T	not provided [RCV002575757]	likely benign	13	20582943	20582943	Human		name
156395892	CV1958939	single nucleotide variant	NM_006531.5(IFT88):c.91-13G>A	not provided [RCV002584355]	likely benign	13	20582944	20582944	Human		name
156246982	CV1969584	single nucleotide variant	NM_006531.5(IFT88):c.698-8T>A	not provided [RCV002597341]	uncertain significance	13	20599443	20599443	Human		name
155919905	CV1991147	single nucleotide variant	NM_006531.5(IFT88):c.-6-11G>A	not provided [RCV002614503]	uncertain significance	13	20574369	20574369	Human		name
156109452	CV2072614	single nucleotide variant	NM_006531.5(IFT88):c.489+4A>C	not provided [RCV002870835]	uncertain significance	13	20596244	20596244	Human		name
156215262	CV2076685	single nucleotide variant	NM_006531.5(IFT88):c.-6-12A>G	not provided [RCV002875648]	uncertain significance	13	20574368	20574368	Human		name
156158297	CV2095013	deletion	NM_006531.5(IFT88):c.154-4del	not provided [RCV002890890]	benign	13	20589804	20589804	Human		name
156366080	CV2177026	single nucleotide variant	NM_006531.5(IFT88):c.265-7T>C	not provided [RCV003049356]	uncertain significance	13	20591611	20591611	Human		name
402516101	CV2856732	single nucleotide variant	NM_006531.5(IFT88):c.595-4T>G	not provided [RCV003575500]	likely benign	13	20598647	20598647	Human		name
405214715	CV3078381	single nucleotide variant	NM_006531.5(IFT88):c.698-7A>G	not provided [RCV003732405]	likely benign	13	20599444	20599444	Human		name
597916078	CV3771499	single nucleotide variant	NM_006531.5(IFT88):c.264+1G>T	not provided [RCV005114430]	uncertain significance	13	20591021	20591021	Human		name
597952157	CV3847563	single nucleotide variant	NM_006531.5(IFT88):c.329-5C>G	not provided [RCV005190545]	uncertain significance	13	20592330	20592330	Human		name
150457299	CV1248764	single nucleotide variant	NM_006531.5(IFT88):c.-7+427A>G	not provided [RCV001668940]	benign	13	20567683	20567683	Human		name
151867693	CV1338217	single nucleotide variant	NM_006531.5(IFT88):c.-7+736A>G	not provided [RCV001884740]	uncertain significance	13	20567992	20567992	Human		name
151844599	CV1457860	single nucleotide variant	NM_006531.5(IFT88):c.1199+5G>A	not provided [RCV001936536]	uncertain significance	13	20615884	20615884	Human		name
151735350	CV1508828	deletion	NM_006531.5(IFT88):c.1299+1del	not provided [RCV002021743]	uncertain significance	13	20625850	20625850	Human		name
152120890	CV1521357	single nucleotide variant	NM_006531.5(IFT88):c.812+15A>G	not provided [RCV002135694]	likely benign	13	20599580	20599580	Human		name
152150030	CV1545500	single nucleotide variant	NM_006531.5(IFT88):c.399-11G>C	not provided [RCV002121610]	likely benign	13	20596139	20596139	Human		name
152117265	CV1566549	single nucleotide variant	NM_006531.5(IFT88):c.490-18G>C	not provided [RCV002153813]	benign	13	20596997	20596997	Human		name
152104529	CV1574805	single nucleotide variant	NM_006531.5(IFT88):c.697+15T>C	not provided [RCV002095974]	benign	13	20598768	20598768	Human		name
152034590	CV1584540	single nucleotide variant	NM_006531.5(IFT88):c.264+18A>G	not provided [RCV002125121]	likely benign	13	20591038	20591038	Human		name
152086574	CV1602320	deletion	NM_006531.5(IFT88):c.153+22del	not provided [RCV002113471]	benign	13	20583034	20583034	Human		name
152147043	CV1615542	duplication	NM_006531.5(IFT88):c.-7+765dup	not provided [RCV002101637]	benign	13	20568013	20568014	Human		name
152136749	CV1625372	single nucleotide variant	NM_006531.5(IFT88):c.328+15C>G	not provided [RCV002137640]	likely benign	13	20591696	20591696	Human		name
152099708	CV1627315	single nucleotide variant	NM_006531.5(IFT88):c.-7+746C>T	not provided [RCV002095356]	likely benign	13	20568002	20568002	Human		name
152114573	CV1651313	single nucleotide variant	NM_006531.5(IFT88):c.490-16A>G	not provided [RCV002153491]	likely benign	13	20596999	20596999	Human		name
152120128	CV1654926	single nucleotide variant	NM_006531.5(IFT88):c.2354-9G>A	not provided [RCV002216663]	benign	13	20691045	20691045	Human		name
156117439	CV1952451	single nucleotide variant	NM_006531.5(IFT88):c.399-19C>T	not provided [RCV002571729]	likely benign	13	20596131	20596131	Human		name
156176470	CV1953152	single nucleotide variant	NM_006531.5(IFT88):c.594+14T>C	not provided [RCV002573977]	likely benign	13	20597133	20597133	Human		name
156373480	CV1953538	single nucleotide variant	NM_006531.5(IFT88):c.153+15T>A	not provided [RCV002582609]	likely benign	13	20583034	20583034	Human		name
156213342	CV1963113	single nucleotide variant	NM_006531.5(IFT88):c.490-12A>G	not provided [RCV002575236]	uncertain significance	13	20597003	20597003	Human		name
156410867	CV1965991	single nucleotide variant	NM_006531.5(IFT88):c.2068+9C>T	not provided [RCV002587295]	likely benign	13	20656439	20656439	Human		name
156222871	CV1981409	single nucleotide variant	NM_006531.5(IFT88):c.697+11A>G	not provided [RCV002626510]	likely benign	13	20598764	20598764	Human		name
156249364	CV1989035	single nucleotide variant	NM_006531.5(IFT88):c.399-17G>A	not provided [RCV002627399]	likely benign	13	20596133	20596133	Human		name
156229887	CV1991766	single nucleotide variant	NM_006531.5(IFT88):c.399-18T>G	not provided [RCV002626754]	likely benign	13	20596132	20596132	Human		name
156266106	CV2011139	single nucleotide variant	NM_006531.5(IFT88):c.398+20G>T	not provided [RCV002714821]	likely benign	13	20592424	20592424	Human		name
155955485	CV2014274	single nucleotide variant	NM_006531.5(IFT88):c.-7+721A>G	not provided [RCV002686243]	uncertain significance	13	20567977	20567977	Human		name
156282338	CV2016407	single nucleotide variant	NM_006531.5(IFT88):c.812+12A>G	not provided [RCV002715343]	likely benign	13	20599577	20599577	Human		name
156234216	CV2021403	single nucleotide variant	NM_006531.5(IFT88):c.1683-5A>G	not provided [RCV002745421]	likely benign	13	20643450	20643450	Human		name
156148942	CV2022969	single nucleotide variant	NM_006531.5(IFT88):c.399-14T>C	not provided [RCV002741160]	likely benign	13	20596136	20596136	Human		name
155910177	CV2041152	single nucleotide variant	NM_006531.5(IFT88):c.2003-2A>G	not provided [RCV002771524]	uncertain significance	13	20656363	20656363	Human		name
155906440	CV2048195	single nucleotide variant	NM_006531.5(IFT88):c.153+14A>T	not provided [RCV002771291]	likely benign	13	20583033	20583033	Human		name
156207188	CV2076775	single nucleotide variant	NM_006531.5(IFT88):c.328+12T>C	not provided [RCV002852688]	likely benign	13	20591693	20591693	Human		name
156249976	CV2097992	single nucleotide variant	NM_006531.5(IFT88):c.265-15C>T	not provided [RCV002895224]	likely benign	13	20591603	20591603	Human		name
156094225	CV2102826	single nucleotide variant	NM_006531.5(IFT88):c.1950-4A>G	IFT88-related disorder [RCV003961167]\|not provided [RCV002913154]	likely benign	13	20653872	20653872	Human		name , trait , alternate_id
156210918	CV2103295	duplication	NM_006531.5(IFT88):c.1683-4dup	not provided [RCV002918158]	likely benign	13	20643450	20643451	Human		name
156225745	CV2115182	single nucleotide variant	NM_006531.5(IFT88):c.264+16G>A	not provided [RCV002918744]	likely benign	13	20591036	20591036	Human		name
156091523	CV2135569	single nucleotide variant	NM_006531.5(IFT88):c.2242+7A>G	not provided [RCV003001850]	likely benign	13	20671046	20671046	Human		name
155943761	CV2154524	duplication	NM_006531.5(IFT88):c.2242+2dup	not provided [RCV003014438]	uncertain significance	13	20671040	20671041	Human		name
156309777	CV2163962	single nucleotide variant	NM_006531.5(IFT88):c.595-17A>G	not provided [RCV003045964]	likely benign	13	20598634	20598634	Human		name
156053436	CV2165387	single nucleotide variant	NM_006531.5(IFT88):c.153+13A>C	not provided [RCV003019476]	likely benign	13	20583032	20583032	Human		name
156019769	CV2174076	single nucleotide variant	NM_006531.5(IFT88):c.1682+8A>G	not provided [RCV003035669]	likely benign	13	20641406	20641406	Human		name
405195192	CV2868705	single nucleotide variant	NM_006531.5(IFT88):c.1683-8T>C	not provided [RCV003550780]	likely benign	13	20643447	20643447	Human		name
402501876	CV2932280	deletion	NM_006531.5(IFT88):c.1042-6del	not provided [RCV003574021]	benign	13	20605026	20605026	Human		name
402515109	CV2936277	single nucleotide variant	NM_006531.5(IFT88):c.210+17T>C	not provided [RCV003662884]	likely benign	13	20589884	20589884	Human		name
405220924	CV2965996	single nucleotide variant	NM_006531.5(IFT88):c.1113-6A>T	not provided [RCV003680667]	uncertain significance	13	20615787	20615787	Human		name
405229233	CV2973769	single nucleotide variant	NM_006531.5(IFT88):c.-7+739A>G	not provided [RCV003681884]	uncertain significance	13	20567995	20567995	Human		name
405214658	CV3078380	single nucleotide variant	NM_006531.5(IFT88):c.-7+751G>A	not provided [RCV003732404]	likely benign	13	20568007	20568007	Human		name
405094648	CV3118984	single nucleotide variant	NM_006531.5(IFT88):c.399-20C>G	not provided [RCV003811435]	likely benign	13	20596130	20596130	Human		name
405194988	CV3146459	single nucleotide variant	NM_006531.5(IFT88):c.698-15A>T	not provided [RCV003843814]	likely benign	13	20599436	20599436	Human		name
405248004	CV3159203	single nucleotide variant	NM_006531.5(IFT88):c.1113-4A>G	not provided [RCV003869348]	likely benign	13	20615789	20615789	Human		name
405244713	CV3161579	single nucleotide variant	NM_006531.5(IFT88):c.1833+1G>C	not provided [RCV003868292]	uncertain significance	13	20643606	20643606	Human		name
405234902	CV3168529	single nucleotide variant	NM_006531.5(IFT88):c.1833+7G>A	not provided [RCV003866003]	likely benign	13	20643612	20643612	Human		name
405255456	CV3172437	single nucleotide variant	NM_006531.5(IFT88):c.328+11C>G	not provided [RCV003872375]	likely benign	13	20591692	20591692	Human		name
405259580	CV3195104	single nucleotide variant	NM_006531.5(IFT88):c.2175+8A>C	IFT88-related disorder [RCV003894301]	likely benign	13	20663612	20663612	Human		name , trait , alternate_id
408383154	CV3504848	single nucleotide variant	NM_006531.5(IFT88):c.1299+1G>T	IFT88-related disorder [RCV004730456]	uncertain significance	13	20625850	20625850	Human		name , trait , alternate_id
597839352	CV3737008	single nucleotide variant	NM_006531.5(IFT88):c.329-16T>C	not provided [RCV005064488]	likely benign	13	20592319	20592319	Human		name
597831967	CV3740092	single nucleotide variant	NM_006531.5(IFT88):c.1682+6T>G	not provided [RCV005062791]	uncertain significance	13	20641404	20641404	Human		name
597958304	CV3755224	single nucleotide variant	NM_006531.5(IFT88):c.1574-1G>A	not provided [RCV005080894]	uncertain significance	13	20641289	20641289	Human		name
597845987	CV3761641	single nucleotide variant	NM_006531.5(IFT88):c.329-18T>C	not provided [RCV005087241]	likely benign	13	20592317	20592317	Human		name
597910381	CV3782126	single nucleotide variant	NM_006531.5(IFT88):c.211-12T>C	not provided [RCV005128618]	uncertain significance	13	20590955	20590955	Human		name
597951261	CV3798315	single nucleotide variant	NM_006531.5(IFT88):c.812+10T>C	not provided [RCV005136095]	likely benign	13	20599575	20599575	Human		name
597951509	CV3798352	single nucleotide variant	NM_006531.5(IFT88):c.1041+1G>C	not provided [RCV005136132]	uncertain significance	13	20601934	20601934	Human		name
597949085	CV3818481	single nucleotide variant	NM_006531.5(IFT88):c.1682+2T>C	not provided [RCV005160742]	uncertain significance	13	20641400	20641400	Human		name
597894540	CV3833560	single nucleotide variant	NM_006531.5(IFT88):c.1683-3A>G	not provided [RCV005180252]	uncertain significance	13	20643452	20643452	Human		name
597911075	CV3854238	single nucleotide variant	NM_006531.5(IFT88):c.210+10T>A	not provided [RCV005203508]	likely benign	13	20589877	20589877	Human		name
152130151	CV1519555	single nucleotide variant	NM_006531.5(IFT88):c.2069-17T>G	not provided [RCV002155418]	likely benign	13	20663481	20663481	Human		name
152071304	CV1552077	single nucleotide variant	NM_006531.5(IFT88):c.1200-16A>G	not provided [RCV002148116]	benign	13	20625734	20625734	Human		name
152127872	CV1554285	single nucleotide variant	NM_006531.5(IFT88):c.1387-17A>G	not provided [RCV002176404]	likely benign	13	20638315	20638315	Human		name
152092953	CV1567886	single nucleotide variant	NM_006531.5(IFT88):c.1573+18A>G	not provided [RCV002212979]	likely benign	13	20638536	20638536	Human		name
152104150	CV1574731	single nucleotide variant	NM_006531.5(IFT88):c.1199+12A>G	not provided [RCV002095921]	benign	13	20615891	20615891	Human		name
152095271	CV1597319	single nucleotide variant	NM_006531.5(IFT88):c.1113-16G>T	not provided [RCV002114619]	likely benign	13	20615777	20615777	Human		name
152151472	CV1598300	single nucleotide variant	NM_006531.5(IFT88):c.1041+12A>G	not provided [RCV002121807]	likely benign	13	20601945	20601945	Human		name
152072986	CV1615325	single nucleotide variant	NM_006531.5(IFT88):c.2175+14G>A	not provided [RCV002091846]	likely benign	13	20663618	20663618	Human		name
152074988	CV1616586	single nucleotide variant	NM_006531.5(IFT88):c.1834-20A>G	not provided [RCV002210474]	benign	13	20644823	20644823	Human		name
152111037	CV1626063	single nucleotide variant	NM_006531.5(IFT88):c.1833+13T>C	not provided [RCV002153057]	likely benign	13	20643618	20643618	Human		name
152131440	CV1631127	single nucleotide variant	NM_006531.5(IFT88):c.2353+16C>G	not provided [RCV002119139]	likely benign	13	20690831	20690831	Human		name
152139169	CV1638056	single nucleotide variant	NM_006531.5(IFT88):c.1299+18T>A	not provided [RCV002177825]	likely benign	13	20625867	20625867	Human		name
152091087	CV1662117	single nucleotide variant	NM_006531.5(IFT88):c.2068+18A>C	not provided [RCV002132052]	benign	13	20656448	20656448	Human		name
152174417	CV1662867	single nucleotide variant	NM_006531.5(IFT88):c.1683-20C>T	not provided [RCV002163152]	likely benign	13	20643435	20643435	Human		name
156390207	CV1869783	duplication	NM_006531.5(IFT88):c.1386+12dup	not provided [RCV003067935]	benign	13	20631107	20631108	Human		name
156437346	CV1937487	single nucleotide variant	NM_006531.5(IFT88):c.1299+10A>T	not provided [RCV003106880]	likely benign	13	20625859	20625859	Human		name
156249924	CV1953782	deletion	NM_006531.5(IFT88):c.1300-16del	not provided [RCV002576506]	uncertain significance	13	20631000	20631000	Human		name
156389940	CV1955236	single nucleotide variant	NM_006531.5(IFT88):c.1300-12T>C	not provided [RCV002583776]	likely benign\|uncertain significance	13	20631004	20631004	Human		name
156373878	CV1963164	single nucleotide variant	NM_006531.5(IFT88):c.1112+11A>T	not provided [RCV002582637]	likely benign	13	20605116	20605116	Human		name
156416156	CV1966497	duplication	NM_006531.5(IFT88):c.1833+12dup	not provided [RCV002589556]	likely benign	13	20643616	20643617	Human		name
156355709	CV1975104	single nucleotide variant	NM_006531.5(IFT88):c.1387-19G>A	not provided [RCV002602146]	likely benign	13	20638313	20638313	Human		name
156416209	CV1984072	single nucleotide variant	NM_006531.5(IFT88):c.1386+16A>G	not provided [RCV002610049]	likely benign	13	20631118	20631118	Human		name
156397526	CV1985355	single nucleotide variant	NM_006531.5(IFT88):c.1834-17C>G	not provided [RCV002635650]	likely benign	13	20644826	20644826	Human		name
156386657	CV1986545	single nucleotide variant	NM_006531.5(IFT88):c.2002+13G>A	not provided [RCV002634658]	likely benign	13	20653941	20653941	Human		name
156351725	CV1997791	single nucleotide variant	NM_006531.5(IFT88):c.2243-10G>A	not provided [RCV002675642]	likely benign	13	20690695	20690695	Human		name
156043964	CV1999158	single nucleotide variant	NM_006531.5(IFT88):c.2353+15C>T	not provided [RCV002659143]	likely benign	13	20690830	20690830	Human		name
155967223	CV2034368	single nucleotide variant	NM_006531.5(IFT88):c.2243-11C>T	not provided [RCV002731451]	likely benign	13	20690694	20690694	Human		name
156016557	CV2035274	single nucleotide variant	NM_006531.5(IFT88):c.2175+10A>G	IFT88-related disorder [RCV003903773]\|not provided [RCV002780436]	likely benign	13	20663614	20663614	Human		name , trait , alternate_id
156213633	CV2037089	single nucleotide variant	NM_006531.5(IFT88):c.1299+17A>T	not provided [RCV002790344]	likely benign	13	20625866	20625866	Human		name
156322233	CV2101119	single nucleotide variant	NM_006531.5(IFT88):c.1683-19T>G	not provided [RCV002899379]	likely benign	13	20643436	20643436	Human		name
155925619	CV2145042	single nucleotide variant	NM_006531.5(IFT88):c.1041+10A>G	not provided [RCV003013391]	likely benign	13	20601943	20601943	Human		name
155912211	CV2153360	single nucleotide variant	NM_006531.5(IFT88):c.1200-11T>C	not provided [RCV003012339]	likely benign	13	20625739	20625739	Human		name
405026236	CV2889849	single nucleotide variant	NM_006531.5(IFT88):c.2354-10C>T	not provided [RCV003578001]	likely benign	13	20691044	20691044	Human		name
402506991	CV2944385	deletion	NM_006531.5(IFT88):c.1386+18del	not provided [RCV003662161]	likely benign	13	20631120	20631120	Human		name
405184008	CV2967494	single nucleotide variant	NM_006531.5(IFT88):c.2243-16A>G	not provided [RCV003676567]	likely benign	13	20690689	20690689	Human		name
402483134	CV3036635	single nucleotide variant	NM_006531.5(IFT88):c.2069-16A>G	not provided [RCV003713048]	likely benign	13	20663482	20663482	Human		name
402484466	CV3036682	single nucleotide variant	NM_006531.5(IFT88):c.1299+18T>C	not provided [RCV003713080]	likely benign	13	20625867	20625867	Human		name
405151389	CV3123394	single nucleotide variant	NM_006531.5(IFT88):c.1041+19T>C	not provided [RCV003817627]	likely benign	13	20601952	20601952	Human		name
405061885	CV3129606	single nucleotide variant	NM_006531.5(IFT88):c.1573+20A>G	not provided [RCV003832875]	likely benign	13	20638538	20638538	Human		name
405186111	CV3160147	single nucleotide variant	NM_006531.5(IFT88):c.2176-13C>T	not provided [RCV003859202]	likely benign	13	20670960	20670960	Human		name
597859932	CV3744704	single nucleotide variant	NM_006531.5(IFT88):c.1683-17A>C	not provided [RCV005067249]	uncertain significance	13	20643438	20643438	Human		name
597960740	CV3756260	single nucleotide variant	NM_006531.5(IFT88):c.1113-19T>G	not provided [RCV005081577]	likely benign	13	20615774	20615774	Human		name
597949405	CV3818556	single nucleotide variant	NM_006531.5(IFT88):c.2354-18A>G	not provided [RCV005160817]	likely benign	13	20691036	20691036	Human		name
12896700	CV390156	single nucleotide variant	NM_006531.5(IFT88):c.1300-15A>T	not provided [RCV002056697]\|not specified [RCV000455700]	benign	13	20631001	20631001	Human		name
152142331	CV1587523	single nucleotide variant	NM_006531.5(IFT88):c.87C>T (p.Ile29=)	not provided [RCV002138334]	likely benign	13	20574472	20574472	Human		name
156317049	CV1975055	single nucleotide variant	NM_006531.5(IFT88):c.54C>T (p.Ser18=)	not provided [RCV002630123]	likely benign	13	20574439	20574439	Human		name
155964736	CV2137118	single nucleotide variant	NM_006531.5(IFT88):c.66C>T (p.Asp22=)	not provided [RCV003015642]	likely benign	13	20574451	20574451	Human		name
405214838	CV2876014	single nucleotide variant	NM_006531.5(IFT88):c.1A>G (p.Met1Val)	not provided [RCV003553082]	uncertain significance	13	20574386	20574386	Human		name
405217127	CV2978282	microsatellite	NM_006531.5(IFT88):c.398+26_398+35del	not provided [RCV003709466]	likely benign	13	20592420	20592429	Human		name
597966622	CV3823834	duplication	NM_006531.5(IFT88):c.399-15_399-12dup	not provided [RCV005165254]	likely benign	13	20596134	20596135	Human		name
152139135	CV1563610	single nucleotide variant	NM_006531.5(IFT88):c.246A>C (p.Pro82=)	not provided [RCV002200348]	benign	13	20591002	20591002	Human		name
152120207	CV1576161	single nucleotide variant	NM_006531.5(IFT88):c.270A>G (p.Gly90=)	not provided [RCV002197946]	likely benign	13	20591623	20591623	Human		name
156019009	CV1909342	single nucleotide variant	NM_006531.5(IFT88):c.243A>G (p.Arg81=)	not provided [RCV002619295]	likely benign	13	20590999	20590999	Human		name
156287885	CV1964718	microsatellite	NM_006531.5(IFT88):c.1574-11_1574-9del	not provided [RCV002577711]	likely benign	13	20641274	20641276	Human		name
156338204	CV1997375	single nucleotide variant	NM_006531.5(IFT88):c.177G>A (p.Thr59=)	not provided [RCV002650180]	likely benign	13	20589834	20589834	Human		name
156199677	CV2024493	single nucleotide variant	NM_006531.5(IFT88):c.18C>G (p.His6Gln)	not provided [RCV002711358]	uncertain significance	13	20574403	20574403	Human		name
401745302	CV2693227	single nucleotide variant	NM_006531.5(IFT88):c.25C>T (p.Pro9Ser)	not specified [RCV004295202]	uncertain significance	13	20574410	20574410	Human		name
405238053	CV2881185	single nucleotide variant	NM_006531.5(IFT88):c.135T>C (p.Ser45=)	not provided [RCV003556684]	likely benign	13	20583001	20583001	Human		name
405172484	CV3122840	single nucleotide variant	NM_006531.5(IFT88):c.210G>A (p.Gly70=)	not provided [RCV003819238]	uncertain significance	13	20589867	20589867	Human		name
597911924	CV3834195	single nucleotide variant	NM_006531.5(IFT88):c.213C>T (p.Ser71=)	not provided [RCV005182957]	uncertain significance	13	20590969	20590969	Human		name
152114737	CV1574977	deletion	NM_006531.5(IFT88):c.2003-14_2003-13del	not provided [RCV002117030]	benign	13	20656351	20656352	Human		name
152153287	CV1577833	single nucleotide variant	NM_006531.5(IFT88):c.86T>C (p.Ile29Thr)	IFT88-related disorder [RCV003958681]\|not provided [RCV002122063]	likely benign	13	20574471	20574471	Human		name , trait , alternate_id
152090074	CV1593987	single nucleotide variant	NM_006531.5(IFT88):c.522A>G (p.Lys174=)	IFT88-related disorder [RCV003933647]\|not provided [RCV002171707]	likely benign	13	20597047	20597047	Human		name , trait , alternate_id
152059400	CV1597599	single nucleotide variant	NM_006531.5(IFT88):c.882A>G (p.Ser294=)	not provided [RCV002128162]	likely benign	13	20601774	20601774	Human		name
152033227	CV1610308	deletion	NM_006531.5(IFT88):c.1199+11_1199+12del	not provided [RCV002124894]	benign	13	20615889	20615890	Human		name
152098735	CV1650407	single nucleotide variant	NM_006531.5(IFT88):c.492C>G (p.Ala164=)	not provided [RCV002115048]	likely benign	13	20597017	20597017	Human		name
152058059	CV1656631	single nucleotide variant	NM_006531.5(IFT88):c.720A>G (p.Gly240=)	not provided [RCV002109785]	likely benign	13	20599473	20599473	Human		name
155954459	CV1915271	single nucleotide variant	NM_006531.5(IFT88):c.92A>T (p.Glu31Val)	not provided [RCV002616399]\|not specified [RCV004070545]	uncertain significance	13	20582958	20582958	Human		name
156418680	CV1918619	single nucleotide variant	NM_006531.5(IFT88):c.88G>A (p.Glu30Lys)	not provided [RCV002611882]	uncertain significance	13	20574473	20574473	Human		name
156419111	CV1929427	single nucleotide variant	NM_006531.5(IFT88):c.924C>G (p.Gly308=)	not provided [RCV002612329]	likely benign	13	20601816	20601816	Human		name
156088717	CV1953458	deletion	NM_006531.5(IFT88):c.1574-20_1574-15del	not provided [RCV002570148]	likely benign	13	20641268	20641273	Human		name
156002881	CV1987940	single nucleotide variant	NM_006531.5(IFT88):c.606T>C (p.Asn202=)	not provided [RCV002618534]	likely benign	13	20598662	20598662	Human		name
156364784	CV2003484	deletion	NM_006531.5(IFT88):c.1386+17_1386+21del	not provided [RCV002676483]	likely benign	13	20631119	20631123	Human		name
156122587	CV2020907	single nucleotide variant	NM_006531.5(IFT88):c.348T>C (p.Leu116=)	not provided [RCV002740256]	likely benign	13	20592354	20592354	Human		name
155904421	CV2031333	single nucleotide variant	NM_006531.5(IFT88):c.68A>G (p.Tyr23Cys)	not provided [RCV002726381]	uncertain significance	13	20574453	20574453	Human		name
156202525	CV2076548	single nucleotide variant	NM_006531.5(IFT88):c.435A>G (p.Val145=)	not provided [RCV002852518]	likely benign	13	20596186	20596186	Human		name
155903323	CV2127098	single nucleotide variant	NM_006531.5(IFT88):c.360G>A (p.Arg120=)	not provided [RCV002967554]	likely benign	13	20592366	20592366	Human		name
156304179	CV2129662	single nucleotide variant	NM_006531.5(IFT88):c.91G>A (p.Glu31Lys)	not provided [RCV002962282]	uncertain significance	13	20582957	20582957	Human		name
155945747	CV2130214	single nucleotide variant	NM_006531.5(IFT88):c.420A>G (p.Gln140=)	not provided [RCV002971570]	likely benign	13	20596171	20596171	Human		name
156349661	CV2146952	single nucleotide variant	NM_006531.5(IFT88):c.79T>G (p.Tyr27Asp)	not provided [RCV003030771]	uncertain significance	13	20574464	20574464	Human		name
156229170	CV2164907	deletion	NM_006531.5(IFT88):c.1042-16_1042-15del	not provided [RCV003043017]	likely benign	13	20605019	20605020	Human		name
156356742	CV2188930	single nucleotide variant	NM_006531.5(IFT88):c.80A>C (p.Tyr27Ser)	not provided [RCV003048740]	uncertain significance	13	20574465	20574465	Human		name
401755489	CV2682501	single nucleotide variant	NM_006531.5(IFT88):c.74C>T (p.Pro25Leu)	not specified [RCV004290521]	uncertain significance	13	20574459	20574459	Human		name
402506811	CV2982452	single nucleotide variant	NM_006531.5(IFT88):c.513A>C (p.Ala171=)	not provided [RCV003689135]	likely benign	13	20597038	20597038	Human		name
404989381	CV2998675	single nucleotide variant	NM_006531.5(IFT88):c.444G>A (p.Leu148=)	not provided [RCV003692141]	likely benign	13	20596195	20596195	Human		name
405245118	CV3054939	single nucleotide variant	NM_006531.5(IFT88):c.933A>C (p.Leu311=)	not provided [RCV003720197]	likely benign	13	20601825	20601825	Human		name
405207886	CV3064729	single nucleotide variant	NM_006531.5(IFT88):c.71A>G (p.Asn24Ser)	not provided [RCV003731572]\|not specified [RCV004374174]	uncertain significance	13	20574456	20574456	Human		name
405266110	CV3221046	single nucleotide variant	NM_006531.5(IFT88):c.660T>C (p.Tyr220=)	IFT88-related disorder [RCV003969178]\|not provided [RCV005102983]	likely benign	13	20598716	20598716	Human		name , trait , alternate_id
408367003	CV3511437	single nucleotide variant	NM_006531.5(IFT88):c.744T>C (p.Asn248=)	IFT88-related disorder [RCV004757736]\|not provided [RCV005103768]	likely benign	13	20599497	20599497	Human		name , trait , alternate_id
597832341	CV3740175	single nucleotide variant	NM_006531.5(IFT88):c.648A>C (p.Ala216=)	not provided [RCV005062874]	likely benign	13	20598704	20598704	Human		name
597920709	CV3811847	deletion	NM_006531.5(IFT88):c.1041+15_1041+16del	not provided [RCV005155678]	likely benign	13	20601947	20601948	Human		name
597968904	CV3821299	single nucleotide variant	NM_006531.5(IFT88):c.62A>G (p.Asn21Ser)	not provided [RCV005165941]	uncertain significance	13	20574447	20574447	Human		name
597911520	CV3826145	single nucleotide variant	NM_006531.5(IFT88):c.450A>G (p.Glu150=)	not provided [RCV005182881]	likely benign	13	20596201	20596201	Human		name
597963915	CV3837796	single nucleotide variant	NM_006531.5(IFT88):c.801T>C (p.Asn267=)	not provided [RCV005193779]	likely benign	13	20599554	20599554	Human		name
598268682	CV3979381	single nucleotide variant	NM_006531.5(IFT88):c.59A>G (p.Tyr20Cys)	not specified [RCV005349755]	uncertain significance	13	20574444	20574444	Human		name
15117919	CV713864	single nucleotide variant	NM_006531.5(IFT88):c.315A>G (p.Lys105=)	not provided [RCV000962284]	benign	13	20591668	20591668	Human		name
151821562	CV1354967	single nucleotide variant	NM_006531.5(IFT88):c.1203C>T (p.Cys401=)	IFT88-related disorder [RCV003923378]\|not provided [RCV001934195]	likely benign\|uncertain significance	13	20625753	20625753	Human		name , trait , alternate_id
151738887	CV1379268	single nucleotide variant	NM_006531.5(IFT88):c.2298C>T (p.Leu766=)	not provided [RCV001911730]	likely benign	13	20690760	20690760	Human		name
151717291	CV1380382	single nucleotide variant	NM_006531.5(IFT88):c.215A>C (p.Lys72Thr)	not provided [RCV002003112]	uncertain significance	13	20590971	20590971	Human		name
151827539	CV1396381	single nucleotide variant	NM_006531.5(IFT88):c.259A>G (p.Ile87Val)	not provided [RCV001934729]	uncertain significance	13	20591015	20591015	Human		name
152082174	CV1525116	single nucleotide variant	NM_006531.5(IFT88):c.1197T>C (p.Asp399=)	not provided [RCV002130959]	likely benign	13	20615877	20615877	Human		name
152027566	CV1529487	single nucleotide variant	NM_006531.5(IFT88):c.2073G>A (p.Leu691=)	not provided [RCV002185545]	benign	13	20663502	20663502	Human		name
152032341	CV1548976	single nucleotide variant	NM_006531.5(IFT88):c.1644A>G (p.Leu548=)	not provided [RCV002086558]	likely benign	13	20641360	20641360	Human		name
152081054	CV1554590	single nucleotide variant	NM_006531.5(IFT88):c.1740T>C (p.Ser580=)	not provided [RCV002193024]	likely benign	13	20643512	20643512	Human		name
152090497	CV1580836	single nucleotide variant	NM_006531.5(IFT88):c.1836A>G (p.Ser612=)	not provided [RCV002094104]	benign	13	20644845	20644845	Human		name
152035370	CV1584932	single nucleotide variant	NM_006531.5(IFT88):c.2284C>T (p.Leu762=)	not provided [RCV002125239]	likely benign	13	20690746	20690746	Human		name
152174536	CV1591169	single nucleotide variant	NM_006531.5(IFT88):c.2454A>G (p.Gly818=)	not provided [RCV002184545]	benign	13	20691154	20691154	Human		name
152026890	CV1593596	single nucleotide variant	NM_006531.5(IFT88):c.1107T>C (p.Arg369=)	not provided [RCV002104709]	likely benign	13	20605100	20605100	Human		name
152175199	CV1602023	single nucleotide variant	NM_006531.5(IFT88):c.1509C>A (p.Ala503=)	not provided [RCV002163414]	likely benign	13	20638454	20638454	Human		name
152162431	CV1606314	single nucleotide variant	NM_006531.5(IFT88):c.1279A>C (p.Arg427=)	not provided [RCV002181158]	likely benign	13	20625829	20625829	Human		name
152147077	CV1608103	single nucleotide variant	NM_006531.5(IFT88):c.244C>T (p.Pro82Ser)	not provided [RCV002178884]	benign	13	20591000	20591000	Human		name
152090299	CV1634150	single nucleotide variant	NM_006531.5(IFT88):c.1656C>T (p.Ala552=)	not provided [RCV002194207]	likely benign	13	20641372	20641372	Human		name
152026168	CV1639306	single nucleotide variant	NM_006531.5(IFT88):c.1272A>T (p.Thr424=)	not provided [RCV002185061]	likely benign	13	20625822	20625822	Human		name
152034593	CV1639509	single nucleotide variant	NM_006531.5(IFT88):c.2238C>T (p.Ser746=)	IFT88-related disorder [RCV003968760]\|not provided [RCV002187282]	benign	13	20671035	20671035	Human		name , trait , alternate_id
152038922	CV1647878	single nucleotide variant	NM_006531.5(IFT88):c.1356T>C (p.Ala452=)	not provided [RCV002087662]	likely benign	13	20631072	20631072	Human		name
152083763	CV1647940	single nucleotide variant	NM_006531.5(IFT88):c.1134T>C (p.Tyr378=)	not provided [RCV002076716]	benign	13	20615814	20615814	Human		name
152028337	CV1655186	single nucleotide variant	NM_006531.5(IFT88):c.250A>G (p.Thr84Ala)	IFT88-related disorder [RCV003903362]\|not provided [RCV002105199]	likely benign	13	20591006	20591006	Human		name , trait , alternate_id
152067433	CV1660101	single nucleotide variant	NM_006531.5(IFT88):c.2416A>C (p.Arg806=)	not provided [RCV002147620]	likely benign	13	20691116	20691116	Human		name
156319818	CV1897744	single nucleotide variant	NM_006531.5(IFT88):c.1020A>G (p.Glu340=)	not provided [RCV002579169]	likely benign	13	20601912	20601912	Human		name
156362256	CV1905072	single nucleotide variant	NM_006531.5(IFT88):c.283A>G (p.Met95Val)	not provided [RCV002602582]	uncertain significance	13	20591636	20591636	Human		name
155953699	CV1915205	single nucleotide variant	NM_006531.5(IFT88):c.226G>A (p.Ala76Thr)	not provided [RCV002616362]	likely benign	13	20590982	20590982	Human		name
156405247	CV1919255	single nucleotide variant	NM_006531.5(IFT88):c.259A>C (p.Ile87Leu)	not provided [RCV002585604]	uncertain significance	13	20591015	20591015	Human		name
156203151	CV1925848	single nucleotide variant	NM_006531.5(IFT88):c.1617C>T (p.Asp539=)	not provided [RCV002643710]	likely benign	13	20641333	20641333	Human		name
156444060	CV1937577	single nucleotide variant	NM_006531.5(IFT88):c.1972C>T (p.Leu658=)	not provided [RCV003114978]	likely benign	13	20653898	20653898	Human		name
156408824	CV1954533	single nucleotide variant	NM_006531.5(IFT88):c.266A>T (p.Asp89Val)	not provided [RCV002586627]	uncertain significance	13	20591619	20591619	Human		name
156231780	CV1956039	single nucleotide variant	NM_006531.5(IFT88):c.1767A>G (p.Leu589=)	not provided [RCV002575900]	likely benign	13	20643539	20643539	Human		name
156071021	CV1959228	single nucleotide variant	NM_006531.5(IFT88):c.1473G>A (p.Gly491=)	not provided [RCV002569604]	likely benign	13	20638418	20638418	Human		name
156354265	CV1962256	single nucleotide variant	NM_006531.5(IFT88):c.206A>T (p.Tyr69Phe)	not provided [RCV002581279]	uncertain significance	13	20589863	20589863	Human		name
156419887	CV1967625	single nucleotide variant	NM_006531.5(IFT88):c.1581C>T (p.Thr527=)	not provided [RCV002613134]	likely benign	13	20641297	20641297	Human		name
156384470	CV1971800	single nucleotide variant	NM_006531.5(IFT88):c.1329A>G (p.Lys443=)	not provided [RCV002604201]	likely benign	13	20631045	20631045	Human		name
155966783	CV1974287	single nucleotide variant	NM_006531.5(IFT88):c.176C>T (p.Thr59Met)	not provided [RCV002616993]	uncertain significance	13	20589833	20589833	Human		name
156082142	CV1982886	single nucleotide variant	NM_006531.5(IFT88):c.1593A>G (p.Leu531=)	IFT88-related disorder [RCV003961098]\|not provided [RCV002638934]	likely benign	13	20641309	20641309	Human		name , trait , alternate_id
156145590	CV2002967	single nucleotide variant	NM_006531.5(IFT88):c.218C>T (p.Thr73Ile)	not provided [RCV002663728]	uncertain significance	13	20590974	20590974	Human		name
155912549	CV2021763	single nucleotide variant	NM_006531.5(IFT88):c.110C>G (p.Ala37Gly)	not provided [RCV002726911]\|not specified [RCV004067750]	uncertain significance	13	20582976	20582976	Human		name
156016405	CV2035237	single nucleotide variant	NM_006531.5(IFT88):c.2262T>C (p.Ser754=)	not provided [RCV002780428]	likely benign	13	20690724	20690724	Human		name
156002333	CV2045640	single nucleotide variant	NM_006531.5(IFT88):c.1119C>T (p.Ala373=)	not provided [RCV002756268]	uncertain significance	13	20615799	20615799	Human		name
155986965	CV2056169	single nucleotide variant	NM_006531.5(IFT88):c.124G>A (p.Val42Met)	not provided [RCV002819024]\|not specified [RCV004927857]	uncertain significance	13	20582990	20582990	Human		name
156203767	CV2076603	duplication	NM_006531.5(IFT88):c.309dup (p.Thr104fs)	not provided [RCV002852560]	uncertain significance	13	20591658	20591659	Human		name
156207128	CV2103801	single nucleotide variant	NM_006531.5(IFT88):c.2064C>T (p.Val688=)	IFT88-related disorder [RCV003926516]\|not provided [RCV002931909]	benign\|likely benign	13	20656426	20656426	Human		name , trait , alternate_id
156214764	CV2106988	single nucleotide variant	NM_006531.5(IFT88):c.1590A>G (p.Lys530=)	not provided [RCV002918314]	likely benign	13	20641306	20641306	Human		name
155940999	CV2119845	single nucleotide variant	NM_006531.5(IFT88):c.1509C>T (p.Ala503=)	not provided [RCV002971284]	likely benign	13	20638454	20638454	Human		name
155995092	CV2122521	single nucleotide variant	NM_006531.5(IFT88):c.2286A>G (p.Leu762=)	not provided [RCV002974911]	likely benign	13	20690748	20690748	Human		name
156026176	CV2131304	single nucleotide variant	NM_006531.5(IFT88):c.2358C>T (p.Ala786=)	not provided [RCV002976397]	likely benign	13	20691058	20691058	Human		name
156085532	CV2144899	single nucleotide variant	NM_006531.5(IFT88):c.1320G>T (p.Val440=)	not provided [RCV003020495]	likely benign	13	20631036	20631036	Human		name
156017279	CV2155210	single nucleotide variant	NM_006531.5(IFT88):c.266A>G (p.Asp89Gly)	not provided [RCV003018056]	uncertain significance	13	20591619	20591619	Human		name
156128733	CV2158624	single nucleotide variant	NM_006531.5(IFT88):c.257C>G (p.Ala86Gly)	not provided [RCV003022092]	uncertain significance	13	20591013	20591013	Human		name
156298836	CV2159477	single nucleotide variant	NM_006531.5(IFT88):c.194T>C (p.Ile65Thr)	not provided [RCV003045454]	uncertain significance	13	20589851	20589851	Human		name
155917194	CV2202254	single nucleotide variant	NM_006531.5(IFT88):c.235A>G (p.Ile79Val)	not provided [RCV005059204]\|not specified [RCV004078194]	uncertain significance	13	20590991	20590991	Human		name
155944879	CV2291870	single nucleotide variant	NM_006531.5(IFT88):c.227C>T (p.Ala76Val)	not specified [RCV004158393]	uncertain significance	13	20590983	20590983	Human		name
401782946	CV2716056	single nucleotide variant	NM_006531.5(IFT88):c.134G>T (p.Ser45Ile)	not specified [RCV004323305]	uncertain significance	13	20583000	20583000	Human		name
405074739	CV2872958	single nucleotide variant	NM_006531.5(IFT88):c.1176A>G (p.Thr392=)	not provided [RCV003548638]	likely benign	13	20615856	20615856	Human		name
405127178	CV2883030	single nucleotide variant	NM_006531.5(IFT88):c.2439T>C (p.Ala813=)	not provided [RCV003559684]	likely benign	13	20691139	20691139	Human		name
405231227	CV2964591	single nucleotide variant	NM_006531.5(IFT88):c.2418G>A (p.Arg806=)	not provided [RCV003682291]	likely benign	13	20691118	20691118	Human		name
405220616	CV2969766	single nucleotide variant	NM_006531.5(IFT88):c.197C>G (p.Ala66Gly)	not provided [RCV003680623]	uncertain significance	13	20589854	20589854	Human		name
405227793	CV2980541	single nucleotide variant	NM_006531.5(IFT88):c.1887T>C (p.Tyr629=)	not provided [RCV003711004]	likely benign	13	20644896	20644896	Human		name
405224116	CV2982995	deletion	NM_006531.5(IFT88):c.569del (p.Asn190fs)	not provided [RCV003681137]	uncertain significance	13	20597091	20597091	Human		name
405227199	CV3039593	single nucleotide variant	NM_006531.5(IFT88):c.1188A>G (p.Ala396=)	not provided [RCV003710909]	uncertain significance	13	20615868	20615868	Human		name
405142407	CV3055973	single nucleotide variant	NM_006531.5(IFT88):c.1383T>C (p.Tyr461=)	not provided [RCV003725766]	likely benign	13	20631099	20631099	Human		name
405212820	CV3078102	single nucleotide variant	NM_006531.5(IFT88):c.1752C>T (p.Thr584=)	not provided [RCV003732246]	likely benign	13	20643524	20643524	Human		name
405192184	CV3145999	single nucleotide variant	NM_006531.5(IFT88):c.1635C>T (p.His545=)	not provided [RCV003843546]	likely benign	13	20641351	20641351	Human		name
405057003	CV3151504	single nucleotide variant	NM_006531.5(IFT88):c.247A>G (p.Met83Val)	not provided [RCV003849914]	uncertain significance	13	20591003	20591003	Human		name
405221226	CV3154733	single nucleotide variant	NM_006531.5(IFT88):c.1668C>T (p.Tyr556=)	not provided [RCV003847228]	likely benign	13	20641384	20641384	Human		name
405248586	CV3169666	single nucleotide variant	NM_006531.5(IFT88):c.135T>G (p.Ser45Arg)	not provided [RCV003869479]	uncertain significance	13	20583001	20583001	Human		name
405277811	CV3196175	single nucleotide variant	NM_006531.5(IFT88):c.1902A>G (p.Gln634=)	IFT88-related disorder [RCV003904689]	likely benign	13	20644911	20644911	Human		name , trait , alternate_id
597922743	CV3738538	single nucleotide variant	NM_006531.5(IFT88):c.1053T>C (p.His351=)	not provided [RCV005074946]	likely benign	13	20605046	20605046	Human		name
597959358	CV3752284	single nucleotide variant	NM_006531.5(IFT88):c.245C>G (p.Pro82Arg)	not provided [RCV005081234]	uncertain significance	13	20591001	20591001	Human		name
597920548	CV3765138	single nucleotide variant	NM_006531.5(IFT88):c.2064C>A (p.Val688=)	not provided [RCV005115155]	likely benign	13	20656426	20656426	Human		name
597921482	CV3777363	single nucleotide variant	NM_006531.5(IFT88):c.1326A>G (p.Glu442=)	not provided [RCV005130292]	likely benign	13	20631042	20631042	Human		name
597933714	CV3793446	single nucleotide variant	NM_006531.5(IFT88):c.129G>T (p.Arg43Ser)	not provided [RCV005132102]	uncertain significance	13	20582995	20582995	Human		name
597961168	CV3794840	single nucleotide variant	NM_006531.5(IFT88):c.2293A>C (p.Arg765=)	not provided [RCV005138745]	likely benign	13	20690755	20690755	Human		name
597875273	CV3813097	single nucleotide variant	NM_006531.5(IFT88):c.1341A>G (p.Arg447=)	not provided [RCV005149033]	likely benign	13	20631057	20631057	Human		name
597878375	CV3813677	single nucleotide variant	NM_006531.5(IFT88):c.2397A>C (p.Pro799=)	not provided [RCV005149419]	likely benign	13	20691097	20691097	Human		name
597947664	CV3817929	deletion	NM_006531.5(IFT88):c.420del (p.Gln140fs)	not provided [RCV005160396]	uncertain significance	13	20596170	20596170	Human		name
597908690	CV3829948	single nucleotide variant	NM_006531.5(IFT88):c.1488A>G (p.Ala496=)	not provided [RCV005182517]	likely benign	13	20638433	20638433	Human		name
127237952	CV1054104	duplication	NM_006531.5(IFT88):c.1082dup (p.Asn361fs)	Rod-cone dystrophy [RCV001376433]\|not provided [RCV001871991]	likely pathogenic\|uncertain significance	13	20605069	20605070	Human	3	name
151841792	CV1379534	single nucleotide variant	NM_006531.5(IFT88):c.356C>T (p.Ser119Leu)	not provided [RCV001936211]	uncertain significance	13	20592362	20592362	Human		name
151889486	CV1398835	single nucleotide variant	NM_006531.5(IFT88):c.962G>A (p.Arg321Gln)	not provided [RCV001942814]	uncertain significance	13	20601854	20601854	Human		name
151743451	CV1431751	single nucleotide variant	NM_006531.5(IFT88):c.715A>G (p.Met239Val)	not provided [RCV001926698]	uncertain significance	13	20599468	20599468	Human		name
151821292	CV1453563	single nucleotide variant	NM_006531.5(IFT88):c.373C>T (p.Pro125Ser)	not provided [RCV001879238]	uncertain significance	13	20592379	20592379	Human		name
151769320	CV1458017	single nucleotide variant	NM_006531.5(IFT88):c.552A>C (p.Gln184His)	not provided [RCV001950002]\|not specified [RCV004927761]	uncertain significance	13	20597077	20597077	Human		name
151790371	CV1475283	single nucleotide variant	NM_006531.5(IFT88):c.652A>T (p.Asn218Tyr)	not provided [RCV001972994]	uncertain significance	13	20598708	20598708	Human		name
151871976	CV1487795	single nucleotide variant	NM_006531.5(IFT88):c.888G>C (p.Glu296Asp)	not provided [RCV001981418]	uncertain significance	13	20601780	20601780	Human		name
151769916	CV1504106	deletion	NM_006531.5(IFT88):c.1250del (p.Leu417fs)	not provided [RCV002045146]	uncertain significance	13	20625800	20625800	Human		name
151728902	CV1515217	single nucleotide variant	NM_006531.5(IFT88):c.354G>T (p.Gln118His)	not provided [RCV002040992]	uncertain significance	13	20592360	20592360	Human		name
152095001	CV1521025	single nucleotide variant	NM_006531.5(IFT88):c.770G>A (p.Arg257Gln)	IFT88-related disorder [RCV003950992]\|not provided [RCV002078223]	likely benign	13	20599523	20599523	Human		name , trait , alternate_id
152111542	CV1551498	single nucleotide variant	NM_006531.5(IFT88):c.342C>A (p.Asp114Glu)	not provided [RCV002196840]	likely benign	13	20592348	20592348	Human		name
152067722	CV1600306	single nucleotide variant	NM_006531.5(IFT88):c.346C>T (p.Leu116Phe)	IFT88-related disorder [RCV003911338]\|not provided [RCV002111019]	benign	13	20592352	20592352	Human		name , trait , alternate_id
156185592	CV1885740	single nucleotide variant	NM_006531.5(IFT88):c.360G>C (p.Arg120Ser)	not provided [RCV003083702]	uncertain significance	13	20592366	20592366	Human		name
156285017	CV1897057	single nucleotide variant	NM_006531.5(IFT88):c.643G>A (p.Glu215Lys)	not provided [RCV003087253]	uncertain significance	13	20598699	20598699	Human		name
156033908	CV1921263	single nucleotide variant	NM_006531.5(IFT88):c.878A>G (p.Asn293Ser)	not provided [RCV002619971]\|not specified [RCV004069081]	uncertain significance	13	20601770	20601770	Human		name
156293170	CV1926141	single nucleotide variant	NM_006531.5(IFT88):c.553G>A (p.Val185Ile)	not provided [RCV002647283]	uncertain significance	13	20597078	20597078	Human		name
156438870	CV1947790	single nucleotide variant	NM_006531.5(IFT88):c.784C>T (p.Gln262Ter)	not provided [RCV003108818]	uncertain significance	13	20599537	20599537	Human		name
156301009	CV1955567	single nucleotide variant	NM_006531.5(IFT88):c.428A>G (p.Lys143Arg)	not provided [RCV002578227]	uncertain significance	13	20596179	20596179	Human		name
156323462	CV1976359	single nucleotide variant	NM_006531.5(IFT88):c.625G>A (p.Val209Ile)	not provided [RCV002600381]	uncertain significance	13	20598681	20598681	Human		name
156308372	CV1976734	single nucleotide variant	NM_006531.5(IFT88):c.683T>C (p.Met228Thr)	not provided [RCV002578557]	uncertain significance	13	20598739	20598739	Human		name
156097310	CV1981037	single nucleotide variant	NM_006531.5(IFT88):c.353A>G (p.Gln118Arg)	not provided [RCV002622082]	uncertain significance	13	20592359	20592359	Human		name
156392993	CV1987835	single nucleotide variant	NM_006531.5(IFT88):c.718G>C (p.Gly240Arg)	not provided [RCV002635168]	uncertain significance	13	20599471	20599471	Human		name
156176063	CV2000415	single nucleotide variant	NM_006531.5(IFT88):c.598C>T (p.Leu200Phe)	not provided [RCV002642875]\|not specified [RCV004632041]	uncertain significance	13	20598654	20598654	Human		name
156284648	CV2001623	single nucleotide variant	NM_006531.5(IFT88):c.661C>G (p.Gln221Glu)	not provided [RCV002646963]	uncertain significance	13	20598717	20598717	Human		name
156161000	CV2009505	single nucleotide variant	NM_006531.5(IFT88):c.544C>T (p.Arg182Ter)	not provided [RCV002710170]	uncertain significance	13	20597069	20597069	Human		name
156084140	CV2023732	single nucleotide variant	NM_006531.5(IFT88):c.746A>T (p.Tyr249Phe)	not provided [RCV002760723]	uncertain significance	13	20599499	20599499	Human		name
156045039	CV2026556	single nucleotide variant	NM_006531.5(IFT88):c.740G>T (p.Arg247Ile)	not provided [RCV002736321]	uncertain significance	13	20599493	20599493	Human		name
156037616	CV2030095	single nucleotide variant	NM_006531.5(IFT88):c.901A>T (p.Met301Leu)	not provided [RCV002736058]	uncertain significance	13	20601793	20601793	Human		name
156330068	CV2061274	single nucleotide variant	NM_006531.5(IFT88):c.841A>G (p.Thr281Ala)	not provided [RCV002810627]	uncertain significance	13	20601733	20601733	Human		name
155971625	CV2062509	single nucleotide variant	NM_006531.5(IFT88):c.757A>G (p.Ile253Val)	not provided [RCV002842106]	uncertain significance	13	20599510	20599510	Human		name
155951398	CV2076405	single nucleotide variant	NM_006531.5(IFT88):c.928A>C (p.Asn310His)	not provided [RCV002862366]	uncertain significance	13	20601820	20601820	Human		name
156049418	CV2093445	single nucleotide variant	NM_006531.5(IFT88):c.659A>G (p.Tyr220Cys)	not provided [RCV002867736]	uncertain significance	13	20598715	20598715	Human		name
156035574	CV2123231	single nucleotide variant	NM_006531.5(IFT88):c.937A>G (p.Ile313Val)	not provided [RCV002949414]\|not specified [RCV004068291]	uncertain significance	13	20601829	20601829	Human		name
156300919	CV2129492	single nucleotide variant	NM_006531.5(IFT88):c.901A>G (p.Met301Val)	not provided [RCV002962140]	uncertain significance	13	20601793	20601793	Human		name
155964485	CV2134701	single nucleotide variant	NM_006531.5(IFT88):c.904G>T (p.Ala302Ser)	not provided [RCV002972542]	uncertain significance	13	20601796	20601796	Human		name
155945633	CV2139421	single nucleotide variant	NM_006531.5(IFT88):c.874A>G (p.Ile292Val)	not provided [RCV002994325]	uncertain significance	13	20601766	20601766	Human		name
156224746	CV2144417	single nucleotide variant	NM_006531.5(IFT88):c.889C>A (p.His297Asn)	not provided [RCV003007518]	uncertain significance	13	20601781	20601781	Human		name
156083590	CV2144651	single nucleotide variant	NM_006531.5(IFT88):c.814A>G (p.Ile272Val)	not provided [RCV003020433]	uncertain significance	13	20601706	20601706	Human		name
155921862	CV2148483	single nucleotide variant	NM_006531.5(IFT88):c.460A>G (p.Ile154Val)	not provided [RCV003013226]	uncertain significance	13	20596211	20596211	Human		name
156188443	CV2148535	single nucleotide variant	NM_006531.5(IFT88):c.818A>C (p.Lys273Thr)	not provided [RCV003005926]	uncertain significance	13	20601710	20601710	Human		name
156018799	CV2151618	single nucleotide variant	NM_006531.5(IFT88):c.881C>T (p.Ser294Leu)	not provided [RCV003018127]	uncertain significance	13	20601773	20601773	Human		name
155989726	CV2170417	single nucleotide variant	NM_006531.5(IFT88):c.683T>G (p.Met228Arg)	not provided [RCV003034272]	uncertain significance	13	20598739	20598739	Human		name
156360303	CV2184120	single nucleotide variant	NM_006531.5(IFT88):c.815T>G (p.Ile272Ser)	not provided [RCV003048978]	uncertain significance	13	20601707	20601707	Human		name
156368083	CV2190448	single nucleotide variant	NM_006531.5(IFT88):c.899G>C (p.Ser300Thr)	not provided [RCV003066088]	uncertain significance	13	20601791	20601791	Human		name
156133227	CV2216731	single nucleotide variant	NM_006531.5(IFT88):c.979G>A (p.Ala327Thr)	not specified [RCV004083179]	uncertain significance	13	20601871	20601871	Human		name
401757913	CV2708027	single nucleotide variant	NM_006531.5(IFT88):c.638A>T (p.Tyr213Phe)	not specified [RCV004309275]	uncertain significance	13	20598694	20598694	Human		name
401867235	CV2777080	single nucleotide variant	NM_006531.5(IFT88):c.641C>T (p.Ala214Val)	not specified [RCV004351866]	uncertain significance	13	20598697	20598697	Human		name
402464575	CV2916340	single nucleotide variant	NM_006531.5(IFT88):c.886G>A (p.Glu296Lys)	not provided [RCV003569043]	uncertain significance	13	20601778	20601778	Human		name
405084232	CV2946459	single nucleotide variant	NM_006531.5(IFT88):c.684G>A (p.Met228Ile)	not provided [RCV003664837]	uncertain significance	13	20598740	20598740	Human		name
402499759	CV2946785	single nucleotide variant	NM_006531.5(IFT88):c.865T>G (p.Ser289Ala)	not provided [RCV003661386]	uncertain significance	13	20601757	20601757	Human		name
402479401	CV2990885	single nucleotide variant	NM_006531.5(IFT88):c.934A>T (p.Thr312Ser)	not provided [RCV003686438]	uncertain significance	13	20601826	20601826	Human		name
402496888	CV3005947	single nucleotide variant	NM_006531.5(IFT88):c.305G>A (p.Gly102Asp)	not provided [RCV003688098]	uncertain significance	13	20591658	20591658	Human		name
405046897	CV3017836	single nucleotide variant	NM_006531.5(IFT88):c.953T>C (p.Ile318Thr)	not provided [RCV003696658]	uncertain significance	13	20601845	20601845	Human		name
405058835	CV3019842	single nucleotide variant	NM_006531.5(IFT88):c.479A>C (p.Asp160Ala)	not provided [RCV003697536]	uncertain significance	13	20596230	20596230	Human		name
405180111	CV3119823	single nucleotide variant	NM_006531.5(IFT88):c.991T>A (p.Leu331Met)	not provided [RCV003819916]	uncertain significance	13	20601883	20601883	Human		name
405217969	CV3139527	duplication	NM_006531.5(IFT88):c.1423dup (p.Ile475fs)	not provided [RCV003824218]	uncertain significance	13	20638367	20638368	Human		name
405243453	CV3164832	single nucleotide variant	NM_006531.5(IFT88):c.896T>C (p.Met299Thr)	not provided [RCV003867913]	uncertain significance	13	20601788	20601788	Human		name
405793025	CV3263907	single nucleotide variant	NM_006531.5(IFT88):c.551A>G (p.Gln184Arg)	not specified [RCV004400377]	uncertain significance	13	20597076	20597076	Human		name
597764109	CV3680018	single nucleotide variant	NM_006531.5(IFT88):c.668T>C (p.Ile223Thr)	not specified [RCV004926510]	uncertain significance	13	20598724	20598724	Human		name
597764118	CV3680020	single nucleotide variant	NM_006531.5(IFT88):c.851A>G (p.Gln284Arg)	not specified [RCV004926512]	uncertain significance	13	20601743	20601743	Human		name
597887166	CV3741902	single nucleotide variant	NM_006531.5(IFT88):c.995T>C (p.Ile332Thr)	not provided [RCV005070622]	uncertain significance	13	20601887	20601887	Human		name
597928371	CV3749128	single nucleotide variant	NM_006531.5(IFT88):c.952A>G (p.Ile318Val)	not provided [RCV005075584]	uncertain significance	13	20601844	20601844	Human		name
597858042	CV3769578	single nucleotide variant	NM_006531.5(IFT88):c.388A>G (p.Lys130Glu)	not provided [RCV005105620]	uncertain significance	13	20592394	20592394	Human		name
597953738	CV3844253	single nucleotide variant	NM_006531.5(IFT88):c.572T>C (p.Ile191Thr)	not provided [RCV005190925]	uncertain significance	13	20597097	20597097	Human		name
597861182	CV3850746	duplication	NM_006531.5(IFT88):c.1462dup (p.Thr488fs)	not provided [RCV005195879]	uncertain significance	13	20638406	20638407	Human		name
597903961	CV3856280	single nucleotide variant	NM_006531.5(IFT88):c.767A>G (p.Tyr256Cys)	not provided [RCV005202508]	uncertain significance	13	20599520	20599520	Human		name
15161203	CV725416	single nucleotide variant	NM_006531.5(IFT88):c.613A>G (p.Ser205Gly)	not provided [RCV000881529]	benign	13	20598669	20598669	Human		name
127237956	CV1054105	single nucleotide variant	NM_006531.5(IFT88):c.1373C>T (p.Ala458Val)	Rod-cone dystrophy [RCV001376434]\|not provided [RCV005057346]	uncertain significance	13	20631089	20631089	Human	3	name
151782379	CV1341998	single nucleotide variant	NM_006531.5(IFT88):c.2423A>C (p.Asp808Ala)	not provided [RCV001897363]	uncertain significance	13	20691123	20691123	Human		name
151857424	CV1348083	single nucleotide variant	NM_006531.5(IFT88):c.1197T>A (p.Asp399Glu)	not provided [RCV001979698]\|not specified [RCV004631874]	uncertain significance	13	20615877	20615877	Human		name
151865017	CV1357558	single nucleotide variant	NM_006531.5(IFT88):c.1641C>G (p.Ile547Met)	not provided [RCV001905778]	uncertain significance	13	20641357	20641357	Human		name
151878894	CV1370181	single nucleotide variant	NM_006531.5(IFT88):c.1424T>C (p.Ile475Thr)	not provided [RCV001961387]\|not specified [RCV004044670]	uncertain significance	13	20638369	20638369	Human		name
151812882	CV1373079	single nucleotide variant	NM_006531.5(IFT88):c.2308C>T (p.Pro770Ser)	not provided [RCV001900124]	uncertain significance	13	20690770	20690770	Human		name
151870655	CV1395641	single nucleotide variant	NM_006531.5(IFT88):c.1829A>G (p.Tyr610Cys)	not provided [RCV002035621]\|not specified [RCV005350844]	uncertain significance	13	20643601	20643601	Human		name
151893361	CV1404746	single nucleotide variant	NM_006531.5(IFT88):c.2422G>A (p.Asp808Asn)	not provided [RCV001944960]\|not specified [RCV004040376]	uncertain significance	13	20691122	20691122	Human		name
151795693	CV1411070	single nucleotide variant	NM_006531.5(IFT88):c.1631T>C (p.Leu544Pro)	not provided [RCV001973456]	uncertain significance	13	20641347	20641347	Human		name
151878076	CV1415987	single nucleotide variant	NM_006531.5(IFT88):c.1223C>G (p.Ser408Cys)	not provided [RCV001926079]	uncertain significance	13	20625773	20625773	Human		name
151775818	CV1424308	single nucleotide variant	NM_006531.5(IFT88):c.1694T>A (p.Met565Lys)	not provided [RCV002025795]	uncertain significance	13	20643466	20643466	Human		name
151740661	CV1425322	single nucleotide variant	NM_006531.5(IFT88):c.1106G>A (p.Arg369His)	not provided [RCV001926437]\|not specified [RCV004044186]	uncertain significance	13	20605099	20605099	Human		name
151746817	CV1428373	single nucleotide variant	NM_006531.5(IFT88):c.1636G>A (p.Ala546Thr)	not provided [RCV001927067]	uncertain significance	13	20641352	20641352	Human		name
151816104	CV1440935	single nucleotide variant	NM_006531.5(IFT88):c.2395C>A (p.Pro799Thr)	not provided [RCV001933688]	uncertain significance	13	20691095	20691095	Human		name
151816818	CV1441062	single nucleotide variant	NM_006531.5(IFT88):c.1918A>G (p.Ile640Val)	not provided [RCV001933754]	uncertain significance	13	20644927	20644927	Human		name
151728634	CV1444459	single nucleotide variant	NM_006531.5(IFT88):c.1090C>G (p.Leu364Val)	not provided [RCV001945813]	uncertain significance	13	20605083	20605083	Human		name
151837421	CV1445169	single nucleotide variant	NM_006531.5(IFT88):c.1619G>A (p.Cys540Tyr)	not provided [RCV001994341]	uncertain significance	13	20641335	20641335	Human		name
151759868	CV1448291	single nucleotide variant	NM_006531.5(IFT88):c.1708C>A (p.Gln570Lys)	not provided [RCV001949011]	uncertain significance	13	20643480	20643480	Human		name
151866062	CV1456265	single nucleotide variant	NM_006531.5(IFT88):c.2363A>G (p.Tyr788Cys)	not provided [RCV002035069]	uncertain significance	13	20691063	20691063	Human		name
151851836	CV1458880	single nucleotide variant	NM_006531.5(IFT88):c.1658A>C (p.Glu553Ala)	not provided [RCV002016690]\|not specified [RCV004046710]	uncertain significance	13	20641374	20641374	Human		name
151850832	CV1460378	single nucleotide variant	NM_006531.5(IFT88):c.1292A>G (p.Tyr431Cys)	not provided [RCV001904073]	uncertain significance	13	20625842	20625842	Human		name
151849914	CV1464816	single nucleotide variant	NM_006531.5(IFT88):c.1502A>T (p.Glu501Val)	not provided [RCV001995826]	uncertain significance	13	20638447	20638447	Human		name
151835998	CV1472837	single nucleotide variant	NM_006531.5(IFT88):c.1722G>T (p.Trp574Cys)	not provided [RCV002051211]	uncertain significance	13	20643494	20643494	Human		name
151882034	CV1484438	single nucleotide variant	NM_006531.5(IFT88):c.1522A>G (p.Lys508Glu)	not provided [RCV001941202]\|not specified [RCV004042050]	uncertain significance	13	20638467	20638467	Human		name
151710063	CV1487180	single nucleotide variant	NM_006531.5(IFT88):c.2083G>T (p.Val695Phe)	not provided [RCV001889183]	uncertain significance	13	20663512	20663512	Human		name
151864882	CV1509606	single nucleotide variant	NM_006531.5(IFT88):c.2043C>G (p.His681Gln)	not provided [RCV001924477]	uncertain significance	13	20656405	20656405	Human		name
151786573	CV1513623	single nucleotide variant	NM_006531.5(IFT88):c.1882G>T (p.Ala628Ser)	not provided [RCV001916384]\|not specified [RCV004042873]	uncertain significance	13	20644891	20644891	Human		name
151870437	CV1515614	single nucleotide variant	NM_006531.5(IFT88):c.1598G>A (p.Arg533Gln)	not provided [RCV001981226]	uncertain significance	13	20641314	20641314	Human		name
152046883	CV1580096	single nucleotide variant	NM_006531.5(IFT88):c.1213G>T (p.Val405Leu)	not provided [RCV002166377]	benign	13	20625763	20625763	Human		name
152170015	CV1592221	single nucleotide variant	NM_006531.5(IFT88):c.1793G>A (p.Arg598His)	not provided [RCV002161630]	benign	13	20643565	20643565	Human		name
152091224	CV1595830	single nucleotide variant	NM_006531.5(IFT88):c.1040G>A (p.Ser347Asn)	not provided [RCV002077739]	benign	13	20601932	20601932	Human		name
152173412	CV1662593	single nucleotide variant	NM_006531.5(IFT88):c.1121T>A (p.Met374Lys)	not provided [RCV002144093]	benign	13	20615801	20615801	Human		name
155958888	CV1873585	single nucleotide variant	NM_006531.5(IFT88):c.2393G>A (p.Arg798Gln)	not provided [RCV003074581]	uncertain significance	13	20691093	20691093	Human		name
156403593	CV1885842	single nucleotide variant	NM_006531.5(IFT88):c.1037C>T (p.Pro346Leu)	See cases [RCV003238156]\|not provided [RCV003069507]	uncertain significance	13	20601929	20601929	Human		name
156042203	CV1887193	single nucleotide variant	NM_006531.5(IFT88):c.1528G>C (p.Ala510Pro)	not provided [RCV003078559]	uncertain significance	13	20638473	20638473	Human		name
156146365	CV1895145	single nucleotide variant	NM_006531.5(IFT88):c.1745T>C (p.Ile582Thr)	not provided [RCV003082394]	uncertain significance	13	20643517	20643517	Human		name
156093787	CV1895769	single nucleotide variant	NM_006531.5(IFT88):c.2470G>C (p.Glu824Gln)	not provided [RCV003080325]\|not specified [RCV005351106]	uncertain significance	13	20691170	20691170	Human		name
156358273	CV1897745	single nucleotide variant	NM_006531.5(IFT88):c.1159G>A (p.Ala387Thr)	not provided [RCV002602318]	uncertain significance	13	20615839	20615839	Human		name
156367742	CV1902907	single nucleotide variant	NM_006531.5(IFT88):c.2075G>A (p.Arg692His)	not provided [RCV003092180]	uncertain significance	13	20663504	20663504	Human		name
156365499	CV1906179	single nucleotide variant	NM_006531.5(IFT88):c.2405C>T (p.Ala802Val)	not provided [RCV003092024]	uncertain significance	13	20691105	20691105	Human		name
156100009	CV1907025	single nucleotide variant	NM_006531.5(IFT88):c.2258A>G (p.Tyr753Cys)	not provided [RCV003080565]	uncertain significance	13	20690720	20690720	Human		name
156020714	CV1911371	single nucleotide variant	NM_006531.5(IFT88):c.1175C>T (p.Thr392Ile)	not provided [RCV002636695]	uncertain significance	13	20615855	20615855	Human		name
156275617	CV1911843	single nucleotide variant	NM_006531.5(IFT88):c.2087G>A (p.Arg696His)	not provided [RCV002628254]	uncertain significance	13	20663516	20663516	Human		name
155951811	CV1942048	single nucleotide variant	NM_006531.5(IFT88):c.1498T>C (p.Tyr500His)	not provided [RCV003111707]\|not specified [RCV004160915]	uncertain significance	13	20638443	20638443	Human		name
156117861	CV1952483	single nucleotide variant	NM_006531.5(IFT88):c.1420G>T (p.Asp474Tyr)	not provided [RCV002571744]	uncertain significance	13	20638365	20638365	Human		name
156343615	CV1958030	single nucleotide variant	NM_006531.5(IFT88):c.2452G>A (p.Gly818Arg)	not provided [RCV002580643]	uncertain significance	13	20691152	20691152	Human		name
156253885	CV1967328	single nucleotide variant	NM_006531.5(IFT88):c.2345A>G (p.Lys782Arg)	not provided [RCV002597560]	uncertain significance	13	20690807	20690807	Human		name
156413139	CV1968961	single nucleotide variant	NM_006531.5(IFT88):c.1016A>T (p.Asp339Val)	not provided [RCV002608753]	uncertain significance	13	20601908	20601908	Human		name
156344421	CV1970432	single nucleotide variant	NM_006531.5(IFT88):c.1708C>G (p.Gln570Glu)	not provided [RCV002601453]	uncertain significance	13	20643480	20643480	Human		name
156378696	CV1971581	single nucleotide variant	NM_006531.5(IFT88):c.1892T>C (p.Ile631Thr)	not provided [RCV002603803]	uncertain significance	13	20644901	20644901	Human		name
155972634	CV1974714	single nucleotide variant	NM_006531.5(IFT88):c.1075A>G (p.Ile359Val)	not provided [RCV002617251]	uncertain significance	13	20605068	20605068	Human		name
156351360	CV1978430	single nucleotide variant	NM_006531.5(IFT88):c.2212C>T (p.Arg738Cys)	not provided [RCV002601850]	uncertain significance	13	20671009	20671009	Human		name
156220465	CV1981268	single nucleotide variant	NM_006531.5(IFT88):c.2279A>C (p.Glu760Ala)	not provided [RCV002626427]	uncertain significance	13	20690741	20690741	Human		name
156341358	CV1984922	single nucleotide variant	NM_006531.5(IFT88):c.2402C>T (p.Thr801Ile)	not provided [RCV002631447]	uncertain significance	13	20691102	20691102	Human		name
156415733	CV1987467	single nucleotide variant	NM_006531.5(IFT88):c.1583A>G (p.Tyr528Cys)	not provided [RCV002609807]	uncertain significance	13	20641299	20641299	Human		name
155992198	CV1990556	single nucleotide variant	NM_006531.5(IFT88):c.1384A>G (p.Met462Val)	not provided [RCV002618069]\|not specified [RCV004065840]	uncertain significance	13	20631100	20631100	Human		name
156148686	CV2003097	single nucleotide variant	NM_006531.5(IFT88):c.1412G>A (p.Ser471Asn)	not provided [RCV002663824]	uncertain significance	13	20638357	20638357	Human		name
156390927	CV2006164	single nucleotide variant	NM_006531.5(IFT88):c.2261G>A (p.Ser754Asn)	not provided [RCV002654374]	uncertain significance	13	20690723	20690723	Human		name
156090565	CV2017651	single nucleotide variant	NM_006531.5(IFT88):c.1087C>T (p.His363Tyr)	not provided [RCV002694926]	uncertain significance	13	20605080	20605080	Human		name
156393229	CV2019066	single nucleotide variant	NM_006531.5(IFT88):c.1382A>G (p.Tyr461Cys)	not provided [RCV002725260]\|not specified [RCV004067626]	uncertain significance	13	20631098	20631098	Human		name
156356644	CV2020065	single nucleotide variant	NM_006531.5(IFT88):c.2318A>G (p.Asn773Ser)	not provided [RCV002720580]	uncertain significance	13	20690780	20690780	Human		name
155919943	CV2032084	single nucleotide variant	NM_006531.5(IFT88):c.2335A>G (p.Ser779Gly)	not provided [RCV002727333]	uncertain significance	13	20690797	20690797	Human		name
155944807	CV2039527	single nucleotide variant	NM_006531.5(IFT88):c.1312T>A (p.Leu438Ile)	not provided [RCV002775416]	uncertain significance	13	20631028	20631028	Human		name
156010686	CV2042960	single nucleotide variant	NM_006531.5(IFT88):c.1147G>T (p.Ala383Ser)	not provided [RCV002756669]	uncertain significance	13	20615827	20615827	Human		name
155936875	CV2044951	single nucleotide variant	NM_006531.5(IFT88):c.1100T>C (p.Met367Thr)	not provided [RCV002774933]	uncertain significance	13	20605093	20605093	Human		name
156226205	CV2048354	single nucleotide variant	NM_006531.5(IFT88):c.2248G>A (p.Gly750Ser)	not provided [RCV002790823]	uncertain significance	13	20690710	20690710	Human		name
156370643	CV2048703	single nucleotide variant	NM_006531.5(IFT88):c.1527G>C (p.Glu509Asp)	not provided [RCV002814255]	uncertain significance	13	20638472	20638472	Human		name
156068995	CV2050891	single nucleotide variant	NM_006531.5(IFT88):c.1940C>G (p.Ser647Cys)	not provided [RCV002797342]	uncertain significance	13	20644949	20644949	Human		name
155996707	CV2056552	single nucleotide variant	NM_006531.5(IFT88):c.2033A>G (p.Lys678Arg)	not provided [RCV002819455]	uncertain significance	13	20656395	20656395	Human		name
156348590	CV2061965	single nucleotide variant	NM_006531.5(IFT88):c.1750A>G (p.Thr584Ala)	not provided [RCV002811612]	uncertain significance	13	20643522	20643522	Human		name
155984018	CV2070269	single nucleotide variant	NM_006531.5(IFT88):c.1042G>A (p.Asp348Asn)	not provided [RCV002842658]	uncertain significance	13	20605035	20605035	Human		name
156324328	CV2072225	single nucleotide variant	NM_006531.5(IFT88):c.1615G>T (p.Asp539Tyr)	not provided [RCV002834915]	uncertain significance	13	20641331	20641331	Human		name
156238314	CV2081950	single nucleotide variant	NM_006531.5(IFT88):c.1090C>A (p.Leu364Ile)	not provided [RCV002876502]	uncertain significance	13	20605083	20605083	Human		name
156049618	CV2093453	single nucleotide variant	NM_006531.5(IFT88):c.1499A>G (p.Tyr500Cys)	not provided [RCV002867742]	uncertain significance	13	20638444	20638444	Human		name
156136180	CV2097363	single nucleotide variant	NM_006531.5(IFT88):c.1229A>G (p.Tyr410Cys)	not provided [RCV002890131]	uncertain significance	13	20625779	20625779	Human		name
156024775	CV2106030	single nucleotide variant	NM_006531.5(IFT88):c.1411A>G (p.Ser471Gly)	not provided [RCV002923238]	uncertain significance	13	20638356	20638356	Human		name
156040768	CV2121544	single nucleotide variant	NM_006531.5(IFT88):c.1984A>G (p.Ser662Gly)	not provided [RCV002923907]	likely benign	13	20653910	20653910	Human		name
156239760	CV2129489	single nucleotide variant	NM_006531.5(IFT88):c.2284C>G (p.Leu762Val)	not provided [RCV002958826]	uncertain significance	13	20690746	20690746	Human		name
156240502	CV2129604	single nucleotide variant	NM_006531.5(IFT88):c.1922A>G (p.Gln641Arg)	not provided [RCV002958850]	uncertain significance	13	20644931	20644931	Human		name
156147893	CV2131049	single nucleotide variant	NM_006531.5(IFT88):c.1325A>C (p.Glu442Ala)	not provided [RCV002982548]	uncertain significance	13	20631041	20631041	Human		name
155945877	CV2139435	single nucleotide variant	NM_006531.5(IFT88):c.2255A>G (p.Asn752Ser)	not provided [RCV002994338]\|not specified [RCV004632137]	uncertain significance	13	20690717	20690717	Human		name
156106015	CV2139900	single nucleotide variant	NM_006531.5(IFT88):c.1309A>C (p.Ile437Leu)	not provided [RCV003002395]\|not specified [RCV004068397]	uncertain significance	13	20631025	20631025	Human		name
156316664	CV2140339	single nucleotide variant	NM_006531.5(IFT88):c.2176C>T (p.Arg726Cys)	not provided [RCV003011428]\|not specified [RCV004927871]	uncertain significance	13	20670973	20670973	Human		name
156136632	CV2141154	single nucleotide variant	NM_006531.5(IFT88):c.2086C>T (p.Arg696Cys)	not provided [RCV002982160]	uncertain significance	13	20663515	20663515	Human		name
155961193	CV2144310	single nucleotide variant	NM_006531.5(IFT88):c.2042A>G (p.His681Arg)	not provided [RCV003015474]	uncertain significance	13	20656404	20656404	Human		name
156096660	CV2152189	single nucleotide variant	NM_006531.5(IFT88):c.1090C>T (p.Leu364Phe)	not provided [RCV003020892]	uncertain significance	13	20605083	20605083	Human		name
156305197	CV2157198	single nucleotide variant	NM_006531.5(IFT88):c.2222G>C (p.Arg741Thr)	not provided [RCV003028287]	uncertain significance	13	20671019	20671019	Human		name
156081850	CV2158625	single nucleotide variant	NM_006531.5(IFT88):c.1529C>G (p.Ala510Gly)	not provided [RCV003037910]	uncertain significance	13	20638474	20638474	Human		name
156247565	CV2168740	single nucleotide variant	NM_006531.5(IFT88):c.1531C>G (p.Leu511Val)	not provided [RCV003026227]\|not specified [RCV004068597]	uncertain significance	13	20638476	20638476	Human		name
156339247	CV2174705	single nucleotide variant	NM_006531.5(IFT88):c.1394A>G (p.Asp465Gly)	not provided [RCV003047651]	uncertain significance	13	20638339	20638339	Human		name
156365159	CV2192069	single nucleotide variant	NM_006531.5(IFT88):c.1222T>A (p.Ser408Thr)	not provided [RCV003065902]	uncertain significance	13	20625772	20625772	Human		name
156054390	CV2243071	single nucleotide variant	NM_006531.5(IFT88):c.1952C>T (p.Pro651Leu)	not provided [RCV003561096]\|not specified [RCV004109988]	uncertain significance	13	20653878	20653878	Human		name
156072916	CV2325379	single nucleotide variant	NM_006531.5(IFT88):c.1379A>G (p.Tyr460Cys)	not specified [RCV004177749]	uncertain significance	13	20631095	20631095	Human		name
155925494	CV2348405	single nucleotide variant	NM_006531.5(IFT88):c.1204G>A (p.Val402Met)	not specified [RCV004193597]	uncertain significance	13	20625754	20625754	Human		name
156391088	CV2385073	single nucleotide variant	NM_006531.5(IFT88):c.2240G>A (p.Gly747Asp)	not specified [RCV004228338]	uncertain significance	13	20671037	20671037	Human		name
156002478	CV2396585	single nucleotide variant	NM_006531.5(IFT88):c.1267G>A (p.Val423Ile)	not specified [RCV004240414]	likely benign	13	20625817	20625817	Human		name
329400224	CV2440780	single nucleotide variant	NM_006531.5(IFT88):c.1657G>C (p.Glu553Gln)	not provided [RCV003779639]\|not specified [RCV004258723]	likely benign\|uncertain significance	13	20641373	20641373	Human		name
329377233	CV2462441	single nucleotide variant	NM_006531.5(IFT88):c.2395C>T (p.Pro799Ser)	not specified [RCV004276632]	uncertain significance	13	20691095	20691095	Human		name
402478855	CV2854661	single nucleotide variant	NM_006531.5(IFT88):c.2177G>A (p.Arg726His)	not provided [RCV003543795]	uncertain significance	13	20670974	20670974	Human		name
402476530	CV2857309	single nucleotide variant	NM_006531.5(IFT88):c.1476T>G (p.Asn492Lys)	not provided [RCV003543466]	uncertain significance	13	20638421	20638421	Human		name
405121308	CV2888098	single nucleotide variant	NM_006531.5(IFT88):c.1630C>T (p.Leu544Phe)	not provided [RCV003559122]	uncertain significance	13	20641346	20641346	Human		name
405165418	CV2905882	single nucleotide variant	NM_006531.5(IFT88):c.2196T>G (p.Asp732Glu)	not provided [RCV003562701]	uncertain significance	13	20670993	20670993	Human		name
405084795	CV2946509	single nucleotide variant	NM_006531.5(IFT88):c.1550G>T (p.Cys517Phe)	not provided [RCV003664875]	uncertain significance	13	20638495	20638495	Human		name
402511516	CV2948333	single nucleotide variant	NM_006531.5(IFT88):c.2230A>C (p.Ser744Arg)	not provided [RCV003662605]	uncertain significance	13	20671027	20671027	Human		name
405118071	CV2949720	single nucleotide variant	NM_006531.5(IFT88):c.1157T>C (p.Ile386Thr)	not provided [RCV003667140]	uncertain significance	13	20615837	20615837	Human		name
405220788	CV2965966	single nucleotide variant	NM_006531.5(IFT88):c.1565A>G (p.Tyr522Cys)	not provided [RCV003680647]	uncertain significance	13	20638510	20638510	Human		name
405184990	CV2967528	single nucleotide variant	NM_006531.5(IFT88):c.1572T>G (p.Ile524Met)	not provided [RCV003676581]	uncertain significance	13	20638517	20638517	Human		name
405243961	CV2971817	single nucleotide variant	NM_006531.5(IFT88):c.1425A>G (p.Ile475Met)	not provided [RCV003684721]	uncertain significance	13	20638370	20638370	Human		name
405194297	CV2985948	single nucleotide variant	NM_006531.5(IFT88):c.1492G>A (p.Gly498Ser)	not provided [RCV003706753]	uncertain significance	13	20638437	20638437	Human		name
404991415	CV2995076	single nucleotide variant	NM_006531.5(IFT88):c.1588A>C (p.Lys530Gln)	not provided [RCV003692263]	uncertain significance	13	20641304	20641304	Human		name
405029215	CV3012472	single nucleotide variant	NM_006531.5(IFT88):c.1325A>G (p.Glu442Gly)	not provided [RCV003695437]	uncertain significance	13	20631041	20631041	Human		name
405159242	CV3021312	single nucleotide variant	NM_006531.5(IFT88):c.1386G>A (p.Met462Ile)	not provided [RCV003703843]	uncertain significance	13	20631102	20631102	Human		name
405138475	CV3029537	single nucleotide variant	NM_006531.5(IFT88):c.1592T>A (p.Leu531Gln)	not provided [RCV003702305]	uncertain significance	13	20641308	20641308	Human		name
405073418	CV3034590	single nucleotide variant	NM_006531.5(IFT88):c.2288G>C (p.Ser763Thr)	not provided [RCV003698455]	uncertain significance	13	20690750	20690750	Human		name
402505238	CV3038961	single nucleotide variant	NM_006531.5(IFT88):c.1439A>G (p.Asp480Gly)	not provided [RCV003715133]	uncertain significance	13	20638384	20638384	Human		name
405180154	CV3060533	single nucleotide variant	NM_006531.5(IFT88):c.1915G>A (p.Ala639Thr)	not provided [RCV003728695]	uncertain significance	13	20644924	20644924	Human		name
405149099	CV3123169	single nucleotide variant	NM_006531.5(IFT88):c.1597C>T (p.Arg533Trp)	not provided [RCV003817402]	uncertain significance	13	20641313	20641313	Human		name
405025097	CV3133033	single nucleotide variant	NM_006531.5(IFT88):c.1767A>T (p.Leu589Phe)	not provided [RCV003830180]	uncertain significance	13	20643539	20643539	Human		name
405016374	CV3139092	single nucleotide variant	NM_006531.5(IFT88):c.1283A>G (p.Gln428Arg)	not provided [RCV003829429]\|not specified [RCV004634367]	uncertain significance	13	20625833	20625833	Human		name
405163729	CV3153219	single nucleotide variant	NM_006531.5(IFT88):c.2239G>A (p.Gly747Ser)	not provided [RCV003840954]	uncertain significance	13	20671036	20671036	Human		name
405244610	CV3161512	single nucleotide variant	NM_006531.5(IFT88):c.2176C>A (p.Arg726Ser)	not provided [RCV003868224]	uncertain significance	13	20670973	20670973	Human		name
405235653	CV3168571	single nucleotide variant	NM_006531.5(IFT88):c.2224G>A (p.Glu742Lys)	not provided [RCV003866045]	uncertain significance	13	20671021	20671021	Human		name
404996723	CV3172909	single nucleotide variant	NM_006531.5(IFT88):c.1420G>C (p.Asp474His)	not provided [RCV003882191]	uncertain significance	13	20638365	20638365	Human		name
405229376	CV3180429	single nucleotide variant	NM_006531.5(IFT88):c.2380C>T (p.Pro794Ser)	not provided [RCV003864850]	uncertain significance	13	20691080	20691080	Human		name
407514738	CV3440698	single nucleotide variant	NM_006531.5(IFT88):c.2309C>T (p.Pro770Leu)	not specified [RCV004627692]	uncertain significance	13	20690771	20690771	Human		name
407514740	CV3440699	single nucleotide variant	NM_006531.5(IFT88):c.1232T>G (p.Val411Gly)	not specified [RCV004627693]	uncertain significance	13	20625782	20625782	Human		name
407514743	CV3440700	single nucleotide variant	NM_006531.5(IFT88):c.1567A>G (p.Asn523Asp)	not specified [RCV004627694]	uncertain significance	13	20638512	20638512	Human		name
408365147	CV3499752	single nucleotide variant	NM_006531.5(IFT88):c.1528G>A (p.Ala510Thr)	Retinitis pigmentosa [RCV004720561]	uncertain significance	13	20638473	20638473	Human	2	name
408383036	CV3504591	single nucleotide variant	NM_006531.5(IFT88):c.1220C>G (p.Ala407Gly)	IFT88-related disorder [RCV004730365]	uncertain significance	13	20625770	20625770	Human		name , trait , alternate_id
597764114	CV3680019	single nucleotide variant	NM_006531.5(IFT88):c.1565A>T (p.Tyr522Phe)	not specified [RCV004926511]	uncertain significance	13	20638510	20638510	Human		name
597845742	CV3736370	single nucleotide variant	NM_006531.5(IFT88):c.1076T>A (p.Ile359Lys)	not provided [RCV005059948]	uncertain significance	13	20605069	20605069	Human		name
597904393	CV3738289	single nucleotide variant	NM_006531.5(IFT88):c.1670A>G (p.Gln557Arg)	not provided [RCV005072711]	uncertain significance	13	20641386	20641386	Human		name
597913002	CV3740443	single nucleotide variant	NM_006531.5(IFT88):c.1678A>G (p.Asn560Asp)	not provided [RCV005073780]	uncertain significance	13	20641394	20641394	Human		name
597885290	CV3741665	single nucleotide variant	NM_006531.5(IFT88):c.1003C>G (p.Pro335Ala)	not provided [RCV005070384]	uncertain significance	13	20601895	20601895	Human		name
597885943	CV3741738	single nucleotide variant	NM_006531.5(IFT88):c.1361C>T (p.Thr454Ile)	not provided [RCV005070457]	uncertain significance	13	20631077	20631077	Human		name
597876943	CV3747921	single nucleotide variant	NM_006531.5(IFT88):c.1105C>T (p.Arg369Cys)	not provided [RCV005069413]	uncertain significance	13	20605098	20605098	Human		name
597909855	CV3749578	single nucleotide variant	NM_006531.5(IFT88):c.2392C>T (p.Arg798Ter)	not provided [RCV005073426]	uncertain significance	13	20691092	20691092	Human		name
597965552	CV3751174	single nucleotide variant	NM_006531.5(IFT88):c.2188G>A (p.Gly730Ser)	not provided [RCV005082736]	uncertain significance	13	20670985	20670985	Human		name
597962765	CV3753657	single nucleotide variant	NM_006531.5(IFT88):c.1051C>T (p.His351Tyr)	not provided [RCV005081961]	uncertain significance	13	20605044	20605044	Human		name
597845234	CV3761535	single nucleotide variant	NM_006531.5(IFT88):c.1213G>A (p.Val405Met)	not provided [RCV005087135]	uncertain significance	13	20625763	20625763	Human		name
597944373	CV3782814	single nucleotide variant	NM_006531.5(IFT88):c.1026A>C (p.Lys342Asn)	not provided [RCV005134354]	uncertain significance	13	20601918	20601918	Human		name
597960823	CV3811969	single nucleotide variant	NM_006531.5(IFT88):c.2390A>G (p.Glu797Gly)	not provided [RCV005163622]	uncertain significance	13	20691090	20691090	Human		name
597842452	CV3831020	single nucleotide variant	NM_006531.5(IFT88):c.2242G>A (p.Asp748Asn)	not provided [RCV005172401]	uncertain significance	13	20671039	20671039	Human		name
597905392	CV3846526	single nucleotide variant	NM_006531.5(IFT88):c.2455G>A (p.Asp819Asn)	not provided [RCV005181953]	uncertain significance	13	20691155	20691155	Human		name
597871707	CV3849366	single nucleotide variant	NM_006531.5(IFT88):c.2282G>A (p.Arg761Gln)	not provided [RCV005197547]	uncertain significance	13	20690744	20690744	Human		name
597920093	CV3851965	single nucleotide variant	NM_006531.5(IFT88):c.1969C>A (p.Gln657Lys)	not provided [RCV005204945]	uncertain significance	13	20653895	20653895	Human		name
597895377	CV3853906	single nucleotide variant	NM_006531.5(IFT88):c.1318G>A (p.Val440Met)	not provided [RCV005201189]	uncertain significance	13	20631034	20631034	Human		name
597864897	CV3861128	single nucleotide variant	NM_006531.5(IFT88):c.1835C>T (p.Ser612Leu)	not provided [RCV005196476]	uncertain significance	13	20644844	20644844	Human		name
597929824	CV3862258	single nucleotide variant	NM_006531.5(IFT88):c.1766T>C (p.Leu589Ser)	not provided [RCV005206499]	uncertain significance	13	20643538	20643538	Human		name
12896236	CV390036	single nucleotide variant	NM_006531.5(IFT88):c.1122G>A (p.Met374Ile)	not provided [RCV002056696]\|not specified [RCV000455077]	benign	13	20615802	20615802	Human	1	name
12896236	CV390036	single nucleotide variant	NM_006531.5(IFT88):c.1122G>A (p.Met374Ile)	not provided [RCV002056696]\|not specified [RCV000455077]	benign	13	20615802	20615803	Human	1	name
12896035	CV390163	single nucleotide variant	NM_006531.5(IFT88):c.1337G>A (p.Ser446Asn)	not provided [RCV002063663]\|not specified [RCV000454792]	benign	13	20631053	20631053	Human		name
598268671	CV3979379	single nucleotide variant	NM_006531.5(IFT88):c.2201G>A (p.Ser734Asn)	not specified [RCV005349753]	uncertain significance	13	20670998	20670998	Human		name
598268676	CV3979380	single nucleotide variant	NM_006531.5(IFT88):c.1044T>A (p.Asp348Glu)	not specified [RCV005349754]	uncertain significance	13	20605037	20605037	Human		name
13467409	CV440213	single nucleotide variant	NM_006531.5(IFT88):c.2087G>C (p.Arg696Pro)	Jeune thoracic dystrophy [RCV000516068]	conflicting interpretations of pathogenicity\|uncertain significance	13	20663516	20663516	Human	1	name
15199839	CV702622	single nucleotide variant	NM_006531.5(IFT88):c.1988G>C (p.Cys663Ser)	not provided [RCV000957156]	benign	13	20653914	20653914	Human		name
15172777	CV738989	single nucleotide variant	NM_006531.5(IFT88):c.1604A>T (p.Asp535Val)	IFT88-related disorder [RCV003977925]\|not provided [RCV000905735]	likely benign	13	20641320	20641320	Human		name , trait , alternate_id
156411731	CV1973675	deletion	NM_006531.5(IFT88):c.252_253del (p.Ala86fs)	not provided [RCV002608338]	uncertain significance	13	20591008	20591009	Human		name
405192597	CV3066153	inversion	NM_006531.5(IFT88):c.230_231inv (p.Ser77Leu)	not provided [RCV003729869]	uncertain significance	13	20590986	20590987	Human		name
156207961	CV2131407	duplication	NM_006531.5(IFT88):c.1789_1814dup (p.Phe606fs)	not provided [RCV002985474]	uncertain significance	13	20643560	20643561	Human		name
155947443	CV2029044	deletion	NM_006531.5(IFT88):c.1057_1060del (p.Thr352_Asn353insTer)	not provided [RCV002730488]	uncertain significance	13	20605047	20605050	Human		name
156143513	CV2122509	insertion	NM_006531.5(IFT88):c.876_877insCTG (p.Ile292_Asn293insLeu)	not provided [RCV002954314]	uncertain significance	13	20601768	20601769	Human		name

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