Taf15 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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186 records found for search term Taf15

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150411484	CV1178150	single nucleotide variant	NM_139215.3(TAF15):c.8-17C>A	not provided [RCV001547186]	likely benign	17	35817699	35817699	Human		name
150418953	CV1181508	single nucleotide variant	NM_139215.3(TAF15):c.8-202A>G	not provided [RCV001550824]	likely benign	17	35817514	35817514	Human		name
150488622	CV1208284	single nucleotide variant	NM_139215.3(TAF15):c.7+288G>A	not provided [RCV001592144]	likely benign	17	35809864	35809864	Human		name
150498340	CV1271494	single nucleotide variant	NM_139215.3(TAF15):c.8-260A>G	not provided [RCV001689184]	benign	17	35817456	35817456	Human		name
405275046	CV3204564	single nucleotide variant	NM_139215.3(TAF15):c.673+6G>C	TAF15-related disorder [RCV003951981]	likely benign	17	35834604	35834604	Human		name , trait , alternate_id
408372694	CV3511902	single nucleotide variant	NM_139215.3(TAF15):c.484+6A>G	TAF15-related disorder [RCV004743795]	likely benign	17	35822839	35822839	Human		name , trait , alternate_id
15176429	CV744963	single nucleotide variant	NM_139215.3(TAF15):c.485-4G>C	TAF15-related disorder [RCV003923081]\|not provided [RCV000906427]	benign\|likely benign	17	35824074	35824074	Human	1	name , trait , alternate_id
150416640	CV1181509	single nucleotide variant	NM_139215.3(TAF15):c.641-29T>C	not provided [RCV001549754]	likely benign	17	35834537	35834537	Human		name
150424913	CV1185245	single nucleotide variant	NM_139215.3(TAF15):c.913+37G>T	not provided [RCV001557304]	likely benign	17	35838590	35838590	Human		name
150504383	CV1211382	single nucleotide variant	NM_139215.3(TAF15):c.291-84G>A	not provided [RCV001595547]	benign	17	35822556	35822556	Human		name
150505659	CV1213581	duplication	NM_139215.3(TAF15):c.913+48dup	not provided [RCV001595837]	benign	17	35838597	35838598	Human		name
150508519	CV1214065	single nucleotide variant	NM_139215.3(TAF15):c.641-50T>C	not provided [RCV001596586]	likely benign	17	35834516	35834516	Human		name
150469752	CV1219126	duplication	NM_139215.3(TAF15):c.673+56dup	not provided [RCV001614878]	benign	17	35834644	35834645	Human		name
150482828	CV1223489	deletion	NM_139215.3(TAF15):c.673+56del	not provided [RCV001617202]	benign	17	35834645	35834645	Human		name
150443660	CV1249310	single nucleotide variant	NM_139215.3(TAF15):c.48-210C>A	not provided [RCV001666742]	benign	17	35819814	35819814	Human		name
150466170	CV1255695	duplication	NM_139215.3(TAF15):c.605+57dup	not provided [RCV001670329]	benign	17	35824241	35824242	Human		name
150521149	CV1290900	single nucleotide variant	NM_139215.3(TAF15):c.185-16C>T	not provided [RCV001732530]	likely benign	17	35820316	35820316	Human		name
405260085	CV3190155	single nucleotide variant	NM_139215.3(TAF15):c.913+10A>T	TAF15-related disorder [RCV003894558]	likely benign	17	35838563	35838563	Human		name , trait , alternate_id
405265683	CV3215596	single nucleotide variant	NM_139215.3(TAF15):c.1006+3A>G	TAF15-related disorder [RCV003946783]	likely benign	17	35842462	35842462	Human		name , trait , alternate_id
150331047	CV1172985	single nucleotide variant	NM_139215.3(TAF15):c.290+157G>A	not provided [RCV001538445]	likely benign	17	35820594	35820594	Human	1	name
150331047	CV1172985	single nucleotide variant	NM_139215.3(TAF15):c.290+157G>A	not provided [RCV001538445]	likely benign	17	35820594	35820595	Human	1	name
150336708	CV1172986	duplication	NM_139215.3(TAF15):c.291-278dup	not provided [RCV001541127]	benign	17	35822344	35822345	Human		name
150332648	CV1172987	single nucleotide variant	NM_139215.3(TAF15):c.606-147C>T	not provided [RCV001539137]	benign	17	35833760	35833760	Human		name
150428369	CV1188523	single nucleotide variant	NM_139215.3(TAF15):c.1089-25G>A	not provided [RCV001562174]	likely benign	17	35844255	35844255	Human		name
150406932	CV1191953	single nucleotide variant	NM_139215.3(TAF15):c.290+106A>T	not provided [RCV001564847]	likely benign	17	35820543	35820543	Human		name
150466333	CV1201227	single nucleotide variant	NM_139215.3(TAF15):c.674-294C>A	not provided [RCV001587707]	likely benign	17	35835838	35835838	Human		name
150449462	CV1202444	single nucleotide variant	NM_139215.3(TAF15):c.673+257C>A	not provided [RCV001585041]	likely benign	17	35834855	35834855	Human		name
150431073	CV1206228	deletion	NM_139215.3(TAF15):c.291-278del	not provided [RCV001580876]	likely benign	17	35822345	35822345	Human		name
150461309	CV1206444	single nucleotide variant	NM_139215.3(TAF15):c.1178-29G>A	not provided [RCV001586845]	likely benign	17	35844448	35844448	Human		name
150513806	CV1210701	single nucleotide variant	NM_139215.3(TAF15):c.914-216G>A	not provided [RCV001598742]	benign	17	35842151	35842151	Human		name
150505918	CV1213648	single nucleotide variant	NM_139215.3(TAF15):c.783+152T>A	not provided [RCV001595904]	benign	17	35836393	35836393	Human		name
150501384	CV1223691	single nucleotide variant	NM_139215.3(TAF15):c.291-142A>G	not provided [RCV001620812]	benign	17	35822498	35822498	Human		name
150434757	CV1231171	single nucleotide variant	NM_139215.3(TAF15):c.783+320G>A	not provided [RCV001643815]	benign	17	35836561	35836561	Human	1	name
150505941	CV1254746	single nucleotide variant	NM_139215.3(TAF15):c.1088+60A>G	not provided [RCV001678051]	benign	17	35844218	35844218	Human		name
150493174	CV1257500	deletion	NM_139215.3(TAF15):c.290+105del	not provided [RCV001675173]	benign	17	35820530	35820530	Human		name
150481564	CV1258941	single nucleotide variant	NM_139215.3(TAF15):c.485-178G>C	not provided [RCV001686071]	benign	17	35823900	35823900	Human		name
150456092	CV1259963	single nucleotide variant	NM_139215.3(TAF15):c.641-289G>A	not provided [RCV001681442]	benign	17	35834277	35834277	Human		name
150443614	CV1266419	single nucleotide variant	NM_139215.3(TAF15):c.485-107G>A	not provided [RCV001690855]	benign	17	35823971	35823971	Human		name
150447065	CV1270251	single nucleotide variant	NM_139215.3(TAF15):c.783+142G>C	not provided [RCV001691385]	benign	17	35836383	35836383	Human		name
407530428	CV3478538	single nucleotide variant	NM_139215.3(TAF15):c.5C>T (p.Ser2Leu)	not specified [RCV004681902]	uncertain significance	17	35809574	35809574	Human		name
405271268	CV3202807	single nucleotide variant	NM_139215.3(TAF15):c.123G>A (p.Thr41=)	TAF15-related disorder [RCV003913873]	likely benign	17	35820187	35820187	Human		name , trait , alternate_id
150494448	CV1204834	deletion	NM_139215.3(TAF15):c.606-321_606-317del	not provided [RCV001593326]	likely benign	17	35833582	35833586	Human		name
150510329	CV1211571	single nucleotide variant	NM_139215.3(TAF15):c.660C>T (p.Pro220=)	TAF15-related disorder [RCV003956286]\|not provided [RCV001597363]	benign\|likely benign	17	35834585	35834585	Human	1	name , trait , alternate_id
408370005	CV3502968	single nucleotide variant	NM_139215.3(TAF15):c.59A>G (p.Tyr20Cys)	not provided [RCV004724089]	uncertain significance	17	35820035	35820035	Human		name
15177983	CV715385	single nucleotide variant	NM_139215.3(TAF15):c.876C>T (p.Asp292=)	TAF15-related disorder [RCV004743232]\|not provided [RCV000973556]	benign\|likely benign	17	35838516	35838516	Human	1	name , trait , alternate_id
15132282	CV740696	single nucleotide variant	NM_139215.3(TAF15):c.726G>A (p.Gly242=)	TAF15-related disorder [RCV003910702]\|not provided [RCV000897929]	benign\|likely benign	17	35836184	35836184	Human	1	name , trait , alternate_id
150485971	CV1223110	single nucleotide variant	NM_139215.3(TAF15):c.1344A>G (p.Gly448=)	TAF15-related disorder [RCV003948648]\|not provided [RCV001617823]	benign\|likely benign	17	35844643	35844643	Human	1	name , trait , alternate_id
150502359	CV1241227	single nucleotide variant	NM_139215.3(TAF15):c.1524C>T (p.Tyr508=)	TAF15-related disorder [RCV003975802]\|not provided [RCV001657123]	benign	17	35844823	35844823	Human	1	name , trait , alternate_id
150485724	CV1262154	single nucleotide variant	NM_139215.3(TAF15):c.1287A>G (p.Gly429=)	TAF15-related disorder [RCV003975943]\|not provided [RCV001686845]	benign	17	35844586	35844586	Human	2	name , trait , alternate_id
150485724	CV1262154	single nucleotide variant	NM_139215.3(TAF15):c.1287A>G (p.Gly429=)	TAF15-related disorder [RCV003975943]\|not provided [RCV001686845]	benign	17	35844586	35844587	Human	2	name , trait , alternate_id
150484974	CV1273874	single nucleotide variant	NM_139215.3(TAF15):c.1332C>T (p.Gly444=)	TAF15-related disorder [RCV003921345]\|not provided [RCV001698616]	benign\|likely benign	17	35844631	35844631	Human	1	name , trait , alternate_id
150549849	CV1299689	single nucleotide variant	NM_139215.3(TAF15):c.223C>G (p.Gln75Glu)	not provided [RCV001752615]	uncertain significance	17	35820370	35820370	Human		name
153303921	CV1690552	single nucleotide variant	NM_139215.3(TAF15):c.143A>G (p.Gln48Arg)	not provided [RCV002269596]	uncertain significance	17	35820207	35820207	Human		name
156055343	CV2243185	single nucleotide variant	NM_139215.3(TAF15):c.122C>T (p.Thr41Met)	not specified [RCV004110080]	uncertain significance	17	35820186	35820186	Human		name
329351538	CV2462088	single nucleotide variant	NM_139215.3(TAF15):c.248A>G (p.Tyr83Cys)	not specified [RCV004266119]	uncertain significance	17	35820395	35820395	Human		name
401798485	CV2742452	single nucleotide variant	NM_139215.3(TAF15):c.227G>T (p.Ser76Ile)	not provided [RCV003324896]	uncertain significance	17	35820374	35820374	Human		name
401903900	CV2811253	single nucleotide variant	NM_139215.3(TAF15):c.1392T>A (p.Gly464=)	not provided [RCV003419711]	likely benign	17	35844691	35844691	Human		name
401903902	CV2811254	single nucleotide variant	NM_139215.3(TAF15):c.1395G>A (p.Gly465=)	not provided [RCV003419712]	likely benign	17	35844694	35844694	Human		name
401914496	CV2811255	single nucleotide variant	NM_139215.3(TAF15):c.1399A>C (p.Arg467=)	not provided [RCV003428231]	likely benign	17	35844698	35844698	Human		name
401914494	CV2811256	single nucleotide variant	NM_139215.3(TAF15):c.1407C>T (p.Gly469=)	TAF15-related disorder [RCV003901050]\|not provided [RCV003428232]	likely benign	17	35844706	35844706	Human	1	name , trait , alternate_id
405256232	CV3203585	single nucleotide variant	NM_139215.3(TAF15):c.1371G>A (p.Gly457=)	TAF15-related disorder [RCV003939825]	likely benign	17	35844670	35844670	Human		name , trait , alternate_id
405274575	CV3208960	single nucleotide variant	NM_139215.3(TAF15):c.1380C>A (p.Gly460=)	TAF15-related disorder [RCV003951735]	likely benign	17	35844679	35844679	Human		name , trait , alternate_id
405262212	CV3212876	single nucleotide variant	NM_139215.3(TAF15):c.1383C>T (p.Gly461=)	TAF15-related disorder [RCV003944752]	likely benign	17	35844682	35844682	Human		name , trait , alternate_id
405265594	CV3215576	single nucleotide variant	NM_139215.3(TAF15):c.205G>T (p.Gly69Cys)	TAF15-related disorder [RCV003946764]	likely benign	17	35820352	35820352	Human		name , trait , alternate_id
405276924	CV3217685	single nucleotide variant	NM_139215.3(TAF15):c.1368T>A (p.Gly456=)	TAF15-related disorder [RCV003974750]	likely benign	17	35844667	35844667	Human		name , trait , alternate_id
408377504	CV3500759	single nucleotide variant	NM_139215.3(TAF15):c.1467C>T (p.Asp489=)	not provided [RCV004722409]	likely benign	17	35844766	35844766	Human		name
408372522	CV3510481	single nucleotide variant	NM_139215.3(TAF15):c.1320T>C (p.Asp440=)	TAF15-related disorder [RCV004743076]	likely benign	17	35844619	35844619	Human		name , trait , alternate_id
408372454	CV3510581	single nucleotide variant	NM_139215.3(TAF15):c.1095C>T (p.Cys365=)	TAF15-related disorder [RCV004743092]	likely benign	17	35844286	35844286	Human		name , trait , alternate_id
408372527	CV3511111	single nucleotide variant	NM_139215.3(TAF15):c.1248C>T (p.Gly416=)	TAF15-related disorder [RCV004743166]	likely benign	17	35844547	35844547	Human		name , trait , alternate_id
408373368	CV3515023	single nucleotide variant	NM_139215.3(TAF15):c.1473T>A (p.Gly491=)	TAF15-related disorder [RCV004744843]	likely benign	17	35844772	35844772	Human		name , trait , alternate_id
408373534	CV3515978	single nucleotide variant	NM_139215.3(TAF15):c.1431T>G (p.Gly477=)	TAF15-related disorder [RCV004745003]	likely benign	17	35844730	35844730	Human		name , trait , alternate_id
408373548	CV3516051	single nucleotide variant	NM_139215.3(TAF15):c.1428A>T (p.Gly476=)	TAF15-related disorder [RCV004745011]	likely benign	17	35844727	35844727	Human		name , trait , alternate_id
408371998	CV3517666	single nucleotide variant	NM_139215.3(TAF15):c.269A>G (p.Gln90Arg)	TAF15-related disorder [RCV004742135]\|not specified [RCV004867940]	uncertain significance	17	35820416	35820416	Human	1	name , trait , alternate_id
596947695	CV3547276	single nucleotide variant	NM_139215.3(TAF15):c.1545T>C (p.Tyr515=)	not provided [RCV004811580]	likely benign	17	35844844	35844844	Human		name
596947812	CV3547396	single nucleotide variant	NM_139215.3(TAF15):c.1563C>T (p.Gly521=)	not provided [RCV004811700]	likely benign	17	35844862	35844862	Human		name
598128813	CV3886611	single nucleotide variant	NM_139215.3(TAF15):c.1485T>A (p.Gly495=)	not provided [RCV005244271]	likely benign	17	35844784	35844784	Human		name
598128868	CV3886667	single nucleotide variant	NM_139215.3(TAF15):c.1491C>T (p.Asp497=)	not provided [RCV005244327]	likely benign	17	35844790	35844790	Human		name
598129023	CV3886826	single nucleotide variant	NM_139215.3(TAF15):c.1500C>T (p.Gly500=)	not provided [RCV005244486]	likely benign	17	35844799	35844799	Human		name
598129940	CV3887364	single nucleotide variant	NM_139215.3(TAF15):c.1479C>T (p.Gly493=)	not provided [RCV005245425]	likely benign	17	35844778	35844778	Human		name
598182034	CV3919872	single nucleotide variant	NM_139215.3(TAF15):c.284C>T (p.Ser95Leu)	not specified [RCV005286857]	uncertain significance	17	35820431	35820431	Human		name
617154576	CV4022307	single nucleotide variant	NM_139215.3(TAF15):c.151A>G (p.Ser51Gly)	not provided [RCV005429663]	uncertain significance	17	35820215	35820215	Human		name
14742622	CV656426	single nucleotide variant	NM_139215.3(TAF15):c.154G>A (p.Gly52Ser)	TAF15-related disorder [RCV003948034]\|not provided [RCV000841520]	likely benign	17	35820218	35820218	Human	1	name , trait , alternate_id
15152434	CV715386	single nucleotide variant	NM_139215.3(TAF15):c.1347C>T (p.Asp449=)	TAF15-related disorder [RCV003916254]\|not provided [RCV000968350]	benign\|likely benign	17	35844646	35844646	Human	1	name , trait , alternate_id
15152438	CV715387	single nucleotide variant	NM_139215.3(TAF15):c.1359T>C (p.Gly453=)	TAF15-related disorder [RCV003916255]\|not provided [RCV000968351]	benign\|likely benign	17	35844658	35844658	Human	1	name , trait , alternate_id
15180366	CV715389	single nucleotide variant	NM_139215.3(TAF15):c.1446T>C (p.Asp482=)	TAF15-related disorder [RCV003962913]\|not provided [RCV000974134]	benign	17	35844745	35844745	Human	1	name , trait , alternate_id
15152443	CV715390	single nucleotide variant	NM_139215.3(TAF15):c.1686A>C (p.Arg562=)	TAF15-related disorder [RCV003905950]\|not provided [RCV000968352]	benign\|likely benign	17	35844985	35844985	Human	1	name , trait , alternate_id
15166805	CV740697	single nucleotide variant	NM_139215.3(TAF15):c.1665T>A (p.Gly555=)	TAF15-related disorder [RCV003950630]\|not provided [RCV000904521]	likely benign	17	35844964	35844964	Human	1	name , trait , alternate_id
15201523	CV755790	single nucleotide variant	NM_139215.3(TAF15):c.1668C>T (p.Gly556=)	TAF15-related disorder [RCV003950779]\|not provided [RCV000913162]	likely benign	17	35844967	35844967	Human	1	name , trait , alternate_id
15194318	CV771444	single nucleotide variant	NM_139215.3(TAF15):c.1248C>A (p.Gly416=)	not provided [RCV000933609]	likely benign	17	35844547	35844547	Human		name
15099141	CV771445	single nucleotide variant	NM_139215.3(TAF15):c.1314C>T (p.Ser438=)	TAF15-related disorder [RCV003970602]\|not provided [RCV000936429]	likely benign	17	35844613	35844613	Human	1	name , trait , alternate_id
15171767	CV771446	single nucleotide variant	NM_139215.3(TAF15):c.1404A>C (p.Gly468=)	TAF15-related disorder [RCV003960465]\|not provided [RCV000927971]	likely benign	17	35844703	35844703	Human	1	name , trait , alternate_id
150549703	CV1299608	single nucleotide variant	NM_139215.3(TAF15):c.436C>A (p.Gln146Lys)	not provided [RCV001752534]	uncertain significance	17	35822785	35822785	Human		name
150527898	CV1300903	single nucleotide variant	NM_139215.3(TAF15):c.927T>A (p.His309Gln)	not provided [RCV001754763]	uncertain significance	17	35842380	35842380	Human		name
150550245	CV1302709	single nucleotide variant	NM_139215.3(TAF15):c.446A>G (p.Tyr149Cys)	not provided [RCV001752831]	uncertain significance	17	35822795	35822795	Human		name
156010685	CV2291057	single nucleotide variant	NM_139215.3(TAF15):c.314A>G (p.Tyr105Cys)	not specified [RCV004151589]	uncertain significance	17	35822663	35822663	Human		name
156383478	CV2361575	single nucleotide variant	NM_139215.3(TAF15):c.530A>G (p.Tyr177Cys)	not specified [RCV004221204]	uncertain significance	17	35824123	35824123	Human		name
329401470	CV2460931	single nucleotide variant	NM_139215.3(TAF15):c.598G>A (p.Gly200Arg)	not specified [RCV004265094]	uncertain significance	17	35824191	35824191	Human		name
401724776	CV2693415	single nucleotide variant	NM_139215.3(TAF15):c.389A>C (p.Asp130Ala)	not specified [RCV004295367]	uncertain significance	17	35822738	35822738	Human		name
401936493	CV2798590	single nucleotide variant	NM_139215.3(TAF15):c.934A>G (p.Ile312Val)	TAF15-related disorder [RCV003414505]\|not specified [RCV004867868]	uncertain significance	17	35842387	35842387	Human	1	name , trait , alternate_id
405277761	CV3196084	single nucleotide variant	NM_139215.3(TAF15):c.329A>G (p.Tyr110Cys)	TAF15-related disorder [RCV003904603]	uncertain significance	17	35822678	35822678	Human		name , trait , alternate_id
405262168	CV3220033	single nucleotide variant	NM_139215.3(TAF15):c.645C>G (p.His215Gln)	TAF15-related disorder [RCV003967179]	likely benign	17	35834570	35834570	Human		name , trait , alternate_id
405745374	CV3331398	single nucleotide variant	NM_139215.3(TAF15):c.416A>G (p.His139Arg)	not specified [RCV004466309]	uncertain significance	17	35822765	35822765	Human		name
405745383	CV3331399	single nucleotide variant	NM_139215.3(TAF15):c.782A>T (p.Lys261Met)	not specified [RCV004466310]	uncertain significance	17	35836240	35836240	Human		name
597781768	CV3615463	single nucleotide variant	NM_139215.3(TAF15):c.670G>T (p.Ala224Ser)	not specified [RCV004874151]	uncertain significance	17	35834595	35834595	Human		name
597794727	CV3615468	single nucleotide variant	NM_139215.3(TAF15):c.986G>C (p.Gly329Ala)	not specified [RCV004877952]	uncertain significance	17	35842439	35842439	Human		name
597781786	CV3615469	single nucleotide variant	NM_139215.3(TAF15):c.478A>C (p.Thr160Pro)	not specified [RCV004874155]	uncertain significance	17	35822827	35822827	Human		name
597715898	CV3708928	single nucleotide variant	NM_139215.3(TAF15):c.305C>T (p.Ala102Val)	Extraskeletal myxoid chondrosarcoma [RCV005010206]	uncertain significance	17	35822654	35822654	Human	1	name
598182030	CV3919871	single nucleotide variant	NM_139215.3(TAF15):c.379G>A (p.Gly127Ser)	not specified [RCV005286856]	uncertain significance	17	35822728	35822728	Human		name
15171321	CV740695	single nucleotide variant	NM_139215.3(TAF15):c.365A>G (p.Tyr122Cys)	TAF15-related disorder [RCV003950649]\|not provided [RCV000905444]	likely benign	17	35822714	35822714	Human	1	name , trait , alternate_id
150424228	CV1185247	single nucleotide variant	NM_139215.3(TAF15):c.1388A>G (p.Tyr463Cys)	not provided [RCV001556387]\|not specified [RCV004039310]	likely benign\|uncertain significance	17	35844687	35844687	Human		name
150453628	CV1205675	single nucleotide variant	NM_139215.3(TAF15):c.1364A>G (p.Tyr455Cys)	TAF15-related disorder [RCV004743554]\|not provided [RCV001585576]	likely benign\|uncertain significance	17	35844663	35844663	Human	1	name , trait , alternate_id
150497382	CV1219397	single nucleotide variant	NM_139215.3(TAF15):c.1163G>A (p.Arg388His)	TAF15-related disorder [RCV003941049]\|not provided [RCV001620066]	benign\|likely benign	17	35844354	35844354	Human	1	name , trait , alternate_id
150530710	CV1293471	single nucleotide variant	NM_139215.3(TAF15):c.1418G>A (p.Gly473Glu)	TAF15-related disorder [RCV003401674]\|not provided [RCV001756692]	uncertain significance	17	35844717	35844717	Human	1	name , trait , alternate_id
150528292	CV1301819	single nucleotide variant	NM_139215.3(TAF15):c.1358G>T (p.Gly453Val)	not provided [RCV001755191]	uncertain significance	17	35844657	35844657	Human		name
152980171	CV1675870	single nucleotide variant	NM_139215.3(TAF15):c.1172G>A (p.Gly391Glu)	not provided [RCV002244461]	uncertain significance	17	35844363	35844363	Human		name
155800568	CV1863695	single nucleotide variant	NM_139215.3(TAF15):c.1331G>A (p.Gly444Asp)	not provided [RCV002474118]	uncertain significance	17	35844630	35844630	Human		name
156145872	CV2196836	single nucleotide variant	NM_139215.3(TAF15):c.1448G>A (p.Arg483Gln)	TAF15-related disorder [RCV003404139]\|not specified [RCV004069845]	uncertain significance	17	35844747	35844747	Human	1	name , trait , alternate_id
155966457	CV2216683	single nucleotide variant	NM_139215.3(TAF15):c.1424G>A (p.Arg475Gln)	not specified [RCV004083137]	uncertain significance	17	35844723	35844723	Human		name
155932523	CV2232109	single nucleotide variant	NM_139215.3(TAF15):c.1603C>G (p.Arg535Gly)	not specified [RCV004093144]	uncertain significance	17	35844902	35844902	Human		name
156273259	CV2277709	single nucleotide variant	NM_139215.3(TAF15):c.1138A>T (p.Asn380Tyr)	not specified [RCV004147153]	uncertain significance	17	35844329	35844329	Human		name
156073954	CV2294691	single nucleotide variant	NM_139215.3(TAF15):c.1012G>A (p.Gly338Arg)	not specified [RCV004161936]	uncertain significance	17	35844082	35844082	Human		name
156356772	CV2318173	single nucleotide variant	NM_139215.3(TAF15):c.1324A>T (p.Ser442Cys)	not specified [RCV004179362]	uncertain significance	17	35844623	35844623	Human		name
156185710	CV2324681	single nucleotide variant	NM_139215.3(TAF15):c.1766A>G (p.Asn589Ser)	not specified [RCV004172925]	uncertain significance	17	35846932	35846932	Human		name
155980504	CV2343531	single nucleotide variant	NM_139215.3(TAF15):c.1604G>A (p.Arg535His)	TAF15-related disorder [RCV003410213]\|not specified [RCV004190567]	uncertain significance	17	35844903	35844903	Human	1	name , trait , alternate_id
156005639	CV2394033	single nucleotide variant	NM_139215.3(TAF15):c.1583G>A (p.Arg528Gln)	not specified [RCV004236251]	uncertain significance	17	35844882	35844882	Human		name
329366067	CV2438064	single nucleotide variant	NM_139215.3(TAF15):c.1447C>G (p.Arg483Gly)	not specified [RCV004256853]	uncertain significance	17	35844746	35844746	Human		name
329393947	CV2449979	single nucleotide variant	NM_139215.3(TAF15):c.1666G>A (p.Gly556Ser)	not specified [RCV004269043]	uncertain significance	17	35844965	35844965	Human		name
329364266	CV2467352	single nucleotide variant	NM_139215.3(TAF15):c.1564T>C (p.Tyr522His)	not specified [RCV004285142]	uncertain significance	17	35844863	35844863	Human		name
329392873	CV2469025	single nucleotide variant	NM_139215.3(TAF15):c.1412A>G (p.Tyr471Cys)	not specified [RCV004274275]	uncertain significance	17	35844711	35844711	Human		name
401727891	CV2678557	single nucleotide variant	NM_139215.3(TAF15):c.1096G>A (p.Gly366Arg)	not specified [RCV004292567]	uncertain significance	17	35844287	35844287	Human		name
401934623	CV2796146	single nucleotide variant	NM_139215.3(TAF15):c.1184G>A (p.Arg395Gln)	TAF15-related disorder [RCV003412046]\|not provided [RCV004798042]	uncertain significance	17	35844483	35844483	Human	1	name , trait , alternate_id
401934660	CV2796265	single nucleotide variant	NM_139215.3(TAF15):c.1222C>T (p.Arg408Cys)	TAF15-related disorder [RCV003412084]	uncertain significance	17	35844521	35844521	Human		name , trait , alternate_id
401903066	CV2797811	single nucleotide variant	NM_139215.3(TAF15):c.1535G>A (p.Arg512Gln)	TAF15-related disorder [RCV003419245]	uncertain significance	17	35844834	35844834	Human		name , trait , alternate_id
401903083	CV2797836	single nucleotide variant	NM_139215.3(TAF15):c.1588G>A (p.Gly530Ser)	TAF15-related disorder [RCV003419254]	uncertain significance	17	35844887	35844887	Human		name , trait , alternate_id
401933769	CV2799780	single nucleotide variant	NM_139215.3(TAF15):c.1634G>A (p.Arg545Gln)	TAF15-related disorder [RCV003410645]	uncertain significance	17	35844933	35844933	Human		name , trait , alternate_id
401923358	CV2803185	single nucleotide variant	NM_139215.3(TAF15):c.1667G>A (p.Gly556Asp)	TAF15-related disorder [RCV003404407]	uncertain significance	17	35844966	35844966	Human		name , trait , alternate_id
405267367	CV3205430	single nucleotide variant	NM_139215.3(TAF15):c.1384G>A (p.Gly462Ser)	TAF15-related disorder [RCV003947353]\|not provided [RCV005422455]	likely benign\|uncertain significance	17	35844683	35844683	Human	1	name , trait , alternate_id
407506342	CV3478537	single nucleotide variant	NM_139215.3(TAF15):c.1312A>G (p.Ser438Gly)	not specified [RCV004671090]	likely benign	17	35844611	35844611	Human		name
408372420	CV3510153	single nucleotide variant	NM_139215.3(TAF15):c.1357G>A (p.Gly453Ser)	TAF15-related disorder [RCV004743011]	uncertain significance	17	35844656	35844656	Human		name , trait , alternate_id
408372380	CV3510196	single nucleotide variant	NM_139215.3(TAF15):c.1739G>A (p.Arg580Lys)	TAF15-related disorder [RCV004743017]	uncertain significance	17	35845038	35845038	Human		name , trait , alternate_id
408372474	CV3510706	single nucleotide variant	NM_139215.3(TAF15):c.1009C>T (p.Arg337Cys)	TAF15-related disorder [RCV004743113]	uncertain significance	17	35844079	35844079	Human		name , trait , alternate_id
408373525	CV3515941	single nucleotide variant	NM_139215.3(TAF15):c.1457A>G (p.Tyr486Cys)	TAF15-related disorder [RCV004744994]	uncertain significance	17	35844756	35844756	Human		name , trait , alternate_id
596930874	CV3529715	single nucleotide variant	NM_139215.3(TAF15):c.1651G>A (p.Gly551Arg)	not provided [RCV004780764]	uncertain significance	17	35844950	35844950	Human		name
596933025	CV3539654	single nucleotide variant	NM_139215.3(TAF15):c.1315G>A (p.Gly439Arg)	not provided [RCV004794279]	uncertain significance	17	35844614	35844614	Human		name
596933026	CV3539655	single nucleotide variant	NM_139215.3(TAF15):c.1318G>A (p.Asp440Asn)	not provided [RCV004794280]	uncertain significance	17	35844617	35844617	Human		name
597632279	CV3552813	single nucleotide variant	NM_139215.3(TAF15):c.1151C>G (p.Pro384Arg)	not provided [RCV004823641]	uncertain significance	17	35844342	35844342	Human		name
597781764	CV3615462	single nucleotide variant	NM_139215.3(TAF15):c.1731G>T (p.Met577Ile)	not specified [RCV004874150]	uncertain significance	17	35845030	35845030	Human		name
597781773	CV3615464	single nucleotide variant	NM_139215.3(TAF15):c.1246G>A (p.Gly416Ser)	not specified [RCV004874152]	uncertain significance	17	35844545	35844545	Human		name
597781777	CV3615465	single nucleotide variant	NM_139215.3(TAF15):c.1363T>A (p.Tyr455Asn)	not specified [RCV004874153]	uncertain significance	17	35844662	35844662	Human		name
597781781	CV3615467	single nucleotide variant	NM_139215.3(TAF15):c.1016G>T (p.Gly339Val)	not specified [RCV004874154]	uncertain significance	17	35844086	35844086	Human		name
597781789	CV3615470	single nucleotide variant	NM_139215.3(TAF15):c.1616G>T (p.Ser539Ile)	not specified [RCV004874156]	uncertain significance	17	35844915	35844915	Human		name
598182038	CV3919873	single nucleotide variant	NM_139215.3(TAF15):c.1037T>C (p.Phe346Ser)	not specified [RCV005286858]	uncertain significance	17	35844107	35844107	Human		name
598182042	CV3919874	single nucleotide variant	NM_139215.3(TAF15):c.1424G>C (p.Arg475Pro)	not specified [RCV005286859]	uncertain significance	17	35844723	35844723	Human		name
598182051	CV3919876	single nucleotide variant	NM_139215.3(TAF15):c.1543T>G (p.Tyr515Asp)	not specified [RCV005286861]	uncertain significance	17	35844842	35844842	Human		name
598182055	CV3919877	single nucleotide variant	NM_139215.3(TAF15):c.1585G>A (p.Gly529Arg)	not specified [RCV005286862]	uncertain significance	17	35844884	35844884	Human		name
15110689	CV727118	single nucleotide variant	NM_139215.3(TAF15):c.1624G>A (p.Gly542Ser)	TAF15-related disorder [RCV003940753]\|not provided [RCV000894119]	benign	17	35844923	35844923	Human	1	name , trait , alternate_id
150428486	CV1188525	deletion	NM_139215.3(TAF15):c.1524_1544del (p.492GGYGGDR[4])	TAF15-related disorder [RCV003966194]\|not provided [RCV001562326]	benign\|likely benign	17	35844803	35844823	Human	1	name , trait , alternate_id
150446472	CV1201730	deletion	NM_139215.3(TAF15):c.1542_1562del (p.492GGYGGDR[4])	TAF15-related disorder [RCV003910911]\|not provided [RCV001584598]	likely benign	17	35844824	35844844	Human	1	name , trait , alternate_id
150514680	CV1228596	duplication	NM_139215.3(TAF15):c.1524_1544dup (p.492GGYGGDR[6])	TAF15-related disorder [RCV003968411]\|not provided [RCV001638584]	benign\|likely benign	17	35844802	35844803	Human	1	name , trait , alternate_id
405274849	CV3204441	deletion	NM_139215.3(TAF15):c.1446_1466del (p.479YGGDRGG[1])	TAF15-related disorder [RCV003951883]	likely benign	17	35844726	35844746	Human		name , trait , alternate_id
150429359	CV1188524	duplication	NM_139215.3(TAF15):c.1392_1415dup (p.454GYGGDRGG[5])	TAF15-related disorder [RCV003956251]\|not provided [RCV001563494]	likely benign	17	35844679	35844680	Human	1	name , trait , alternate_id
150529762	CV1293168	deletion	NM_139215.3(TAF15):c.1380_1403del (p.454GYGGDRGG[3])	TAF15-related disorder [RCV003941118]\|not provided [RCV001756386]	benign\|likely benign	17	35844659	35844682	Human	1	name , trait , alternate_id
401920534	CV2804100	deletion	NM_139215.3(TAF15):c.1407_1430del (p.454GYGGDRGG[3])	TAF15-related disorder [RCV003402665]	uncertain significance	17	35844699	35844722	Human		name , trait , alternate_id
405264361	CV3189932	deletion	NM_139215.3(TAF15):c.1674_1697del (p.557GYGGDRGG[1])	TAF15-related disorder [RCV003896977]	uncertain significance	17	35844968	35844991	Human		name , trait , alternate_id
405275308	CV3204763	deletion	NM_139215.3(TAF15):c.1692_1715del (p.557GYGGDRGG[1])	TAF15-related disorder [RCV003952144]	likely benign	17	35844974	35844997	Human		name , trait , alternate_id
408373010	CV3513819	deletion	NM_139215.3(TAF15):c.1368_1415del (p.454GYGGDRGG[2])	TAF15-related disorder [RCV004744121]	uncertain significance	17	35844659	35844706	Human		name , trait , alternate_id
150425155	CV1185246	duplication	NM_139215.3(TAF15):c.1344_1370dup (p.442SGGGYGGDR[3])	TAF15-related disorder [RCV003921216]\|not provided [RCV001557630]	likely benign	17	35844631	35844632	Human	1	name , trait , alternate_id
150450336	CV1232668	deletion	NM_139215.3(TAF15):c.1351_1377del (p.442SGGGYGGDR[1])	TAF15-related disorder [RCV003931256]\|not provided [RCV001647743]	benign\|likely benign	17	35844644	35844670	Human	1	name , trait , alternate_id
150553992	CV1298392	deletion	NM_139215.3(TAF15):c.1320_1346del (p.442SGGGYGGDR[1])	not provided [RCV001770591]	uncertain significance	17	35844614	35844640	Human		name
405271556	CV3209483	deletion	NM_139215.3(TAF15):c.1344_1370del (p.442SGGGYGGDR[1])	TAF15-related disorder [RCV003949798]	benign	17	35844632	35844658	Human		name , trait , alternate_id
405270460	CV3211454	deletion	NM_139215.3(TAF15):c.1332_1358del (p.442SGGGYGGDR[1])	TAF15-related disorder [RCV003949343]\|not provided [RCV004780688]	likely benign\|uncertain significance	17	35844620	35844646	Human	1	name , trait , alternate_id
150495759	CV1205897	deletion	NM_139215.3(TAF15):c.1287_1370del (p.Ser432_Arg459del)	not provided [RCV001593579]	uncertain significance	17	35844545	35844628	Human		name
150551368	CV1297328	duplication	NM_139215.3(TAF15):c.1269_1295dup (p.Gly424_Ser432dup)	TAF15-related disorder [RCV003948706]\|not provided [RCV001767010]	likely benign\|uncertain significance	17	35844547	35844548	Human	1	name , trait , alternate_id
401933959	CV2797814	deletion	NM_139215.3(TAF15):c.1605_1685del (p.Ser539_Gly565del)	TAF15-related disorder [RCV003410714]\|not provided [RCV003481505]	uncertain significance	17	35844887	35844967	Human	1	name , trait , alternate_id
405286176	CV3192073	deletion	NM_139215.3(TAF15):c.1269_1295del (p.Gly424_Ser432del)	TAF15-related disorder [RCV003923995]	likely benign	17	35844548	35844574	Human		name , trait , alternate_id
405270244	CV3198070	deletion	NM_139215.3(TAF15):c.1278_1304del (p.Tyr427_Gly435del)	TAF15-related disorder [RCV003899880]	likely benign	17	35844572	35844598	Human		name , trait , alternate_id
408365635	CV3500031	indel	NM_139215.3(TAF15):c.1338_1341delinsCAGC (p.Gly447Ser)	not provided [RCV004722074]	uncertain significance	17	35844637	35844640	Human		name
15168610	CV715388	deletion	NM_139215.3(TAF15):c.1392_1415del (p.454_461GYGGDRGG[3])	TAF15-related disorder [RCV003918470]\|not provided [RCV000971649]	benign	17	35844680	35844703	Human	1	name , trait , alternate_id
15200150	CV727117	deletion	NM_139215.3(TAF15):c.1422_1445del (p.454_461GYGGDRGG[3])	TAF15-related disorder [RCV003930789]\|not provided [RCV000890833]	benign\|likely benign	17	35844707	35844730	Human	1	name , trait , alternate_id
405262093	CV3220011	deletion	NM_139215.3(TAF15):c.1428_1472del (p.478GYGGDRGGYGGDRGG[1])	TAF15-related disorder [RCV003967159]\|not provided [RCV004759343]	likely benign\|uncertain significance	17	35844707	35844751	Human	1	name , trait , alternate_id
405258838	CV3215116	duplication	NM_139215.3(TAF15):c.1542_1562dup (p.Arg526_Ser527insGlyGlyTyrGlyGlyAspArg)	TAF15-related disorder [RCV003942171]	likely benign	17	35844823	35844824	Human		name , trait , alternate_id
408372614	CV3511543	duplication	NM_139215.3(TAF15):c.1380_1403dup (p.Gly485_Tyr486insGlyTyrGlyGlyAspArgGlyGly)	TAF15-related disorder [RCV004743744]	uncertain significance	17	35844658	35844659	Human		name , trait , alternate_id
405291714	CV3206048	duplication	NM_139215.3(TAF15):c.1351_1377dup (p.Arg459_Gly460insSerGlyGlyGlyTyrGlyGlyAspArg)	TAF15-related disorder [RCV003964136]	likely benign	17	35844643	35844644	Human		name , trait , alternate_id
405274487	CV3208795	duplication	NM_139215.3(TAF15):c.1332_1358dup (p.Arg459_Gly460insSerGlyGlyGlyTyrGlyGlyAspArg)	TAF15-related disorder [RCV003951600]\|not provided [RCV005052077]	likely benign\|uncertain significance	17	35844619	35844620	Human	1	name , trait , alternate_id
405261366	CV3209907	duplication	NM_139215.3(TAF15):c.1428_1472dup (p.Gly507_Tyr508insGlyTyrGlyGlyAspArgGlyGlyTyrGlyGlyAspArgGlyGly)	TAF15-related disorder [RCV003944509]	likely benign	17	35844706	35844707	Human		name , trait , alternate_id
401936201	CV2802829	microsatellite	NM_139215.3(TAF15):c.1542TTATGGAGGAGATCGAGGAGG[3] (p.Arg526_Ser527insGlyGlyTyrGlyGlyAspArgGlyGlyTyrGlyGlyAspArg)	TAF15-related disorder [RCV003414178]	uncertain significance	17	35844823	35844824	Human		name , trait , alternate_id

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