Kcnh3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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91 records found for search term Kcnh3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15156827	CV760014	single nucleotide variant	NM_012284.3(KCNH3):c.1919-9T>C	not provided [RCV000924742]	benign	12	49554328	49554328	Human		name
597787997	CV3687456	single nucleotide variant	NM_012284.3(KCNH3):c.20T>G (p.Leu7Arg)	not specified [RCV004932614]	uncertain significance	12	49539436	49539436	Human		name
150483642	CV1280258	single nucleotide variant	NM_012284.3(KCNH3):c.939A>G (p.Ala313=)	not provided [RCV001715222]	benign	12	49544030	49544030	Human		name
41406067	CV980260	single nucleotide variant	NM_012284.3(KCNH3):c.74C>T (p.Thr25Met)	not provided [RCV001280696]	uncertain significance	12	49539490	49539490	Human		name
329359748	CV2446289	single nucleotide variant	NM_012284.3(KCNH3):c.251G>A (p.Arg84His)	not specified [RCV004249424]	uncertain significance	12	49541073	49541073	Human		name
597788016	CV3687460	single nucleotide variant	NM_012284.3(KCNH3):c.197C>A (p.Ala66Asp)	not specified [RCV004932618]	uncertain significance	12	49541019	49541019	Human		name
597788036	CV3687465	single nucleotide variant	NM_012284.3(KCNH3):c.1113G>A (p.Ala371=)	not specified [RCV004932623]	likely benign	12	49544306	49544306	Human		name
598259632	CV3976067	single nucleotide variant	NM_012284.3(KCNH3):c.239G>A (p.Arg80His)	not specified [RCV005347466]	uncertain significance	12	49541061	49541061	Human		name
15135122	CV713557	single nucleotide variant	NM_012284.3(KCNH3):c.2004C>T (p.Cys668=)	not provided [RCV000965235]	benign	12	49554422	49554422	Human		name
15179134	CV725132	single nucleotide variant	NM_012284.3(KCNH3):c.1110C>T (p.Leu370=)	not provided [RCV000885222]	benign	12	49544303	49544303	Human		name
15192876	CV738684	single nucleotide variant	NM_012284.3(KCNH3):c.2796C>T (p.Ser932=)	not provided [RCV000910673]	benign	12	49557497	49557497	Human		name
15156821	CV753438	single nucleotide variant	NM_012284.3(KCNH3):c.1068C>T (p.Ser356=)	not provided [RCV000924741]	benign	12	49544261	49544261	Human		name
8634702	CV89922	single nucleotide variant	NM_012284.1(KCNH3):c.1846C>T (p.Leu616=)	Malignant melanoma [RCV000070019]	not provided	12	49550257	49550257	Human		name
155994530	CV2253701	single nucleotide variant	NM_012284.3(KCNH3):c.775G>A (p.Gly259Ser)	not specified [RCV004127157]	uncertain significance	12	49543470	49543470	Human		name
156357554	CV2254052	single nucleotide variant	NM_012284.3(KCNH3):c.535G>A (p.Gly179Arg)	not specified [RCV004129501]	uncertain significance	12	49542795	49542795	Human		name
156033791	CV2275160	single nucleotide variant	NM_012284.3(KCNH3):c.484G>A (p.Gly162Ser)	not specified [RCV004136958]	uncertain significance	12	49542744	49542744	Human		name
156033477	CV2376595	single nucleotide variant	NM_012284.3(KCNH3):c.640C>T (p.Pro214Ser)	not specified [RCV004220756]	uncertain significance	12	49543335	49543335	Human		name
155967765	CV2391383	single nucleotide variant	NM_012284.3(KCNH3):c.736G>A (p.Val246Met)	not specified [RCV004239788]	uncertain significance	12	49543431	49543431	Human		name
401738720	CV2721957	single nucleotide variant	NM_012284.3(KCNH3):c.457C>T (p.Arg153Cys)	not specified [RCV004326453]	uncertain significance	12	49542717	49542717	Human		name
401880443	CV2792850	single nucleotide variant	NM_012284.3(KCNH3):c.560G>A (p.Gly187Asp)	not specified [RCV004365595]	uncertain significance	12	49542820	49542820	Human		name
405806558	CV3268597	single nucleotide variant	NM_012284.3(KCNH3):c.472G>A (p.Ala158Thr)	not specified [RCV004406111]	uncertain significance	12	49542732	49542732	Human		name
597787962	CV3687448	single nucleotide variant	NM_012284.3(KCNH3):c.853G>A (p.Val285Met)	not specified [RCV004932606]	uncertain significance	12	49543944	49543944	Human		name
597787989	CV3687454	single nucleotide variant	NM_012284.3(KCNH3):c.485G>T (p.Gly162Val)	not specified [RCV004932612]	uncertain significance	12	49542745	49542745	Human		name
597788012	CV3687459	single nucleotide variant	NM_012284.3(KCNH3):c.554C>G (p.Pro185Arg)	not specified [RCV004932617]	uncertain significance	12	49542814	49542814	Human		name
597788020	CV3687461	single nucleotide variant	NM_012284.3(KCNH3):c.475C>G (p.Arg159Gly)	not specified [RCV004932619]	likely benign	12	49542735	49542735	Human		name
597788028	CV3687463	single nucleotide variant	NM_012284.3(KCNH3):c.427G>A (p.Asp143Asn)	not specified [RCV004932621]	uncertain significance	12	49541746	49541746	Human		name
598259611	CV3976058	single nucleotide variant	NM_012284.3(KCNH3):c.470G>A (p.Arg157Gln)	not specified [RCV005347463]	uncertain significance	12	49542730	49542730	Human		name
598235009	CV3976059	single nucleotide variant	NM_012284.3(KCNH3):c.461G>A (p.Arg154Gln)	not specified [RCV005363600]	uncertain significance	12	49542721	49542721	Human		name
598212913	CV3976063	single nucleotide variant	NM_012284.3(KCNH3):c.580G>A (p.Gly194Arg)	not specified [RCV005358898]	uncertain significance	12	49543275	49543275	Human		name
598259626	CV3976065	single nucleotide variant	NM_012284.3(KCNH3):c.410A>G (p.Lys137Arg)	not specified [RCV005347465]	uncertain significance	12	49541729	49541729	Human		name
156318462	CV2200317	single nucleotide variant	NM_012284.3(KCNH3):c.2498G>C (p.Gly833Ala)	not specified [RCV004076650]	uncertain significance	12	49556399	49556399	Human		name
156372861	CV2204622	single nucleotide variant	NM_012284.3(KCNH3):c.1256G>C (p.Gly419Ala)	not specified [RCV004081729]	uncertain significance	12	49548961	49548961	Human		name
156332625	CV2220715	single nucleotide variant	NM_012284.3(KCNH3):c.2333G>A (p.Arg778His)	not specified [RCV004097885]	uncertain significance	12	49555816	49555816	Human		name
156194444	CV2223346	single nucleotide variant	NM_012284.3(KCNH3):c.1910C>T (p.Ala637Val)	not specified [RCV004105949]	uncertain significance	12	49550321	49550321	Human		name
156067161	CV2236957	single nucleotide variant	NM_012284.3(KCNH3):c.2240A>C (p.Asp747Ala)	not specified [RCV004112952]	uncertain significance	12	49555723	49555723	Human		name
156161670	CV2246436	single nucleotide variant	NM_012284.3(KCNH3):c.1129G>A (p.Val377Ile)	not specified [RCV004110206]	likely benign	12	49544322	49544322	Human		name
156040109	CV2261264	single nucleotide variant	NM_012284.3(KCNH3):c.1798C>T (p.Pro600Ser)	not specified [RCV004128136]	uncertain significance	12	49550209	49550209	Human		name
156007949	CV2288420	single nucleotide variant	NM_012284.3(KCNH3):c.1222A>T (p.Thr408Ser)	not specified [RCV004151968]	uncertain significance	12	49548927	49548927	Human		name
156161664	CV2311756	single nucleotide variant	NM_012284.3(KCNH3):c.2315G>A (p.Arg772Gln)	not specified [RCV004170617]	uncertain significance	12	49555798	49555798	Human		name
156047198	CV2319148	single nucleotide variant	NM_012284.3(KCNH3):c.1073T>C (p.Val358Ala)	not specified [RCV004178214]	uncertain significance	12	49544266	49544266	Human		name
156165844	CV2330078	single nucleotide variant	NM_012284.3(KCNH3):c.2246C>T (p.Pro749Leu)	not specified [RCV004185569]	uncertain significance	12	49555729	49555729	Human		name
156363864	CV2330097	single nucleotide variant	NM_012284.3(KCNH3):c.1187T>C (p.Ile396Thr)	not specified [RCV004185587]	uncertain significance	12	49544380	49544380	Human		name
156039071	CV2332679	single nucleotide variant	NM_012284.3(KCNH3):c.2501C>T (p.Ser834Leu)	not specified [RCV004189356]	uncertain significance	12	49556402	49556402	Human		name
156071681	CV2353214	single nucleotide variant	NM_012284.3(KCNH3):c.1069G>A (p.Ala357Thr)	not specified [RCV004203682]	uncertain significance	12	49544262	49544262	Human		name
156074171	CV2365508	single nucleotide variant	NM_012284.3(KCNH3):c.2740A>G (p.Arg914Gly)	not specified [RCV004211625]	likely benign	12	49557441	49557441	Human		name
156074194	CV2365510	single nucleotide variant	NM_012284.3(KCNH3):c.2887C>T (p.His963Tyr)	not specified [RCV004211627]	uncertain significance	12	49557588	49557588	Human		name
156390700	CV2383328	single nucleotide variant	NM_012284.3(KCNH3):c.2804T>A (p.Leu935Gln)	not specified [RCV004222369]	uncertain significance	12	49557505	49557505	Human		name
155954705	CV2389809	single nucleotide variant	NM_012284.3(KCNH3):c.2777C>T (p.Pro926Leu)	not specified [RCV004236035]	uncertain significance	12	49557478	49557478	Human		name
401731487	CV2674390	single nucleotide variant	NM_012284.3(KCNH3):c.2578A>C (p.Ser860Arg)	not specified [RCV004289260]	uncertain significance	12	49557185	49557185	Human		name
401771321	CV2675550	single nucleotide variant	NM_012284.3(KCNH3):c.2525G>A (p.Arg842His)	not specified [RCV004295165]	uncertain significance	12	49556426	49556426	Human		name
401724676	CV2677954	single nucleotide variant	NM_012284.3(KCNH3):c.2786C>T (p.Ala929Val)	not specified [RCV004296487]	uncertain significance	12	49557487	49557487	Human		name
401732059	CV2677985	single nucleotide variant	NM_012284.3(KCNH3):c.2395G>A (p.Ala799Thr)	not specified [RCV004296515]	uncertain significance	12	49555878	49555878	Human		name
401718107	CV2689617	single nucleotide variant	NM_012284.3(KCNH3):c.2129C>G (p.Ser710Cys)	not specified [RCV004309034]	uncertain significance	12	49554547	49554547	Human		name
401750244	CV2695991	single nucleotide variant	NM_012284.3(KCNH3):c.1295G>A (p.Ser432Asn)	not specified [RCV004308253]	uncertain significance	12	49549000	49549000	Human		name
401866116	CV2762531	single nucleotide variant	NM_012284.3(KCNH3):c.1168G>A (p.Glu390Lys)	not specified [RCV004338065]	uncertain significance	12	49544361	49544361	Human		name
401887264	CV2773272	single nucleotide variant	NM_012284.3(KCNH3):c.1649A>G (p.Asn550Ser)	not specified [RCV004353943]	uncertain significance	12	49549621	49549621	Human		name
401891499	CV2779169	single nucleotide variant	NM_012284.3(KCNH3):c.1151G>A (p.Arg384Gln)	not specified [RCV004349079]	likely benign	12	49544344	49544344	Human		name
401874907	CV2781359	single nucleotide variant	NM_012284.3(KCNH3):c.2645G>A (p.Arg882Gln)	not specified [RCV004352368]	uncertain significance	12	49557252	49557252	Human		name
405806495	CV3268588	single nucleotide variant	NM_012284.3(KCNH3):c.1237G>C (p.Val413Leu)	not specified [RCV004406102]	uncertain significance	12	49548942	49548942	Human		name
405806497	CV3268589	single nucleotide variant	NM_012284.3(KCNH3):c.2126G>C (p.Gly709Ala)	not specified [RCV004406103]	uncertain significance	12	49554544	49554544	Human		name
405806499	CV3268590	single nucleotide variant	NM_012284.3(KCNH3):c.2219C>T (p.Thr740Met)	not specified [RCV004406104]	uncertain significance	12	49555702	49555702	Human		name
405806503	CV3268592	single nucleotide variant	NM_012284.3(KCNH3):c.2581G>A (p.Gly861Ser)	not specified [RCV004406106]	uncertain significance	12	49557188	49557188	Human		name
405806550	CV3268593	single nucleotide variant	NM_012284.3(KCNH3):c.2797G>C (p.Gly933Arg)	not specified [RCV004406107]	uncertain significance	12	49557498	49557498	Human		name
405806552	CV3268594	single nucleotide variant	NM_012284.3(KCNH3):c.2984C>T (p.Thr995Ile)	not specified [RCV004406108]	uncertain significance	12	49557685	49557685	Human		name
407467997	CV3445002	single nucleotide variant	NM_012284.3(KCNH3):c.2524C>T (p.Arg842Cys)	not specified [RCV004636105]	uncertain significance	12	49556425	49556425	Human		name
407468003	CV3445005	single nucleotide variant	NM_012284.3(KCNH3):c.2326C>T (p.Arg776Trp)	not specified [RCV004636107]	uncertain significance	12	49555809	49555809	Human		name
597787942	CV3687443	single nucleotide variant	NM_012284.3(KCNH3):c.2404C>T (p.Arg802Trp)	not specified [RCV004932601]	uncertain significance	12	49555887	49555887	Human		name
597787945	CV3687444	single nucleotide variant	NM_012284.3(KCNH3):c.1952G>A (p.Arg651Gln)	not specified [RCV004932602]	uncertain significance	12	49554370	49554370	Human		name
597787950	CV3687445	single nucleotide variant	NM_012284.3(KCNH3):c.2758C>T (p.Arg920Trp)	not specified [RCV004932603]	uncertain significance	12	49557459	49557459	Human		name
597787966	CV3687449	single nucleotide variant	NM_012284.3(KCNH3):c.2090G>A (p.Arg697Gln)	not specified [RCV004932607]	uncertain significance	12	49554508	49554508	Human		name
597787970	CV3687450	single nucleotide variant	NM_012284.3(KCNH3):c.2048C>T (p.Ala683Val)	not specified [RCV004932608]	uncertain significance	12	49554466	49554466	Human		name
597787974	CV3687451	single nucleotide variant	NM_012284.3(KCNH3):c.1569C>G (p.Asp523Glu)	not specified [RCV004932609]	uncertain significance	12	49549541	49549541	Human		name
597787978	CV3687452	single nucleotide variant	NM_012284.3(KCNH3):c.1462A>C (p.Ile488Leu)	not specified [RCV004932610]	uncertain significance	12	49549167	49549167	Human		name
597787985	CV3687453	single nucleotide variant	NM_012284.3(KCNH3):c.1763G>A (p.Arg588His)	not specified [RCV004932611]	uncertain significance	12	49550174	49550174	Human		name
597787993	CV3687455	single nucleotide variant	NM_012284.3(KCNH3):c.1108C>A (p.Leu370Ile)	not specified [RCV004932613]	uncertain significance	12	49544301	49544301	Human		name
597788001	CV3687457	single nucleotide variant	NM_012284.3(KCNH3):c.1666G>A (p.Glu556Lys)	not specified [RCV004932615]	uncertain significance	12	49549638	49549638	Human		name
597788024	CV3687462	single nucleotide variant	NM_012284.3(KCNH3):c.2707C>T (p.Arg903Cys)	not specified [RCV004932620]	uncertain significance	12	49557408	49557408	Human		name
597788032	CV3687464	single nucleotide variant	NM_012284.3(KCNH3):c.1030C>T (p.Arg344Cys)	not specified [RCV004932622]	uncertain significance	12	49544223	49544223	Human		name
598259605	CV3976057	single nucleotide variant	NM_012284.3(KCNH3):c.2312G>A (p.Arg771His)	not specified [RCV005347462]	uncertain significance	12	49555795	49555795	Human		name
598212899	CV3976060	single nucleotide variant	NM_012284.3(KCNH3):c.1043G>A (p.Arg348Gln)	not specified [RCV005358896]	uncertain significance	12	49544236	49544236	Human		name
598259618	CV3976062	single nucleotide variant	NM_012284.3(KCNH3):c.1567G>C (p.Asp523His)	not specified [RCV005347464]	uncertain significance	12	49549539	49549539	Human		name
598235024	CV3976066	single nucleotide variant	NM_012284.3(KCNH3):c.1096G>A (p.Val366Met)	not specified [RCV005363602]	uncertain significance	12	49544289	49544289	Human		name
329399618	CV2443495	single nucleotide variant	NM_012284.3(KCNH3):c.3065A>G (p.Glu1022Gly)	not specified [RCV004262330]	uncertain significance	12	49557766	49557766	Human		name
401763281	CV2720261	single nucleotide variant	NM_012284.3(KCNH3):c.3088G>A (p.Ala1030Thr)	not specified [RCV004325593]	uncertain significance	12	49557789	49557789	Human		name
401760873	CV2726567	single nucleotide variant	NM_012284.3(KCNH3):c.3148G>A (p.Gly1050Ser)	not specified [RCV004329061]	uncertain significance	12	49557849	49557849	Human		name
401880712	CV2792945	single nucleotide variant	NM_012284.3(KCNH3):c.3146G>A (p.Gly1049Glu)	not specified [RCV004365671]	uncertain significance	12	49557847	49557847	Human		name
405806554	CV3268595	single nucleotide variant	NM_012284.3(KCNH3):c.3139G>A (p.Gly1047Arg)	not specified [RCV004406109]	uncertain significance	12	49557840	49557840	Human		name
405806556	CV3268596	single nucleotide variant	NM_012284.3(KCNH3):c.3173A>C (p.His1058Pro)	not specified [RCV004406110]	uncertain significance	12	49557874	49557874	Human		name
407511754	CV3445004	single nucleotide variant	NM_012284.3(KCNH3):c.3059C>T (p.Pro1020Leu)	not specified [RCV004626567]	uncertain significance	12	49557760	49557760	Human		name
597787951	CV3687446	single nucleotide variant	NM_012284.3(KCNH3):c.3247G>A (p.Val1083Ile)	not specified [RCV004932604]	uncertain significance	12	49557948	49557948	Human		name
598212906	CV3976061	single nucleotide variant	NM_012284.3(KCNH3):c.3101G>A (p.Ser1034Asn)	not specified [RCV005358897]	uncertain significance	12	49557802	49557802	Human		name

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