Tet1 Variant Search Result - Rat Genome Database

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183 records found for search term Tet1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401938352	CV2813225	single nucleotide variant	NM_030625.3(TET1):c.5053-3C>T	not provided [RCV003417448]	likely benign	10	68686353	68686353	Human		name
598225100	CV3920480	single nucleotide variant	NM_030625.3(TET1):c.16C>T (p.His6Tyr)	not specified [RCV005294230]	uncertain significance	10	68572354	68572354	Human		name
598164814	CV3920481	single nucleotide variant	NM_030625.3(TET1):c.20C>T (p.Ala7Val)	not specified [RCV005283360]	uncertain significance	10	68572358	68572358	Human		name
329360436	CV2458742	single nucleotide variant	NM_030625.3(TET1):c.38T>C (p.Val13Ala)	not specified [RCV004270179]	uncertain significance	10	68572376	68572376	Human		name
405285080	CV3202435	single nucleotide variant	NM_030625.3(TET1):c.732T>C (p.Ala244=)	TET1-related disorder [RCV003909701]	likely benign	10	68573070	68573070	Human		name , trait , alternate_id
15112675	CV767874	single nucleotide variant	NM_030625.3(TET1):c.516A>C (p.Leu172=)	TET1-related disorder [RCV003942951]\|not provided [RCV000938984]	benign\|likely benign	10	68572854	68572854	Human		name , trait , alternate_id
150434850	CV1244053	single nucleotide variant	NM_030625.3(TET1):c.2751G>A (p.Glu917=)	not provided [RCV001665260]	benign	10	68645480	68645480	Human	1	name
150434850	CV1244053	single nucleotide variant	NM_030625.3(TET1):c.2751G>A (p.Glu917=)	not provided [RCV001665260]	benign	10	68645480	68645481	Human	1	name
156302003	CV2241701	single nucleotide variant	NM_030625.3(TET1):c.242G>C (p.Arg81Pro)	not specified [RCV004106646]	uncertain significance	10	68572580	68572580	Human		name
156199274	CV2331266	single nucleotide variant	NM_030625.3(TET1):c.176A>G (p.Lys59Arg)	not specified [RCV004181867]	uncertain significance	10	68572514	68572514	Human		name
401892882	CV2758183	single nucleotide variant	NM_030625.3(TET1):c.253G>A (p.Asp85Asn)	not specified [RCV004341553]	uncertain significance	10	68572591	68572591	Human		name
401938351	CV2813224	single nucleotide variant	NM_030625.3(TET1):c.2823C>T (p.Leu941=)	not provided [RCV003417447]	likely benign	10	68645552	68645552	Human		name
405284680	CV3190467	single nucleotide variant	NM_030625.3(TET1):c.2298A>G (p.Leu766=)	TET1-related disorder [RCV003909276]	likely benign	10	68645027	68645027	Human		name , trait , alternate_id
405291755	CV3206098	single nucleotide variant	NM_030625.3(TET1):c.2328A>G (p.Lys776=)	TET1-related disorder [RCV003964177]	benign	10	68645057	68645057	Human		name , trait , alternate_id
405288084	CV3211137	single nucleotide variant	NM_030625.3(TET1):c.260C>G (p.Thr87Ser)	TET1-related disorder [RCV003924748]	likely benign	10	68572598	68572598	Human		name , trait , alternate_id
405283444	CV3218622	single nucleotide variant	NM_030625.3(TET1):c.1644C>T (p.Val548=)	TET1-related disorder [RCV003957392]	likely benign	10	68573982	68573982	Human		name , trait , alternate_id
405781710	CV3325116	single nucleotide variant	NM_030625.3(TET1):c.103A>G (p.Asn35Asp)	not specified [RCV004472073]	uncertain significance	10	68572441	68572441	Human		name
597783547	CV3609965	single nucleotide variant	NM_030625.3(TET1):c.257G>A (p.Arg86Lys)	not specified [RCV004874594]	uncertain significance	10	68572595	68572595	Human		name
597783556	CV3609967	single nucleotide variant	NM_030625.3(TET1):c.199C>T (p.Pro67Ser)	not specified [RCV004874596]	uncertain significance	10	68572537	68572537	Human		name
597783560	CV3609968	single nucleotide variant	NM_030625.3(TET1):c.171T>A (p.Asp57Glu)	not specified [RCV004874597]	uncertain significance	10	68572509	68572509	Human		name
15112682	CV767875	single nucleotide variant	NM_030625.3(TET1):c.2406C>T (p.Asn802=)	TET1-related disorder [RCV003970614]\|not provided [RCV000938985]	benign\|likely benign	10	68645135	68645135	Human		name , trait , alternate_id
156266064	CV2247106	single nucleotide variant	NM_030625.3(TET1):c.686C>T (p.Ser229Phe)	not specified [RCV004114642]	uncertain significance	10	68573024	68573024	Human		name
156183781	CV2292183	single nucleotide variant	NM_030625.3(TET1):c.788A>G (p.Gln263Arg)	not specified [RCV004148237]	uncertain significance	10	68573126	68573126	Human		name
156184370	CV2292228	single nucleotide variant	NM_030625.3(TET1):c.695C>T (p.Thr232Ile)	not specified [RCV004148270]	uncertain significance	10	68573033	68573033	Human		name
155906197	CV2393898	single nucleotide variant	NM_030625.3(TET1):c.664C>T (p.Arg222Cys)	not specified [RCV004233720]	likely benign	10	68573002	68573002	Human		name
329394351	CV2450152	single nucleotide variant	NM_030625.3(TET1):c.419G>A (p.Cys140Tyr)	not specified [RCV004270976]	uncertain significance	10	68572757	68572757	Human		name
401760756	CV2695149	single nucleotide variant	NM_030625.3(TET1):c.830T>C (p.Val277Ala)	not specified [RCV004303302]	uncertain significance	10	68573168	68573168	Human		name
401864640	CV2791212	single nucleotide variant	NM_030625.3(TET1):c.418T>C (p.Cys140Arg)	not specified [RCV004356853]	uncertain significance	10	68572756	68572756	Human		name
401938350	CV2813223	single nucleotide variant	NM_030625.3(TET1):c.775A>G (p.Lys259Glu)	not provided [RCV003417446]	uncertain significance	10	68573113	68573113	Human		name
405260400	CV3204005	single nucleotide variant	NM_030625.3(TET1):c.6084C>T (p.His2028=)	TET1-related disorder [RCV003943892]	likely benign	10	68691487	68691487	Human		name , trait , alternate_id
405290783	CV3207631	single nucleotide variant	NM_030625.3(TET1):c.5541C>T (p.Gly1847=)	TET1-related disorder [RCV003927197]	likely benign	10	68690944	68690944	Human		name , trait , alternate_id
405281638	CV3210085	single nucleotide variant	NM_030625.3(TET1):c.5916C>T (p.Asp1972=)	TET1-related disorder [RCV003907385]	likely benign	10	68691319	68691319	Human		name , trait , alternate_id
405282339	CV3212817	single nucleotide variant	NM_030625.3(TET1):c.4215C>T (p.Asn1405=)	TET1-related disorder [RCV003956961]	likely benign	10	68646944	68646944	Human		name , trait , alternate_id
405279412	CV3217504	single nucleotide variant	NM_030625.3(TET1):c.5106T>C (p.Asp1702=)	TET1-related disorder [RCV003976903]	likely benign	10	68686409	68686409	Human		name , trait , alternate_id
405271011	CV3218887	single nucleotide variant	NM_030625.3(TET1):c.5496G>A (p.Ser1832=)	TET1-related disorder [RCV003971633]	likely benign	10	68690899	68690899	Human		name , trait , alternate_id
405781839	CV3342418	single nucleotide variant	NM_030625.3(TET1):c.364G>A (p.Val122Ile)	not specified [RCV004472094]	likely benign	10	68572702	68572702	Human		name
405781863	CV3342422	single nucleotide variant	NM_030625.3(TET1):c.470C>T (p.Ser157Leu)	not specified [RCV004472098]	uncertain significance	10	68572808	68572808	Human		name
405781912	CV3342430	single nucleotide variant	NM_030625.3(TET1):c.629C>T (p.Ala210Val)	not specified [RCV004472106]	uncertain significance	10	68572967	68572967	Human		name
405781918	CV3342431	single nucleotide variant	NM_030625.3(TET1):c.778G>A (p.Val260Ile)	not specified [RCV004472107]	uncertain significance	10	68573116	68573116	Human		name
407519874	CV3482448	single nucleotide variant	NM_030625.3(TET1):c.899C>A (p.Ser300Tyr)	not specified [RCV004676732]	uncertain significance	10	68573237	68573237	Human		name
597783605	CV3609980	single nucleotide variant	NM_030625.3(TET1):c.944T>C (p.Leu315Ser)	not specified [RCV004874608]	uncertain significance	10	68573282	68573282	Human		name
15193600	CV701410	single nucleotide variant	NM_030625.3(TET1):c.5763C>T (p.Leu1921=)	not provided [RCV000955417]	benign	10	68691166	68691166	Human		name
15201443	CV701411	single nucleotide variant	NM_030625.3(TET1):c.5904G>A (p.Glu1968=)	not provided [RCV000957624]	benign	10	68691307	68691307	Human		name
15159355	CV701412	single nucleotide variant	NM_030625.3(TET1):c.6387G>A (p.Ala2129=)	not provided [RCV000947258]	benign	10	68691790	68691790	Human		name
15168212	CV712435	single nucleotide variant	NM_030625.3(TET1):c.4509G>C (p.Arg1503=)	TET1-related disorder [RCV003936124]\|not provided [RCV000971567]	benign	10	68667092	68667092	Human		name , trait , alternate_id
15169265	CV712436	single nucleotide variant	NM_030625.3(TET1):c.5235G>A (p.Thr1745=)	not provided [RCV000971777]	benign\|likely benign	10	68686538	68686538	Human		name
15117570	CV737557	single nucleotide variant	NM_030625.3(TET1):c.496C>T (p.Leu166Phe)	TET1-related disorder [RCV003940770]\|not provided [RCV000895400]	benign	10	68572834	68572834	Human		name , trait , alternate_id
156316270	CV2193031	single nucleotide variant	NM_030625.3(TET1):c.1534A>G (p.Thr512Ala)	not specified [RCV004069579]	uncertain significance	10	68573872	68573872	Human		name
155923294	CV2217600	single nucleotide variant	NM_030625.3(TET1):c.1444A>C (p.Asn482His)	not specified [RCV004090123]	uncertain significance	10	68573782	68573782	Human		name
155935179	CV2225517	single nucleotide variant	NM_030625.3(TET1):c.2288T>A (p.Val763Glu)	not specified [RCV004100904]	uncertain significance	10	68645017	68645017	Human		name
156084464	CV2249264	single nucleotide variant	NM_030625.3(TET1):c.2914G>T (p.Gly972Trp)	not specified [RCV004118296]	uncertain significance	10	68645643	68645643	Human		name
156121633	CV2276025	single nucleotide variant	NM_030625.3(TET1):c.2912A>G (p.Asn971Ser)	not specified [RCV004141702]	uncertain significance	10	68645641	68645641	Human		name
156240380	CV2286042	single nucleotide variant	NM_030625.3(TET1):c.1284C>G (p.Asp428Glu)	not specified [RCV004143942]	uncertain significance	10	68573622	68573622	Human		name
156065767	CV2317791	single nucleotide variant	NM_030625.3(TET1):c.2029T>A (p.Cys677Ser)	not specified [RCV004175040]	uncertain significance	10	68644758	68644758	Human		name
156258705	CV2322170	single nucleotide variant	NM_030625.3(TET1):c.1150G>T (p.Val384Phe)	not specified [RCV004175951]	uncertain significance	10	68573488	68573488	Human		name
156354166	CV2324218	single nucleotide variant	NM_030625.3(TET1):c.2198C>T (p.Ala733Val)	not specified [RCV004176958]	uncertain significance	10	68644927	68644927	Human		name
155920477	CV2343357	single nucleotide variant	NM_030625.3(TET1):c.2464G>A (p.Val822Ile)	not specified [RCV004194971]	uncertain significance	10	68645193	68645193	Human		name
156099362	CV2367377	single nucleotide variant	NM_030625.3(TET1):c.2164G>A (p.Val722Met)	not specified [RCV004209280]	uncertain significance	10	68644893	68644893	Human		name
156163037	CV2368371	single nucleotide variant	NM_030625.3(TET1):c.2164G>T (p.Val722Leu)	not specified [RCV004219145]	uncertain significance	10	68644893	68644893	Human		name
155954559	CV2389785	single nucleotide variant	NM_030625.3(TET1):c.1897G>A (p.Val633Ile)	not specified [RCV004236014]	uncertain significance	10	68574235	68574235	Human		name
156099218	CV2392847	single nucleotide variant	NM_030625.3(TET1):c.1277T>C (p.Val426Ala)	not specified [RCV004247206]	likely benign	10	68573615	68573615	Human		name
401747866	CV2698864	single nucleotide variant	NM_030625.3(TET1):c.2372A>T (p.Tyr791Phe)	not specified [RCV004301631]	uncertain significance	10	68645101	68645101	Human		name
401758373	CV2704468	single nucleotide variant	NM_030625.3(TET1):c.2759A>C (p.Glu920Ala)	not specified [RCV004313213]	uncertain significance	10	68645488	68645488	Human		name
401758376	CV2704470	single nucleotide variant	NM_030625.3(TET1):c.2760G>T (p.Glu920Asp)	not specified [RCV004313215]	uncertain significance	10	68645489	68645489	Human		name
401763749	CV2717109	single nucleotide variant	NM_030625.3(TET1):c.2030G>A (p.Cys677Tyr)	not specified [RCV004330124]	uncertain significance	10	68644759	68644759	Human		name
401892066	CV2777205	single nucleotide variant	NM_030625.3(TET1):c.2774G>A (p.Ser925Asn)	not specified [RCV004354240]	uncertain significance	10	68645503	68645503	Human		name
401875759	CV2789156	single nucleotide variant	NM_030625.3(TET1):c.1454A>C (p.Lys485Thr)	not specified [RCV004365206]	uncertain significance	10	68573792	68573792	Human		name
405781705	CV3325115	single nucleotide variant	NM_030625.3(TET1):c.1022C>T (p.Ala341Val)	not specified [RCV004472072]	uncertain significance	10	68573360	68573360	Human		name
405781715	CV3325117	single nucleotide variant	NM_030625.3(TET1):c.1043C>G (p.Ala348Gly)	not specified [RCV004472074]	uncertain significance	10	68573381	68573381	Human		name
405781721	CV3325118	single nucleotide variant	NM_030625.3(TET1):c.1822T>G (p.Tyr608Asp)	not specified [RCV004472075]	uncertain significance	10	68574160	68574160	Human		name
405781728	CV3325119	single nucleotide variant	NM_030625.3(TET1):c.2038G>T (p.Gly680Trp)	not specified [RCV004472076]	uncertain significance	10	68644767	68644767	Human		name
405781734	CV3325120	single nucleotide variant	NM_030625.3(TET1):c.2219A>G (p.Glu740Gly)	not specified [RCV004472077]	uncertain significance	10	68644948	68644948	Human		name
405781741	CV3325121	single nucleotide variant	NM_030625.3(TET1):c.2255T>G (p.Phe752Cys)	not specified [RCV004472078]	uncertain significance	10	68644984	68644984	Human		name
405781748	CV3325122	single nucleotide variant	NM_030625.3(TET1):c.2554G>A (p.Glu852Lys)	not specified [RCV004472079]	uncertain significance	10	68645283	68645283	Human		name
405781755	CV3325123	single nucleotide variant	NM_030625.3(TET1):c.2586A>G (p.Ile862Met)	not specified [RCV004472080]	uncertain significance	10	68645315	68645315	Human		name
405781760	CV3325124	single nucleotide variant	NM_030625.3(TET1):c.2746G>T (p.Asp916Tyr)	not specified [RCV004472081]	uncertain significance	10	68645475	68645475	Human		name
405781768	CV3325125	single nucleotide variant	NM_030625.3(TET1):c.2770G>C (p.Ala924Pro)	not specified [RCV004472082]	uncertain significance	10	68645499	68645499	Human		name
405781774	CV3325126	single nucleotide variant	NM_030625.3(TET1):c.2851C>A (p.Pro951Thr)	not specified [RCV004472083]	uncertain significance	10	68645580	68645580	Human		name
405781779	CV3325127	single nucleotide variant	NM_030625.3(TET1):c.2961C>A (p.Asn987Lys)	not specified [RCV004472084]	uncertain significance	10	68645690	68645690	Human		name
405781791	CV3325129	single nucleotide variant	NM_030625.3(TET1):c.2965G>A (p.Ala989Thr)	not specified [RCV004472086]	uncertain significance	10	68645694	68645694	Human		name
407518485	CV3482454	single nucleotide variant	NM_030625.3(TET1):c.1703T>C (p.Met568Thr)	not specified [RCV004675993]	uncertain significance	10	68574041	68574041	Human		name
407519880	CV3482456	single nucleotide variant	NM_030625.3(TET1):c.2003A>T (p.Lys668Met)	not specified [RCV004676735]	uncertain significance	10	68644732	68644732	Human		name
408367063	CV3511842	single nucleotide variant	NM_030625.3(TET1):c.2047C>G (p.Gln683Glu)	TET1-related disorder [RCV004757761]	likely benign	10	68644776	68644776	Human		name , trait , alternate_id
597783527	CV3609960	single nucleotide variant	NM_030625.3(TET1):c.2234G>A (p.Arg745Gln)	not specified [RCV004874589]	likely benign	10	68644963	68644963	Human		name
597783543	CV3609964	single nucleotide variant	NM_030625.3(TET1):c.2347G>A (p.Gly783Ser)	not specified [RCV004874593]	uncertain significance	10	68645076	68645076	Human		name
597783551	CV3609966	single nucleotide variant	NM_030625.3(TET1):c.1702A>G (p.Met568Val)	not specified [RCV004874595]	uncertain significance	10	68574040	68574040	Human		name
597783564	CV3609969	single nucleotide variant	NM_030625.3(TET1):c.2403A>C (p.Lys801Asn)	not specified [RCV004874598]	likely benign	10	68645132	68645132	Human		name
597783597	CV3609978	single nucleotide variant	NM_030625.3(TET1):c.2197G>A (p.Ala733Thr)	not specified [RCV004874606]	uncertain significance	10	68644926	68644926	Human		name
598225112	CV3920484	single nucleotide variant	NM_030625.3(TET1):c.1319T>C (p.Ile440Thr)	not specified [RCV005294232]	uncertain significance	10	68573657	68573657	Human		name
598225136	CV3920487	single nucleotide variant	NM_030625.3(TET1):c.1705G>A (p.Val569Ile)	not specified [RCV005294235]	uncertain significance	10	68574043	68574043	Human		name
598164827	CV3920488	single nucleotide variant	NM_030625.3(TET1):c.1538A>G (p.Gln513Arg)	not specified [RCV005283362]	uncertain significance	10	68573876	68573876	Human		name
15193596	CV701407	single nucleotide variant	NM_030625.3(TET1):c.1303G>A (p.Val435Ile)	not provided [RCV000955416]	benign	10	68573641	68573641	Human		name
15101519	CV701408	single nucleotide variant	NM_030625.3(TET1):c.2495G>A (p.Cys832Tyr)	not provided [RCV000959108]	benign	10	68645224	68645224	Human		name
15101523	CV701409	single nucleotide variant	NM_030625.3(TET1):c.2953G>T (p.Ala985Ser)	TET1-related disorder [RCV003926098]\|not provided [RCV000959109]	benign	10	68645682	68645682	Human		name , trait , alternate_id
15107327	CV712433	single nucleotide variant	NM_030625.3(TET1):c.2102G>A (p.Ser701Asn)	not provided [RCV000960268]	benign	10	68644831	68644831	Human		name
155946135	CV2238080	single nucleotide variant	NM_030625.3(TET1):c.3877A>T (p.Asn1293Tyr)	not specified [RCV004111100]	uncertain significance	10	68646606	68646606	Human		name
155989051	CV2251275	single nucleotide variant	NM_030625.3(TET1):c.5714G>A (p.Gly1905Asp)	not specified [RCV004115491]	uncertain significance	10	68691117	68691117	Human		name
156219584	CV2254068	single nucleotide variant	NM_030625.3(TET1):c.4910A>G (p.Asn1637Ser)	not specified [RCV004129516]	uncertain significance	10	68681484	68681484	Human		name
156171687	CV2267755	single nucleotide variant	NM_030625.3(TET1):c.3346T>C (p.Tyr1116His)	not specified [RCV004134286]	uncertain significance	10	68646075	68646075	Human		name
156232056	CV2273636	single nucleotide variant	NM_030625.3(TET1):c.3364A>G (p.Thr1122Ala)	not specified [RCV004132306]	uncertain significance	10	68646093	68646093	Human		name
155917880	CV2275096	single nucleotide variant	NM_030625.3(TET1):c.5165A>G (p.Lys1722Arg)	not specified [RCV004136905]	likely benign	10	68686468	68686468	Human		name
155967218	CV2280291	single nucleotide variant	NM_030625.3(TET1):c.5596G>C (p.Ala1866Pro)	not specified [RCV004140492]	uncertain significance	10	68690999	68690999	Human		name
155990062	CV2285202	single nucleotide variant	NM_030625.3(TET1):c.4067T>C (p.Val1356Ala)	not specified [RCV004145409]	uncertain significance	10	68646796	68646796	Human		name
156163564	CV2305512	single nucleotide variant	NM_030625.3(TET1):c.4046C>T (p.Ser1349Leu)	not specified [RCV004165223]	uncertain significance	10	68646775	68646775	Human		name
155912469	CV2308858	single nucleotide variant	NM_030625.3(TET1):c.5687C>T (p.Ala1896Val)	not specified [RCV004169157]	likely benign	10	68691090	68691090	Human		name
155951948	CV2309853	single nucleotide variant	NM_030625.3(TET1):c.3742C>G (p.Pro1248Ala)	not specified [RCV004160963]	uncertain significance	10	68646471	68646471	Human		name
155916240	CV2336112	single nucleotide variant	NM_030625.3(TET1):c.4040C>G (p.Pro1347Arg)	not specified [RCV004189707]	uncertain significance	10	68646769	68646769	Human		name
155924797	CV2348213	single nucleotide variant	NM_030625.3(TET1):c.5509G>A (p.Ala1837Thr)	not specified [RCV004191256]	uncertain significance	10	68690912	68690912	Human		name
156240935	CV2350379	single nucleotide variant	NM_030625.3(TET1):c.3545T>G (p.Met1182Arg)	not specified [RCV004202323]	uncertain significance	10	68646274	68646274	Human		name
156173890	CV2377133	single nucleotide variant	NM_030625.3(TET1):c.3508G>C (p.Glu1170Gln)	not specified [RCV004231811]	uncertain significance	10	68646237	68646237	Human		name
156091945	CV2389522	single nucleotide variant	NM_030625.3(TET1):c.5234C>T (p.Thr1745Met)	not specified [RCV004243596]	uncertain significance	10	68686537	68686537	Human		name
156005107	CV2393956	single nucleotide variant	NM_030625.3(TET1):c.3214C>A (p.Gln1072Lys)	not specified [RCV004236185]	likely benign	10	68645943	68645943	Human		name
156448753	CV2402164	single nucleotide variant	NM_030625.3(TET1):c.3974T>A (p.Val1325Asp)	not provided [RCV003120323]	uncertain significance	10	68646703	68646703	Human		name
329361889	CV2437788	single nucleotide variant	NM_030625.3(TET1):c.4085G>A (p.Gly1362Asp)	not specified [RCV004261088]	uncertain significance	10	68646814	68646814	Human		name
329360736	CV2439652	single nucleotide variant	NM_030625.3(TET1):c.3866C>T (p.Thr1289Met)	not specified [RCV004255667]	uncertain significance	10	68646595	68646595	Human		name
329371906	CV2454981	single nucleotide variant	NM_030625.3(TET1):c.4317C>G (p.His1439Gln)	not specified [RCV004272247]	uncertain significance	10	68651886	68651886	Human		name
329396755	CV2459008	single nucleotide variant	NM_030625.3(TET1):c.5776C>G (p.Pro1926Ala)	not specified [RCV004272487]	uncertain significance	10	68691179	68691179	Human		name
329399742	CV2467627	single nucleotide variant	NM_030625.3(TET1):c.5891C>T (p.Ser1964Phe)	not specified [RCV004287483]	uncertain significance	10	68691294	68691294	Human		name
329388937	CV2469645	single nucleotide variant	NM_030625.3(TET1):c.3091T>C (p.Cys1031Arg)	not specified [RCV004283068]	uncertain significance	10	68645820	68645820	Human		name
401741748	CV2676517	single nucleotide variant	NM_030625.3(TET1):c.3062T>C (p.Ile1021Thr)	not specified [RCV004288712]	uncertain significance	10	68645791	68645791	Human		name
401781664	CV2682087	single nucleotide variant	NM_030625.3(TET1):c.3826G>A (p.Ala1276Thr)	not specified [RCV004290148]	uncertain significance	10	68646555	68646555	Human		name
401754589	CV2682243	single nucleotide variant	NM_030625.3(TET1):c.5173A>G (p.Met1725Val)	not specified [RCV004297202]	uncertain significance	10	68686476	68686476	Human		name
401729039	CV2693999	single nucleotide variant	NM_030625.3(TET1):c.5060C>G (p.Thr1687Ser)	not specified [RCV004300285]	uncertain significance	10	68686363	68686363	Human		name
401747869	CV2698865	single nucleotide variant	NM_030625.3(TET1):c.5362A>G (p.Thr1788Ala)	not specified [RCV004301632]	uncertain significance	10	68686665	68686665	Human		name
401720198	CV2705749	single nucleotide variant	NM_030625.3(TET1):c.3840A>C (p.Lys1280Asn)	not specified [RCV004318587]	uncertain significance	10	68646569	68646569	Human		name
401779478	CV2731842	single nucleotide variant	NM_030625.3(TET1):c.3473G>A (p.Arg1158Gln)	not specified [RCV004333094]	uncertain significance	10	68646202	68646202	Human		name
401898849	CV2782756	single nucleotide variant	NM_030625.3(TET1):c.5994G>C (p.Glu1998Asp)	not specified [RCV004359754]	uncertain significance	10	68691397	68691397	Human		name
401943187	CV2839918	single nucleotide variant	NM_030625.3(TET1):c.5422G>A (p.Val1808Met)	TET1-related disorder [RCV003939050]\|not provided [RCV003456705]	likely benign	10	68690825	68690825	Human		name , trait , alternate_id
404994816	CV2851263	single nucleotide variant	NM_030625.3(TET1):c.5716G>A (p.Glu1906Lys)	not provided [RCV003491666]	uncertain significance	10	68691119	68691119	Human		name
405265917	CV3220971	single nucleotide variant	NM_030625.3(TET1):c.3998G>A (p.Arg1333Lys)	TET1-related disorder [RCV003969122]	likely benign	10	68646727	68646727	Human		name , trait , alternate_id
405781797	CV3325130	single nucleotide variant	NM_030625.3(TET1):c.3162C>G (p.Ser1054Arg)	not specified [RCV004472087]	uncertain significance	10	68645891	68645891	Human		name
405781803	CV3325131	single nucleotide variant	NM_030625.3(TET1):c.3205A>T (p.Thr1069Ser)	not specified [RCV004472088]	uncertain significance	10	68645934	68645934	Human		name
405781809	CV3325132	single nucleotide variant	NM_030625.3(TET1):c.3283C>T (p.Pro1095Ser)	not specified [RCV004472089]	likely benign	10	68646012	68646012	Human		name
405781815	CV3342414	single nucleotide variant	NM_030625.3(TET1):c.3448A>G (p.Thr1150Ala)	not specified [RCV004472090]	uncertain significance	10	68646177	68646177	Human		name
405781821	CV3342415	single nucleotide variant	NM_030625.3(TET1):c.3454T>C (p.Ser1152Pro)	not specified [RCV004472091]	uncertain significance	10	68646183	68646183	Human		name
405781828	CV3342416	single nucleotide variant	NM_030625.3(TET1):c.3502T>G (p.Tyr1168Asp)	not specified [RCV004472092]	uncertain significance	10	68646231	68646231	Human		name
405781833	CV3342417	single nucleotide variant	NM_030625.3(TET1):c.3518G>T (p.Arg1173Leu)	not specified [RCV004472093]	uncertain significance	10	68646247	68646247	Human		name
405781845	CV3342419	single nucleotide variant	NM_030625.3(TET1):c.3788T>C (p.Leu1263Pro)	not specified [RCV004472095]	uncertain significance	10	68646517	68646517	Human		name
405781852	CV3342420	single nucleotide variant	NM_030625.3(TET1):c.3982C>A (p.Gln1328Lys)	not specified [RCV004472096]	uncertain significance	10	68646711	68646711	Human		name
405781857	CV3342421	single nucleotide variant	NM_030625.3(TET1):c.3989T>C (p.Met1330Thr)	not specified [RCV004472097]	uncertain significance	10	68646718	68646718	Human		name
405781870	CV3342423	single nucleotide variant	NM_030625.3(TET1):c.5249C>T (p.Pro1750Leu)	not specified [RCV004472099]	uncertain significance	10	68686552	68686552	Human		name
405781875	CV3342424	single nucleotide variant	NM_030625.3(TET1):c.5270A>G (p.Lys1757Arg)	not specified [RCV004472100]	uncertain significance	10	68686573	68686573	Human		name
405781882	CV3342425	single nucleotide variant	NM_030625.3(TET1):c.5320G>C (p.Glu1774Gln)	not specified [RCV004472101]	uncertain significance	10	68686623	68686623	Human		name
405781888	CV3342426	single nucleotide variant	NM_030625.3(TET1):c.5324A>G (p.Lys1775Arg)	not specified [RCV004472102]	uncertain significance	10	68686627	68686627	Human		name
405781896	CV3342427	single nucleotide variant	NM_030625.3(TET1):c.5365A>C (p.Thr1789Pro)	not specified [RCV004472103]	uncertain significance	10	68686668	68686668	Human		name
405781900	CV3342428	single nucleotide variant	NM_030625.3(TET1):c.5630G>A (p.Ser1877Asn)	not specified [RCV004472104]	uncertain significance	10	68691033	68691033	Human		name
405781906	CV3342429	single nucleotide variant	NM_030625.3(TET1):c.5654C>T (p.Ser1885Leu)	not specified [RCV004472105]	likely benign	10	68691057	68691057	Human		name
407518469	CV3482447	single nucleotide variant	NM_030625.3(TET1):c.5659A>G (p.Arg1887Gly)	not specified [RCV004675988]	uncertain significance	10	68691062	68691062	Human		name
407518472	CV3482449	single nucleotide variant	NM_030625.3(TET1):c.3442A>C (p.Lys1148Gln)	not specified [RCV004675989]	uncertain significance	10	68646171	68646171	Human		name
407518475	CV3482450	single nucleotide variant	NM_030625.3(TET1):c.4841A>G (p.Asp1614Gly)	not specified [RCV004675990]	uncertain significance	10	68681415	68681415	Human		name
407518478	CV3482451	single nucleotide variant	NM_030625.3(TET1):c.4661C>A (p.Thr1554Asn)	not specified [RCV004675991]	uncertain significance	10	68667244	68667244	Human		name
407518482	CV3482452	single nucleotide variant	NM_030625.3(TET1):c.6041C>G (p.Ala2014Gly)	not specified [RCV004675992]	uncertain significance	10	68691444	68691444	Human		name
407519876	CV3482453	single nucleotide variant	NM_030625.3(TET1):c.5264G>T (p.Gly1755Val)	not specified [RCV004676733]	uncertain significance	10	68686567	68686567	Human		name
407519878	CV3482455	single nucleotide variant	NM_030625.3(TET1):c.5167G>C (p.Glu1723Gln)	not specified [RCV004676734]	uncertain significance	10	68686470	68686470	Human		name
407518488	CV3482458	single nucleotide variant	NM_030625.3(TET1):c.5953G>C (p.Glu1985Gln)	not specified [RCV004675994]	uncertain significance	10	68691356	68691356	Human		name
407518492	CV3482459	single nucleotide variant	NM_030625.3(TET1):c.3218T>C (p.Ile1073Thr)	not specified [RCV004675995]	uncertain significance	10	68645947	68645947	Human		name
408383878	CV3505970	single nucleotide variant	NM_030625.3(TET1):c.5822A>T (p.His1941Leu)	TET1-related disorder [RCV004731358]	uncertain significance	10	68691225	68691225	Human		name , trait , alternate_id
597783531	CV3609961	single nucleotide variant	NM_030625.3(TET1):c.3287A>C (p.Glu1096Ala)	not specified [RCV004874590]	uncertain significance	10	68646016	68646016	Human		name
597783535	CV3609962	single nucleotide variant	NM_030625.3(TET1):c.4915G>C (p.Val1639Leu)	not specified [RCV004874591]	uncertain significance	10	68682836	68682836	Human		name
597783539	CV3609963	single nucleotide variant	NM_030625.3(TET1):c.6116A>G (p.Asn2039Ser)	not specified [RCV004874592]	uncertain significance	10	68691519	68691519	Human		name
597783567	CV3609971	single nucleotide variant	NM_030625.3(TET1):c.5636C>A (p.Pro1879His)	not specified [RCV004874599]	uncertain significance	10	68691039	68691039	Human		name
597783571	CV3609972	single nucleotide variant	NM_030625.3(TET1):c.5843C>G (p.Ser1948Cys)	not specified [RCV004874600]	uncertain significance	10	68691246	68691246	Human		name
597783575	CV3609973	single nucleotide variant	NM_030625.3(TET1):c.3361G>T (p.Gly1121Cys)	not specified [RCV004874601]	uncertain significance	10	68646090	68646090	Human		name
597783580	CV3609974	single nucleotide variant	NM_030625.3(TET1):c.3529G>C (p.Glu1177Gln)	not specified [RCV004874602]	uncertain significance	10	68646258	68646258	Human		name
597783585	CV3609975	single nucleotide variant	NM_030625.3(TET1):c.6105C>A (p.His2035Gln)	not specified [RCV004874603]	uncertain significance	10	68691508	68691508	Human		name
597783589	CV3609976	single nucleotide variant	NM_030625.3(TET1):c.3821G>A (p.Gly1274Glu)	not specified [RCV004874604]	uncertain significance	10	68646550	68646550	Human		name
597783593	CV3609977	single nucleotide variant	NM_030625.3(TET1):c.4009T>A (p.Leu1337Met)	not specified [RCV004874605]	uncertain significance	10	68646738	68646738	Human		name
597783601	CV3609979	single nucleotide variant	NM_030625.3(TET1):c.5090G>C (p.Gly1697Ala)	not specified [RCV004874607]	uncertain significance	10	68686393	68686393	Human		name
597783612	CV3609982	single nucleotide variant	NM_030625.3(TET1):c.3475C>T (p.Arg1159Trp)	not specified [RCV004874610]	uncertain significance	10	68646204	68646204	Human		name
597783616	CV3609983	single nucleotide variant	NM_030625.3(TET1):c.6198T>G (p.Ile2066Met)	not specified [RCV004874611]	uncertain significance	10	68691601	68691601	Human		name
598225106	CV3920482	single nucleotide variant	NM_030625.3(TET1):c.4450A>G (p.Ile1484Val)	not specified [RCV005294231]	likely benign	10	68652583	68652583	Human		name
598164822	CV3920483	single nucleotide variant	NM_030625.3(TET1):c.5840C>T (p.Thr1947Ile)	not specified [RCV005283361]	uncertain significance	10	68691243	68691243	Human		name
598225120	CV3920485	single nucleotide variant	NM_030625.3(TET1):c.5573C>T (p.Thr1858Ile)	not specified [RCV005294233]	uncertain significance	10	68690976	68690976	Human		name
598225127	CV3920486	single nucleotide variant	NM_030625.3(TET1):c.5425C>A (p.Gln1809Lys)	not specified [RCV005294234]	uncertain significance	10	68690828	68690828	Human		name
598225142	CV3920489	single nucleotide variant	NM_030625.3(TET1):c.3961T>G (p.Phe1321Val)	not specified [RCV005294236]	uncertain significance	10	68646690	68646690	Human		name
598225148	CV3920490	single nucleotide variant	NM_030625.3(TET1):c.5649G>T (p.Met1883Ile)	not specified [RCV005294237]	uncertain significance	10	68691052	68691052	Human		name
598164833	CV3920491	single nucleotide variant	NM_030625.3(TET1):c.6299A>T (p.Glu2100Val)	not specified [RCV005283363]	uncertain significance	10	68691702	68691702	Human		name
598225155	CV3920492	single nucleotide variant	NM_030625.3(TET1):c.4372G>C (p.Gly1458Arg)	not specified [RCV005294238]	uncertain significance	10	68652505	68652505	Human		name
598225161	CV3920493	single nucleotide variant	NM_030625.3(TET1):c.5696C>T (p.Pro1899Leu)	not specified [RCV005294239]	uncertain significance	10	68691099	68691099	Human		name
598164839	CV3920494	single nucleotide variant	NM_030625.3(TET1):c.5492A>G (p.Tyr1831Cys)	not specified [RCV005283364]	uncertain significance	10	68690895	68690895	Human		name
15138054	CV712434	single nucleotide variant	NM_030625.3(TET1):c.4261A>G (p.Thr1421Ala)	TET1-related disorder [RCV003926263]\|not provided [RCV000965723]	benign	10	68646990	68646990	Human		name , trait , alternate_id
15196917	CV724017	single nucleotide variant	NM_030625.3(TET1):c.5378G>A (p.Ser1793Asn)	not provided [RCV000889904]	benign	10	68686681	68686681	Human		name
596947451	CV3549006	microsatellite	NM_030625.3(TET1):c.3332_3336del (p.Asn1111fs)	not provided [RCV004811330]	uncertain significance	10	68646056	68646060	Human		name

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