Scn3b Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

317 records found for search term Scn3b

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
11666084	CV325183	single nucleotide variant	NM_018400.3(SCN3B):c.-43G>A	Brugada syndrome [RCV000314924]	uncertain significance	11	123653844	123653844	Human		name
11666510	CV326028	single nucleotide variant	NM_018400.3(SCN3B):c.-85G>T	Brugada syndrome [RCV000351102]	uncertain significance	11	123653886	123653886	Human		name
11666915	CV312996	single nucleotide variant	NM_018400.3(SCN3B):c.*930A>G	Brugada syndrome [RCV000393413]	uncertain significance	11	123632869	123632869	Human		name
11666107	CV312997	single nucleotide variant	NM_018400.3(SCN3B):c.*131T>A	Brugada syndrome [RCV000316430]	uncertain significance	11	123633668	123633668	Human		name
11665661	CV313001	single nucleotide variant	NM_018400.3(SCN3B):c.*103C>T	Brugada syndrome [RCV000285896]	uncertain significance	11	123633696	123633696	Human		name
11665900	CV313014	single nucleotide variant	NM_018400.3(SCN3B):c.-736G>C	Brugada syndrome [RCV000301262]	uncertain significance	11	123654537	123654537	Human		name
11666679	CV318998	single nucleotide variant	NM_018400.3(SCN3B):c.*696A>G	Brugada syndrome [RCV000368721]	uncertain significance	11	123633103	123633103	Human		name
11666146	CV319000	single nucleotide variant	NM_018400.3(SCN3B):c.*548C>T	Brugada syndrome [RCV000319881]	uncertain significance	11	123633251	123633251	Human		name
11665860	CV319007	single nucleotide variant	NM_018400.3(SCN3B):c.-249G>T	Brugada syndrome [RCV000298482]	uncertain significance	11	123654050	123654050	Human		name
11666188	CV319008	single nucleotide variant	NM_018400.3(SCN3B):c.-332G>A	Brugada syndrome [RCV000322983]	uncertain significance	11	123654133	123654133	Human		name
11665802	CV319011	single nucleotide variant	NM_018400.3(SCN3B):c.-557C>T	Brugada syndrome [RCV000295234]	uncertain significance	11	123654358	123654358	Human		name
11666304	CV325181	single nucleotide variant	NM_018400.3(SCN3B):c.*855A>C	Brugada syndrome [RCV000332871]	likely benign	11	123632944	123632944	Human		name
11665997	CV325997	single nucleotide variant	NM_018400.3(SCN3B):c.*892C>A	Brugada syndrome [RCV000308397]	likely benign	11	123632907	123632907	Human		name
11666629	CV326008	single nucleotide variant	NM_018400.3(SCN3B):c.*888A>G	Brugada syndrome [RCV000363105]	uncertain significance	11	123632911	123632911	Human		name
11665531	CV326009	single nucleotide variant	NM_018400.3(SCN3B):c.*869A>G	Brugada syndrome [RCV000277890]	uncertain significance	11	123632930	123632930	Human		name
11665475	CV326012	single nucleotide variant	NM_018400.3(SCN3B):c.*657A>G	Brugada syndrome [RCV000274119]	uncertain significance	11	123633142	123633142	Human		name
11666784	CV326022	single nucleotide variant	NM_018400.3(SCN3B):c.*104G>A	Brugada syndrome [RCV000380303]	uncertain significance	11	123633695	123633695	Human		name
11666529	CV326030	single nucleotide variant	NM_018400.3(SCN3B):c.-252G>T	Brugada syndrome [RCV000353285]	uncertain significance	11	123654053	123654053	Human		name
11665373	CV326034	single nucleotide variant	NM_018400.3(SCN3B):c.-253G>C	Brugada syndrome [RCV000267772]	uncertain significance	11	123654054	123654054	Human		name
11666262	CV326036	single nucleotide variant	NM_018400.3(SCN3B):c.-393C>A	Brugada syndrome [RCV000329162]	uncertain significance	11	123654194	123654194	Human		name
11666454	CV326039	single nucleotide variant	NM_018400.3(SCN3B):c.-489G>T	Brugada syndrome [RCV000344417]	uncertain significance	11	123654290	123654290	Human		name
11666870	CV326040	single nucleotide variant	NM_018400.3(SCN3B):c.-538G>A	Brugada syndrome [RCV000389630]	uncertain significance	11	123654339	123654339	Human		name
14717869	CV665582	single nucleotide variant	NM_018400.3(SCN3B):c.-951C>G	not provided [RCV000830204]	benign	11	123654752	123654752	Human		name
14717865	CV665587	single nucleotide variant	NM_018400.3(SCN3B):c.-955A>C	not provided [RCV000830203]	benign	11	123654756	123654756	Human		name
401868867	CV2787592	single nucleotide variant	NM_001040151.2(SCN3B):c.-4G>T	Cardiovascular phenotype [RCV003380368]	uncertain significance	11	123653805	123653805	Human		name
11665556	CV312955	single nucleotide variant	NM_018400.3(SCN3B):c.*4523A>G	Brugada syndrome [RCV000279220]	uncertain significance	11	123629276	123629276	Human		name
11666733	CV312959	single nucleotide variant	NM_018400.3(SCN3B):c.*4395G>A	Brugada syndrome [RCV000374933]	uncertain significance	11	123629404	123629404	Human		name
11665988	CV312961	single nucleotide variant	NM_018400.3(SCN3B):c.*4334C>T	Brugada syndrome [RCV000307145]	uncertain significance	11	123629465	123629465	Human		name
11666542	CV312968	single nucleotide variant	NM_018400.3(SCN3B):c.*3306G>A	Brugada syndrome [RCV000354654]	uncertain significance	11	123630493	123630493	Human		name
11665329	CV312969	single nucleotide variant	NM_018400.3(SCN3B):c.*3060G>T	Brugada syndrome [RCV000265561]	likely benign	11	123630739	123630739	Human		name
11666796	CV312971	single nucleotide variant	NM_018400.3(SCN3B):c.*2561C>T	Brugada syndrome [RCV000381223]	likely benign	11	123631238	123631238	Human		name
11666936	CV312973	single nucleotide variant	NM_018400.3(SCN3B):c.*2242C>T	Brugada syndrome [RCV000397169]	likely benign	11	123631557	123631557	Human		name
11666246	CV312982	single nucleotide variant	NM_018400.3(SCN3B):c.*1856A>G	Brugada syndrome [RCV000328113]	likely benign	11	123631943	123631943	Human		name
11666637	CV312985	single nucleotide variant	NM_018400.3(SCN3B):c.*1808G>A	Brugada syndrome [RCV000363845]	uncertain significance	11	123631991	123631991	Human		name
11665599	CV312986	single nucleotide variant	NM_018400.3(SCN3B):c.*1318G>A	Brugada syndrome [RCV000281342]	uncertain significance	11	123632481	123632481	Human		name
11666341	CV312992	single nucleotide variant	NM_018400.3(SCN3B):c.*1290G>A	Brugada syndrome [RCV000336535]	likely benign	11	123632509	123632509	Human		name
11666992	CV312993	single nucleotide variant	NM_018400.3(SCN3B):c.*1289C>T	Brugada syndrome [RCV000404215]	likely benign	11	123632510	123632510	Human		name
11666417	CV312995	single nucleotide variant	NM_018400.3(SCN3B):c.*1232G>A	Brugada syndrome [RCV000342379]	likely benign	11	123632567	123632567	Human		name
11666946	CV318963	single nucleotide variant	NM_018400.3(SCN3B):c.*4361T>C	Brugada syndrome [RCV000398050]	uncertain significance	11	123629438	123629438	Human		name
11666667	CV318964	single nucleotide variant	NM_018400.3(SCN3B):c.*3748G>A	Brugada syndrome [RCV000367584]	likely benign	11	123630051	123630051	Human		name
11665220	CV318965	single nucleotide variant	NM_018400.3(SCN3B):c.*3282T>C	Brugada syndrome [RCV000260002]	uncertain significance	11	123630517	123630517	Human		name
11666209	CV318967	single nucleotide variant	NM_018400.3(SCN3B):c.*3242G>A	Brugada syndrome [RCV000324533]	uncertain significance	11	123630557	123630557	Human		name
11666768	CV318968	single nucleotide variant	NM_018400.3(SCN3B):c.*3076C>T	Brugada syndrome [RCV000378753]	uncertain significance	11	123630723	123630723	Human		name
11666502	CV318969	single nucleotide variant	NM_018400.3(SCN3B):c.*2462G>A	Brugada syndrome [RCV000350578]	likely benign	11	123631337	123631337	Human		name
11666935	CV318972	single nucleotide variant	NM_018400.3(SCN3B):c.*2429C>T	Brugada syndrome [RCV000397161]	uncertain significance	11	123631370	123631370	Human		name
11666367	CV318978	single nucleotide variant	NM_018400.3(SCN3B):c.*2266G>A	Brugada syndrome [RCV000338230]	uncertain significance	11	123631533	123631533	Human		name
11665858	CV318981	single nucleotide variant	NM_018400.3(SCN3B):c.*2203C>A	Brugada syndrome [RCV000298432]	uncertain significance	11	123631596	123631596	Human		name
11666528	CV318983	single nucleotide variant	NM_018400.3(SCN3B):c.*2178T>A	Brugada syndrome [RCV000353187]	uncertain significance	11	123631621	123631621	Human	1	name
11666528	CV318983	single nucleotide variant	NM_018400.3(SCN3B):c.*2178T>A	Brugada syndrome [RCV000353187]	uncertain significance	11	123631621	123631622	Human	1	name
11665452	CV318984	single nucleotide variant	NM_018400.3(SCN3B):c.*1927A>G	Brugada syndrome [RCV000273003]	uncertain significance	11	123631872	123631872	Human		name
11665406	CV318991	single nucleotide variant	NM_018400.3(SCN3B):c.*1746G>A	Brugada syndrome [RCV000269489]	likely benign	11	123632053	123632053	Human		name
11666276	CV318992	single nucleotide variant	NM_018400.3(SCN3B):c.*1508A>G	Brugada syndrome [RCV000330588]	uncertain significance	11	123632291	123632291	Human		name
11665682	CV318995	single nucleotide variant	NM_018400.3(SCN3B):c.*1257G>A	Brugada syndrome [RCV000287380]	likely benign	11	123632542	123632542	Human		name
11666913	CV318996	single nucleotide variant	NM_018400.3(SCN3B):c.*1151G>A	Brugada syndrome [RCV000393409]	uncertain significance	11	123632648	123632648	Human		name
11665754	CV325091	single nucleotide variant	NM_018400.3(SCN3B):c.*4394C>T	Brugada syndrome [RCV000292027]	likely benign	11	123629405	123629405	Human		name
11666459	CV325100	single nucleotide variant	NM_018400.3(SCN3B):c.*4390C>T	Brugada syndrome [RCV000346900]	uncertain significance	11	123629409	123629409	Human		name
11666524	CV325104	single nucleotide variant	NM_018400.3(SCN3B):c.*4265C>A	Brugada syndrome [RCV000352626]	uncertain significance	11	123629534	123629534	Human		name
11666945	CV325105	single nucleotide variant	NM_018400.3(SCN3B):c.*4191C>A	Brugada syndrome [RCV000398022]	uncertain significance	11	123629608	123629608	Human		name
11666825	CV325107	single nucleotide variant	NM_018400.3(SCN3B):c.*2722G>A	Brugada syndrome [RCV000384476]	likely benign	11	123631077	123631077	Human		name
11665725	CV325108	single nucleotide variant	NM_018400.3(SCN3B):c.*2629C>T	Brugada syndrome [RCV000290259]	uncertain significance	11	123631170	123631170	Human		name
11666441	CV325117	single nucleotide variant	NM_018400.3(SCN3B):c.*2603T>A	Brugada syndrome [RCV000345178]	uncertain significance	11	123631196	123631196	Human		name
11665821	CV325124	single nucleotide variant	NM_018400.3(SCN3B):c.*2516G>A	Brugada syndrome [RCV000296205]	likely benign	11	123631283	123631283	Human		name
11666318	CV325140	single nucleotide variant	NM_018400.3(SCN3B):c.*1686T>C	Brugada syndrome [RCV000333908]	likely benign	11	123632113	123632113	Human		name
11665786	CV325157	single nucleotide variant	NM_018400.3(SCN3B):c.*1542A>C	Brugada syndrome [RCV000294242]	uncertain significance	11	123632257	123632257	Human		name
11666743	CV325171	single nucleotide variant	NM_018400.3(SCN3B):c.*1434G>A	Brugada syndrome [RCV000375738]	uncertain significance	11	123632365	123632365	Human		name
11665924	CV325174	single nucleotide variant	NM_018400.3(SCN3B):c.*1095G>A	Brugada syndrome [RCV000302670]	uncertain significance	11	123632704	123632704	Human		name
11666197	CV325964	single nucleotide variant	NM_018400.3(SCN3B):c.*4541A>G	Brugada syndrome [RCV000323705]	uncertain significance	11	123629258	123629258	Human		name
11666788	CV325965	single nucleotide variant	NM_018400.3(SCN3B):c.*4537C>T	Brugada syndrome [RCV000380588]	uncertain significance	11	123629262	123629262	Human		name
11666343	CV325966	single nucleotide variant	NM_018400.3(SCN3B):c.*4450G>A	Brugada syndrome [RCV000336641]	uncertain significance	11	123629349	123629349	Human		name
11665288	CV325974	single nucleotide variant	NM_018400.3(SCN3B):c.*3612A>G	Brugada syndrome [RCV000263597]	uncertain significance	11	123630187	123630187	Human		name
11665879	CV325975	single nucleotide variant	NM_018400.3(SCN3B):c.*3444A>T	Brugada syndrome [RCV000299781]	likely benign	11	123630355	123630355	Human		name
11666962	CV325980	duplication	NM_018400.3(SCN3B):c.*2174dup	Brugada syndrome [RCV000400711]	likely benign	11	123631624	123631625	Human		name
11665940	CV325981	single nucleotide variant	NM_018400.3(SCN3B):c.*2056C>G	Brugada syndrome [RCV000303510]	uncertain significance	11	123631743	123631743	Human		name
11666858	CV325991	single nucleotide variant	NM_018400.3(SCN3B):c.*1685A>G	Brugada syndrome [RCV000388346]	uncertain significance	11	123632114	123632114	Human		name
11666487	CV326026	single nucleotide variant	NM_001040151.2(SCN3B):c.-9C>T	not specified [RCV000431664]	benign\|uncertain significance	11	123653810	123653810	Human		name
150458885	CV1263925	single nucleotide variant	NM_001040151.2(SCN3B):c.*26G>A	not provided [RCV001681839]	benign	11	123633773	123633773	Human		name
11665709	CV313011	deletion	NM_001040151.2(SCN3B):c.-62del	Brugada syndrome 7 [RCV002487351]\|Brugada syndrome [RCV000289193]	uncertain significance	11	123654262	123654262	Human	2	name
11666820	CV326037	single nucleotide variant	NM_001040151.2(SCN3B):c.-32G>A	not provided [RCV001684890]	benign\|uncertain significance	11	123654232	123654232	Human		name
150415187	CV1191164	single nucleotide variant	NM_001040151.2(SCN3B):c.-277C>G	not provided [RCV001567871]	likely benign	11	123654477	123654477	Human		name
150487957	CV1225987	single nucleotide variant	NM_001040151.2(SCN3B):c.*153C>T	not provided [RCV001618148]	benign	11	123633646	123633646	Human		name
151807107	CV1382270	single nucleotide variant	NM_001040151.2(SCN3B):c.55+3A>G	Brugada syndrome 7 [RCV002028622]\|Cardiovascular phenotype [RCV003170489]	uncertain significance	11	123653744	123653744	Human	1	name
11667017	CV319012	single nucleotide variant	NM_001040151.2(SCN3B):c.-326C>G	Brugada syndrome [RCV000406653]	uncertain significance	11	123654526	123654526	Human	1	name
11666730	CV325182	single nucleotide variant	NM_001040151.2(SCN3B):c.*509G>A	not provided [RCV001540261]	benign\|likely benign	11	123633290	123633290	Human		name
11666501	CV325197	single nucleotide variant	NM_001040151.2(SCN3B):c.-293G>C	not provided [RCV001684317]	benign\|likely benign	11	123654493	123654493	Human		name
11665575	CV326015	single nucleotide variant	NM_001040151.2(SCN3B):c.*447C>A	Brugada syndrome [RCV000280076]	uncertain significance	11	123633352	123633352	Human	1	name
11666356	CV326045	single nucleotide variant	NM_001040151.2(SCN3B):c.-364G>A	not provided [RCV001639651]	benign\|likely benign	11	123654564	123654564	Human		name
12843129	CV372041	single nucleotide variant	NM_001040151.2(SCN3B):c.55+7A>G	Brugada syndrome 7 [RCV002522416]\|not specified [RCV000435668]	likely benign	11	123653740	123653740	Human	1	name
15132122	CV760015	single nucleotide variant	NM_001040151.2(SCN3B):c.55+8C>G	not provided [RCV000920285]	likely benign	11	123653739	123653739	Human		name
127275706	CV1099600	single nucleotide variant	NM_001040151.2(SCN3B):c.446-7C>G	Brugada syndrome 7 [RCV001432490]	likely benign	11	123638331	123638331	Human	1	name
150493736	CV1238728	single nucleotide variant	NM_001040151.2(SCN3B):c.55+44C>T	not provided [RCV001655272]	benign	11	123653703	123653703	Human		name
151808221	CV1362726	single nucleotide variant	NM_001040151.2(SCN3B):c.219+2T>C	Brugada syndrome 7 [RCV001991573]	uncertain significance	11	123645585	123645585	Human	1	name
151740914	CV1455389	duplication	NM_001040151.2(SCN3B):c.584+2dup	Brugada syndrome 7 [RCV002005812]	uncertain significance	11	123638183	123638184	Human	1	name
152089225	CV1550332	single nucleotide variant	NM_001040151.2(SCN3B):c.584+9A>C	Brugada syndrome 7 [RCV002131833]	likely benign	11	123638177	123638177	Human	1	name
152034098	CV1669452	single nucleotide variant	NM_001040151.2(SCN3B):c.585-2A>G	not provided [RCV002223443]	uncertain significance	11	123634208	123634208	Human		name
155942009	CV1910298	single nucleotide variant	NM_001040151.2(SCN3B):c.585-1G>C	Brugada syndrome 7 [RCV002615698]	uncertain significance	11	123634207	123634207	Human	1	name
156446120	CV1951145	single nucleotide variant	NM_001040151.2(SCN3B):c.55+11G>A	Brugada syndrome 7 [RCV003117084]	likely benign	11	123653736	123653736	Human	1	name
11665347	CV312954	single nucleotide variant	NM_001040151.2(SCN3B):c.*4588T>C	Brugada syndrome [RCV000266188]	uncertain significance	11	123629211	123629211	Human	1	name
11665767	CV312972	single nucleotide variant	NM_001040151.2(SCN3B):c.*2366G>A	Brugada syndrome [RCV000292638]	uncertain significance	11	123631433	123631433	Human	1	name
11666658	CV325175	duplication	NM_001040151.2(SCN3B):c.*1007dup	Brugada syndrome [RCV000366696]	uncertain significance	11	123632791	123632792	Human	1	name
405724225	CV3381565	single nucleotide variant	NM_001040151.2(SCN3B):c.584+1G>A	Cardiovascular phenotype [RCV004524258]	uncertain significance	11	123638185	123638185	Human		name
12838672	CV372253	single nucleotide variant	NM_001040151.2(SCN3B):c.445+3G>A	Cardiovascular phenotype [RCV004022303]\|not specified [RCV000427385]	likely benign\|uncertain significance	11	123642443	123642443	Human		name
13533256	CV510259	single nucleotide variant	NM_001040151.2(SCN3B):c.585-4A>G	Brugada syndrome 7 [RCV000983797]\|Cardiovascular phenotype [RCV000617294]	likely benign\|uncertain significance	11	123634210	123634210	Human	1	name
14723445	CV665581	single nucleotide variant	NM_001040151.2(SCN3B):c.55+66T>C	not provided [RCV000832537]	likely benign	11	123653681	123653681	Human		name
15118303	CV759940	single nucleotide variant	NM_001040151.2(SCN3B):c.445+8T>C	Brugada syndrome 7 [RCV000917949]	likely benign	11	123642438	123642438	Human	1	name
15179305	CV775782	single nucleotide variant	NM_001040151.2(SCN3B):c.446-4T>G	not provided [RCV000929607]	likely benign	11	123638328	123638328	Human		name
150424469	CV1184486	deletion	NM_001040151.2(SCN3B):c.56-310del	not provided [RCV001556697]	likely benign	11	123646060	123646060	Human		name
150506380	CV1226333	single nucleotide variant	NM_001040151.2(SCN3B):c.55+160A>T	not provided [RCV001635701]	benign	11	123653587	123653587	Human		name
8692771	CV142738	single nucleotide variant	NM_001040151.2(SCN3B):c.*22+16A>C	not specified [RCV000127951]	benign	11	123634105	123634105	Human		name
152170549	CV1578181	single nucleotide variant	NM_001040151.2(SCN3B):c.585-16C>T	Brugada syndrome 7 [RCV002183190]	likely benign	11	123634222	123634222	Human	1	name
11665308	CV313006	single nucleotide variant	NM_001040151.2(SCN3B):c.-26+61G>A	not provided [RCV001568073]	likely benign	11	123654165	123654165	Human		name
405194940	CV3167709	single nucleotide variant	NM_001040151.2(SCN3B):c.445+20T>G	Brugada syndrome 7 [RCV003860115]	likely benign	11	123642426	123642426	Human	1	name
11666761	CV326035	single nucleotide variant	NM_001040151.2(SCN3B):c.-26+86C>G	not provided [RCV001537285]	benign\|uncertain significance	11	123654140	123654140	Human		name
12839152	CV372032	single nucleotide variant	NM_001040151.2(SCN3B):c.*23-15T>A	not specified [RCV000428298]	likely benign	11	123633791	123633791	Human		name
12843846	CV372034	single nucleotide variant	NM_001040151.2(SCN3B):c.219+18C>T	not specified [RCV000436962]	likely benign	11	123645569	123645569	Human		name
12844927	CV372252	single nucleotide variant	NM_001040151.2(SCN3B):c.584+12G>A	not specified [RCV000438878]	likely benign	11	123638174	123638174	Human		name
14714612	CV656035	single nucleotide variant	NM_001040151.2(SCN3B):c.-26+17C>G	not provided [RCV000829095]	likely benign	11	123654209	123654209	Human		name
14743681	CV656036	single nucleotide variant	NM_001040151.2(SCN3B):c.-26+12T>C	not provided [RCV000842226]	likely benign	11	123654214	123654214	Human		name
14728373	CV664962	single nucleotide variant	NM_001040151.2(SCN3B):c.584+52T>C	not provided [RCV000834743]	benign	11	123638134	123638134	Human		name
14717615	CV665579	single nucleotide variant	NM_001040151.2(SCN3B):c.585-45G>C	Brugada syndrome 7 [RCV001807357]\|not provided [RCV000830122]	benign	11	123634251	123634251	Human	1	name
14746024	CV665649	single nucleotide variant	NM_001040151.2(SCN3B):c.56-254A>C	not provided [RCV000843999]	benign	11	123646004	123646004	Human		name
14717608	CV665825	single nucleotide variant	NM_001040151.2(SCN3B):c.584+91C>T	not provided [RCV000830120]	likely benign	11	123638095	123638095	Human		name
150424075	CV1184485	single nucleotide variant	NM_001040151.2(SCN3B):c.585-190T>A	not provided [RCV001556180]	likely benign	11	123634396	123634396	Human		name
150407706	CV1194456	single nucleotide variant	NM_001040151.2(SCN3B):c.-25-158C>T	not provided [RCV001572417]	likely benign	11	123653984	123653984	Human		name
150432708	CV1200763	single nucleotide variant	NM_001040151.2(SCN3B):c.585-156A>G	not provided [RCV001581487]	likely benign	11	123634362	123634362	Human		name
150507676	CV1211235	deletion	NM_001040151.2(SCN3B):c.220-148del	not provided [RCV001596354]	likely benign	11	123642819	123642819	Human		name
150461982	CV1264672	single nucleotide variant	NM_001040151.2(SCN3B):c.445+197T>C	not provided [RCV001682296]	benign	11	123642249	123642249	Human		name
155716173	CV1785115	deletion	NM_001040151.2(SCN3B):c.31_55+2del	Cardiovascular phenotype [RCV002325975]	uncertain significance	11	123653745	123653771	Human		name
11666943	CV325190	single nucleotide variant	NM_001040151.2(SCN3B):c.-25-154C>T	not provided [RCV001691438]	benign\|likely benign	11	123653980	123653980	Human		name
11666033	CV325191	single nucleotide variant	NM_001040151.2(SCN3B):c.-25-156A>G	not provided [RCV001695296]	benign\|likely benign	11	123653982	123653982	Human		name
11666560	CV325193	single nucleotide variant	NM_001040151.2(SCN3B):c.-25-169G>T	not provided [RCV001564656]	likely benign	11	123653995	123653995	Human		name
11665261	CV325196	single nucleotide variant	NM_001040151.2(SCN3B):c.-26+191G>A	not provided [RCV001667742]	benign\|likely benign	11	123654035	123654035	Human		name
14720054	CV664951	single nucleotide variant	NM_001040151.2(SCN3B):c.*22+156G>C	not provided [RCV000831049]	benign	11	123633965	123633965	Human		name
14720052	CV664953	single nucleotide variant	NM_001040151.2(SCN3B):c.585-185G>A	not provided [RCV000831048]	benign	11	123634391	123634391	Human		name
14725880	CV664964	single nucleotide variant	NM_001040151.2(SCN3B):c.220-133C>T	not provided [RCV000833631]	likely benign	11	123642804	123642804	Human		name
14713384	CV665580	single nucleotide variant	NM_001040151.2(SCN3B):c.220-281A>G	not provided [RCV000828702]	likely benign	11	123642952	123642952	Human		name
14720920	CV665629	single nucleotide variant	NM_001040151.2(SCN3B):c.585-130T>C	not provided [RCV000831444]	likely benign	11	123634336	123634336	Human		name
14728376	CV665639	single nucleotide variant	NM_001040151.2(SCN3B):c.584+206C>A	not provided [RCV000834744]	benign	11	123637980	123637980	Human		name
14717612	CV665641	single nucleotide variant	NM_001040151.2(SCN3B):c.584+130C>T	not provided [RCV000830121]	likely benign	11	123638056	123638056	Human		name
14728371	CV665642	single nucleotide variant	NM_001040151.2(SCN3B):c.446-204C>T	not provided [RCV000834742]	benign	11	123638528	123638528	Human		name
14725582	CV665827	single nucleotide variant	NM_001040151.2(SCN3B):c.220-132C>T	not provided [RCV000833503]	likely benign	11	123642803	123642803	Human		name
11666049	CV312966	deletion	NM_018400.3(SCN3B):c.3973_3976del	Brugada syndrome [RCV000312802]	likely benign	11	123629823	123629826	Human		name
11666155	CV325976	microsatellite	NM_001040151.2(SCN3B):c.*2795GAA[1]	Brugada syndrome [RCV000320548]	uncertain significance	11	123630999	123631001	Human		name
11666584	CV325982	microsatellite	NM_001040151.2(SCN3B):c.*1948TATT[2]	Brugada syndrome [RCV000358241]	uncertain significance	11	123631840	123631843	Human		name
14394386	CV609783	single nucleotide variant	NM_001040151.2(SCN3B):c.6T>C (p.Pro2=)	Brugada syndrome 7 [RCV001441804]\|Cardiovascular phenotype [RCV002360869]\|not provided [RCV000757739]	likely benign	11	123653796	123653796	Human	1	name
127307734	CV1156626	single nucleotide variant	NM_001040151.2(SCN3B):c.15T>C (p.Asn5=)	Brugada syndrome 7 [RCV001517234]\|Cardiovascular phenotype [RCV002405211]	benign\|likely benign	11	123653787	123653787	Human	1	name
155956508	CV2078313	single nucleotide variant	NM_001040151.2(SCN3B):c.27C>T (p.Pro9=)	Brugada syndrome 7 [RCV002880794]	likely benign	11	123653775	123653775	Human	1	name
127275802	CV1099603	single nucleotide variant	NM_001040151.2(SCN3B):c.99G>A (p.Thr33=)	Brugada syndrome 7 [RCV001443488]\|Cardiovascular phenotype [RCV003160785]	likely benign	11	123645707	123645707	Human	1	name
152053218	CV1575014	single nucleotide variant	NM_001040151.2(SCN3B):c.66C>T (p.Cys22=)	Brugada syndrome 7 [RCV002109236]\|Cardiovascular phenotype [RCV004046499]	likely benign	11	123645740	123645740	Human	1	name
155698014	CV1816822	single nucleotide variant	NM_001040151.2(SCN3B):c.81G>C (p.Val27=)	Cardiovascular phenotype [RCV002427919]	likely benign	11	123645725	123645725	Human		name
155726996	CV1822372	single nucleotide variant	NM_001040151.2(SCN3B):c.69C>T (p.Phe23=)	Cardiovascular phenotype [RCV002364742]	likely benign	11	123645737	123645737	Human		name
404995115	CV3014119	single nucleotide variant	NM_001040151.2(SCN3B):c.39C>T (p.Leu13=)	Brugada syndrome 7 [RCV003604990]	likely benign	11	123653763	123653763	Human	1	name
11665721	CV313002	single nucleotide variant	NM_001040151.2(SCN3B):c.93G>A (p.Ser31=)	Brugada syndrome 7 [RCV001303529]\|Cardiovascular phenotype [RCV002374517]	likely benign\|uncertain significance	11	123645713	123645713	Human	1	name
597682001	CV3598128	single nucleotide variant	NM_001040151.2(SCN3B):c.99G>C (p.Thr33=)	Cardiovascular phenotype [RCV004983483]	likely benign	11	123645707	123645707	Human		name
126751263	CV1030124	single nucleotide variant	NM_001040151.2(SCN3B):c.14A>G (p.Asn5Ser)	Brugada syndrome 7 [RCV001352405]\|Cardiovascular phenotype [RCV002395785]	uncertain significance	11	123653788	123653788	Human	1	name
127233564	CV1077939	single nucleotide variant	NM_001040151.2(SCN3B):c.198C>A (p.Pro66=)	Brugada syndrome 7 [RCV001413945]\|Cardiovascular phenotype [RCV002420931]	likely benign	11	123645608	123645608	Human	1	name
127265550	CV1099602	single nucleotide variant	NM_001040151.2(SCN3B):c.111G>A (p.Gln37=)	Brugada syndrome 7 [RCV001429114]	likely benign	11	123645695	123645695	Human	1	name
127336481	CV1121136	single nucleotide variant	NM_001040151.2(SCN3B):c.174G>A (p.Thr58=)	Brugada syndrome 7 [RCV001474970]\|Cardiovascular phenotype [RCV002405122]	likely benign	11	123645632	123645632	Human	1	name
8696337	CV150291	single nucleotide variant	NM_001040151.2(SCN3B):c.17G>A (p.Arg6Lys)	Atrial fibrillation, familial, 16 [RCV000128815]	pathogenic	11	123653785	123653785	Human	1	name
155744174	CV1842966	single nucleotide variant	NM_001040151.2(SCN3B):c.193A>C (p.Arg65=)	Cardiovascular phenotype [RCV002413147]	likely benign	11	123645613	123645613	Human		name
155695481	CV1844637	single nucleotide variant	NM_001040151.2(SCN3B):c.225C>T (p.Tyr75=)	Brugada syndrome 7 [RCV003101175]\|Cardiovascular phenotype [RCV002443686]	likely benign	11	123642666	123642666	Human	1	name
155671552	CV1845613	single nucleotide variant	NM_001040151.2(SCN3B):c.258C>T (p.Ser86=)	Brugada syndrome 7 [RCV003101996]\|Cardiovascular phenotype [RCV002437089]	likely benign	11	123642633	123642633	Human	1	name
155726855	CV1851219	single nucleotide variant	NM_001040151.2(SCN3B):c.240C>T (p.Gly80=)	Brugada syndrome 7 [RCV003497959]\|Cardiovascular phenotype [RCV002450319]	likely benign	11	123642651	123642651	Human	1	name
10044390	CV188507	single nucleotide variant	NM_001040151.2(SCN3B):c.198C>T (p.Pro66=)	Brugada syndrome 7 [RCV000233030]\|Cardiovascular phenotype [RCV000249174]\|not provided [RCV001812148]\|not specified [RCV000171067]	benign\|likely benign	11	123645608	123645608	Human	1	name
156413865	CV1905643	single nucleotide variant	NM_001040151.2(SCN3B):c.135C>T (p.Cys45=)	Brugada syndrome 7 [RCV003073476]	likely benign	11	123645671	123645671	Human	1	name
11543732	CV258685	single nucleotide variant	NM_001040151.2(SCN3B):c.105C>T (p.Ala35=)	Brugada syndrome 7 [RCV000461565]\|Cardiovascular phenotype [RCV000242852]\|not provided [RCV001651297]\|not specified [RCV003401209]	benign\|likely benign	11	123645701	123645701	Human	1	name
405114196	CV2883889	single nucleotide variant	NM_001040151.2(SCN3B):c.192C>T (p.Tyr64=)	Brugada syndrome 7 [RCV003499841]	likely benign	11	123645614	123645614	Human	1	name
404984001	CV3061549	single nucleotide variant	NM_001040151.2(SCN3B):c.13A>G (p.Asn5Asp)	Brugada syndrome 7 [RCV003603695]\|Cardiovascular phenotype [RCV004374202]	uncertain significance	11	123653789	123653789	Human	1	name
597681992	CV3598125	single nucleotide variant	NM_001040151.2(SCN3B):c.153A>G (p.Arg51=)	Cardiovascular phenotype [RCV004983481]	likely benign	11	123645653	123645653	Human		name
597681998	CV3598127	single nucleotide variant	NM_001040151.2(SCN3B):c.108G>T (p.Val36=)	Cardiovascular phenotype [RCV004983482]	likely benign	11	123645698	123645698	Human		name
597682007	CV3598129	single nucleotide variant	NM_001040151.2(SCN3B):c.105C>G (p.Ala35=)	Cardiovascular phenotype [RCV004983484]	likely benign	11	123645701	123645701	Human		name
597835536	CV3760976	single nucleotide variant	NM_001040151.2(SCN3B):c.20T>G (p.Leu7Trp)	Brugada syndrome 7 [RCV005085527]	uncertain significance	11	123653782	123653782	Human	1	name
598234854	CV3910453	single nucleotide variant	NM_001040151.2(SCN3B):c.204C>T (p.Gly68=)	Cardiovascular phenotype [RCV005275141]	uncertain significance	11	123645602	123645602	Human		name
13487467	CV461292	single nucleotide variant	NM_001040151.2(SCN3B):c.249G>A (p.Glu83=)	Brugada syndrome 7 [RCV000554297]\|Cardiovascular phenotype [RCV002431667]	benign\|likely benign	11	123642642	123642642	Human	1	name
8626929	CV82073	single nucleotide variant	NM_018400.3(SCN3B):c.449G>A (p.Gly150Glu)	Malignant melanoma [RCV000062152]	not provided	11	123638321	123638321	Human		name
127267466	CV1077938	single nucleotide variant	NM_001040151.2(SCN3B):c.630G>A (p.Ala210=)	Brugada syndrome 7 [RCV001404110]\|Cardiovascular phenotype [RCV002357339]	likely benign	11	123634161	123634161	Human	1	name
127279030	CV1099601	single nucleotide variant	NM_001040151.2(SCN3B):c.423C>T (p.Ile141=)	Brugada syndrome 7 [RCV001445493]	likely benign	11	123642468	123642468	Human	1	name
127304051	CV1121135	single nucleotide variant	NM_001040151.2(SCN3B):c.570A>G (p.Ala190=)	Brugada syndrome 7 [RCV001462087]\|Cardiovascular phenotype [RCV002350939]\|not provided [RCV001702099]\|not specified [RCV001699790]	benign\|likely benign	11	123638200	123638200	Human	1	name
127286452	CV1141994	single nucleotide variant	NM_001040151.2(SCN3B):c.561C>T (p.Ala187=)	Brugada syndrome 7 [RCV001494209]\|Cardiovascular phenotype [RCV002343663]\|SCN3B-related disorder [RCV003908768]	likely benign	11	123638209	123638209	Human	1	name , trait , alternate_id
127307772	CV1141995	single nucleotide variant	NM_001040151.2(SCN3B):c.309G>A (p.Val103=)	Brugada syndrome 7 [RCV001480394]\|Cardiovascular phenotype [RCV003375317]	likely benign	11	123642582	123642582	Human	1	name
151777718	CV1337011	deletion	NM_001040151.2(SCN3B):c.256del (p.Ser86fs)	Brugada syndrome 7 [RCV002025962]\|Cardiovascular phenotype [RCV002425402]	uncertain significance	11	123642635	123642635	Human	1	name
151857225	CV1377617	single nucleotide variant	NM_001040151.2(SCN3B):c.38T>C (p.Leu13Pro)	Brugada syndrome 7 [RCV001923548]	uncertain significance	11	123653764	123653764	Human	1	name
151719952	CV1396481	single nucleotide variant	NM_001040151.2(SCN3B):c.31G>A (p.Ala11Thr)	Brugada syndrome 7 [RCV001890935]	uncertain significance	11	123653771	123653771	Human	1	name
151788104	CV1419708	single nucleotide variant	NM_001040151.2(SCN3B):c.46A>G (p.Ile16Val)	Brugada syndrome 7 [RCV001951768]	uncertain significance	11	123653756	123653756	Human	1	name
8692769	CV142736	single nucleotide variant	NM_001040151.2(SCN3B):c.390G>A (p.Ala130=)	Brugada syndrome 7 [RCV000471206]\|Cardiovascular phenotype [RCV000253821]\|not provided [RCV001701682]\|not specified [RCV000127949]	benign\|likely benign	11	123642501	123642501	Human	1	name
8692770	CV142737	single nucleotide variant	NM_001040151.2(SCN3B):c.438C>A (p.Thr146=)	not specified [RCV000127950]	benign	11	123642453	123642453	Human		name
152038012	CV1669208	deletion	NM_001040151.2(SCN3B):c.186del (p.Trp62fs)	not provided [RCV002224260]	uncertain significance	11	123645620	123645620	Human		name
8595788	CV17509	single nucleotide variant	NM_001040151.2(SCN3B):c.29T>C (p.Leu10Pro)	Atrial fibrillation, familial, 16 [RCV000128811]\|Brugada syndrome 7 [RCV000002574]\|Brugada syndrome [RCV000171567]\|Cardiovascular phenotype [RCV000250087]\|not provided [RCV000171069]\|not specified [RCV000220802]	pathogenic\|likely pathogenic\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance\|no classifications from unflagged records	11	123653773	123653773	Human	3	name
155719081	CV1788742	single nucleotide variant	NM_001040151.2(SCN3B):c.333T>C (p.Thr111=)	Cardiovascular phenotype [RCV002326584]	likely benign	11	123642558	123642558	Human		name
155726462	CV1791073	single nucleotide variant	NM_001040151.2(SCN3B):c.420G>T (p.Leu140=)	Cardiovascular phenotype [RCV002327951]	likely benign	11	123642471	123642471	Human		name
155692084	CV1794803	single nucleotide variant	NM_001040151.2(SCN3B):c.312C>T (p.Ser104=)	Cardiovascular phenotype [RCV002320567]	likely benign	11	123642579	123642579	Human		name
155682888	CV1801159	single nucleotide variant	NM_001040151.2(SCN3B):c.62T>C (p.Val21Ala)	Cardiovascular phenotype [RCV002353956]	uncertain significance	11	123645744	123645744	Human		name
155719993	CV1805333	single nucleotide variant	NM_001040151.2(SCN3B):c.47T>C (p.Ile16Thr)	Cardiovascular phenotype [RCV002337870]	uncertain significance	11	123653755	123653755	Human		name
155731419	CV1814324	single nucleotide variant	NM_001040151.2(SCN3B):c.83A>G (p.Glu28Gly)	Cardiovascular phenotype [RCV002434891]	uncertain significance	11	123645723	123645723	Human		name
155718801	CV1819441	single nucleotide variant	NM_001040151.2(SCN3B):c.73G>C (p.Val25Leu)	Cardiovascular phenotype [RCV002380526]	uncertain significance	11	123645733	123645733	Human		name
155703064	CV1852283	deletion	NM_001040151.2(SCN3B):c.266del (p.Gln89fs)	Cardiovascular phenotype [RCV002428796]	uncertain significance	11	123642625	123642625	Human		name
155698500	CV1855073	single nucleotide variant	NM_001040151.2(SCN3B):c.306C>T (p.Asp102=)	Cardiovascular phenotype [RCV002444312]	likely benign	11	123642585	123642585	Human		name
10044389	CV188504	single nucleotide variant	NM_001040151.2(SCN3B):c.582C>T (p.Asn194=)	Brugada syndrome 7 [RCV000463466]\|Cardiovascular phenotype [RCV000622088]\|not provided [RCV001723742]\|not specified [RCV000171065]	benign\|likely benign	11	123638188	123638188	Human	1	name
10044941	CV188508	single nucleotide variant	NM_001040151.2(SCN3B):c.59G>A (p.Ser20Asn)	Cardiovascular phenotype [RCV002354424]\|not provided [RCV000171070]	uncertain significance	11	123645747	123645747	Human		name
156300191	CV2017277	single nucleotide variant	NM_001040151.2(SCN3B):c.50A>G (p.Tyr17Cys)	Brugada syndrome 7 [RCV002716022]	uncertain significance	11	123653752	123653752	Human	1	name
156024873	CV2020064	single nucleotide variant	NM_001040151.2(SCN3B):c.95A>G (p.Glu32Gly)	Brugada syndrome 7 [RCV002691176]	uncertain significance	11	123645711	123645711	Human	1	name
156391487	CV2118726	single nucleotide variant	NM_001040151.2(SCN3B):c.92C>T (p.Ser31Leu)	Brugada syndrome 7 [RCV002943950]\|Cardiovascular phenotype [RCV004983224]	uncertain significance	11	123645714	123645714	Human	1	name
156110896	CV2121150	single nucleotide variant	NM_001040151.2(SCN3B):c.411G>A (p.Thr137=)	Brugada syndrome 7 [RCV002953109]\|Cardiovascular phenotype [RCV003377806]	likely benign	11	123642480	123642480	Human	1	name
156121622	CV2128555	single nucleotide variant	NM_001040151.2(SCN3B):c.519G>T (p.Leu173=)	Brugada syndrome 7 [RCV002953520]	likely benign	11	123638251	123638251	Human	1	name
11040172	CV224415	single nucleotide variant	NM_001040151.2(SCN3B):c.60T>G (p.Ser20Arg)	not specified [RCV000208517]	likely benign\|conflicting interpretations of pathogenicity	11	123645746	123645746	Human		name
329364926	CV2425840	single nucleotide variant	NM_001040151.2(SCN3B):c.399C>A (p.Pro133=)	Cardiovascular phenotype [RCV003181803]	likely benign	11	123642492	123642492	Human		name
11542753	CV254022	single nucleotide variant	NM_001040151.2(SCN3B):c.438C>T (p.Thr146=)	Brugada syndrome 7 [RCV000860457]\|Cardiovascular phenotype [RCV000241560]\|not provided [RCV001636803]\|not specified [RCV000244052]	benign\|likely benign	11	123642453	123642453	Human	5	name
11542753	CV254022	single nucleotide variant	NM_001040151.2(SCN3B):c.438C>T (p.Thr146=)	Brugada syndrome 7 [RCV000860457]\|Cardiovascular phenotype [RCV000241560]\|not provided [RCV001636803]\|not specified [RCV000244052]	benign\|likely benign	11	123642453	123642454	Human	5	name
11545825	CV258683	single nucleotide variant	NM_001040151.2(SCN3B):c.390G>T (p.Ala130=)	Brugada syndrome 7 [RCV001521817]\|Cardiovascular phenotype [RCV000245661]\|not provided [RCV003422186]\|not specified [RCV000437142]	benign\|likely benign	11	123642501	123642501	Human	1	name
11549148	CV258684	single nucleotide variant	NM_001040151.2(SCN3B):c.363T>C (p.Asn121=)	Cardiovascular phenotype [RCV000250033]	likely benign	11	123642528	123642528	Human		name
401765958	CV2724546	single nucleotide variant	NM_001040151.2(SCN3B):c.74T>C (p.Val25Ala)	Cardiovascular phenotype [RCV003301648]	uncertain significance	11	123645732	123645732	Human		name
401868871	CV2787594	single nucleotide variant	NM_001040151.2(SCN3B):c.330C>T (p.Val110=)	Cardiovascular phenotype [RCV003380370]	likely benign	11	123642561	123642561	Human		name
405109962	CV2879374	single nucleotide variant	NM_001040151.2(SCN3B):c.525C>T (p.Ile175=)	Brugada syndrome 7 [RCV003499112]	likely benign	11	123638245	123638245	Human	1	name
405183430	CV3124066	single nucleotide variant	NM_001040151.2(SCN3B):c.624C>T (p.Asn208=)	Brugada syndrome 7 [RCV003820262]	likely benign	11	123634167	123634167	Human	1	name
405724230	CV3381566	single nucleotide variant	NM_001040151.2(SCN3B):c.597T>C (p.Leu199=)	Cardiovascular phenotype [RCV004524259]	likely benign	11	123634194	123634194	Human		name
405724239	CV3381567	single nucleotide variant	NM_001040151.2(SCN3B):c.621G>A (p.Glu207=)	Cardiovascular phenotype [RCV004524260]	likely benign	11	123634170	123634170	Human		name
12847824	CV373926	single nucleotide variant	NM_001040151.2(SCN3B):c.489C>T (p.Tyr163=)	Cardiovascular phenotype [RCV002339079]\|not specified [RCV000444171]	likely benign	11	123638281	123638281	Human		name
597930096	CV3745805	single nucleotide variant	NM_001040151.2(SCN3B):c.354C>T (p.Tyr118=)	Brugada syndrome 7 [RCV005075790]	likely benign	11	123642537	123642537	Human	1	name
597899103	CV3782865	single nucleotide variant	NM_001040151.2(SCN3B):c.65G>A (p.Cys22Tyr)	Brugada syndrome 7 [RCV005126885]	uncertain significance	11	123645741	123645741	Human	1	name
597959052	CV3815017	single nucleotide variant	NM_001040151.2(SCN3B):c.309G>T (p.Val103=)	Brugada syndrome 7 [RCV005163143]	likely benign	11	123642582	123642582	Human	1	name
597877130	CV3860220	single nucleotide variant	NM_001040151.2(SCN3B):c.82G>C (p.Glu28Gln)	Brugada syndrome 7 [RCV005198429]	uncertain significance	11	123645724	123645724	Human	1	name
598234842	CV3910450	single nucleotide variant	NM_001040151.2(SCN3B):c.82G>T (p.Glu28Ter)	Cardiovascular phenotype [RCV005275138]	uncertain significance	11	123645724	123645724	Human		name
598234859	CV3910454	single nucleotide variant	NM_001040151.2(SCN3B):c.336G>A (p.Leu112=)	Cardiovascular phenotype [RCV005275142]	likely benign	11	123642555	123642555	Human		name
12891436	CV398081	single nucleotide variant	NM_001040151.2(SCN3B):c.327C>T (p.Asn109=)	Brugada syndrome 7 [RCV000476588]\|Cardiovascular phenotype [RCV002446906]\|SCN3B-related disorder [RCV003932762]\|not provided [RCV001567043]	likely benign	11	123642564	123642564	Human	1	name , trait , alternate_id
13535532	CV503505	single nucleotide variant	NM_001040151.2(SCN3B):c.339C>T (p.Asn113=)	Brugada syndrome 7 [RCV002066736]\|Cardiovascular phenotype [RCV002457956]\|not specified [RCV000607842]	likely benign	11	123642552	123642552	Human	1	name
13529682	CV510260	single nucleotide variant	NM_001040151.2(SCN3B):c.537T>C (p.Tyr179=)	Brugada syndrome 7 [RCV001510932]\|Cardiovascular phenotype [RCV000621836]	benign\|likely benign	11	123638233	123638233	Human	1	name
13534933	CV510262	single nucleotide variant	NM_001040151.2(SCN3B):c.414G>A (p.Thr138=)	Cardiovascular phenotype [RCV000619211]	likely benign	11	123642477	123642477	Human		name
13817207	CV564503	single nucleotide variant	NM_001040151.2(SCN3B):c.98C>T (p.Thr33Met)	Brugada syndrome 7 [RCV000706863]\|Cardiovascular phenotype [RCV002386276]	uncertain significance	11	123645708	123645708	Human	1	name
15118793	CV684238	single nucleotide variant	NM_001040151.2(SCN3B):c.396G>T (p.Arg132=)	Brugada syndrome 7 [RCV000861375]\|Cardiovascular phenotype [RCV002372396]	likely benign	11	123642495	123642495	Human	1	name
126726498	CV994378	single nucleotide variant	NM_001040151.2(SCN3B):c.73G>T (p.Val25Leu)	Brugada syndrome 7 [RCV001302904]\|Cardiovascular phenotype [RCV002384364]\|not provided [RCV001586116]	likely benign\|uncertain significance	11	123645733	123645733	Human	1	name
150556102	CV1295486	single nucleotide variant	NM_001040151.2(SCN3B):c.205G>A (p.Gly69Ser)	Brugada syndrome 7 [RCV002032825]\|Cardiovascular phenotype [RCV002421252]\|not provided [RCV001773921]	uncertain significance	11	123645601	123645601	Human	1	name
151879677	CV1388299	single nucleotide variant	NM_001040151.2(SCN3B):c.260C>G (p.Pro87Arg)	Brugada syndrome 7 [RCV001982351]\|Cardiovascular phenotype [RCV002425309]	uncertain significance	11	123642631	123642631	Human	1	name
151890252	CV1448035	single nucleotide variant	NM_001040151.2(SCN3B):c.232C>T (p.Arg78Trp)	Brugada syndrome 7 [RCV001942991]\|Cardiovascular phenotype [RCV002449576]\|not specified [RCV004587253]	uncertain significance	11	123642659	123642659	Human	1	name
151760055	CV1448351	single nucleotide variant	NM_001040151.2(SCN3B):c.295G>A (p.Asp99Asn)	Brugada syndrome 7 [RCV001949029]	uncertain significance	11	123642596	123642596	Human	1	name
151875517	CV1466818	single nucleotide variant	NM_001040151.2(SCN3B):c.106G>A (p.Val36Met)	Brugada syndrome 7 [RCV001885810]\|Cardiovascular phenotype [RCV003164240]	likely benign\|uncertain significance	11	123645700	123645700	Human	1	name
151711183	CV1497184	single nucleotide variant	NM_001040151.2(SCN3B):c.233G>A (p.Arg78Gln)	Brugada syndrome 7 [RCV002001999]\|Cardiovascular phenotype [RCV002442904]	uncertain significance	11	123642658	123642658	Human	1	name
8696334	CV150288	single nucleotide variant	NM_001040151.2(SCN3B):c.161T>G (p.Val54Gly)	Brugada syndrome 7 [RCV001243331]\|Cardiovascular phenotype [RCV002399507]\|not provided [RCV000128812]	conflicting interpretations of pathogenicity\|uncertain significance	11	123645645	123645645	Human	1	name
155686139	CV1771117	single nucleotide variant	NM_001040151.2(SCN3B):c.241C>T (p.His81Tyr)	Brugada syndrome 7 [RCV002298983]	uncertain significance	11	123642650	123642650	Human	1	name
155682636	CV1801009	single nucleotide variant	NM_001040151.2(SCN3B):c.121A>G (p.Met41Val)	Cardiovascular phenotype [RCV002353915]	uncertain significance	11	123645685	123645685	Human		name
155740158	CV1809249	single nucleotide variant	NM_001040151.2(SCN3B):c.118C>A (p.Pro40Thr)	Cardiovascular phenotype [RCV002342841]	uncertain significance	11	123645688	123645688	Human		name
155682950	CV1839875	single nucleotide variant	NM_001040151.2(SCN3B):c.197C>T (p.Pro66Leu)	Cardiovascular phenotype [RCV002423651]	uncertain significance	11	123645609	123645609	Human		name
155672317	CV1853936	single nucleotide variant	NM_001040151.2(SCN3B):c.272G>A (p.Arg91His)	Brugada syndrome 7 [RCV003102152]\|Cardiovascular phenotype [RCV002437470]	uncertain significance	11	123642619	123642619	Human	1	name
155671116	CV1853941	single nucleotide variant	NM_001040151.2(SCN3B):c.272G>T (p.Arg91Leu)	Cardiovascular phenotype [RCV002453233]	uncertain significance	11	123642619	123642619	Human		name
10046877	CV189327	single nucleotide variant	NM_001040151.2(SCN3B):c.217C>A (p.Leu73Ile)	not provided [RCV000171693]	uncertain significance	11	123645589	123645589	Human		name
156303663	CV1898406	single nucleotide variant	NM_001040151.2(SCN3B):c.139T>A (p.Ser47Thr)	Brugada syndrome 7 [RCV003088062]	uncertain significance	11	123645667	123645667	Human	1	name
156045526	CV2157748	single nucleotide variant	NM_001040151.2(SCN3B):c.244C>T (p.Gln82Ter)	Brugada syndrome 7 [RCV003019218]	uncertain significance	11	123642647	123642647	Human	1	name
329363639	CV2425839	single nucleotide variant	NM_001040151.2(SCN3B):c.253G>C (p.Glu85Gln)	Cardiovascular phenotype [RCV003168307]	uncertain significance	11	123642638	123642638	Human		name
329364922	CV2425843	single nucleotide variant	NM_001040151.2(SCN3B):c.291C>G (p.Ser97Arg)	Brugada syndrome 7 [RCV005101019]\|Cardiovascular phenotype [RCV003181806]	uncertain significance	11	123642600	123642600	Human	1	name
401868870	CV2787593	single nucleotide variant	NM_001040151.2(SCN3B):c.130C>T (p.Arg44Cys)	Brugada syndrome 7 [RCV005104236]\|Cardiovascular phenotype [RCV003380369]	uncertain significance	11	123645676	123645676	Human	1	name
401910233	CV2809964	single nucleotide variant	NM_001040151.2(SCN3B):c.214T>A (p.Phe72Ile)	not provided [RCV003424870]	uncertain significance	11	123645592	123645592	Human		name
405104214	CV2900361	single nucleotide variant	NM_001040151.2(SCN3B):c.173C>T (p.Thr58Met)	Brugada syndrome 7 [RCV003497547]	uncertain significance	11	123645633	123645633	Human	1	name
404994846	CV3013502	single nucleotide variant	NM_001040151.2(SCN3B):c.117C>G (p.Asn39Lys)	Brugada syndrome 7 [RCV003604961]	uncertain significance	11	123645689	123645689	Human	1	name
405724194	CV3381560	single nucleotide variant	NM_001040151.2(SCN3B):c.110A>G (p.Gln37Arg)	Cardiovascular phenotype [RCV004524253]	uncertain significance	11	123645696	123645696	Human		name
407506938	CV3496211	single nucleotide variant	NM_001040151.2(SCN3B):c.133T>C (p.Cys45Arg)	not provided [RCV004698052]	uncertain significance	11	123645673	123645673	Human		name
597682716	CV3598130	single nucleotide variant	NM_001040151.2(SCN3B):c.131G>A (p.Arg44His)	Cardiovascular phenotype [RCV004983485]	uncertain significance	11	123645675	123645675	Human		name
13211841	CV425910	single nucleotide variant	NM_001040151.2(SCN3B):c.199G>A (p.Glu67Lys)	Brugada syndrome 7 [RCV001372816]\|Cardiovascular phenotype [RCV004023335]\|Long QT syndrome [RCV003318378]\|not provided [RCV000497982]	uncertain significance	11	123645607	123645607	Human	3	name
13528108	CV510258	duplication	NM_001040151.2(SCN3B):c.591dup (p.Tyr198fs)	Cardiovascular phenotype [RCV000620529]	uncertain significance	11	123634199	123634200	Human		name
26902880	CV858252	single nucleotide variant	NM_001040151.2(SCN3B):c.118C>T (p.Pro40Ser)	Brugada syndrome [RCV001089637]	uncertain significance	11	123645688	123645688	Human	1	name
38461451	CV947354	single nucleotide variant	NM_001040151.2(SCN3B):c.160G>A (p.Val54Met)	Brugada syndrome 7 [RCV001229539]\|Cardiovascular phenotype [RCV005268985]	uncertain significance	11	123645646	123645646	Human	1	name
126923163	CV1047100	single nucleotide variant	NM_001040151.2(SCN3B):c.446C>G (p.Ala149Gly)	Brugada syndrome 7 [RCV001365529]	uncertain significance	11	123638324	123638324	Human	1	name
151235849	CV1319276	single nucleotide variant	NM_001040151.2(SCN3B):c.389C>A (p.Ala130Glu)	Cardiovascular phenotype [RCV004040854]\|not provided [RCV001797221]	uncertain significance	11	123642502	123642502	Human		name
151772096	CV1410987	single nucleotide variant	NM_001040151.2(SCN3B):c.392A>G (p.His131Arg)	Brugada syndrome 7 [RCV001971282]	uncertain significance	11	123642499	123642499	Human	1	name
8696335	CV150289	single nucleotide variant	NM_001040151.2(SCN3B):c.389C>T (p.Ala130Val)	Atrial fibrillation, familial, 16 [RCV000128813]\|Brugada syndrome 7 [RCV001320720]\|not provided [RCV000480040]	pathogenic\|uncertain significance	11	123642502	123642502	Human	1	name
8696336	CV150290	single nucleotide variant	NM_001040151.2(SCN3B):c.482T>C (p.Met161Thr)	Atrial fibrillation, familial, 16 [RCV000128814]	pathogenic	11	123638288	123638288	Human	1	name
152037828	CV1669178	single nucleotide variant	NM_001040151.2(SCN3B):c.341A>T (p.Asp114Val)	not provided [RCV002224230]	uncertain significance	11	123642550	123642550	Human		name
155729495	CV1786248	single nucleotide variant	NM_001040151.2(SCN3B):c.354C>G (p.Tyr118Ter)	Cardiovascular phenotype [RCV002339727]	uncertain significance	11	123642537	123642537	Human		name
155664972	CV1786694	single nucleotide variant	NM_001040151.2(SCN3B):c.371G>A (p.Arg124Gln)	Brugada syndrome 7 [RCV003094326]\|Cardiovascular phenotype [RCV002349076]	uncertain significance	11	123642520	123642520	Human	1	name
155701673	CV1791320	single nucleotide variant	NM_001040151.2(SCN3B):c.439G>A (p.Glu147Lys)	Cardiovascular phenotype [RCV002333706]	uncertain significance	11	123642452	123642452	Human		name
155724503	CV1799439	single nucleotide variant	NM_001040151.2(SCN3B):c.517C>G (p.Leu173Val)	Cardiovascular phenotype [RCV002338432]	uncertain significance	11	123638253	123638253	Human		name
155669936	CV1800456	single nucleotide variant	NM_001040151.2(SCN3B):c.574C>G (p.Gln192Glu)	Brugada syndrome 7 [RCV003096864]\|Cardiovascular phenotype [RCV002349920]	uncertain significance	11	123638196	123638196	Human	1	name
155672605	CV1801084	single nucleotide variant	NM_001040151.2(SCN3B):c.628G>A (p.Ala210Thr)	Cardiovascular phenotype [RCV002368731]	uncertain significance	11	123634163	123634163	Human		name
155737374	CV1801894	single nucleotide variant	NM_001040151.2(SCN3B):c.484A>G (p.Met162Val)	Cardiovascular phenotype [RCV002330799]	uncertain significance	11	123638286	123638286	Human		name
155733411	CV1802043	single nucleotide variant	NM_001040151.2(SCN3B):c.486G>A (p.Met162Ile)	Cardiovascular phenotype [RCV002340406]	uncertain significance	11	123638284	123638284	Human		name
155745425	CV1802819	single nucleotide variant	NM_001040151.2(SCN3B):c.535T>C (p.Tyr179His)	Brugada syndrome 7 [RCV003096710]\|Cardiovascular phenotype [RCV002347028]	uncertain significance	11	123638235	123638235	Human	1	name
155743846	CV1803199	single nucleotide variant	NM_001040151.2(SCN3B):c.562G>A (p.Glu188Lys)	Cardiovascular phenotype [RCV002345075]	uncertain significance	11	123638208	123638208	Human		name
155735167	CV1804872	single nucleotide variant	NM_001040151.2(SCN3B):c.454G>A (p.Asp152Asn)	Cardiovascular phenotype [RCV002330344]	uncertain significance	11	123638316	123638316	Human		name
155668544	CV1856159	single nucleotide variant	NM_001040151.2(SCN3B):c.301C>A (p.Gln101Lys)	Brugada syndrome 7 [RCV003102978]\|Cardiovascular phenotype [RCV002435861]	uncertain significance	11	123642590	123642590	Human	1	name
156239587	CV1882355	single nucleotide variant	NM_001040151.2(SCN3B):c.601A>G (p.Ile201Val)	Brugada syndrome 7 [RCV003085692]	uncertain significance	11	123634190	123634190	Human	1	name
10044706	CV188503	single nucleotide variant	NM_001040151.2(SCN3B):c.629C>T (p.Ala210Val)	Brugada syndrome 7 [RCV002054024]\|Cardiovascular phenotype [RCV003165348]\|not provided [RCV004700526]	benign\|likely benign\|uncertain significance	11	123634162	123634162	Human	1	name
10044942	CV188505	single nucleotide variant	NM_001040151.2(SCN3B):c.416G>A (p.Arg139Gln)	Brugada syndrome 7 [RCV001221228]\|Cardiovascular phenotype [RCV002326936]\|not provided [RCV000171071]\|not specified [RCV001000945]	benign\|uncertain significance	11	123642475	123642475	Human	1	name
10044707	CV188506	single nucleotide variant	NM_001040151.2(SCN3B):c.328G>A (p.Val110Ile)	Brugada syndrome 7 [RCV001087315]\|Cardiomyopathy [RCV000852659]\|Cardiovascular phenotype [RCV000621217]\|Death in infancy [RCV000234992]\|SCN3B-related disorder [RCV003937532]\|not provided [RCV000171068]\|not specified [RCV000185522]	pathogenic\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	123642563	123642563	Human	5	name , trait , alternate_id
156166187	CV1929985	single nucleotide variant	NM_001040151.2(SCN3B):c.407A>G (p.Lys136Arg)	Brugada syndrome 7 [RCV002624558]	uncertain significance	11	123642484	123642484	Human	1	name
156374709	CV1963408	single nucleotide variant	NM_001040151.2(SCN3B):c.436A>G (p.Thr146Ala)	Brugada syndrome 7 [RCV002582703]	uncertain significance	11	123642455	123642455	Human	1	name
156343376	CV1981671	single nucleotide variant	NM_001040151.2(SCN3B):c.584C>T (p.Ala195Val)	Brugada syndrome 7 [RCV002631545]	uncertain significance	11	123638186	123638186	Human	1	name
156375579	CV2000164	single nucleotide variant	NM_001040151.2(SCN3B):c.541T>A (p.Tyr181Asn)	Brugada syndrome 7 [RCV002653265]	uncertain significance	11	123638229	123638229	Human	1	name
156212772	CV2018948	single nucleotide variant	NM_001040151.2(SCN3B):c.618G>C (p.Lys206Asn)	Brugada syndrome 7 [RCV002700690]	uncertain significance	11	123634173	123634173	Human	1	name
156115578	CV2173930	single nucleotide variant	NM_001040151.2(SCN3B):c.322C>T (p.Leu108Phe)	Brugada syndrome 7 [RCV003055261]	uncertain significance	11	123642569	123642569	Human	1	name
11039996	CV224414	single nucleotide variant	NM_001040151.2(SCN3B):c.587C>G (p.Ser196Cys)	Sudden cardiac death [RCV000208160]	uncertain significance	11	123634204	123634204	Human	2	name
11522989	CV226503	single nucleotide variant	NM_001040151.2(SCN3B):c.423C>G (p.Ile141Met)	Brugada syndrome 7 [RCV002515579]\|Cardiac arrhythmia [RCV001842965]	pathogenic\|uncertain significance	11	123642468	123642468	Human	3	name
329364924	CV2425841	single nucleotide variant	NM_001040151.2(SCN3B):c.565G>A (p.Glu189Lys)	Cardiovascular phenotype [RCV003181804]	uncertain significance	11	123638205	123638205	Human		name
329364923	CV2425842	single nucleotide variant	NM_001040151.2(SCN3B):c.384T>G (p.Phe128Leu)	Cardiovascular phenotype [RCV003181805]	uncertain significance	11	123642507	123642507	Human		name
329390160	CV2465709	single nucleotide variant	NM_001040151.2(SCN3B):c.608C>T (p.Ser203Phe)	Brugada syndrome 7 [RCV005101374]\|Cardiovascular phenotype [RCV003216614]	uncertain significance	11	123634183	123634183	Human	1	name
401765957	CV2724545	single nucleotide variant	NM_001040151.2(SCN3B):c.441G>T (p.Glu147Asp)	Cardiovascular phenotype [RCV003301647]	uncertain significance	11	123642450	123642450	Human		name
401765960	CV2724547	single nucleotide variant	NM_001040151.2(SCN3B):c.631G>A (p.Val211Ile)	Cardiovascular phenotype [RCV003301649]	uncertain significance	11	123634160	123634160	Human		name
401865901	CV2778941	single nucleotide variant	NM_001040151.2(SCN3B):c.370C>T (p.Arg124Trp)	Cardiovascular phenotype [RCV004348604]	uncertain significance	11	123642521	123642521	Human		name
405724200	CV3381561	single nucleotide variant	NM_001040151.2(SCN3B):c.334C>G (p.Leu112Val)	Cardiovascular phenotype [RCV004524254]	uncertain significance	11	123642557	123642557	Human		name
405724205	CV3381562	single nucleotide variant	NM_001040151.2(SCN3B):c.380A>G (p.Glu127Gly)	Cardiovascular phenotype [RCV004524255]	uncertain significance	11	123642511	123642511	Human		name
405724211	CV3381563	single nucleotide variant	NM_001040151.2(SCN3B):c.391C>A (p.His131Asn)	Cardiovascular phenotype [RCV004524256]	uncertain significance	11	123642500	123642500	Human		name
405724218	CV3381564	single nucleotide variant	NM_001040151.2(SCN3B):c.404T>C (p.Val135Ala)	Cardiovascular phenotype [RCV004524257]	uncertain significance	11	123642487	123642487	Human		name
407461601	CV3480107	single nucleotide variant	NM_001040151.2(SCN3B):c.368C>T (p.Ser123Phe)	Cardiovascular phenotype [RCV004658768]	uncertain significance	11	123642523	123642523	Human		name
407461603	CV3480108	single nucleotide variant	NM_001040151.2(SCN3B):c.331A>C (p.Thr111Pro)	Cardiovascular phenotype [RCV004658769]	uncertain significance	11	123642560	123642560	Human		name
597681981	CV3598123	single nucleotide variant	NM_001040151.2(SCN3B):c.308T>C (p.Val103Ala)	Cardiovascular phenotype [RCV004983479]	uncertain significance	11	123642583	123642583	Human		name
597681988	CV3598124	single nucleotide variant	NM_001040151.2(SCN3B):c.572C>T (p.Ala191Val)	Cardiovascular phenotype [RCV004983480]	uncertain significance	11	123638198	123638198	Human		name
597872471	CV3747174	single nucleotide variant	NM_001040151.2(SCN3B):c.460A>G (p.Thr154Ala)	Brugada syndrome 7 [RCV005068858]	uncertain significance	11	123638310	123638310	Human	1	name
597910262	CV3782106	single nucleotide variant	NM_001040151.2(SCN3B):c.331A>T (p.Thr111Ser)	Brugada syndrome 7 [RCV005128598]	uncertain significance	11	123642560	123642560	Human	1	name
597954201	CV3795725	single nucleotide variant	NM_001040151.2(SCN3B):c.340G>A (p.Asp114Asn)	Brugada syndrome 7 [RCV005136735]	uncertain significance	11	123642551	123642551	Human	1	name
12907044	CV415256	single nucleotide variant	NM_001040151.2(SCN3B):c.614A>G (p.Asn205Ser)	Brugada syndrome 7 [RCV002489198]\|Cardiovascular phenotype [RCV002356802]\|not provided [RCV000489960]	uncertain significance	11	123634177	123634177	Human	1	name
13534667	CV510261	single nucleotide variant	NM_001040151.2(SCN3B):c.415C>T (p.Arg139Trp)	Brugada syndrome 7 [RCV001855267]\|Cardiovascular phenotype [RCV000618849]	benign\|uncertain significance	11	123642476	123642476	Human	1	name
13821503	CV564502	single nucleotide variant	NM_001040151.2(SCN3B):c.632T>G (p.Val211Gly)	Brugada syndrome 7 [RCV000695978]	uncertain significance	11	123634159	123634159	Human	1	name
14718427	CV639813	single nucleotide variant	NM_001040151.2(SCN3B):c.583G>A (p.Ala195Thr)	Brugada syndrome 7 [RCV000795798]\|Cardiovascular phenotype [RCV002352331]\|not provided [RCV001700306]\|not specified [RCV001002066]	likely benign\|uncertain significance	11	123638187	123638187	Human	1	name
14723712	CV639814	single nucleotide variant	NM_001040151.2(SCN3B):c.395G>A (p.Arg132Gln)	Brugada syndrome 7 [RCV000798076]\|Cardiovascular phenotype [RCV004027942]	uncertain significance	11	123642496	123642496	Human	1	name
14729491	CV639815	single nucleotide variant	NM_001040151.2(SCN3B):c.394C>T (p.Arg132Trp)	Brugada syndrome 7 [RCV000800514]\|Cardiac arrhythmia [RCV001841980]\|Cardiovascular phenotype [RCV002352355]	uncertain significance	11	123642497	123642497	Human	3	name
21074143	CV796535	single nucleotide variant	NM_001040151.2(SCN3B):c.413C>T (p.Thr138Met)	Brugada syndrome 7 [RCV005056728]\|Cardiovascular phenotype [RCV002327222]\|not provided [RCV000994748]	uncertain significance	11	123642478	123642478	Human	1	name
38489978	CV926151	single nucleotide variant	NM_001040151.2(SCN3B):c.410C>T (p.Thr137Met)	Brugada syndrome 7 [RCV001221947]	uncertain significance	11	123642481	123642481	Human	1	name
41405887	CV981735	single nucleotide variant	NM_001040151.2(SCN3B):c.568G>A (p.Ala190Thr)	not provided [RCV001810629]	uncertain significance	11	123638202	123638202	Human		name
40887936	CV973786	microsatellite	NM_001040151.2(SCN3B):c.409ACG[1] (p.Thr138del)	Brugada syndrome 7 [RCV003770397]\|Inborn genetic diseases [RCV001267470]	uncertain significance	11	123642477	123642479	Human		name
155741925	CV1791189	indel	NM_001040151.2(SCN3B):c.438_439delinsTA (p.Glu147Lys)	Cardiovascular phenotype [RCV002333575]	uncertain significance	11	123642452	123642453	Human		name
151828446	CV1468523	deletion	NM_001040151.2(SCN3B):c.392_397del (p.His131_Arg132del)	Brugada syndrome 7 [RCV002030565]\|Cardiovascular phenotype [RCV003303576]	uncertain significance	11	123642494	123642499	Human	1	name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message