Brwd3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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804 records found for search term Brwd3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
13213421	CV430949	single nucleotide variant	NM_153252.5(BRWD3):c.-8G>C	not specified [RCV000499996]	uncertain significance	X	80809479	80809479	Human		name
596924431	CV3531827	deletion	NM_153252.4(BRWD3):c.593del	not provided [RCV004781389]	pathogenic	X	80744252	80744252	Human		name
126744572	CV1019090	single nucleotide variant	NM_153252.5(BRWD3):c.90+5G>A	Intellectual disability, X-linked 93 [RCV001330467]	uncertain significance	X	80809241	80809241	Human	1	name
11627270	CV349101	single nucleotide variant	NM_153252.5(BRWD3):c.*121C>G	Intellectual disability, X-linked 93 [RCV000278679]	uncertain significance	X	80676488	80676488	Human	1	name
28877928	CV903235	single nucleotide variant	NM_153252.5(BRWD3):c.*847G>A	Intellectual disability, X-linked 93 [RCV001166592]	uncertain significance	X	80675762	80675762	Human	1	name
28877932	CV903236	single nucleotide variant	NM_153252.5(BRWD3):c.*802A>G	Intellectual disability, X-linked 93 [RCV001166593]	uncertain significance	X	80675807	80675807	Human	1	name
38598639	CV903237	single nucleotide variant	NM_153252.5(BRWD3):c.*799C>A	Intellectual disability, X-linked 93 [RCV001253927]	uncertain significance	X	80675810	80675810	Human	1	name
38598640	CV903238	single nucleotide variant	NM_153252.5(BRWD3):c.*575G>T	Intellectual disability, X-linked 93 [RCV001253928]	benign	X	80676034	80676034	Human	1	name
28877935	CV903239	single nucleotide variant	NM_153252.5(BRWD3):c.*248C>T	Intellectual disability, X-linked 93 [RCV001166594]	uncertain significance	X	80676361	80676361	Human	1	name
28878144	CV903249	single nucleotide variant	NM_153252.5(BRWD3):c.-229C>T	Intellectual disability, X-linked 93 [RCV001166658]	benign	X	80809700	80809700	Human	1	name
28878149	CV903492	single nucleotide variant	NM_153252.5(BRWD3):c.-267C>T	Intellectual disability, X-linked 93 [RCV001166659]	uncertain significance	X	80809738	80809738	Human	1	name
127244085	CV1056813	single nucleotide variant	NM_153252.5(BRWD3):c.331+1G>A	not provided [RCV001377206]	likely pathogenic	X	80793621	80793621	Human		name
150331937	CV1173610	single nucleotide variant	NM_153252.5(BRWD3):c.91-94A>G	not provided [RCV001538838]	benign	X	80809136	80809136	Human		name
150411513	CV1182509	duplication	NM_153252.5(BRWD3):c.31+23dup	Intellectual disability, X-linked 93 [RCV001553919]\|not provided [RCV001673197]	benign	X	80809411	80809412	Human	1	name
150426689	CV1189173	single nucleotide variant	NM_153252.5(BRWD3):c.591+4A>C	not provided [RCV001559896]	uncertain significance	X	80745565	80745565	Human		name
156248145	CV1953642	single nucleotide variant	NM_153252.5(BRWD3):c.32-13C>T	not provided [RCV002576452]	benign	X	80809317	80809317	Human		name
156395774	CV1958920	single nucleotide variant	NM_153252.5(BRWD3):c.32-16C>T	not provided [RCV002584345]	likely benign	X	80809320	80809320	Human		name
156151698	CV2125005	single nucleotide variant	NM_153252.5(BRWD3):c.120+6G>T	not provided [RCV002928925]	uncertain significance	X	80809007	80809007	Human		name
405268292	CV3187009	single nucleotide variant	NM_153252.5(BRWD3):c.121-4C>T	not provided [RCV003887092]	uncertain significance	X	80808602	80808602	Human		name
11625058	CV339571	single nucleotide variant	NM_153252.5(BRWD3):c.*6640T>A	Intellectual disability, X-linked 93 [RCV000394522]	benign\|likely benign	X	80669969	80669969	Human	1	name
11618108	CV339572	single nucleotide variant	NM_153252.5(BRWD3):c.*6439G>A	Intellectual disability, X-linked 93 [RCV000310851]\|not provided [RCV003221964]	likely benign\|uncertain significance	X	80670170	80670170	Human	1	name
11613966	CV339575	single nucleotide variant	NM_153252.5(BRWD3):c.*5993G>C	Intellectual disability, X-linked 93 [RCV000273349]	benign	X	80670616	80670616	Human	1	name
11623450	CV339580	single nucleotide variant	NM_153252.5(BRWD3):c.*5333G>T	Intellectual disability, X-linked 93 [RCV000372780]	benign\|likely benign	X	80671276	80671276	Human	1	name
11619381	CV339584	single nucleotide variant	NM_153252.5(BRWD3):c.*5133G>T	Intellectual disability, X-linked 93 [RCV000324640]	benign\|likely benign	X	80671476	80671476	Human	1	name
11615685	CV339591	single nucleotide variant	NM_153252.5(BRWD3):c.*4194C>A	Intellectual disability, X-linked 93 [RCV000288046]\|not provided [RCV004703899]	likely benign	X	80672415	80672415	Human	1	name
11621169	CV339593	single nucleotide variant	NM_153252.5(BRWD3):c.*3850G>C	Intellectual disability, X-linked 93 [RCV000345459]\|not provided [RCV004713906]	benign	X	80672759	80672759	Human	1	name
11617444	CV339599	single nucleotide variant	NM_153252.5(BRWD3):c.*2626C>T	Intellectual disability, X-linked 93 [RCV000304344]	uncertain significance	X	80673983	80673983	Human	1	name
11619383	CV339600	single nucleotide variant	NM_153252.5(BRWD3):c.*1895C>G	Intellectual disability, X-linked 93 [RCV000325051]	uncertain significance	X	80674714	80674714	Human	1	name
11624134	CV339601	single nucleotide variant	NM_153252.5(BRWD3):c.*1703T>C	Intellectual disability, X-linked 93 [RCV000382019]	uncertain significance	X	80674906	80674906	Human	1	name
11624425	CV339603	single nucleotide variant	NM_153252.5(BRWD3):c.*1372T>A	Intellectual disability, X-linked 93 [RCV000386110]\|not provided [RCV004713910]	benign	X	80675237	80675237	Human	1	name
407426947	CV3411747	single nucleotide variant	NM_153252.5(BRWD3):c.431-5T>C	not provided [RCV004590925]	uncertain significance	X	80745734	80745734	Human		name
11630120	CV349050	single nucleotide variant	NM_153252.5(BRWD3):c.*6957C>G	Intellectual disability, X-linked 93 [RCV000341927]	uncertain significance	X	80669652	80669652	Human	1	name
11632107	CV349051	single nucleotide variant	NM_153252.5(BRWD3):c.*6197T>C	Intellectual disability, X-linked 93 [RCV000398724]	uncertain significance	X	80670412	80670412	Human	1	name
11629039	CV349056	single nucleotide variant	NM_153252.5(BRWD3):c.*6157C>T	Intellectual disability, X-linked 93 [RCV000314296]	benign	X	80670452	80670452	Human	1	name
11628981	CV349057	single nucleotide variant	NM_153252.5(BRWD3):c.*5790G>A	Intellectual disability, X-linked 93 [RCV000312200]\|not provided [RCV003437159]	likely benign\|uncertain significance	X	80670819	80670819	Human	1	name
11632121	CV349059	single nucleotide variant	NM_153252.5(BRWD3):c.*3787T>C	Intellectual disability, X-linked 93 [RCV000399001]	benign	X	80672822	80672822	Human	1	name
11628884	CV349062	single nucleotide variant	NM_153252.5(BRWD3):c.*3483G>A	Intellectual disability, X-linked 93 [RCV000311372]\|not provided [RCV004713907]	benign	X	80673126	80673126	Human	1	name
11630429	CV349065	single nucleotide variant	NM_153252.5(BRWD3):c.*3083G>T	Intellectual disability, X-linked 93 [RCV000349897]	uncertain significance	X	80673526	80673526	Human	1	name
11632205	CV349067	single nucleotide variant	NM_153252.5(BRWD3):c.*2877G>A	Intellectual disability, X-linked 93 [RCV000401149]\|not provided [RCV004696182]	likely benign\|uncertain significance	X	80673732	80673732	Human	1	name
11628366	CV349071	single nucleotide variant	NM_153252.5(BRWD3):c.*2831C>T	Intellectual disability, X-linked 93 [RCV000300650]\|not provided [RCV004713908]	benign	X	80673778	80673778	Human	1	name
11630859	CV349072	single nucleotide variant	NM_153252.5(BRWD3):c.*2594T>C	Intellectual disability, X-linked 93 [RCV000361422]	uncertain significance	X	80674015	80674015	Human	1	name
11629367	CV349075	single nucleotide variant	NM_153252.5(BRWD3):c.*2323G>A	Intellectual disability, X-linked 93 [RCV000321421]	benign\|likely benign	X	80674286	80674286	Human	1	name
11628063	CV349082	single nucleotide variant	NM_153252.5(BRWD3):c.*1592G>C	Intellectual disability, X-linked 93 [RCV000294816]	benign\|likely benign	X	80675017	80675017	Human	1	name
11629774	CV349093	single nucleotide variant	NM_153252.5(BRWD3):c.*1473T>A	Intellectual disability, X-linked 93 [RCV000333380]	uncertain significance	X	80675136	80675136	Human	1	name
11631555	CV352448	single nucleotide variant	NM_153252.5(BRWD3):c.*6902G>A	Intellectual disability, X-linked 93 [RCV000380586]	benign\|likely benign	X	80669707	80669707	Human	1	name
11627540	CV352449	single nucleotide variant	NM_153252.5(BRWD3):c.*6871G>T	Intellectual disability, X-linked 93 [RCV000283815]	likely benign\|uncertain significance	X	80669738	80669738	Human	1	name
11626371	CV352450	single nucleotide variant	NM_153252.5(BRWD3):c.*5481A>C	Intellectual disability, X-linked 93 [RCV000262882]\|not provided [RCV004713903]	benign	X	80671128	80671128	Human	1	name
11626607	CV352451	single nucleotide variant	NM_153252.5(BRWD3):c.*5264G>T	Intellectual disability, X-linked 93 [RCV000267167]	benign\|uncertain significance	X	80671345	80671345	Human	1	name
11631393	CV352452	single nucleotide variant	NM_153252.5(BRWD3):c.*4809T>G	Intellectual disability, X-linked 93 [RCV000376873]	benign\|likely benign	X	80671800	80671800	Human	1	name
11627620	CV352453	single nucleotide variant	NM_153252.5(BRWD3):c.*4581C>T	Intellectual disability, X-linked 93 [RCV000284648]	uncertain significance	X	80672028	80672028	Human	1	name
11630598	CV352454	single nucleotide variant	NM_153252.5(BRWD3):c.*2744A>G	Intellectual disability, X-linked 93 [RCV000353435]	likely benign	X	80673865	80673865	Human	1	name
11630965	CV352455	single nucleotide variant	NM_153252.5(BRWD3):c.*2154A>G	Intellectual disability, X-linked 93 [RCV000364544]\|not provided [RCV004696183]	likely benign\|uncertain significance	X	80674455	80674455	Human	1	name
11628028	CV352456	single nucleotide variant	NM_153252.5(BRWD3):c.*1036A>C	Intellectual disability, X-linked 93 [RCV000294164]\|not provided [RCV004713911]	benign	X	80675573	80675573	Human	1	name
11630094	CV352952	single nucleotide variant	NM_153252.5(BRWD3):c.*6862T>C	Intellectual disability, X-linked 93 [RCV000341194]	benign	X	80669747	80669747	Human	2	name
11630094	CV352952	single nucleotide variant	NM_153252.5(BRWD3):c.*6862T>C	Intellectual disability, X-linked 93 [RCV000341194]	benign	X	80669747	80669748	Human	2	name
11630226	CV352953	single nucleotide variant	NM_153252.5(BRWD3):c.*6248A>G	Intellectual disability, X-linked 93 [RCV000344697]	uncertain significance	X	80670361	80670361	Human	1	name
11631178	CV352954	duplication	NM_153252.5(BRWD3):c.*6025dup	Non-syndromic X-linked intellectual disability [RCV000370337]	likely benign	X	80670583	80670584	Human	1	name
11630639	CV352955	single nucleotide variant	NM_153252.5(BRWD3):c.*5514T>C	Intellectual disability, X-linked 93 [RCV000355293]	uncertain significance	X	80671095	80671095	Human	1	name
11629109	CV352956	single nucleotide variant	NM_153252.5(BRWD3):c.*5461T>G	Intellectual disability, X-linked 93 [RCV000315808]\|not provided [RCV004713904]	benign	X	80671148	80671148	Human	1	name
11630290	CV352957	single nucleotide variant	NM_153252.5(BRWD3):c.*4272C>T	Intellectual disability, X-linked 93 [RCV000346649]	benign\|likely benign	X	80672337	80672337	Human	1	name
11631657	CV352958	single nucleotide variant	NM_153252.5(BRWD3):c.*4223C>T	Intellectual disability, X-linked 93 [RCV000384804]\|not provided [RCV004713905]	benign	X	80672386	80672386	Human	1	name
11626304	CV352959	single nucleotide variant	NM_153252.5(BRWD3):c.*2710G>A	Intellectual disability, X-linked 93 [RCV000260924]	uncertain significance	X	80673899	80673899	Human	1	name
11626476	CV352960	single nucleotide variant	NM_153252.5(BRWD3):c.*2329A>T	Intellectual disability, X-linked 93 [RCV000263968]	uncertain significance	X	80674280	80674280	Human	1	name
11626937	CV352961	single nucleotide variant	NM_153252.5(BRWD3):c.*1992G>A	Intellectual disability, X-linked 93 [RCV000272289]\|not provided [RCV004713909]	benign\|likely benign	X	80674617	80674617	Human	1	name
11626796	CV352963	single nucleotide variant	NM_153252.5(BRWD3):c.814-8T>A	Intellectual disability, X-linked 93 [RCV000269755]	uncertain significance	X	80736096	80736096	Human	1	name
597916360	CV3737401	duplication	NM_153252.5(BRWD3):c.91-17dup	not provided [RCV005074190]	likely benign	X	80809058	80809059	Human		name
597917065	CV3737471	single nucleotide variant	NM_153252.5(BRWD3):c.986-7C>A	not provided [RCV005074260]	benign	X	80734225	80734225	Human		name
597841554	CV3752854	single nucleotide variant	NM_153252.5(BRWD3):c.915-8A>C	not provided [RCV005086583]	likely benign	X	80735205	80735205	Human		name
597943499	CV3812351	single nucleotide variant	NM_153252.5(BRWD3):c.32-12C>T	not provided [RCV005159561]	likely benign	X	80809316	80809316	Human		name
597926571	CV3855384	single nucleotide variant	NM_153252.5(BRWD3):c.331+6A>T	not provided [RCV005205983]	uncertain significance	X	80793616	80793616	Human		name
597867191	CV3861730	single nucleotide variant	NM_153252.5(BRWD3):c.986-3T>C	not provided [RCV005196871]	uncertain significance	X	80734221	80734221	Human		name
13510026	CV482266	single nucleotide variant	NM_153252.5(BRWD3):c.986-9A>G	not provided [RCV000579312]	uncertain significance	X	80734227	80734227	Human		name
13828331	CV581095	deletion	NM_153252.5(BRWD3):c.814-4del	Inborn genetic diseases [RCV002312345]\|not provided [RCV001672930]	benign	X	80736092	80736092	Human	1	name
13829028	CV581199	single nucleotide variant	NM_153252.5(BRWD3):c.814-4T>A	BRWD3-related disorder [RCV004535782]\|Inborn genetic diseases [RCV002314446]	likely benign\|uncertain significance	X	80736092	80736092	Human	2	name , trait , alternate_id
15146276	CV745398	single nucleotide variant	NM_153252.5(BRWD3):c.986-4C>T	not provided [RCV000900298]	likely benign	X	80734222	80734222	Human		name
25317071	CV805062	single nucleotide variant	NM_153252.5(BRWD3):c.592-3T>C	Intellectual disability, X-linked 93 [RCV001007815]	uncertain significance	X	80744256	80744256	Human	1	name
28883388	CV903216	single nucleotide variant	NM_153252.5(BRWD3):c.*6692A>G	Intellectual disability, X-linked 93 [RCV001168194]	uncertain significance	X	80669917	80669917	Human	1	name
28883392	CV903217	single nucleotide variant	NM_153252.5(BRWD3):c.*6451T>C	Intellectual disability, X-linked 93 [RCV001168195]	uncertain significance	X	80670158	80670158	Human	1	name
28883396	CV903218	single nucleotide variant	NM_153252.5(BRWD3):c.*6331C>G	Intellectual disability, X-linked 93 [RCV001168196]	benign	X	80670278	80670278	Human	1	name
28886037	CV903219	single nucleotide variant	NM_153252.5(BRWD3):c.*5773A>C	Intellectual disability, X-linked 93 [RCV001168948]\|not provided [RCV003438710]	likely benign\|uncertain significance	X	80670836	80670836	Human	1	name
28886040	CV903220	single nucleotide variant	NM_153252.5(BRWD3):c.*5741G>T	Intellectual disability, X-linked 93 [RCV001168949]	benign	X	80670868	80670868	Human	1	name
28876117	CV903221	single nucleotide variant	NM_153252.5(BRWD3):c.*5142A>G	Intellectual disability, X-linked 93 [RCV001166054]\|not provided [RCV003438698]	likely benign\|uncertain significance	X	80671467	80671467	Human	1	name
28876121	CV903222	single nucleotide variant	NM_153252.5(BRWD3):c.*4661A>G	Intellectual disability, X-linked 93 [RCV001166055]	uncertain significance	X	80671948	80671948	Human	1	name
28881426	CV903223	single nucleotide variant	NM_153252.5(BRWD3):c.*4139T>C	Intellectual disability, X-linked 93 [RCV001167623]	uncertain significance	X	80672470	80672470	Human	1	name
28881432	CV903224	single nucleotide variant	NM_153252.5(BRWD3):c.*3738A>G	Intellectual disability, X-linked 93 [RCV001167624]	uncertain significance	X	80672871	80672871	Human	1	name
28881434	CV903225	single nucleotide variant	NM_153252.5(BRWD3):c.*3594T>C	Intellectual disability, X-linked 93 [RCV001167625]	uncertain significance	X	80673015	80673015	Human	1	name
28883635	CV903226	single nucleotide variant	NM_153252.5(BRWD3):c.*3447G>A	Intellectual disability, X-linked 93 [RCV001168267]	benign	X	80673162	80673162	Human	1	name
28883638	CV903227	single nucleotide variant	NM_153252.5(BRWD3):c.*3377T>G	Intellectual disability, X-linked 93 [RCV001168268]	uncertain significance	X	80673232	80673232	Human	1	name
28883641	CV903228	single nucleotide variant	NM_153252.5(BRWD3):c.*3293C>A	Intellectual disability, X-linked 93 [RCV001168269]	uncertain significance	X	80673316	80673316	Human	1	name
28883645	CV903229	single nucleotide variant	NM_153252.5(BRWD3):c.*3252T>C	Intellectual disability, X-linked 93 [RCV001168270]	uncertain significance	X	80673357	80673357	Human	1	name
28883650	CV903230	single nucleotide variant	NM_153252.5(BRWD3):c.*2875A>G	Intellectual disability, X-linked 93 [RCV001168271]	uncertain significance	X	80673734	80673734	Human	1	name
28886246	CV903231	single nucleotide variant	NM_153252.5(BRWD3):c.*2723A>G	Intellectual disability, X-linked 93 [RCV001169008]	benign	X	80673886	80673886	Human	1	name
28886251	CV903232	single nucleotide variant	NM_153252.5(BRWD3):c.*2413T>A	Intellectual disability, X-linked 93 [RCV001169009]	uncertain significance	X	80674196	80674196	Human	1	name
28876300	CV903233	single nucleotide variant	NM_153252.5(BRWD3):c.*1820G>C	Intellectual disability, X-linked 93 [RCV001166104]	uncertain significance	X	80674789	80674789	Human	1	name
28876305	CV903234	single nucleotide variant	NM_153252.5(BRWD3):c.*1394G>C	Intellectual disability, X-linked 93 [RCV001166105]	uncertain significance	X	80675215	80675215	Human	1	name
8643429	CV102412	single nucleotide variant	NM_153252.5(BRWD3):c.813+10G>C	BRWD3-related disorder [RCV004529871]\|Intellectual disability, X-linked 93 [RCV000327216]\|not provided [RCV001588908]\|not specified [RCV000082671]	benign\|likely benign	X	80744022	80744022	Human	1	name , trait , alternate_id
150419383	CV1195824	single nucleotide variant	NM_153252.5(BRWD3):c.3729-1G>C	not provided [RCV001569661]	pathogenic	X	80689847	80689847	Human		name
150536763	CV1314263	single nucleotide variant	NM_153252.5(BRWD3):c.1522-1G>C	Intellectual disability, X-linked 93 [RCV001780688]	likely pathogenic	X	80723877	80723877	Human	1	name
151885602	CV1451780	single nucleotide variant	NM_153252.5(BRWD3):c.2835+5T>C	not provided [RCV002000517]	uncertain significance	X	80703475	80703475	Human		name
152039498	CV1592758	single nucleotide variant	NM_153252.5(BRWD3):c.4397+6A>G	not provided [RCV002188043]	benign	X	80682459	80682459	Human		name
155697206	CV1794010	single nucleotide variant	NM_153252.5(BRWD3):c.4006-8C>T	Inborn genetic diseases [RCV002375689]	uncertain significance	X	80685544	80685544	Human	1	name
155671412	CV1847571	single nucleotide variant	NM_153252.5(BRWD3):c.2232-3T>C	Inborn genetic diseases [RCV002420143]\|not provided [RCV003660960]	uncertain significance	X	80716253	80716253	Human	1	name
155799446	CV1862496	single nucleotide variant	NM_153252.5(BRWD3):c.1387-5T>C	Intellectual disability, X-linked 93 [RCV002471902]	uncertain significance	X	80725072	80725072	Human	1	name
156359523	CV1908337	single nucleotide variant	NM_153252.5(BRWD3):c.1386+9T>C	not provided [RCV002602398]	likely benign	X	80728743	80728743	Human		name
156116980	CV1952418	single nucleotide variant	NM_153252.5(BRWD3):c.431-13G>A	not provided [RCV002571712]	likely benign	X	80745742	80745742	Human		name
10049272	CV196349	duplication	NM_153252.5(BRWD3):c.814-16dup	Intellectual disability, X-linked 93 [RCV002485185]\|not provided [RCV001610500]\|not specified [RCV000180706]	benign\|likely benign	X	80736091	80736092	Human	1	name
156156264	CV1987799	single nucleotide variant	NM_153252.5(BRWD3):c.331+19A>G	not provided [RCV002642242]	likely benign	X	80793603	80793603	Human		name
156289849	CV1998130	single nucleotide variant	NM_153252.5(BRWD3):c.4398-3T>C	not provided [RCV002647149]	conflicting interpretations of pathogenicity\|uncertain significance	X	80682097	80682097	Human		name
156069525	CV2032517	single nucleotide variant	NM_153252.5(BRWD3):c.4655-8T>A	not provided [RCV002760277]	likely benign	X	80677371	80677371	Human		name
156020585	CV2040580	single nucleotide variant	NM_153252.5(BRWD3):c.915-16T>A	not provided [RCV002795565]	benign	X	80735213	80735213	Human		name
156287961	CV2047065	single nucleotide variant	NM_153252.5(BRWD3):c.3151+8T>C	not provided [RCV002770644]	likely benign	X	80695900	80695900	Human		name
156377394	CV2050577	single nucleotide variant	NM_153252.5(BRWD3):c.985+20G>C	not provided [RCV002814809]	likely benign	X	80735107	80735107	Human		name
156339372	CV2055268	single nucleotide variant	NM_153252.5(BRWD3):c.3152-6T>C	not provided [RCV002811112]	uncertain significance	X	80693057	80693057	Human		name
156149288	CV2128565	single nucleotide variant	NM_153252.5(BRWD3):c.1877-5T>C	not provided [RCV002928844]	likely benign	X	80719661	80719661	Human		name
156169267	CV2184915	deletion	NM_153252.5(BRWD3):c.180+14del	not provided [RCV003057168]	benign	X	80808525	80808525	Human		name
11525830	CV247209	single nucleotide variant	NM_153252.5(BRWD3):c.2325+5G>A	Inborn genetic diseases [RCV002311364]\|Intellectual disability, X-linked 93 [RCV000990889]\|not provided [RCV000890603]\|not specified [RCV000238931]	benign\|likely benign	X	80716152	80716152	Human	2	name
8561923	CV25841	single nucleotide variant	NM_153252.5(BRWD3):c.3325+1G>T	Intellectual disability, X-linked 93 [RCV000011549]	pathogenic	X	80692088	80692088	Human	1	name
401857082	CV2752089	single nucleotide variant	NM_153252.5(BRWD3):c.4006-1G>A	Intellectual disability, X-linked 93 [RCV003335966]	likely pathogenic	X	80685537	80685537	Human	1	name
401903643	CV2800058	single nucleotide variant	NM_153252.5(BRWD3):c.2721+5G>A	BRWD3-related disorder [RCV004536770]	uncertain significance	X	80704673	80704673	Human		name , trait , alternate_id
401916458	CV2831093	single nucleotide variant	NM_153252.5(BRWD3):c.2943+4A>G	not provided [RCV003443362]	uncertain significance	X	80699953	80699953	Human		name
405146662	CV2881514	single nucleotide variant	NM_153252.5(BRWD3):c.1086+7G>C	not provided [RCV003561415]	likely benign	X	80734111	80734111	Human		name
405236669	CV2884706	deletion	NM_153252.5(BRWD3):c.1127+6del	not provided [RCV003556538]	benign	X	80733450	80733450	Human		name
405219356	CV2903895	single nucleotide variant	NM_153252.5(BRWD3):c.2231+9A>G	not provided [RCV003568172]	likely benign	X	80717564	80717564	Human		name
405215085	CV2925279	single nucleotide variant	NM_153252.5(BRWD3):c.121-19C>A	not provided [RCV003567655]	likely benign	X	80808617	80808617	Human		name
405193303	CV2975065	single nucleotide variant	NM_153252.5(BRWD3):c.3808-5T>G	not provided [RCV003677407]	uncertain significance	X	80688130	80688130	Human		name
405195289	CV2975802	single nucleotide variant	NM_153252.5(BRWD3):c.1128-5T>C	not provided [RCV003677593]	likely benign	X	80730025	80730025	Human		name
405053741	CV3151351	single nucleotide variant	NM_153252.5(BRWD3):c.813+10G>A	not provided [RCV003849760]	likely benign	X	80744022	80744022	Human		name
405157086	CV3152561	single nucleotide variant	NM_153252.5(BRWD3):c.180+15C>A	not provided [RCV003840488]	benign	X	80808524	80808524	Human		name
405266966	CV3186740	single nucleotide variant	NM_153252.5(BRWD3):c.2232-4T>C	not provided [RCV003886821]	uncertain significance	X	80716254	80716254	Human		name
11620464	CV339605	microsatellite	NM_153252.5(BRWD3):c.*265AC[4]	Non-syndromic X-linked intellectual disability [RCV000337357]\|not provided [RCV001613251]	benign	X	80676333	80676336	Human		name
11631995	CV349099	microsatellite	NM_153252.5(BRWD3):c.*244CA[2]	Non-syndromic X-linked intellectual disability [RCV000395426]	uncertain significance	X	80676358	80676361	Human		name
11631280	CV349108	microsatellite	NM_153252.5(BRWD3):c.-239TC[6]	Non-syndromic X-linked intellectual disability [RCV000373735]\|not provided [RCV001643124]	benign	X	80809700	80809701	Human		name
11627407	CV352964	microsatellite	NM_153252.5(BRWD3):c.-265TC[7]	Non-syndromic X-linked intellectual disability [RCV000281658]	uncertain significance	X	80809721	80809722	Human		name
11665939	CV353868	microsatellite	NM_153252.5(BRWD3):c.-283CT[8]	Non-syndromic X-linked intellectual disability [RCV000303458]\|not provided [RCV001653779]	benign	X	80809737	80809738	Human		name
597839349	CV3758371	single nucleotide variant	NM_153252.5(BRWD3):c.1522-8A>G	not provided [RCV005086206]	benign	X	80723884	80723884	Human		name
597844075	CV3827404	single nucleotide variant	NM_153252.5(BRWD3):c.2325+3A>G	not provided [RCV005172675]	uncertain significance	X	80716154	80716154	Human		name
597857904	CV3850134	single nucleotide variant	NM_153252.5(BRWD3):c.3729-2A>G	not provided [RCV005195466]	likely pathogenic	X	80689848	80689848	Human		name
598126716	CV3882172	single nucleotide variant	NM_153252.5(BRWD3):c.3152-5T>A	not provided [RCV005233723]	uncertain significance	X	80693056	80693056	Human		name
598124862	CV3883711	single nucleotide variant	NM_153252.5(BRWD3):c.1876+5G>A	not provided [RCV005236065]	uncertain significance	X	80722557	80722557	Human		name
598222134	CV3893839	single nucleotide variant	NM_153252.5(BRWD3):c.814-17A>G	not provided [RCV005257082]	likely benign	X	80736105	80736105	Human		name
616939615	CV4014112	single nucleotide variant	NM_153252.5(BRWD3):c.4233+8T>A	not provided [RCV005413604]	likely benign	X	80684002	80684002	Human		name
617150263	CV4021690	single nucleotide variant	NM_153252.5(BRWD3):c.3264-1G>T	not provided [RCV005425659]	pathogenic	X	80692151	80692151	Human		name
13214158	CV430946	single nucleotide variant	NM_153252.5(BRWD3):c.4398-7C>T	not specified [RCV000500918]	uncertain significance	X	80682101	80682101	Human		name
13483761	CV446793	single nucleotide variant	NM_153252.5(BRWD3):c.2553-3C>G	not provided [RCV000522144]	uncertain significance	X	80704849	80704849	Human		name
15182449	CV731489	duplication	NM_153252.5(BRWD3):c.431-10dup	not provided [RCV000885994]	benign	X	80745732	80745733	Human		name
150405810	CV1178805	single nucleotide variant	NM_153252.5(BRWD3):c.2836-55A>T	not provided [RCV001545027]	likely benign	X	80700119	80700119	Human		name
150411507	CV1182507	single nucleotide variant	NM_153252.5(BRWD3):c.1087-23G>C	Intellectual disability, X-linked 93 [RCV001553917]\|not provided [RCV001619978]	benign	X	80733519	80733519	Human	1	name
150420570	CV1195825	single nucleotide variant	NM_153252.5(BRWD3):c.1386+76A>T	not provided [RCV001570178]	likely benign	X	80728676	80728676	Human		name
150418069	CV1199556	single nucleotide variant	NM_153252.5(BRWD3):c.4496-81A>T	not provided [RCV001576583]	likely benign	X	80681580	80681580	Human		name
150440262	CV1221423	single nucleotide variant	NM_153252.5(BRWD3):c.814-167G>A	not provided [RCV001610118]	benign	X	80736255	80736255	Human		name
150484322	CV1222466	single nucleotide variant	NM_153252.5(BRWD3):c.813+185T>A	not provided [RCV001617469]	benign	X	80743847	80743847	Human		name
8587665	CV122296	single nucleotide variant	NM_153252.4(BRWD3):c.985+341C>T	Lung cancer [RCV000102816]	uncertain significance	X	80734786	80734786	Human		name
150450503	CV1232688	deletion	NM_153252.5(BRWD3):c.4398-30del	not provided [RCV001647763]	benign	X	80682124	80682124	Human		name
150432114	CV1236654	single nucleotide variant	NM_153252.5(BRWD3):c.914+315C>T	not provided [RCV001642058]	benign	X	80735673	80735673	Human		name
150440824	CV1246636	duplication	NM_153252.5(BRWD3):c.914+167dup	not provided [RCV001666289]	benign	X	80735803	80735804	Human		name
150489822	CV1250924	single nucleotide variant	NM_153252.5(BRWD3):c.1651-46T>A	not provided [RCV001674591]	benign	X	80722833	80722833	Human		name
150483305	CV1261764	single nucleotide variant	NM_153252.5(BRWD3):c.4398-24G>A	not provided [RCV001686368]	benign	X	80682118	80682118	Human		name
150463400	CV1263800	single nucleotide variant	NM_153252.5(BRWD3):c.1650+57T>C	not provided [RCV001682501]	benign	X	80723691	80723691	Human		name
150460664	CV1264206	single nucleotide variant	NM_153252.5(BRWD3):c.331+123G>A	not provided [RCV001682123]	benign	X	80793499	80793499	Human		name
150441928	CV1264352	single nucleotide variant	NM_153252.5(BRWD3):c.1386+32G>A	not provided [RCV001679335]	benign	X	80728720	80728720	Human		name
150494117	CV1267287	single nucleotide variant	NM_153252.5(BRWD3):c.914+235T>G	not provided [RCV001688315]	benign	X	80735753	80735753	Human		name
150504158	CV1285901	single nucleotide variant	NM_153252.5(BRWD3):c.4496-86C>T	not provided [RCV001719324]	benign	X	80681585	80681585	Human		name
152061703	CV1611228	single nucleotide variant	NM_153252.5(BRWD3):c.1127+19T>C	not provided [RCV002146852]	benign	X	80733437	80733437	Human		name
152121863	CV1631702	single nucleotide variant	NM_153252.5(BRWD3):c.1087-14G>C	not provided [RCV002117951]	benign	X	80733510	80733510	Human		name
156202569	CV1952575	single nucleotide variant	NM_153252.5(BRWD3):c.3481+11T>C	not provided [RCV002574832]	benign	X	80691812	80691812	Human		name
156408518	CV1954420	single nucleotide variant	NM_153252.5(BRWD3):c.3729-19G>A	not provided [RCV002586538]	likely benign	X	80689865	80689865	Human		name
156111999	CV1961725	single nucleotide variant	NM_153252.5(BRWD3):c.1522-12T>C	not provided [RCV002592809]	benign	X	80723888	80723888	Human		name
156411893	CV1972844	single nucleotide variant	NM_153252.5(BRWD3):c.2325+16C>T	not provided [RCV002587640]	benign	X	80716141	80716141	Human		name
156189436	CV1997980	single nucleotide variant	NM_153252.5(BRWD3):c.2325+18A>G	not provided [RCV002643267]	likely benign	X	80716139	80716139	Human		name
156302164	CV1998453	single nucleotide variant	NM_153252.5(BRWD3):c.2944-14A>T	not provided [RCV002671210]	likely benign	X	80696877	80696877	Human		name
156369256	CV2021185	single nucleotide variant	NM_153252.5(BRWD3):c.4398-16A>G	not provided [RCV002721402]	benign	X	80682110	80682110	Human		name
156312839	CV2078985	single nucleotide variant	NM_153252.5(BRWD3):c.4234-19A>G	not provided [RCV002898817]	likely benign	X	80682647	80682647	Human		name
156212930	CV2087309	single nucleotide variant	NM_153252.5(BRWD3):c.3482-12A>C	not provided [RCV002852898]	likely benign	X	80691185	80691185	Human		name
156209062	CV2160362	single nucleotide variant	NM_153252.5(BRWD3):c.1128-18T>G	not provided [RCV003042261]	likely benign	X	80730038	80730038	Human		name
405221506	CV2908182	single nucleotide variant	NM_153252.5(BRWD3):c.4495+16G>A	not provided [RCV003568509]	likely benign	X	80681981	80681981	Human		name
405032321	CV2926216	single nucleotide variant	NM_153252.5(BRWD3):c.1233-19T>A	not provided [RCV003578332]	likely benign	X	80728924	80728924	Human		name
405110795	CV2942096	single nucleotide variant	NM_153252.5(BRWD3):c.4655-17C>T	not provided [RCV003666281]	likely benign	X	80677380	80677380	Human		name
405118803	CV2957429	single nucleotide variant	NM_153252.5(BRWD3):c.4005+12G>C	not provided [RCV003667216]	likely benign	X	80686851	80686851	Human		name
405207201	CV2994509	single nucleotide variant	NM_153252.5(BRWD3):c.3068+12T>G	not provided [RCV003678889]	uncertain significance	X	80696727	80696727	Human		name
405249756	CV3000868	single nucleotide variant	NM_153252.5(BRWD3):c.2476-19T>C	not provided [RCV003721429]	likely benign	X	80707522	80707522	Human		name
405172127	CV3026586	single nucleotide variant	NM_153252.5(BRWD3):c.3326-13A>T	not provided [RCV003704768]	likely benign	X	80691991	80691991	Human		name
405093898	CV3118928	single nucleotide variant	NM_153252.5(BRWD3):c.1086+20G>A	not provided [RCV003811379]	benign	X	80734098	80734098	Human		name
405085018	CV3121993	single nucleotide variant	NM_153252.5(BRWD3):c.3068+12T>C	not provided [RCV003810748]	benign	X	80696727	80696727	Human		name
405146047	CV3126494	single nucleotide variant	NM_153252.5(BRWD3):c.3808-18T>C	not provided [RCV003817221]	benign	X	80688143	80688143	Human		name
405146163	CV3126502	single nucleotide variant	NM_153252.5(BRWD3):c.1386+11T>C	not provided [RCV003817229]	benign	X	80728741	80728741	Human		name
404977047	CV3127074	single nucleotide variant	NM_153252.5(BRWD3):c.3264-13T>C	not provided [RCV003825297]	benign	X	80692163	80692163	Human		name
405122252	CV3131672	single nucleotide variant	NM_153252.5(BRWD3):c.2553-13G>T	not provided [RCV003837536]	uncertain significance	X	80704859	80704859	Human		name
405106147	CV3136073	single nucleotide variant	NM_153252.5(BRWD3):c.3864+20G>C	not provided [RCV003835419]	benign	X	80688049	80688049	Human		name
405003117	CV3184110	single nucleotide variant	NM_153252.5(BRWD3):c.3152-17A>G	not provided [RCV003882693]	benign	X	80693068	80693068	Human		name
11625593	CV339609	deletion	NM_153252.5(BRWD3):c.3326-14del	Non-syndromic X-linked intellectual disability [RCV000401000]\|not provided [RCV001556730]	benign\|likely benign\|uncertain significance	X	80691992	80691992	Human	1	name
11622271	CV339610	duplication	NM_153252.5(BRWD3):c.3326-26dup	Non-syndromic X-linked intellectual disability [RCV000358530]\|not provided [RCV002058834]	benign\|uncertain significance	X	80691991	80691992	Human	1	name
408391392	CV3523173	single nucleotide variant	NM_153252.5(BRWD3):c.4234-13T>G	not provided [RCV004770545]	uncertain significance	X	80682641	80682641	Human		name
597848180	CV3736781	duplication	NM_153252.5(BRWD3):c.3602+14dup	not provided [RCV005065940]	benign	X	80691038	80691039	Human		name
597962408	CV3753697	single nucleotide variant	NM_153252.5(BRWD3):c.1232+20G>A	not provided [RCV005082001]	benign	X	80729896	80729896	Human		name
597956084	CV3787269	single nucleotide variant	NM_153252.5(BRWD3):c.4005+15G>T	not provided [RCV005122154]	likely benign	X	80686848	80686848	Human		name
21069737	CV789392	single nucleotide variant	NM_153252.5(BRWD3):c.3602+20C>G	Developmental delay [RCV003153882]\|Intellectual disability, X-linked 93 [RCV000984902]	uncertain significance	X	80691033	80691033	Human	3	name
28886492	CV903487	single nucleotide variant	NM_153252.5(BRWD3):c.3602+15A>C	Intellectual disability, X-linked 93 [RCV001169077]\|not provided [RCV002067831]	benign	X	80691038	80691038	Human	1	name
28886495	CV903488	single nucleotide variant	NM_153252.5(BRWD3):c.3602+14T>A	Intellectual disability, X-linked 93 [RCV001169078]\|not provided [RCV001615130]	benign	X	80691039	80691039	Human	1	name
28886505	CV903489	single nucleotide variant	NM_153252.5(BRWD3):c.2943+13A>G	Intellectual disability, X-linked 93 [RCV001169080]	uncertain significance	X	80699944	80699944	Human	1	name
28886510	CV903490	single nucleotide variant	NM_153252.5(BRWD3):c.2326-14C>A	Intellectual disability, X-linked 93 [RCV001169081]	uncertain significance	X	80709591	80709591	Human	1	name
28886513	CV903491	single nucleotide variant	NM_153252.5(BRWD3):c.2044+13A>G	Intellectual disability, X-linked 93 [RCV001169082]\|not provided [RCV002559624]	benign	X	80719476	80719476	Human	1	name
150422095	CV1182173	single nucleotide variant	NM_153252.5(BRWD3):c.3263+186C>A	not provided [RCV001552339]	likely benign	X	80692754	80692754	Human		name
150425980	CV1185868	single nucleotide variant	NM_153252.5(BRWD3):c.3807+129G>A	not provided [RCV001558745]	likely benign	X	80689639	80689639	Human		name
150427128	CV1189172	single nucleotide variant	NM_153252.5(BRWD3):c.4081-248A>T	not provided [RCV001560523]	likely benign	X	80684410	80684410	Human		name
150409889	CV1192577	single nucleotide variant	NM_153252.5(BRWD3):c.1128-111A>G	not provided [RCV001565816]	likely benign	X	80730131	80730131	Human		name
150405278	CV1195823	single nucleotide variant	NM_153252.5(BRWD3):c.3808-169A>C	not provided [RCV001571557]	likely benign	X	80688294	80688294	Human		name
150420076	CV1199557	single nucleotide variant	NM_153252.5(BRWD3):c.2552+161A>G	not provided [RCV001577453]	likely benign	X	80707266	80707266	Human		name
150414065	CV1199558	single nucleotide variant	NM_153252.5(BRWD3):c.2326-125A>G	not provided [RCV001574816]	likely benign	X	80709702	80709702	Human		name
150447318	CV1201872	duplication	NM_153252.5(BRWD3):c.1087-113dup	not provided [RCV001584741]	likely benign	X	80733595	80733596	Human		name
150448579	CV1202055	single nucleotide variant	NM_153252.5(BRWD3):c.3865-296G>A	not provided [RCV001584925]	likely benign	X	80687299	80687299	Human		name
150475693	CV1202281	single nucleotide variant	NM_153252.5(BRWD3):c.1522-160G>A	not provided [RCV001589524]	likely benign	X	80724036	80724036	Human		name
150480836	CV1222047	single nucleotide variant	NM_153252.5(BRWD3):c.3481+136G>T	not provided [RCV001616844]	benign	X	80691687	80691687	Human		name
8587664	CV122295	single nucleotide variant	NM_153252.4(BRWD3):c.1876+303A>T	Lung cancer [RCV000102815]	uncertain significance	X	80722259	80722259	Human		name
150482846	CV1223492	single nucleotide variant	NM_153252.5(BRWD3):c.1232+303T>C	not provided [RCV001617205]	benign	X	80729613	80729613	Human		name
150493244	CV1225627	single nucleotide variant	NM_153252.5(BRWD3):c.1650+220A>G	not provided [RCV001619143]	benign	X	80723528	80723528	Human		name
150515061	CV1228719	single nucleotide variant	NM_153252.5(BRWD3):c.1876+155G>A	not provided [RCV001638707]	benign	X	80722407	80722407	Human		name
150435604	CV1233903	single nucleotide variant	NM_153252.5(BRWD3):c.2326-322C>A	not provided [RCV001644030]	benign	X	80709899	80709899	Human		name
150462739	CV1234956	single nucleotide variant	NM_153252.5(BRWD3):c.3865-293G>C	not provided [RCV001649538]	benign	X	80687296	80687296	Human		name
150504639	CV1240794	single nucleotide variant	NM_153252.5(BRWD3):c.2836-245C>T	not provided [RCV001657637]	benign	X	80700309	80700309	Human		name
150506865	CV1242318	single nucleotide variant	NM_153252.5(BRWD3):c.3264-184G>A	not provided [RCV001658673]	benign	X	80692334	80692334	Human		name
150431132	CV1243594	deletion	NM_153252.5(BRWD3):c.1087-100del	not provided [RCV001663214]	benign	X	80733596	80733596	Human		name
150459517	CV1248679	single nucleotide variant	NM_153252.5(BRWD3):c.3151+178T>A	not provided [RCV001669289]	benign	X	80695730	80695730	Human		name
150456662	CV1249963	single nucleotide variant	NM_153252.5(BRWD3):c.1386+307G>A	not provided [RCV001668860]	benign	X	80728445	80728445	Human		name
150502659	CV1254588	single nucleotide variant	NM_153252.5(BRWD3):c.3152-330G>C	not provided [RCV001677290]	benign	X	80693381	80693381	Human		name
150452079	CV1254912	single nucleotide variant	NM_153252.5(BRWD3):c.1128-122G>T	not provided [RCV001667971]	benign	X	80730142	80730142	Human		name
150505632	CV1255522	single nucleotide variant	NM_153252.5(BRWD3):c.3603-311T>A	not provided [RCV001677969]	benign	X	80690403	80690403	Human		name
150503980	CV1257904	single nucleotide variant	NM_153252.5(BRWD3):c.4233+271G>A	not provided [RCV001677592]	benign	X	80683739	80683739	Human		name
150472095	CV1259238	single nucleotide variant	NM_153252.5(BRWD3):c.4496-135A>G	not provided [RCV001684484]	benign	X	80681634	80681634	Human		name
150450105	CV1260914	single nucleotide variant	NM_153252.5(BRWD3):c.2722-152G>A	not provided [RCV001680583]	benign	X	80703745	80703745	Human		name
150490292	CV1267584	single nucleotide variant	NM_153252.5(BRWD3):c.4081-253T>C	not provided [RCV001687608]	benign	X	80684415	80684415	Human		name
150464043	CV1273240	single nucleotide variant	NM_153252.5(BRWD3):c.3263+275T>C	not provided [RCV001693997]	benign	X	80692665	80692665	Human		name
150453265	CV1276824	single nucleotide variant	NM_153252.5(BRWD3):c.2553-277C>T	not provided [RCV001708614]	benign	X	80705123	80705123	Human		name
150467323	CV1277551	single nucleotide variant	NM_153252.5(BRWD3):c.4398-114C>A	not provided [RCV001710846]	benign	X	80682208	80682208	Human		name
150444084	CV1277944	single nucleotide variant	NM_153252.5(BRWD3):c.1128-152T>G	not provided [RCV001707087]	benign	X	80730172	80730172	Human		name
405255433	CV3172414	microsatellite	NM_153252.5(BRWD3):c.2475+3TA[6]	not provided [RCV003872352]	benign	X	80709415	80709416	Human		name
11629698	CV349107	duplication	NM_153252.5(BRWD3):c.-229_-228dup	Non-syndromic X-linked intellectual disability [RCV000330803]	uncertain significance	X	80809698	80809699	Human	1	name
21073760	CV792512	microsatellite	NM_153252.5(BRWD3):c.3865-119TA[9]	Intellectual disability, X-linked 93 [RCV000990888]\|not provided [RCV001615099]	benign	X	80687101	80687104	Human		name
150340131	CV1168501	microsatellite	NM_153252.5(BRWD3):c.3068+176GT[19]	not provided [RCV001535019]	benign	X	80696520	80696525	Human		name
150423124	CV1185867	microsatellite	NM_153252.5(BRWD3):c.3865-119TA[12]	not provided [RCV001554905]	likely benign	X	80687100	80687101	Human		name
150507347	CV1226569	microsatellite	NM_153252.5(BRWD3):c.3865-119TA[10]	not provided [RCV001635937]	benign	X	80687101	80687102	Human		name
150456157	CV1236848	microsatellite	NM_153252.5(BRWD3):c.3068+176GT[24]	not provided [RCV001648584]	benign	X	80696519	80696520	Human		name
150464429	CV1241287	microsatellite	NM_153252.5(BRWD3):c.3068+176GT[21]	not provided [RCV001649798]	benign	X	80696520	80696521	Human		name
150465545	CV1252899	microsatellite	NM_153252.5(BRWD3):c.3068+176GT[18]	not provided [RCV001670223]	benign	X	80696520	80696527	Human		name
150451087	CV1254188	microsatellite	NM_153252.5(BRWD3):c.3068+176GT[20]	not provided [RCV001667827]	benign	X	80696520	80696523	Human		name
150456938	CV1278565	microsatellite	NM_153252.5(BRWD3):c.3068+176GT[23]	not provided [RCV001709180]	benign	X	80696519	80696520	Human		name
405287895	CV3203195	duplication	NM_153252.5(BRWD3):c.814-5_814-4dup	BRWD3-related disorder [RCV004532152]	likely benign	X	80736091	80736092	Human		name , trait , alternate_id
15192922	CV774264	single nucleotide variant	NM_153252.5(BRWD3):c.6G>A (p.Ala2=)	not provided [RCV000933219]	likely benign	X	80809466	80809466	Human		name
156408431	CV1957841	single nucleotide variant	NM_153252.5(BRWD3):c.18C>T (p.Thr6=)	not provided [RCV002586516]	likely benign	X	80809454	80809454	Human		name
150411510	CV1182508	duplication	NM_153252.5(BRWD3):c.592-47_592-45dup	Intellectual disability, X-linked 93 [RCV001553918]\|not provided [RCV001615307]	benign	X	80744297	80744298	Human	1	name
156413216	CV1887757	duplication	NM_153252.5(BRWD3):c.2475+2_2475+3dup	not provided [RCV003073204]	benign	X	80709424	80709425	Human		name
10048214	CV192585	single nucleotide variant	NM_153252.5(BRWD3):c.33G>A (p.Glu11=)	Inborn genetic diseases [RCV002314615]\|Intellectual disability, X-linked 93 [RCV000277974]\|not provided [RCV000973061]\|not specified [RCV000175993]	benign\|likely benign\|conflicting interpretations of pathogenicity	X	80809303	80809303	Human	2	name
401918284	CV2831271	microsatellite	NM_153252.5(BRWD3):c.1233-7_1233-3del	Intellectual disability, X-linked 93 [RCV003444036]	uncertain significance	X	80728908	80728912	Human		name
596921730	CV3535356	single nucleotide variant	NM_153252.5(BRWD3):c.2T>C (p.Met1Thr)	Intellectual disability, X-linked 93 [RCV004784911]	likely pathogenic	X	80809470	80809470	Human	1	name
13526295	CV508435	duplication	NM_153252.5(BRWD3):c.2721+4_2721+7dup	not specified [RCV000603945]	likely benign	X	80704670	80704671	Human		name
28878142	CV903248	single nucleotide variant	NM_153252.5(BRWD3):c.96A>G (p.Leu32=)	Intellectual disability, X-linked 93 [RCV001166657]\|not provided [RCV002558632]	likely benign\|uncertain significance	X	80809037	80809037	Human	1	name
155684670	CV1827080	single nucleotide variant	NM_153252.5(BRWD3):c.14C>G (p.Pro5Arg)	Inborn genetic diseases [RCV002389891]\|not provided [RCV003095244]	benign\|uncertain significance	X	80809458	80809458	Human	1	name
155695619	CV1844669	single nucleotide variant	NM_153252.5(BRWD3):c.225T>C (p.Ile75=)	Inborn genetic diseases [RCV002443718]	likely benign	X	80793728	80793728	Human	1	name
155799443	CV1862495	single nucleotide variant	NM_153252.5(BRWD3):c.11C>T (p.Ala4Val)	Intellectual disability, X-linked 93 [RCV002471901]\|not provided [RCV005098457]	uncertain significance	X	80809461	80809461	Human	1	name
156364544	CV2176805	single nucleotide variant	NM_153252.5(BRWD3):c.186A>C (p.Ala62=)	not provided [RCV003049249]	benign	X	80793767	80793767	Human		name
401869353	CV2750167	duplication	NM_153252.5(BRWD3):c.94dup (p.Leu32fs)	Intellectual disability, X-linked 93 [RCV003333612]	likely pathogenic	X	80809038	80809039	Human	1	name
407496249	CV3496533	single nucleotide variant	NM_153252.5(BRWD3):c.11C>A (p.Ala4Glu)	not provided [RCV004696734]	uncertain significance	X	80809461	80809461	Human		name
150483719	CV1222348	microsatellite	NM_153252.5(BRWD3):c.914+147_914+149del	not provided [RCV001617351]	benign	X	80735839	80735841	Human		name
151353649	CV1327201	single nucleotide variant	NM_153252.5(BRWD3):c.369G>A (p.Ala123=)	not provided [RCV002542515]\|not specified [RCV001817145]	uncertain significance	X	80791915	80791915	Human		name
152116544	CV1611018	microsatellite	NM_153252.5(BRWD3):c.3264-15_3264-13del	not provided [RCV002135165]	benign	X	80692163	80692165	Human		name
153001934	CV1682736	single nucleotide variant	NM_153252.5(BRWD3):c.67G>C (p.Gly23Arg)	not provided [RCV002251815]	uncertain significance	X	80809269	80809269	Human		name
156297044	CV1894421	single nucleotide variant	NM_153252.5(BRWD3):c.657T>G (p.Arg219=)	not provided [RCV003087738]	likely benign	X	80744188	80744188	Human		name
156116998	CV1994005	single nucleotide variant	NM_153252.5(BRWD3):c.759T>C (p.Thr253=)	not provided [RCV002662705]	likely benign	X	80744086	80744086	Human		name
156022469	CV2019439	single nucleotide variant	NM_153252.5(BRWD3):c.429G>C (p.Val143=)	not provided [RCV002691067]	benign\|likely benign	X	80791855	80791855	Human		name
10403747	CV209307	single nucleotide variant	NM_153252.5(BRWD3):c.597A>C (p.Ser199=)	Inborn genetic diseases [RCV002311289]\|Intellectual disability, X-linked 93 [RCV000370145]\|not provided [RCV000960089]\|not specified [RCV000193303]	benign\|likely benign\|uncertain significance	X	80744248	80744248	Human	2	name
156255837	CV2098237	single nucleotide variant	NM_153252.5(BRWD3):c.915A>G (p.Arg305=)	Inborn genetic diseases [RCV004065994]\|not provided [RCV002895411]	benign\|likely benign	X	80735197	80735197	Human	1	name
156145697	CV2122790	single nucleotide variant	NM_153252.5(BRWD3):c.348A>G (p.Leu116=)	not provided [RCV002954389]	likely benign	X	80791936	80791936	Human		name
401929096	CV2826578	single nucleotide variant	NM_153252.5(BRWD3):c.318A>T (p.Leu106=)	not provided [RCV003439717]	likely benign	X	80793635	80793635	Human		name
402496019	CV2942744	single nucleotide variant	NM_153252.5(BRWD3):c.411T>C (p.Tyr137=)	not provided [RCV003661113]	likely benign	X	80791873	80791873	Human		name
405217972	CV2988165	single nucleotide variant	NM_153252.5(BRWD3):c.873A>C (p.Thr291=)	not provided [RCV003709490]	likely benign	X	80736029	80736029	Human		name
405044467	CV3141554	single nucleotide variant	NM_153252.5(BRWD3):c.501C>T (p.Tyr167=)	not provided [RCV003831655]	likely benign	X	80745659	80745659	Human		name
405045105	CV3150355	single nucleotide variant	NM_153252.5(BRWD3):c.417A>G (p.Lys139=)	not provided [RCV003849149]	likely benign	X	80791867	80791867	Human		name
596947491	CV3549047	single nucleotide variant	NM_153252.5(BRWD3):c.346C>T (p.Leu116=)	not provided [RCV004811371]	uncertain significance	X	80791938	80791938	Human		name
597897340	CV3773898	single nucleotide variant	NM_153252.5(BRWD3):c.50C>A (p.Ala17Asp)	not provided [RCV005111619]	uncertain significance	X	80809286	80809286	Human		name
597896099	CV3810494	deletion	NM_153252.5(BRWD3):c.2721+20_2721+22del	not provided [RCV005152019]	likely benign	X	80704656	80704658	Human		name
597914794	CV3833975	single nucleotide variant	NM_153252.5(BRWD3):c.318A>G (p.Leu106=)	not provided [RCV005183334]	likely benign	X	80793635	80793635	Human		name
597946987	CV3841786	single nucleotide variant	NM_153252.5(BRWD3):c.453A>G (p.Gln151=)	not provided [RCV005189220]	likely benign	X	80745707	80745707	Human		name
597861089	CV3880781	deletion	NM_153252.5(BRWD3):c.263del (p.Pro88fs)	Intellectual disability, X-linked 93 [RCV005229615]	pathogenic	X	80793690	80793690	Human	1	name
598125127	CV3885601	single nucleotide variant	NM_153252.5(BRWD3):c.85G>T (p.Ala29Ser)	not specified [RCV005240179]	uncertain significance	X	80809251	80809251	Human		name
617150266	CV4021691	single nucleotide variant	NM_153252.5(BRWD3):c.894T>C (p.His298=)	not provided [RCV005425660]	likely benign	X	80736008	80736008	Human		name
13214927	CV430948	single nucleotide variant	NM_153252.5(BRWD3):c.573C>T (p.Ser191=)	BRWD3-related disorder [RCV004535589]\|not provided [RCV002056839]\|not specified [RCV000501761]	benign\|likely benign	X	80745587	80745587	Human	1	name , trait , alternate_id
13830039	CV581161	single nucleotide variant	NM_153252.5(BRWD3):c.381A>G (p.Arg127=)	Inborn genetic diseases [RCV002318831]	likely benign	X	80791903	80791903	Human	1	name
15131501	CV717871	variation	NM_153252.5(BRWD3):c.3863= (p.Lys1288=)	not provided [RCV000964613]	benign	X	80688070	80688070	Human		name
15201907	CV729721	single nucleotide variant	NM_153252.5(BRWD3):c.858T>C (p.Thr286=)	not provided [RCV000891328]	likely benign	X	80736044	80736044	Human		name
15161858	CV758677	single nucleotide variant	NM_153252.5(BRWD3):c.459C>T (p.Thr153=)	not provided [RCV000925771]	likely benign	X	80745701	80745701	Human		name
15157945	CV758678	single nucleotide variant	NM_153252.5(BRWD3):c.423A>T (p.Pro141=)	not provided [RCV000924967]	likely benign	X	80791861	80791861	Human		name
15182769	CV774263	single nucleotide variant	NM_153252.5(BRWD3):c.492A>G (p.Ser164=)	BRWD3-related disorder [RCV004533581]\|Inborn genetic diseases [RCV004029565]\|not provided [RCV000930437]	benign\|likely benign	X	80745668	80745668	Human	2	name , trait , alternate_id
15124575	CV786937	single nucleotide variant	NM_153252.5(BRWD3):c.435T>C (p.Asn145=)	not provided [RCV000980036]	likely benign	X	80745725	80745725	Human		name
28876509	CV903246	single nucleotide variant	NM_153252.5(BRWD3):c.957C>A (p.Val319=)	Intellectual disability, X-linked 93 [RCV001166165]\|not provided [RCV005056972]	benign	X	80735155	80735155	Human	1	name
151350813	CV1324842	single nucleotide variant	NM_153252.5(BRWD3):c.187G>T (p.Ala63Ser)	Intellectual disability, X-linked 93 [RCV001809287]	uncertain significance	X	80793766	80793766	Human	1	name
151350588	CV1325614	single nucleotide variant	NM_153252.5(BRWD3):c.164G>A (p.Arg55Lys)	not provided [RCV001814901]	uncertain significance	X	80808555	80808555	Human		name
151356273	CV1329037	single nucleotide variant	NM_153252.5(BRWD3):c.1002A>C (p.Thr334=)	not provided [RCV002542668]\|not specified [RCV001822626]	benign\|likely benign	X	80734202	80734202	Human		name
152099907	CV1524697	single nucleotide variant	NM_153252.5(BRWD3):c.2733G>T (p.Leu911=)	not provided [RCV002172957]	likely benign	X	80703582	80703582	Human		name
152034500	CV1610605	single nucleotide variant	NM_153252.5(BRWD3):c.2346T>C (p.Cys782=)	Inborn genetic diseases [RCV002443189]\|not provided [RCV002125107]	benign\|likely benign	X	80709557	80709557	Human	1	name
155644850	CV1708831	single nucleotide variant	NM_153252.5(BRWD3):c.144G>A (p.Trp48Ter)	Intellectual disability, X-linked 93 [RCV002291428]	likely pathogenic	X	80808575	80808575	Human	1	name
155715591	CV1812295	single nucleotide variant	NM_153252.5(BRWD3):c.1233C>T (p.Gly411=)	Inborn genetic diseases [RCV002362343]	likely benign	X	80728905	80728905	Human	1	name
155685038	CV1827202	single nucleotide variant	NM_153252.5(BRWD3):c.1506G>T (p.Arg502=)	Inborn genetic diseases [RCV002390013]\|not provided [RCV003439014]	likely benign	X	80724948	80724948	Human	1	name
155714406	CV1841857	single nucleotide variant	NM_153252.5(BRWD3):c.2502C>T (p.Asp834=)	Inborn genetic diseases [RCV002431115]\|not provided [RCV005098167]	benign\|likely benign	X	80707477	80707477	Human	1	name
155795435	CV1861297	single nucleotide variant	NM_153252.5(BRWD3):c.269G>A (p.Ser90Asn)	not provided [RCV002469579]	uncertain significance	X	80793684	80793684	Human		name
156408480	CV1911635	single nucleotide variant	NM_153252.5(BRWD3):c.1407C>T (p.Phe469=)	not provided [RCV002607246]	likely benign	X	80725047	80725047	Human		name
156437573	CV1947580	single nucleotide variant	NM_153252.5(BRWD3):c.1758T>A (p.Pro586=)	not provided [RCV003107112]	benign	X	80722680	80722680	Human		name
156287440	CV1964678	single nucleotide variant	NM_153252.5(BRWD3):c.2967A>T (p.Val989=)	not provided [RCV002577693]	likely benign	X	80696840	80696840	Human		name
155901489	CV1975673	single nucleotide variant	NM_153252.5(BRWD3):c.1998A>C (p.Gly666=)	not provided [RCV002613416]	likely benign	X	80719535	80719535	Human		name
155965990	CV1978045	single nucleotide variant	NM_153252.5(BRWD3):c.2655C>T (p.Ser885=)	not provided [RCV002616957]	likely benign	X	80704744	80704744	Human		name
156255216	CV1981785	single nucleotide variant	NM_153252.5(BRWD3):c.2979T>C (p.Tyr993=)	not provided [RCV002646029]	likely benign	X	80696828	80696828	Human		name
156351515	CV1997731	single nucleotide variant	NM_153252.5(BRWD3):c.1545G>A (p.Ala515=)	not provided [RCV002675628]	likely benign	X	80723853	80723853	Human		name
156142507	CV2002820	single nucleotide variant	NM_153252.5(BRWD3):c.2799C>T (p.Pro933=)	not provided [RCV002663619]	likely benign	X	80703516	80703516	Human		name
155943572	CV2032500	single nucleotide variant	NM_153252.5(BRWD3):c.2274C>T (p.Ile758=)	not provided [RCV002730273]	likely benign	X	80716208	80716208	Human		name
156084760	CV2060452	single nucleotide variant	NM_153252.5(BRWD3):c.1329C>T (p.Asn443=)	not provided [RCV002823973]	likely benign	X	80728809	80728809	Human		name
156169733	CV2075478	single nucleotide variant	NM_153252.5(BRWD3):c.1311A>G (p.Thr437=)	not provided [RCV002851492]	likely benign	X	80728827	80728827	Human		name
10407009	CV209306	single nucleotide variant	NM_153252.5(BRWD3):c.1755T>G (p.Pro585=)	not specified [RCV000195075]	uncertain significance	X	80722683	80722683	Human		name
156051797	CV2187399	single nucleotide variant	NM_153252.5(BRWD3):c.1929T>C (p.Asp643=)	not provided [RCV003036934]	likely benign	X	80719604	80719604	Human		name
243064962	CV2409553	single nucleotide variant	NM_153252.5(BRWD3):c.250G>C (p.Asp84His)	Intellectual disability, X-linked 93 [RCV003143825]	uncertain significance	X	80793703	80793703	Human	1	name
8561924	CV25842	duplication	NM_153252.5(BRWD3):c.946dup (p.Arg316fs)	Intellectual disability, X-linked 93 [RCV000011550]	pathogenic	X	80735165	80735166	Human	1	name
401929090	CV2826576	single nucleotide variant	NM_153252.5(BRWD3):c.1716A>C (p.Val572=)	not provided [RCV003439715]	benign\|likely benign	X	80722722	80722722	Human		name
401964101	CV2845020	single nucleotide variant	NM_153252.5(BRWD3):c.296G>T (p.Gly99Val)	Intellectual disability, X-linked 93 [RCV003484585]	uncertain significance	X	80793657	80793657	Human	1	name
405206027	CV2913356	single nucleotide variant	NM_153252.5(BRWD3):c.2685A>G (p.Glu895=)	not provided [RCV003566513]	benign	X	80704714	80704714	Human		name
405091241	CV3044852	single nucleotide variant	NM_153252.5(BRWD3):c.2613A>C (p.Pro871=)	not provided [RCV003717835]	benign	X	80704786	80704786	Human		name
405254540	CV3055453	single nucleotide variant	NM_153252.5(BRWD3):c.2151G>A (p.Arg717=)	not provided [RCV003723057]	likely benign	X	80717653	80717653	Human		name
405151728	CV3063826	single nucleotide variant	NM_153252.5(BRWD3):c.2823A>G (p.Gln941=)	not provided [RCV003726469]	likely benign	X	80703492	80703492	Human		name
402464486	CV3081148	duplication	NM_153252.5(BRWD3):c.439dup (p.Thr147fs)	Intellectual disability, X-linked 93 [RCV003622411]	likely pathogenic	X	80745720	80745721	Human	1	name
405192723	CV3128421	single nucleotide variant	NM_153252.5(BRWD3):c.2508G>A (p.Ser836=)	not provided [RCV003821158]	benign	X	80707471	80707471	Human		name
405129818	CV3133313	single nucleotide variant	NM_153252.5(BRWD3):c.2604A>G (p.Leu868=)	not provided [RCV003838283]	likely benign	X	80704795	80704795	Human		name
405074380	CV3140672	single nucleotide variant	NM_153252.5(BRWD3):c.2784C>A (p.Ile928=)	not provided [RCV003833635]	benign	X	80703531	80703531	Human		name
405162099	CV3160068	single nucleotide variant	NM_153252.5(BRWD3):c.1380A>G (p.Thr460=)	not provided [RCV003857139]	likely benign	X	80728758	80728758	Human		name
405249727	CV3180526	single nucleotide variant	NM_153252.5(BRWD3):c.1590C>T (p.Cys530=)	not provided [RCV003869803]	likely benign	X	80723808	80723808	Human		name
405260163	CV3190208	single nucleotide variant	NM_153252.5(BRWD3):c.1308C>T (p.Thr436=)	BRWD3-related disorder [RCV004534661]	likely benign	X	80728830	80728830	Human		name , trait , alternate_id
11622944	CV339611	single nucleotide variant	NM_153252.5(BRWD3):c.2184G>A (p.Ala728=)	Inborn genetic diseases [RCV002429334]\|Intellectual disability, X-linked 93 [RCV000366434]\|not provided [RCV001726151]\|not specified [RCV000502732]	benign\|likely benign\|uncertain significance	X	80717620	80717620	Human	2	name
408376243	CV3505709	single nucleotide variant	NM_153252.5(BRWD3):c.134G>C (p.Arg45Pro)	BRWD3-related disorder [RCV004726658]	uncertain significance	X	80808585	80808585	Human		name , trait , alternate_id
597898863	CV3740875	single nucleotide variant	NM_153252.5(BRWD3):c.1533A>G (p.Gln511=)	not provided [RCV005072038]	likely benign	X	80723865	80723865	Human		name
597970106	CV3750114	single nucleotide variant	NM_153252.5(BRWD3):c.1344A>G (p.Lys448=)	not provided [RCV005084055]	likely benign	X	80728794	80728794	Human		name
597970760	CV3750143	single nucleotide variant	NM_153252.5(BRWD3):c.1629A>G (p.Gly543=)	not provided [RCV005084084]	likely benign	X	80723769	80723769	Human		name
597971218	CV3750660	single nucleotide variant	NM_153252.5(BRWD3):c.1155T>C (p.Asp385=)	not provided [RCV005084404]	likely benign	X	80729993	80729993	Human		name
597936277	CV3777633	single nucleotide variant	NM_153252.5(BRWD3):c.2718G>A (p.Lys906=)	not provided [RCV005132546]	likely benign	X	80704681	80704681	Human		name
597884740	CV3780646	single nucleotide variant	NM_153252.5(BRWD3):c.2199G>A (p.Val733=)	not provided [RCV005124774]	likely benign	X	80717605	80717605	Human		name
597938859	CV3808329	single nucleotide variant	NM_153252.5(BRWD3):c.2868T>C (p.Tyr956=)	not provided [RCV005158517]	likely benign	X	80700032	80700032	Human		name
597836646	CV3828468	single nucleotide variant	NM_153252.5(BRWD3):c.2577T>C (p.Asp859=)	not provided [RCV005171361]	likely benign	X	80704822	80704822	Human		name
13830242	CV581158	single nucleotide variant	NM_153252.5(BRWD3):c.1962G>A (p.Leu654=)	Inborn genetic diseases [RCV002316858]	likely benign	X	80719571	80719571	Human	1	name
13830257	CV581159	single nucleotide variant	NM_153252.5(BRWD3):c.1761A>G (p.Pro587=)	Inborn genetic diseases [RCV002316873]	likely benign	X	80722677	80722677	Human	1	name
14399318	CV614613	single nucleotide variant	NM_153252.5(BRWD3):c.256G>A (p.Glu86Lys)	Intellectual disability, X-linked 93 [RCV000768432]	likely pathogenic	X	80793697	80793697	Human	1	name
15198679	CV729720	single nucleotide variant	NM_153252.5(BRWD3):c.1404A>G (p.Val468=)	not provided [RCV000890427]	likely benign	X	80725050	80725050	Human		name
15100880	CV774261	single nucleotide variant	NM_153252.5(BRWD3):c.2941A>C (p.Arg981=)	not provided [RCV000936695]	likely benign	X	80699959	80699959	Human		name
15139167	CV774262	single nucleotide variant	NM_153252.5(BRWD3):c.1674C>T (p.His558=)	not provided [RCV000943510]	likely benign	X	80722764	80722764	Human		name
15143882	CV786936	single nucleotide variant	NM_153252.5(BRWD3):c.1416A>G (p.Glu472=)	not provided [RCV000983400]	likely benign	X	80725038	80725038	Human		name
21075146	CV798417	single nucleotide variant	NM_153252.5(BRWD3):c.1413A>C (p.Leu471=)	not provided [RCV000995980]	likely benign	X	80725041	80725041	Human		name
40886725	CV974440	single nucleotide variant	NM_153252.5(BRWD3):c.1086G>A (p.Thr362=)	Inborn genetic diseases [RCV001265916]\|Intellectual disability, X-linked 93 [RCV005002000]	uncertain significance	X	80734118	80734118	Human	2	name
40890010	CV975653	single nucleotide variant	NM_153252.5(BRWD3):c.100C>T (p.Gln34Ter)	not provided [RCV001268573]	likely pathogenic	X	80809033	80809033	Human		name
126732076	CV1001294	single nucleotide variant	NM_153252.5(BRWD3):c.872C>A (p.Thr291Lys)	not provided [RCV001310739]	uncertain significance	X	80736030	80736030	Human		name
8643428	CV102411	single nucleotide variant	NM_153252.5(BRWD3):c.4377A>G (p.Leu1459=)	not provided [RCV000082670]	conflicting interpretations of pathogenicity\|uncertain significance	X	80682485	80682485	Human		name
150338138	CV1173841	single nucleotide variant	NM_153252.5(BRWD3):c.424A>C (p.Asn142His)	not provided [RCV001542074]	uncertain significance	X	80791860	80791860	Human		name
150428347	CV1189171	deletion	NM_153252.5(BRWD3):c.4234-140_4234-137del	not provided [RCV001562145]	likely benign	X	80682765	80682768	Human		name
150556264	CV1296822	single nucleotide variant	NM_153252.5(BRWD3):c.684G>T (p.Met228Ile)	not provided [RCV001774112]	uncertain significance	X	80744161	80744161	Human		name
150555334	CV1297784	single nucleotide variant	NM_153252.5(BRWD3):c.577A>G (p.Arg193Gly)	not provided [RCV001772692]	uncertain significance	X	80745583	80745583	Human		name
150540794	CV1298520	single nucleotide variant	NM_153252.5(BRWD3):c.371C>G (p.Ala124Gly)	not provided [RCV001760668]	uncertain significance	X	80791913	80791913	Human		name
8659106	CV133980	single nucleotide variant	NM_153252.5(BRWD3):c.5100T>C (p.Gly1700=)	Inborn genetic diseases [RCV002312042]\|Intellectual disability, X-linked 93 [RCV000399425]\|not provided [RCV000951362]\|not specified [RCV000116503]	benign\|likely benign	X	80676918	80676918	Human	2	name
151814197	CV1348963	single nucleotide variant	NM_153252.5(BRWD3):c.4233G>A (p.Arg1411=)	not provided [RCV001918918]	uncertain significance	X	80684010	80684010	Human		name
151807109	CV1400222	single nucleotide variant	NM_153252.5(BRWD3):c.3264C>T (p.His1088=)	not provided [RCV002012089]	uncertain significance	X	80692150	80692150	Human		name
152053016	CV1651396	single nucleotide variant	NM_153252.5(BRWD3):c.436A>G (p.Ile146Val)	BRWD3-related disorder [RCV004543890]\|Inborn genetic diseases [RCV004603171]\|not provided [RCV002145916]	likely benign\|uncertain significance	X	80745724	80745724	Human	2	name , trait , alternate_id
153348622	CV1692666	single nucleotide variant	NM_153252.5(BRWD3):c.513G>C (p.Lys171Asn)	not provided [RCV002274521]	uncertain significance	X	80745647	80745647	Human		name
153350035	CV1693996	single nucleotide variant	NM_153252.5(BRWD3):c.3363C>T (p.Val1121=)	not provided [RCV002276472]	likely benign	X	80691941	80691941	Human		name
155265571	CV1695715	single nucleotide variant	NM_153252.5(BRWD3):c.329A>G (p.Lys110Arg)	not provided [RCV002280446]	uncertain significance	X	80793624	80793624	Human		name
155267131	CV1699445	single nucleotide variant	NM_153252.5(BRWD3):c.993G>A (p.Met331Ile)	not provided [RCV002283240]	uncertain significance	X	80734211	80734211	Human		name
155701790	CV1776188	single nucleotide variant	NM_153252.5(BRWD3):c.598G>C (p.Asp200His)	not provided [RCV002300009]	uncertain significance	X	80744247	80744247	Human		name
155691697	CV1778036	single nucleotide variant	NM_153252.5(BRWD3):c.989G>A (p.Gly330Asp)	not provided [RCV002299341]	uncertain significance	X	80734215	80734215	Human		name
155686347	CV1789885	single nucleotide variant	NM_153252.5(BRWD3):c.3837C>T (p.Asp1279=)	Inborn genetic diseases [RCV002355427]\|not provided [RCV003718492]	benign\|likely benign	X	80688096	80688096	Human	1	name
155687097	CV1796831	single nucleotide variant	NM_153252.5(BRWD3):c.3936A>G (p.Leu1312=)	Inborn genetic diseases [RCV002373244]\|not provided [RCV005096441]	benign\|likely benign	X	80686932	80686932	Human	1	name
155733539	CV1802073	single nucleotide variant	NM_153252.5(BRWD3):c.4872C>T (p.Asp1624=)	Inborn genetic diseases [RCV002340432]\|not provided [RCV005058389]	likely benign	X	80677146	80677146	Human	1	name
155707893	CV1823167	single nucleotide variant	NM_153252.5(BRWD3):c.763G>A (p.Ala255Thr)	Inborn genetic diseases [RCV002396349]	uncertain significance	X	80744082	80744082	Human	1	name
156268767	CV1915162	single nucleotide variant	NM_153252.5(BRWD3):c.5229A>G (p.Arg1743=)	not provided [RCV002628018]	benign	X	80676789	80676789	Human		name
10049205	CV196081	single nucleotide variant	NM_153252.5(BRWD3):c.769G>A (p.Val257Ile)	Inborn genetic diseases [RCV002399642]\|Intellectual disability, X-linked 93 [RCV001166166]\|not provided [RCV000514166]\|not specified [RCV000180381]	benign\|likely benign	X	80744076	80744076	Human	2	name
156354165	CV1962247	single nucleotide variant	NM_153252.5(BRWD3):c.4644A>G (p.Pro1548=)	not provided [RCV002581272]	likely benign	X	80681351	80681351	Human		name
156397755	CV1965764	single nucleotide variant	NM_153252.5(BRWD3):c.4815G>A (p.Glu1605=)	not provided [RCV002584547]	likely benign	X	80677203	80677203	Human		name
156252662	CV1967277	single nucleotide variant	NM_153252.5(BRWD3):c.4524A>T (p.Leu1508=)	not provided [RCV002597521]	benign	X	80681471	80681471	Human		name
156312369	CV1969777	single nucleotide variant	NM_153252.5(BRWD3):c.4125G>A (p.Val1375=)	not provided [RCV002578764]	likely benign	X	80684118	80684118	Human		name
156048368	CV1978149	single nucleotide variant	NM_153252.5(BRWD3):c.4566G>A (p.Ser1522=)	not provided [RCV002590577]	likely benign	X	80681429	80681429	Human		name
156253455	CV1985021	single nucleotide variant	NM_153252.5(BRWD3):c.299T>A (p.Val100Asp)	not provided [RCV002645971]\|not specified [RCV004700794]	uncertain significance	X	80793654	80793654	Human		name
156191757	CV1994672	single nucleotide variant	NM_153252.5(BRWD3):c.3549T>C (p.Ala1183=)	not provided [RCV002643334]	likely benign	X	80691106	80691106	Human		name
156218802	CV1995614	single nucleotide variant	NM_153252.5(BRWD3):c.3297A>G (p.Pro1099=)	not provided [RCV002667145]	likely benign	X	80692117	80692117	Human		name
156029678	CV2001042	single nucleotide variant	NM_153252.5(BRWD3):c.736G>A (p.Val246Ile)	not provided [RCV002658606]	likely benign	X	80744109	80744109	Human		name
156170902	CV2016137	single nucleotide variant	NM_153252.5(BRWD3):c.682A>G (p.Met228Val)	not provided [RCV002710481]	benign	X	80744163	80744163	Human		name
155982154	CV2025351	single nucleotide variant	NM_153252.5(BRWD3):c.5118G>T (p.Gly1706=)	not provided [RCV002755378]	likely benign	X	80676900	80676900	Human		name
156024773	CV2077977	single nucleotide variant	NM_153252.5(BRWD3):c.3093T>C (p.Ile1031=)	not provided [RCV002866781]	likely benign	X	80695966	80695966	Human		name
10406730	CV209302	single nucleotide variant	NM_153252.5(BRWD3):c.3690A>G (p.Ala1230=)	not provided [RCV000921416]\|not specified [RCV000193883]	likely benign\|uncertain significance	X	80690005	80690005	Human		name
10404079	CV209304	single nucleotide variant	NM_153252.5(BRWD3):c.3324A>G (p.Gly1108=)	not provided [RCV005055697]\|not specified [RCV000194130]	likely benign\|uncertain significance	X	80692090	80692090	Human		name
155943107	CV2154446	single nucleotide variant	NM_153252.5(BRWD3):c.469C>T (p.Arg157Cys)	not provided [RCV003014397]	uncertain significance	X	80745691	80745691	Human		name
156183466	CV2178510	single nucleotide variant	NM_153252.5(BRWD3):c.4017G>A (p.Glu1339=)	not provided [RCV003057602]	likely benign	X	80685525	80685525	Human		name
156256622	CV2219781	single nucleotide variant	NM_153252.5(BRWD3):c.746G>A (p.Trp249Ter)	Inborn genetic diseases [RCV002702770]	pathogenic	X	80744099	80744099	Human	1	name
156382118	CV2227202	single nucleotide variant	NM_153252.5(BRWD3):c.392C>T (p.Pro131Leu)	Inborn genetic diseases [RCV002722710]	uncertain significance	X	80791892	80791892	Human	1	name
243064961	CV2409552	single nucleotide variant	NM_153252.5(BRWD3):c.869G>A (p.Gly290Glu)	Intellectual disability, X-linked 93 [RCV003143824]	uncertain significance	X	80736033	80736033	Human	1	name
243054070	CV2416497	single nucleotide variant	NM_153252.5(BRWD3):c.379A>G (p.Arg127Gly)	not provided [RCV003149558]	uncertain significance	X	80791905	80791905	Human		name
329350114	CV2477276	single nucleotide variant	NM_153252.5(BRWD3):c.652C>T (p.Leu218Phe)	not provided [RCV003221601]	uncertain significance	X	80744193	80744193	Human		name
401797705	CV2741062	single nucleotide variant	NM_153252.5(BRWD3):c.602A>T (p.Asp201Val)	not provided [RCV003322226]	uncertain significance	X	80744243	80744243	Human		name
401856216	CV2752380	single nucleotide variant	NM_153252.5(BRWD3):c.463T>G (p.Cys155Gly)	Intellectual disability, X-linked 93 [RCV003340717]	uncertain significance	X	80745697	80745697	Human	1	name
401861211	CV2769576	single nucleotide variant	NM_153252.5(BRWD3):c.309G>C (p.Gln103His)	Inborn genetic diseases [RCV003357711]	likely benign	X	80793644	80793644	Human	1	name
401929076	CV2826572	single nucleotide variant	NM_153252.5(BRWD3):c.4426T>C (p.Leu1476=)	not provided [RCV003439711]	likely benign	X	80682066	80682066	Human		name
401929084	CV2826574	single nucleotide variant	NM_153252.5(BRWD3):c.3759T>C (p.Thr1253=)	not provided [RCV003439713]	likely benign	X	80689816	80689816	Human		name
405224731	CV2885433	single nucleotide variant	NM_153252.5(BRWD3):c.3480G>A (p.Leu1160=)	not provided [RCV003554393]	uncertain significance	X	80691824	80691824	Human		name
402475048	CV2916042	single nucleotide variant	NM_153252.5(BRWD3):c.4575T>C (p.Gly1525=)	not provided [RCV003571283]	likely benign	X	80681420	80681420	Human		name
405178472	CV2959859	single nucleotide variant	NM_153252.5(BRWD3):c.368C>T (p.Ala123Val)	not provided [RCV003676045]	uncertain significance	X	80791916	80791916	Human		name
402524642	CV3007774	single nucleotide variant	NM_153252.5(BRWD3):c.3633C>G (p.Arg1211=)	not provided [RCV003716690]	likely benign	X	80690062	80690062	Human		name
405242134	CV3014437	single nucleotide variant	NM_153252.5(BRWD3):c.5247A>G (p.Thr1749=)	not provided [RCV003719285]	likely benign	X	80676771	80676771	Human		name
405071639	CV3034426	single nucleotide variant	NM_153252.5(BRWD3):c.464G>A (p.Cys155Tyr)	not provided [RCV003698357]	uncertain significance	X	80745696	80745696	Human		name
402498962	CV3038300	single nucleotide variant	NM_153252.5(BRWD3):c.5055A>G (p.Gly1685=)	not provided [RCV003714542]	benign	X	80676963	80676963	Human		name
405221178	CV3060138	single nucleotide variant	NM_153252.5(BRWD3):c.3180C>T (p.Asp1060=)	not provided [RCV003733334]	likely benign	X	80693023	80693023	Human		name
405202148	CV3067018	single nucleotide variant	NM_153252.5(BRWD3):c.560C>T (p.Ala187Val)	not provided [RCV003730880]	uncertain significance	X	80745600	80745600	Human		name
405017085	CV3124875	single nucleotide variant	NM_153252.5(BRWD3):c.5178A>C (p.Ala1726=)	not provided [RCV003829500]	benign	X	80676840	80676840	Human		name
405027601	CV3129770	single nucleotide variant	NM_153252.5(BRWD3):c.4293C>A (p.Ile1431=)	not provided [RCV003830368]	likely benign	X	80682569	80682569	Human		name
405143870	CV3155736	single nucleotide variant	NM_153252.5(BRWD3):c.409T>A (p.Tyr137Asn)	Inborn genetic diseases [RCV004605063]\|not provided [RCV003855778]	benign\|likely benign	X	80791875	80791875	Human	1	name
405082371	CV3166813	single nucleotide variant	NM_153252.5(BRWD3):c.3006C>T (p.Cys1002=)	not provided [RCV003851587]	likely benign	X	80696801	80696801	Human		name
405228618	CV3180401	single nucleotide variant	NM_153252.5(BRWD3):c.4089A>G (p.Gln1363=)	not provided [RCV003864822]	likely benign	X	80684154	80684154	Human		name
404981018	CV3183364	single nucleotide variant	NM_153252.5(BRWD3):c.3489C>T (p.Ala1163=)	not provided [RCV003880387]	benign	X	80691166	80691166	Human		name
405270583	CV3212014	single nucleotide variant	NM_153252.5(BRWD3):c.3084G>A (p.Pro1028=)	BRWD3-related disorder [RCV004543928]	likely benign	X	80695975	80695975	Human		name , trait , alternate_id
11629885	CV349104	single nucleotide variant	NM_153252.5(BRWD3):c.5130G>T (p.Gly1710=)	BRWD3-related disorder [RCV004530495]\|Inborn genetic diseases [RCV002317882]\|Intellectual disability, X-linked 93 [RCV000336048]\|not provided [RCV000909425]	benign\|likely benign	X	80676888	80676888	Human	2	name , trait , alternate_id
408387184	CV3518737	single nucleotide variant	NM_153252.5(BRWD3):c.764C>T (p.Ala255Val)	not provided [RCV004761056]	uncertain significance	X	80744081	80744081	Human		name
408390194	CV3519246	single nucleotide variant	NM_153252.5(BRWD3):c.760T>G (p.Cys254Gly)	not provided [RCV004762555]	uncertain significance	X	80744085	80744085	Human		name
408393823	CV3519946	single nucleotide variant	NM_153252.5(BRWD3):c.622G>T (p.Ala208Ser)	not provided [RCV004764242]	uncertain significance	X	80744223	80744223	Human		name
408380974	CV3523721	single nucleotide variant	NM_153252.5(BRWD3):c.5073C>T (p.Gly1691=)	not provided [RCV004766119]	uncertain significance	X	80676945	80676945	Human		name
408390250	CV3525000	single nucleotide variant	NM_153252.5(BRWD3):c.907A>C (p.Lys303Gln)	not provided [RCV004769895]	uncertain significance	X	80735995	80735995	Human		name
408392319	CV3528090	single nucleotide variant	NM_153252.5(BRWD3):c.964T>C (p.Ser322Pro)	not provided [RCV004775858]	uncertain significance	X	80735148	80735148	Human		name
408386464	CV3528939	single nucleotide variant	NM_153252.5(BRWD3):c.592G>A (p.Gly198Ser)	not provided [RCV004772772]	uncertain significance	X	80744253	80744253	Human		name
11628618	CV352962	single nucleotide variant	NM_153252.5(BRWD3):c.4263C>T (p.Ala1421=)	Intellectual disability, X-linked 93 [RCV000305786]	uncertain significance	X	80682599	80682599	Human	1	name
596920462	CV3534666	single nucleotide variant	NM_153252.5(BRWD3):c.608T>G (p.Leu203Ter)	Intellectual disability, X-linked 93 [RCV004782233]	likely pathogenic	X	80744237	80744237	Human	1	name
596922588	CV3537297	single nucleotide variant	NM_153252.5(BRWD3):c.319C>T (p.Arg107Trp)	not provided [RCV004787267]	uncertain significance	X	80793634	80793634	Human		name
12741944	CV361256	single nucleotide variant	NM_153252.5(BRWD3):c.568C>T (p.Arg190Ter)	Intellectual disability, X-linked 93 [RCV000415462]	pathogenic	X	80745592	80745592	Human	1	name
597637424	CV3637310	single nucleotide variant	NM_153252.5(BRWD3):c.560C>G (p.Ala187Gly)	Inborn genetic diseases [RCV004970197]	uncertain significance	X	80745600	80745600	Human	1	name
597655863	CV3731521	single nucleotide variant	NM_153252.5(BRWD3):c.952G>A (p.Gly318Arg)	not provided [RCV005001702]	uncertain significance	X	80735160	80735160	Human		name
597878703	CV3744405	single nucleotide variant	NM_153252.5(BRWD3):c.4491T>C (p.Ser1497=)	not provided [RCV005069619]	benign	X	80682001	80682001	Human		name
597928001	CV3749081	single nucleotide variant	NM_153252.5(BRWD3):c.398T>A (p.Leu133Gln)	not provided [RCV005075537]	uncertain significance	X	80791886	80791886	Human		name
597966046	CV3751485	single nucleotide variant	NM_153252.5(BRWD3):c.656G>A (p.Arg219His)	not provided [RCV005082854]	uncertain significance	X	80744189	80744189	Human		name
597945653	CV3755410	single nucleotide variant	NM_153252.5(BRWD3):c.3669A>G (p.Pro1223=)	not provided [RCV005078419]	likely benign	X	80690026	80690026	Human		name
597946302	CV3774845	single nucleotide variant	NM_153252.5(BRWD3):c.421C>G (p.Pro141Ala)	not provided [RCV005119942]	uncertain significance	X	80791863	80791863	Human		name
597919747	CV3781158	single nucleotide variant	NM_153252.5(BRWD3):c.4044T>C (p.Val1348=)	not provided [RCV005130040]	likely benign	X	80685498	80685498	Human		name
597898255	CV3782536	single nucleotide variant	NM_153252.5(BRWD3):c.4704G>A (p.Arg1568=)	not provided [RCV005126761]	likely benign	X	80677314	80677314	Human		name
12838171	CV379482	single nucleotide variant	NM_153252.5(BRWD3):c.478C>T (p.His160Tyr)	not provided [RCV000426469]	uncertain significance	X	80745682	80745682	Human		name
12844338	CV379484	single nucleotide variant	NM_153252.5(BRWD3):c.460G>A (p.Gly154Ser)	not provided [RCV000437817]	uncertain significance	X	80745700	80745700	Human		name
597952333	CV3795105	single nucleotide variant	NM_153252.5(BRWD3):c.3252T>C (p.Cys1084=)	not provided [RCV005136317]	likely benign	X	80692951	80692951	Human		name
597853416	CV3805801	single nucleotide variant	NM_153252.5(BRWD3):c.3972A>G (p.Pro1324=)	not provided [RCV005145731]	benign	X	80686896	80686896	Human		name
597968957	CV3821321	single nucleotide variant	NM_153252.5(BRWD3):c.5079A>G (p.Gly1693=)	not provided [RCV005165963]	likely benign	X	80676939	80676939	Human		name
597957194	CV3838450	single nucleotide variant	NM_153252.5(BRWD3):c.4023G>A (p.Glu1341=)	not provided [RCV005191825]	likely benign	X	80685519	80685519	Human		name
597918972	CV3842494	single nucleotide variant	NM_153252.5(BRWD3):c.4491T>A (p.Ser1497=)	not provided [RCV005183979]	likely benign	X	80682001	80682001	Human		name
597896861	CV3854116	single nucleotide variant	NM_153252.5(BRWD3):c.5355G>A (p.Val1785=)	not provided [RCV005201400]	likely benign	X	80676663	80676663	Human		name
598127261	CV3882540	single nucleotide variant	NM_153252.5(BRWD3):c.752T>C (p.Leu251Pro)	not provided [RCV005234092]	uncertain significance	X	80744093	80744093	Human		name
598159253	CV3897052	single nucleotide variant	NM_153252.5(BRWD3):c.854C>T (p.Ser285Phe)	not provided [RCV005368026]	uncertain significance	X	80736048	80736048	Human		name
598210978	CV3939086	single nucleotide variant	NM_153252.5(BRWD3):c.335G>A (p.Cys112Tyr)	Inborn genetic diseases [RCV005315943]	uncertain significance	X	80791949	80791949	Human	1	name
598174728	CV3939088	single nucleotide variant	NM_153252.5(BRWD3):c.413T>C (p.Val138Ala)	Inborn genetic diseases [RCV005309753]	uncertain significance	X	80791871	80791871	Human	1	name
616935312	CV4009452	single nucleotide variant	NM_153252.5(BRWD3):c.340A>C (p.Ser114Arg)	not provided [RCV005402624]	uncertain significance	X	80791944	80791944	Human		name
616936236	CV4016252	single nucleotide variant	NM_153252.5(BRWD3):c.3603G>A (p.Arg1201=)	not provided [RCV005415118]	uncertain significance	X	80690092	80690092	Human		name
617152621	CV4017872	single nucleotide variant	NM_153252.5(BRWD3):c.590C>T (p.Thr197Ile)	Intellectual disability, X-linked 93 [RCV005417662]	uncertain significance	X	80745570	80745570	Human	1	name
12900767	CV411501	single nucleotide variant	NM_153252.5(BRWD3):c.638G>A (p.Arg213His)	not provided [RCV000483139]	uncertain significance	X	80744207	80744207	Human		name
13480851	CV446795	single nucleotide variant	NM_153252.5(BRWD3):c.488C>T (p.Pro163Leu)	not provided [RCV000521343]	uncertain significance	X	80745672	80745672	Human		name
15191743	CV743487	single nucleotide variant	NM_153252.5(BRWD3):c.4572C>T (p.Phe1524=)	BRWD3-related disorder [RCV004541937]\|Inborn genetic diseases [RCV002336895]\|Intellectual disability, X-linked 93 [RCV002502730]\|not provided [RCV000910335]	benign\|likely benign	X	80681423	80681423	Human	2	name , trait , alternate_id
15165937	CV743488	single nucleotide variant	NM_153252.5(BRWD3):c.4524A>G (p.Leu1508=)	BRWD3-related disorder [RCV004541906]\|not provided [RCV000904333]	likely benign	X	80681471	80681471	Human	1	name , trait , alternate_id
15183242	CV743489	single nucleotide variant	NM_153252.5(BRWD3):c.4314C>T (p.Ile1438=)	not provided [RCV000908016]	likely benign	X	80682548	80682548	Human		name
15184987	CV774260	single nucleotide variant	NM_153252.5(BRWD3):c.3672C>T (p.Asp1224=)	not provided [RCV000930937]	likely benign	X	80690023	80690023	Human		name
21075142	CV798413	single nucleotide variant	NM_153252.5(BRWD3):c.4137G>A (p.Leu1379=)	not provided [RCV000995976]	uncertain significance	X	80684106	80684106	Human		name
21075143	CV798414	single nucleotide variant	NM_153252.5(BRWD3):c.3432C>T (p.Asp1144=)	not provided [RCV000995977]	benign\|likely benign	X	80691872	80691872	Human		name
28883884	CV903242	single nucleotide variant	NM_153252.5(BRWD3):c.3939G>A (p.Leu1313=)	Intellectual disability, X-linked 93 [RCV001168338]\|not provided [RCV002559613]	benign	X	80686929	80686929	Human	1	name
28886499	CV903243	single nucleotide variant	NM_153252.5(BRWD3):c.3318A>G (p.Pro1106=)	BRWD3-related disorder [RCV004545097]\|Inborn genetic diseases [RCV002451349]\|Intellectual disability, X-linked 93 [RCV001169079]\|not provided [RCV002557463]	benign\|likely benign	X	80692096	80692096	Human	2	name , trait , alternate_id
28876511	CV903247	single nucleotide variant	NM_153252.5(BRWD3):c.637C>T (p.Arg213Cys)	Intellectual disability, X-linked 93 [RCV001166167]	uncertain significance	X	80744208	80744208	Human	1	name
40887380	CV974441	single nucleotide variant	NM_153252.5(BRWD3):c.473T>C (p.Phe158Ser)	Inborn genetic diseases [RCV001266941]	uncertain significance	X	80745687	80745687	Human	1	name
126744557	CV1019089	single nucleotide variant	NM_153252.5(BRWD3):c.2689A>T (p.Arg897Trp)	Intellectual disability, X-linked 93 [RCV001330464]	uncertain significance	X	80704710	80704710	Human	1	name
150554217	CV1296618	single nucleotide variant	NM_153252.5(BRWD3):c.1282A>G (p.Met428Val)	not provided [RCV001770855]	uncertain significance	X	80728856	80728856	Human		name
150531053	CV1299265	single nucleotide variant	NM_153252.5(BRWD3):c.2304G>C (p.Lys768Asn)	not provided [RCV001756958]	uncertain significance	X	80716178	80716178	Human		name
150549573	CV1299529	single nucleotide variant	NM_153252.5(BRWD3):c.1823G>A (p.Arg608Gln)	not provided [RCV001752455]	uncertain significance	X	80722615	80722615	Human		name
150550491	CV1300277	single nucleotide variant	NM_153252.5(BRWD3):c.2114T>C (p.Ile705Thr)	not provided [RCV001765747]	uncertain significance	X	80717690	80717690	Human		name
150556407	CV1303084	single nucleotide variant	NM_153252.5(BRWD3):c.2633C>T (p.Thr878Ile)	not provided [RCV001774277]	uncertain significance	X	80704766	80704766	Human		name
150535752	CV1312017	single nucleotide variant	NM_153252.5(BRWD3):c.2083A>C (p.Asn695His)	not provided [RCV001779828]	uncertain significance	X	80717721	80717721	Human		name
151235513	CV1318838	single nucleotide variant	NM_153252.5(BRWD3):c.2096G>A (p.Arg699Gln)	not provided [RCV001795657]	uncertain significance	X	80717708	80717708	Human		name
151234535	CV1320303	single nucleotide variant	NM_153252.5(BRWD3):c.2315C>T (p.Thr772Ile)	not provided [RCV001799927]	uncertain significance	X	80716167	80716167	Human		name
151747242	CV1364845	single nucleotide variant	NM_153252.5(BRWD3):c.1384T>A (p.Ser462Thr)	not provided [RCV001985876]	uncertain significance	X	80728754	80728754	Human		name
151836210	CV1383019	single nucleotide variant	NM_153252.5(BRWD3):c.1738G>A (p.Ala580Thr)	not provided [RCV001935585]	uncertain significance	X	80722700	80722700	Human		name
152034974	CV1670069	single nucleotide variant	NM_153252.5(BRWD3):c.2443G>A (p.Gly815Ser)	not provided [RCV002223603]	uncertain significance	X	80709460	80709460	Human		name
152980598	CV1676019	single nucleotide variant	NM_153252.5(BRWD3):c.1789C>T (p.His597Tyr)	not provided [RCV002245088]	uncertain significance	X	80722649	80722649	Human		name
153001952	CV1682741	single nucleotide variant	NM_153252.5(BRWD3):c.1685G>A (p.Arg562His)	not provided [RCV002251820]	uncertain significance	X	80722753	80722753	Human		name
155641793	CV1706048	single nucleotide variant	NM_153252.5(BRWD3):c.1799A>T (p.Lys600Ile)	not provided [RCV002286910]	uncertain significance	X	80722639	80722639	Human		name
155642309	CV1706221	single nucleotide variant	NM_153252.5(BRWD3):c.2632A>G (p.Thr878Ala)	not provided [RCV002287084]	uncertain significance	X	80704767	80704767	Human		name
155726558	CV1812013	single nucleotide variant	NM_153252.5(BRWD3):c.1227G>A (p.Met409Ile)	Inborn genetic diseases [RCV002364636]\|not provided [RCV003669283]	likely benign\|uncertain significance	X	80729921	80729921	Human	1	name
155678794	CV1851891	single nucleotide variant	NM_153252.5(BRWD3):c.2542A>G (p.Ser848Gly)	Inborn genetic diseases [RCV002455795]\|not provided [RCV003101947]	benign\|likely benign	X	80707437	80707437	Human	1	name
155798227	CV1859655	single nucleotide variant	NM_153252.5(BRWD3):c.2656T>C (p.Ser886Pro)	Intellectual disability, X-linked 93 [RCV002465447]	uncertain significance	X	80704743	80704743	Human	1	name
155797869	CV1860535	single nucleotide variant	NM_153252.5(BRWD3):c.2165C>A (p.Thr722Asn)	not provided [RCV002467177]	uncertain significance	X	80717639	80717639	Human		name
155953056	CV1896420	single nucleotide variant	NM_153252.5(BRWD3):c.2261G>C (p.Gly754Ala)	not provided [RCV003095436]	uncertain significance	X	80716221	80716221	Human		name
10050590	CV192155	single nucleotide variant	NM_153252.5(BRWD3):c.2083A>G (p.Asn695Asp)	not provided [RCV000175490]	uncertain significance	X	80717721	80717721	Human		name
155946860	CV1935683	single nucleotide variant	NM_153252.5(BRWD3):c.1684C>T (p.Arg562Cys)	not provided [RCV002511433]	uncertain significance	X	80722754	80722754	Human		name
156445171	CV1945169	single nucleotide variant	NM_153252.5(BRWD3):c.2012T>C (p.Leu671Ser)	not provided [RCV003116109]	likely benign	X	80719521	80719521	Human		name
156161340	CV1977813	single nucleotide variant	NM_153252.5(BRWD3):c.2378G>A (p.Arg793His)	Inborn genetic diseases [RCV004965956]\|not provided [RCV002594478]	benign\|likely benign	X	80709525	80709525	Human	1	name
155911874	CV2021697	single nucleotide variant	NM_153252.5(BRWD3):c.2671T>G (p.Leu891Val)	not provided [RCV002726866]	likely benign	X	80704728	80704728	Human		name
156259943	CV2037628	single nucleotide variant	NM_153252.5(BRWD3):c.2039A>T (p.Asn680Ile)	not provided [RCV002806293]	likely benign	X	80719494	80719494	Human		name
155967197	CV2049035	single nucleotide variant	NM_153252.5(BRWD3):c.2843A>G (p.Tyr948Cys)	Intellectual disability, X-linked 93 [RCV002776560]	uncertain significance	X	80700057	80700057	Human	1	name
10406469	CV209305	single nucleotide variant	NM_153252.5(BRWD3):c.2105G>A (p.Ser702Asn)	not specified [RCV000192738]	likely benign	X	80717699	80717699	Human		name
156351631	CV2157570	single nucleotide variant	NM_153252.5(BRWD3):c.2413C>T (p.His805Tyr)	not provided [RCV003030917]	uncertain significance	X	80709490	80709490	Human		name
156275916	CV2209718	single nucleotide variant	NM_153252.5(BRWD3):c.2479G>T (p.Asp827Tyr)	Inborn genetic diseases [RCV002669845]\|not provided [RCV003777609]	uncertain significance	X	80707500	80707500	Human	1	name
155915460	CV2243784	single nucleotide variant	NM_153252.5(BRWD3):c.1943A>T (p.Asp648Val)	Inborn genetic diseases [RCV002772217]	uncertain significance	X	80719590	80719590	Human	1	name
155923681	CV2248575	single nucleotide variant	NM_153252.5(BRWD3):c.2183C>T (p.Ala728Val)	Inborn genetic diseases [RCV002773347]	uncertain significance	X	80717621	80717621	Human	1	name
156259913	CV2274151	single nucleotide variant	NM_153252.5(BRWD3):c.1490G>A (p.Arg497Gln)	Inborn genetic diseases [RCV002831645]	likely benign	X	80724964	80724964	Human	1	name
243063760	CV2405160	single nucleotide variant	NM_153252.5(BRWD3):c.2722A>G (p.Lys908Glu)	Intellectual disability, X-linked 93 [RCV003142292]	uncertain significance	X	80703593	80703593	Human	1	name
243064958	CV2409549	single nucleotide variant	NM_153252.5(BRWD3):c.2678C>T (p.Ser893Phe)	Intellectual disability, X-linked 93 [RCV003143821]	uncertain significance	X	80704721	80704721	Human	1	name
243062215	CV2414451	single nucleotide variant	NM_153252.5(BRWD3):c.2095C>T (p.Arg699Ter)	Intellectual disability, X-linked 93 [RCV003139521]	likely pathogenic	X	80717709	80717709	Human	1	name
243051544	CV2415907	duplication	NM_153252.5(BRWD3):c.3899dup (p.Cys1300fs)	Intellectual disability, X-linked 93 [RCV003148525]	likely pathogenic	X	80686968	80686969	Human	1	name
329351109	CV2476261	single nucleotide variant	NM_153252.5(BRWD3):c.2864C>G (p.Ala955Gly)	Intellectual disability, X-linked 93 [RCV003222502]	pathogenic	X	80700036	80700036	Human	1	name
329349576	CV2477121	single nucleotide variant	NM_153252.5(BRWD3):c.1696C>T (p.Arg566Cys)	not provided [RCV003221446]	uncertain significance	X	80722742	80722742	Human		name
329954445	CV2669130	single nucleotide variant	NM_153252.5(BRWD3):c.2062A>T (p.Met688Leu)	not provided [RCV003232963]	uncertain significance	X	80717742	80717742	Human		name
329952380	CV2671730	single nucleotide variant	NM_153252.5(BRWD3):c.1489C>G (p.Arg497Gly)	not provided [RCV003237126]	uncertain significance	X	80724965	80724965	Human		name
401758775	CV2705124	single nucleotide variant	NM_153252.5(BRWD3):c.2698A>G (p.Lys900Glu)	Inborn genetic diseases [RCV003256589]	uncertain significance	X	80704701	80704701	Human	1	name
401740357	CV2738708	single nucleotide variant	NM_153252.5(BRWD3):c.1875T>A (p.Asn625Lys)	not provided [RCV003318102]	uncertain significance	X	80722563	80722563	Human		name
401799234	CV2741812	single nucleotide variant	NM_153252.5(BRWD3):c.2065G>C (p.Asp689His)	not provided [RCV003323220]	uncertain significance	X	80717739	80717739	Human		name
401829976	CV2744099	single nucleotide variant	NM_153252.5(BRWD3):c.2945A>G (p.Glu982Gly)	not provided [RCV003327244]	uncertain significance	X	80696862	80696862	Human		name
401871893	CV2749602	single nucleotide variant	NM_153252.5(BRWD3):c.2861A>G (p.Glu954Gly)	not provided [RCV003332730]	uncertain significance	X	80700039	80700039	Human		name
401859991	CV2794444	single nucleotide variant	NM_153252.5(BRWD3):c.2691G>T (p.Arg897Ser)	not provided [RCV003387612]	uncertain significance	X	80704708	80704708	Human		name
401933304	CV2797601	single nucleotide variant	NM_153252.5(BRWD3):c.2387C>G (p.Thr796Ser)	BRWD3-related disorder [RCV004531718]	uncertain significance	X	80709516	80709516	Human		name , trait , alternate_id
401933502	CV2802194	single nucleotide variant	NM_153252.5(BRWD3):c.2219A>G (p.Asn740Ser)	BRWD3-related disorder [RCV004534248]	uncertain significance	X	80717585	80717585	Human		name , trait , alternate_id
401929087	CV2826575	single nucleotide variant	NM_153252.5(BRWD3):c.2350C>T (p.Arg784Cys)	not provided [RCV003439714]	uncertain significance	X	80709553	80709553	Human		name
401929093	CV2826577	single nucleotide variant	NM_153252.5(BRWD3):c.1586C>T (p.Ala529Val)	not provided [RCV003439716]	uncertain significance	X	80723812	80723812	Human		name
401912945	CV2830104	single nucleotide variant	NM_153252.5(BRWD3):c.2872C>T (p.Arg958Trp)	not provided [RCV003441318]	uncertain significance	X	80700028	80700028	Human		name
401944966	CV2840766	single nucleotide variant	NM_153252.5(BRWD3):c.2233G>A (p.Val745Ile)	not provided [RCV003457610]	uncertain significance	X	80716249	80716249	Human		name
405053886	CV2890102	single nucleotide variant	NM_153252.5(BRWD3):c.2779T>A (p.Trp927Arg)	not provided [RCV003579991]	uncertain significance	X	80703536	80703536	Human		name
405119266	CV2891471	single nucleotide variant	NM_153252.5(BRWD3):c.1085C>T (p.Thr362Met)	not provided [RCV003558884]	uncertain significance	X	80734119	80734119	Human		name
405184365	CV2920434	duplication	NM_153252.5(BRWD3):c.4288dup (p.Ile1430fs)	not provided [RCV003564312]	pathogenic	X	80682573	80682574	Human		name
405135877	CV2958113	single nucleotide variant	NM_153252.5(BRWD3):c.2314A>G (p.Thr772Ala)	not provided [RCV003672812]	benign	X	80716168	80716168	Human		name
404985447	CV2979855	single nucleotide variant	NM_153252.5(BRWD3):c.1467C>G (p.Asn489Lys)	not provided [RCV003691777]	uncertain significance	X	80724987	80724987	Human		name
404978733	CV3013111	single nucleotide variant	NM_153252.5(BRWD3):c.1888G>A (p.Val630Ile)	not provided [RCV003690843]	uncertain significance	X	80719645	80719645	Human		name
405045798	CV3017809	single nucleotide variant	NM_153252.5(BRWD3):c.1340T>G (p.Leu447Trp)	not provided [RCV003696646]	uncertain significance	X	80728798	80728798	Human		name
405063135	CV3020615	single nucleotide variant	NM_153252.5(BRWD3):c.2675A>G (p.Lys892Arg)	not provided [RCV003697832]	uncertain significance	X	80704724	80704724	Human		name
405176355	CV3023774	deletion	NM_153252.5(BRWD3):c.3448del (p.Val1150fs)	not provided [RCV003705126]	pathogenic	X	80691856	80691856	Human		name
405069536	CV3031085	single nucleotide variant	NM_153252.5(BRWD3):c.1397A>G (p.Asp466Gly)	not provided [RCV003698235]	uncertain significance	X	80725057	80725057	Human		name
405088721	CV3044586	single nucleotide variant	NM_153252.5(BRWD3):c.2535A>T (p.Gln845His)	Inborn genetic diseases [RCV004963784]\|not provided [RCV003717663]	uncertain significance	X	80707444	80707444	Human	1	name
405130105	CV3050946	single nucleotide variant	NM_153252.5(BRWD3):c.2740A>G (p.Ile914Val)	not provided [RCV003724750]	uncertain significance	X	80703575	80703575	Human		name
404992485	CV3132381	single nucleotide variant	NM_153252.5(BRWD3):c.2150G>A (p.Arg717Gln)	not provided [RCV003827319]	benign	X	80717654	80717654	Human		name
405036397	CV3140554	single nucleotide variant	NM_153252.5(BRWD3):c.1706A>G (p.Asn569Ser)	not provided [RCV003831036]	uncertain significance	X	80722732	80722732	Human		name
405133636	CV3163911	single nucleotide variant	NM_153252.5(BRWD3):c.2315C>G (p.Thr772Ser)	not provided [RCV003854899]	uncertain significance	X	80716167	80716167	Human		name
405091567	CV3167938	single nucleotide variant	NM_153252.5(BRWD3):c.1408G>A (p.Val470Ile)	not provided [RCV003852328]	benign	X	80725046	80725046	Human		name
405261205	CV3186104	single nucleotide variant	NM_153252.5(BRWD3):c.2464A>G (p.Ser822Gly)	Inborn genetic diseases [RCV004968557]\|not provided [RCV003885180]	uncertain significance	X	80709439	80709439	Human	1	name
405261762	CV3219894	single nucleotide variant	NM_153252.5(BRWD3):c.2296A>G (p.Lys766Glu)	BRWD3-related disorder [RCV004540758]	uncertain significance	X	80716186	80716186	Human		name , trait , alternate_id
405709014	CV3298348	single nucleotide variant	NM_153252.5(BRWD3):c.1663A>G (p.Met555Val)	Inborn genetic diseases [RCV004426518]	uncertain significance	X	80722775	80722775	Human	1	name
405709021	CV3298349	single nucleotide variant	NM_153252.5(BRWD3):c.1834A>G (p.Lys612Glu)	Inborn genetic diseases [RCV004426519]	uncertain significance	X	80722604	80722604	Human	1	name
405709028	CV3298350	single nucleotide variant	NM_153252.5(BRWD3):c.2311T>C (p.Tyr771His)	Inborn genetic diseases [RCV004426520]	uncertain significance	X	80716171	80716171	Human	1	name
405709033	CV3298351	single nucleotide variant	NM_153252.5(BRWD3):c.2339C>A (p.Pro780His)	Inborn genetic diseases [RCV004426521]	uncertain significance	X	80709564	80709564	Human	1	name
407457223	CV3416082	single nucleotide variant	NM_153252.5(BRWD3):c.2415T>A (p.His805Gln)	not provided [RCV004598959]	uncertain significance	X	80709488	80709488	Human		name
408373209	CV3502216	single nucleotide variant	NM_153252.5(BRWD3):c.2654G>T (p.Ser885Ile)	not provided [RCV004725803]	uncertain significance	X	80704745	80704745	Human		name
408368630	CV3514476	single nucleotide variant	NM_153252.5(BRWD3):c.2830G>A (p.Asp944Asn)	BRWD3-related disorder [RCV004735369]	uncertain significance	X	80703485	80703485	Human		name , trait , alternate_id
408394669	CV3518350	duplication	NM_153252.5(BRWD3):c.4888dup (p.Arg1630fs)	Intellectual disability, X-linked 93 [RCV004759673]	uncertain significance	X	80677129	80677130	Human	1	name
408385476	CV3520192	single nucleotide variant	NM_153252.5(BRWD3):c.1298G>A (p.Arg433His)	not provided [RCV004760013]	uncertain significance	X	80728840	80728840	Human		name
408388093	CV3520636	single nucleotide variant	NM_153252.5(BRWD3):c.2624C>T (p.Thr875Ile)	not provided [RCV004761469]	uncertain significance	X	80704775	80704775	Human		name
408391095	CV3521092	single nucleotide variant	NM_153252.5(BRWD3):c.1300T>A (p.Tyr434Asn)	not provided [RCV004762914]	uncertain significance	X	80728838	80728838	Human		name
408392837	CV3525370	single nucleotide variant	NM_153252.5(BRWD3):c.2050A>G (p.Arg684Gly)	not provided [RCV004771256]	uncertain significance	X	80717754	80717754	Human		name
408386149	CV3528807	single nucleotide variant	NM_153252.5(BRWD3):c.2212C>A (p.Leu738Ile)	not provided [RCV004772640]	uncertain significance	X	80717592	80717592	Human		name
408386406	CV3528910	single nucleotide variant	NM_153252.5(BRWD3):c.2194A>G (p.Arg732Gly)	not provided [RCV004772743]	uncertain significance	X	80717610	80717610	Human		name
408389360	CV3529351	single nucleotide variant	NM_153252.5(BRWD3):c.2540A>G (p.Glu847Gly)	not provided [RCV004774173]	uncertain significance	X	80707439	80707439	Human		name
596926066	CV3530684	single nucleotide variant	NM_153252.5(BRWD3):c.1609T>A (p.Leu537Met)	not provided [RCV004778269]	uncertain significance	X	80723789	80723789	Human		name
596929215	CV3531011	single nucleotide variant	NM_153252.5(BRWD3):c.2669A>C (p.Asn890Thr)	not provided [RCV004779585]	uncertain significance	X	80704730	80704730	Human		name
596931188	CV3531521	single nucleotide variant	NM_153252.5(BRWD3):c.1581T>G (p.His527Gln)	not provided [RCV004781083]	uncertain significance	X	80723817	80723817	Human		name
596921919	CV3535548	single nucleotide variant	NM_153252.5(BRWD3):c.2803C>T (p.Arg935Cys)	Intellectual disability, X-linked 93 [RCV004785103]	uncertain significance	X	80703512	80703512	Human	1	name
596927205	CV3536521	single nucleotide variant	NM_153252.5(BRWD3):c.2473G>T (p.Glu825Ter)	Intellectual disability, X-linked 93 [RCV004789930]	pathogenic	X	80709430	80709430	Human	1	name
596943937	CV3543049	single nucleotide variant	NM_153252.5(BRWD3):c.1519A>G (p.Met507Val)	not provided [RCV004798634]	uncertain significance	X	80724935	80724935	Human		name
596944928	CV3543582	single nucleotide variant	NM_153252.5(BRWD3):c.2555A>T (p.Asp852Val)	not provided [RCV004801704]	uncertain significance	X	80704844	80704844	Human		name
597630981	CV3552519	deletion	NM_153252.5(BRWD3):c.4186del (p.Gln1396fs)	Intellectual disability, X-linked 93 [RCV004823272]	likely pathogenic	X	80684057	80684057	Human	1	name
597637421	CV3637308	single nucleotide variant	NM_153252.5(BRWD3):c.2251A>G (p.Thr751Ala)	Inborn genetic diseases [RCV004970196]	uncertain significance	X	80716231	80716231	Human	1	name
597660486	CV3731829	single nucleotide variant	NM_153252.5(BRWD3):c.1150C>T (p.Arg384Ter)	Intellectual disability, X-linked 93 [RCV005002049]	likely pathogenic	X	80729998	80729998	Human	1	name
597843261	CV3735878	single nucleotide variant	NM_153252.5(BRWD3):c.2554G>A (p.Asp852Asn)	not provided [RCV005065227]	uncertain significance	X	80704845	80704845	Human		name
597920491	CV3765128	single nucleotide variant	NM_153252.5(BRWD3):c.2441C>T (p.Ser814Leu)	not provided [RCV005115145]	uncertain significance	X	80709462	80709462	Human		name
597871671	CV3768372	single nucleotide variant	NM_153252.5(BRWD3):c.2254G>A (p.Ala752Thr)	not provided [RCV005122751]	uncertain significance	X	80716228	80716228	Human		name
597925228	CV3772643	single nucleotide variant	NM_153252.5(BRWD3):c.2248C>T (p.Arg750Ter)	not provided [RCV005115793]	pathogenic	X	80716234	80716234	Human		name
597906786	CV3781385	single nucleotide variant	NM_153252.5(BRWD3):c.2814T>A (p.Phe938Leu)	not provided [RCV005128073]	benign	X	80703501	80703501	Human		name
597899736	CV3782927	single nucleotide variant	NM_153252.5(BRWD3):c.1658A>T (p.Asp553Val)	not provided [RCV005126947]	uncertain significance	X	80722780	80722780	Human		name
597894673	CV3785627	single nucleotide variant	NM_153252.5(BRWD3):c.2150G>T (p.Arg717Leu)	not provided [RCV005126213]	uncertain significance	X	80717654	80717654	Human		name
597972409	CV3790263	single nucleotide variant	NM_153252.5(BRWD3):c.1228A>G (p.Thr410Ala)	not provided [RCV005142686]	uncertain significance	X	80729920	80729920	Human		name
12833181	CV379476	single nucleotide variant	NM_153252.5(BRWD3):c.2327A>T (p.Asn776Ile)	not provided [RCV000418033]	uncertain significance	X	80709576	80709576	Human		name
12846884	CV379480	single nucleotide variant	NM_153252.5(BRWD3):c.1808G>A (p.Arg603Gln)	not provided [RCV000442499]	uncertain significance	X	80722630	80722630	Human		name
597961836	CV3795277	single nucleotide variant	NM_153252.5(BRWD3):c.1421A>G (p.His474Arg)	not provided [RCV005138969]	uncertain significance	X	80725033	80725033	Human		name
12839541	CV379553	single nucleotide variant	NM_153252.5(BRWD3):c.1792C>G (p.Pro598Ala)	not provided [RCV000429005]	uncertain significance	X	80722646	80722646	Human		name
12838712	CV379556	single nucleotide variant	NM_153252.5(BRWD3):c.1645G>A (p.Glu549Lys)	not provided [RCV000427455]	uncertain significance	X	80723753	80723753	Human		name
597958756	CV3797361	single nucleotide variant	NM_153252.5(BRWD3):c.2501A>T (p.Asp834Val)	not provided [RCV005138048]	uncertain significance	X	80707478	80707478	Human		name
597956808	CV3800304	single nucleotide variant	NM_153252.5(BRWD3):c.2407A>G (p.Ile803Val)	not provided [RCV005137396]	uncertain significance	X	80709496	80709496	Human		name
597857957	CV3822339	single nucleotide variant	NM_153252.5(BRWD3):c.2273T>C (p.Ile758Thr)	not provided [RCV005174637]	uncertain significance	X	80716209	80716209	Human		name
597915629	CV3845632	single nucleotide variant	NM_153252.5(BRWD3):c.2463C>G (p.Asp821Glu)	not provided [RCV005183427]	uncertain significance	X	80709440	80709440	Human		name
598126281	CV3886179	single nucleotide variant	NM_153252.5(BRWD3):c.1577A>C (p.Asn526Thr)	not provided [RCV005241982]	uncertain significance	X	80723821	80723821	Human		name
598127756	CV3888314	single nucleotide variant	NM_153252.5(BRWD3):c.2147C>T (p.Pro716Leu)	not provided [RCV005243000]	uncertain significance	X	80717657	80717657	Human		name
598202411	CV3892837	single nucleotide variant	NM_153252.5(BRWD3):c.1563T>G (p.Phe521Leu)	not provided [RCV005255167]	uncertain significance	X	80723835	80723835	Human		name
598236330	CV3893489	single nucleotide variant	NM_153252.5(BRWD3):c.2777A>C (p.Gln926Pro)	not provided [RCV005256222]	uncertain significance	X	80703538	80703538	Human		name
598174743	CV3939091	single nucleotide variant	NM_153252.5(BRWD3):c.2009A>G (p.His670Arg)	Inborn genetic diseases [RCV005309756]	uncertain significance	X	80719524	80719524	Human	1	name
598174746	CV3939092	single nucleotide variant	NM_153252.5(BRWD3):c.2696A>G (p.Lys899Arg)	Inborn genetic diseases [RCV005309757]	uncertain significance	X	80704703	80704703	Human	1	name
598174751	CV3939093	single nucleotide variant	NM_153252.5(BRWD3):c.1490G>C (p.Arg497Pro)	Inborn genetic diseases [RCV005309758]	uncertain significance	X	80724964	80724964	Human	1	name
616939383	CV4015714	single nucleotide variant	NM_153252.5(BRWD3):c.2221G>A (p.Gly741Arg)	Intellectual disability, X-linked 93 [RCV005413226]	uncertain significance	X	80717583	80717583	Human	1	name
616935874	CV4015949	single nucleotide variant	NM_153252.5(BRWD3):c.2035G>A (p.Val679Ile)	not provided [RCV005414813]	uncertain significance	X	80719498	80719498	Human		name
617150952	CV4021953	single nucleotide variant	NM_153252.5(BRWD3):c.2932A>G (p.Met978Val)	not provided [RCV005426914]	uncertain significance	X	80699968	80699968	Human		name
12902390	CV411500	single nucleotide variant	NM_153252.5(BRWD3):c.1633A>G (p.Ser545Gly)	not provided [RCV000486984]	uncertain significance	X	80723765	80723765	Human		name
13211340	CV426496	single nucleotide variant	NM_153252.5(BRWD3):c.2535A>C (p.Gln845His)	not provided [RCV000497311]	uncertain significance	X	80707444	80707444	Human		name
13215741	CV430947	single nucleotide variant	NM_153252.5(BRWD3):c.1300T>C (p.Tyr434His)	Inborn genetic diseases [RCV000623943]\|not provided [RCV005091086]\|not specified [RCV000502884]	benign\|likely benign\|uncertain significance	X	80728838	80728838	Human	1	name
13488423	CV446794	single nucleotide variant	NM_153252.5(BRWD3):c.2551A>G (p.Ser851Gly)	not provided [RCV000523558]	uncertain significance	X	80707428	80707428	Human		name
13830792	CV581012	single nucleotide variant	NM_153252.5(BRWD3):c.2729G>C (p.Gly910Ala)	Inborn genetic diseases [RCV002318869]\|not provided [RCV000922929]	benign	X	80703586	80703586	Human	1	name
13829061	CV581015	single nucleotide variant	NM_153252.5(BRWD3):c.2300A>C (p.Lys767Thr)	Inborn genetic diseases [RCV002314478]	uncertain significance	X	80716182	80716182	Human	1	name
13829911	CV581198	single nucleotide variant	NM_153252.5(BRWD3):c.1505G>A (p.Arg502Gln)	History of neurodevelopmental disorder [RCV000719144]\|not provided [RCV003225116]	uncertain significance	X	80724949	80724949	Human		name
13836901	CV588184	single nucleotide variant	NM_153252.5(BRWD3):c.1858C>A (p.Leu620Met)	not provided [RCV000733148]	uncertain significance	X	80722580	80722580	Human		name
14981534	CV613548	deletion	NM_153252.5(BRWD3):c.3791del (p.Ser1264fs)	Intellectual disability [RCV000850218]	pathogenic	X	80689784	80689784	Human	2	name
14746761	CV672121	single nucleotide variant	NM_153252.5(BRWD3):c.2878G>A (p.Val960Ile)	BRWD3-related disorder [RCV000844959]\|not provided [RCV001759635]	uncertain significance\|not provided	X	80700022	80700022	Human	1	name , trait , alternate_id
21073761	CV792513	single nucleotide variant	NM_153252.5(BRWD3):c.1690C>T (p.Leu564Phe)	Intellectual disability, X-linked 93 [RCV000990890]	likely pathogenic\|uncertain significance	X	80722748	80722748	Human	1	name
21075145	CV798416	single nucleotide variant	NM_153252.5(BRWD3):c.1919A>G (p.Asn640Ser)	not provided [RCV000995979]	uncertain significance	X	80719614	80719614	Human		name
28876501	CV903244	single nucleotide variant	NM_153252.5(BRWD3):c.2026G>A (p.Ala676Thr)	Intellectual disability, X-linked 93 [RCV001166163]	uncertain significance	X	80719507	80719507	Human	1	name
28876505	CV903245	single nucleotide variant	NM_153252.5(BRWD3):c.1384T>C (p.Ser462Pro)	Intellectual disability, X-linked 93 [RCV001166164]\|not provided [RCV002558621]	likely benign\|uncertain significance	X	80728754	80728754	Human	1	name
38596409	CV964007	single nucleotide variant	NM_153252.5(BRWD3):c.2377C>T (p.Arg793Cys)	Intellectual disability [RCV001251697]\|not provided [RCV003669215]	likely benign\|uncertain significance	X	80709526	80709526	Human	2	name
40903444	CV977312	single nucleotide variant	NM_153252.5(BRWD3):c.1118A>G (p.Asn373Ser)	BRWD3-related X-linked syndromic intellectual disability [RCV001270718]	uncertain significance	X	80733465	80733465	Human		name , trait
126744568	CV1019087	single nucleotide variant	NM_153252.5(BRWD3):c.4705A>G (p.Thr1569Ala)	Intellectual disability, X-linked 93 [RCV001330466]\|not provided [RCV001751644]	uncertain significance	X	80677313	80677313	Human	1	name
126744564	CV1019088	single nucleotide variant	NM_153252.5(BRWD3):c.4138G>A (p.Glu1380Lys)	Intellectual disability, X-linked 93 [RCV001330465]	uncertain significance	X	80684105	80684105	Human	1	name
150332916	CV1164613	single nucleotide variant	NM_153252.5(BRWD3):c.4339C>T (p.Arg1447Trp)	not provided [RCV001528547]	uncertain significance	X	80682523	80682523	Human		name
150336106	CV1166493	single nucleotide variant	NM_153252.5(BRWD3):c.4786A>C (p.Lys1596Gln)	not provided [RCV001531794]	uncertain significance	X	80677232	80677232	Human		name
150425022	CV1185865	single nucleotide variant	NM_153252.5(BRWD3):c.5173C>T (p.Arg1725Ter)	not provided [RCV001557451]	likely pathogenic	X	80676845	80676845	Human		name
150425124	CV1185866	single nucleotide variant	NM_153252.5(BRWD3):c.5081G>A (p.Arg1694Gln)	not provided [RCV001557594]	uncertain significance	X	80676937	80676937	Human		name
150521340	CV1289060	single nucleotide variant	NM_153252.5(BRWD3):c.5273T>C (p.Leu1758Ser)	not provided [RCV001725824]	uncertain significance	X	80676745	80676745	Human		name
150533253	CV1294143	single nucleotide variant	NM_153252.5(BRWD3):c.4955G>C (p.Arg1652Thr)	not provided [RCV001758161]	uncertain significance	X	80677063	80677063	Human		name
150556123	CV1297986	single nucleotide variant	NM_153252.5(BRWD3):c.3557C>G (p.Thr1186Ser)	not provided [RCV001773950]	uncertain significance	X	80691098	80691098	Human		name
150541062	CV1298653	single nucleotide variant	NM_153252.5(BRWD3):c.5078G>T (p.Gly1693Val)	not provided [RCV001760801]	uncertain significance	X	80676940	80676940	Human		name
150556524	CV1303217	single nucleotide variant	NM_153252.5(BRWD3):c.4345A>G (p.Arg1449Gly)	Inborn genetic diseases [RCV003346685]\|not provided [RCV001774410]	uncertain significance	X	80682517	80682517	Human	1	name
150553586	CV1303595	single nucleotide variant	NM_153252.5(BRWD3):c.3397C>T (p.Pro1133Ser)	not provided [RCV001769285]	uncertain significance	X	80691907	80691907	Human		name
150547998	CV1303968	single nucleotide variant	NM_153252.5(BRWD3):c.3083C>T (p.Pro1028Leu)	not provided [RCV001764071]	uncertain significance	X	80695976	80695976	Human		name
150555828	CV1305314	single nucleotide variant	NM_153252.5(BRWD3):c.3873C>G (p.Cys1291Trp)	not provided [RCV001773247]	uncertain significance	X	80686995	80686995	Human		name
150555838	CV1305327	single nucleotide variant	NM_153252.5(BRWD3):c.5208G>C (p.Met1736Ile)	not provided [RCV001773260]	uncertain significance	X	80676810	80676810	Human		name
150544017	CV1310066	single nucleotide variant	NM_153252.5(BRWD3):c.4228T>G (p.Ser1410Ala)	not provided [RCV003238070]	likely pathogenic	X	80684015	80684015	Human		name
150544033	CV1310073	single nucleotide variant	NM_153252.5(BRWD3):c.3232C>A (p.Pro1078Thr)	not provided [RCV003238075]	uncertain significance	X	80692971	80692971	Human		name
151235431	CV1318745	single nucleotide variant	NM_153252.5(BRWD3):c.3730G>C (p.Asp1244His)	Intellectual disability, X-linked 93 [RCV001795563]	uncertain significance	X	80689845	80689845	Human	1	name
151352275	CV1322361	single nucleotide variant	NM_153252.5(BRWD3):c.4645G>A (p.Val1549Ile)	not provided [RCV001806985]	uncertain significance	X	80681350	80681350	Human		name
151755856	CV1334841	single nucleotide variant	NM_153252.5(BRWD3):c.3893T>A (p.Leu1298Ter)	Intellectual disability, X-linked 93 [RCV001843797]	likely pathogenic	X	80686975	80686975	Human	1	name
151864307	CV1336814	single nucleotide variant	NM_153252.5(BRWD3):c.4211A>G (p.Tyr1404Cys)	not provided [RCV002034852]	uncertain significance	X	80684032	80684032	Human		name
151741988	CV1386767	single nucleotide variant	NM_153252.5(BRWD3):c.4635A>T (p.Arg1545Ser)	not provided [RCV001893355]	conflicting interpretations of pathogenicity\|uncertain significance	X	80681360	80681360	Human		name
151730573	CV1517812	single nucleotide variant	NM_153252.5(BRWD3):c.3976C>T (p.Arg1326Ter)	Intellectual disability, X-linked 93 [RCV002052427]	pathogenic	X	80686892	80686892	Human	1	name
151730578	CV1517813	single nucleotide variant	NM_153252.5(BRWD3):c.3413G>T (p.Trp1138Leu)	Intellectual disability, X-linked 93 [RCV002052428]	pathogenic	X	80691891	80691891	Human	1	name
153304183	CV1690644	single nucleotide variant	NM_153252.5(BRWD3):c.3591T>A (p.Asn1197Lys)	not provided [RCV002269688]	uncertain significance	X	80691064	80691064	Human		name
155267196	CV1699479	single nucleotide variant	NM_153252.5(BRWD3):c.3146A>G (p.Gln1049Arg)	not provided [RCV002283274]	uncertain significance	X	80695913	80695913	Human		name
155641819	CV1707145	single nucleotide variant	NM_153252.5(BRWD3):c.5233C>T (p.Pro1745Ser)	not provided [RCV002288075]	uncertain significance	X	80676785	80676785	Human		name
155747052	CV1778202	single nucleotide variant	NM_153252.5(BRWD3):c.3965C>G (p.Ser1322Trp)	not provided [RCV002303559]	uncertain significance	X	80686903	80686903	Human		name
155715790	CV1780423	single nucleotide variant	NM_153252.5(BRWD3):c.4472C>G (p.Thr1491Ser)	not provided [RCV002306028]	uncertain significance	X	80682020	80682020	Human		name
155733881	CV1788105	single nucleotide variant	NM_153252.5(BRWD3):c.4253G>A (p.Arg1418Gln)	Inborn genetic diseases [RCV002329883]	uncertain significance	X	80682609	80682609	Human	1	name
155683246	CV1792410	single nucleotide variant	NM_153252.5(BRWD3):c.3445C>T (p.Arg1149Trp)	Inborn genetic diseases [RCV002457157]\|not provided [RCV005254064]	uncertain significance	X	80691859	80691859	Human	1	name
155730319	CV1796094	single nucleotide variant	NM_153252.5(BRWD3):c.3596T>A (p.Phe1199Tyr)	Inborn genetic diseases [RCV002339847]	uncertain significance	X	80691059	80691059	Human	1	name
155738164	CV1805038	single nucleotide variant	NM_153252.5(BRWD3):c.4576G>T (p.Gly1526Ter)	Inborn genetic diseases [RCV002342162]	pathogenic	X	80681419	80681419	Human	1	name
155738335	CV1805116	single nucleotide variant	NM_153252.5(BRWD3):c.4586G>A (p.Arg1529Gln)	Inborn genetic diseases [RCV002342240]\|Intellectual disability, X-linked 93 [RCV003146544]\|not provided [RCV005096602]	benign\|uncertain significance	X	80681409	80681409	Human	2	name
155803794	CV1858360	single nucleotide variant	NM_153252.5(BRWD3):c.4631A>G (p.Asn1544Ser)	not provided [RCV002462670]	uncertain significance	X	80681364	80681364	Human		name
155798214	CV1863506	single nucleotide variant	NM_153252.5(BRWD3):c.3605G>T (p.Arg1202Ile)	not provided [RCV002473401]	likely pathogenic\|uncertain significance	X	80690090	80690090	Human		name
156050040	CV1867661	single nucleotide variant	NM_153252.5(BRWD3):c.4208C>T (p.Ala1403Val)	not provided [RCV002510133]	uncertain significance	X	80684035	80684035	Human		name
156390839	CV1869902	single nucleotide variant	NM_153252.5(BRWD3):c.4384A>G (p.Ser1462Gly)	Intellectual disability, X-linked 93 [RCV003985112]\|not provided [RCV003067998]\|not specified [RCV003155509]	benign\|uncertain significance	X	80682478	80682478	Human	1	name
156407503	CV1918144	single nucleotide variant	NM_153252.5(BRWD3):c.3761A>T (p.Tyr1254Phe)	not provided [RCV002606913]	likely benign	X	80689814	80689814	Human		name
155945891	CV1935621	single nucleotide variant	NM_153252.5(BRWD3):c.3899G>A (p.Cys1300Tyr)	not provided [RCV002511369]	uncertain significance	X	80686969	80686969	Human		name
156394596	CV1983671	single nucleotide variant	NM_153252.5(BRWD3):c.4553C>A (p.Pro1518Gln)	not provided [RCV002605017]	benign	X	80681442	80681442	Human		name
156254513	CV2003658	single nucleotide variant	NM_153252.5(BRWD3):c.4234A>C (p.Ile1412Leu)	Inborn genetic diseases [RCV002653067]\|not provided [RCV002627561]	benign\|likely benign	X	80682628	80682628	Human	1	name
156223487	CV2080500	single nucleotide variant	NM_153252.5(BRWD3):c.3397C>A (p.Pro1133Thr)	not provided [RCV002875961]	likely benign	X	80691907	80691907	Human		name
10404515	CV209301	single nucleotide variant	NM_153252.5(BRWD3):c.5101G>A (p.Gly1701Arg)	Inborn genetic diseases [RCV002345688]\|Intellectual disability [RCV001251698]\|Intellectual disability, X-linked 93 [RCV000599839]\|not provided [RCV001701635]\|not specified [RCV000195263]	likely pathogenic\|likely benign\|uncertain significance	X	80676917	80676917	Human	4	name
10406579	CV209303	single nucleotide variant	NM_153252.5(BRWD3):c.3541G>A (p.Val1181Ile)	not specified [RCV000193229]	uncertain significance	X	80691114	80691114	Human		name
156355014	CV2129822	single nucleotide variant	NM_153252.5(BRWD3):c.3007T>G (p.Leu1003Val)	Inborn genetic diseases [RCV002966589]\|not provided [RCV002966588]	uncertain significance	X	80696800	80696800	Human	1	name
156014430	CV2133993	single nucleotide variant	NM_153252.5(BRWD3):c.4214C>A (p.Thr1405Asn)	not provided [RCV003017918]	uncertain significance	X	80684029	80684029	Human		name
10405918	CV213673	single nucleotide variant	NM_153252.5(BRWD3):c.4255T>G (p.Leu1419Val)	Intellectual disability, X-linked 93 [RCV000199586]\|not specified [RCV003235122]	likely pathogenic\|uncertain significance	X	80682607	80682607	Human	1	name
156143597	CV2163968	single nucleotide variant	NM_153252.5(BRWD3):c.3553C>T (p.Pro1185Ser)	not provided [RCV003022608]	uncertain significance	X	80691102	80691102	Human		name
156228215	CV2212947	single nucleotide variant	NM_153252.5(BRWD3):c.4123G>A (p.Val1375Met)	Inborn genetic diseases [RCV002712580]	uncertain significance	X	80684120	80684120	Human	1	name
156359564	CV2257779	single nucleotide variant	NM_153252.5(BRWD3):c.4102A>T (p.Thr1368Ser)	Inborn genetic diseases [RCV002812610]	uncertain significance	X	80684141	80684141	Human	1	name
155904943	CV2285747	single nucleotide variant	NM_153252.5(BRWD3):c.4791G>T (p.Glu1597Asp)	Inborn genetic diseases [RCV002837069]	uncertain significance	X	80677227	80677227	Human	1	name
155906425	CV2357321	single nucleotide variant	NM_153252.5(BRWD3):c.3875G>A (p.Arg1292Gln)	Inborn genetic diseases [RCV002990556]	likely benign	X	80686993	80686993	Human	1	name
156305037	CV2369308	single nucleotide variant	NM_153252.5(BRWD3):c.3578G>A (p.Arg1193Gln)	Inborn genetic diseases [RCV003010635]\|not provided [RCV003565607]	benign\|likely benign	X	80691077	80691077	Human	1	name
11350953	CV237187	single nucleotide variant	NM_153252.5(BRWD3):c.3718C>T (p.Arg1240Ter)	Intellectual disability, X-linked 93 [RCV001814124]\|not provided [RCV000224684]	pathogenic\|likely pathogenic	X	80689977	80689977	Human	1	name
156440140	CV2401825	single nucleotide variant	NM_153252.5(BRWD3):c.4502A>T (p.Asp1501Val)	not provided [RCV003110113]	uncertain significance	X	80681493	80681493	Human		name
156434517	CV2402978	single nucleotide variant	NM_153252.5(BRWD3):c.4823A>G (p.Glu1608Gly)	not provided [RCV003126406]	uncertain significance	X	80677195	80677195	Human		name
156435406	CV2403545	single nucleotide variant	NM_153252.5(BRWD3):c.4510G>A (p.Glu1504Lys)	Autism spectrum disorder [RCV003128007]	uncertain significance	X	80681485	80681485	Human	2	name
243052370	CV2404368	single nucleotide variant	NM_153252.5(BRWD3):c.3053A>C (p.Glu1018Ala)	not provided [RCV003129394]	uncertain significance	X	80696754	80696754	Human		name
243064959	CV2409550	single nucleotide variant	NM_153252.5(BRWD3):c.4025G>A (p.Gly1342Glu)	Intellectual disability, X-linked 93 [RCV003143822]	uncertain significance	X	80685517	80685517	Human	1	name
243064960	CV2409551	single nucleotide variant	NM_153252.5(BRWD3):c.5206A>T (p.Met1736Leu)	Intellectual disability, X-linked 93 [RCV003143823]	uncertain significance	X	80676812	80676812	Human	1	name
243064963	CV2409554	single nucleotide variant	NM_153252.5(BRWD3):c.4784C>T (p.Thr1595Ile)	Intellectual disability, X-linked 93 [RCV003143826]	uncertain significance	X	80677234	80677234	Human	1	name
243064964	CV2409555	single nucleotide variant	NM_153252.5(BRWD3):c.3119A>G (p.Tyr1040Cys)	Intellectual disability, X-linked 93 [RCV003143827]	uncertain significance	X	80695940	80695940	Human	1	name
243050112	CV2415374	single nucleotide variant	NM_153252.5(BRWD3):c.3724A>G (p.Ile1242Val)	Inborn genetic diseases [RCV003164866]\|Intellectual disability, X-linked 93 [RCV003147889]	uncertain significance	X	80689971	80689971	Human	2	name
243049837	CV2417207	single nucleotide variant	NM_153252.5(BRWD3):c.3171A>G (p.Ile1057Met)	not provided [RCV003152078]	uncertain significance	X	80693032	80693032	Human		name
329350628	CV2421753	single nucleotide variant	NM_153252.5(BRWD3):c.4798C>G (p.His1600Asp)	not provided [RCV003159456]	uncertain significance	X	80677220	80677220	Human		name
329350571	CV2477389	single nucleotide variant	NM_153252.5(BRWD3):c.4004C>T (p.Pro1335Leu)	not provided [RCV003221714]	uncertain significance	X	80686864	80686864	Human		name
329847402	CV2524238	single nucleotide variant	NM_153252.5(BRWD3):c.3784C>T (p.Arg1262Ter)	not provided [RCV003227130]	likely pathogenic	X	80689791	80689791	Human		name
329847671	CV2524419	single nucleotide variant	NM_153252.5(BRWD3):c.4855T>C (p.Cys1619Arg)	not provided [RCV003227311]	uncertain significance	X	80677163	80677163	Human		name
8561925	CV25843	single nucleotide variant	NM_153252.5(BRWD3):c.4786A>G (p.Lys1596Glu)	Intellectual disability, X-linked 93 [RCV000011551]	pathogenic	X	80677232	80677232	Human	1	name
11635938	CV264927	single nucleotide variant	NM_153252.5(BRWD3):c.4309G>A (p.Ala1437Thr)	Inborn genetic diseases [RCV004021052]\|not provided [RCV000727485]	conflicting interpretations of pathogenicity\|uncertain significance	X	80682553	80682553	Human	1	name
11642235	CV265317	single nucleotide variant	NM_153252.5(BRWD3):c.3863A>G (p.Lys1288Arg)	Intellectual disability, X-linked 93 [RCV001553916]\|not provided [RCV001668619]\|not specified [RCV000371280]	benign	X	80688070	80688070	Human	1	name
401737127	CV2699679	single nucleotide variant	NM_153252.5(BRWD3):c.4573G>A (p.Gly1525Ser)	Inborn genetic diseases [RCV003250204]\|not provided [RCV004809990]	likely benign	X	80681422	80681422	Human	1	name
401718702	CV2704759	single nucleotide variant	NM_153252.5(BRWD3):c.3607A>T (p.Ile1203Leu)	Inborn genetic diseases [RCV003266631]	uncertain significance	X	80690088	80690088	Human	1	name
401741365	CV2738817	single nucleotide variant	NM_153252.5(BRWD3):c.5020G>A (p.Gly1674Ser)	not provided [RCV003318211]	uncertain significance	X	80676998	80676998	Human		name
401796866	CV2739841	single nucleotide variant	NM_153252.5(BRWD3):c.3799G>A (p.Ala1267Thr)	not provided [RCV003319802]	uncertain significance	X	80689776	80689776	Human		name
401799171	CV2741748	single nucleotide variant	NM_153252.5(BRWD3):c.3100C>T (p.Leu1034Phe)	not provided [RCV003323156]	uncertain significance	X	80695959	80695959	Human		name
401829548	CV2747454	single nucleotide variant	NM_153252.5(BRWD3):c.3413G>C (p.Trp1138Ser)	not provided [RCV003328919]	uncertain significance	X	80691891	80691891	Human		name
401870523	CV2769281	single nucleotide variant	NM_153252.5(BRWD3):c.4651C>G (p.Gln1551Glu)	Inborn genetic diseases [RCV003346164]	likely benign	X	80681344	80681344	Human	1	name
401859221	CV2771482	single nucleotide variant	NM_153252.5(BRWD3):c.4546G>C (p.Asp1516His)	Inborn genetic diseases [RCV003357042]	likely benign	X	80681449	80681449	Human	1	name
401915964	CV2795351	single nucleotide variant	NM_153252.5(BRWD3):c.3413G>A (p.Trp1138Ter)	Neurodevelopmental disorder [RCV003389186]\|not provided [RCV004593283]	pathogenic\|likely pathogenic	X	80691891	80691891	Human	1	name
401938007	CV2797382	single nucleotide variant	NM_153252.5(BRWD3):c.3785G>A (p.Arg1262Gln)	BRWD3-related disorder [RCV004531689]\|not provided [RCV005062898]	benign\|uncertain significance	X	80689790	80689790	Human	1	name , trait , alternate_id
401919443	CV2798362	single nucleotide variant	NM_153252.5(BRWD3):c.4432C>T (p.Pro1478Ser)	BRWD3-related disorder [RCV004527883]\|not provided [RCV005061390]	uncertain significance	X	80682060	80682060	Human	1	name , trait , alternate_id
401929071	CV2826570	single nucleotide variant	NM_153252.5(BRWD3):c.4702C>T (p.Arg1568Trp)	not provided [RCV003439709]	likely benign	X	80677316	80677316	Human		name
401929073	CV2826571	single nucleotide variant	NM_153252.5(BRWD3):c.4642C>G (p.Pro1548Ala)	not provided [RCV003439710]	uncertain significance	X	80681353	80681353	Human		name
401929080	CV2826573	single nucleotide variant	NM_153252.5(BRWD3):c.4340G>A (p.Arg1447Gln)	not provided [RCV003439712]	uncertain significance	X	80682522	80682522	Human		name
401916213	CV2829425	single nucleotide variant	NM_153252.5(BRWD3):c.3635A>G (p.Tyr1212Cys)	not provided [RCV003443274]	uncertain significance	X	80690060	80690060	Human		name
401912993	CV2830137	single nucleotide variant	NM_153252.5(BRWD3):c.4236C>G (p.Ile1412Met)	not provided [RCV003441352]	uncertain significance	X	80682626	80682626	Human		name
401913536	CV2830442	single nucleotide variant	NM_153252.5(BRWD3):c.4006G>C (p.Gly1336Arg)	not provided [RCV003441657]	uncertain significance	X	80685536	80685536	Human		name
401916243	CV2831014	single nucleotide variant	NM_153252.5(BRWD3):c.4693A>G (p.Arg1565Gly)	not provided [RCV003443283]	uncertain significance	X	80677325	80677325	Human		name
405869504	CV2832023	single nucleotide variant	NM_153252.5(BRWD3):c.3121A>C (p.Asn1041His)	not provided [RCV004573034]	uncertain significance	X	80695938	80695938	Human		name
405223666	CV2919151	single nucleotide variant	NM_153252.5(BRWD3):c.4310C>G (p.Ala1437Gly)	not provided [RCV003568808]	uncertain significance	X	80682552	80682552	Human		name
405227828	CV2980548	single nucleotide variant	NM_153252.5(BRWD3):c.3943C>T (p.Leu1315Phe)	not provided [RCV003711010]	uncertain significance	X	80686925	80686925	Human		name
402491371	CV3011945	single nucleotide variant	NM_153252.5(BRWD3):c.3583C>G (p.Leu1195Val)	not provided [RCV003687567]	uncertain significance	X	80691072	80691072	Human		name
405069383	CV3030949	single nucleotide variant	NM_153252.5(BRWD3):c.4286A>G (p.Asn1429Ser)	not provided [RCV003698146]	uncertain significance	X	80682576	80682576	Human		name
405114895	CV3134079	single nucleotide variant	NM_153252.5(BRWD3):c.3164G>A (p.Arg1055His)	not provided [RCV003836681]	likely benign	X	80693039	80693039	Human		name
405232645	CV3144919	single nucleotide variant	NM_153252.5(BRWD3):c.4907T>G (p.Val1636Gly)	not provided [RCV003853176]	uncertain significance	X	80677111	80677111	Human		name
402471154	CV3171499	single nucleotide variant	NM_153252.5(BRWD3):c.3955C>T (p.Arg1319Cys)	not provided [RCV003874283]	uncertain significance	X	80686913	80686913	Human		name
405270323	CV3187687	single nucleotide variant	NM_153252.5(BRWD3):c.3714A>C (p.Leu1238Phe)	not provided [RCV003887771]	uncertain significance	X	80689981	80689981	Human		name
405288998	CV3193939	single nucleotide variant	NM_153252.5(BRWD3):c.3179A>T (p.Asp1060Val)	BRWD3-related disorder [RCV004544156]	uncertain significance	X	80693024	80693024	Human		name , trait , alternate_id
405709041	CV3298352	single nucleotide variant	NM_153252.5(BRWD3):c.4235T>C (p.Ile1412Thr)	Inborn genetic diseases [RCV004426522]	uncertain significance	X	80682627	80682627	Human	1	name
407426566	CV3411398	single nucleotide variant	NM_153252.5(BRWD3):c.3890C>G (p.Ser1297Cys)	not provided [RCV004590575]	uncertain significance	X	80686978	80686978	Human		name
407488521	CV3421563	single nucleotide variant	NM_153252.5(BRWD3):c.4234A>G (p.Ile1412Val)	Inborn genetic diseases [RCV004603989]	uncertain significance	X	80682628	80682628	Human	1	name
407574544	CV3499555	single nucleotide variant	NM_153252.5(BRWD3):c.3409G>A (p.Glu1137Lys)	not provided [RCV004719550]	uncertain significance	X	80691895	80691895	Human		name
408371080	CV3504662	single nucleotide variant	NM_153252.5(BRWD3):c.3709G>A (p.Val1237Ile)	BRWD3-related disorder [RCV004724372]\|not provided [RCV005103657]	uncertain significance	X	80689986	80689986	Human	1	name , trait , alternate_id
408386719	CV3518508	single nucleotide variant	NM_153252.5(BRWD3):c.4406G>A (p.Gly1469Glu)	not provided [RCV004760826]	uncertain significance	X	80682086	80682086	Human		name
408392954	CV3519628	single nucleotide variant	NM_153252.5(BRWD3):c.3593G>A (p.Arg1198His)	not provided [RCV004763924]	uncertain significance	X	80691062	80691062	Human		name
408388652	CV3522712	single nucleotide variant	NM_153252.5(BRWD3):c.3073C>G (p.His1025Asp)	not provided [RCV004769093]	uncertain significance	X	80695986	80695986	Human		name
408389526	CV3524599	single nucleotide variant	NM_153252.5(BRWD3):c.4441G>C (p.Asp1481His)	not provided [RCV004769494]	uncertain significance	X	80682051	80682051	Human		name
408381538	CV3526528	single nucleotide variant	NM_153252.5(BRWD3):c.4731T>G (p.Ser1577Arg)	not provided [RCV004771841]	uncertain significance	X	80677287	80677287	Human		name
596931432	CV3531768	single nucleotide variant	NM_153252.5(BRWD3):c.3149T>C (p.Ile1050Thr)	not provided [RCV004781330]	uncertain significance	X	80695910	80695910	Human		name
596920945	CV3534317	single nucleotide variant	NM_153252.5(BRWD3):c.4562C>T (p.Ser1521Leu)	not specified [RCV004783536]	uncertain significance	X	80681433	80681433	Human		name
596921856	CV3535483	single nucleotide variant	NM_153252.5(BRWD3):c.5357G>A (p.Arg1786His)	Intellectual disability, X-linked 93 [RCV004785038]	uncertain significance	X	80676661	80676661	Human	1	name
596927208	CV3536522	single nucleotide variant	NM_153252.5(BRWD3):c.3962A>T (p.Asp1321Val)	Intellectual disability, X-linked 93 [RCV004789931]	uncertain significance	X	80686906	80686906	Human	1	name
596923043	CV3537527	single nucleotide variant	NM_153252.5(BRWD3):c.4446G>C (p.Gln1482His)	not provided [RCV004787497]	uncertain significance	X	80682046	80682046	Human		name
596943957	CV3543041	single nucleotide variant	NM_153252.5(BRWD3):c.3556A>G (p.Thr1186Ala)	not provided [RCV004798626]	uncertain significance	X	80691099	80691099	Human		name
596945022	CV3543679	single nucleotide variant	NM_153252.5(BRWD3):c.4151A>G (p.Tyr1384Cys)	not provided [RCV004801801]	uncertain significance	X	80684092	80684092	Human		name
596942226	CV3544023	single nucleotide variant	NM_153252.5(BRWD3):c.3780A>C (p.Glu1260Asp)	not specified [RCV004800013]	uncertain significance	X	80689795	80689795	Human		name
596940228	CV3550842	single nucleotide variant	NM_153252.5(BRWD3):c.3050G>C (p.Gly1017Ala)	not provided [RCV004814742]	uncertain significance	X	80696757	80696757	Human		name
597637414	CV3637306	single nucleotide variant	NM_153252.5(BRWD3):c.4370G>A (p.Ser1457Asn)	Inborn genetic diseases [RCV004970194]	uncertain significance	X	80682492	80682492	Human	1	name
597637417	CV3637307	single nucleotide variant	NM_153252.5(BRWD3):c.3731A>G (p.Asp1244Gly)	Inborn genetic diseases [RCV004970195]	uncertain significance	X	80689844	80689844	Human	1	name
597637428	CV3637311	single nucleotide variant	NM_153252.5(BRWD3):c.3082C>G (p.Pro1028Ala)	Inborn genetic diseases [RCV004970198]	uncertain significance	X	80695977	80695977	Human	1	name
597637432	CV3637312	single nucleotide variant	NM_153252.5(BRWD3):c.4168T>C (p.Phe1390Leu)	Inborn genetic diseases [RCV004970199]	uncertain significance	X	80684075	80684075	Human	1	name
597658390	CV3729936	single nucleotide variant	NM_153252.5(BRWD3):c.3196A>G (p.Thr1066Ala)	Intellectual disability, X-linked 93 [RCV005041915]	uncertain significance	X	80693007	80693007	Human	1	name
597834245	CV3735218	single nucleotide variant	NM_153252.5(BRWD3):c.3476C>G (p.Ser1159Cys)	not provided [RCV005054951]	uncertain significance	X	80691828	80691828	Human		name
597834942	CV3735815	single nucleotide variant	NM_153252.5(BRWD3):c.3603G>C (p.Arg1201Ser)	not provided [RCV005063678]	uncertain significance	X	80690092	80690092	Human		name
597906538	CV3738772	single nucleotide variant	NM_153252.5(BRWD3):c.4565C>T (p.Ser1522Leu)	not provided [RCV005073007]	benign	X	80681430	80681430	Human		name
597837316	CV3740185	single nucleotide variant	NM_153252.5(BRWD3):c.4062A>C (p.Gln1354His)	not provided [RCV005064213]	benign	X	80685480	80685480	Human		name
597890053	CV3749243	single nucleotide variant	NM_153252.5(BRWD3):c.3838G>A (p.Gly1280Ser)	not provided [RCV005071027]	uncertain significance	X	80688095	80688095	Human		name
597952428	CV3756624	single nucleotide variant	NM_153252.5(BRWD3):c.4537G>C (p.Asp1513His)	not provided [RCV005079682]	uncertain significance	X	80681458	80681458	Human		name
597862380	CV3766490	single nucleotide variant	NM_153252.5(BRWD3):c.4656T>A (p.Asp1552Glu)	not provided [RCV005106215]	uncertain significance	X	80677362	80677362	Human		name
597909700	CV3770277	single nucleotide variant	NM_153252.5(BRWD3):c.3435A>C (p.Glu1145Asp)	not provided [RCV005113578]	uncertain significance	X	80691869	80691869	Human		name
597897308	CV3773894	single nucleotide variant	NM_153252.5(BRWD3):c.4907T>C (p.Val1636Ala)	not provided [RCV005111615]	uncertain significance	X	80677111	80677111	Human		name
597897324	CV3773896	single nucleotide variant	NM_153252.5(BRWD3):c.4469G>A (p.Arg1490Lys)	not provided [RCV005111617]	uncertain significance	X	80682023	80682023	Human		name
597897332	CV3773897	single nucleotide variant	NM_153252.5(BRWD3):c.4055G>C (p.Arg1352Thr)	not provided [RCV005111618]	uncertain significance	X	80685487	80685487	Human		name
597939928	CV3785234	single nucleotide variant	NM_153252.5(BRWD3):c.5108G>A (p.Gly1703Asp)	not provided [RCV005133339]	uncertain significance	X	80676910	80676910	Human		name
12836719	CV379474	single nucleotide variant	NM_153252.5(BRWD3):c.4732G>A (p.Ala1578Thr)	not provided [RCV000423891]	uncertain significance	X	80677286	80677286	Human		name
12840096	CV379551	single nucleotide variant	NM_153252.5(BRWD3):c.5237G>A (p.Arg1746Gln)	not provided [RCV000430053]	uncertain significance	X	80676781	80676781	Human		name
12844403	CV379552	single nucleotide variant	NM_153252.5(BRWD3):c.4757G>A (p.Gly1586Glu)	not provided [RCV000437933]	uncertain significance	X	80677261	80677261	Human		name
12847166	CV380132	single nucleotide variant	NM_153252.5(BRWD3):c.5117G>A (p.Gly1706Glu)	not provided [RCV000442988]	uncertain significance	X	80676901	80676901	Human		name
597970826	CV3802103	single nucleotide variant	NM_153252.5(BRWD3):c.4526A>G (p.Tyr1509Cys)	not provided [RCV005141895]	uncertain significance	X	80681469	80681469	Human		name
597939395	CV3818637	single nucleotide variant	NM_153252.5(BRWD3):c.5179C>T (p.Arg1727Cys)	not provided [RCV005158643]	uncertain significance	X	80676839	80676839	Human		name
597967187	CV3823852	single nucleotide variant	NM_153252.5(BRWD3):c.4312A>G (p.Ile1438Val)	not provided [RCV005165272]	uncertain significance	X	80682550	80682550	Human		name
597961635	CV3844087	single nucleotide variant	NM_153252.5(BRWD3):c.4760G>A (p.Gly1587Glu)	not provided [RCV005192933]	uncertain significance	X	80677258	80677258	Human		name
597874528	CV3846386	single nucleotide variant	NM_153252.5(BRWD3):c.4628G>A (p.Arg1543Gln)	not provided [RCV005177269]	benign	X	80681367	80681367	Human		name
597936116	CV3863714	single nucleotide variant	NM_153252.5(BRWD3):c.4667A>G (p.Asp1556Gly)	not provided [RCV005207527]	uncertain significance	X	80677351	80677351	Human		name
598122314	CV3884330	single nucleotide variant	NM_153252.5(BRWD3):c.3071A>G (p.Tyr1024Cys)	not specified [RCV005237021]	uncertain significance	X	80695988	80695988	Human		name
598125685	CV3885894	single nucleotide variant	NM_153252.5(BRWD3):c.3016G>T (p.Ala1006Ser)	not provided [RCV005241697]	uncertain significance	X	80696791	80696791	Human		name
598200486	CV3892663	single nucleotide variant	NM_153252.5(BRWD3):c.5286T>G (p.Asp1762Glu)	not provided [RCV005254496]	uncertain significance	X	80676732	80676732	Human		name
598233149	CV3893211	single nucleotide variant	NM_153252.5(BRWD3):c.3034T>A (p.Ser1012Thr)	Intellectual disability, X-linked 93 [RCV005255977]	uncertain significance	X	80696773	80696773	Human	1	name
598160566	CV3897301	single nucleotide variant	NM_153252.5(BRWD3):c.5143G>A (p.Gly1715Ser)	Intellectual disability, X-linked 93 [RCV005368270]	uncertain significance	X	80676875	80676875	Human	1	name
598174733	CV3939089	single nucleotide variant	NM_153252.5(BRWD3):c.3358C>T (p.Pro1120Ser)	Inborn genetic diseases [RCV005309754]	uncertain significance	X	80691946	80691946	Human	1	name
598174737	CV3939090	single nucleotide variant	NM_153252.5(BRWD3):c.4000T>G (p.Tyr1334Asp)	Inborn genetic diseases [RCV005309755]	uncertain significance	X	80686868	80686868	Human	1	name
598210980	CV3939094	single nucleotide variant	NM_153252.5(BRWD3):c.4969C>A (p.Gln1657Lys)	Inborn genetic diseases [RCV005315944]	uncertain significance	X	80677049	80677049	Human	1	name
616934486	CV4012491	single nucleotide variant	NM_153252.5(BRWD3):c.4207G>A (p.Ala1403Thr)	not specified [RCV005409528]	uncertain significance	X	80684036	80684036	Human		name
616939220	CV4015550	single nucleotide variant	NM_153252.5(BRWD3):c.3733C>A (p.Gln1245Lys)	not provided [RCV005413062]	uncertain significance	X	80689842	80689842	Human		name
12900398	CV411499	single nucleotide variant	NM_153252.5(BRWD3):c.3359C>T (p.Pro1120Leu)	not provided [RCV000482323]	uncertain significance	X	80691945	80691945	Human		name
12906217	CV415817	single nucleotide variant	NM_153252.5(BRWD3):c.3433G>A (p.Glu1145Lys)	not provided [RCV000488959]	uncertain significance	X	80691871	80691871	Human		name
13445732	CV438458	single nucleotide variant	NM_153252.5(BRWD3):c.4849A>T (p.Ser1617Cys)	not provided [RCV000512790]	uncertain significance	X	80677169	80677169	Human		name
13489202	CV446792	single nucleotide variant	NM_153252.5(BRWD3):c.4994G>A (p.Trp1665Ter)	not provided [RCV000523814]	uncertain significance	X	80677024	80677024	Human		name
13798038	CV553163	single nucleotide variant	NM_153252.5(BRWD3):c.5236C>T (p.Arg1746Ter)	Intellectual disability, X-linked 93 [RCV000681484]	uncertain significance	X	80676782	80676782	Human	1	name
14395958	CV611960	single nucleotide variant	NM_153252.5(BRWD3):c.5089C>T (p.Arg1697Ter)	not provided [RCV000760679]	pathogenic\|likely pathogenic	X	80676929	80676929	Human		name
14395868	CV611961	single nucleotide variant	NM_153252.5(BRWD3):c.4054A>T (p.Arg1352Ter)	not provided [RCV000760583]	pathogenic	X	80685488	80685488	Human		name
14396107	CV611962	single nucleotide variant	NM_153252.5(BRWD3):c.4015G>T (p.Glu1339Ter)	not provided [RCV000760840]	pathogenic	X	80685527	80685527	Human		name
15104740	CV774259	single nucleotide variant	NM_153252.5(BRWD3):c.4088A>G (p.Gln1363Arg)	Inborn genetic diseases [RCV003169403]\|not provided [RCV000937444]	benign\|likely benign	X	80684155	80684155	Human	1	name
21075141	CV798412	single nucleotide variant	NM_153252.5(BRWD3):c.5297A>T (p.Asp1766Val)	Inborn genetic diseases [RCV002346203]\|not provided [RCV000995975]	uncertain significance	X	80676721	80676721	Human	1	name
28888147	CV860938	single nucleotide variant	NM_153252.5(BRWD3):c.3031A>G (p.Ile1011Val)	not provided [RCV001092038]	uncertain significance	X	80696776	80696776	Human		name
28883874	CV903240	single nucleotide variant	NM_153252.5(BRWD3):c.4328G>C (p.Arg1443Thr)	Inborn genetic diseases [RCV004601378]\|Intellectual disability, X-linked 93 [RCV001168336]	uncertain significance	X	80682534	80682534	Human	2	name
28883879	CV903241	single nucleotide variant	NM_153252.5(BRWD3):c.3965C>T (p.Ser1322Leu)	Intellectual disability, X-linked 93 [RCV001168337]\|not provided [RCV003727934]	uncertain significance	X	80686903	80686903	Human	1	name
8637934	CV93160	single nucleotide variant	NM_153252.4(BRWD3):c.4736C>T (p.Ser1579Leu)	Malignant melanoma [RCV000073258]	not provided	X	80677282	80677282	Human		name
38596408	CV964006	single nucleotide variant	NM_153252.5(BRWD3):c.4184G>A (p.Arg1395His)	Intellectual disability [RCV001251696]	likely benign	X	80684059	80684059	Human	2	name
40815325	CV971232	single nucleotide variant	NM_153252.5(BRWD3):c.5080C>T (p.Arg1694Ter)	not provided [RCV003156332]	pathogenic\|uncertain significance\|no classifications from unflagged records	X	80676938	80676938	Human		name
40886609	CV974439	single nucleotide variant	NM_153252.5(BRWD3):c.3886C>T (p.Gln1296Ter)	Inborn genetic diseases [RCV001265773]	pathogenic	X	80686982	80686982	Human	1	name
40889992	CV975652	single nucleotide variant	NM_153252.5(BRWD3):c.3208C>T (p.Gln1070Ter)	not provided [RCV001268546]	pathogenic	X	80692995	80692995	Human		name
40904227	CV976691	single nucleotide variant	NM_153252.5(BRWD3):c.5345C>A (p.Ser1782Ter)	Intellectual disability, X-linked 93 [RCV001270390]	uncertain significance	X	80676673	80676673	Human	1	name
156436192	CV2403653	duplication	NM_153252.5(BRWD3):c.828_829dup (p.Lys277fs)	Intellectual disability, X-linked 93 [RCV003128101]	pathogenic	X	80736072	80736073	Human	1	name
408394710	CV3521991	microsatellite	NM_153252.5(BRWD3):c.665_666del (p.Ser222fs)	Intellectual disability, X-linked 93 [RCV004764812]	pathogenic	X	80744179	80744180	Human		name
617152614	CV4017876	deletion	NM_153252.5(BRWD3):c.824_827del (p.Ser275fs)	Intellectual disability, X-linked 93 [RCV005417666]	likely pathogenic	X	80736075	80736078	Human	1	name
151767427	CV1341203	microsatellite	NM_153252.5(BRWD3):c.2557TCA[1] (p.Ser855del)	not provided [RCV001863748]	uncertain significance	X	80704837	80704839	Human		name
21075144	CV798415	microsatellite	NM_153252.5(BRWD3):c.2295GAA[1] (p.Lys768del)	not provided [RCV000995978]	uncertain significance	X	80716182	80716184	Human		name
153302279	CV1689534	microsatellite	NM_153252.5(BRWD3):c.4057CAA[1] (p.Gln1354del)	not provided [RCV002267485]	uncertain significance	X	80685480	80685482	Human		name
405219757	CV2870250	deletion	NM_153252.5(BRWD3):c.2103_2104del (p.His701fs)	not provided [RCV003553703]	pathogenic	X	80717700	80717701	Human		name
408389629	CV3524672	microsatellite	NM_153252.5(BRWD3):c.3762TAA[1] (p.Asn1255del)	not provided [RCV004769567]	uncertain significance	X	80689808	80689810	Human		name
12742165	CV360695	duplication	NM_153252.5(BRWD3):c.2598_2601dup (p.Leu868fs)	not provided [RCV000413023]	pathogenic	X	80704797	80704798	Human		name
401913684	CV2799587	deletion	NM_153252.5(BRWD3):c.4273_4274del (p.His1426fs)	BRWD3-related disorder [RCV004534299]	likely pathogenic	X	80682588	80682589	Human		name , trait , alternate_id
408371068	CV3504754	deletion	NM_153252.5(BRWD3):c.4345_4351del (p.Arg1449fs)	BRWD3-related disorder [RCV004724435]	likely pathogenic	X	80682511	80682517	Human		name , trait , alternate_id
14396612	CV612340	microsatellite	NM_153252.5(BRWD3):c.3200_3201del (p.Val1067fs)	Intellectual disability, X-linked 93 [RCV000761506]	pathogenic	X	80693002	80693003	Human		name
151349420	CV1325339	deletion	NM_153252.5(BRWD3):c.3697_3699del (p.Ile1233del)	Intellectual disability, X-linked 93 [RCV001814629]	uncertain significance	X	80689996	80689998	Human	1	name
402488733	CV2856546	indel	NM_153252.5(BRWD3):c.845_846delinsTT (p.Tyr282Phe)	not provided [RCV003572795]	uncertain significance	X	80736056	80736057	Human		name
150438286	CV1286822	indel	NM_153252.5(BRWD3):c.4887delinsAGATCA (p.Arg1630fs)	Intellectual disability, X-linked 93 [RCV001724768]	uncertain significance	X	80677131	80677131	Human		name
150547978	CV1303944	indel	NM_153252.5(BRWD3):c.4598_4599delinsTT (p.Ser1533Ile)	not provided [RCV001764047]	uncertain significance	X	80681396	80681397	Human		name
402506494	CV3039166	indel	NM_153252.5(BRWD3):c.4968_4969delinsAA (p.Gln1657Lys)	not provided [RCV003715251]	uncertain significance	X	80677049	80677050	Human		name
408393383	CV3519795	indel	NM_153252.5(BRWD3):c.4177_4178delinsTT (p.Asp1393Phe)	not provided [RCV004764091]	uncertain significance	X	80684065	80684066	Human		name
407502348	CV3495670	duplication	NM_153252.5(BRWD3):c.5039dup (p.Gly1680_Arg1681insTer)	not provided [RCV004697510]	likely pathogenic	X	80676978	80676979	Human		name
408388559	CV3529022	deletion	NM_153252.5(BRWD3):c.2615_2623del (p.Lys872_Gln874del)	not provided [RCV004773844]	uncertain significance	X	80704776	80704784	Human		name
401797912	CV2739138	deletion	NM_153252.5(BRWD3):c.4666_4677del (p.Asp1556_Leu1559del)	not provided [RCV003318785]	uncertain significance	X	80677341	80677352	Human		name
243049862	CV2417103	microsatellite	NM_153252.5(BRWD3):c.4057CAA[4] (p.Gln1354_Asp1355insGlnGln)	not provided [RCV003151973]	uncertain significance	X	80685479	80685480	Human		name
150405392	CV1178804	insertion	NM_153252.5(BRWD3):c.4006-137_4006-136insAGAATGACGAATGTACAATTT	not provided [RCV001544843]	likely benign	X	80685672	80685673	Human		name
598228216	CV3894604	deletion	NM_153252.5(BRWD3):c.3255_3256del (p.Tyr1085_Ser1086delinsTer)	not provided [RCV005257848]	pathogenic	X	80692947	80692948	Human		name
155957516	CV2066408	microsatellite	NM_153252.5(BRWD3):c.4866CTCTGA[3] (p.Ser1625_Glu1626insAspSer)	not provided [RCV002816598]	uncertain significance	X	80677140	80677141	Human		name

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