Wiz Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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95 records found for search term Wiz

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8636641	CV91866	single nucleotide variant	NM_021241.2(WIZ):c.683G>A (p.Arg228Gln)	Malignant melanoma [RCV000071964]	not provided	19	15427380	15427380	Human		name
401880782	CV2780335	single nucleotide variant	NM_001371589.1(WIZ):c.71C>T (p.Pro24Leu)	not specified [RCV004357740]	uncertain significance	19	15448237	15448237	Human		name
156037801	CV2218683	single nucleotide variant	NM_001371589.1(WIZ):c.133C>T (p.Arg45Trp)	not specified [RCV004090932]	uncertain significance	19	15448175	15448175	Human		name
329393252	CV2466821	single nucleotide variant	NM_001371589.1(WIZ):c.145T>C (p.Tyr49His)	not specified [RCV004280763]	uncertain significance	19	15448163	15448163	Human		name
597739899	CV3630324	single nucleotide variant	NM_001371589.1(WIZ):c.194G>T (p.Gly65Val)	not specified [RCV004890426]	uncertain significance	19	15448114	15448114	Human		name
401937104	CV2811760	single nucleotide variant	NM_001371589.1(WIZ):c.3681C>A (p.Pro1227=)	not provided [RCV003415124]	likely benign	19	15428243	15428243	Human		name
405811838	CV3352796	single nucleotide variant	NM_001371589.1(WIZ):c.4503G>A (p.Ser1501=)	not specified [RCV004482994]	likely benign	19	15425632	15425632	Human		name
156179435	CV2298377	single nucleotide variant	NM_001371589.1(WIZ):c.2461T>A (p.Phe821Ile)	not specified [RCV004160268]	uncertain significance	19	15437085	15437085	Human		name
401908519	CV2811761	single nucleotide variant	NM_001371589.1(WIZ):c.1825C>T (p.Arg609Trp)	not provided [RCV003423417]	likely benign	19	15439169	15439169	Human		name
407465463	CV3487903	single nucleotide variant	NM_001371589.1(WIZ):c.2626C>G (p.Arg876Gly)	not specified [RCV004688775]	uncertain significance	19	15436920	15436920	Human		name
597739904	CV3630325	single nucleotide variant	NM_001371589.1(WIZ):c.2506G>A (p.Ala836Thr)	not specified [RCV004890427]	uncertain significance	19	15437040	15437040	Human		name
156399754	CV2202196	single nucleotide variant	NM_001371589.1(WIZ):c.4117C>T (p.Pro1373Ser)	not specified [RCV004078143]	uncertain significance	19	15427231	15427231	Human		name
156366668	CV2203374	single nucleotide variant	NM_001371589.1(WIZ):c.4621G>A (p.Ala1541Thr)	not specified [RCV004072603]	uncertain significance	19	15425514	15425514	Human		name
155978388	CV2222677	single nucleotide variant	NM_001371589.1(WIZ):c.4136C>T (p.Pro1379Leu)	not specified [RCV004101539]	uncertain significance	19	15427212	15427212	Human		name
156252918	CV2232456	single nucleotide variant	NM_001371589.1(WIZ):c.5437C>T (p.Pro1813Ser)	not specified [RCV004099073]	uncertain significance	19	15424256	15424256	Human		name
156019068	CV2233359	single nucleotide variant	NM_001371589.1(WIZ):c.5002G>A (p.Val1668Ile)	not specified [RCV004105724]	uncertain significance	19	15424925	15424925	Human		name
156124640	CV2237395	single nucleotide variant	NM_001371589.1(WIZ):c.5600C>G (p.Ser1867Cys)	not specified [RCV004106367]	uncertain significance	19	15423146	15423146	Human		name
156181105	CV2246152	single nucleotide variant	NM_001371589.1(WIZ):c.5575C>T (p.Arg1859Trp)	not specified [RCV004114048]	uncertain significance	19	15423171	15423171	Human		name
156098033	CV2253235	single nucleotide variant	NM_001371589.1(WIZ):c.3899C>T (p.Ala1300Val)	not specified [RCV004122779]	uncertain significance	19	15427449	15427449	Human		name
155993962	CV2253638	single nucleotide variant	NM_001371589.1(WIZ):c.4372C>T (p.Arg1458Trp)	not specified [RCV004125316]	uncertain significance	19	15425763	15425763	Human		name
156359845	CV2257981	single nucleotide variant	NM_001371589.1(WIZ):c.5222C>G (p.Ala1741Gly)	not specified [RCV004129789]	uncertain significance	19	15424705	15424705	Human		name
156340993	CV2268205	single nucleotide variant	NM_001371589.1(WIZ):c.5069A>G (p.Tyr1690Cys)	not specified [RCV004138511]	uncertain significance	19	15424858	15424858	Human		name
156291287	CV2296622	single nucleotide variant	NM_001371589.1(WIZ):c.5267C>T (p.Pro1756Leu)	not specified [RCV004154680]	uncertain significance	19	15424660	15424660	Human		name
155912594	CV2308912	single nucleotide variant	NM_001371589.1(WIZ):c.4109A>C (p.His1370Pro)	not specified [RCV004169202]	uncertain significance	19	15427239	15427239	Human		name
156274141	CV2320235	single nucleotide variant	NM_001371589.1(WIZ):c.4010C>T (p.Pro1337Leu)	not specified [RCV004169853]	uncertain significance	19	15427338	15427338	Human		name
156295651	CV2321525	single nucleotide variant	NM_001371589.1(WIZ):c.4387C>T (p.Arg1463Cys)	not specified [RCV004177492]	uncertain significance	19	15425748	15425748	Human		name
156354779	CV2324348	single nucleotide variant	NM_001371589.1(WIZ):c.4373G>A (p.Arg1458Gln)	not specified [RCV004178853]	uncertain significance	19	15425762	15425762	Human		name
156190122	CV2325445	single nucleotide variant	NM_001371589.1(WIZ):c.5416C>G (p.Pro1806Ala)	not specified [RCV004179900]	uncertain significance	19	15424277	15424277	Human		name
156178634	CV2327477	single nucleotide variant	NM_001371589.1(WIZ):c.5335C>T (p.Arg1779Cys)	not specified [RCV004174888]	uncertain significance	19	15424358	15424358	Human		name
155973726	CV2332432	single nucleotide variant	NM_001371589.1(WIZ):c.4139C>G (p.Pro1380Arg)	not specified [RCV004196163]	uncertain significance	19	15427209	15427209	Human		name
156067632	CV2340983	single nucleotide variant	NM_001371589.1(WIZ):c.4291G>A (p.Ala1431Thr)	not specified [RCV004181475]	uncertain significance	19	15427057	15427057	Human		name
156221091	CV2345112	single nucleotide variant	NM_001371589.1(WIZ):c.4655C>T (p.Ser1552Leu)	not specified [RCV004193384]	uncertain significance	19	15425480	15425480	Human		name
156188669	CV2346857	single nucleotide variant	NM_001371589.1(WIZ):c.5089G>A (p.Gly1697Ser)	not specified [RCV004199854]	uncertain significance	19	15424838	15424838	Human		name
156189151	CV2356588	single nucleotide variant	NM_001371589.1(WIZ):c.5150C>T (p.Pro1717Leu)	not specified [RCV004201954]	uncertain significance	19	15424777	15424777	Human		name
155995695	CV2375847	single nucleotide variant	NM_001371589.1(WIZ):c.4738G>C (p.Ala1580Pro)	not specified [RCV004217696]	uncertain significance	19	15425397	15425397	Human		name
156265960	CV2389114	single nucleotide variant	NM_001371589.1(WIZ):c.5137A>G (p.Ser1713Gly)	not specified [RCV004235447]	likely benign	19	15424790	15424790	Human		name
156089567	CV2392088	single nucleotide variant	NM_001371589.1(WIZ):c.5186T>G (p.Val1729Gly)	not specified [RCV004237983]	uncertain significance	19	15424741	15424741	Human		name
329373009	CV2439245	single nucleotide variant	NM_001371589.1(WIZ):c.4724C>T (p.Thr1575Met)	not specified [RCV004255528]	uncertain significance	19	15425411	15425411	Human		name
329399364	CV2446854	single nucleotide variant	NM_001371589.1(WIZ):c.4286C>T (p.Pro1429Leu)	not specified [RCV004257707]	uncertain significance	19	15427062	15427062	Human		name
401723823	CV2684879	single nucleotide variant	NM_001371589.1(WIZ):c.5353G>A (p.Ala1785Thr)	not specified [RCV004296384]	uncertain significance	19	15424340	15424340	Human		name
401782880	CV2716024	single nucleotide variant	NM_001371589.1(WIZ):c.5614C>T (p.Pro1872Ser)	not specified [RCV004323280]	uncertain significance	19	15423132	15423132	Human		name
401773334	CV2716530	single nucleotide variant	NM_001371589.1(WIZ):c.5615C>T (p.Pro1872Leu)	not specified [RCV004327611]	uncertain significance	19	15423131	15423131	Human		name
401749920	CV2719449	single nucleotide variant	NM_001371589.1(WIZ):c.4658C>T (p.Pro1553Leu)	not specified [RCV004326848]	uncertain significance	19	15425477	15425477	Human		name
401781739	CV2722249	single nucleotide variant	NM_001371589.1(WIZ):c.4717A>G (p.Ser1573Gly)	not specified [RCV004328807]	uncertain significance	19	15425418	15425418	Human		name
401751603	CV2727066	single nucleotide variant	NM_001371589.1(WIZ):c.3845G>A (p.Arg1282His)	not specified [RCV004325440]	uncertain significance	19	15427503	15427503	Human		name
401895607	CV2774522	single nucleotide variant	NM_001371589.1(WIZ):c.4649C>T (p.Pro1550Leu)	not specified [RCV004350009]	uncertain significance	19	15425486	15425486	Human		name
401862491	CV2775329	single nucleotide variant	NM_001371589.1(WIZ):c.3835C>G (p.Arg1279Gly)	not specified [RCV004348440]	uncertain significance	19	15427513	15427513	Human		name
401892514	CV2782116	single nucleotide variant	NM_001371589.1(WIZ):c.5246A>G (p.Glu1749Gly)	not specified [RCV004359107]	uncertain significance	19	15424681	15424681	Human		name
401877923	CV2786863	single nucleotide variant	NM_001371589.1(WIZ):c.5087G>A (p.Gly1696Asp)	not specified [RCV004366016]	uncertain significance	19	15424840	15424840	Human		name
401867012	CV2792581	single nucleotide variant	NM_001371589.1(WIZ):c.4663G>T (p.Ala1555Ser)	not specified [RCV004363613]	uncertain significance	19	15425472	15425472	Human		name
405811840	CV3352797	single nucleotide variant	NM_001371589.1(WIZ):c.4633G>A (p.Val1545Met)	not specified [RCV004482995]	likely benign	19	15425502	15425502	Human		name
405811842	CV3352798	single nucleotide variant	NM_001371589.1(WIZ):c.4669C>T (p.Arg1557Trp)	not specified [RCV004482996]	uncertain significance	19	15425466	15425466	Human		name
405811844	CV3352799	single nucleotide variant	NM_001371589.1(WIZ):c.5188G>A (p.Gly1730Ser)	not specified [RCV004482997]	uncertain significance	19	15424739	15424739	Human		name
405811950	CV3352800	single nucleotide variant	NM_001371589.1(WIZ):c.5300G>A (p.Arg1767Gln)	not specified [RCV004482998]	uncertain significance	19	15424627	15424627	Human		name
405811848	CV3352801	single nucleotide variant	NM_001371589.1(WIZ):c.5338C>T (p.Pro1780Ser)	not specified [RCV004482999]	uncertain significance	19	15424355	15424355	Human		name
405811850	CV3352802	single nucleotide variant	NM_001371589.1(WIZ):c.5407C>T (p.Arg1803Trp)	not specified [RCV004483000]	uncertain significance	19	15424286	15424286	Human		name
405811852	CV3352803	single nucleotide variant	NM_001371589.1(WIZ):c.5443C>G (p.Leu1815Val)	not specified [RCV004483001]	uncertain significance	19	15424250	15424250	Human		name
405811854	CV3352804	single nucleotide variant	NM_001371589.1(WIZ):c.5456C>G (p.Pro1819Arg)	not specified [RCV004483002]	uncertain significance	19	15424237	15424237	Human		name
405811857	CV3352806	single nucleotide variant	NM_001371589.1(WIZ):c.5617C>T (p.Pro1873Ser)	not specified [RCV004483004]	uncertain significance	19	15423129	15423129	Human		name
405811859	CV3352807	single nucleotide variant	NM_001371589.1(WIZ):c.3850G>C (p.Glu1284Gln)	not specified [RCV004483005]	uncertain significance	19	15427498	15427498	Human		name
405811861	CV3352808	single nucleotide variant	NM_001371589.1(WIZ):c.3986G>A (p.Arg1329Gln)	not specified [RCV004483006]	uncertain significance	19	15427362	15427362	Human		name
405811863	CV3352809	single nucleotide variant	NM_001371589.1(WIZ):c.4090C>T (p.Arg1364Cys)	not specified [RCV004483007]	uncertain significance	19	15427258	15427258	Human		name
405811867	CV3352811	single nucleotide variant	NM_001371589.1(WIZ):c.4091G>A (p.Arg1364His)	not specified [RCV004483009]	uncertain significance	19	15427257	15427257	Human		name
405811869	CV3352812	single nucleotide variant	NM_001371589.1(WIZ):c.4135C>T (p.Pro1379Ser)	not specified [RCV004483010]	uncertain significance	19	15427213	15427213	Human		name
405811870	CV3352813	single nucleotide variant	NM_001371589.1(WIZ):c.4145C>T (p.Pro1382Leu)	not specified [RCV004483011]	uncertain significance	19	15427203	15427203	Human		name
405854088	CV3395843	single nucleotide variant	NM_001371589.1(WIZ):c.4637A>G (p.Gln1546Arg)	Bladder exstrophy-epispadias-cloacal extrophy complex [RCV004556174]	uncertain significance	19	15425498	15425498	Human	1	name
407465459	CV3487902	single nucleotide variant	NM_001371589.1(WIZ):c.4033C>T (p.Pro1345Ser)	not specified [RCV004688774]	uncertain significance	19	15427315	15427315	Human		name
407524639	CV3487904	single nucleotide variant	NM_001371589.1(WIZ):c.4171A>C (p.Thr1391Pro)	not specified [RCV004678503]	uncertain significance	19	15427177	15427177	Human		name
407524642	CV3487905	single nucleotide variant	NM_001371589.1(WIZ):c.4333G>T (p.Ala1445Ser)	not specified [RCV004678504]	uncertain significance	19	15427015	15427015	Human		name
407524646	CV3487907	single nucleotide variant	NM_001371589.1(WIZ):c.5662G>T (p.Ala1888Ser)	not specified [RCV004678505]	uncertain significance	19	15423084	15423084	Human		name
597792405	CV3630311	single nucleotide variant	NM_001371589.1(WIZ):c.4186C>T (p.Pro1396Ser)	not specified [RCV004876991]	uncertain significance	19	15427162	15427162	Human		name
597792408	CV3630312	single nucleotide variant	NM_001371589.1(WIZ):c.5615C>A (p.Pro1872Gln)	not specified [RCV004876992]	uncertain significance	19	15423131	15423131	Human		name
597792411	CV3630313	single nucleotide variant	NM_001371589.1(WIZ):c.4000C>T (p.Pro1334Ser)	not specified [RCV004876993]	uncertain significance	19	15427348	15427348	Human		name
597792414	CV3630314	single nucleotide variant	NM_001371589.1(WIZ):c.4670G>A (p.Arg1557Gln)	not specified [RCV004876994]	uncertain significance	19	15425465	15425465	Human		name
597792418	CV3630315	single nucleotide variant	NM_001371589.1(WIZ):c.4520G>A (p.Arg1507Gln)	not specified [RCV004876995]	uncertain significance	19	15425615	15425615	Human		name
597739889	CV3630316	single nucleotide variant	NM_001371589.1(WIZ):c.3940G>A (p.Val1314Ile)	not specified [RCV004890424]	uncertain significance	19	15427408	15427408	Human		name
597792420	CV3630317	single nucleotide variant	NM_001371589.1(WIZ):c.4786C>A (p.Pro1596Thr)	not specified [RCV004876996]	uncertain significance	19	15425349	15425349	Human		name
597792423	CV3630318	single nucleotide variant	NM_001371589.1(WIZ):c.4199A>G (p.Lys1400Arg)	not specified [RCV004876997]	uncertain significance	19	15427149	15427149	Human		name
597739895	CV3630319	single nucleotide variant	NM_001371589.1(WIZ):c.4571C>T (p.Pro1524Leu)	not specified [RCV004890425]	uncertain significance	19	15425564	15425564	Human		name
597792426	CV3630320	single nucleotide variant	NM_001371589.1(WIZ):c.5429G>A (p.Arg1810Gln)	not specified [RCV004876998]	uncertain significance	19	15424264	15424264	Human		name
597792429	CV3630321	single nucleotide variant	NM_001371589.1(WIZ):c.4802G>A (p.Arg1601His)	not specified [RCV004876999]	uncertain significance	19	15425333	15425333	Human		name
597792432	CV3630322	single nucleotide variant	NM_001371589.1(WIZ):c.4259G>A (p.Arg1420Gln)	not specified [RCV004877000]	uncertain significance	19	15427089	15427089	Human		name
597792437	CV3630323	single nucleotide variant	NM_001371589.1(WIZ):c.4960G>A (p.Ala1654Thr)	not specified [RCV004877001]	uncertain significance	19	15424967	15424967	Human		name
597739908	CV3630326	single nucleotide variant	NM_001371589.1(WIZ):c.4783C>T (p.Arg1595Trp)	not specified [RCV004890428]	uncertain significance	19	15425352	15425352	Human		name
597739914	CV3630327	single nucleotide variant	NM_001371589.1(WIZ):c.5057A>G (p.Lys1686Arg)	not specified [RCV004890429]	uncertain significance	19	15424870	15424870	Human		name
598233267	CV3929750	single nucleotide variant	NM_001371589.1(WIZ):c.5645A>G (p.Gln1882Arg)	not specified [RCV005295541]	uncertain significance	19	15423101	15423101	Human		name
598233274	CV3929751	single nucleotide variant	NM_001371589.1(WIZ):c.3850G>A (p.Glu1284Lys)	not specified [RCV005295542]	uncertain significance	19	15427498	15427498	Human		name
598267306	CV3929752	single nucleotide variant	NM_001371589.1(WIZ):c.4298A>C (p.His1433Pro)	not specified [RCV005302150]	uncertain significance	19	15427050	15427050	Human		name
598267311	CV3929753	single nucleotide variant	NM_001371589.1(WIZ):c.5260G>A (p.Ala1754Thr)	not specified [RCV005302151]	uncertain significance	19	15424667	15424667	Human		name
598267316	CV3929754	single nucleotide variant	NM_001371589.1(WIZ):c.4254A>C (p.Gln1418His)	not specified [RCV005302152]	uncertain significance	19	15427094	15427094	Human		name
598267322	CV3929755	single nucleotide variant	NM_001371589.1(WIZ):c.4657C>T (p.Pro1553Ser)	not specified [RCV005302153]	uncertain significance	19	15425478	15425478	Human		name
598233280	CV3929756	single nucleotide variant	NM_001371589.1(WIZ):c.4094G>C (p.Ser1365Thr)	not specified [RCV005295543]	uncertain significance	19	15427254	15427254	Human		name
598233285	CV3929757	single nucleotide variant	NM_001371589.1(WIZ):c.5435T>G (p.Val1812Gly)	not specified [RCV005295544]	uncertain significance	19	15424258	15424258	Human		name
598233291	CV3929758	single nucleotide variant	NM_001371589.1(WIZ):c.5633C>T (p.Ala1878Val)	not specified [RCV005295545]	uncertain significance	19	15423113	15423113	Human		name
598267329	CV3929759	single nucleotide variant	NM_001371589.1(WIZ):c.3998G>A (p.Arg1333Gln)	not specified [RCV005302154]	uncertain significance	19	15427350	15427350	Human		name

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