Wap Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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84 records found for search term Wap

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
13794918	CV513825	single nucleotide variant	NM_015045.5(WAPL):c.2192G>A (p.Arg731His)	WAPL-related disorder [RCV000680250]	uncertain significance	10	86467457	86467457	Human		name , trait
401779496	CV2676589	single nucleotide variant	NM_015045.5(WAPL):c.67G>A (p.Val23Ile)	not specified [RCV004288773]	uncertain significance	10	86518003	86518003	Human		name
156178236	CV2331301	single nucleotide variant	NM_015045.5(WAPL):c.163A>G (p.Ile55Val)	not specified [RCV004181901]	uncertain significance	10	86517907	86517907	Human		name
405665357	CV3338825	single nucleotide variant	NM_015045.5(WAPL):c.242C>A (p.Ser81Tyr)	not specified [RCV004485355]	uncertain significance	10	86517828	86517828	Human		name
597689249	CV3623636	single nucleotide variant	NM_015045.5(WAPL):c.164T>C (p.Ile55Thr)	not specified [RCV004884454]	uncertain significance	10	86517906	86517906	Human		name
597700448	CV3623639	single nucleotide variant	NM_015045.5(WAPL):c.164T>G (p.Ile55Ser)	not specified [RCV004885614]	uncertain significance	10	86517906	86517906	Human		name
598256688	CV3936771	single nucleotide variant	NM_015045.5(WAPL):c.274G>A (p.Val92Ile)	not specified [RCV005299673]	uncertain significance	10	86517796	86517796	Human		name
8633747	CV88963	single nucleotide variant	NM_015045.2(WAPAL):c.639C>T (p.Ser213=)	Malignant melanoma [RCV000069060]	not provided	10	86500604	86500604	Human		name
155921413	CV2207192	single nucleotide variant	NM_015045.5(WAPL):c.982G>A (p.Glu328Lys)	not specified [RCV004087925]	uncertain significance	10	86500261	86500261	Human		name
156040903	CV2219518	single nucleotide variant	NM_015045.5(WAPL):c.536A>G (p.Asn179Ser)	not specified [RCV004095264]	uncertain significance	10	86500707	86500707	Human		name
156002899	CV2347730	single nucleotide variant	NM_015045.5(WAPL):c.610A>G (p.Ile204Val)	not specified [RCV004202698]	uncertain significance	10	86500633	86500633	Human		name
156194524	CV2350817	single nucleotide variant	NM_015045.5(WAPL):c.850G>A (p.Val284Ile)	not specified [RCV004207145]	uncertain significance	10	86500393	86500393	Human		name
156179964	CV2356053	single nucleotide variant	NM_015045.5(WAPL):c.740G>C (p.Arg247Thr)	not specified [RCV004203470]	uncertain significance	10	86500503	86500503	Human		name
329400748	CV2438738	single nucleotide variant	NM_015045.5(WAPL):c.949G>A (p.Gly317Ser)	not specified [RCV004261887]	uncertain significance	10	86500294	86500294	Human		name
329362823	CV2464776	single nucleotide variant	NM_015045.5(WAPL):c.629C>G (p.Thr210Ser)	not specified [RCV004284734]	uncertain significance	10	86500614	86500614	Human		name
329388583	CV2469397	single nucleotide variant	NM_015045.5(WAPL):c.385G>C (p.Val129Leu)	not specified [RCV004281027]	uncertain significance	10	86517685	86517685	Human		name
401777824	CV2704373	single nucleotide variant	NM_015045.5(WAPL):c.409G>A (p.Glu137Lys)	not specified [RCV004311343]	uncertain significance	10	86517661	86517661	Human		name
405665386	CV3338831	single nucleotide variant	NM_015045.5(WAPL):c.508G>C (p.Glu170Gln)	not specified [RCV004485361]	uncertain significance	10	86500735	86500735	Human		name
405665390	CV3338832	single nucleotide variant	NM_015045.5(WAPL):c.956G>T (p.Ser319Ile)	not specified [RCV004485362]	uncertain significance	10	86500287	86500287	Human		name
405665395	CV3338833	single nucleotide variant	NM_015045.5(WAPL):c.986C>T (p.Ser329Leu)	not specified [RCV004485363]	uncertain significance	10	86500257	86500257	Human		name
407450925	CV3491698	single nucleotide variant	NM_015045.5(WAPL):c.995A>G (p.Asp332Gly)	not specified [RCV004683481]	uncertain significance	10	86500248	86500248	Human		name
407465171	CV3491704	single nucleotide variant	NM_015045.5(WAPL):c.554A>G (p.Lys185Arg)	not specified [RCV004688699]	uncertain significance	10	86500689	86500689	Human		name
597689196	CV3623627	single nucleotide variant	NM_015045.5(WAPL):c.802T>C (p.Phe268Leu)	not specified [RCV004884448]	likely benign	10	86500441	86500441	Human		name
597689206	CV3623628	single nucleotide variant	NM_015045.5(WAPL):c.719A>G (p.Asp240Gly)	not specified [RCV004884449]	uncertain significance	10	86500524	86500524	Human		name
597689215	CV3623629	single nucleotide variant	NM_015045.5(WAPL):c.832G>A (p.Ala278Thr)	not specified [RCV004884450]	uncertain significance	10	86500411	86500411	Human		name
597700422	CV3623632	single nucleotide variant	NM_015045.5(WAPL):c.956G>A (p.Ser319Asn)	not specified [RCV004885611]	uncertain significance	10	86500287	86500287	Human		name
597689231	CV3623634	single nucleotide variant	NM_015045.5(WAPL):c.380C>G (p.Thr127Ser)	not specified [RCV004884452]	likely benign	10	86517690	86517690	Human		name
598218743	CV3936765	single nucleotide variant	NM_015045.5(WAPL):c.392A>T (p.Asp131Val)	not specified [RCV005293216]	uncertain significance	10	86517678	86517678	Human		name
598256670	CV3936766	single nucleotide variant	NM_015045.5(WAPL):c.826A>C (p.Asn276His)	not specified [RCV005299670]	uncertain significance	10	86500417	86500417	Human		name
598256677	CV3936767	single nucleotide variant	NM_015045.5(WAPL):c.641A>G (p.Gln214Arg)	not specified [RCV005299671]	uncertain significance	10	86500602	86500602	Human		name
598218748	CV3936768	single nucleotide variant	NM_015045.5(WAPL):c.504A>C (p.Lys168Asn)	not specified [RCV005293217]	uncertain significance	10	86500739	86500739	Human		name
598256683	CV3936769	single nucleotide variant	NM_015045.5(WAPL):c.778C>T (p.Leu260Phe)	not specified [RCV005299672]	uncertain significance	10	86500465	86500465	Human		name
598218756	CV3936770	single nucleotide variant	NM_015045.5(WAPL):c.530A>T (p.Glu177Val)	not specified [RCV005293218]	uncertain significance	10	86500713	86500713	Human		name
598256701	CV3936773	single nucleotide variant	NM_015045.5(WAPL):c.563A>G (p.Asp188Gly)	not specified [RCV005299675]	uncertain significance	10	86500680	86500680	Human		name
598218762	CV3936774	single nucleotide variant	NM_015045.5(WAPL):c.647G>A (p.Gly216Glu)	not specified [RCV005293219]	uncertain significance	10	86500596	86500596	Human		name
155965307	CV2206420	single nucleotide variant	NM_015045.5(WAPL):c.1136G>A (p.Arg379His)	not specified [RCV004078742]	uncertain significance	10	86500107	86500107	Human		name
156358331	CV2251018	single nucleotide variant	NM_015045.5(WAPL):c.1438A>G (p.Thr480Ala)	not specified [RCV004123582]	uncertain significance	10	86499805	86499805	Human		name
155948282	CV2272064	single nucleotide variant	NM_015045.5(WAPL):c.1244C>T (p.Pro415Leu)	not specified [RCV004124860]	uncertain significance	10	86499999	86499999	Human		name
156274175	CV2277895	single nucleotide variant	NM_015045.5(WAPL):c.1152C>G (p.Phe384Leu)	not specified [RCV004147305]	uncertain significance	10	86500091	86500091	Human		name
156264263	CV2312067	single nucleotide variant	NM_015045.5(WAPL):c.1270G>A (p.Val424Ile)	not specified [RCV004164994]	uncertain significance	10	86499973	86499973	Human		name
156194196	CV2322072	single nucleotide variant	NM_015045.5(WAPL):c.2529A>T (p.Lys843Asn)	not specified [RCV004173815]	uncertain significance	10	86460450	86460450	Human		name
156036092	CV2335054	single nucleotide variant	NM_015045.5(WAPL):c.1439C>A (p.Thr480Asn)	not specified [RCV004184593]	uncertain significance	10	86499804	86499804	Human		name
156057296	CV2343536	single nucleotide variant	NM_015045.5(WAPL):c.2699G>A (p.Arg900His)	not specified [RCV004190571]	uncertain significance	10	86453790	86453790	Human		name
156099451	CV2392867	single nucleotide variant	NM_015045.5(WAPL):c.1582A>G (p.Ile528Val)	not specified [RCV004247220]	uncertain significance	10	86497263	86497263	Human		name
329399761	CV2444147	single nucleotide variant	NM_015045.5(WAPL):c.1471C>A (p.Pro491Thr)	not specified [RCV004260885]	uncertain significance	10	86499772	86499772	Human		name
401751855	CV2702927	single nucleotide variant	NM_015045.5(WAPL):c.1831A>G (p.Ile611Val)	not specified [RCV004321256]	uncertain significance	10	86472674	86472674	Human		name
401771748	CV2711876	single nucleotide variant	NM_015045.5(WAPL):c.1546G>C (p.Asp516His)	not specified [RCV004309502]	uncertain significance	10	86497299	86497299	Human		name
401727268	CV2722099	single nucleotide variant	NM_015045.5(WAPL):c.1009G>A (p.Ala337Thr)	not specified [RCV004328360]	uncertain significance	10	86500234	86500234	Human		name
401774398	CV2727829	single nucleotide variant	NM_015045.5(WAPL):c.1457C>T (p.Pro486Leu)	not specified [RCV004323851]	uncertain significance	10	86499786	86499786	Human		name
401734158	CV2736953	single nucleotide variant	NM_015045.5(WAPL):c.2020C>T (p.Arg674Cys)	Clubfoot [RCV003313716]	uncertain significance	10	86472218	86472218	Human	2	name
401860383	CV2768573	single nucleotide variant	NM_015045.5(WAPL):c.1503T>G (p.Ser501Arg)	not specified [RCV004344437]	uncertain significance	10	86499740	86499740	Human		name
405665326	CV3338818	single nucleotide variant	NM_015045.5(WAPL):c.1270G>T (p.Val424Phe)	not specified [RCV004485348]	uncertain significance	10	86499973	86499973	Human		name
405665331	CV3338819	single nucleotide variant	NM_015045.5(WAPL):c.1300C>A (p.His434Asn)	not specified [RCV004485349]	uncertain significance	10	86499943	86499943	Human		name
405665335	CV3338820	single nucleotide variant	NM_015045.5(WAPL):c.1420A>C (p.Lys474Gln)	not specified [RCV004485350]	uncertain significance	10	86499823	86499823	Human		name
405665340	CV3338821	single nucleotide variant	NM_015045.5(WAPL):c.1519A>G (p.Asn507Asp)	not specified [RCV004485351]	uncertain significance	10	86499724	86499724	Human		name
405665343	CV3338822	single nucleotide variant	NM_015045.5(WAPL):c.1768C>A (p.Gln590Lys)	not specified [RCV004485352]	uncertain significance	10	86472737	86472737	Human		name
405665353	CV3338824	single nucleotide variant	NM_015045.5(WAPL):c.1831A>T (p.Ile611Leu)	not specified [RCV004485354]	uncertain significance	10	86472674	86472674	Human		name
405665362	CV3338826	single nucleotide variant	NM_015045.5(WAPL):c.2764G>T (p.Val922Leu)	not specified [RCV004485356]	uncertain significance	10	86453725	86453725	Human		name
407450932	CV3491701	single nucleotide variant	NM_015045.5(WAPL):c.2771A>C (p.Lys924Thr)	not specified [RCV004683484]	uncertain significance	10	86453718	86453718	Human		name
407450935	CV3491702	single nucleotide variant	NM_015045.5(WAPL):c.1813G>A (p.Val605Met)	not specified [RCV004683485]	uncertain significance	10	86472692	86472692	Human		name
597689222	CV3623630	single nucleotide variant	NM_015045.5(WAPL):c.1019G>C (p.Gly340Ala)	not specified [RCV004884451]	uncertain significance	10	86500224	86500224	Human		name
597700412	CV3623631	single nucleotide variant	NM_015045.5(WAPL):c.1340A>C (p.Asn447Thr)	not specified [RCV004885610]	uncertain significance	10	86499903	86499903	Human		name
597700431	CV3623633	single nucleotide variant	NM_015045.5(WAPL):c.2267C>T (p.Ser756Leu)	not specified [RCV004885612]	uncertain significance	10	86467382	86467382	Human		name
597689239	CV3623635	single nucleotide variant	NM_015045.5(WAPL):c.2890T>A (p.Cys964Ser)	not specified [RCV004884453]	uncertain significance	10	86453279	86453279	Human		name
597689257	CV3623637	single nucleotide variant	NM_015045.5(WAPL):c.2690A>G (p.Gln897Arg)	not specified [RCV004884455]	uncertain significance	10	86453799	86453799	Human		name
597700440	CV3623638	single nucleotide variant	NM_015045.5(WAPL):c.2738T>C (p.Leu913Pro)	not specified [RCV004885613]	uncertain significance	10	86453751	86453751	Human		name
597689277	CV3623641	single nucleotide variant	NM_015045.5(WAPL):c.1129A>G (p.Met377Val)	not specified [RCV004884457]	uncertain significance	10	86500114	86500114	Human		name
598218767	CV3936775	single nucleotide variant	NM_015045.5(WAPL):c.2708A>G (p.Asp903Gly)	not specified [RCV005293220]	uncertain significance	10	86453781	86453781	Human		name
8633746	CV88962	single nucleotide variant	NM_015045.2(WAPAL):c.799G>A (p.Asp267Asn)	Malignant melanoma [RCV000069059]	not provided	10	86500444	86500444	Human		name
8633748	CV88964	single nucleotide variant	NM_015045.2(WAPAL):c.638C>T (p.Ser213Phe)	Malignant melanoma [RCV000069061]	not provided	10	86500605	86500605	Human		name
156229082	CV2199460	single nucleotide variant	NM_015045.5(WAPL):c.3013A>G (p.Met1005Val)	not specified [RCV004071018]	uncertain significance	10	86452068	86452068	Human		name
156053753	CV2243005	single nucleotide variant	NM_015045.5(WAPL):c.3180T>A (p.Asp1060Glu)	not specified [RCV004107880]	uncertain significance	10	86446384	86446384	Human		name
156301588	CV2258512	single nucleotide variant	NM_015045.5(WAPL):c.3362T>C (p.Val1121Ala)	not specified [RCV004116004]	uncertain significance	10	86443324	86443324	Human		name
156249153	CV2264071	single nucleotide variant	NM_015045.5(WAPL):c.3133C>T (p.Arg1045Trp)	not specified [RCV004138082]	uncertain significance	10	86446431	86446431	Human		name
329356166	CV2430613	single nucleotide variant	NM_015045.5(WAPL):c.3061G>A (p.Asp1021Asn)	not specified [RCV004253807]	uncertain significance	10	86452020	86452020	Human		name
401775981	CV2692558	single nucleotide variant	NM_015045.5(WAPL):c.3080G>A (p.Gly1027Asp)	not specified [RCV004312301]	uncertain significance	10	86452001	86452001	Human		name
405665367	CV3338827	single nucleotide variant	NM_015045.5(WAPL):c.3011A>G (p.Asn1004Ser)	not specified [RCV004485357]	uncertain significance	10	86452070	86452070	Human		name
405665370	CV3338828	single nucleotide variant	NM_015045.5(WAPL):c.3023C>G (p.Ser1008Trp)	not specified [RCV004485358]	uncertain significance	10	86452058	86452058	Human		name
405665376	CV3338829	single nucleotide variant	NM_015045.5(WAPL):c.3043A>G (p.Ile1015Val)	not specified [RCV004485359]	uncertain significance	10	86452038	86452038	Human		name
405665381	CV3338830	single nucleotide variant	NM_015045.5(WAPL):c.3044T>C (p.Ile1015Thr)	not specified [RCV004485360]	uncertain significance	10	86452037	86452037	Human		name
407450928	CV3491699	single nucleotide variant	NM_015045.5(WAPL):c.3460A>G (p.Ile1154Val)	not specified [RCV004683482]	uncertain significance	10	86437967	86437967	Human		name
407450930	CV3491700	single nucleotide variant	NM_015045.5(WAPL):c.3002G>T (p.Cys1001Phe)	not specified [RCV004683483]	uncertain significance	10	86452079	86452079	Human		name
597689267	CV3623640	single nucleotide variant	NM_015045.5(WAPL):c.3094G>A (p.Ala1032Thr)	not specified [RCV004884456]	uncertain significance	10	86451987	86451987	Human		name
156391079	CV2385070	microsatellite	NM_015045.5(WAPL):c.2175_2178dup (p.Leu727fs)	not specified [RCV004228335]	uncertain significance	10	86467470	86467471	Human		name

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