Calm1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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169 records found for search term Calm1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
127267669	CV1080825	single nucleotide variant	NM_006888.6(CALM1):c.4-9T>A	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001404174]	likely benign	14	90400056	90400056	Human	1	name
155701946	CV1791358	single nucleotide variant	NM_006888.6(CALM1):c.4-3T>C	Cardiovascular phenotype [RCV002333744]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003775885]	uncertain significance	14	90400062	90400062	Human	2	name
156118004	CV2081418	single nucleotide variant	NM_006888.6(CALM1):c.4-6A>T	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002889446]	likely benign	14	90400059	90400059	Human	1	name
156373749	CV2123889	single nucleotide variant	NM_006888.6(CALM1):c.4-7C>T	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002942538]	likely benign	14	90400058	90400058	Human	1	name
597837550	CV3866823	single nucleotide variant	NM_006888.6(CALM1):c.4-9T>C	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005225814]	likely benign	14	90400056	90400056	Human	1	name
597860467	CV3879910	single nucleotide variant	NM_006888.6(CALM1):c.4-6A>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005229490]	likely benign	14	90400059	90400059	Human	1	name
598203656	CV3942901	single nucleotide variant	NM_006888.6(CALM1):c.4-4A>G	Cardiovascular phenotype [RCV005314661]	uncertain significance	14	90400061	90400061	Human		name
13541418	CV505565	single nucleotide variant	NM_006888.6(CALM1):c.-32C>T	not specified [RCV000616131]	likely benign	14	90397199	90397199	Human		name
14726584	CV656269	single nucleotide variant	NM_006888.6(CALM1):c.-86G>A	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001554674]\|not provided [RCV000833933]	benign	14	90397145	90397145	Human	1	name
150478000	CV1207593	single nucleotide variant	NM_006888.6(CALM1):c.-123G>T	not provided [RCV001589868]	likely benign	14	90397108	90397108	Human		name
150471541	CV1209568	single nucleotide variant	NM_006888.6(CALM1):c.-161C>T	not provided [RCV001588679]	likely benign	14	90397070	90397070	Human		name
152052639	CV1607270	single nucleotide variant	NM_006888.6(CALM1):c.3+13T>C	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002109168]	likely benign	14	90397246	90397246	Human	1	name
156327668	CV1990670	single nucleotide variant	NM_006888.6(CALM1):c.3+10G>C	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002630745]	likely benign	14	90397243	90397243	Human	1	name
405017391	CV3091600	single nucleotide variant	NM_006888.6(CALM1):c.3+14G>T	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003795267]	likely benign	14	90397247	90397247	Human	1	name
12847273	CV374397	single nucleotide variant	NM_006888.6(CALM1):c.4-10C>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000652518]\|not provided [RCV001698290]\|not specified [RCV004767259]	benign\|likely benign	14	90400055	90400055	Human	1	name
597856325	CV3870748	single nucleotide variant	NM_006888.6(CALM1):c.3+15G>A	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005228949]	likely benign	14	90397248	90397248	Human	1	name
597838162	CV3871006	deletion	NM_006888.6(CALM1):c.4-15del	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005210665]	benign	14	90400047	90400047	Human	1	name
14737037	CV656268	single nucleotide variant	NM_006888.6(CALM1):c.-168C>T	not provided [RCV000838758]	likely benign	14	90397063	90397063	Human		name
14714771	CV667119	single nucleotide variant	NM_006888.4(CALM1):c.-390C>T	not provided [RCV000829147]	benign	14	90396841	90396841	Human		name
14745506	CV667125	single nucleotide variant	NM_006888.4(CALM1):c.-372G>T	not provided [RCV000843445]	benign	14	90396859	90396859	Human		name
14723962	CV667423	single nucleotide variant	NM_006888.4(CALM1):c.-540G>T	not provided [RCV000832770]	benign	14	90396691	90396691	Human		name
14726587	CV667624	single nucleotide variant	NM_006888.6(CALM1):c.4-63C>T	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001554796]\|not provided [RCV000833934]	benign	14	90400002	90400002	Human	1	name
127280396	CV1080826	duplication	NM_006888.6(CALM1):c.421+6dup	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001409753]	likely benign	14	90404516	90404517	Human	1	name
150422213	CV1194887	single nucleotide variant	NM_006888.6(CALM1):c.3+331C>A	not provided [RCV001570915]	likely benign	14	90397564	90397564	Human		name
150544324	CV1297817	single nucleotide variant	NM_006888.6(CALM1):c.422-6T>G	not provided [RCV001772725]	uncertain significance	14	90404683	90404683	Human		name
152094993	CV1521023	single nucleotide variant	NM_006888.6(CALM1):c.34+16C>T	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002078222]	likely benign	14	90400111	90400111	Human	1	name
152136031	CV1634550	single nucleotide variant	NM_006888.6(CALM1):c.34+12A>C	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002218727]	likely benign	14	90400107	90400107	Human	1	name
156387899	CV1875719	single nucleotide variant	NM_006888.6(CALM1):c.179-4C>T	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003051018]	likely benign	14	90403858	90403858	Human	1	name
155944134	CV1878982	single nucleotide variant	NM_006888.6(CALM1):c.34+12A>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003073737]	likely benign	14	90400107	90400107	Human	1	name
155946609	CV2062254	single nucleotide variant	NM_006888.6(CALM1):c.35-14A>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002816020]	likely benign	14	90401245	90401245	Human	1	name
156215699	CV2070645	single nucleotide variant	NM_006888.6(CALM1):c.35-19G>A	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002829486]	likely benign	14	90401240	90401240	Human	1	name
329365426	CV2433471	single nucleotide variant	NM_006888.6(CALM1):c.179-3G>A	Cardiovascular phenotype [RCV003182228]	uncertain significance	14	90403859	90403859	Human		name
402486931	CV3090459	duplication	NM_006888.6(CALM1):c.179-9dup	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003787120]	benign	14	90403847	90403848	Human	1	name
405126357	CV3111936	single nucleotide variant	NM_006888.6(CALM1):c.286-9T>C	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003815409]	likely benign	14	90404370	90404370	Human	1	name
597925714	CV3877315	single nucleotide variant	NM_006888.6(CALM1):c.422-8C>T	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005224011]	likely benign	14	90404681	90404681	Human	1	name
597842999	CV3878394	single nucleotide variant	NM_006888.6(CALM1):c.35-11T>A	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005226884]	likely benign	14	90401248	90401248	Human	1	name
13526805	CV504653	single nucleotide variant	NM_006888.6(CALM1):c.34+19G>T	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005223066]\|not specified [RCV000604632]	likely benign	14	90400114	90400114	Human	1	name
13540149	CV505141	deletion	NM_006888.6(CALM1):c.35-13del	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003767648]\|not specified [RCV000614298]	likely benign	14	90401246	90401246	Human	1	name
14714784	CV667491	single nucleotide variant	NM_006888.6(CALM1):c.3+298G>T	not provided [RCV000829151]	benign	14	90397531	90397531	Human		name
14730680	CV667496	single nucleotide variant	NM_006888.6(CALM1):c.34+29G>A	not provided [RCV000835790]	benign	14	90400124	90400124	Human		name
14745518	CV667831	single nucleotide variant	NM_006888.6(CALM1):c.3+293C>T	not provided [RCV000843457]	benign	14	90397526	90397526	Human		name
14730678	CV667833	single nucleotide variant	NM_006888.6(CALM1):c.4-129A>G	not provided [RCV000835789]	benign	14	90399936	90399936	Human		name
152053905	CV1523791	single nucleotide variant	NM_006888.6(CALM1):c.285+20G>T	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002127548]	likely benign	14	90403988	90403988	Human	1	name
152163556	CV1575464	single nucleotide variant	NM_006888.6(CALM1):c.422-20T>C	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002181356]	likely benign	14	90404669	90404669	Human	1	name
152040660	CV1577643	single nucleotide variant	NM_006888.6(CALM1):c.285+17A>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002107692]	likely benign	14	90403985	90403985	Human	1	name
9691246	CV171782	single nucleotide variant	NM_006888.6(CALM1):c.421+16C>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005222769]\|not provided [RCV000149484]	benign\|likely benign	14	90404530	90404530	Human	1	name
156163615	CV1933338	single nucleotide variant	NM_006888.6(CALM1):c.285+12T>A	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002624467]	likely benign	14	90403980	90403980	Human	1	name
156385919	CV1998105	single nucleotide variant	NM_006888.6(CALM1):c.421+10A>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002653988]	likely benign	14	90404524	90404524	Human	1	name
156259137	CV2057013	single nucleotide variant	NM_006888.6(CALM1):c.179-14T>C	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002791955]	likely benign	14	90403848	90403848	Human	1	name
156079555	CV2098565	single nucleotide variant	NM_006888.6(CALM1):c.285+15A>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002912653]	likely benign	14	90403983	90403983	Human	1	name
156108038	CV2140007	single nucleotide variant	NM_006888.6(CALM1):c.178+20G>T	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003002476]	likely benign	14	90401422	90401422	Human	1	name
405024919	CV3082013	single nucleotide variant	NM_006888.6(CALM1):c.179-17T>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003785619]	likely benign	14	90403845	90403845	Human	1	name
405029388	CV3082559	single nucleotide variant	NM_006888.6(CALM1):c.422-15T>C	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003786010]	likely benign	14	90404674	90404674	Human	1	name
404996918	CV3085533	single nucleotide variant	NM_006888.6(CALM1):c.178+16C>A	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003783064]	likely benign	14	90401418	90401418	Human	1	name
405001129	CV3095456	single nucleotide variant	NM_006888.6(CALM1):c.422-19A>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003793759]	likely benign	14	90404670	90404670	Human	1	name
12841431	CV373234	single nucleotide variant	NM_006888.6(CALM1):c.178+18A>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002059953]\|not specified [RCV000432574]	benign\|likely benign	14	90401420	90401420	Human	1	name
597891720	CV3867939	single nucleotide variant	NM_006888.6(CALM1):c.286-20C>T	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005218967]	likely benign	14	90404359	90404359	Human	1	name
597890663	CV3871627	single nucleotide variant	NM_006888.6(CALM1):c.286-18A>G	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005218795]	likely benign	14	90404361	90404361	Human	1	name
597926389	CV3873978	single nucleotide variant	NM_006888.6(CALM1):c.422-10G>A	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005224249]	likely benign	14	90404679	90404679	Human	1	name
13526270	CV504894	deletion	NM_006888.6(CALM1):c.179-15del	not specified [RCV000603916]	likely benign	14	90403847	90403847	Human		name
13534700	CV505566	duplication	NM_006888.6(CALM1):c.422-16dup	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002531653]\|not specified [RCV000607409]	likely benign	14	90404672	90404673	Human	1	name
14727278	CV666718	single nucleotide variant	NM_006888.6(CALM1):c.179-88G>A	not provided [RCV000834241]	likely benign	14	90403774	90403774	Human		name
150418448	CV1181199	deletion	NM_006888.6(CALM1):c.178+269del	not provided [RCV001550606]	likely benign	14	90401655	90401655	Human		name
150416480	CV1181200	single nucleotide variant	NM_006888.6(CALM1):c.286-141A>C	not provided [RCV001549661]	likely benign	14	90404238	90404238	Human		name
150433410	CV1203665	single nucleotide variant	NM_006888.6(CALM1):c.285+110G>A	not provided [RCV001581821]	likely benign	14	90404078	90404078	Human		name
150443861	CV1205185	single nucleotide variant	NM_006888.6(CALM1):c.285+168C>T	not provided [RCV001584028]	likely benign	14	90404136	90404136	Human		name
150499498	CV1224600	duplication	NM_006888.6(CALM1):c.178+269dup	not provided [RCV001620431]	benign	14	90401654	90401655	Human		name
150494446	CV1224901	single nucleotide variant	NM_006888.6(CALM1):c.179-108T>C	not provided [RCV001619379]	benign	14	90403754	90403754	Human		name
12901039	CV409165	duplication	NM_006888.6(CALM1):c.-37_-36dup	not specified [RCV000483763]	likely benign	14	90397192	90397193	Human		name
14710343	CV667628	single nucleotide variant	NM_006888.6(CALM1):c.179-293C>T	not provided [RCV000827673]	benign	14	90403569	90403569	Human	1	name
14710343	CV667628	single nucleotide variant	NM_006888.6(CALM1):c.179-293C>T	not provided [RCV000827673]	benign	14	90403569	90403570	Human	1	name
597909129	CV3867144	duplication	NM_006888.6(CALM1):c.35-44_77dup	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005221609]	uncertain significance	14	90401212	90401213	Human	1	name
150405926	CV1191623	single nucleotide variant	NM_001363669.2(CALM1):c.-106+211G>C	not provided [RCV001564509]	likely benign	14	90396869	90396869	Human		name
152084031	CV1533394	deletion	NM_006888.6(CALM1):c.421+8_421+9del	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002093230]	likely benign	14	90404522	90404523	Human	1	name
597726835	CV3647371	single nucleotide variant	NM_006888.6(CALM1):c.6T>C (p.Ala2=)	Cardiovascular phenotype [RCV004994941]	likely benign	14	90400067	90400067	Human		name
155733559	CV1842649	single nucleotide variant	NM_006888.6(CALM1):c.18C>G (p.Thr6=)	Cardiovascular phenotype [RCV002408220]	likely benign	14	90400079	90400079	Human		name
405024494	CV3085057	single nucleotide variant	NM_006888.6(CALM1):c.27G>A (p.Gln9=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003795923]	likely benign	14	90400088	90400088	Human	1	name
12839109	CV374404	single nucleotide variant	NM_006888.6(CALM1):c.18C>T (p.Thr6=)	Cardiovascular phenotype [RCV002411409]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001495669]\|not provided [RCV000868494]	likely benign	14	90400079	90400079	Human	2	name
12900931	CV409168	deletion	NM_006888.6(CALM1):c.421+7_421+10del	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002063819]\|not specified [RCV000483518]	likely benign	14	90404519	90404522	Human	1	name
127331634	CV1124061	single nucleotide variant	NM_006888.6(CALM1):c.90A>C (p.Thr30=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001471704]	likely benign	14	90401314	90401314	Human	1	name
150411543	CV1191624	deletion	NM_006888.6(CALM1):c.35-290_35-288del	not provided [RCV001566627]	likely benign	14	90400957	90400959	Human		name
150455032	CV1220396	deletion	NM_006888.6(CALM1):c.35-289_35-288del	not provided [RCV001612489]	benign	14	90400957	90400958	Human		name
152129435	CV1583895	single nucleotide variant	NM_006888.6(CALM1):c.87A>C (p.Thr29=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002199124]	likely benign	14	90401311	90401311	Human	1	name
9691247	CV171781	single nucleotide variant	NM_006888.6(CALM1):c.72C>T (p.Gly24=)	Cardiovascular phenotype [RCV000620499]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000652516]\|not provided [RCV000149485]	benign\|likely benign\|uncertain significance	14	90401296	90401296	Human	2	name
155704217	CV1810648	single nucleotide variant	NM_006888.6(CALM1):c.57A>G (p.Leu19=)	Cardiovascular phenotype [RCV002359837]	likely benign	14	90401281	90401281	Human		name
155713002	CV1824358	single nucleotide variant	NM_006888.6(CALM1):c.84C>T (p.Ile28=)	Cardiovascular phenotype [RCV002447708]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003103511]	likely benign	14	90401308	90401308	Human	2	name
597850280	CV3876946	deletion	NM_006888.6(CALM1):c.422-16_422-12del	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005228174]	likely benign	14	90404669	90404673	Human	1	name
13484048	CV464413	single nucleotide variant	NM_006888.6(CALM1):c.69T>C (p.Asp23=)	Cardiovascular phenotype [RCV000621045]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000530152]	likely benign	14	90401293	90401293	Human	2	name
13500500	CV464415	single nucleotide variant	NM_006888.6(CALM1):c.78C>T (p.Gly26=)	Cardiovascular phenotype [RCV004609437]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000540449]	likely benign\|uncertain significance	14	90401302	90401302	Human	2	name
127297488	CV1124062	single nucleotide variant	NM_006888.6(CALM1):c.267A>G (p.Ala89=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001460258]	likely benign	14	90403950	90403950	Human	1	name
152129212	CV1549218	single nucleotide variant	NM_006888.6(CALM1):c.225A>G (p.Arg75=)	Cardiovascular phenotype [RCV002443211]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002099254]\|not provided [RCV004704772]	likely benign	14	90403908	90403908	Human	2	name
152068889	CV1571315	single nucleotide variant	NM_006888.6(CALM1):c.108C>T (p.Val36=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002129339]	likely benign	14	90401332	90401332	Human	1	name
152037068	CV1605506	single nucleotide variant	NM_006888.6(CALM1):c.183T>C (p.Asn61=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002087395]	likely benign	14	90403866	90403866	Human	1	name
152130390	CV1630956	single nucleotide variant	NM_006888.6(CALM1):c.118C>T (p.Leu40=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002119011]	likely benign	14	90401342	90401342	Human	1	name
155746191	CV1838998	single nucleotide variant	NM_006888.6(CALM1):c.186C>T (p.Gly62=)	Cardiovascular phenotype [RCV002415069]	likely benign	14	90403869	90403869	Human		name
156405236	CV1893708	single nucleotide variant	NM_006888.6(CALM1):c.234A>G (p.Lys78=)	Cardiovascular phenotype [RCV004071882]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003069959]	likely benign	14	90403917	90403917	Human	2	name
156393582	CV1934021	single nucleotide variant	NM_006888.6(CALM1):c.198C>T (p.Phe66=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002654637]	likely benign	14	90403881	90403881	Human	1	name
155937648	CV2045984	single nucleotide variant	NM_006888.6(CALM1):c.213T>C (p.Thr71=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002751570]	likely benign	14	90403896	90403896	Human	1	name
401861938	CV2760273	single nucleotide variant	NM_006888.6(CALM1):c.264G>A (p.Glu88=)	Cardiovascular phenotype [RCV003358233]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003777452]	likely benign	14	90403947	90403947	Human	2	name
405009503	CV3083254	single nucleotide variant	NM_006888.6(CALM1):c.150G>A (p.Gln50=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003784201]	likely benign	14	90401374	90401374	Human	1	name
404988579	CV3084005	single nucleotide variant	NM_006888.6(CALM1):c.237T>C (p.Asp79=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003782197]	likely benign	14	90403920	90403920	Human	1	name
597834030	CV3864205	single nucleotide variant	NM_006888.6(CALM1):c.243T>C (p.Asp81=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005209841]	likely benign	14	90403926	90403926	Human	1	name
597837582	CV3866829	single nucleotide variant	NM_006888.6(CALM1):c.258C>A (p.Ile86=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005225820]	likely benign	14	90403941	90403941	Human	1	name
597862897	CV3875292	single nucleotide variant	NM_006888.6(CALM1):c.240A>G (p.Thr80=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005214469]	likely benign	14	90403923	90403923	Human	1	name
13624655	CV528408	single nucleotide variant	NM_006888.6(CALM1):c.273A>G (p.Arg91=)	Cardiovascular phenotype [RCV004025870]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000652519]	likely benign	14	90403956	90403956	Human	2	name
15145530	CV714260	single nucleotide variant	NM_006888.6(CALM1):c.201C>T (p.Pro67=)	Cardiovascular phenotype [RCV003169484]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002547295]	likely benign	14	90403884	90403884	Human	2	name
127296883	CV1124063	single nucleotide variant	NM_006888.6(CALM1):c.426C>T (p.Phe142=)	Cardiovascular phenotype [RCV004038514]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001452878]	likely benign	14	90404693	90404693	Human	2	name
150501056	CV1256218	deletion	NM_006888.6(CALM1):c.178+266_178+269del	not provided [RCV001676842]	benign	14	90401655	90401658	Human		name
151771377	CV1380357	single nucleotide variant	NM_006888.6(CALM1):c.402C>T (p.Asp134=)	Cardiovascular phenotype [RCV004990531]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002025391]	likely benign	14	90404495	90404495	Human	2	name
152135984	CV1624707	single nucleotide variant	NM_006888.6(CALM1):c.417T>C (p.Tyr139=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002177423]	likely benign	14	90404510	90404510	Human	1	name
152072335	CV1643730	single nucleotide variant	NM_006888.6(CALM1):c.390T>C (p.Asp130=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002111625]	likely benign	14	90404483	90404483	Human	1	name
155672759	CV1801140	single nucleotide variant	NM_006888.6(CALM1):c.62A>G (p.Asp21Gly)	Cardiovascular phenotype [RCV002368771]	uncertain significance	14	90401286	90401286	Human		name
156029889	CV2121140	single nucleotide variant	NM_006888.6(CALM1):c.70G>A (p.Gly24Ser)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002923465]	uncertain significance	14	90401294	90401294	Human	1	name
329365427	CV2433472	single nucleotide variant	NM_006888.6(CALM1):c.414C>T (p.Asn138=)	Cardiovascular phenotype [RCV003182229]	likely benign	14	90404507	90404507	Human		name
401797145	CV2741976	single nucleotide variant	NM_006888.6(CALM1):c.309A>T (p.Ala103=)	not specified [RCV003324152]	likely benign	14	90404402	90404402	Human		name
405021672	CV3088114	single nucleotide variant	NM_006888.6(CALM1):c.327C>T (p.Val109=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003795674]	likely benign	14	90404420	90404420	Human	1	name
405012850	CV3093508	single nucleotide variant	NM_006888.6(CALM1):c.336C>T (p.Asn112=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003784512]	likely benign	14	90404429	90404429	Human	1	name
405854222	CV3393836	single nucleotide variant	NM_006888.6(CALM1):c.318A>G (p.Leu106=)	not provided [RCV004547062]	likely benign	14	90404411	90404411	Human		name
596926625	CV3530855	single nucleotide variant	NM_006888.6(CALM1):c.28A>G (p.Ile10Val)	not provided [RCV004778440]	uncertain significance	14	90400089	90400089	Human		name
12849518	CV373937	single nucleotide variant	NM_006888.6(CALM1):c.88A>C (p.Thr30Pro)	not provided [RCV000431318]	likely pathogenic	14	90401312	90401312	Human		name
12845577	CV373940	single nucleotide variant	NM_006888.6(CALM1):c.324C>T (p.His108=)	CALM1-related disorder [RCV003959980]\|Cardiovascular phenotype [RCV000621603]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000556220]\|not provided [RCV001698289]	likely benign	14	90404417	90404417	Human	2	name , trait , alternate_id
597924371	CV3877281	single nucleotide variant	NM_006888.6(CALM1):c.411C>A (p.Val137=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005223977]	likely benign	14	90404504	90404504	Human	1	name
597913341	CV3879977	single nucleotide variant	NM_006888.6(CALM1):c.405A>G (p.Gly135=)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005222216]	likely benign	14	90404498	90404498	Human	1	name
12901112	CV409166	single nucleotide variant	NM_006888.6(CALM1):c.67G>T (p.Asp23Tyr)	not provided [RCV000483941]	uncertain significance	14	90401291	90401291	Human		name
13501833	CV464422	single nucleotide variant	NM_006888.6(CALM1):c.303C>T (p.Ile101=)	CALM1-related disorder [RCV003945313]\|Cardiovascular phenotype [RCV000618235]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000541358]\|not provided [RCV000615644]\|not specified [RCV001700161]	benign\|likely benign	14	90404396	90404396	Human	2	name , trait , alternate_id
13624656	CV528802	single nucleotide variant	NM_006888.6(CALM1):c.411C>G (p.Val137=)	Cardiovascular phenotype [RCV002325311]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000652520]	likely benign	14	90404504	90404504	Human	2	name
152080284	CV1666931	single nucleotide variant	NM_006888.6(CALM1):c.287A>G (p.Asp96Gly)	not provided [RCV002211276]	uncertain significance	14	90404380	90404380	Human		name
9834938	CV181365	single nucleotide variant	NM_006888.6(CALM1):c.268T>C (p.Phe90Leu)	Long QT syndrome 14 [RCV000162064]	pathogenic\|likely pathogenic	14	90403951	90403951	Human	1	name
155671665	CV1845907	single nucleotide variant	NM_006888.6(CALM1):c.260G>A (p.Arg87His)	Cardiovascular phenotype [RCV002437171]\|not provided [RCV004812451]	uncertain significance	14	90403943	90403943	Human		name
156172819	CV1867156	single nucleotide variant	NM_006888.6(CALM1):c.210G>T (p.Leu70Phe)	not provided [RCV002508709]	uncertain significance	14	90403893	90403893	Human		name
156240338	CV2154857	single nucleotide variant	NM_006888.6(CALM1):c.286G>T (p.Asp96Tyr)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003025983]	pathogenic	14	90404379	90404379	Human	1	name
408387167	CV3524428	single nucleotide variant	NM_006888.6(CALM1):c.275T>C (p.Val92Ala)	not provided [RCV004768302]	uncertain significance	14	90403958	90403958	Human		name
597835099	CV3864407	single nucleotide variant	NM_006888.6(CALM1):c.154A>G (p.Met52Val)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005210043]	uncertain significance	14	90401378	90401378	Human	1	name
597909149	CV3867147	single nucleotide variant	NM_006888.6(CALM1):c.293A>T (p.Asn98Ile)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005221612]	uncertain significance	14	90404386	90404386	Human	1	name
597906881	CV3870250	single nucleotide variant	NM_006888.6(CALM1):c.199C>T (p.Pro67Ser)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005221301]	uncertain significance	14	90403882	90403882	Human	1	name
597886943	CV3876440	indel	NM_006888.6(CALM1):c.35-12_35-11delinsCC	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005218186]	uncertain significance	14	90401247	90401248	Human		name
617148327	CV4018691	single nucleotide variant	NM_006888.6(CALM1):c.133A>G (p.Thr45Ala)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV005420482]	uncertain significance	14	90401357	90401357	Human	1	name
617150663	CV4018868	single nucleotide variant	NM_006888.6(CALM1):c.172G>A (p.Ala58Thr)	not provided [RCV005423276]	uncertain significance	14	90401396	90401396	Human		name
617150752	CV4019220	single nucleotide variant	NM_006888.6(CALM1):c.272G>A (p.Arg91Gln)	not provided [RCV005423628]	uncertain significance	14	90403955	90403955	Human		name
13474032	CV464421	single nucleotide variant	NM_006888.6(CALM1):c.157A>G (p.Ile53Val)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000548067]	uncertain significance	14	90401381	90401381	Human	1	name
8604349	CV48356	single nucleotide variant	NM_006888.6(CALM1):c.161A>T (p.Asn54Ile)	Catecholaminergic polymorphic ventricular tachycardia 1 [RCV000157133]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000032976]	pathogenic\|likely pathogenic	14	90401385	90401385	Human	2	name
8604350	CV48357	single nucleotide variant	NM_006888.6(CALM1):c.293A>G (p.Asn98Ser)	CALM1-related disorder [RCV004758616]\|Cardiovascular phenotype [RCV002433484]\|Catecholaminergic polymorphic ventricular tachycardia 1 [RCV000157134]\|Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000032977]\|Catecholaminergic polymorphic ventricular ... (more) tachycardia 4 [RCV000526484]\|Catecholaminergic polymorphic ventricular tachycardia [RCV000714909]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity	14	90404386	90404386	Human	5	name , trait , alternate_id
26896677	CV841903	single nucleotide variant	NM_006888.6(CALM1):c.106G>C (p.Val36Leu)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001048231]	uncertain significance	14	90401330	90401330	Human	1	name
38477942	CV927193	single nucleotide variant	NM_006888.6(CALM1):c.280G>C (p.Asp94His)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001216383]	uncertain significance	14	90403963	90403963	Human	1	name
151661750	CV1329981	single nucleotide variant	NM_006888.6(CALM1):c.319C>T (p.Arg107Cys)	not provided [RCV001823392]	uncertain significance	14	90404412	90404412	Human		name
151827077	CV1396302	single nucleotide variant	NM_006888.6(CALM1):c.395A>G (p.Asp132Gly)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001934687]	pathogenic	14	90404488	90404488	Human	1	name
151842278	CV1438335	single nucleotide variant	NM_006888.6(CALM1):c.328A>C (p.Met110Leu)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001921674]	uncertain significance	14	90404421	90404421	Human	1	name
152038111	CV1669223	single nucleotide variant	NM_006888.6(CALM1):c.322C>G (p.His108Asp)	not provided [RCV002224275]	uncertain significance	14	90404415	90404415	Human		name
155714351	CV1760341	single nucleotide variant	NM_006888.6(CALM1):c.299A>G (p.Tyr100Cys)	not provided [RCV002300847]	uncertain significance	14	90404392	90404392	Human		name
155695264	CV1771999	single nucleotide variant	NM_006888.6(CALM1):c.358G>A (p.Glu120Lys)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV002299569]	uncertain significance	14	90404451	90404451	Human	1	name
9834936	CV181363	single nucleotide variant	NM_006888.6(CALM1):c.389A>G (p.Asp130Gly)	Long QT syndrome 14 [RCV000162062]\|not provided [RCV001781506]	pathogenic\|likely pathogenic	14	90404482	90404482	Human	1	name
9834937	CV181364	single nucleotide variant	NM_006888.6(CALM1):c.426C>G (p.Phe142Leu)	Long QT syndrome 14 [RCV000162063]	pathogenic	14	90404693	90404693	Human	1	name
156160946	CV2191825	single nucleotide variant	NM_006888.6(CALM1):c.402C>G (p.Asp134Glu)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003040707]	uncertain significance	14	90404495	90404495	Human	1	name
401899378	CV2793819	single nucleotide variant	NM_006888.6(CALM1):c.392T>C (p.Ile131Thr)	Cardiovascular phenotype [RCV003377564]	uncertain significance	14	90404485	90404485	Human		name
405107434	CV3113802	single nucleotide variant	NM_006888.6(CALM1):c.398G>C (p.Gly133Ala)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV003812925]	uncertain significance	14	90404491	90404491	Human	1	name
408391870	CV3496998	single nucleotide variant	NM_006888.6(CALM1):c.398G>T (p.Gly133Val)	Long QT syndrome [RCV004775600]	likely pathogenic	14	90404491	90404491	Human	2	name
408385582	CV3520246	single nucleotide variant	NM_006888.6(CALM1):c.419A>C (p.Glu140Ala)	not provided [RCV004760067]	uncertain significance	14	90404512	90404512	Human		name
408391280	CV3523133	single nucleotide variant	NM_006888.6(CALM1):c.382G>C (p.Glu128Gln)	not provided [RCV004770505]	uncertain significance	14	90404475	90404475	Human		name
12850196	CV373939	single nucleotide variant	NM_006888.6(CALM1):c.313G>A (p.Glu105Lys)	not provided [RCV000442999]	likely pathogenic	14	90404406	90404406	Human		name
12894617	CV409167	single nucleotide variant	NM_006888.6(CALM1):c.419A>T (p.Glu140Val)	not provided [RCV000483471]	likely pathogenic	14	90404512	90404512	Human		name
12906702	CV415407	single nucleotide variant	NM_006888.6(CALM1):c.424T>C (p.Phe142Leu)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001856891]\|not provided [RCV000489543]	pathogenic\|likely pathogenic	14	90404691	90404691	Human	1	name
13624653	CV528327	single nucleotide variant	NM_006888.6(CALM1):c.398G>A (p.Gly133Glu)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000652517]	likely pathogenic	14	90404491	90404491	Human	1	name
14723777	CV642780	single nucleotide variant	NM_006888.6(CALM1):c.301A>G (p.Ile101Val)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000798107]	uncertain significance	14	90404394	90404394	Human	1	name
14709203	CV642781	single nucleotide variant	NM_006888.6(CALM1):c.394G>A (p.Asp132Asn)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV000792817]	pathogenic	14	90404487	90404487	Human	1	name
38484491	CV927194	single nucleotide variant	NM_006888.6(CALM1):c.395A>T (p.Asp132Val)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001219455]	pathogenic	14	90404488	90404488	Human	1	name
38482030	CV948723	single nucleotide variant	NM_006888.6(CALM1):c.426C>A (p.Phe142Leu)	Catecholaminergic polymorphic ventricular tachycardia 4 [RCV001235389]	pathogenic	14	90404693	90404693	Human	1	name
38457614	CV962908	single nucleotide variant	NM_006888.6(CALM1):c.422A>G (p.Glu141Gly)	Long QT syndrome 14 [RCV001250791]	pathogenic	14	90404689	90404689	Human	1	name
38457822	CV962909	single nucleotide variant	NM_006888.6(CALM1):c.422A>T (p.Glu141Val)	Long QT syndrome 14 [RCV001250792]	pathogenic	14	90404689	90404689	Human	1	name
150528264	CV1301787	deletion	NM_006888.6(CALM1):c.144_146del (p.Leu49del)	not provided [RCV001755159]	uncertain significance	14	90401368	90401370	Human		name

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