Utp20 Variant Search Result - Rat Genome Database

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252 records found for search term Utp20

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15186554	CV778011	single nucleotide variant	NM_014503.3(UTP20):c.735+8A>C	not provided [RCV000953318]	benign	12	101290282	101290282	Human		name
155921330	CV2240510	single nucleotide variant	NM_014503.3(UTP20):c.7A>C (p.Thr3Pro)	not specified [RCV004119175]	likely benign	12	101280289	101280289	Human		name
15149030	CV724829	single nucleotide variant	NM_014503.3(UTP20):c.54A>G (p.Thr18=)	not provided [RCV000879077]	benign	12	101281124	101281124	Human		name
405801310	CV3348491	single nucleotide variant	NM_014503.3(UTP20):c.23A>G (p.His8Arg)	not specified [RCV004477754]	uncertain significance	12	101280305	101280305	Human		name
597803400	CV3623438	single nucleotide variant	NM_014503.3(UTP20):c.22C>T (p.His8Tyr)	not specified [RCV004881717]	uncertain significance	12	101280304	101280304	Human		name
405801391	CV3348536	single nucleotide variant	NM_014503.3(UTP20):c.97C>T (p.Arg33Trp)	not specified [RCV004477799]	uncertain significance	12	101281167	101281167	Human		name
15151991	CV713274	single nucleotide variant	NM_014503.3(UTP20):c.405G>A (p.Ser135=)	not provided [RCV000968258]	benign\|likely benign	12	101286399	101286399	Human		name
15125479	CV713276	single nucleotide variant	NM_014503.3(UTP20):c.912C>T (p.His304=)	not provided [RCV000963586]	benign	12	101291762	101291762	Human		name
15122447	CV768853	single nucleotide variant	NM_014503.3(UTP20):c.819C>T (p.Leu273=)	not provided [RCV000940686]	likely benign	12	101290816	101290816	Human		name
156341706	CV2344915	single nucleotide variant	NM_014503.3(UTP20):c.262A>G (p.Ile88Val)	not specified [RCV004191047]	uncertain significance	12	101285817	101285817	Human		name
597803375	CV3623423	single nucleotide variant	NM_014503.3(UTP20):c.2830T>C (p.Leu944=)	not specified [RCV004881705]	likely benign	12	101320852	101320852	Human		name
597803425	CV3632963	single nucleotide variant	NM_014503.3(UTP20):c.151G>A (p.Gly51Ser)	not specified [RCV004881729]	uncertain significance	12	101285594	101285594	Human		name
617152297	CV4020672	single nucleotide variant	NM_014503.3(UTP20):c.2160G>A (p.Pro720=)	not provided [RCV005427929]	benign	12	101309768	101309768	Human		name
156062389	CV2203579	single nucleotide variant	NM_014503.3(UTP20):c.500T>C (p.Met167Thr)	not specified [RCV004072775]	uncertain significance	12	101286494	101286494	Human		name
156090806	CV2206640	single nucleotide variant	NM_014503.3(UTP20):c.319C>G (p.Leu107Val)	not specified [RCV004080979]	uncertain significance	12	101285874	101285874	Human		name
156279148	CV2210118	single nucleotide variant	NM_014503.3(UTP20):c.958A>C (p.Lys320Gln)	not specified [RCV004078585]	uncertain significance	12	101291808	101291808	Human		name
155930040	CV2224653	single nucleotide variant	NM_014503.3(UTP20):c.835T>A (p.Ser279Thr)	not specified [RCV004092498]	uncertain significance	12	101290832	101290832	Human		name
156217979	CV2253908	single nucleotide variant	NM_014503.3(UTP20):c.809G>A (p.Gly270Glu)	not specified [RCV004127588]	uncertain significance	12	101290806	101290806	Human		name
156051280	CV2386303	single nucleotide variant	NM_014503.3(UTP20):c.755G>A (p.Arg252Gln)	not specified [RCV004228646]	likely benign	12	101290752	101290752	Human		name
329363508	CV2471700	single nucleotide variant	NM_014503.3(UTP20):c.415A>G (p.Thr139Ala)	not specified [RCV004286980]	uncertain significance	12	101286409	101286409	Human		name
401746855	CV2732000	single nucleotide variant	NM_014503.3(UTP20):c.553A>G (p.Ile185Val)	not specified [RCV004333235]	uncertain significance	12	101288997	101288997	Human		name
401857505	CV2760196	single nucleotide variant	NM_014503.3(UTP20):c.653C>G (p.Pro218Arg)	not specified [RCV004347373]	uncertain significance	12	101290192	101290192	Human		name
401898639	CV2782568	single nucleotide variant	NM_014503.3(UTP20):c.796T>C (p.Trp266Arg)	not specified [RCV004359602]	uncertain significance	12	101290793	101290793	Human		name
401932302	CV2816775	single nucleotide variant	NM_014503.3(UTP20):c.8131T>C (p.Leu2711=)	not provided [RCV003391956]	likely benign	12	101385657	101385657	Human		name
405801470	CV3348499	single nucleotide variant	NM_014503.3(UTP20):c.349G>T (p.Asp117Tyr)	not specified [RCV004477762]	uncertain significance	12	101286343	101286343	Human		name
405801334	CV3348504	single nucleotide variant	NM_014503.3(UTP20):c.404C>T (p.Ser135Leu)	not specified [RCV004477767]	uncertain significance	12	101286398	101286398	Human		name
405801390	CV3348535	single nucleotide variant	NM_014503.3(UTP20):c.972A>T (p.Glu324Asp)	not specified [RCV004477798]	uncertain significance	12	101291822	101291822	Human		name
407529163	CV3487814	single nucleotide variant	NM_014503.3(UTP20):c.658A>G (p.Lys220Glu)	not specified [RCV004680761]	uncertain significance	12	101290197	101290197	Human		name
597799351	CV3623408	single nucleotide variant	NM_014503.3(UTP20):c.394A>T (p.Thr132Ser)	not specified [RCV004879634]	uncertain significance	12	101286388	101286388	Human		name
597799353	CV3623409	single nucleotide variant	NM_014503.3(UTP20):c.838A>G (p.Thr280Ala)	not specified [RCV004879635]	uncertain significance	12	101290835	101290835	Human		name
597803402	CV3623439	single nucleotide variant	NM_014503.3(UTP20):c.358A>T (p.Met120Leu)	not specified [RCV004881718]	uncertain significance	12	101286352	101286352	Human		name
598204888	CV3933083	single nucleotide variant	NM_014503.3(UTP20):c.421G>A (p.Asp141Asn)	not specified [RCV005290764]	uncertain significance	12	101286415	101286415	Human		name
598204897	CV3933084	single nucleotide variant	NM_014503.3(UTP20):c.602C>T (p.Ser201Phe)	not specified [RCV005290765]	uncertain significance	12	101290141	101290141	Human		name
598239412	CV3933088	single nucleotide variant	NM_014503.3(UTP20):c.968T>G (p.Leu323Trp)	not specified [RCV005296585]	uncertain significance	12	101291818	101291818	Human		name
15174877	CV702057	single nucleotide variant	NM_014503.3(UTP20):c.6345G>A (p.Val2115=)	not provided [RCV000950444]	benign	12	101367937	101367937	Human		name
15118984	CV713275	single nucleotide variant	NM_014503.3(UTP20):c.501G>A (p.Met167Ile)	not provided [RCV000962474]	benign	12	101286495	101286495	Human		name
15106185	CV724831	single nucleotide variant	NM_014503.3(UTP20):c.3906T>C (p.His1302=)	not provided [RCV000893231]	benign	12	101338850	101338850	Human		name
15181701	CV724835	single nucleotide variant	NM_014503.3(UTP20):c.6159A>G (p.Leu2053=)	not provided [RCV000885825]	benign	12	101366591	101366591	Human		name
15113354	CV724836	single nucleotide variant	NM_014503.3(UTP20):c.7797G>A (p.Ala2599=)	not provided [RCV000894649]	benign\|likely benign	12	101383181	101383181	Human		name
15118692	CV768854	single nucleotide variant	NM_014503.3(UTP20):c.6198T>C (p.Val2066=)	not provided [RCV000940055]	likely benign	12	101366630	101366630	Human		name
156247471	CV2215338	single nucleotide variant	NM_014503.3(UTP20):c.2761G>A (p.Val921Ile)	not specified [RCV004089153]	uncertain significance	12	101319567	101319567	Human		name
155939579	CV2225576	single nucleotide variant	NM_014503.3(UTP20):c.2566C>T (p.Pro856Ser)	not specified [RCV004100955]	uncertain significance	12	101317491	101317491	Human		name
156225668	CV2226240	single nucleotide variant	NM_014503.3(UTP20):c.2093A>G (p.His698Arg)	not specified [RCV004099493]	uncertain significance	12	101308282	101308282	Human		name
155950724	CV2238638	single nucleotide variant	NM_014503.3(UTP20):c.1934T>G (p.Ile645Ser)	not specified [RCV004107541]	uncertain significance	12	101306700	101306700	Human		name
156152088	CV2245270	single nucleotide variant	NM_014503.3(UTP20):c.2995G>A (p.Val999Ile)	not specified [RCV004107035]	uncertain significance	12	101321583	101321583	Human		name
156034640	CV2256749	single nucleotide variant	NM_014503.3(UTP20):c.1763G>T (p.Arg588Leu)	not specified [RCV004120698]	uncertain significance	12	101302535	101302535	Human		name
156254414	CV2325632	single nucleotide variant	NM_014503.3(UTP20):c.1052C>T (p.Thr351Ile)	not specified [RCV004180044]	uncertain significance	12	101291983	101291983	Human		name
156136124	CV2357123	single nucleotide variant	NM_014503.3(UTP20):c.2929A>T (p.Arg977Trp)	not specified [RCV004206917]	uncertain significance	12	101321517	101321517	Human		name
329390894	CV2437402	single nucleotide variant	NM_014503.3(UTP20):c.2724G>C (p.Arg908Ser)	not specified [RCV004256271]	uncertain significance	12	101317649	101317649	Human		name
329360010	CV2446520	single nucleotide variant	NM_014503.3(UTP20):c.1661G>A (p.Gly554Glu)	not specified [RCV004251420]	uncertain significance	12	101300047	101300047	Human		name
401721310	CV2673673	single nucleotide variant	NM_014503.3(UTP20):c.1618G>A (p.Val540Ile)	not specified [RCV004282404]	uncertain significance	12	101300004	101300004	Human		name
401730773	CV2677339	single nucleotide variant	NM_014503.3(UTP20):c.2897C>T (p.Pro966Leu)	not specified [RCV004295954]	uncertain significance	12	101320919	101320919	Human		name
401752693	CV2707094	single nucleotide variant	NM_014503.3(UTP20):c.2618G>A (p.Gly873Glu)	not specified [RCV004321677]	uncertain significance	12	101317543	101317543	Human		name
401863491	CV2765851	single nucleotide variant	NM_014503.3(UTP20):c.2603G>A (p.Arg868Gln)	not specified [RCV004337889]	uncertain significance	12	101317528	101317528	Human		name
405801299	CV3348485	single nucleotide variant	NM_014503.3(UTP20):c.1024G>A (p.Ala342Thr)	not specified [RCV004477748]	uncertain significance	12	101291874	101291874	Human		name
405801301	CV3348486	single nucleotide variant	NM_014503.3(UTP20):c.2152G>C (p.Glu718Gln)	not specified [RCV004477749]	uncertain significance	12	101308341	101308341	Human		name
405801303	CV3348487	single nucleotide variant	NM_014503.3(UTP20):c.2242C>T (p.His748Tyr)	not specified [RCV004477750]	uncertain significance	12	101311729	101311729	Human		name
405801304	CV3348488	single nucleotide variant	NM_014503.3(UTP20):c.2245G>A (p.Glu749Lys)	not specified [RCV004477751]	uncertain significance	12	101311732	101311732	Human		name
405801306	CV3348489	single nucleotide variant	NM_014503.3(UTP20):c.2279A>G (p.Tyr760Cys)	not specified [RCV004477752]	uncertain significance	12	101311766	101311766	Human		name
405801308	CV3348490	single nucleotide variant	NM_014503.3(UTP20):c.2398C>G (p.Leu800Val)	not specified [RCV004477753]	uncertain significance	12	101312122	101312122	Human		name
405801313	CV3348493	single nucleotide variant	NM_014503.3(UTP20):c.2773T>G (p.Phe925Val)	not specified [RCV004477756]	uncertain significance	12	101319579	101319579	Human		name
405801315	CV3348494	single nucleotide variant	NM_014503.3(UTP20):c.2848C>G (p.Gln950Glu)	not specified [RCV004477757]	uncertain significance	12	101320870	101320870	Human		name
405801317	CV3348495	single nucleotide variant	NM_014503.3(UTP20):c.2947A>C (p.Ser983Arg)	not specified [RCV004477758]	uncertain significance	12	101321535	101321535	Human		name
407529145	CV3487804	single nucleotide variant	NM_014503.3(UTP20):c.1674A>T (p.Lys558Asn)	not specified [RCV004680752]	uncertain significance	12	101300060	101300060	Human		name
407529157	CV3487810	single nucleotide variant	NM_014503.3(UTP20):c.1769A>G (p.Lys590Arg)	not specified [RCV004680758]	uncertain significance	12	101302541	101302541	Human		name
407464700	CV3487813	single nucleotide variant	NM_014503.3(UTP20):c.2186A>G (p.Tyr729Cys)	not specified [RCV004688575]	uncertain significance	12	101309794	101309794	Human		name
407529165	CV3487815	single nucleotide variant	NM_014503.3(UTP20):c.2176G>A (p.Gly726Ser)	not specified [RCV004680762]	uncertain significance	12	101309784	101309784	Human		name
407529176	CV3487820	single nucleotide variant	NM_014503.3(UTP20):c.1982C>G (p.Pro661Arg)	not specified [RCV004680767]	uncertain significance	12	101306748	101306748	Human		name
407529186	CV3487826	single nucleotide variant	NM_014503.3(UTP20):c.2962A>G (p.Ile988Val)	not specified [RCV004680772]	uncertain significance	12	101321550	101321550	Human		name
407529189	CV3487828	single nucleotide variant	NM_014503.3(UTP20):c.1361C>T (p.Ala454Val)	not specified [RCV004680774]	uncertain significance	12	101295589	101295589	Human		name
597799356	CV3623410	single nucleotide variant	NM_014503.3(UTP20):c.2513G>A (p.Arg838Gln)	not specified [RCV004879636]	uncertain significance	12	101312237	101312237	Human		name
597799359	CV3623412	single nucleotide variant	NM_014503.3(UTP20):c.1445A>T (p.Gln482Leu)	not specified [RCV004879638]	uncertain significance	12	101299696	101299696	Human		name
597799361	CV3623413	single nucleotide variant	NM_014503.3(UTP20):c.1681T>G (p.Leu561Val)	not specified [RCV004879639]	uncertain significance	12	101302453	101302453	Human		name
597697354	CV3623417	single nucleotide variant	NM_014503.3(UTP20):c.2567C>T (p.Pro856Leu)	not specified [RCV004885258]	uncertain significance	12	101317492	101317492	Human		name
597803371	CV3623418	single nucleotide variant	NM_014503.3(UTP20):c.2248A>G (p.Met750Val)	not specified [RCV004881703]	uncertain significance	12	101311735	101311735	Human		name
597803379	CV3623425	single nucleotide variant	NM_014503.3(UTP20):c.1298T>C (p.Ile433Thr)	not specified [RCV004881707]	uncertain significance	12	101295526	101295526	Human		name
597803381	CV3623427	single nucleotide variant	NM_014503.3(UTP20):c.1027G>C (p.Asp343His)	not specified [RCV004881708]	uncertain significance	12	101291877	101291877	Human		name
597803392	CV3623433	single nucleotide variant	NM_014503.3(UTP20):c.2363G>T (p.Ser788Ile)	not specified [RCV004881713]	uncertain significance	12	101312087	101312087	Human		name
597803394	CV3623434	single nucleotide variant	NM_014503.3(UTP20):c.2543G>A (p.Arg848Lys)	not specified [RCV004881714]	uncertain significance	12	101312267	101312267	Human		name
597803404	CV3623440	single nucleotide variant	NM_014503.3(UTP20):c.2906T>A (p.Leu969His)	not specified [RCV004881719]	uncertain significance	12	101320928	101320928	Human		name
597697421	CV3623442	single nucleotide variant	NM_014503.3(UTP20):c.1000A>C (p.Ser334Arg)	not specified [RCV004885265]	uncertain significance	12	101291850	101291850	Human		name
597803411	CV3632954	single nucleotide variant	NM_014503.3(UTP20):c.1702G>A (p.Val568Ile)	not specified [RCV004881722]	uncertain significance	12	101302474	101302474	Human		name
597803414	CV3632958	single nucleotide variant	NM_014503.3(UTP20):c.2375C>T (p.Thr792Ile)	not specified [RCV004881724]	uncertain significance	12	101312099	101312099	Human		name
597803418	CV3632960	single nucleotide variant	NM_014503.3(UTP20):c.1027G>A (p.Asp343Asn)	not specified [RCV004881726]	uncertain significance	12	101291877	101291877	Human		name
597803429	CV3632965	single nucleotide variant	NM_014503.3(UTP20):c.2327A>C (p.Asn776Thr)	not specified [RCV004881731]	uncertain significance	12	101312051	101312051	Human		name
598204837	CV3933074	single nucleotide variant	NM_014503.3(UTP20):c.2726G>C (p.Arg909Thr)	not specified [RCV005290757]	uncertain significance	12	101317651	101317651	Human		name
598239387	CV3933075	single nucleotide variant	NM_014503.3(UTP20):c.2727A>T (p.Arg909Ser)	not specified [RCV005296580]	uncertain significance	12	101317652	101317652	Human		name
598239390	CV3933077	single nucleotide variant	NM_014503.3(UTP20):c.1451A>C (p.Lys484Thr)	not specified [RCV005296581]	uncertain significance	12	101299702	101299702	Human		name
598239401	CV3933086	single nucleotide variant	NM_014503.3(UTP20):c.1019C>T (p.Thr340Met)	not specified [RCV005296583]	likely benign	12	101291869	101291869	Human		name
598239423	CV3933092	single nucleotide variant	NM_014503.3(UTP20):c.1495C>G (p.His499Asp)	not specified [RCV005296587]	uncertain significance	12	101299746	101299746	Human		name
598204921	CV3933097	single nucleotide variant	NM_014503.3(UTP20):c.1373C>T (p.Thr458Ile)	not specified [RCV005290769]	uncertain significance	12	101295601	101295601	Human		name
598239443	CV3933099	single nucleotide variant	NM_014503.3(UTP20):c.2902G>A (p.Val968Ile)	not specified [RCV005296591]	likely benign	12	101320924	101320924	Human		name
598239449	CV3933100	single nucleotide variant	NM_014503.3(UTP20):c.1121T>A (p.Leu374Gln)	not specified [RCV005296592]	uncertain significance	12	101292052	101292052	Human		name
15126209	CV713277	single nucleotide variant	NM_014503.3(UTP20):c.1015C>A (p.Pro339Thr)	not provided [RCV000963707]	benign	12	101291865	101291865	Human		name
15149033	CV724830	single nucleotide variant	NM_014503.3(UTP20):c.1129A>T (p.Asn377Tyr)	not provided [RCV000879078]	benign	12	101292060	101292060	Human		name
156066262	CV2193296	single nucleotide variant	NM_014503.3(UTP20):c.7807G>A (p.Gly2603Arg)	not specified [RCV004071604]	likely benign	12	101383191	101383191	Human		name
156398721	CV2194747	single nucleotide variant	NM_014503.3(UTP20):c.5216C>T (p.Pro1739Leu)	not specified [RCV004075296]	likely benign	12	101354940	101354940	Human		name
156269344	CV2195082	single nucleotide variant	NM_014503.3(UTP20):c.4342G>A (p.Val1448Ile)	not specified [RCV004077992]	uncertain significance	12	101342986	101342986	Human		name
156135890	CV2196125	single nucleotide variant	NM_014503.3(UTP20):c.5993G>A (p.Arg1998Gln)	not specified [RCV004073487]	uncertain significance	12	101365493	101365493	Human		name
156068849	CV2203731	single nucleotide variant	NM_014503.3(UTP20):c.6629A>G (p.Tyr2210Cys)	not specified [RCV004074378]	uncertain significance	12	101370505	101370505	Human		name
156069085	CV2203754	single nucleotide variant	NM_014503.3(UTP20):c.5110G>A (p.Ala1704Thr)	not specified [RCV004074397]	likely benign	12	101354834	101354834	Human		name
156222116	CV2208915	single nucleotide variant	NM_014503.3(UTP20):c.3887G>A (p.Gly1296Glu)	not specified [RCV004085280]	uncertain significance	12	101338831	101338831	Human		name
156039309	CV2215152	single nucleotide variant	NM_014503.3(UTP20):c.4480A>G (p.Ser1494Gly)	not specified [RCV004086872]	uncertain significance	12	101344625	101344625	Human		name
155922885	CV2215323	single nucleotide variant	NM_014503.3(UTP20):c.5324C>T (p.Thr1775Ile)	not specified [RCV004087350]	uncertain significance	12	101355048	101355048	Human		name
156092107	CV2216728	single nucleotide variant	NM_014503.3(UTP20):c.3250G>A (p.Asp1084Asn)	not specified [RCV004083175]	uncertain significance	12	101329282	101329282	Human		name
156341122	CV2225761	single nucleotide variant	NM_014503.3(UTP20):c.4586G>T (p.Gly1529Val)	not specified [RCV004103173]	uncertain significance	12	101344731	101344731	Human		name
156071121	CV2229120	single nucleotide variant	NM_014503.3(UTP20):c.3924G>T (p.Gln1308His)	not specified [RCV004099167]	uncertain significance	12	101338868	101338868	Human		name
155941401	CV2229121	single nucleotide variant	NM_014503.3(UTP20):c.3925T>A (p.Tyr1309Asn)	not specified [RCV004099168]	uncertain significance	12	101338869	101338869	Human		name
156388876	CV2229720	single nucleotide variant	NM_014503.3(UTP20):c.6200G>A (p.Arg2067Gln)	not specified [RCV004103521]	uncertain significance	12	101366632	101366632	Human		name
156251126	CV2232270	single nucleotide variant	NM_014503.3(UTP20):c.8332C>G (p.Leu2778Val)	not specified [RCV004105053]	uncertain significance	12	101386097	101386097	Human		name
156029156	CV2238289	single nucleotide variant	NM_014503.3(UTP20):c.6104C>G (p.Pro2035Arg)	not specified [RCV004113367]	uncertain significance	12	101365604	101365604	Human		name
156297359	CV2240848	single nucleotide variant	NM_014503.3(UTP20):c.3473T>C (p.Met1158Thr)	not specified [RCV004102137]	uncertain significance	12	101333356	101333356	Human		name
156073212	CV2251540	single nucleotide variant	NM_014503.3(UTP20):c.3670C>G (p.Pro1224Ala)	not specified [RCV004117497]	uncertain significance	12	101338079	101338079	Human		name
156077426	CV2251541	single nucleotide variant	NM_014503.3(UTP20):c.7634T>G (p.Leu2545Trp)	not specified [RCV004117498]	uncertain significance	12	101381189	101381189	Human		name
156031417	CV2274928	single nucleotide variant	NM_014503.3(UTP20):c.6724G>A (p.Asp2242Asn)	not specified [RCV004134988]	uncertain significance	12	101371094	101371094	Human		name
156177894	CV2298249	single nucleotide variant	NM_014503.3(UTP20):c.6862A>T (p.Met2288Leu)	not specified [RCV004160168]	uncertain significance	12	101372947	101372947	Human		name
156073098	CV2299145	single nucleotide variant	NM_014503.3(UTP20):c.3767T>C (p.Val1256Ala)	not specified [RCV004152490]	likely benign	12	101338176	101338176	Human		name
156042202	CV2310953	single nucleotide variant	NM_014503.3(UTP20):c.6737G>A (p.Arg2246Gln)	not specified [RCV004163987]	uncertain significance	12	101371107	101371107	Human		name
156263108	CV2314946	single nucleotide variant	NM_014503.3(UTP20):c.3689A>G (p.Asp1230Gly)	not specified [RCV004171049]	uncertain significance	12	101338098	101338098	Human		name
156258351	CV2322138	single nucleotide variant	NM_014503.3(UTP20):c.5195G>A (p.Ser1732Asn)	not specified [RCV004175922]	uncertain significance	12	101354919	101354919	Human		name
156278033	CV2330886	single nucleotide variant	NM_014503.3(UTP20):c.5093T>C (p.Ile1698Thr)	not specified [RCV004185939]	uncertain significance	12	101353115	101353115	Human		name
156284318	CV2334752	single nucleotide variant	NM_014503.3(UTP20):c.5225C>T (p.Pro1742Leu)	not specified [RCV004188729]	uncertain significance	12	101354949	101354949	Human		name
156287362	CV2336091	single nucleotide variant	NM_014503.3(UTP20):c.4235C>T (p.Thr1412Met)	not specified [RCV004189687]	uncertain significance	12	101342579	101342579	Human		name
155976045	CV2342732	single nucleotide variant	NM_014503.3(UTP20):c.5954A>G (p.Lys1985Arg)	not specified [RCV004196804]	uncertain significance	12	101363739	101363739	Human		name
156218406	CV2344745	single nucleotide variant	NM_014503.3(UTP20):c.7492G>A (p.Glu2498Lys)	not specified [RCV004190899]	uncertain significance	12	101379466	101379466	Human		name
156075660	CV2350894	single nucleotide variant	NM_014503.3(UTP20):c.4887T>A (p.His1629Gln)	not specified [RCV004211731]	uncertain significance	12	101352057	101352057	Human		name
156154755	CV2359645	single nucleotide variant	NM_014503.3(UTP20):c.3458G>A (p.Arg1153His)	not specified [RCV004210473]	uncertain significance	12	101333341	101333341	Human		name
156212989	CV2367013	single nucleotide variant	NM_014503.3(UTP20):c.7994C>T (p.Pro2665Leu)	not specified [RCV004215464]	uncertain significance	12	101383607	101383607	Human		name
156256811	CV2369211	single nucleotide variant	NM_014503.3(UTP20):c.3781A>G (p.Asn1261Asp)	not specified [RCV004208130]	uncertain significance	12	101338190	101338190	Human		name
156384225	CV2371331	single nucleotide variant	NM_014503.3(UTP20):c.4209C>A (p.Asn1403Lys)	not specified [RCV004223340]	uncertain significance	12	101342553	101342553	Human		name
156387347	CV2372717	single nucleotide variant	NM_014503.3(UTP20):c.4180A>G (p.Ile1394Val)	not specified [RCV004221909]	uncertain significance	12	101342524	101342524	Human		name
156387439	CV2372746	single nucleotide variant	NM_014503.3(UTP20):c.6266G>A (p.Arg2089Gln)	not specified [RCV004221934]	uncertain significance	12	101366698	101366698	Human		name
156387847	CV2383400	single nucleotide variant	NM_014503.3(UTP20):c.6154C>T (p.Arg2052Cys)	not specified [RCV004222424]	uncertain significance	12	101366586	101366586	Human		name
329400045	CV2440434	single nucleotide variant	NM_014503.3(UTP20):c.7729A>G (p.Lys2577Glu)	not specified [RCV004256369]	likely benign	12	101383113	101383113	Human		name
329402589	CV2451101	single nucleotide variant	NM_014503.3(UTP20):c.4040A>G (p.Glu1347Gly)	not specified [RCV004270041]	uncertain significance	12	101340549	101340549	Human		name
329386925	CV2452688	single nucleotide variant	NM_014503.3(UTP20):c.4717G>C (p.Asp1573His)	not specified [RCV004275247]	uncertain significance	12	101345665	101345665	Human		name
329386359	CV2455888	single nucleotide variant	NM_014503.3(UTP20):c.5590A>G (p.Ile1864Val)	not specified [RCV004279161]	uncertain significance	12	101356981	101356981	Human		name
329359923	CV2462379	single nucleotide variant	NM_014503.3(UTP20):c.5345C>G (p.Thr1782Ser)	not specified [RCV004268144]	uncertain significance	12	101355069	101355069	Human		name
329399753	CV2467632	single nucleotide variant	NM_014503.3(UTP20):c.3050A>G (p.Tyr1017Cys)	not specified [RCV004287487]	uncertain significance	12	101327089	101327089	Human		name
329353358	CV2468982	single nucleotide variant	NM_014503.3(UTP20):c.6058G>A (p.Glu2020Lys)	not specified [RCV004274245]	uncertain significance	12	101365558	101365558	Human		name
329375046	CV2470976	single nucleotide variant	NM_014503.3(UTP20):c.5619A>G (p.Ile1873Met)	not specified [RCV004276157]	uncertain significance	12	101357010	101357010	Human		name
401742304	CV2673750	single nucleotide variant	NM_014503.3(UTP20):c.3715C>A (p.Leu1239Ile)	not specified [RCV004291094]	uncertain significance	12	101338124	101338124	Human		name
401742374	CV2673766	single nucleotide variant	NM_014503.3(UTP20):c.3158T>C (p.Ile1053Thr)	not specified [RCV004293153]	uncertain significance	12	101327197	101327197	Human		name
401742824	CV2677689	single nucleotide variant	NM_014503.3(UTP20):c.8215C>A (p.Pro2739Thr)	not specified [RCV004291774]	uncertain significance	12	101385980	101385980	Human		name
401743341	CV2684680	single nucleotide variant	NM_014503.3(UTP20):c.4523A>C (p.Asn1508Thr)	not specified [RCV004293776]	uncertain significance	12	101344668	101344668	Human		name
401770664	CV2685828	single nucleotide variant	NM_014503.3(UTP20):c.4339G>A (p.Asp1447Asn)	not specified [RCV004294814]	uncertain significance	12	101342983	101342983	Human		name
401775974	CV2692556	single nucleotide variant	NM_014503.3(UTP20):c.6196G>T (p.Val2066Phe)	not specified [RCV004312299]	uncertain significance	12	101366628	101366628	Human		name
401783184	CV2703859	single nucleotide variant	NM_014503.3(UTP20):c.4078C>T (p.Leu1360Phe)	not specified [RCV004306723]	uncertain significance	12	101340587	101340587	Human		name
401779208	CV2713335	single nucleotide variant	NM_014503.3(UTP20):c.3324T>G (p.Ile1108Met)	not specified [RCV004318636]	uncertain significance	12	101329356	101329356	Human		name
401780529	CV2716819	single nucleotide variant	NM_014503.3(UTP20):c.7000A>G (p.Thr2334Ala)	not specified [RCV004329635]	uncertain significance	12	101373636	101373636	Human		name
401888836	CV2764973	single nucleotide variant	NM_014503.3(UTP20):c.8179C>T (p.Arg2727Trp)	not specified [RCV004335052]	uncertain significance	12	101385705	101385705	Human		name
401860894	CV2772290	single nucleotide variant	NM_014503.3(UTP20):c.5560C>T (p.Leu1854Phe)	not specified [RCV004353311]	uncertain significance	12	101356951	101356951	Human		name
401887613	CV2773546	single nucleotide variant	NM_014503.3(UTP20):c.3684A>C (p.Glu1228Asp)	not specified [RCV004355955]	uncertain significance	12	101338093	101338093	Human		name
401873949	CV2773609	single nucleotide variant	NM_014503.3(UTP20):c.5755G>A (p.Gly1919Arg)	not specified [RCV004356304]	uncertain significance	12	101362025	101362025	Human		name
401892820	CV2791815	single nucleotide variant	NM_014503.3(UTP20):c.4112T>C (p.Val1371Ala)	not specified [RCV004359266]	uncertain significance	12	101342456	101342456	Human		name
401932301	CV2816774	single nucleotide variant	NM_014503.3(UTP20):c.7840G>A (p.Gly2614Ser)	not provided [RCV003391955]	likely benign	12	101383224	101383224	Human		name
405801319	CV3348496	single nucleotide variant	NM_014503.3(UTP20):c.3244G>A (p.Asp1082Asn)	not specified [RCV004477759]	uncertain significance	12	101329276	101329276	Human		name
405801321	CV3348497	single nucleotide variant	NM_014503.3(UTP20):c.3278G>A (p.Arg1093His)	not specified [RCV004477760]	uncertain significance	12	101329310	101329310	Human		name
405801323	CV3348498	single nucleotide variant	NM_014503.3(UTP20):c.3388G>A (p.Val1130Ile)	not specified [RCV004477761]	uncertain significance	12	101329420	101329420	Human		name
405801328	CV3348501	single nucleotide variant	NM_014503.3(UTP20):c.3796G>A (p.Glu1266Lys)	not specified [RCV004477764]	uncertain significance	12	101338205	101338205	Human		name
405801330	CV3348502	single nucleotide variant	NM_014503.3(UTP20):c.3963A>T (p.Lys1321Asn)	not specified [RCV004477765]	uncertain significance	12	101338907	101338907	Human		name
405801332	CV3348503	single nucleotide variant	NM_014503.3(UTP20):c.3997C>A (p.Leu1333Ile)	not specified [RCV004477766]	uncertain significance	12	101338941	101338941	Human		name
405801336	CV3348505	single nucleotide variant	NM_014503.3(UTP20):c.4268G>T (p.Gly1423Val)	not specified [RCV004477768]	uncertain significance	12	101342809	101342809	Human		name
405801340	CV3348507	single nucleotide variant	NM_014503.3(UTP20):c.4362G>C (p.Gln1454His)	not specified [RCV004477770]	uncertain significance	12	101343006	101343006	Human		name
405801341	CV3348508	single nucleotide variant	NM_014503.3(UTP20):c.4375T>A (p.Tyr1459Asn)	not specified [RCV004477771]	uncertain significance	12	101343019	101343019	Human		name
405801343	CV3348509	single nucleotide variant	NM_014503.3(UTP20):c.4437C>A (p.Phe1479Leu)	not specified [RCV004477772]	uncertain significance	12	101343081	101343081	Human		name
405801345	CV3348510	single nucleotide variant	NM_014503.3(UTP20):c.4558C>T (p.Arg1520Cys)	not specified [RCV004477773]	uncertain significance	12	101344703	101344703	Human		name
405801347	CV3348511	single nucleotide variant	NM_014503.3(UTP20):c.4724T>C (p.Phe1575Ser)	not specified [RCV004477774]	uncertain significance	12	101345672	101345672	Human		name
405801348	CV3348512	single nucleotide variant	NM_014503.3(UTP20):c.4808T>C (p.Val1603Ala)	not specified [RCV004477775]	uncertain significance	12	101346512	101346512	Human		name
405801352	CV3348514	single nucleotide variant	NM_014503.3(UTP20):c.5015T>C (p.Leu1672Pro)	not specified [RCV004477777]	uncertain significance	12	101352185	101352185	Human		name
405801354	CV3348515	single nucleotide variant	NM_014503.3(UTP20):c.5399A>C (p.Lys1800Thr)	not specified [RCV004477778]	uncertain significance	12	101356558	101356558	Human		name
405801356	CV3348516	single nucleotide variant	NM_014503.3(UTP20):c.5666A>G (p.Gln1889Arg)	not specified [RCV004477779]	uncertain significance	12	101357057	101357057	Human		name
405801358	CV3348517	single nucleotide variant	NM_014503.3(UTP20):c.5762T>G (p.Leu1921Trp)	not specified [RCV004477780]	uncertain significance	12	101362032	101362032	Human		name
405801360	CV3348518	single nucleotide variant	NM_014503.3(UTP20):c.5792T>C (p.Ile1931Thr)	not specified [RCV004477781]	uncertain significance	12	101363577	101363577	Human		name
405801363	CV3348520	single nucleotide variant	NM_014503.3(UTP20):c.6014G>A (p.Arg2005His)	not specified [RCV004477783]	uncertain significance	12	101365514	101365514	Human		name
405801365	CV3348521	single nucleotide variant	NM_014503.3(UTP20):c.6143C>T (p.Ala2048Val)	not specified [RCV004477784]	uncertain significance	12	101366575	101366575	Human		name
405801367	CV3348522	single nucleotide variant	NM_014503.3(UTP20):c.6418G>A (p.Val2140Ile)	not specified [RCV004477785]	uncertain significance	12	101369754	101369754	Human		name
405801472	CV3348523	single nucleotide variant	NM_014503.3(UTP20):c.6499G>A (p.Ala2167Thr)	not specified [RCV004477786]	uncertain significance	12	101369835	101369835	Human		name
405801370	CV3348524	single nucleotide variant	NM_014503.3(UTP20):c.6514G>A (p.Ala2172Thr)	not specified [RCV004477787]	uncertain significance	12	101369850	101369850	Human		name
405801372	CV3348525	single nucleotide variant	NM_014503.3(UTP20):c.6545A>G (p.Asn2182Ser)	not specified [RCV004477788]	uncertain significance	12	101369881	101369881	Human		name
405801374	CV3348526	single nucleotide variant	NM_014503.3(UTP20):c.7063G>C (p.Gly2355Arg)	not specified [RCV004477789]	uncertain significance	12	101373699	101373699	Human		name
405801375	CV3348527	single nucleotide variant	NM_014503.3(UTP20):c.7205G>T (p.Arg2402Ile)	not specified [RCV004477790]	uncertain significance	12	101374881	101374881	Human		name
405801377	CV3348528	single nucleotide variant	NM_014503.3(UTP20):c.7361T>A (p.Phe2454Tyr)	not specified [RCV004477791]	uncertain significance	12	101375721	101375721	Human		name
405801379	CV3348529	single nucleotide variant	NM_014503.3(UTP20):c.7398T>A (p.Ser2466Arg)	not specified [RCV004477792]	uncertain significance	12	101379372	101379372	Human		name
405801381	CV3348530	single nucleotide variant	NM_014503.3(UTP20):c.7669T>G (p.Leu2557Val)	not specified [RCV004477793]	uncertain significance	12	101383053	101383053	Human		name
405801382	CV3348531	single nucleotide variant	NM_014503.3(UTP20):c.7882C>T (p.Arg2628Trp)	not specified [RCV004477794]	uncertain significance	12	101383266	101383266	Human		name
405801384	CV3348532	single nucleotide variant	NM_014503.3(UTP20):c.7979T>C (p.Ile2660Thr)	not specified [RCV004477795]	uncertain significance	12	101383592	101383592	Human		name
405801386	CV3348533	single nucleotide variant	NM_014503.3(UTP20):c.8279A>G (p.Lys2760Arg)	not specified [RCV004477796]	uncertain significance	12	101386044	101386044	Human		name
405801388	CV3348534	single nucleotide variant	NM_014503.3(UTP20):c.8353G>C (p.Glu2785Gln)	not specified [RCV004477797]	uncertain significance	12	101386118	101386118	Human		name
407529143	CV3487803	single nucleotide variant	NM_014503.3(UTP20):c.7967T>C (p.Met2656Thr)	not specified [RCV004680751]	uncertain significance	12	101383580	101383580	Human		name
407529147	CV3487805	single nucleotide variant	NM_014503.3(UTP20):c.5752G>A (p.Val1918Ile)	not specified [RCV004680753]	uncertain significance	12	101362022	101362022	Human		name
407529149	CV3487806	single nucleotide variant	NM_014503.3(UTP20):c.7510A>G (p.Asn2504Asp)	not specified [RCV004680754]	uncertain significance	12	101379484	101379484	Human		name
407529151	CV3487807	single nucleotide variant	NM_014503.3(UTP20):c.7549G>A (p.Ala2517Thr)	not specified [RCV004680755]	uncertain significance	12	101379523	101379523	Human		name
407529153	CV3487808	single nucleotide variant	NM_014503.3(UTP20):c.5893T>C (p.Tyr1965His)	not specified [RCV004680756]	uncertain significance	12	101363678	101363678	Human		name
407529155	CV3487809	single nucleotide variant	NM_014503.3(UTP20):c.3007G>A (p.Ala1003Thr)	not specified [RCV004680757]	uncertain significance	12	101321595	101321595	Human		name
407529159	CV3487811	single nucleotide variant	NM_014503.3(UTP20):c.6255G>C (p.Glu2085Asp)	not specified [RCV004680759]	uncertain significance	12	101366687	101366687	Human		name
407529167	CV3487816	single nucleotide variant	NM_014503.3(UTP20):c.7399C>T (p.His2467Tyr)	not specified [RCV004680763]	uncertain significance	12	101379373	101379373	Human		name
407529169	CV3487817	single nucleotide variant	NM_014503.3(UTP20):c.7883G>A (p.Arg2628Gln)	not specified [RCV004680764]	uncertain significance	12	101383267	101383267	Human		name
407529172	CV3487818	single nucleotide variant	NM_014503.3(UTP20):c.4040A>C (p.Glu1347Ala)	not specified [RCV004680765]	uncertain significance	12	101340549	101340549	Human		name
407529174	CV3487819	single nucleotide variant	NM_014503.3(UTP20):c.5488C>A (p.Leu1830Ile)	not specified [RCV004680766]	uncertain significance	12	101356647	101356647	Human		name
407529178	CV3487821	single nucleotide variant	NM_014503.3(UTP20):c.5545A>G (p.Lys1849Glu)	not specified [RCV004680768]	uncertain significance	12	101356936	101356936	Human		name
407529181	CV3487823	single nucleotide variant	NM_014503.3(UTP20):c.3271T>G (p.Leu1091Val)	not specified [RCV004680770]	uncertain significance	12	101329303	101329303	Human		name
407464704	CV3487824	single nucleotide variant	NM_014503.3(UTP20):c.5272A>G (p.Ile1758Val)	not specified [RCV004688576]	uncertain significance	12	101354996	101354996	Human		name
407529183	CV3487825	single nucleotide variant	NM_014503.3(UTP20):c.6214G>T (p.Ala2072Ser)	not specified [RCV004680771]	uncertain significance	12	101366646	101366646	Human		name
407529187	CV3487827	single nucleotide variant	NM_014503.3(UTP20):c.5004C>G (p.Ile1668Met)	not specified [RCV004680773]	uncertain significance	12	101352174	101352174	Human		name
597799347	CV3623406	single nucleotide variant	NM_014503.3(UTP20):c.3136G>T (p.Ala1046Ser)	not specified [RCV004879632]	uncertain significance	12	101327175	101327175	Human		name
597799349	CV3623407	single nucleotide variant	NM_014503.3(UTP20):c.3301C>T (p.Leu1101Phe)	not specified [RCV004879633]	uncertain significance	12	101329333	101329333	Human		name
597799357	CV3623411	single nucleotide variant	NM_014503.3(UTP20):c.3367C>G (p.Leu1123Val)	not specified [RCV004879637]	uncertain significance	12	101329399	101329399	Human		name
597799366	CV3623415	single nucleotide variant	NM_014503.3(UTP20):c.3457C>T (p.Arg1153Cys)	not specified [RCV004879641]	uncertain significance	12	101333340	101333340	Human		name
597697343	CV3623416	single nucleotide variant	NM_014503.3(UTP20):c.3286G>A (p.Gly1096Ser)	not specified [RCV004885257]	uncertain significance	12	101329318	101329318	Human		name
597803373	CV3623419	single nucleotide variant	NM_014503.3(UTP20):c.6535C>G (p.Leu2179Val)	not specified [RCV004881704]	uncertain significance	12	101369871	101369871	Human		name
597697364	CV3623420	single nucleotide variant	NM_014503.3(UTP20):c.4310A>G (p.Asp1437Gly)	not specified [RCV004885259]	uncertain significance	12	101342954	101342954	Human		name
597697375	CV3623421	single nucleotide variant	NM_014503.3(UTP20):c.5063A>G (p.His1688Arg)	not specified [RCV004885260]	uncertain significance	12	101353085	101353085	Human		name
597697384	CV3623422	single nucleotide variant	NM_014503.3(UTP20):c.6355A>G (p.Ile2119Val)	not specified [RCV004885261]	uncertain significance	12	101367947	101367947	Human		name
597697393	CV3623426	single nucleotide variant	NM_014503.3(UTP20):c.6866T>C (p.Leu2289Pro)	not specified [RCV004885262]	uncertain significance	12	101372951	101372951	Human		name
597697405	CV3623428	single nucleotide variant	NM_014503.3(UTP20):c.7531C>G (p.His2511Asp)	not specified [RCV004885263]	uncertain significance	12	101379505	101379505	Human		name
597803383	CV3623429	single nucleotide variant	NM_014503.3(UTP20):c.7743C>G (p.Asp2581Glu)	not specified [RCV004881709]	uncertain significance	12	101383127	101383127	Human		name
597803385	CV3623430	single nucleotide variant	NM_014503.3(UTP20):c.3467T>C (p.Ile1156Thr)	not specified [RCV004881710]	uncertain significance	12	101333350	101333350	Human		name
597803388	CV3623431	single nucleotide variant	NM_014503.3(UTP20):c.7603G>A (p.Ala2535Thr)	not specified [RCV004881711]	uncertain significance	12	101381158	101381158	Human		name
597803390	CV3623432	single nucleotide variant	NM_014503.3(UTP20):c.4856C>T (p.Thr1619Ile)	not specified [RCV004881712]	uncertain significance	12	101346560	101346560	Human		name
597803398	CV3623436	single nucleotide variant	NM_014503.3(UTP20):c.6245T>C (p.Ile2082Thr)	not specified [RCV004881716]	uncertain significance	12	101366677	101366677	Human		name
597697413	CV3623437	single nucleotide variant	NM_014503.3(UTP20):c.3649C>A (p.Pro1217Thr)	not specified [RCV004885264]	uncertain significance	12	101338058	101338058	Human		name
597803407	CV3623441	single nucleotide variant	NM_014503.3(UTP20):c.3364A>T (p.Ile1122Leu)	not specified [RCV004881720]	uncertain significance	12	101329396	101329396	Human		name
597803409	CV3632953	single nucleotide variant	NM_014503.3(UTP20):c.3826G>A (p.Val1276Ile)	not specified [RCV004881721]	uncertain significance	12	101338235	101338235	Human		name
597803412	CV3632955	single nucleotide variant	NM_014503.3(UTP20):c.5618T>C (p.Ile1873Thr)	not specified [RCV004881723]	uncertain significance	12	101357009	101357009	Human		name
597697441	CV3632957	single nucleotide variant	NM_014503.3(UTP20):c.7702G>A (p.Glu2568Lys)	not specified [RCV004885267]	uncertain significance	12	101383086	101383086	Human		name
597803416	CV3632959	single nucleotide variant	NM_014503.3(UTP20):c.4895T>C (p.Ile1632Thr)	not specified [RCV004881725]	uncertain significance	12	101352065	101352065	Human		name
597803421	CV3632961	single nucleotide variant	NM_014503.3(UTP20):c.6017G>A (p.Arg2006Gln)	not specified [RCV004881727]	uncertain significance	12	101365517	101365517	Human		name
597803423	CV3632962	single nucleotide variant	NM_014503.3(UTP20):c.6619C>G (p.Leu2207Val)	not specified [RCV004881728]	uncertain significance	12	101370495	101370495	Human		name
597803427	CV3632964	single nucleotide variant	NM_014503.3(UTP20):c.6541G>T (p.Val2181Phe)	not specified [RCV004881730]	uncertain significance	12	101369877	101369877	Human		name
598126552	CV3882001	single nucleotide variant	NM_014503.3(UTP20):c.4108G>A (p.Glu1370Lys)	not provided [RCV005233553]	uncertain significance	12	101342452	101342452	Human		name
598204844	CV3933076	single nucleotide variant	NM_014503.3(UTP20):c.7007A>G (p.Asn2336Ser)	not specified [RCV005290758]	uncertain significance	12	101373643	101373643	Human		name
598204853	CV3933078	single nucleotide variant	NM_014503.3(UTP20):c.7022C>T (p.Thr2341Met)	not specified [RCV005290759]	likely benign	12	101373658	101373658	Human		name
598204861	CV3933079	single nucleotide variant	NM_014503.3(UTP20):c.8090T>C (p.Ile2697Thr)	not specified [RCV005290760]	uncertain significance	12	101385616	101385616	Human		name
598204868	CV3933080	single nucleotide variant	NM_014503.3(UTP20):c.5821G>A (p.Ala1941Thr)	not specified [RCV005290761]	uncertain significance	12	101363606	101363606	Human		name
598204874	CV3933081	single nucleotide variant	NM_014503.3(UTP20):c.3759G>A (p.Met1253Ile)	not specified [RCV005290762]	uncertain significance	12	101338168	101338168	Human		name
598204880	CV3933082	single nucleotide variant	NM_014503.3(UTP20):c.3086A>T (p.Gln1029Leu)	not specified [RCV005290763]	uncertain significance	12	101327125	101327125	Human		name
598239396	CV3933085	single nucleotide variant	NM_014503.3(UTP20):c.5459G>A (p.Arg1820Gln)	not specified [RCV005296582]	uncertain significance	12	101356618	101356618	Human		name
598239407	CV3933087	single nucleotide variant	NM_014503.3(UTP20):c.6150T>G (p.Asp2050Glu)	not specified [RCV005296584]	uncertain significance	12	101366582	101366582	Human		name
598204904	CV3933089	single nucleotide variant	NM_014503.3(UTP20):c.7235A>G (p.Lys2412Arg)	not specified [RCV005290766]	uncertain significance	12	101374911	101374911	Human		name
598239417	CV3933091	single nucleotide variant	NM_014503.3(UTP20):c.5167G>A (p.Glu1723Lys)	not specified [RCV005296586]	uncertain significance	12	101354891	101354891	Human		name
598239427	CV3933093	single nucleotide variant	NM_014503.3(UTP20):c.5995A>C (p.Lys1999Gln)	not specified [RCV005296588]	uncertain significance	12	101365495	101365495	Human		name
598239432	CV3933094	single nucleotide variant	NM_014503.3(UTP20):c.3350C>T (p.Pro1117Leu)	not specified [RCV005296589]	uncertain significance	12	101329382	101329382	Human		name
598239438	CV3933095	single nucleotide variant	NM_014503.3(UTP20):c.5392A>G (p.Thr1798Ala)	not specified [RCV005296590]	uncertain significance	12	101355116	101355116	Human		name
598204915	CV3933096	single nucleotide variant	NM_014503.3(UTP20):c.4630A>G (p.Ile1544Val)	not specified [RCV005290768]	uncertain significance	12	101345578	101345578	Human		name
598204926	CV3933098	single nucleotide variant	NM_014503.3(UTP20):c.3949G>T (p.Ala1317Ser)	not specified [RCV005290770]	uncertain significance	12	101338893	101338893	Human		name
598239456	CV3933102	single nucleotide variant	NM_014503.3(UTP20):c.4308C>G (p.Phe1436Leu)	not specified [RCV005296593]	uncertain significance	12	101342952	101342952	Human		name
15201609	CV702058	single nucleotide variant	NM_014503.3(UTP20):c.6383A>G (p.Lys2128Arg)	not provided [RCV000957672]	benign	12	101367975	101367975	Human		name
15149036	CV724832	single nucleotide variant	NM_014503.3(UTP20):c.5713G>A (p.Val1905Ile)	not provided [RCV000879079]	likely benign	12	101361983	101361983	Human		name
15181692	CV724833	single nucleotide variant	NM_014503.3(UTP20):c.5801A>G (p.His1934Arg)	not provided [RCV000885823]	benign	12	101363586	101363586	Human		name
15181697	CV724834	single nucleotide variant	NM_014503.3(UTP20):c.5935A>G (p.Lys1979Glu)	not provided [RCV000885824]	benign	12	101363720	101363720	Human		name
15161298	CV738379	single nucleotide variant	NM_014503.3(UTP20):c.6517A>G (p.Arg2173Gly)	not provided [RCV000903319]	benign	12	101369853	101369853	Human		name

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