Iws1 Variant Search Result - Rat Genome Database

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55 records found for search term Iws1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329379727	CV2443531	single nucleotide variant	NM_017969.3(IWS1):c.6C>G (p.Asp2Glu)	not specified [RCV004262361]	uncertain significance	2	127526203	127526203	Human		name
597776797	CV3684007	single nucleotide variant	NM_017969.3(IWS1):c.25G>C (p.Asp9His)	not specified [RCV004929700]	uncertain significance	2	127526184	127526184	Human		name
405794819	CV3264888	single nucleotide variant	NM_017969.3(IWS1):c.67C>T (p.Arg23Trp)	not specified [RCV004400975]	uncertain significance	2	127523759	127523759	Human		name
15155803	CV707710	single nucleotide variant	NM_017969.3(IWS1):c.867G>A (p.Ser289=)	not provided [RCV000968990]	benign	2	127505036	127505036	Human		name
156343436	CV2232739	single nucleotide variant	NM_017969.3(IWS1):c.115G>C (p.Gly39Arg)	not specified [RCV004101391]	uncertain significance	2	127523711	127523711	Human		name
155954905	CV2302292	single nucleotide variant	NM_017969.3(IWS1):c.218A>G (p.Glu73Gly)	not specified [RCV004161058]	uncertain significance	2	127505685	127505685	Human		name
405794828	CV3264885	single nucleotide variant	NM_017969.3(IWS1):c.224T>C (p.Leu75Ser)	not specified [RCV004400972]	likely benign	2	127505679	127505679	Human		name
407466869	CV3448006	single nucleotide variant	NM_017969.3(IWS1):c.167G>A (p.Arg56Gln)	not specified [RCV004635664]	uncertain significance	2	127505736	127505736	Human		name
597776804	CV3684009	single nucleotide variant	NM_017969.3(IWS1):c.140G>A (p.Arg47His)	not specified [RCV004929702]	uncertain significance	2	127523686	127523686	Human		name
15183565	CV697005	single nucleotide variant	NM_017969.3(IWS1):c.1278A>G (p.Ser426=)	not provided [RCV000952495]	benign	2	127503518	127503518	Human		name
156378752	CV2207797	single nucleotide variant	NM_017969.3(IWS1):c.299G>A (p.Arg100His)	not specified [RCV004084233]	likely benign	2	127505604	127505604	Human		name
156336294	CV2228518	single nucleotide variant	NM_017969.3(IWS1):c.660G>C (p.Gln220His)	not specified [RCV004092761]	uncertain significance	2	127505243	127505243	Human		name
156275801	CV2287657	single nucleotide variant	NM_017969.3(IWS1):c.341A>T (p.Asn114Ile)	not specified [RCV004141087]	uncertain significance	2	127505562	127505562	Human		name
156205092	CV2297850	single nucleotide variant	NM_017969.3(IWS1):c.819C>G (p.Ile273Met)	not specified [RCV004157792]	uncertain significance	2	127505084	127505084	Human		name
401756325	CV2687091	single nucleotide variant	NM_017969.3(IWS1):c.596A>C (p.Glu199Ala)	not specified [RCV004304406]	uncertain significance	2	127505307	127505307	Human		name
401781652	CV2722206	single nucleotide variant	NM_017969.3(IWS1):c.391A>G (p.Ser131Gly)	not specified [RCV004328771]	uncertain significance	2	127505512	127505512	Human		name
401719329	CV2729148	single nucleotide variant	NM_017969.3(IWS1):c.355G>A (p.Asp119Asn)	not specified [RCV004332688]	uncertain significance	2	127505548	127505548	Human		name
401866370	CV2762622	single nucleotide variant	NM_017969.3(IWS1):c.697C>G (p.Gln233Glu)	not specified [RCV004340188]	uncertain significance	2	127505206	127505206	Human		name
401870697	CV2769306	single nucleotide variant	NM_017969.3(IWS1):c.572C>T (p.Pro191Leu)	not specified [RCV004357307]	uncertain significance	2	127505331	127505331	Human		name
401899163	CV2783715	single nucleotide variant	NM_017969.3(IWS1):c.638G>A (p.Ser213Asn)	not specified [RCV004360635]	uncertain significance	2	127505265	127505265	Human		name
405794825	CV3264886	single nucleotide variant	NM_017969.3(IWS1):c.616C>G (p.Pro206Ala)	not specified [RCV004400973]	uncertain significance	2	127505287	127505287	Human		name
405794822	CV3264887	single nucleotide variant	NM_017969.3(IWS1):c.638G>T (p.Ser213Ile)	not specified [RCV004400974]	uncertain significance	2	127505265	127505265	Human		name
405794816	CV3264889	single nucleotide variant	NM_017969.3(IWS1):c.827C>T (p.Ser276Leu)	not specified [RCV004400976]	uncertain significance	2	127505076	127505076	Human		name
597776789	CV3684005	single nucleotide variant	NM_017969.3(IWS1):c.653A>G (p.Lys218Arg)	not specified [RCV004929698]	uncertain significance	2	127505250	127505250	Human		name
597776808	CV3684010	single nucleotide variant	NM_017969.3(IWS1):c.884C>T (p.Pro295Leu)	not specified [RCV004929703]	uncertain significance	2	127505019	127505019	Human		name
597776812	CV3684011	single nucleotide variant	NM_017969.3(IWS1):c.433G>C (p.Asp145His)	not specified [RCV004929704]	uncertain significance	2	127505470	127505470	Human		name
598258433	CV3969204	single nucleotide variant	NM_017969.3(IWS1):c.811C>A (p.Pro271Thr)	not specified [RCV005347198]	uncertain significance	2	127505092	127505092	Human		name
156115088	CV2221379	single nucleotide variant	NM_017969.3(IWS1):c.2336C>T (p.Ala779Val)	not specified [RCV004096678]	uncertain significance	2	127481168	127481168	Human		name
156158950	CV2262531	single nucleotide variant	NM_017969.3(IWS1):c.1039G>A (p.Asp347Asn)	not specified [RCV004130746]	uncertain significance	2	127504864	127504864	Human		name
156171058	CV2286598	single nucleotide variant	NM_017969.3(IWS1):c.1450G>A (p.Glu484Lys)	not specified [RCV004142449]	uncertain significance	2	127502832	127502832	Human		name
156202938	CV2313261	single nucleotide variant	NM_017969.3(IWS1):c.1994A>G (p.Tyr665Cys)	not specified [RCV004161509]	uncertain significance	2	127492024	127492024	Human		name
156218064	CV2344701	single nucleotide variant	NM_017969.3(IWS1):c.1004G>A (p.Arg335Lys)	not specified [RCV004190861]	uncertain significance	2	127504899	127504899	Human		name
156196101	CV2367211	single nucleotide variant	NM_017969.3(IWS1):c.1131T>G (p.Ser377Arg)	not specified [RCV004215637]	uncertain significance	2	127504772	127504772	Human		name
155938632	CV2380840	single nucleotide variant	NM_017969.3(IWS1):c.1325A>G (p.Glu442Gly)	not specified [RCV004218396]	uncertain significance	2	127503471	127503471	Human		name
156097635	CV2392714	single nucleotide variant	NM_017969.3(IWS1):c.1764A>C (p.Leu588Phe)	not specified [RCV004247089]	uncertain significance	2	127494907	127494907	Human		name
329380661	CV2444499	single nucleotide variant	NM_017969.3(IWS1):c.1235G>A (p.Arg412His)	not specified [RCV004263228]	uncertain significance	2	127503561	127503561	Human		name
401729783	CV2683795	single nucleotide variant	NM_017969.3(IWS1):c.1357A>G (p.Asn453Asp)	not specified [RCV004284526]	uncertain significance	2	127503439	127503439	Human		name
401771879	CV2693569	single nucleotide variant	NM_017969.3(IWS1):c.1253A>G (p.Asp418Gly)	not specified [RCV004297545]	uncertain significance	2	127503543	127503543	Human		name
405794836	CV3264882	single nucleotide variant	NM_017969.3(IWS1):c.1412A>C (p.Asn471Thr)	not specified [RCV004400969]	uncertain significance	2	127502870	127502870	Human		name
405794834	CV3264883	single nucleotide variant	NM_017969.3(IWS1):c.1906G>A (p.Glu636Lys)	not specified [RCV004400970]	uncertain significance	2	127493304	127493304	Human		name
405794831	CV3264884	single nucleotide variant	NM_017969.3(IWS1):c.2147G>A (p.Arg716Gln)	not specified [RCV004400971]	uncertain significance	2	127489844	127489844	Human		name
407466565	CV3448007	single nucleotide variant	NM_017969.3(IWS1):c.1327G>C (p.Glu443Gln)	not specified [RCV004635665]	uncertain significance	2	127503469	127503469	Human		name
407466567	CV3448008	single nucleotide variant	NM_017969.3(IWS1):c.1482A>T (p.Glu494Asp)	not specified [RCV004635666]	uncertain significance	2	127498223	127498223	Human		name
407466571	CV3448009	single nucleotide variant	NM_017969.3(IWS1):c.1837A>T (p.Met613Leu)	not specified [RCV004635667]	uncertain significance	2	127493373	127493373	Human		name
407511579	CV3448010	single nucleotide variant	NM_017969.3(IWS1):c.2413G>C (p.Ala805Pro)	not specified [RCV004626508]	uncertain significance	2	127481091	127481091	Human		name
597776767	CV3683999	single nucleotide variant	NM_017969.3(IWS1):c.1648G>A (p.Gly550Ser)	not specified [RCV004929692]	uncertain significance	2	127496066	127496066	Human		name
597776769	CV3684000	single nucleotide variant	NM_017969.3(IWS1):c.2309T>C (p.Val770Ala)	not specified [RCV004929693]	uncertain significance	2	127486572	127486572	Human		name
597776773	CV3684001	single nucleotide variant	NM_017969.3(IWS1):c.2150G>A (p.Arg717Lys)	not specified [RCV004929694]	uncertain significance	2	127489841	127489841	Human		name
597776778	CV3684002	single nucleotide variant	NM_017969.3(IWS1):c.2269C>T (p.Pro757Ser)	not specified [RCV004929695]	uncertain significance	2	127486612	127486612	Human		name
597776781	CV3684003	single nucleotide variant	NM_017969.3(IWS1):c.2065A>G (p.Ile689Val)	not specified [RCV004929696]	uncertain significance	2	127489926	127489926	Human		name
597776792	CV3684006	single nucleotide variant	NM_017969.3(IWS1):c.1469G>T (p.Gly490Val)	not specified [RCV004929699]	uncertain significance	2	127498236	127498236	Human		name
597776800	CV3684008	single nucleotide variant	NM_017969.3(IWS1):c.1291A>G (p.Lys431Glu)	not specified [RCV004929701]	uncertain significance	2	127503505	127503505	Human		name
598172120	CV3969201	single nucleotide variant	NM_017969.3(IWS1):c.1616T>G (p.Met539Arg)	not specified [RCV005370714]	uncertain significance	2	127496098	127496098	Human		name
598258426	CV3969202	single nucleotide variant	NM_017969.3(IWS1):c.1620T>A (p.Ser540Arg)	not specified [RCV005347196]	uncertain significance	2	127496094	127496094	Human		name
598258430	CV3969203	single nucleotide variant	NM_017969.3(IWS1):c.1372C>G (p.Leu458Val)	not specified [RCV005347197]	uncertain significance	2	127503424	127503424	Human		name

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