Shroom2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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218 records found for search term Shroom2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405292237	CV3199780	single nucleotide variant	NM_001649.4(SHROOM2):c.4311+10T>A	SHROOM2-related disorder [RCV003964411]	benign	X	9939376	9939376	Human		name , trait , alternate_id
8587856	CV122491	single nucleotide variant	NM_001649.2(SHROOM2):c.3587+757G>C	Lung cancer [RCV000103011]	uncertain significance	X	9933627	9933627	Human		name
156088400	CV2295508	single nucleotide variant	NM_001649.4(SHROOM2):c.17C>T (p.Pro6Leu)	not specified [RCV004160614]	uncertain significance	X	9786562	9786562	Human		name
405288323	CV3197286	single nucleotide variant	NM_001649.4(SHROOM2):c.222C>T (p.Ile74=)	SHROOM2-related disorder [RCV003982382]	likely benign	X	9873708	9873708	Human		name , trait , alternate_id
407519210	CV3480597	single nucleotide variant	NM_001649.4(SHROOM2):c.10G>A (p.Ala4Thr)	not specified [RCV004676393]	uncertain significance	X	9786555	9786555	Human		name
156037440	CV2218599	single nucleotide variant	NM_001649.4(SHROOM2):c.73C>A (p.Arg25Ser)	not specified [RCV004090860]	uncertain significance	X	9786618	9786618	Human		name
401931162	CV2823824	single nucleotide variant	NM_001649.4(SHROOM2):c.390G>A (p.Ala130=)	not provided [RCV003440942]	likely benign	X	9891049	9891049	Human		name
405276021	CV3193206	single nucleotide variant	NM_001649.4(SHROOM2):c.399A>G (p.Pro133=)	SHROOM2-related disorder [RCV003974372]	benign	X	9891058	9891058	Human		name , trait , alternate_id
405285669	CV3206587	single nucleotide variant	NM_001649.4(SHROOM2):c.783G>A (p.Ser261=)	SHROOM2-related disorder [RCV003981273]	benign	X	9894691	9894691	Human		name , trait , alternate_id
405257911	CV3207953	single nucleotide variant	NM_001649.4(SHROOM2):c.960T>A (p.Pro320=)	SHROOM2-related disorder [RCV003941422]	likely benign	X	9894868	9894868	Human		name , trait , alternate_id
405287685	CV3210703	single nucleotide variant	NM_001649.4(SHROOM2):c.483G>A (p.Glu161=)	SHROOM2-related disorder [RCV003924463]	benign	X	9894391	9894391	Human		name , trait , alternate_id
405272402	CV3221638	single nucleotide variant	NM_001649.4(SHROOM2):c.411C>T (p.Thr137=)	SHROOM2-related disorder [RCV003972130]	benign	X	9891070	9891070	Human		name , trait , alternate_id
156186256	CV2236169	single nucleotide variant	NM_001649.4(SHROOM2):c.188C>T (p.Ala63Val)	not specified [RCV004107882]	uncertain significance	X	9873674	9873674	Human		name
401728352	CV2686021	single nucleotide variant	NM_001649.4(SHROOM2):c.164A>G (p.Lys55Arg)	not specified [RCV004297036]	uncertain significance	X	9786709	9786709	Human		name
401931160	CV2823826	single nucleotide variant	NM_001649.4(SHROOM2):c.2379G>A (p.Thr793=)	not provided [RCV003440944]	likely benign	X	9896287	9896287	Human		name
405280243	CV3191699	single nucleotide variant	NM_001649.4(SHROOM2):c.2859A>G (p.Ala953=)	SHROOM2-related disorder [RCV003919833]	benign	X	9898258	9898258	Human		name , trait , alternate_id
405266330	CV3201910	single nucleotide variant	NM_001649.4(SHROOM2):c.1827G>A (p.Pro609=)	SHROOM2-related disorder [RCV003911399]	likely benign	X	9895735	9895735	Human		name , trait , alternate_id
405277217	CV3210564	single nucleotide variant	NM_001649.4(SHROOM2):c.2889G>A (p.Pro963=)	SHROOM2-related disorder [RCV003917386]	benign	X	9898288	9898288	Human		name , trait , alternate_id
405283260	CV3216999	single nucleotide variant	NM_001649.4(SHROOM2):c.1164A>G (p.Pro388=)	SHROOM2-related disorder [RCV003979146]	benign	X	9895072	9895072	Human		name , trait , alternate_id
405271558	CV3219137	single nucleotide variant	NM_001649.4(SHROOM2):c.2694G>A (p.Ala898=)	SHROOM2-related disorder [RCV003971831]	likely benign	X	9896602	9896602	Human		name , trait , alternate_id
405278213	CV3221743	single nucleotide variant	NM_001649.4(SHROOM2):c.2535C>T (p.Thr845=)	SHROOM2-related disorder [RCV003976329]	likely benign	X	9896443	9896443	Human		name , trait , alternate_id
405733183	CV3311251	single nucleotide variant	NM_001649.4(SHROOM2):c.266C>T (p.Ala89Val)	not specified [RCV004451293]	uncertain significance	X	9873752	9873752	Human		name
408367530	CV3517763	single nucleotide variant	NM_001649.4(SHROOM2):c.1590C>T (p.Arg530=)	SHROOM2-related disorder [RCV004758582]	likely benign	X	9895498	9895498	Human		name , trait , alternate_id
597719262	CV3598912	single nucleotide variant	NM_001649.4(SHROOM2):c.233A>G (p.Asn78Ser)	not specified [RCV004861855]	uncertain significance	X	9873719	9873719	Human		name
597719376	CV3598925	single nucleotide variant	NM_001649.4(SHROOM2):c.100G>T (p.Gly34Cys)	not specified [RCV004861868]	uncertain significance	X	9786645	9786645	Human		name
151235768	CV1163104	single nucleotide variant	NM_001649.4(SHROOM2):c.631G>A (p.Gly211Ser)	Meniere disease [RCV001797192]	likely pathogenic	X	9894539	9894539	Human	1	name
156018762	CV2233252	single nucleotide variant	NM_001649.4(SHROOM2):c.351G>T (p.Trp117Cys)	not specified [RCV004105637]	uncertain significance	X	9891010	9891010	Human		name
156079326	CV2248500	single nucleotide variant	NM_001649.4(SHROOM2):c.433G>A (p.Gly145Ser)	not specified [RCV004119629]	likely benign	X	9891092	9891092	Human		name
155984186	CV2274498	single nucleotide variant	NM_001649.4(SHROOM2):c.777G>C (p.Gln259His)	not specified [RCV004137122]	uncertain significance	X	9894685	9894685	Human		name
155928358	CV2281088	single nucleotide variant	NM_001649.4(SHROOM2):c.617G>T (p.Arg206Leu)	not specified [RCV004147357]	uncertain significance	X	9894525	9894525	Human		name
329351826	CV2455357	single nucleotide variant	NM_001649.4(SHROOM2):c.619G>A (p.Asp207Asn)	not specified [RCV004274857]	uncertain significance	X	9894527	9894527	Human		name
401729146	CV2673168	single nucleotide variant	NM_001649.4(SHROOM2):c.820G>A (p.Gly274Ser)	not specified [RCV004284148]	likely benign	X	9894728	9894728	Human		name
401760358	CV2709797	single nucleotide variant	NM_001649.4(SHROOM2):c.385C>A (p.Leu129Ile)	not specified [RCV004320776]	uncertain significance	X	9891044	9891044	Human		name
401931156	CV2823829	single nucleotide variant	NM_001649.4(SHROOM2):c.3699C>T (p.Ala1233=)	not provided [RCV003440947]	likely benign	X	9937245	9937245	Human		name
401931155	CV2823830	single nucleotide variant	NM_001649.4(SHROOM2):c.4152C>T (p.Pro1384=)	SHROOM2-related disorder [RCV003929191]\|not provided [RCV003440948]	likely benign	X	9939207	9939207	Human		name , trait , alternate_id
405265278	CV3195641	single nucleotide variant	NM_001649.4(SHROOM2):c.409A>G (p.Thr137Ala)	SHROOM2-related disorder [RCV003897335]	benign	X	9891068	9891068	Human		name , trait , alternate_id
405275327	CV3196260	single nucleotide variant	NM_001649.4(SHROOM2):c.3210C>T (p.Arg1070=)	SHROOM2-related disorder [RCV003974129]	likely benign	X	9932493	9932493	Human		name , trait , alternate_id
405294178	CV3203498	single nucleotide variant	NM_001649.4(SHROOM2):c.3948G>A (p.Ser1316=)	SHROOM2-related disorder [RCV003934027]	likely benign	X	9937494	9937494	Human		name , trait , alternate_id
405273214	CV3210354	single nucleotide variant	NM_001649.4(SHROOM2):c.3489G>A (p.Thr1163=)	SHROOM2-related disorder [RCV003914579]	benign	X	9932772	9932772	Human		name , trait , alternate_id
405255740	CV3210847	single nucleotide variant	NM_001649.4(SHROOM2):c.4383C>T (p.Asp1461=)	SHROOM2-related disorder [RCV003939353]	benign	X	9944712	9944712	Human		name , trait , alternate_id
405262176	CV3212832	single nucleotide variant	NM_001649.4(SHROOM2):c.4464C>T (p.Phe1488=)	SHROOM2-related disorder [RCV003944742]	likely benign	X	9944793	9944793	Human		name , trait , alternate_id
405284308	CV3213649	single nucleotide variant	NM_001649.4(SHROOM2):c.4662C>T (p.Arg1554=)	SHROOM2-related disorder [RCV003922219]	likely benign	X	9946748	9946748	Human		name , trait , alternate_id
405260959	CV3215555	single nucleotide variant	NM_001649.4(SHROOM2):c.3237C>T (p.Asp1079=)	SHROOM2-related disorder [RCV003944286]	likely benign	X	9932520	9932520	Human		name , trait , alternate_id
405278600	CV3220343	single nucleotide variant	NM_001649.4(SHROOM2):c.3756A>G (p.Thr1252=)	SHROOM2-related disorder [RCV003976570]	benign	X	9937302	9937302	Human		name , trait , alternate_id
405733260	CV3311261	single nucleotide variant	NM_001649.4(SHROOM2):c.616C>T (p.Arg206Cys)	not specified [RCV004451303]	uncertain significance	X	9894524	9894524	Human		name
405733267	CV3311262	single nucleotide variant	NM_001649.4(SHROOM2):c.682G>A (p.Asp228Asn)	not specified [RCV004451304]	uncertain significance	X	9894590	9894590	Human		name
405733271	CV3311263	single nucleotide variant	NM_001649.4(SHROOM2):c.913C>A (p.Pro305Thr)	not specified [RCV004451305]	uncertain significance	X	9894821	9894821	Human		name
405733277	CV3311264	single nucleotide variant	NM_001649.4(SHROOM2):c.950C>T (p.Pro317Leu)	not specified [RCV004451306]	uncertain significance	X	9894858	9894858	Human		name
408367363	CV3511386	single nucleotide variant	NM_001649.4(SHROOM2):c.3342C>T (p.Ser1114=)	SHROOM2-related disorder [RCV004758407]	likely benign	X	9932625	9932625	Human		name , trait , alternate_id
597719117	CV3598894	single nucleotide variant	NM_001649.4(SHROOM2):c.532G>A (p.Val178Ile)	not specified [RCV004861837]	uncertain significance	X	9894440	9894440	Human		name
597719125	CV3598895	single nucleotide variant	NM_001649.4(SHROOM2):c.748C>T (p.Arg250Trp)	not specified [RCV004861838]	uncertain significance	X	9894656	9894656	Human		name
597719135	CV3598896	single nucleotide variant	NM_001649.4(SHROOM2):c.566C>T (p.Ser189Leu)	not specified [RCV004861839]	uncertain significance	X	9894474	9894474	Human		name
597719216	CV3598906	single nucleotide variant	NM_001649.4(SHROOM2):c.416G>A (p.Gly139Asp)	not specified [RCV004861849]	uncertain significance	X	9891075	9891075	Human		name
597719244	CV3598910	single nucleotide variant	NM_001649.4(SHROOM2):c.964C>T (p.Arg322Cys)	not specified [RCV004861853]	uncertain significance	X	9894872	9894872	Human		name
597719287	CV3598915	single nucleotide variant	NM_001649.4(SHROOM2):c.937T>C (p.Ser313Pro)	not specified [RCV004861858]	uncertain significance	X	9894845	9894845	Human		name
597719368	CV3598924	single nucleotide variant	NM_001649.4(SHROOM2):c.820G>T (p.Gly274Cys)	not specified [RCV004861867]	uncertain significance	X	9894728	9894728	Human		name
597719394	CV3598927	single nucleotide variant	NM_001649.4(SHROOM2):c.859G>A (p.Glu287Lys)	not specified [RCV004861870]	uncertain significance	X	9894767	9894767	Human		name
598242288	CV3914302	single nucleotide variant	NM_001649.4(SHROOM2):c.896G>A (p.Gly299Glu)	not specified [RCV005276500]	uncertain significance	X	9894804	9894804	Human		name
15203252	CV706340	single nucleotide variant	NM_001649.4(SHROOM2):c.3774G>C (p.Ser1258=)	SHROOM2-related disorder [RCV003915969]\|not provided [RCV000958309]	benign	X	9937320	9937320	Human		name , trait , alternate_id
155923941	CV2217759	single nucleotide variant	NM_001649.4(SHROOM2):c.2864G>A (p.Arg955Gln)	not specified [RCV004083939]	uncertain significance	X	9898263	9898263	Human		name
155970316	CV2241350	single nucleotide variant	NM_001649.4(SHROOM2):c.2956G>T (p.Ala986Ser)	not specified [RCV004102484]	uncertain significance	X	9932239	9932239	Human		name
156082926	CV2244437	single nucleotide variant	NM_001649.4(SHROOM2):c.1669C>T (p.Arg557Cys)	not specified [RCV004100404]	uncertain significance	X	9895577	9895577	Human		name
156240749	CV2265593	single nucleotide variant	NM_001649.4(SHROOM2):c.1175A>G (p.His392Arg)	not specified [RCV004124329]	likely benign	X	9895083	9895083	Human		name
156070831	CV2267190	single nucleotide variant	NM_001649.4(SHROOM2):c.1460C>T (p.Ala487Val)	not specified [RCV004133876]	likely benign	X	9895368	9895368	Human		name
155900985	CV2298119	single nucleotide variant	NM_001649.4(SHROOM2):c.1153C>T (p.Pro385Ser)	not specified [RCV004159785]	likely benign	X	9895061	9895061	Human		name
156054423	CV2308669	single nucleotide variant	NM_001649.4(SHROOM2):c.2486C>G (p.Pro829Arg)	not specified [RCV004167217]	uncertain significance	X	9896394	9896394	Human		name
156300490	CV2322494	single nucleotide variant	NM_001649.4(SHROOM2):c.1452C>G (p.Asp484Glu)	not specified [RCV004180615]	uncertain significance	X	9895360	9895360	Human		name
155976343	CV2324676	single nucleotide variant	NM_001649.4(SHROOM2):c.1681G>C (p.Ala561Pro)	not specified [RCV004172920]	uncertain significance	X	9895589	9895589	Human		name
156253125	CV2325474	single nucleotide variant	NM_001649.4(SHROOM2):c.2992T>A (p.Cys998Ser)	not specified [RCV004179926]	likely benign	X	9932275	9932275	Human		name
156191628	CV2325620	single nucleotide variant	NM_001649.4(SHROOM2):c.1719T>A (p.Asp573Glu)	not specified [RCV004180036]	uncertain significance	X	9895627	9895627	Human		name
156082264	CV2368895	single nucleotide variant	NM_001649.4(SHROOM2):c.1178C>A (p.Ala393Glu)	not provided [RCV003435948]\|not specified [RCV004207851]	likely benign\|uncertain significance	X	9895086	9895086	Human		name
156209375	CV2370102	single nucleotide variant	NM_001649.4(SHROOM2):c.1495A>G (p.Thr499Ala)	not specified [RCV004210993]	uncertain significance	X	9895403	9895403	Human		name
156261019	CV2381269	single nucleotide variant	NM_001649.4(SHROOM2):c.1600C>T (p.Arg534Trp)	not specified [RCV004227331]	uncertain significance	X	9895508	9895508	Human		name
156391795	CV2382611	single nucleotide variant	NM_001649.4(SHROOM2):c.1532C>T (p.Thr511Met)	not specified [RCV004232935]	uncertain significance	X	9895440	9895440	Human		name
156053204	CV2388518	single nucleotide variant	NM_001649.4(SHROOM2):c.2858C>A (p.Ala953Glu)	not specified [RCV004237370]	uncertain significance	X	9898257	9898257	Human		name
329374370	CV2443865	single nucleotide variant	NM_001649.4(SHROOM2):c.1301A>G (p.Asp434Gly)	not specified [RCV004258204]	uncertain significance	X	9895209	9895209	Human		name
329380360	CV2466580	single nucleotide variant	NM_001649.4(SHROOM2):c.1030G>A (p.Ala344Thr)	not specified [RCV004274112]	uncertain significance	X	9894938	9894938	Human		name
329392826	CV2468977	single nucleotide variant	NM_001649.4(SHROOM2):c.2863C>G (p.Arg955Gly)	not specified [RCV004274242]	uncertain significance	X	9898262	9898262	Human		name
401768724	CV2686351	single nucleotide variant	NM_001649.4(SHROOM2):c.1680A>T (p.Lys560Asn)	not specified [RCV004297426]	uncertain significance	X	9895588	9895588	Human		name
401767104	CV2721534	single nucleotide variant	NM_001649.4(SHROOM2):c.1994C>T (p.Ala665Val)	not specified [RCV004316050]	likely benign	X	9895902	9895902	Human		name
401729375	CV2733000	single nucleotide variant	NM_001649.4(SHROOM2):c.1004C>T (p.Ala335Val)	not specified [RCV004331174]	uncertain significance	X	9894912	9894912	Human		name
401866259	CV2762584	single nucleotide variant	NM_001649.4(SHROOM2):c.1685G>T (p.Ser562Ile)	not specified [RCV004338108]	uncertain significance	X	9895593	9895593	Human		name
401866262	CV2762585	single nucleotide variant	NM_001649.4(SHROOM2):c.1746G>C (p.Gln582His)	not specified [RCV004338109]	uncertain significance	X	9895654	9895654	Human		name
401931161	CV2823825	single nucleotide variant	NM_001649.4(SHROOM2):c.1840G>A (p.Ala614Thr)	not provided [RCV003440943]	likely benign	X	9895748	9895748	Human		name
401931158	CV2823827	single nucleotide variant	NM_001649.4(SHROOM2):c.2558A>G (p.Asn853Ser)	not provided [RCV003440945]\|not specified [RCV004364634]	likely benign	X	9896466	9896466	Human		name
401931157	CV2823828	single nucleotide variant	NM_001649.4(SHROOM2):c.2810G>A (p.Arg937Gln)	not provided [RCV003440946]	likely benign	X	9898209	9898209	Human		name
405292713	CV3192590	single nucleotide variant	NM_001649.4(SHROOM2):c.2458G>A (p.Gly820Arg)	SHROOM2-related disorder [RCV003929839]	benign	X	9896366	9896366	Human		name , trait , alternate_id
405275821	CV3199497	single nucleotide variant	NM_001649.4(SHROOM2):c.1789C>T (p.Arg597Trp)	SHROOM2-related disorder [RCV003916896]\|not specified [RCV004858014]	likely benign\|uncertain significance	X	9895697	9895697	Human		name , trait , alternate_id
405275924	CV3199505	single nucleotide variant	NM_001649.4(SHROOM2):c.2794G>T (p.Ala932Ser)	SHROOM2-related disorder [RCV003916904]	benign	X	9898193	9898193	Human		name , trait , alternate_id
405260910	CV3204384	single nucleotide variant	NM_001649.4(SHROOM2):c.2569G>A (p.Ala857Thr)	SHROOM2-related disorder [RCV003944210]	likely benign	X	9896477	9896477	Human		name , trait , alternate_id
405276374	CV3206671	single nucleotide variant	NM_001649.4(SHROOM2):c.1318G>A (p.Ala440Thr)	SHROOM2-related disorder [RCV003917111]	likely benign	X	9895226	9895226	Human		name , trait , alternate_id
405292936	CV3207051	single nucleotide variant	NM_001649.4(SHROOM2):c.2693C>T (p.Ala898Val)	SHROOM2-related disorder [RCV003931465]	benign	X	9896601	9896601	Human		name , trait , alternate_id
405293392	CV3207389	single nucleotide variant	NM_001649.4(SHROOM2):c.1639G>A (p.Ala547Thr)	SHROOM2-related disorder [RCV003931771]	benign	X	9895547	9895547	Human		name , trait , alternate_id
405256162	CV3208668	single nucleotide variant	NM_001649.4(SHROOM2):c.1426G>C (p.Gly476Arg)	SHROOM2-related disorder [RCV003939730]	benign	X	9895334	9895334	Human		name , trait , alternate_id
405288740	CV3209878	single nucleotide variant	NM_001649.4(SHROOM2):c.2453T>C (p.Leu818Pro)	SHROOM2-related disorder [RCV003961377]\|not specified [RCV004674006]	likely benign\|uncertain significance	X	9896361	9896361	Human		name , trait , alternate_id
405286982	CV3213845	single nucleotide variant	NM_001649.4(SHROOM2):c.1549C>T (p.Arg517Cys)	SHROOM2-related disorder [RCV003924241]	benign	X	9895457	9895457	Human		name , trait , alternate_id
405270949	CV3218786	single nucleotide variant	NM_001649.4(SHROOM2):c.2453T>G (p.Leu818Arg)	SHROOM2-related disorder [RCV003971553]\|not provided [RCV004703359]	likely benign	X	9896361	9896361	Human		name , trait , alternate_id
405279022	CV3220539	single nucleotide variant	NM_001649.4(SHROOM2):c.2826C>A (p.Asp942Glu)	SHROOM2-related disorder [RCV003976718]	benign	X	9898225	9898225	Human		name , trait , alternate_id
405266020	CV3220992	single nucleotide variant	NM_001649.4(SHROOM2):c.1985G>A (p.Arg662His)	SHROOM2-related disorder [RCV003969135]\|not specified [RCV005281524]	likely benign\|uncertain significance	X	9895893	9895893	Human		name , trait , alternate_id
405293052	CV3221235	single nucleotide variant	NM_001649.4(SHROOM2):c.2573C>G (p.Ala858Gly)	SHROOM2-related disorder [RCV003966769]	benign	X	9896481	9896481	Human		name , trait , alternate_id
405733171	CV3311249	single nucleotide variant	NM_001649.4(SHROOM2):c.2573C>T (p.Ala858Val)	not specified [RCV004451291]	uncertain significance	X	9896481	9896481	Human		name
405733177	CV3311250	single nucleotide variant	NM_001649.4(SHROOM2):c.2611G>A (p.Gly871Ser)	not specified [RCV004451292]	uncertain significance	X	9896519	9896519	Human		name
405733191	CV3311252	single nucleotide variant	NM_001649.4(SHROOM2):c.2833G>A (p.Glu945Lys)	not specified [RCV004451294]	uncertain significance	X	9898232	9898232	Human		name
405733197	CV3311253	single nucleotide variant	NM_001649.4(SHROOM2):c.2911C>T (p.Arg971Trp)	not specified [RCV004451295]	likely benign	X	9932194	9932194	Human		name
405733210	CV3311254	single nucleotide variant	NM_001649.4(SHROOM2):c.2960C>T (p.Pro987Leu)	not specified [RCV004451296]	uncertain significance	X	9932243	9932243	Human		name
405733118	CV3314699	single nucleotide variant	NM_001649.4(SHROOM2):c.1058C>T (p.Ala353Val)	not specified [RCV004451284]	uncertain significance	X	9894966	9894966	Human		name
405733126	CV3314700	single nucleotide variant	NM_001649.4(SHROOM2):c.1061A>G (p.Gln354Arg)	not specified [RCV004451285]	likely benign	X	9894969	9894969	Human		name
405733133	CV3314701	single nucleotide variant	NM_001649.4(SHROOM2):c.1114T>C (p.Ser372Pro)	not specified [RCV004451286]	uncertain significance	X	9895022	9895022	Human		name
405733141	CV3314702	single nucleotide variant	NM_001649.4(SHROOM2):c.1135G>A (p.Gly379Arg)	not specified [RCV004451287]	uncertain significance	X	9895043	9895043	Human		name
405733146	CV3314703	single nucleotide variant	NM_001649.4(SHROOM2):c.1742C>T (p.Pro581Leu)	not specified [RCV004451288]	uncertain significance	X	9895650	9895650	Human		name
405733156	CV3314704	single nucleotide variant	NM_001649.4(SHROOM2):c.1984C>T (p.Arg662Cys)	not specified [RCV004451289]	uncertain significance	X	9895892	9895892	Human		name
405733165	CV3314705	single nucleotide variant	NM_001649.4(SHROOM2):c.2311G>A (p.Glu771Lys)	not specified [RCV004451290]	uncertain significance	X	9896219	9896219	Human		name
407501154	CV3480596	single nucleotide variant	NM_001649.4(SHROOM2):c.1275C>A (p.Ser425Arg)	not specified [RCV004669730]	uncertain significance	X	9895183	9895183	Human		name
407501160	CV3480598	single nucleotide variant	NM_001649.4(SHROOM2):c.2869G>A (p.Glu957Lys)	not specified [RCV004669731]	likely benign	X	9898268	9898268	Human		name
407519212	CV3480599	single nucleotide variant	NM_001649.4(SHROOM2):c.1730G>T (p.Ser577Ile)	not specified [RCV004676394]	uncertain significance	X	9895638	9895638	Human		name
407501169	CV3480601	single nucleotide variant	NM_001649.4(SHROOM2):c.1619A>G (p.Lys540Arg)	not specified [RCV004669733]	likely benign	X	9895527	9895527	Human		name
407519216	CV3480605	single nucleotide variant	NM_001649.4(SHROOM2):c.1000A>G (p.Lys334Glu)	not specified [RCV004676396]	uncertain significance	X	9894908	9894908	Human		name
407501184	CV3480607	single nucleotide variant	NM_001649.4(SHROOM2):c.1685G>C (p.Ser562Thr)	not specified [RCV004669736]	uncertain significance	X	9895593	9895593	Human		name
407501193	CV3480609	single nucleotide variant	NM_001649.4(SHROOM2):c.1693C>G (p.Leu565Val)	not specified [RCV004669738]	uncertain significance	X	9895601	9895601	Human		name
597719101	CV3598892	single nucleotide variant	NM_001649.4(SHROOM2):c.2489G>A (p.Arg830Gln)	not specified [RCV004861835]	likely benign	X	9896397	9896397	Human		name
597719142	CV3598897	single nucleotide variant	NM_001649.4(SHROOM2):c.2702T>A (p.Ile901Asn)	not specified [RCV004861840]	uncertain significance	X	9896610	9896610	Human		name
597719151	CV3598898	single nucleotide variant	NM_001649.4(SHROOM2):c.1121A>G (p.His374Arg)	not specified [RCV004861841]	likely benign	X	9895029	9895029	Human		name
597719167	CV3598900	single nucleotide variant	NM_001649.4(SHROOM2):c.1673C>T (p.Ala558Val)	not specified [RCV004861843]	likely benign	X	9895581	9895581	Human		name
597719175	CV3598901	single nucleotide variant	NM_001649.4(SHROOM2):c.1786C>T (p.Arg596Cys)	not specified [RCV004861844]	uncertain significance	X	9895694	9895694	Human		name
597719202	CV3598904	single nucleotide variant	NM_001649.4(SHROOM2):c.1862G>A (p.Arg621Gln)	not specified [RCV004861847]	uncertain significance	X	9895770	9895770	Human		name
597719232	CV3598908	single nucleotide variant	NM_001649.4(SHROOM2):c.2099G>A (p.Arg700His)	not specified [RCV004861851]	uncertain significance	X	9896007	9896007	Human		name
597719254	CV3598911	single nucleotide variant	NM_001649.4(SHROOM2):c.1475C>T (p.Ala492Val)	not specified [RCV004861854]	uncertain significance	X	9895383	9895383	Human		name
597719277	CV3598914	single nucleotide variant	NM_001649.4(SHROOM2):c.2486C>T (p.Pro829Leu)	not specified [RCV004861857]	uncertain significance	X	9896394	9896394	Human		name
597719313	CV3598918	single nucleotide variant	NM_001649.4(SHROOM2):c.2324C>G (p.Thr775Arg)	not specified [RCV004861861]	uncertain significance	X	9896232	9896232	Human		name
597719330	CV3598920	single nucleotide variant	NM_001649.4(SHROOM2):c.1426G>A (p.Gly476Ser)	not specified [RCV004861863]	likely benign	X	9895334	9895334	Human		name
597719340	CV3598921	single nucleotide variant	NM_001649.4(SHROOM2):c.1717G>C (p.Asp573His)	not specified [RCV004861864]	uncertain significance	X	9895625	9895625	Human		name
597719349	CV3598922	single nucleotide variant	NM_001649.4(SHROOM2):c.1183G>A (p.Gly395Ser)	not specified [RCV004861865]	uncertain significance	X	9895091	9895091	Human		name
597719403	CV3598928	single nucleotide variant	NM_001649.4(SHROOM2):c.1801A>G (p.Ser601Gly)	not specified [RCV004861871]	uncertain significance	X	9895709	9895709	Human		name
597719411	CV3598929	single nucleotide variant	NM_001649.4(SHROOM2):c.2900A>T (p.Asp967Val)	not specified [RCV004861872]	uncertain significance	X	9932183	9932183	Human		name
597719419	CV3598930	single nucleotide variant	NM_001649.4(SHROOM2):c.1028C>T (p.Ala343Val)	not specified [RCV004861873]	likely benign	X	9894936	9894936	Human		name
598242278	CV3914300	single nucleotide variant	NM_001649.4(SHROOM2):c.2602C>T (p.Arg868Trp)	not specified [RCV005276498]	uncertain significance	X	9896510	9896510	Human		name
598242313	CV3914307	single nucleotide variant	NM_001649.4(SHROOM2):c.1846G>A (p.Val616Met)	not specified [RCV005276505]	uncertain significance	X	9895754	9895754	Human		name
598242318	CV3914308	single nucleotide variant	NM_001649.4(SHROOM2):c.2680C>A (p.Arg894Ser)	not specified [RCV005276506]	uncertain significance	X	9896588	9896588	Human		name
598242324	CV3914309	single nucleotide variant	NM_001649.4(SHROOM2):c.1033G>A (p.Ala345Thr)	not specified [RCV005276507]	likely benign	X	9894941	9894941	Human		name
598242329	CV3914310	single nucleotide variant	NM_001649.4(SHROOM2):c.1093C>T (p.Leu365Phe)	not specified [RCV005276508]	uncertain significance	X	9895001	9895001	Human		name
598242353	CV3914315	single nucleotide variant	NM_001649.4(SHROOM2):c.2084C>T (p.Thr695Met)	not specified [RCV005276513]	uncertain significance	X	9895992	9895992	Human		name
598242359	CV3914316	single nucleotide variant	NM_001649.4(SHROOM2):c.2858C>T (p.Ala953Val)	not specified [RCV005276514]	uncertain significance	X	9898257	9898257	Human		name
15104588	CV706339	single nucleotide variant	NM_001649.4(SHROOM2):c.2195T>A (p.Leu732Gln)	SHROOM2-related disorder [RCV003916008]\|not provided [RCV000959716]	benign	X	9896103	9896103	Human		name , trait , alternate_id
15136841	CV717882	single nucleotide variant	NM_001649.4(SHROOM2):c.2495C>T (p.Ala832Val)	SHROOM2-related disorder [RCV003926260]\|not provided [RCV000965516]	benign	X	9896403	9896403	Human		name , trait , alternate_id
8628755	CV83899	single nucleotide variant	NM_001649.2(SHROOM2):c.1192C>T (p.Pro398Ser)	Malignant melanoma [RCV000063980]	not provided	X	9895100	9895100	Human		name
8628756	CV83900	single nucleotide variant	NM_001649.2(SHROOM2):c.1193C>T (p.Pro398Leu)	Malignant melanoma [RCV000063981]	not provided	X	9895101	9895101	Human		name
155265090	CV1695469	single nucleotide variant	NM_001649.4(SHROOM2):c.3811G>C (p.Glu1271Gln)	not provided [RCV002280032]	uncertain significance	X	9937357	9937357	Human		name
155265337	CV1695530	single nucleotide variant	NM_001649.4(SHROOM2):c.4769G>A (p.Arg1590Gln)	not provided [RCV002280262]\|not specified [RCV004857895]	uncertain significance	X	9946855	9946855	Human		name
156200184	CV2237673	single nucleotide variant	NM_001649.4(SHROOM2):c.3176G>A (p.Arg1059Lys)	not specified [RCV004106598]	uncertain significance	X	9932459	9932459	Human		name
156267384	CV2243982	single nucleotide variant	NM_001649.4(SHROOM2):c.4366G>A (p.Glu1456Lys)	not specified [RCV004108480]	uncertain significance	X	9944695	9944695	Human		name
155924751	CV2248857	single nucleotide variant	NM_001649.4(SHROOM2):c.3573T>A (p.Asp1191Glu)	not specified [RCV004115869]	uncertain significance	X	9932856	9932856	Human		name
156085875	CV2249364	single nucleotide variant	NM_001649.4(SHROOM2):c.3808C>T (p.Pro1270Ser)	not specified [RCV004118376]	uncertain significance	X	9937354	9937354	Human		name
156315730	CV2250813	single nucleotide variant	NM_001649.4(SHROOM2):c.3266T>A (p.Val1089Asp)	not specified [RCV004129673]	uncertain significance	X	9932549	9932549	Human		name
156253395	CV2284049	single nucleotide variant	NM_001649.4(SHROOM2):c.3478C>G (p.Arg1160Gly)	not specified [RCV004144655]	uncertain significance	X	9932761	9932761	Human		name
156237966	CV2285845	single nucleotide variant	NM_001649.4(SHROOM2):c.3661C>A (p.Pro1221Thr)	not specified [RCV004143788]	uncertain significance	X	9937207	9937207	Human		name
156017231	CV2295537	single nucleotide variant	NM_001649.4(SHROOM2):c.3571G>A (p.Asp1191Asn)	not specified [RCV004160637]	uncertain significance	X	9932854	9932854	Human		name
156296449	CV2297575	single nucleotide variant	NM_001649.4(SHROOM2):c.3322C>T (p.Arg1108Cys)	not specified [RCV004155278]	uncertain significance	X	9932605	9932605	Human		name
156242127	CV2346974	single nucleotide variant	NM_001649.4(SHROOM2):c.3065C>T (p.Ser1022Leu)	not specified [RCV004202419]	uncertain significance	X	9932348	9932348	Human		name
155905480	CV2349774	single nucleotide variant	NM_001649.4(SHROOM2):c.3050G>A (p.Arg1017Gln)	not specified [RCV004204186]	uncertain significance	X	9932333	9932333	Human		name
155992357	CV2379303	single nucleotide variant	NM_001649.4(SHROOM2):c.4411G>A (p.Glu1471Lys)	not specified [RCV004223770]	uncertain significance	X	9944740	9944740	Human		name
156451073	CV2402450	single nucleotide variant	NM_001649.4(SHROOM2):c.4121C>T (p.Pro1374Leu)	not provided [RCV003123251]	uncertain significance	X	9937667	9937667	Human		name
329370868	CV2435711	single nucleotide variant	NM_001649.4(SHROOM2):c.3209G>A (p.Arg1070His)	not specified [RCV004254943]	uncertain significance	X	9932492	9932492	Human		name
329353720	CV2439585	single nucleotide variant	NM_001649.4(SHROOM2):c.3025C>T (p.Arg1009Trp)	not specified [RCV004255605]	uncertain significance	X	9932308	9932308	Human		name
329365918	CV2441232	single nucleotide variant	NM_001649.4(SHROOM2):c.4105C>A (p.Pro1369Thr)	not specified [RCV004263621]	uncertain significance	X	9937651	9937651	Human		name
329372586	CV2443179	single nucleotide variant	NM_001649.4(SHROOM2):c.4294G>A (p.Asp1432Asn)	not specified [RCV004255372]	uncertain significance	X	9939349	9939349	Human		name
329394708	CV2461541	single nucleotide variant	NM_001649.4(SHROOM2):c.3172A>G (p.Lys1058Glu)	not specified [RCV004269458]	uncertain significance	X	9932455	9932455	Human		name
329352813	CV2470559	single nucleotide variant	NM_001649.4(SHROOM2):c.4019T>C (p.Ile1340Thr)	not specified [RCV004273563]	uncertain significance	X	9937565	9937565	Human		name
329376614	CV2472268	single nucleotide variant	NM_001649.4(SHROOM2):c.3464A>T (p.Lys1155Met)	not specified [RCV004283374]	uncertain significance	X	9932747	9932747	Human		name
401731493	CV2674392	single nucleotide variant	NM_001649.4(SHROOM2):c.3401G>A (p.Arg1134His)	not specified [RCV004289262]	uncertain significance	X	9932684	9932684	Human		name
401741542	CV2677382	single nucleotide variant	NM_001649.4(SHROOM2):c.3421G>A (p.Gly1141Arg)	not specified [RCV004289463]	uncertain significance	X	9932704	9932704	Human		name
401719084	CV2679412	single nucleotide variant	NM_001649.4(SHROOM2):c.3880C>T (p.Arg1294Cys)	not specified [RCV004285939]	uncertain significance	X	9937426	9937426	Human		name
401727286	CV2684551	single nucleotide variant	NM_001649.4(SHROOM2):c.3966G>C (p.Glu1322Asp)	not specified [RCV004293662]	uncertain significance	X	9937512	9937512	Human		name
401782286	CV2686655	single nucleotide variant	NM_001649.4(SHROOM2):c.3533C>G (p.Pro1178Arg)	not specified [RCV004300068]	uncertain significance	X	9932816	9932816	Human		name
401741507	CV2697564	single nucleotide variant	NM_001649.4(SHROOM2):c.3238G>A (p.Gly1080Ser)	not specified [RCV004298320]	likely benign	X	9932521	9932521	Human		name
401729647	CV2733211	single nucleotide variant	NM_001649.4(SHROOM2):c.4576G>A (p.Gly1526Ser)	not specified [RCV004332129]	uncertain significance	X	9944905	9944905	Human		name
401879308	CV2758267	single nucleotide variant	NM_001649.4(SHROOM2):c.4168G>A (p.Val1390Met)	not specified [RCV004341625]	uncertain significance	X	9939223	9939223	Human		name
401876230	CV2777716	single nucleotide variant	NM_001649.4(SHROOM2):c.3529G>A (p.Ala1177Thr)	not specified [RCV004345552]	uncertain significance	X	9932812	9932812	Human		name
401890723	CV2778315	single nucleotide variant	NM_001649.4(SHROOM2):c.3380C>T (p.Pro1127Leu)	not specified [RCV004350368]	uncertain significance	X	9932663	9932663	Human		name
401897519	CV2787125	single nucleotide variant	NM_001649.4(SHROOM2):c.3537G>C (p.Gln1179His)	not specified [RCV004360559]	uncertain significance	X	9932820	9932820	Human		name
401875360	CV2789029	single nucleotide variant	NM_001649.4(SHROOM2):c.3553C>A (p.Pro1185Thr)	not specified [RCV004363335]	uncertain significance	X	9932836	9932836	Human		name
404993569	CV2851008	single nucleotide variant	NM_001649.4(SHROOM2):c.4718C>T (p.Ala1573Val)	not provided [RCV003491479]	uncertain significance	X	9946804	9946804	Human		name
405272296	CV3199311	single nucleotide variant	NM_001649.4(SHROOM2):c.4423A>G (p.Ile1475Val)	SHROOM2-related disorder [RCV003914261]	benign	X	9944752	9944752	Human		name , trait , alternate_id
405285154	CV3202472	single nucleotide variant	NM_001649.4(SHROOM2):c.3657C>A (p.Ser1219Arg)	SHROOM2-related disorder [RCV003909735]	likely benign	X	9937203	9937203	Human		name , trait , alternate_id
405271565	CV3209486	single nucleotide variant	NM_001649.4(SHROOM2):c.3991G>T (p.Ala1331Ser)	SHROOM2-related disorder [RCV003949801]	likely benign	X	9937537	9937537	Human		name , trait , alternate_id
405265633	CV3215610	single nucleotide variant	NM_001649.4(SHROOM2):c.4163C>T (p.Ala1388Val)	SHROOM2-related disorder [RCV003946793]	likely benign	X	9939218	9939218	Human		name , trait , alternate_id
405287597	CV3217860	single nucleotide variant	NM_001649.4(SHROOM2):c.4821G>C (p.Leu1607Phe)	SHROOM2-related disorder [RCV003981983]	benign	X	9946907	9946907	Human		name , trait , alternate_id
405272979	CV3220449	single nucleotide variant	NM_001649.4(SHROOM2):c.3854G>T (p.Gly1285Val)	SHROOM2-related disorder [RCV003972267]	benign	X	9937400	9937400	Human		name , trait , alternate_id
405733217	CV3311255	single nucleotide variant	NM_001649.4(SHROOM2):c.3125A>G (p.His1042Arg)	not specified [RCV004451297]	uncertain significance	X	9932408	9932408	Human		name
405733225	CV3311256	single nucleotide variant	NM_001649.4(SHROOM2):c.3604G>A (p.Asp1202Asn)	not specified [RCV004451298]	uncertain significance	X	9937150	9937150	Human		name
405733239	CV3311258	single nucleotide variant	NM_001649.4(SHROOM2):c.3752G>A (p.Ser1251Asn)	not specified [RCV004451300]	uncertain significance	X	9937298	9937298	Human		name
405733246	CV3311259	single nucleotide variant	NM_001649.4(SHROOM2):c.4355G>A (p.Arg1452Gln)	not specified [RCV004451301]	uncertain significance	X	9944684	9944684	Human		name
405733253	CV3311260	single nucleotide variant	NM_001649.4(SHROOM2):c.4746G>T (p.Lys1582Asn)	not specified [RCV004451302]	uncertain significance	X	9946832	9946832	Human		name
407501164	CV3480600	single nucleotide variant	NM_001649.4(SHROOM2):c.4184A>G (p.Asn1395Ser)	not specified [RCV004669732]	uncertain significance	X	9939239	9939239	Human		name
407519214	CV3480602	single nucleotide variant	NM_001649.4(SHROOM2):c.3847C>A (p.Pro1283Thr)	not specified [RCV004676395]	uncertain significance	X	9937393	9937393	Human		name
407501173	CV3480603	single nucleotide variant	NM_001649.4(SHROOM2):c.3038G>A (p.Gly1013Glu)	not specified [RCV004669734]	uncertain significance	X	9932321	9932321	Human		name
407519218	CV3480606	single nucleotide variant	NM_001649.4(SHROOM2):c.4118C>A (p.Ser1373Tyr)	not specified [RCV004676397]	uncertain significance	X	9937664	9937664	Human		name
407501188	CV3480608	single nucleotide variant	NM_001649.4(SHROOM2):c.3062A>C (p.Tyr1021Ser)	not specified [RCV004669737]	uncertain significance	X	9932345	9932345	Human		name
407501198	CV3480610	single nucleotide variant	NM_001649.4(SHROOM2):c.4109A>G (p.Lys1370Arg)	not specified [RCV004669739]	uncertain significance	X	9937655	9937655	Human		name
597719159	CV3598899	single nucleotide variant	NM_001649.4(SHROOM2):c.3814G>T (p.Ala1272Ser)	not specified [RCV004861842]	uncertain significance	X	9937360	9937360	Human		name
597719184	CV3598902	single nucleotide variant	NM_001649.4(SHROOM2):c.4156G>A (p.Val1386Met)	not specified [RCV004861845]	uncertain significance	X	9939211	9939211	Human		name
597719209	CV3598905	single nucleotide variant	NM_001649.4(SHROOM2):c.3479G>A (p.Arg1160His)	not specified [RCV004861848]	uncertain significance	X	9932762	9932762	Human		name
597719225	CV3598907	single nucleotide variant	NM_001649.4(SHROOM2):c.3614C>A (p.Thr1205Asn)	not specified [RCV004861850]	uncertain significance	X	9937160	9937160	Human		name
597719238	CV3598909	single nucleotide variant	NM_001649.4(SHROOM2):c.4363C>T (p.Arg1455Cys)	not specified [RCV004861852]	uncertain significance	X	9944692	9944692	Human		name
597719295	CV3598916	single nucleotide variant	NM_001649.4(SHROOM2):c.4294G>C (p.Asp1432His)	not specified [RCV004861859]	uncertain significance	X	9939349	9939349	Human		name
597719304	CV3598917	single nucleotide variant	NM_001649.4(SHROOM2):c.3439C>G (p.Leu1147Val)	not specified [RCV004861860]	uncertain significance	X	9932722	9932722	Human		name
597719321	CV3598919	single nucleotide variant	NM_001649.4(SHROOM2):c.3986C>T (p.Ser1329Phe)	not specified [RCV004861862]	uncertain significance	X	9937532	9937532	Human		name
597719386	CV3598926	single nucleotide variant	NM_001649.4(SHROOM2):c.4267G>A (p.Glu1423Lys)	not specified [RCV004861869]	uncertain significance	X	9939322	9939322	Human		name
598242267	CV3914297	single nucleotide variant	NM_001649.4(SHROOM2):c.3032G>T (p.Arg1011Leu)	not specified [RCV005276496]	uncertain significance	X	9932315	9932315	Human		name
598199336	CV3914298	single nucleotide variant	NM_001649.4(SHROOM2):c.4282G>A (p.Asp1428Asn)	not specified [RCV005268379]	uncertain significance	X	9939337	9939337	Human		name
598242271	CV3914299	single nucleotide variant	NM_001649.4(SHROOM2):c.4336C>T (p.Arg1446Cys)	not specified [RCV005276497]	uncertain significance	X	9944665	9944665	Human		name
598242282	CV3914301	single nucleotide variant	NM_001649.4(SHROOM2):c.3241G>A (p.Ala1081Thr)	not specified [RCV005276499]	likely benign	X	9932524	9932524	Human		name
598242294	CV3914303	single nucleotide variant	NM_001649.4(SHROOM2):c.4069C>T (p.Leu1357Phe)	not specified [RCV005276501]	uncertain significance	X	9937615	9937615	Human		name
598242298	CV3914304	single nucleotide variant	NM_001649.4(SHROOM2):c.3545C>T (p.Thr1182Met)	not specified [RCV005276502]	uncertain significance	X	9932828	9932828	Human		name
598242304	CV3914305	single nucleotide variant	NM_001649.4(SHROOM2):c.3884G>T (p.Cys1295Phe)	not specified [RCV005276503]	uncertain significance	X	9937430	9937430	Human		name
598242308	CV3914306	single nucleotide variant	NM_001649.4(SHROOM2):c.4354C>T (p.Arg1452Trp)	not specified [RCV005276504]	uncertain significance	X	9944683	9944683	Human		name
598242342	CV3914313	single nucleotide variant	NM_001649.4(SHROOM2):c.3433C>T (p.Arg1145Cys)	not specified [RCV005276511]	likely benign	X	9932716	9932716	Human		name
598242347	CV3914314	single nucleotide variant	NM_001649.4(SHROOM2):c.3286A>T (p.Thr1096Ser)	not specified [RCV005276512]	uncertain significance	X	9932569	9932569	Human		name
598242364	CV3914317	single nucleotide variant	NM_001649.4(SHROOM2):c.3912G>A (p.Met1304Ile)	not specified [RCV005276515]	uncertain significance	X	9937458	9937458	Human		name

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