Steap3 Variant Search Result - Rat Genome Database

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123 records found for search term Steap3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405029036	CV2925927	single nucleotide variant	NM_182915.3(STEAP3):c.523-4G>A	STEAP3-related disorder [RCV003946754]\|not provided [RCV003578219]	benign\|likely benign	2	119247675	119247675	Human	1	name , trait , alternate_id
156131963	CV2037510	single nucleotide variant	NM_182915.3(STEAP3):c.1051-20T>C	not provided [RCV002800648]	benign	2	119254664	119254664	Human		name
156015534	CV2087083	single nucleotide variant	NM_182915.3(STEAP3):c.1050+12A>G	not provided [RCV002866336]	likely benign	2	119248218	119248218	Human		name
126738440	CV1019450	single nucleotide variant	NM_182915.3(STEAP3):c.1215+2654A>T	Hypochromic microcytic anemia with iron overload 2 [RCV001335521]	pathogenic	2	119257502	119257502	Human		name
401924750	CV2812267	single nucleotide variant	NM_182915.3(STEAP3):c.1215+2604C>T	STEAP3-related disorder [RCV003980912]\|not provided [RCV003436127]	likely benign	2	119257452	119257452	Human	1	name , trait , alternate_id
405294932	CV3214964	single nucleotide variant	NM_182915.3(STEAP3):c.1215+2737C>T	STEAP3-related disorder [RCV003936822]	benign	2	119257585	119257585	Human		name , trait , alternate_id
405278917	CV3220474	single nucleotide variant	NM_182915.3(STEAP3):c.1215+2773A>T	STEAP3-related disorder [RCV003976666]	benign	2	119257621	119257621	Human		name , trait , alternate_id
408367077	CV3512072	single nucleotide variant	NM_182915.3(STEAP3):c.1215+2650C>A	STEAP3-related disorder [RCV004757774]	likely benign	2	119257498	119257498	Human		name , trait , alternate_id
598178525	CV4008453	single nucleotide variant	NM_182915.3(STEAP3):c.1215+2771C>G	Severe congenital hypochromic anemia with ringed sideroblasts [RCV005393972]	uncertain significance	2	119257619	119257619	Human	1	name
401916820	CV2812262	single nucleotide variant	NM_182915.3(STEAP3):c.81C>T (p.Ser27=)	not provided [RCV003429253]	likely benign	2	119245547	119245547	Human		name
597703690	CV3618590	single nucleotide variant	NM_182915.3(STEAP3):c.5C>T (p.Ser2Leu)	not specified [RCV004860219]	uncertain significance	2	119231017	119231017	Human		name
329401181	CV2446238	single nucleotide variant	NM_182915.3(STEAP3):c.10C>A (p.Gln4Lys)	not specified [RCV004264632]	uncertain significance	2	119231022	119231022	Human		name
405113493	CV2939180	single nucleotide variant	NM_182915.3(STEAP3):c.129C>T (p.Ile43=)	not provided [RCV003666621]	likely benign	2	119245595	119245595	Human		name
405259572	CV3194796	single nucleotide variant	NM_182915.3(STEAP3):c.105C>T (p.Pro35=)	STEAP3-related disorder [RCV003894184]	likely benign	2	119245571	119245571	Human		name , trait , alternate_id
15156122	CV696989	single nucleotide variant	NM_182915.3(STEAP3):c.282G>A (p.Pro94=)	not provided [RCV000946632]	benign	2	119245748	119245748	Human		name
152162281	CV1543918	single nucleotide variant	NM_182915.3(STEAP3):c.837C>T (p.Leu279=)	STEAP3-related disorder [RCV003968723]\|not provided [RCV002159854]	benign	2	119247993	119247993	Human	1	name , trait , alternate_id
401924761	CV2812265	single nucleotide variant	NM_182915.3(STEAP3):c.615G>A (p.Leu205=)	not provided [RCV003436125]	likely benign	2	119247771	119247771	Human		name
401924749	CV2812266	single nucleotide variant	NM_182915.3(STEAP3):c.645C>T (p.Pro215=)	not provided [RCV003436126]	likely benign	2	119247801	119247801	Human		name
405265425	CV3185651	single nucleotide variant	NM_182915.3(STEAP3):c.978C>T (p.His326=)	not provided [RCV003886215]	likely benign	2	119248134	119248134	Human		name
405286264	CV3218730	single nucleotide variant	NM_182915.3(STEAP3):c.351G>A (p.Ala117=)	STEAP3-related disorder [RCV003959448]	likely benign	2	119245817	119245817	Human		name , trait , alternate_id
405740076	CV3334360	single nucleotide variant	NM_182915.3(STEAP3):c.46G>T (p.Asp16Tyr)	not specified [RCV004465573]	uncertain significance	2	119245512	119245512	Human		name
15162885	CV732731	single nucleotide variant	NM_182915.3(STEAP3):c.43A>G (p.Met15Val)	not provided [RCV000903653]	likely benign	2	119245509	119245509	Human		name
15162891	CV732732	single nucleotide variant	NM_182915.3(STEAP3):c.645C>G (p.Pro215=)	not provided [RCV000903654]	benign	2	119247801	119247801	Human		name
15164374	CV746747	single nucleotide variant	NM_182915.3(STEAP3):c.648G>A (p.Leu216=)	not provided [RCV000926366]	likely benign	2	119247804	119247804	Human		name
152128783	CV1583799	single nucleotide variant	NM_182915.3(STEAP3):c.1002G>A (p.Pro334=)	not provided [RCV002199044]	likely benign	2	119248158	119248158	Human		name
152034229	CV1610550	single nucleotide variant	NM_182915.3(STEAP3):c.1203C>T (p.Phe401=)	not provided [RCV002125064]	benign	2	119254836	119254836	Human		name
155935660	CV2221779	single nucleotide variant	NM_182915.3(STEAP3):c.217C>T (p.Arg73Cys)	not provided [RCV003574987]\|not specified [RCV004102816]	uncertain significance	2	119245683	119245683	Human		name
155928663	CV2224415	single nucleotide variant	NM_182915.3(STEAP3):c.245C>A (p.Ala82Asp)	not specified [RCV004098022]	uncertain significance	2	119245711	119245711	Human		name
156288649	CV2332930	single nucleotide variant	NM_182915.3(STEAP3):c.151C>T (p.Arg51Cys)	not specified [RCV004192187]	uncertain significance	2	119245617	119245617	Human		name
155927935	CV2349885	single nucleotide variant	NM_182915.3(STEAP3):c.260A>G (p.Gln87Arg)	not provided [RCV003546944]\|not specified [RCV004206306]	uncertain significance	2	119245726	119245726	Human		name
156158942	CV2361404	single nucleotide variant	NM_182915.3(STEAP3):c.254C>T (p.Thr85Ile)	not specified [RCV004221052]	uncertain significance	2	119245720	119245720	Human		name
156031441	CV2376361	single nucleotide variant	NM_182915.3(STEAP3):c.152G>A (p.Arg51His)	not specified [RCV004220556]	uncertain significance	2	119245618	119245618	Human		name
156194720	CV2395720	single nucleotide variant	NM_182915.3(STEAP3):c.204C>A (p.Ser68Arg)	not specified [RCV004235258]	uncertain significance	2	119245670	119245670	Human		name
401731114	CV2674265	single nucleotide variant	NM_182915.3(STEAP3):c.281C>T (p.Pro94Leu)	not provided [RCV005102530]\|not specified [RCV004289149]	uncertain significance	2	119245747	119245747	Human		name
401924767	CV2812263	single nucleotide variant	NM_182915.3(STEAP3):c.106G>A (p.Asp36Asn)	not provided [RCV003436123]	likely benign	2	119245572	119245572	Human		name
401924754	CV2812269	single nucleotide variant	NM_182915.3(STEAP3):c.1479G>A (p.Glu493=)	not provided [RCV003436129]	likely benign	2	119263320	119263320	Human		name
405146760	CV3024036	single nucleotide variant	NM_182915.3(STEAP3):c.1422C>G (p.Gly474=)	not provided [RCV003702989]	likely benign	2	119263263	119263263	Human		name
407496154	CV3485431	single nucleotide variant	NM_182915.3(STEAP3):c.182G>A (p.Gly61Asp)	not specified [RCV004668056]	uncertain significance	2	119245648	119245648	Human		name
597747275	CV3618584	single nucleotide variant	NM_182915.3(STEAP3):c.166C>T (p.Arg56Cys)	not specified [RCV004866034]	uncertain significance	2	119245632	119245632	Human		name
597703681	CV3618585	single nucleotide variant	NM_182915.3(STEAP3):c.206G>A (p.Arg69His)	not specified [RCV004860218]	uncertain significance	2	119245672	119245672	Human		name
597747290	CV3618589	single nucleotide variant	NM_182915.3(STEAP3):c.262G>C (p.Glu88Gln)	not specified [RCV004866037]	uncertain significance	2	119245728	119245728	Human		name
597747295	CV3618591	single nucleotide variant	NM_182915.3(STEAP3):c.113C>A (p.Ala38Asp)	not specified [RCV004866038]	uncertain significance	2	119245579	119245579	Human		name
597887500	CV3741973	single nucleotide variant	NM_182915.3(STEAP3):c.1302C>T (p.Tyr434=)	not provided [RCV005070693]	likely benign	2	119263143	119263143	Human		name
598251288	CV3919578	single nucleotide variant	NM_182915.3(STEAP3):c.251T>C (p.Val84Ala)	not specified [RCV005277857]	uncertain significance	2	119245717	119245717	Human		name
15165445	CV707693	single nucleotide variant	NM_182915.3(STEAP3):c.1218C>T (p.Ser406=)	not provided [RCV000970950]	benign	2	119263059	119263059	Human		name
15175536	CV719208	single nucleotide variant	NM_182915.3(STEAP3):c.1011C>T (p.Arg337=)	not provided [RCV000884390]	benign	2	119248167	119248167	Human		name
15163158	CV732735	single nucleotide variant	NM_182915.3(STEAP3):c.1338G>A (p.Leu446=)	not provided [RCV000903710]	benign	2	119263179	119263179	Human		name
15134879	CV746748	single nucleotide variant	NM_182915.3(STEAP3):c.1023C>T (p.Tyr341=)	not provided [RCV000920760]	likely benign	2	119248179	119248179	Human		name
15106308	CV780818	single nucleotide variant	NM_182915.3(STEAP3):c.1269C>T (p.Tyr423=)	not provided [RCV000976606]	benign	2	119263110	119263110	Human		name
152159584	CV1588157	single nucleotide variant	NM_182915.3(STEAP3):c.580G>A (p.Ala194Thr)	not provided [RCV002180696]	benign	2	119247736	119247736	Human		name
152114702	CV1659678	single nucleotide variant	NM_182915.3(STEAP3):c.830T>C (p.Leu277Pro)	not provided [RCV002080732]	likely benign	2	119247986	119247986	Human		name
156366029	CV1909275	single nucleotide variant	NM_182915.3(STEAP3):c.813C>A (p.Cys271Ter)	not provided [RCV002602833]	likely benign	2	119247969	119247969	Human		name
156104117	CV1956801	single nucleotide variant	NM_182915.3(STEAP3):c.637G>A (p.Ala213Thr)	not provided [RCV002570955]	uncertain significance	2	119247793	119247793	Human		name
156376088	CV2210446	single nucleotide variant	NM_182915.3(STEAP3):c.967G>A (p.Ala323Thr)	not specified [RCV004089585]	uncertain significance	2	119248123	119248123	Human		name
155913131	CV2245760	single nucleotide variant	NM_182915.3(STEAP3):c.556C>T (p.Arg186Cys)	not specified [RCV004111621]	uncertain significance	2	119247712	119247712	Human		name
156178620	CV2258253	single nucleotide variant	NM_182915.3(STEAP3):c.407G>A (p.Arg136His)	not specified [RCV004121623]	uncertain significance	2	119245873	119245873	Human		name
155996814	CV2288550	single nucleotide variant	NM_182915.3(STEAP3):c.815T>A (p.Val272Glu)	not specified [RCV004152076]	uncertain significance	2	119247971	119247971	Human		name
156010035	CV2290962	single nucleotide variant	NM_182915.3(STEAP3):c.559G>T (p.Ala187Ser)	not specified [RCV004151516]	uncertain significance	2	119247715	119247715	Human		name
155909207	CV2307231	single nucleotide variant	NM_182915.3(STEAP3):c.526C>G (p.Pro176Ala)	not specified [RCV004159693]	uncertain significance	2	119247682	119247682	Human		name
155976162	CV2324608	single nucleotide variant	NM_182915.3(STEAP3):c.436C>A (p.Leu146Ile)	not specified [RCV004172862]	uncertain significance	2	119245902	119245902	Human		name
156051067	CV2336636	single nucleotide variant	NM_182915.3(STEAP3):c.421G>A (p.Glu141Lys)	not provided [RCV003575010]\|not specified [RCV004196878]	uncertain significance	2	119245887	119245887	Human		name
156173923	CV2355216	single nucleotide variant	NM_182915.3(STEAP3):c.944T>C (p.Ile315Thr)	not provided [RCV003699008]\|not specified [RCV004198591]	uncertain significance	2	119248100	119248100	Human		name
156065415	CV2376083	single nucleotide variant	NM_182915.3(STEAP3):c.379C>G (p.Pro127Ala)	not specified [RCV004220319]	uncertain significance	2	119245845	119245845	Human		name
156000955	CV2378761	single nucleotide variant	NM_182915.3(STEAP3):c.898C>T (p.Arg300Cys)	not specified [RCV004231214]	uncertain significance	2	119248054	119248054	Human		name
156048651	CV2382693	single nucleotide variant	NM_182915.3(STEAP3):c.746A>C (p.Tyr249Ser)	not specified [RCV004233006]	uncertain significance	2	119247902	119247902	Human		name
156098534	CV2385083	single nucleotide variant	NM_182915.3(STEAP3):c.700G>A (p.Val234Ile)	not specified [RCV004228348]	likely benign	2	119247856	119247856	Human		name
329355375	CV2445397	single nucleotide variant	NM_182915.3(STEAP3):c.470A>G (p.Asn157Ser)	not specified [RCV004257471]	uncertain significance	2	119245936	119245936	Human		name
401893791	CV2759825	single nucleotide variant	NM_182915.3(STEAP3):c.719A>G (p.Asn240Ser)	not provided [RCV003549073]\|not specified [RCV004343259]	likely benign\|uncertain significance	2	119247875	119247875	Human		name
401924766	CV2812264	single nucleotide variant	NM_182915.3(STEAP3):c.575C>T (p.Ala192Val)	not provided [RCV003436124]	likely benign	2	119247731	119247731	Human		name
402506675	CV2880779	single nucleotide variant	NM_182915.3(STEAP3):c.598G>A (p.Val200Met)	not provided [RCV003546432]\|not specified [RCV004369129]	likely benign\|uncertain significance	2	119247754	119247754	Human		name
405215394	CV2911159	single nucleotide variant	NM_182915.3(STEAP3):c.776A>G (p.Lys259Arg)	not provided [RCV003567715]	uncertain significance	2	119247932	119247932	Human		name
402508614	CV2986051	single nucleotide variant	NM_182915.3(STEAP3):c.522G>C (p.Gln174His)	not provided [RCV003689316]	uncertain significance	2	119245988	119245988	Human		name
402499193	CV3016093	single nucleotide variant	NM_182915.3(STEAP3):c.632T>C (p.Val211Ala)	not provided [RCV003688316]	uncertain significance	2	119247788	119247788	Human		name
405220403	CV3059783	single nucleotide variant	NM_182915.3(STEAP3):c.649C>A (p.Arg217Ser)	not provided [RCV003733156]\|not specified [RCV005273856]	uncertain significance	2	119247805	119247805	Human		name
405740082	CV3334361	single nucleotide variant	NM_182915.3(STEAP3):c.613C>G (p.Leu205Val)	not specified [RCV004465574]	uncertain significance	2	119247769	119247769	Human		name
405740095	CV3334363	single nucleotide variant	NM_182915.3(STEAP3):c.814G>A (p.Val272Met)	not specified [RCV004465576]	uncertain significance	2	119247970	119247970	Human		name
407496147	CV3485429	single nucleotide variant	NM_182915.3(STEAP3):c.853G>A (p.Val285Met)	not specified [RCV004668054]	uncertain significance	2	119248009	119248009	Human		name
597747300	CV3618592	single nucleotide variant	NM_182915.3(STEAP3):c.977A>G (p.His326Arg)	not specified [RCV004866039]	uncertain significance	2	119248133	119248133	Human		name
597969036	CV3761317	single nucleotide variant	NM_182915.3(STEAP3):c.838G>A (p.Val280Met)	not provided [RCV005083704]	uncertain significance	2	119247994	119247994	Human		name
598251262	CV3919574	single nucleotide variant	NM_182915.3(STEAP3):c.503C>A (p.Pro168Gln)	not specified [RCV005277853]	uncertain significance	2	119245969	119245969	Human		name
598251269	CV3919575	single nucleotide variant	NM_182915.3(STEAP3):c.746A>G (p.Tyr249Cys)	not specified [RCV005277854]	uncertain significance	2	119247902	119247902	Human		name
598251277	CV3919576	single nucleotide variant	NM_182915.3(STEAP3):c.556C>A (p.Arg186Ser)	not specified [RCV005277855]	uncertain significance	2	119247712	119247712	Human		name
598251283	CV3919577	single nucleotide variant	NM_182915.3(STEAP3):c.496G>T (p.Ala166Ser)	not specified [RCV005277856]	likely benign	2	119245962	119245962	Human		name
598251295	CV3919579	single nucleotide variant	NM_182915.3(STEAP3):c.436C>T (p.Leu146Phe)	not specified [RCV005277858]	uncertain significance	2	119245902	119245902	Human		name
598178532	CV4008454	single nucleotide variant	NM_182915.3(STEAP3):c.745T>C (p.Tyr249His)	Severe congenital hypochromic anemia with ringed sideroblasts [RCV005393973]	uncertain significance	2	119247901	119247901	Human	1	name
8572428	CV59495	single nucleotide variant	NM_182915.3(STEAP3):c.330C>A (p.Cys110Ter)	Severe congenital hypochromic anemia with ringed sideroblasts [RCV000043521]	pathogenic	2	119245796	119245796	Human	1	name
15163190	CV707692	single nucleotide variant	NM_182915.3(STEAP3):c.881G>A (p.Arg294His)	not provided [RCV000970428]	benign	2	119248037	119248037	Human		name
15159364	CV719206	single nucleotide variant	NM_182915.3(STEAP3):c.535G>A (p.Gly179Ser)	not provided [RCV000881181]	benign	2	119247691	119247691	Human		name
15102593	CV719207	single nucleotide variant	NM_182915.3(STEAP3):c.677C>T (p.Thr226Ile)	not provided [RCV000892509]	likely benign	2	119247833	119247833	Human		name
15169075	CV732733	single nucleotide variant	NM_182915.3(STEAP3):c.899G>A (p.Arg300His)	not provided [RCV000904986]	benign	2	119248055	119248055	Human		name
151795068	CV1434398	single nucleotide variant	NM_182915.3(STEAP3):c.1156G>A (p.Val386Met)	not provided [RCV001866606]\|not specified [RCV004039005]	uncertain significance	2	119254789	119254789	Human		name
152999714	CV1683282	single nucleotide variant	NM_182915.3(STEAP3):c.1135G>T (p.Gly379Cys)	See cases [RCV002252466]\|not provided [RCV003120854]	uncertain significance	2	119254768	119254768	Human		name
156356048	CV1880340	single nucleotide variant	NM_182915.3(STEAP3):c.1259C>T (p.Thr420Met)	not provided [RCV003065246]	likely benign	2	119263100	119263100	Human		name
156196133	CV1912327	single nucleotide variant	NM_182915.3(STEAP3):c.1468G>A (p.Ala490Thr)	not provided [RCV002595542]	uncertain significance	2	119263309	119263309	Human		name
156234951	CV2108793	single nucleotide variant	NM_182915.3(STEAP3):c.1007G>A (p.Arg336His)	not provided [RCV002932982]\|not specified [RCV004067050]	uncertain significance	2	119248163	119248163	Human		name
156310903	CV2119994	single nucleotide variant	NM_182915.3(STEAP3):c.1210G>A (p.Val404Ile)	not provided [RCV002962612]	uncertain significance	2	119254843	119254843	Human		name
156230939	CV2235105	single nucleotide variant	NM_182915.3(STEAP3):c.1430G>A (p.Arg477Lys)	not specified [RCV004113281]	likely benign	2	119263271	119263271	Human		name
329362560	CV2438883	single nucleotide variant	NM_182915.3(STEAP3):c.1270G>A (p.Gly424Ser)	not specified [RCV004264414]	uncertain significance	2	119263111	119263111	Human		name
401726568	CV2695724	single nucleotide variant	NM_182915.3(STEAP3):c.1280G>C (p.Arg427Pro)	not specified [RCV004299525]	uncertain significance	2	119263121	119263121	Human		name
401924752	CV2812268	single nucleotide variant	NM_182915.3(STEAP3):c.1330C>G (p.Leu444Val)	not provided [RCV003436128]	uncertain significance	2	119263171	119263171	Human		name
405022353	CV2877514	single nucleotide variant	NM_182915.3(STEAP3):c.1006C>T (p.Arg336Cys)	not provided [RCV003577712]	uncertain significance	2	119248162	119248162	Human		name
405245506	CV2969232	single nucleotide variant	NM_182915.3(STEAP3):c.1099A>C (p.Met367Leu)	not provided [RCV003685184]	uncertain significance	2	119254732	119254732	Human		name
405168013	CV3153619	single nucleotide variant	NM_182915.3(STEAP3):c.1240G>A (p.Val414Met)	not provided [RCV003841164]	uncertain significance	2	119263081	119263081	Human		name
405740039	CV3334355	single nucleotide variant	NM_182915.3(STEAP3):c.1001C>T (p.Pro334Leu)	not provided [RCV005104725]\|not specified [RCV004465568]	likely benign\|uncertain significance	2	119248157	119248157	Human		name
405740047	CV3334356	single nucleotide variant	NM_182915.3(STEAP3):c.1031T>A (p.Val344Asp)	not specified [RCV004465569]	uncertain significance	2	119248187	119248187	Human		name
405740423	CV3334357	single nucleotide variant	NM_182915.3(STEAP3):c.1033A>T (p.Asn345Tyr)	not specified [RCV004465570]	uncertain significance	2	119248189	119248189	Human		name
405740062	CV3334358	single nucleotide variant	NM_182915.3(STEAP3):c.1310A>G (p.Tyr437Cys)	not specified [RCV004465571]	uncertain significance	2	119263151	119263151	Human		name
407496151	CV3485430	single nucleotide variant	NM_182915.3(STEAP3):c.1169C>T (p.Pro390Leu)	not specified [RCV004668055]	uncertain significance	2	119254802	119254802	Human		name
407496157	CV3485432	single nucleotide variant	NM_182915.3(STEAP3):c.1396C>T (p.Arg466Cys)	not provided [RCV005059730]\|not specified [RCV004668057]	uncertain significance	2	119263237	119263237	Human		name
597747266	CV3618581	single nucleotide variant	NM_182915.3(STEAP3):c.1477G>A (p.Glu493Lys)	not specified [RCV004866032]	uncertain significance	2	119263318	119263318	Human		name
597703668	CV3618582	single nucleotide variant	NM_182915.3(STEAP3):c.1397G>A (p.Arg466His)	not specified [RCV004860217]	uncertain significance	2	119263238	119263238	Human		name
597747271	CV3618583	single nucleotide variant	NM_182915.3(STEAP3):c.1460C>T (p.Thr487Ile)	not specified [RCV004866033]	uncertain significance	2	119263301	119263301	Human		name
597747280	CV3618586	single nucleotide variant	NM_182915.3(STEAP3):c.1426G>A (p.Glu476Lys)	not specified [RCV004866035]	uncertain significance	2	119263267	119263267	Human		name
597747285	CV3618588	single nucleotide variant	NM_182915.3(STEAP3):c.1234G>T (p.Ala412Ser)	not specified [RCV004866036]	uncertain significance	2	119263075	119263075	Human		name
597905767	CV3803973	single nucleotide variant	NM_182915.3(STEAP3):c.1484C>T (p.Thr495Met)	not provided [RCV005153519]	benign	2	119263325	119263325	Human		name
597955561	CV3841267	single nucleotide variant	NM_182915.3(STEAP3):c.1414C>T (p.Arg472Trp)	not provided [RCV005191386]	uncertain significance	2	119263255	119263255	Human		name
598213763	CV3919573	single nucleotide variant	NM_182915.3(STEAP3):c.1345C>A (p.Pro449Thr)	not specified [RCV005271116]	uncertain significance	2	119263186	119263186	Human		name
15153701	CV719209	single nucleotide variant	NM_182915.3(STEAP3):c.1019G>A (p.Arg340His)	STEAP3-related disorder [RCV003955801]\|not provided [RCV000880063]	likely benign	2	119248175	119248175	Human	1	name , trait , alternate_id
15125248	CV732734	single nucleotide variant	NM_182915.3(STEAP3):c.1196G>A (p.Arg399Lys)	STEAP3-related disorder [RCV003920848]\|not provided [RCV000896729]	likely benign	2	119254829	119254829	Human	1	name , trait , alternate_id
15157625	CV732736	single nucleotide variant	NM_182915.3(STEAP3):c.1451C>T (p.Thr484Met)	STEAP3-related disorder [RCV003958163]\|not provided [RCV000902567]	benign\|likely benign	2	119263292	119263292	Human	1	name , trait , alternate_id
8625115	CV80234	single nucleotide variant	NM_001008410.1(STEAP3):c.52G>A (p.Asp18Asn)	Malignant melanoma [RCV000060310]	not provided	2	119245548	119245548	Human		name
8629810	CV84957	single nucleotide variant	NM_001008410.1(STEAP3):c.693C>T (p.Phe231=)	Malignant melanoma [RCV000065039]	not provided	2	119247879	119247879	Human		name
407487428	CV3414948	microsatellite	NM_182915.3(STEAP3):c.959TCT[1] (p.Phe321del)	not specified [RCV004597283]	uncertain significance	2	119248113	119248115	Human		name

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