Smoc2 Variant Search Result - Rat Genome Database

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145 records found for search term Smoc2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150492466	CV1225479	single nucleotide variant	NM_001166412.2(SMOC2):c.-37A>G	not provided [RCV001618994]	benign	6	168441334	168441334	Human		name
150460174	CV1264132	single nucleotide variant	NM_001166412.2(SMOC2):c.-104C>T	not provided [RCV001682047]	benign	6	168441267	168441267	Human		name
8581736	CV116181	single nucleotide variant	NM_022138.2(SMOC2):c.1043+728G>A	Lung cancer [RCV000096704]	uncertain significance	6	168651511	168651511	Human		name
151661770	CV1330001	deletion	NM_001166412.2(SMOC2):c.825-9del	not provided [RCV001823412]	benign	6	168608143	168608143	Human		name
156296255	CV1924131	single nucleotide variant	NM_001166412.2(SMOC2):c.824+4A>G	not provided [RCV002629028]	uncertain significance	6	168599008	168599008	Human		name
156237753	CV2047060	single nucleotide variant	NM_001166412.2(SMOC2):c.511+7A>G	not provided [RCV002805560]	likely benign	6	168543679	168543679	Human		name
156090668	CV2109977	single nucleotide variant	NM_001166412.2(SMOC2):c.824+3A>G	not provided [RCV002952345]	likely benign	6	168599007	168599007	Human		name
402504874	CV2879870	single nucleotide variant	NM_001166412.2(SMOC2):c.825-6C>G	not provided [RCV003546161]	likely benign	6	168608151	168608151	Human		name
405034144	CV3130444	single nucleotide variant	NM_001166412.2(SMOC2):c.363+7G>A	not provided [RCV003830851]	likely benign	6	168526459	168526459	Human		name
597850930	CV3761790	single nucleotide variant	NM_001166412.2(SMOC2):c.85-17T>C	not provided [RCV005087886]	benign	6	168509898	168509898	Human		name
8581734	CV116179	single nucleotide variant	NM_022138.2(SMOC2):c.670+20848C>G	Lung cancer [RCV000096702]	uncertain significance	6	168570051	168570051	Human		name
8581735	CV116180	single nucleotide variant	NM_022138.2(SMOC2):c.940+20471C>T	Lung cancer [RCV000096703]	uncertain significance	6	168628710	168628710	Human		name
150502652	CV1212286	single nucleotide variant	NM_001166412.2(SMOC2):c.363+81G>A	not provided [RCV001595160]	benign	6	168526533	168526533	Human		name
150434697	CV1231156	single nucleotide variant	NM_001166412.2(SMOC2):c.364-83G>A	not provided [RCV001643800]	benign	6	168527545	168527545	Human		name
150471587	CV1270106	single nucleotide variant	NM_001166412.2(SMOC2):c.85-152C>G	not provided [RCV001695394]	benign	6	168509763	168509763	Human		name
150451475	CV1276601	single nucleotide variant	NM_001166412.2(SMOC2):c.364-57C>T	not provided [RCV001708390]	benign	6	168527571	168527571	Human		name
156046234	CV1868730	single nucleotide variant	NM_001166412.2(SMOC2):c.512-30C>T	not provided [RCV003052836]	uncertain significance	6	168547089	168547089	Human		name
155955372	CV2040096	duplication	NM_001166412.2(SMOC2):c.824+26dup	not provided [RCV002775992]	benign	6	168599022	168599023	Human		name
156242049	CV2043749	duplication	NM_001166412.2(SMOC2):c.1286-9dup	not provided [RCV002805712]	benign	6	168664055	168664056	Human		name
405125172	CV2889529	single nucleotide variant	NM_001166412.2(SMOC2):c.512-14C>T	not provided [RCV003559420]	likely benign	6	168547105	168547105	Human		name
405126702	CV3132816	deletion	NM_001166412.2(SMOC2):c.1286-9del	not provided [RCV003837979]	benign	6	168664056	168664056	Human		name
404991129	CV3176280	single nucleotide variant	NM_001166412.2(SMOC2):c.364-11C>T	not provided [RCV003881605]	benign	6	168527617	168527617	Human		name
405712588	CV3329806	single nucleotide variant	NM_001166412.2(SMOC2):c.512-13G>A	not specified [RCV004462007]	uncertain significance	6	168547106	168547106	Human		name
597838179	CV3740291	deletion	NM_001166412.2(SMOC2):c.824+26del	not provided [RCV005064319]	likely benign	6	168599023	168599023	Human		name
150503436	CV1212482	single nucleotide variant	NM_001166412.2(SMOC2):c.908-195A>G	not provided [RCV001595357]	benign	6	168650486	168650486	Human		name
150438821	CV1221218	single nucleotide variant	NM_001166412.2(SMOC2):c.562+206G>A	not provided [RCV001609912]	benign	6	168547375	168547375	Human		name
150458851	CV1235996	single nucleotide variant	NM_001166412.2(SMOC2):c.562+237C>G	not provided [RCV001648967]	benign	6	168547406	168547406	Human		name
150481432	CV1243309	single nucleotide variant	NM_001166412.2(SMOC2):c.363+317T>C	not provided [RCV001652945]	benign	6	168526769	168526769	Human		name
150440271	CV1247835	single nucleotide variant	NM_001166412.2(SMOC2):c.562+107G>C	not provided [RCV001666202]	benign	6	168547276	168547276	Human		name
150458373	CV1248923	single nucleotide variant	NM_001166412.2(SMOC2):c.256+254T>A	not provided [RCV001669099]	benign	6	168510340	168510340	Human		name
150463211	CV1263773	single nucleotide variant	NM_001166412.2(SMOC2):c.463+112C>T	not provided [RCV001682474]	benign	6	168527839	168527839	Human		name
150466161	CV1268728	single nucleotide variant	NM_001166412.2(SMOC2):c.257-241G>A	not provided [RCV001694424]	benign	6	168526105	168526105	Human		name
150457071	CV1269160	single nucleotide variant	NM_001166412.2(SMOC2):c.908-210G>A	not provided [RCV001692984]	benign	6	168650471	168650471	Human		name
150477263	CV1272021	single nucleotide variant	NM_001166412.2(SMOC2):c.512-261T>C	not provided [RCV001696306]	benign	6	168546858	168546858	Human		name
150467776	CV1277630	single nucleotide variant	NM_001166412.2(SMOC2):c.562+238G>C	not provided [RCV001710925]	benign	6	168547407	168547407	Human		name
156132301	CV2037531	single nucleotide variant	NM_001166412.2(SMOC2):c.1285+20C>T	not provided [RCV002800659]	benign	6	168653248	168653248	Human		name
405011452	CV3128062	single nucleotide variant	NM_001166412.2(SMOC2):c.1010+13C>T	not provided [RCV003828942]	likely benign	6	168650796	168650796	Human		name
150441439	CV1265783	single nucleotide variant	NM_001166412.2(SMOC2):c.1285+139C>T	not provided [RCV001690508]	benign	6	168653367	168653367	Human		name
150464865	CV1277142	single nucleotide variant	NM_001166412.2(SMOC2):c.1323+142T>C	not provided [RCV001710436]	benign	6	168664253	168664253	Human		name
405114308	CV3115417	microsatellite	NM_001166412.2(SMOC2):c.638-17CTT[2]	SMOC2-related disorder [RCV003929356]\|not provided [RCV003814099]	likely benign	6	168598801	168598803	Human		name , trait , alternate_id
150437129	CV1249819	single nucleotide variant	NM_001166412.2(SMOC2):c.63T>G (p.Ala21=)	not provided [RCV001665733]	benign	6	168441433	168441433	Human		name
155906545	CV2130813	single nucleotide variant	NM_001166412.2(SMOC2):c.60C>G (p.Pro20=)	SMOC2-related disorder [RCV003963525]\|not provided [RCV002967746]	likely benign	6	168441430	168441430	Human	1	name , trait , alternate_id
405087269	CV2862358	single nucleotide variant	NM_001166412.2(SMOC2):c.57G>T (p.Val19=)	not provided [RCV003549651]	likely benign	6	168441427	168441427	Human		name
597929928	CV3789226	single nucleotide variant	NM_001166412.2(SMOC2):c.99T>C (p.Asp33=)	not provided [RCV005131507]	benign	6	168509929	168509929	Human		name
156354556	CV1920926	single nucleotide variant	NM_001166412.2(SMOC2):c.243A>G (p.Arg81=)	not provided [RCV002632230]	likely benign	6	168510073	168510073	Human		name
155923757	CV2099447	single nucleotide variant	NM_001166412.2(SMOC2):c.285G>A (p.Lys95=)	not provided [RCV002903471]	benign	6	168526374	168526374	Human		name
405076966	CV3031717	single nucleotide variant	NM_001166412.2(SMOC2):c.13C>T (p.Gln5Ter)	not provided [RCV003698656]	pathogenic	6	168441383	168441383	Human		name
597905190	CV3784796	single nucleotide variant	NM_001166412.2(SMOC2):c.141G>A (p.Ser47=)	not provided [RCV005127847]	likely benign	6	168509971	168509971	Human		name
8631919	CV87125	single nucleotide variant	NM_022138.2(SMOC2):c.375C>G (p.His125Gln)	Malignant melanoma [RCV000067216]	not provided	6	168527639	168527639	Human		name
155927267	CV1912157	single nucleotide variant	NM_001166412.2(SMOC2):c.729C>T (p.Gly243=)	not provided [RCV002614825]	likely benign	6	168598909	168598909	Human		name
156417343	CV1913365	single nucleotide variant	NM_001166412.2(SMOC2):c.435C>T (p.Ala145=)	not provided [RCV002610666]	likely benign	6	168527699	168527699	Human		name
156302481	CV1998514	single nucleotide variant	NM_001166412.2(SMOC2):c.348C>T (p.Asp116=)	not provided [RCV002671224]	likely benign	6	168526437	168526437	Human		name
155977374	CV2100160	single nucleotide variant	NM_001166412.2(SMOC2):c.810C>T (p.Pro270=)	not provided [RCV002881767]	benign	6	168598990	168598990	Human		name
155990724	CV2116159	single nucleotide variant	NM_001166412.2(SMOC2):c.870C>T (p.Ala290=)	not provided [RCV002947318]	benign	6	168608202	168608202	Human		name
401745687	CV2693329	single nucleotide variant	NM_001166412.2(SMOC2):c.77C>T (p.Ala26Val)	not specified [RCV004295292]	uncertain significance	6	168441447	168441447	Human		name
401889685	CV2766829	single nucleotide variant	NM_001166412.2(SMOC2):c.52C>G (p.Pro18Ala)	not specified [RCV004349214]	uncertain significance	6	168441422	168441422	Human		name
405278019	CV3221686	single nucleotide variant	NM_001166412.2(SMOC2):c.582T>A (p.Pro194=)	SMOC2-related disorder [RCV003976290]	likely benign	6	168549148	168549148	Human		name , trait , alternate_id
597727211	CV3597220	single nucleotide variant	NM_001166412.2(SMOC2):c.62C>A (p.Ala21Asp)	not specified [RCV004862656]	uncertain significance	6	168441432	168441432	Human		name
597831497	CV3759770	single nucleotide variant	NM_001166412.2(SMOC2):c.531G>A (p.Ala177=)	not provided [RCV005084708]	likely benign	6	168547138	168547138	Human		name
597925400	CV3840547	single nucleotide variant	NM_001166412.2(SMOC2):c.468C>T (p.Ser156=)	not provided [RCV005185018]	likely benign	6	168543629	168543629	Human		name
598238213	CV3915176	single nucleotide variant	NM_001166412.2(SMOC2):c.72C>G (p.Phe24Leu)	not specified [RCV005275796]	uncertain significance	6	168441442	168441442	Human		name
15199086	CV721882	single nucleotide variant	NM_001166412.2(SMOC2):c.966G>A (p.Thr322=)	not provided [RCV000890536]	benign\|likely benign	6	168650739	168650739	Human		name
15122541	CV782493	single nucleotide variant	NM_001166412.2(SMOC2):c.357C>T (p.Tyr119=)	not provided [RCV000979663]	likely benign	6	168526446	168526446	Human		name
8631920	CV87126	single nucleotide variant	NM_022138.2(SMOC2):c.1057G>A (p.Asp353Asn)	Malignant melanoma [RCV000067217]	not provided	6	168652967	168652967	Human		name
156373417	CV1953519	single nucleotide variant	NM_001166412.2(SMOC2):c.187C>T (p.Arg63Cys)	not provided [RCV002582605]	uncertain significance	6	168510017	168510017	Human		name
156309459	CV2111191	single nucleotide variant	NM_001166412.2(SMOC2):c.1242C>T (p.Gly414=)	not provided [RCV002937080]	benign	6	168653185	168653185	Human		name
156331265	CV2112676	single nucleotide variant	NM_001166412.2(SMOC2):c.134C>T (p.Ala45Val)	not provided [RCV002938380]	uncertain significance	6	168509964	168509964	Human		name
156084574	CV2249272	single nucleotide variant	NM_001166412.2(SMOC2):c.233T>C (p.Ile78Thr)	not specified [RCV004118302]	uncertain significance	6	168510063	168510063	Human		name
156188532	CV2375369	single nucleotide variant	NM_001166412.2(SMOC2):c.136G>A (p.Gly46Ser)	not specified [RCV004232769]	uncertain significance	6	168509966	168509966	Human		name
329382478	CV2424481	single nucleotide variant	NM_001166412.2(SMOC2):c.140C>T (p.Ser47Leu)	not specified [RCV004252370]	uncertain significance	6	168509970	168509970	Human		name
401741509	CV2680423	single nucleotide variant	NM_001166412.2(SMOC2):c.242G>A (p.Arg81Gln)	not specified [RCV004288663]	uncertain significance	6	168510072	168510072	Human		name
405259216	CV3215293	single nucleotide variant	NM_001166412.2(SMOC2):c.1053G>A (p.Val351=)	SMOC2-related disorder [RCV003942326]	likely benign	6	168652996	168652996	Human		name , trait , alternate_id
405712560	CV3329802	single nucleotide variant	NM_001166412.2(SMOC2):c.203G>A (p.Arg68His)	not specified [RCV004462003]	uncertain significance	6	168510033	168510033	Human		name
407503259	CV3474451	single nucleotide variant	NM_001166412.2(SMOC2):c.296A>G (p.Glu99Gly)	not specified [RCV004670191]	uncertain significance	6	168526385	168526385	Human		name
407452464	CV3474453	single nucleotide variant	NM_001166412.2(SMOC2):c.152C>T (p.Pro51Leu)	not specified [RCV004684057]	uncertain significance	6	168509982	168509982	Human		name
407452466	CV3474455	single nucleotide variant	NM_001166412.2(SMOC2):c.254A>C (p.Lys85Thr)	not specified [RCV004684058]	uncertain significance	6	168510084	168510084	Human		name
597962892	CV3795858	single nucleotide variant	NM_001166412.2(SMOC2):c.1002G>A (p.Ser334=)	not provided [RCV005139348]	benign	6	168650775	168650775	Human		name
598170287	CV3915168	single nucleotide variant	NM_001166412.2(SMOC2):c.133G>A (p.Ala45Thr)	not specified [RCV005284556]	uncertain significance	6	168509963	168509963	Human		name
13212345	CV425681	single nucleotide variant	NM_001166412.2(SMOC2):c.269G>A (p.Cys90Tyr)	not provided [RCV000498688]	uncertain significance	6	168526358	168526358	Human		name
15197361	CV699453	single nucleotide variant	NM_001166412.2(SMOC2):c.1155C>T (p.Pro385=)	not provided [RCV000956444]	benign	6	168653098	168653098	Human		name
15151270	CV710332	single nucleotide variant	NM_001166412.2(SMOC2):c.1092T>C (p.Ser364=)	not provided [RCV000968104]	benign	6	168653035	168653035	Human		name
126737071	CV1016691	single nucleotide variant	NM_001166412.2(SMOC2):c.400G>A (p.Val134Ile)	Dentin dysplasia type I [RCV001328672]\|not specified [RCV005278826]	uncertain significance	6	168527664	168527664	Human	1	name
150457248	CV1278601	deletion	NM_001166412.2(SMOC2):c.1323+291_1323+305del	not provided [RCV001709216]	benign	6	168664385	168664399	Human		name
152977970	CV1671331	single nucleotide variant	NM_001166412.2(SMOC2):c.842G>A (p.Cys281Tyr)	Dentin dysplasia type I [RCV002227005]	uncertain significance	6	168608174	168608174	Human	1	name
156025150	CV2112400	single nucleotide variant	NM_001166412.2(SMOC2):c.544C>G (p.Pro182Ala)	not provided [RCV002909802]\|not specified [RCV004067040]	uncertain significance	6	168547151	168547151	Human		name
156062808	CV2199789	single nucleotide variant	NM_001166412.2(SMOC2):c.449C>T (p.Thr150Met)	not specified [RCV004073992]	uncertain significance	6	168527713	168527713	Human		name
155914514	CV2242745	single nucleotide variant	NM_001166412.2(SMOC2):c.520G>A (p.Ala174Thr)	not specified [RCV004113775]	uncertain significance	6	168547127	168547127	Human		name
156317139	CV2251007	single nucleotide variant	NM_001166412.2(SMOC2):c.832C>A (p.Gln278Lys)	not specified [RCV004123574]	uncertain significance	6	168608164	168608164	Human		name
401780841	CV2681786	single nucleotide variant	NM_001166412.2(SMOC2):c.304C>T (p.Arg102Trp)	not specified [RCV004296789]	uncertain significance	6	168526393	168526393	Human		name
401737595	CV2695841	single nucleotide variant	NM_001166412.2(SMOC2):c.328A>T (p.Ile110Phe)	not specified [RCV004308123]	uncertain significance	6	168526417	168526417	Human		name
401765154	CV2733519	single nucleotide variant	NM_001166412.2(SMOC2):c.865C>T (p.Pro289Ser)	not specified [RCV004330416]	uncertain significance	6	168608197	168608197	Human		name
401893392	CV2756515	single nucleotide variant	NM_001166412.2(SMOC2):c.797G>A (p.Gly266Glu)	not specified [RCV004345046]	uncertain significance	6	168598977	168598977	Human		name
401896146	CV2773666	single nucleotide variant	NM_001166412.2(SMOC2):c.994T>C (p.Ser332Pro)	not specified [RCV004356353]	uncertain significance	6	168650767	168650767	Human		name
401898172	CV2781029	single nucleotide variant	NM_001166412.2(SMOC2):c.341A>G (p.Asn114Ser)	not specified [RCV004354552]	uncertain significance	6	168526430	168526430	Human		name
401882830	CV2788611	single nucleotide variant	NM_001166412.2(SMOC2):c.592A>G (p.Thr198Ala)	not specified [RCV004361104]	uncertain significance	6	168549158	168549158	Human		name
405712534	CV3329798	single nucleotide variant	NM_001166412.2(SMOC2):c.967G>A (p.Asp323Asn)	not specified [RCV004461999]	uncertain significance	6	168650740	168650740	Human		name
405712565	CV3329803	single nucleotide variant	NM_001166412.2(SMOC2):c.302C>T (p.Ala101Val)	not specified [RCV004462004]	uncertain significance	6	168526391	168526391	Human		name
405712571	CV3329804	single nucleotide variant	NM_001166412.2(SMOC2):c.412G>A (p.Gly138Arg)	not specified [RCV004462005]	uncertain significance	6	168527676	168527676	Human		name
405712579	CV3329805	single nucleotide variant	NM_001166412.2(SMOC2):c.506A>G (p.Lys169Arg)	not specified [RCV004462006]	uncertain significance	6	168543667	168543667	Human		name
405712595	CV3329807	single nucleotide variant	NM_001166412.2(SMOC2):c.605A>G (p.Lys202Arg)	not specified [RCV004462008]	uncertain significance	6	168549171	168549171	Human		name
405712602	CV3329808	single nucleotide variant	NM_001166412.2(SMOC2):c.811G>C (p.Gly271Arg)	not specified [RCV004462009]	uncertain significance	6	168598991	168598991	Human		name
405712609	CV3329809	single nucleotide variant	NM_001166412.2(SMOC2):c.829G>C (p.Glu277Gln)	not specified [RCV004462010]	uncertain significance	6	168608161	168608161	Human		name
405712615	CV3329810	single nucleotide variant	NM_001166412.2(SMOC2):c.878G>A (p.Arg293Gln)	not specified [RCV004462011]	uncertain significance	6	168608210	168608210	Human		name
405712621	CV3329811	single nucleotide variant	NM_001166412.2(SMOC2):c.914C>T (p.Pro305Leu)	not specified [RCV004462012]	uncertain significance	6	168650687	168650687	Human		name
405712627	CV3329812	single nucleotide variant	NM_001166412.2(SMOC2):c.928C>G (p.His310Asp)	not specified [RCV004462013]	uncertain significance	6	168650701	168650701	Human		name
405712633	CV3329813	single nucleotide variant	NM_001166412.2(SMOC2):c.944G>A (p.Ser315Asn)	not specified [RCV004462014]	uncertain significance	6	168650717	168650717	Human		name
407452455	CV3474448	single nucleotide variant	NM_001166412.2(SMOC2):c.611G>A (p.Arg204Gln)	not specified [RCV004684053]	uncertain significance	6	168549177	168549177	Human		name
407452459	CV3474450	single nucleotide variant	NM_001166412.2(SMOC2):c.454C>T (p.Arg152Trp)	not specified [RCV004684055]	uncertain significance	6	168527718	168527718	Human		name
597744019	CV3597212	single nucleotide variant	NM_001166412.2(SMOC2):c.851C>T (p.Thr284Met)	not specified [RCV004865377]	uncertain significance	6	168608183	168608183	Human		name
597744029	CV3597214	single nucleotide variant	NM_001166412.2(SMOC2):c.421A>G (p.Ile141Val)	not specified [RCV004865379]	uncertain significance	6	168527685	168527685	Human		name
597744034	CV3597216	single nucleotide variant	NM_001166412.2(SMOC2):c.965C>T (p.Thr322Met)	not specified [RCV004865380]	uncertain significance	6	168650738	168650738	Human		name
597744038	CV3597217	single nucleotide variant	NM_001166412.2(SMOC2):c.461C>T (p.Pro154Leu)	not specified [RCV004865381]	uncertain significance	6	168527725	168527725	Human		name
597744042	CV3597218	single nucleotide variant	NM_001166412.2(SMOC2):c.982G>A (p.Ala328Thr)	not specified [RCV004865382]	uncertain significance	6	168650755	168650755	Human		name
597744047	CV3597219	single nucleotide variant	NM_001166412.2(SMOC2):c.820A>G (p.Thr274Ala)	not specified [RCV004865383]	uncertain significance	6	168599000	168599000	Human		name
597727220	CV3597221	single nucleotide variant	NM_001166412.2(SMOC2):c.905A>C (p.Gln302Pro)	not specified [RCV004862657]	uncertain significance	6	168608237	168608237	Human		name
597727230	CV3597222	single nucleotide variant	NM_001166412.2(SMOC2):c.722C>T (p.Ala241Val)	not specified [RCV004862658]	uncertain significance	6	168598902	168598902	Human		name
597727239	CV3597223	single nucleotide variant	NM_001166412.2(SMOC2):c.568G>A (p.Ala190Thr)	not specified [RCV004862659]	uncertain significance	6	168549134	168549134	Human		name
598170293	CV3915170	single nucleotide variant	NM_001166412.2(SMOC2):c.664T>A (p.Ser222Thr)	not specified [RCV005284558]	uncertain significance	6	168598844	168598844	Human		name
598170296	CV3915171	single nucleotide variant	NM_001166412.2(SMOC2):c.727G>A (p.Gly243Ser)	not specified [RCV005284559]	uncertain significance	6	168598907	168598907	Human		name
598170299	CV3915172	single nucleotide variant	NM_001166412.2(SMOC2):c.358A>C (p.Ser120Arg)	not specified [RCV005284560]	uncertain significance	6	168526447	168526447	Human		name
13211822	CV425682	deletion	NM_001166412.2(SMOC2):c.1122del (p.Phe375fs)	not provided [RCV000497956]	likely pathogenic	6	168653063	168653063	Human		name
15160001	CV721881	single nucleotide variant	NM_001166412.2(SMOC2):c.635C>T (p.Ser212Leu)	not provided [RCV000881300]\|not specified [RCV004857737]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	6	168549201	168549201	Human		name
156338164	CV2179523	single nucleotide variant	NM_001166412.2(SMOC2):c.1265C>T (p.Ala422Val)	not provided [RCV003030135]	benign	6	168653208	168653208	Human		name
156021035	CV2226626	single nucleotide variant	NM_001166412.2(SMOC2):c.1028C>T (p.Pro343Leu)	not specified [RCV004101873]	uncertain significance	6	168652971	168652971	Human		name
156083418	CV2298982	single nucleotide variant	NM_001166412.2(SMOC2):c.1086C>G (p.Asn362Lys)	not specified [RCV004158509]	uncertain significance	6	168653029	168653029	Human		name
405712541	CV3329799	single nucleotide variant	NM_001166412.2(SMOC2):c.1001C>T (p.Ser334Leu)	not specified [RCV004462000]	uncertain significance	6	168650774	168650774	Human		name
405712546	CV3329800	single nucleotide variant	NM_001166412.2(SMOC2):c.1199A>G (p.Asn400Ser)	not specified [RCV004462001]	uncertain significance	6	168653142	168653142	Human		name
405712554	CV3329801	single nucleotide variant	NM_001166412.2(SMOC2):c.1303G>A (p.Glu435Lys)	not specified [RCV004462002]	uncertain significance	6	168664091	168664091	Human		name
407503255	CV3474447	single nucleotide variant	NM_001166412.2(SMOC2):c.1048C>T (p.Arg350Trp)	not specified [RCV004670190]	uncertain significance	6	168652991	168652991	Human		name
407452461	CV3474452	single nucleotide variant	NM_001166412.2(SMOC2):c.1135C>T (p.Leu379Phe)	not specified [RCV004684056]	uncertain significance	6	168653078	168653078	Human		name
407503262	CV3474454	single nucleotide variant	NM_001166412.2(SMOC2):c.1060T>G (p.Trp354Gly)	not specified [RCV004670192]	uncertain significance	6	168653003	168653003	Human		name
597688607	CV3537577	single nucleotide variant	NM_001166412.2(SMOC2):c.1138C>T (p.Arg380Cys)	Dentin dysplasia type I [RCV005411262]\|not specified [RCV004867950]	uncertain significance	6	168653081	168653081	Human	1	name
597727201	CV3597215	single nucleotide variant	NM_001166412.2(SMOC2):c.1192G>A (p.Val398Met)	not specified [RCV004862655]	uncertain significance	6	168653135	168653135	Human		name
598170302	CV3915173	single nucleotide variant	NM_001166412.2(SMOC2):c.1325C>G (p.Pro442Arg)	not specified [RCV005284561]	uncertain significance	6	168666422	168666422	Human		name
598170305	CV3915174	single nucleotide variant	NM_001166412.2(SMOC2):c.1310C>T (p.Thr437Met)	not specified [RCV005284562]	uncertain significance	6	168664098	168664098	Human		name
598170308	CV3915175	single nucleotide variant	NM_001166412.2(SMOC2):c.1066T>A (p.Phe356Ile)	not specified [RCV005284563]	uncertain significance	6	168653009	168653009	Human		name
598170312	CV3915177	single nucleotide variant	NM_001166412.2(SMOC2):c.1049G>A (p.Arg350Gln)	not specified [RCV005284564]	uncertain significance	6	168652992	168652992	Human		name
598170316	CV3915178	single nucleotide variant	NM_001166412.2(SMOC2):c.1307G>C (p.Ser436Thr)	not specified [RCV005284565]	uncertain significance	6	168664095	168664095	Human		name
15122247	CV710333	single nucleotide variant	NM_001166412.2(SMOC2):c.1243G>A (p.Val415Met)	SMOC2-related disorder [RCV003916108]\|not provided [RCV000963040]	likely benign	6	168653186	168653186	Human	2	name , trait , alternate_id
15122247	CV710333	single nucleotide variant	NM_001166412.2(SMOC2):c.1243G>A (p.Val415Met)	SMOC2-related disorder [RCV003916108]\|not provided [RCV000963040]	likely benign	6	168653186	168653187	Human	2	name , trait , alternate_id
15123176	CV710334	single nucleotide variant	NM_001166412.2(SMOC2):c.1315A>G (p.Asn439Asp)	not provided [RCV000963194]	benign\|likely benign	6	168664103	168664103	Human		name
150503525	CV1212500	insertion	NM_001166412.2(SMOC2):c.1011-101_1011-100insGG	not provided [RCV001595375]	benign	6	168652852	168652853	Human		name
155794460	CV1858584	insertion	NM_001166412.2(SMOC2):c.907+15386_907+15387insTGTAATTACTACCAGCGTGGAATAAAAACACC	Schizophrenia [RCV002463546]	uncertain significance	6	168623621	168623622	Human	2	name
8568492	CV39614	single nucleotide variant	NM_001166412.2(SMOC2):c.84+1G>T AND DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA	DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH [RCV000023634]\|not provided [RCV001090786]	pathogenic	6	168441455	168441455	Human	1	name
11087844	CV227500	single nucleotide variant	NM_001166412.2(SMOC2):c.648T>A (p.Cys216Ter) AND DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA	DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH [RCV000210957]	pathogenic	6	168598828	168598828	Human	1	name

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