Grwd1 Variant Search Result - Rat Genome Database

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77 records found for search term Grwd1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405271444	CV3219083	single nucleotide variant	NM_031485.4(GRWD1):c.*4G>A	GRWD1-related disorder [RCV003971791]	likely benign	19	48453029	48453029	Human		name , trait , alternate_id
405261165	CV3212439	single nucleotide variant	NM_031485.4(GRWD1):c.1024-10C>A	GRWD1-related disorder [RCV003944413]	likely benign	19	48452698	48452698	Human		name , trait , alternate_id
405257998	CV3207997	single nucleotide variant	NM_031485.4(GRWD1):c.100C>T (p.Leu34=)	GRWD1-related disorder [RCV003941463]	likely benign	19	48446105	48446105	Human		name , trait , alternate_id
405772275	CV3259000	single nucleotide variant	NM_031485.4(GRWD1):c.10C>T (p.Arg4Cys)	not specified [RCV004396141]	uncertain significance	19	48446015	48446015	Human		name
407504391	CV3433389	single nucleotide variant	NM_031485.4(GRWD1):c.13A>G (p.Lys5Glu)	not specified [RCV004624061]	uncertain significance	19	48446018	48446018	Human		name
156098258	CV2392771	single nucleotide variant	NM_031485.4(GRWD1):c.55G>A (p.Ala19Thr)	not specified [RCV004247137]	uncertain significance	19	48446060	48446060	Human		name
405280806	CV3195731	single nucleotide variant	NM_031485.4(GRWD1):c.741C>T (p.Gly247=)	GRWD1-related disorder [RCV003906963]	likely benign	19	48450724	48450724	Human		name , trait , alternate_id
405295450	CV3204706	single nucleotide variant	NM_031485.4(GRWD1):c.849C>T (p.Asp283=)	GRWD1-related disorder [RCV003937355]\|not specified [RCV005353327]	likely benign	19	48451057	48451057	Human	1	name , trait , alternate_id
405294557	CV3208880	single nucleotide variant	NM_031485.4(GRWD1):c.930C>T (p.Asp310=)	GRWD1-related disorder [RCV003934459]	likely benign	19	48451138	48451138	Human		name , trait , alternate_id
405272736	CV3210132	single nucleotide variant	NM_031485.4(GRWD1):c.753C>T (p.His251=)	GRWD1-related disorder [RCV003914380]	likely benign	19	48450736	48450736	Human		name , trait , alternate_id
405293650	CV3214358	single nucleotide variant	NM_031485.4(GRWD1):c.876G>A (p.Arg292=)	GRWD1-related disorder [RCV003932049]	likely benign	19	48451084	48451084	Human		name , trait , alternate_id
597771323	CV3688511	single nucleotide variant	NM_031485.4(GRWD1):c.43G>A (p.Glu15Lys)	not specified [RCV004928435]	uncertain significance	19	48446048	48446048	Human		name
598235018	CV3978321	single nucleotide variant	NM_031485.4(GRWD1):c.65G>A (p.Gly22Asp)	not specified [RCV005342993]	uncertain significance	19	48446070	48446070	Human		name
156352016	CV2323880	single nucleotide variant	NM_031485.4(GRWD1):c.211A>G (p.Ile71Val)	not specified [RCV004176411]	uncertain significance	19	48446408	48446408	Human		name
405267867	CV3198440	single nucleotide variant	NM_031485.4(GRWD1):c.1098C>T (p.Ser366=)	GRWD1-related disorder [RCV003911808]	likely benign	19	48452782	48452782	Human		name , trait , alternate_id
405292899	CV3210453	single nucleotide variant	NM_031485.4(GRWD1):c.224A>G (p.His75Arg)	GRWD1-related disorder [RCV003931417]	likely benign	19	48446421	48446421	Human		name , trait , alternate_id
405772318	CV3259007	single nucleotide variant	NM_031485.4(GRWD1):c.232G>A (p.Asp78Asn)	not specified [RCV004396148]	uncertain significance	19	48446429	48446429	Human		name
598189223	CV3978319	single nucleotide variant	NM_031485.4(GRWD1):c.131G>A (p.Gly44Glu)	not specified [RCV005353964]	uncertain significance	19	48446136	48446136	Human		name
150470110	CV1268208	single nucleotide variant	NM_031485.4(GRWD1):c.956G>A (p.Arg319Gln)	not provided [RCV001695072]	benign	19	48451164	48451164	Human		name
9687095	CV171637	single nucleotide variant	NM_031485.4(GRWD1):c.593G>A (p.Arg198Gln)	Prostate cancer [RCV000149314]\|not specified [RCV004019790]	uncertain significance	19	48450437	48450437	Human	2	name
156261526	CV2216460	single nucleotide variant	NM_031485.4(GRWD1):c.859C>T (p.Arg287Cys)	not specified [RCV004097274]	uncertain significance	19	48451067	48451067	Human		name
156255673	CV2264748	single nucleotide variant	NM_031485.4(GRWD1):c.908C>T (p.Thr303Ile)	not specified [RCV004132727]	uncertain significance	19	48451116	48451116	Human		name
156019212	CV2272544	single nucleotide variant	NM_031485.4(GRWD1):c.754G>A (p.Val252Met)	not specified [RCV004133441]	uncertain significance	19	48450737	48450737	Human		name
156031735	CV2274958	single nucleotide variant	NM_031485.4(GRWD1):c.703T>C (p.Cys235Arg)	not specified [RCV004135008]	uncertain significance	19	48450686	48450686	Human		name
156281378	CV2316058	single nucleotide variant	NM_031485.4(GRWD1):c.454A>G (p.Ile152Val)	not specified [RCV004165935]	uncertain significance	19	48446829	48446829	Human		name
155913563	CV2341808	single nucleotide variant	NM_031485.4(GRWD1):c.782C>T (p.Thr261Ile)	not specified [RCV004184764]	uncertain significance	19	48450765	48450765	Human		name
156063859	CV2349692	single nucleotide variant	NM_031485.4(GRWD1):c.739G>A (p.Gly247Ser)	not specified [RCV004204108]	uncertain significance	19	48450722	48450722	Human		name
156223974	CV2355621	single nucleotide variant	NM_031485.4(GRWD1):c.686G>A (p.Arg229His)	not specified [RCV004205462]	uncertain significance	19	48450669	48450669	Human		name
329392740	CV2439151	single nucleotide variant	NM_031485.4(GRWD1):c.545G>A (p.Arg182Gln)	not specified [RCV004266432]	uncertain significance	19	48450389	48450389	Human		name
401746561	CV2691935	single nucleotide variant	NM_031485.4(GRWD1):c.916G>A (p.Ala306Thr)	not specified [RCV004301669]	uncertain significance	19	48451124	48451124	Human		name
401781498	CV2731634	single nucleotide variant	NM_031485.4(GRWD1):c.953G>A (p.Arg318His)	not specified [RCV004331741]	uncertain significance	19	48451161	48451161	Human		name
401868032	CV2767134	single nucleotide variant	NM_031485.4(GRWD1):c.784C>T (p.Arg262Cys)	not specified [RCV004347533]	uncertain significance	19	48450767	48450767	Human		name
401896601	CV2791729	single nucleotide variant	NM_031485.4(GRWD1):c.671C>A (p.Pro224His)	not specified [RCV004353057]	uncertain significance	19	48450515	48450515	Human		name
405772323	CV3259008	single nucleotide variant	NM_031485.4(GRWD1):c.352C>A (p.Pro118Thr)	not specified [RCV004396149]	uncertain significance	19	48446727	48446727	Human		name
405772330	CV3259009	single nucleotide variant	NM_031485.4(GRWD1):c.389A>T (p.Asp130Val)	not specified [RCV004396150]	uncertain significance	19	48446764	48446764	Human		name
405772336	CV3259010	single nucleotide variant	NM_031485.4(GRWD1):c.397G>A (p.Asp133Asn)	not specified [RCV004396151]	uncertain significance	19	48446772	48446772	Human		name
405772343	CV3259011	single nucleotide variant	NM_031485.4(GRWD1):c.403G>A (p.Glu135Lys)	not specified [RCV004396152]	uncertain significance	19	48446778	48446778	Human		name
405772349	CV3259012	single nucleotide variant	NM_031485.4(GRWD1):c.580G>A (p.Ala194Thr)	not specified [RCV004396153]	uncertain significance	19	48450424	48450424	Human		name
405772361	CV3259014	single nucleotide variant	NM_031485.4(GRWD1):c.668C>G (p.Ser223Cys)	not specified [RCV004396155]	uncertain significance	19	48450512	48450512	Human		name
405772369	CV3259015	single nucleotide variant	NM_031485.4(GRWD1):c.676G>A (p.Val226Met)	not specified [RCV004396156]	uncertain significance	19	48450520	48450520	Human		name
405772374	CV3259016	single nucleotide variant	NM_031485.4(GRWD1):c.697G>A (p.Gly233Ser)	not specified [RCV004396157]	uncertain significance	19	48450680	48450680	Human		name
405772386	CV3259018	single nucleotide variant	NM_031485.4(GRWD1):c.812C>T (p.Pro271Leu)	not specified [RCV004396159]	uncertain significance	19	48450795	48450795	Human		name
405772392	CV3259019	single nucleotide variant	NM_031485.4(GRWD1):c.860G>A (p.Arg287His)	not specified [RCV004396160]	uncertain significance	19	48451068	48451068	Human		name
405772398	CV3259020	single nucleotide variant	NM_031485.4(GRWD1):c.875G>A (p.Arg292Gln)	not specified [RCV004396161]	uncertain significance	19	48451083	48451083	Human		name
405772402	CV3259021	single nucleotide variant	NM_031485.4(GRWD1):c.878C>T (p.Ala293Val)	not specified [RCV004396162]	uncertain significance	19	48451086	48451086	Human		name
405772408	CV3259022	single nucleotide variant	NM_031485.4(GRWD1):c.974G>A (p.Ser325Asn)	not specified [RCV004396163]	uncertain significance	19	48451182	48451182	Human		name
405772420	CV3259024	single nucleotide variant	NM_031485.4(GRWD1):c.979G>A (p.Gly327Arg)	not specified [RCV004396165]	uncertain significance	19	48451187	48451187	Human		name
597625469	CV3410868	single nucleotide variant	NM_031485.4(GRWD1):c.920A>G (p.His307Arg)	Congenital diarrhea [RCV004994442]\|DIARRHEA 14, CONGENITAL [RCV005256515]	pathogenic\|likely pathogenic	19	48451128	48451128	Human	2	name
407463903	CV3433390	single nucleotide variant	NM_031485.4(GRWD1):c.365G>C (p.Ser122Thr)	not specified [RCV004634946]	uncertain significance	19	48446740	48446740	Human		name
597771329	CV3688509	single nucleotide variant	NM_031485.4(GRWD1):c.541C>G (p.Arg181Gly)	not specified [RCV004928434]	uncertain significance	19	48450385	48450385	Human		name
597756215	CV3688510	single nucleotide variant	NM_031485.4(GRWD1):c.592C>T (p.Arg198Trp)	not specified [RCV004924821]	uncertain significance	19	48450436	48450436	Human		name
597756219	CV3688512	single nucleotide variant	NM_031485.4(GRWD1):c.674G>A (p.Arg225Gln)	not specified [RCV004924822]	uncertain significance	19	48450518	48450518	Human		name
597771101	CV3688517	single nucleotide variant	NM_031485.4(GRWD1):c.431C>T (p.Ala144Val)	not specified [RCV004928439]	uncertain significance	19	48446806	48446806	Human		name
598189215	CV3978318	single nucleotide variant	NM_031485.4(GRWD1):c.604G>A (p.Ala202Thr)	not specified [RCV005353963]	uncertain significance	19	48450448	48450448	Human		name
598189237	CV3978322	single nucleotide variant	NM_031485.4(GRWD1):c.634G>A (p.Gly212Arg)	not specified [RCV005353966]	uncertain significance	19	48450478	48450478	Human		name
598235026	CV3978323	single nucleotide variant	NM_031485.4(GRWD1):c.415C>A (p.Pro139Thr)	not specified [RCV005342994]	uncertain significance	19	48446790	48446790	Human		name
598189245	CV3978324	single nucleotide variant	NM_031485.4(GRWD1):c.668C>T (p.Ser223Phe)	not specified [RCV005353967]	uncertain significance	19	48450512	48450512	Human		name
598189251	CV3978325	single nucleotide variant	NM_031485.4(GRWD1):c.976G>A (p.Gly326Ser)	not specified [RCV005353968]	uncertain significance	19	48451184	48451184	Human		name
156168352	CV2197680	single nucleotide variant	NM_031485.4(GRWD1):c.1039G>A (p.Ala347Thr)	not specified [RCV004074888]	uncertain significance	19	48452723	48452723	Human		name
156400467	CV2199200	single nucleotide variant	NM_031485.4(GRWD1):c.1168G>C (p.Glu390Gln)	not specified [RCV004080587]	uncertain significance	19	48452852	48452852	Human		name
155978357	CV2247041	single nucleotide variant	NM_031485.4(GRWD1):c.1017G>C (p.Gln339His)	not specified [RCV004114597]	uncertain significance	19	48451225	48451225	Human		name
156124615	CV2285770	single nucleotide variant	NM_031485.4(GRWD1):c.1225T>G (p.Phe409Val)	not specified [RCV004141907]	uncertain significance	19	48452909	48452909	Human		name
401859987	CV2765426	single nucleotide variant	NM_031485.4(GRWD1):c.1325G>A (p.Arg442His)	not provided [RCV004696503]\|not specified [RCV004341745]	uncertain significance	19	48453009	48453009	Human		name
401887563	CV2772015	single nucleotide variant	NM_031485.4(GRWD1):c.1108G>C (p.Ala370Pro)	not specified [RCV004344693]	uncertain significance	19	48452792	48452792	Human		name
405295062	CV3210959	single nucleotide variant	NM_031485.4(GRWD1):c.1057G>A (p.Val353Met)	GRWD1-related disorder [RCV003936968]	benign	19	48452741	48452741	Human		name , trait , alternate_id
405772281	CV3259001	single nucleotide variant	NM_031485.4(GRWD1):c.1114T>G (p.Ser372Ala)	not specified [RCV004396142]	uncertain significance	19	48452798	48452798	Human		name
405772287	CV3259002	single nucleotide variant	NM_031485.4(GRWD1):c.1160G>A (p.Arg387Gln)	not specified [RCV004396143]	uncertain significance	19	48452844	48452844	Human		name
405772293	CV3259003	single nucleotide variant	NM_031485.4(GRWD1):c.1172C>T (p.Ala391Val)	not specified [RCV004396144]	uncertain significance	19	48452856	48452856	Human		name
405772299	CV3259004	single nucleotide variant	NM_031485.4(GRWD1):c.1180G>A (p.Val394Met)	not specified [RCV004396145]	uncertain significance	19	48452864	48452864	Human		name
405772305	CV3259005	single nucleotide variant	NM_031485.4(GRWD1):c.1324C>T (p.Arg442Cys)	not specified [RCV004396146]	uncertain significance	19	48453008	48453008	Human		name
597625473	CV3410869	single nucleotide variant	NM_031485.4(GRWD1):c.1102G>T (p.Val368Phe)	Congenital diarrhea [RCV004994443]\|DIARRHEA 14, CONGENITAL [RCV005256516]	pathogenic\|likely pathogenic	19	48452786	48452786	Human	2	name
597771208	CV3688513	single nucleotide variant	NM_031485.4(GRWD1):c.1271C>T (p.Pro424Leu)	not specified [RCV004928436]	uncertain significance	19	48452955	48452955	Human		name
597771092	CV3688514	single nucleotide variant	NM_031485.4(GRWD1):c.1069A>G (p.Thr357Ala)	not specified [RCV004928437]	uncertain significance	19	48452753	48452753	Human		name
597771096	CV3688515	single nucleotide variant	NM_031485.4(GRWD1):c.1189G>A (p.Asp397Asn)	not specified [RCV004928438]	uncertain significance	19	48452873	48452873	Human		name
597756222	CV3688516	single nucleotide variant	NM_031485.4(GRWD1):c.1297A>G (p.Thr433Ala)	not specified [RCV004924823]	uncertain significance	19	48452981	48452981	Human		name
597756226	CV3688518	single nucleotide variant	NM_031485.4(GRWD1):c.1012C>G (p.Arg338Gly)	not specified [RCV004924824]	uncertain significance	19	48451220	48451220	Human		name
598189229	CV3978320	single nucleotide variant	NM_031485.4(GRWD1):c.1246G>A (p.Glu416Lys)	not specified [RCV005353965]	uncertain significance	19	48452930	48452930	Human		name

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