Dnah12 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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333 records found for search term Dnah12

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
616938121	CV4015775	variation	DNAH12, ILE816MET	SPERMATOGENIC FAILURE 100 [RCV005414307]	pathogenic				Human		name
616938119	CV4015773	single nucleotide variant	DNAH12, GLN2077TER	SPERMATOGENIC FAILURE 100 [RCV005414305]	pathogenic				Human	1	name
616938120	CV4015774	variation	DNAH12, ARG3002CYS	SPERMATOGENIC FAILURE 100 [RCV005414306]	pathogenic				Human		name
616938122	CV4015776	single nucleotide variant	DNAH12, IVS, G-C, -1	SPERMATOGENIC FAILURE 100 [RCV005414308]	pathogenic				Human	1	name
616938123	CV4015777	single nucleotide variant	DNAH12, IVS, G-A, +5	SPERMATOGENIC FAILURE 100 [RCV005414309]	pathogenic				Human	1	name
616938125	CV4015778	deletion	DNAH12, 2-BP DEL, 944TT	SPERMATOGENIC FAILURE 100 [RCV005414310]	pathogenic				Human	1	name
12895827	CV389580	single nucleotide variant	NM_001366028.2(DNAH12):c.3053+9A>G	not provided [RCV004716478]\|not specified [RCV000454507]	benign	3	57458090	57458090	Human		name
12896136	CV389593	single nucleotide variant	NM_001366028.2(DNAH12):c.1912-8A>G	not provided [RCV004716479]\|not specified [RCV000454929]	benign	3	57470644	57470644	Human		name
12896646	CV389651	single nucleotide variant	NM_001366028.2(DNAH12):c.1650+6G>A	not provided [RCV004716480]\|not specified [RCV000455634]	benign	3	57483370	57483370	Human		name
12896371	CV390440	single nucleotide variant	NM_001366028.2(DNAH12):c.6948+922=	not provided [RCV004716473]\|not specified [RCV000455257]	benign	3	57402387	57402387	Human		name
156091085	CV2389414	single nucleotide variant	NM_001366028.2(DNAH12):c.5253+240T>G	not specified [RCV004238145]	uncertain significance	3	57428393	57428393	Human		name
597712633	CV3656041	single nucleotide variant	NM_001366028.2(DNAH12):c.6948+896C>T	not specified [RCV004917957]	uncertain significance	3	57402413	57402413	Human		name
12896909	CV389575	single nucleotide variant	NM_001366028.2(DNAH12):c.5253+289C>T	not provided [RCV004717602]\|not specified [RCV000455980]	benign	3	57428344	57428344	Human		name
12896078	CV389589	single nucleotide variant	NM_001366028.2(DNAH12):c.5253+263A>T	not provided [RCV004716474]\|not specified [RCV000454852]	benign	3	57428370	57428370	Human		name
8630925	CV86081	single nucleotide variant	NM_198564.3(DNAH12):c.161A>T (p.Asn54Ile)	Malignant melanoma [RCV000066165]	not provided	3	57542710	57542710	Human		name
155976290	CV2338584	single nucleotide variant	NM_001366028.2(DNAH12):c.65C>T (p.Pro22Leu)	not specified [RCV004182175]	uncertain significance	3	57542806	57542806	Human		name
405709316	CV3247245	single nucleotide variant	NM_001366028.2(DNAH12):c.70G>T (p.Val24Phe)	not specified [RCV004376388]	uncertain significance	3	57542801	57542801	Human		name
8625649	CV80773	single nucleotide variant	NM_198564.3(DNAH12):c.1055G>A (p.Ser352Asn)	Malignant melanoma [RCV000060850]	not provided	3	57504047	57504047	Human		name
156184460	CV2239206	single nucleotide variant	NM_001366028.2(DNAH12):c.158T>G (p.Ile53Ser)	not specified [RCV004112186]	uncertain significance	3	57542713	57542713	Human		name
329373340	CV2456038	single nucleotide variant	NM_001366028.2(DNAH12):c.137C>G (p.Ser46Cys)	not specified [RCV004272939]	uncertain significance	3	57542734	57542734	Human		name
401922318	CV2827502	single nucleotide variant	NM_001366028.2(DNAH12):c.2751C>G (p.Arg917=)	not provided [RCV003433636]	likely benign	3	57459772	57459772	Human		name
405672368	CV3237634	single nucleotide variant	NM_001366028.2(DNAH12):c.161A>C (p.Asn54Thr)	not specified [RCV004368953]	uncertain significance	3	57542710	57542710	Human		name
405672373	CV3237635	single nucleotide variant	NM_001366028.2(DNAH12):c.181G>T (p.Ala61Ser)	not specified [RCV004368954]	uncertain significance	3	57523874	57523874	Human		name
405672398	CV3237640	single nucleotide variant	NM_001366028.2(DNAH12):c.229C>T (p.Pro77Ser)	not specified [RCV004368959]	uncertain significance	3	57523826	57523826	Human		name
156278126	CV2330893	single nucleotide variant	NM_001366028.2(DNAH12):c.763G>A (p.Ala255Thr)	not specified [RCV004185946]	uncertain significance	3	57507777	57507777	Human		name
156008554	CV2365280	single nucleotide variant	NM_001366028.2(DNAH12):c.857A>T (p.Asp286Val)	not specified [RCV004209374]	uncertain significance	3	57507683	57507683	Human		name
156176751	CV2374469	single nucleotide variant	NM_001366028.2(DNAH12):c.763G>T (p.Ala255Ser)	not specified [RCV004231976]	uncertain significance	3	57507777	57507777	Human		name
329392161	CV2441280	single nucleotide variant	NM_001366028.2(DNAH12):c.418C>T (p.Leu140Phe)	not specified [RCV004257100]	uncertain significance	3	57510841	57510841	Human		name
329378631	CV2447064	single nucleotide variant	NM_001366028.2(DNAH12):c.973A>G (p.Ile325Val)	not specified [RCV004259939]	uncertain significance	3	57504129	57504129	Human		name
401752953	CV2681068	single nucleotide variant	NM_001366028.2(DNAH12):c.632T>C (p.Met211Thr)	not specified [RCV004296129]	uncertain significance	3	57508451	57508451	Human		name
405709198	CV3247229	single nucleotide variant	NM_001366028.2(DNAH12):c.538C>T (p.Pro180Ser)	not specified [RCV004376372]	uncertain significance	3	57509144	57509144	Human		name
405709268	CV3247237	single nucleotide variant	NM_001366028.2(DNAH12):c.646G>A (p.Asp216Asn)	not specified [RCV004376380]	uncertain significance	3	57508437	57508437	Human		name
405709274	CV3247238	single nucleotide variant	NM_001366028.2(DNAH12):c.673A>G (p.Thr225Ala)	not specified [RCV004376381]	uncertain significance	3	57508410	57508410	Human		name
405709402	CV3247258	single nucleotide variant	NM_001366028.2(DNAH12):c.874G>A (p.Val292Ile)	not specified [RCV004376401]	uncertain significance	3	57507666	57507666	Human		name
597641320	CV3656047	single nucleotide variant	NM_001366028.2(DNAH12):c.541G>A (p.Val181Ile)	not specified [RCV004909154]	uncertain significance	3	57509141	57509141	Human		name
597641430	CV3656071	single nucleotide variant	NM_001366028.2(DNAH12):c.527T>C (p.Leu176Ser)	not specified [RCV004909174]	uncertain significance	3	57509155	57509155	Human		name
597641484	CV3656082	single nucleotide variant	NM_001366028.2(DNAH12):c.328C>G (p.Pro110Ala)	not specified [RCV004909184]	uncertain significance	3	57510931	57510931	Human		name
12896334	CV389596	single nucleotide variant	NM_001366028.2(DNAH12):c.672T>G (p.Asp224Glu)	not provided [RCV004716482]\|not specified [RCV000455207]	benign	3	57508411	57508411	Human		name
12896126	CV389618	single nucleotide variant	NM_001366028.2(DNAH12):c.4338C>T (p.Tyr1446=)	not provided [RCV004716476]\|not specified [RCV000454916]	benign	3	57445261	57445261	Human		name
12896597	CV389622	single nucleotide variant	NM_001366028.2(DNAH12):c.3952C>T (p.Leu1318=)	not provided [RCV004716477]\|not specified [RCV000455566]	benign	3	57446258	57446258	Human		name
12895908	CV390439	single nucleotide variant	NM_001366028.2(DNAH12):c.9639G>C (p.Leu3213=)	not provided [RCV004716472]\|not specified [RCV000454622]	benign	3	57352120	57352120	Human		name
598265225	CV3956838	single nucleotide variant	NM_001366028.2(DNAH12):c.479T>C (p.Val160Ala)	not specified [RCV005326303]	uncertain significance	3	57509203	57509203	Human		name
616939713	CV4014211	single nucleotide variant	NM_001366028.2(DNAH12):c.6024C>T (p.Tyr2008=)	not provided [RCV005413704]	likely benign	3	57408532	57408532	Human		name
156152540	CV2194291	single nucleotide variant	NM_001366028.2(DNAH12):c.1163T>G (p.Val388Gly)	not specified [RCV004079408]	uncertain significance	3	57502403	57502403	Human		name
156084728	CV2205610	single nucleotide variant	NM_001366028.2(DNAH12):c.2845C>A (p.Gln949Lys)	not specified [RCV004082528]	uncertain significance	3	57459678	57459678	Human		name
156019291	CV2229986	single nucleotide variant	NM_001366028.2(DNAH12):c.2411A>G (p.Gln804Arg)	not specified [RCV004105794]	uncertain significance	3	57462814	57462814	Human		name
156079408	CV2300922	single nucleotide variant	NM_001366028.2(DNAH12):c.1906C>G (p.Gln636Glu)	not specified [RCV004158112]	uncertain significance	3	57471477	57471477	Human		name
156205337	CV2311350	single nucleotide variant	NM_001366028.2(DNAH12):c.1204C>T (p.Arg402Trp)	not specified [RCV004166418]	uncertain significance	3	57502362	57502362	Human		name
156341545	CV2344845	single nucleotide variant	NM_001366028.2(DNAH12):c.2653C>G (p.Gln885Glu)	not specified [RCV004190986]	uncertain significance	3	57461572	57461572	Human		name
156229954	CV2353030	single nucleotide variant	NM_001366028.2(DNAH12):c.2387G>A (p.Gly796Glu)	not specified [RCV004201058]	uncertain significance	3	57462838	57462838	Human		name
156194973	CV2400444	single nucleotide variant	NM_001366028.2(DNAH12):c.1943G>A (p.Arg648His)	not specified [RCV004246650]	uncertain significance	3	57470605	57470605	Human		name
156170940	CV2400626	single nucleotide variant	NM_001366028.2(DNAH12):c.2425G>C (p.Val809Leu)	not specified [RCV004242311]	uncertain significance	3	57462800	57462800	Human		name
329388092	CV2437039	single nucleotide variant	NM_001366028.2(DNAH12):c.2186A>G (p.Lys729Arg)	not specified [RCV004262852]	uncertain significance	3	57468899	57468899	Human		name
329376483	CV2438243	single nucleotide variant	NM_001366028.2(DNAH12):c.2882T>C (p.Val961Ala)	not specified [RCV004257007]	uncertain significance	3	57459641	57459641	Human		name
329354585	CV2448449	single nucleotide variant	NM_001366028.2(DNAH12):c.1613G>A (p.Arg538Gln)	not specified [RCV004256728]	uncertain significance	3	57483413	57483413	Human		name
329360656	CV2452368	single nucleotide variant	NM_001366028.2(DNAH12):c.2164G>A (p.Glu722Lys)	not specified [RCV004272690]	uncertain significance	3	57468921	57468921	Human		name
401767246	CV2681554	single nucleotide variant	NM_001366028.2(DNAH12):c.1660C>T (p.Arg554Cys)	not specified [RCV004292082]	uncertain significance	3	57472662	57472662	Human		name
401775407	CV2692364	single nucleotide variant	NM_001366028.2(DNAH12):c.2692A>G (p.Met898Val)	not specified [RCV004310345]	uncertain significance	3	57461533	57461533	Human		name
401773670	CV2695323	single nucleotide variant	NM_001366028.2(DNAH12):c.1408C>T (p.Arg470Cys)	not specified [RCV004305234]	uncertain significance	3	57489615	57489615	Human		name
401778848	CV2705772	single nucleotide variant	NM_001366028.2(DNAH12):c.1067G>A (p.Arg356Gln)	not specified [RCV004318608]	uncertain significance	3	57504035	57504035	Human		name
401774502	CV2713508	single nucleotide variant	NM_001366028.2(DNAH12):c.2780A>C (p.Glu927Ala)	not specified [RCV004319109]	uncertain significance	3	57459743	57459743	Human		name
401725131	CV2725712	single nucleotide variant	NM_001366028.2(DNAH12):c.2017T>C (p.Tyr673His)	not specified [RCV004322407]	uncertain significance	3	57470531	57470531	Human		name
401778836	CV2732919	single nucleotide variant	NM_001366028.2(DNAH12):c.2311A>G (p.Met771Val)	not specified [RCV004331098]	uncertain significance	3	57468774	57468774	Human		name
401888839	CV2764977	single nucleotide variant	NM_001366028.2(DNAH12):c.1661G>A (p.Arg554His)	not specified [RCV004335056]	uncertain significance	3	57472661	57472661	Human		name
401891964	CV2775851	single nucleotide variant	NM_001366028.2(DNAH12):c.1751A>G (p.Asn584Ser)	not specified [RCV004344886]	uncertain significance	3	57472571	57472571	Human		name
405263844	CV3185241	single nucleotide variant	NM_001366028.2(DNAH12):c.10836C>T (p.Pro3612=)	not provided [RCV003885805]	likely benign	3	57310777	57310777	Human		name
405672339	CV3237628	single nucleotide variant	NM_001366028.2(DNAH12):c.1003G>A (p.Asp335Asn)	not specified [RCV004368947]	uncertain significance	3	57504099	57504099	Human		name
405672343	CV3237629	single nucleotide variant	NM_001366028.2(DNAH12):c.1016T>C (p.Phe339Ser)	not specified [RCV004368948]	uncertain significance	3	57504086	57504086	Human		name
405672348	CV3237630	single nucleotide variant	NM_001366028.2(DNAH12):c.1246G>A (p.Glu416Lys)	not specified [RCV004368949]	uncertain significance	3	57501410	57501410	Human		name
405672353	CV3237631	single nucleotide variant	NM_001366028.2(DNAH12):c.1277C>T (p.Ala426Val)	not specified [RCV004368950]	uncertain significance	3	57501379	57501379	Human		name
405672358	CV3237632	single nucleotide variant	NM_001366028.2(DNAH12):c.1409G>A (p.Arg470His)	not specified [RCV004368951]	uncertain significance	3	57489614	57489614	Human		name
405672377	CV3237636	single nucleotide variant	NM_001366028.2(DNAH12):c.1865G>A (p.Arg622His)	not specified [RCV004368955]	uncertain significance	3	57471518	57471518	Human		name
405672382	CV3237637	single nucleotide variant	NM_001366028.2(DNAH12):c.2093G>A (p.Arg698Gln)	not specified [RCV004368956]	uncertain significance	3	57470455	57470455	Human		name
405672387	CV3237638	single nucleotide variant	NM_001366028.2(DNAH12):c.2104C>T (p.Arg702Trp)	not specified [RCV004368957]	uncertain significance	3	57470444	57470444	Human		name
405672392	CV3237639	single nucleotide variant	NM_001366028.2(DNAH12):c.2215A>C (p.Lys739Gln)	not specified [RCV004368958]	uncertain significance	3	57468870	57468870	Human		name
405672401	CV3237641	single nucleotide variant	NM_001366028.2(DNAH12):c.2518A>G (p.Ser840Gly)	not specified [RCV004368960]	uncertain significance	3	57462707	57462707	Human		name
405672406	CV3237642	single nucleotide variant	NM_001366028.2(DNAH12):c.2524G>A (p.Gly842Ser)	not specified [RCV004368961]	uncertain significance	3	57462701	57462701	Human		name
405672412	CV3237643	single nucleotide variant	NM_001366028.2(DNAH12):c.2599A>G (p.Ile867Val)	not specified [RCV004368962]	uncertain significance	3	57461626	57461626	Human		name
405672416	CV3237644	single nucleotide variant	NM_001366028.2(DNAH12):c.2609A>G (p.Tyr870Cys)	not specified [RCV004368963]	uncertain significance	3	57461616	57461616	Human		name
405672421	CV3237645	single nucleotide variant	NM_001366028.2(DNAH12):c.2759G>A (p.Arg920Gln)	not specified [RCV004368964]	uncertain significance	3	57459764	57459764	Human		name
405672424	CV3237646	single nucleotide variant	NM_001366028.2(DNAH12):c.2932G>T (p.Val978Phe)	not specified [RCV004368965]	uncertain significance	3	57458220	57458220	Human		name
407453483	CV3441023	single nucleotide variant	NM_001366028.2(DNAH12):c.1298T>C (p.Phe433Ser)	not specified [RCV004609058]	uncertain significance	3	57501358	57501358	Human		name
407453499	CV3441027	single nucleotide variant	NM_001366028.2(DNAH12):c.2558T>C (p.Met853Thr)	not specified [RCV004609062]	uncertain significance	3	57461667	57461667	Human		name
407453513	CV3441032	single nucleotide variant	NM_001366028.2(DNAH12):c.1862G>A (p.Arg621His)	not specified [RCV004609067]	uncertain significance	3	57471521	57471521	Human		name
407453515	CV3441033	single nucleotide variant	NM_001366028.2(DNAH12):c.1723A>G (p.Thr575Ala)	not specified [RCV004609068]	likely benign	3	57472599	57472599	Human		name
407453521	CV3441035	single nucleotide variant	NM_001366028.2(DNAH12):c.1321G>A (p.Asp441Asn)	not specified [RCV004609070]	uncertain significance	3	57501335	57501335	Human		name
407453523	CV3441036	single nucleotide variant	NM_001366028.2(DNAH12):c.1817T>C (p.Met606Thr)	not specified [RCV004609071]	uncertain significance	3	57471566	57471566	Human		name
407453539	CV3441042	single nucleotide variant	NM_001366028.2(DNAH12):c.2254C>T (p.Arg752Trp)	not specified [RCV004609077]	uncertain significance	3	57468831	57468831	Human		name
597641359	CV3656057	single nucleotide variant	NM_001366028.2(DNAH12):c.1360G>A (p.Ala454Thr)	not specified [RCV004909161]	uncertain significance	3	57489663	57489663	Human		name
597641396	CV3656064	single nucleotide variant	NM_001366028.2(DNAH12):c.2576C>G (p.Thr859Ser)	not specified [RCV004909168]	uncertain significance	3	57461649	57461649	Human		name
597641412	CV3656067	single nucleotide variant	NM_001366028.2(DNAH12):c.2765A>C (p.Gln922Pro)	not specified [RCV004909171]	uncertain significance	3	57459758	57459758	Human		name
597641418	CV3656069	single nucleotide variant	NM_001366028.2(DNAH12):c.1546C>A (p.His516Asn)	not specified [RCV004909172]	uncertain significance	3	57483480	57483480	Human		name
597641453	CV3656075	single nucleotide variant	NM_001366028.2(DNAH12):c.1022C>T (p.Pro341Leu)	not specified [RCV004909178]	uncertain significance	3	57504080	57504080	Human		name
597641475	CV3656079	single nucleotide variant	NM_001366028.2(DNAH12):c.2694G>A (p.Met898Ile)	not specified [RCV004909182]	uncertain significance	3	57461531	57461531	Human		name
597641496	CV3656084	single nucleotide variant	NM_001366028.2(DNAH12):c.2412G>C (p.Gln804His)	not specified [RCV004909186]	uncertain significance	3	57462813	57462813	Human		name
597712741	CV3656090	single nucleotide variant	NM_001366028.2(DNAH12):c.2507T>C (p.Phe836Ser)	not specified [RCV004917967]	uncertain significance	3	57462718	57462718	Human		name
12895834	CV389594	single nucleotide variant	NM_001366028.2(DNAH12):c.1399A>C (p.Thr467Pro)	not provided [RCV004716481]\|not specified [RCV000454517]	benign	3	57489624	57489624	Human		name
598265049	CV3956803	single nucleotide variant	NM_001366028.2(DNAH12):c.1537A>G (p.Ile513Val)	not specified [RCV005326268]	uncertain significance	3	57483489	57483489	Human		name
598265067	CV3956806	single nucleotide variant	NM_001366028.2(DNAH12):c.2866C>T (p.Arg956Cys)	not specified [RCV005326271]	uncertain significance	3	57459657	57459657	Human		name
598265078	CV3956808	single nucleotide variant	NM_001366028.2(DNAH12):c.2168T>A (p.Phe723Tyr)	not specified [RCV005326273]	uncertain significance	3	57468917	57468917	Human		name
598265083	CV3956809	single nucleotide variant	NM_001366028.2(DNAH12):c.1861C>T (p.Arg621Cys)	not specified [RCV005326274]	uncertain significance	3	57471522	57471522	Human		name
598265088	CV3956810	single nucleotide variant	NM_001366028.2(DNAH12):c.2778T>A (p.Asp926Glu)	not specified [RCV005326275]	uncertain significance	3	57459745	57459745	Human		name
598265098	CV3956812	single nucleotide variant	NM_001366028.2(DNAH12):c.2057A>G (p.Tyr686Cys)	not specified [RCV005326277]	uncertain significance	3	57470491	57470491	Human		name
598265104	CV3956813	single nucleotide variant	NM_001366028.2(DNAH12):c.2629A>G (p.Ile877Val)	not specified [RCV005326278]	uncertain significance	3	57461596	57461596	Human		name
598265109	CV3956814	single nucleotide variant	NM_001366028.2(DNAH12):c.1280T>G (p.Val427Gly)	not specified [RCV005326279]	uncertain significance	3	57501376	57501376	Human		name
598265120	CV3956816	single nucleotide variant	NM_001366028.2(DNAH12):c.2794C>G (p.Gln932Glu)	not specified [RCV005326281]	uncertain significance	3	57459729	57459729	Human		name
598265125	CV3956817	single nucleotide variant	NM_001366028.2(DNAH12):c.2750G>A (p.Arg917His)	not specified [RCV005326282]	uncertain significance	3	57459773	57459773	Human		name
598265163	CV3956825	single nucleotide variant	NM_001366028.2(DNAH12):c.2714A>G (p.Lys905Arg)	not specified [RCV005326290]	uncertain significance	3	57461511	57461511	Human		name
598265168	CV3956826	single nucleotide variant	NM_001366028.2(DNAH12):c.1295C>T (p.Thr432Ile)	not specified [RCV005326291]	uncertain significance	3	57501361	57501361	Human		name
598265195	CV3956832	single nucleotide variant	NM_001366028.2(DNAH12):c.1634T>G (p.Leu545Trp)	not specified [RCV005326297]	uncertain significance	3	57483392	57483392	Human		name
598265266	CV3956846	single nucleotide variant	NM_001366028.2(DNAH12):c.2114A>G (p.Asp705Gly)	not specified [RCV005326311]	uncertain significance	3	57468971	57468971	Human		name
598265271	CV3956847	single nucleotide variant	NM_001366028.2(DNAH12):c.2818C>G (p.Pro940Ala)	not specified [RCV005326312]	uncertain significance	3	57459705	57459705	Human		name
156372706	CV2194531	single nucleotide variant	NM_001366028.2(DNAH12):c.5885G>A (p.Arg1962His)	not specified [RCV004081597]	uncertain significance	3	57413881	57413881	Human		name
156192201	CV2223163	single nucleotide variant	NM_001366028.2(DNAH12):c.4798A>T (p.Met1600Leu)	not specified [RCV004104008]	uncertain significance	3	57433686	57433686	Human		name
156120260	CV2233633	single nucleotide variant	NM_001366028.2(DNAH12):c.5996G>A (p.Arg1999Gln)	not specified [RCV004100092]	uncertain significance	3	57413770	57413770	Human		name
156051803	CV2238100	single nucleotide variant	NM_001366028.2(DNAH12):c.6386G>C (p.Arg2129Thr)	not specified [RCV004111116]	uncertain significance	3	57405843	57405843	Human		name
156065472	CV2240298	single nucleotide variant	NM_001366028.2(DNAH12):c.3675G>C (p.Glu1225Asp)	not specified [RCV004112857]	uncertain significance	3	57452954	57452954	Human		name
155948550	CV2245953	single nucleotide variant	NM_001366028.2(DNAH12):c.5546A>G (p.Tyr1849Cys)	not specified [RCV004113576]	uncertain significance	3	57421534	57421534	Human		name
156206678	CV2249976	single nucleotide variant	NM_001366028.2(DNAH12):c.6699G>C (p.Gln2233His)	not specified [RCV004122944]	uncertain significance	3	57405025	57405025	Human		name
156099622	CV2250688	single nucleotide variant	NM_001366028.2(DNAH12):c.5185G>A (p.Ala1729Thr)	not specified [RCV004129310]	uncertain significance	3	57428701	57428701	Human		name
155962295	CV2254378	single nucleotide variant	NM_001366028.2(DNAH12):c.5752T>C (p.Ser1918Pro)	not specified [RCV004123768]	uncertain significance	3	57415527	57415527	Human		name
156105245	CV2260643	single nucleotide variant	NM_001366028.2(DNAH12):c.5162C>T (p.Pro1721Leu)	not specified [RCV004123401]	uncertain significance	3	57428724	57428724	Human		name
156260010	CV2274158	single nucleotide variant	NM_001366028.2(DNAH12):c.5480A>T (p.Asp1827Val)	not specified [RCV004134794]	uncertain significance	3	57421600	57421600	Human		name
156273361	CV2277727	single nucleotide variant	NM_001366028.2(DNAH12):c.3118G>A (p.Val1040Ile)	not specified [RCV004147168]	uncertain significance	3	57457939	57457939	Human		name
156258273	CV2277728	single nucleotide variant	NM_001366028.2(DNAH12):c.4711G>A (p.Ala1571Thr)	not specified [RCV004147169]	uncertain significance	3	57433773	57433773	Human		name
156251247	CV2286823	single nucleotide variant	NM_001366028.2(DNAH12):c.9685G>C (p.Glu3229Gln)	not specified [RCV004142625]	uncertain significance	3	57334930	57334930	Human		name
156276932	CV2287786	single nucleotide variant	NM_001366028.2(DNAH12):c.3922T>G (p.Tyr1308Asp)	not specified [RCV004143234]	uncertain significance	3	57446554	57446554	Human		name
156002565	CV2288064	single nucleotide variant	NM_001366028.2(DNAH12):c.5387T>C (p.Phe1796Ser)	not specified [RCV004147817]	uncertain significance	3	57421693	57421693	Human		name
156146212	CV2289163	single nucleotide variant	NM_001366028.2(DNAH12):c.4247C>T (p.Ser1416Phe)	not specified [RCV004150383]	uncertain significance	3	57445352	57445352	Human		name
155906799	CV2303383	single nucleotide variant	NM_001366028.2(DNAH12):c.3400A>C (p.Ile1134Leu)	not specified [RCV004159115]	uncertain significance	3	57454831	57454831	Human		name
155956736	CV2304067	single nucleotide variant	NM_001366028.2(DNAH12):c.6172A>G (p.Met2058Val)	not specified [RCV004170112]	uncertain significance	3	57408384	57408384	Human		name
156061099	CV2305462	single nucleotide variant	NM_001366028.2(DNAH12):c.3818C>A (p.Ala1273Asp)	not specified [RCV004165181]	uncertain significance	3	57446658	57446658	Human		name
156168485	CV2315388	single nucleotide variant	NM_001366028.2(DNAH12):c.6010T>G (p.Cys2004Gly)	not specified [RCV004167356]	uncertain significance	3	57413756	57413756	Human		name
156048547	CV2319247	single nucleotide variant	NM_001366028.2(DNAH12):c.9955C>G (p.Leu3319Val)	not specified [RCV004178291]	uncertain significance	3	57334488	57334488	Human		name
156061366	CV2323166	single nucleotide variant	NM_001366028.2(DNAH12):c.4250A>G (p.Tyr1417Cys)	not specified [RCV004187569]	uncertain significance	3	57445349	57445349	Human		name
156072137	CV2325288	single nucleotide variant	NM_001366028.2(DNAH12):c.5494C>T (p.Pro1832Ser)	not specified [RCV004177683]	uncertain significance	3	57421586	57421586	Human		name
156081278	CV2333743	single nucleotide variant	NM_001366028.2(DNAH12):c.6419G>A (p.Arg2140His)	not specified [RCV004181254]	uncertain significance	3	57405810	57405810	Human		name
155919693	CV2343205	single nucleotide variant	NM_001366028.2(DNAH12):c.4054A>C (p.Ile1352Leu)	not specified [RCV004194835]	uncertain significance	3	57446156	57446156	Human		name
156244724	CV2347182	single nucleotide variant	NM_001366028.2(DNAH12):c.4990A>T (p.Met1664Leu)	not specified [RCV004204655]	uncertain significance	3	57429765	57429765	Human		name
156077512	CV2351045	single nucleotide variant	NM_001366028.2(DNAH12):c.6196G>C (p.Val2066Leu)	not specified [RCV004211867]	uncertain significance	3	57408360	57408360	Human		name
156137705	CV2354446	single nucleotide variant	NM_001366028.2(DNAH12):c.6181A>G (p.Ile2061Val)	not specified [RCV004202440]	uncertain significance	3	57408375	57408375	Human		name
156016058	CV2360384	single nucleotide variant	NM_001366028.2(DNAH12):c.4597G>A (p.Val1533Ile)	not specified [RCV004208714]	uncertain significance	3	57437009	57437009	Human		name
155930493	CV2361162	single nucleotide variant	NM_001366028.2(DNAH12):c.6271A>G (p.Met2091Val)	not specified [RCV004216350]	uncertain significance	3	57408285	57408285	Human		name
156211614	CV2370377	single nucleotide variant	NM_001366028.2(DNAH12):c.3623A>G (p.His1208Arg)	not specified [RCV004213277]	uncertain significance	3	57453006	57453006	Human		name
156401870	CV2371071	single nucleotide variant	NM_001366028.2(DNAH12):c.3935G>A (p.Gly1312Glu)	not specified [RCV004220827]	uncertain significance	3	57446541	57446541	Human		name
155957542	CV2387512	single nucleotide variant	NM_001366028.2(DNAH12):c.4702C>T (p.His1568Tyr)	not specified [RCV004240365]	uncertain significance	3	57433782	57433782	Human		name
155957552	CV2387513	single nucleotide variant	NM_001366028.2(DNAH12):c.4703A>T (p.His1568Leu)	not specified [RCV004240366]	uncertain significance	3	57433781	57433781	Human		name
156170959	CV2400627	single nucleotide variant	NM_001366028.2(DNAH12):c.4516G>A (p.Gly1506Ser)	not specified [RCV004242312]	uncertain significance	3	57444726	57444726	Human		name
329385889	CV2428132	single nucleotide variant	NM_001366028.2(DNAH12):c.3251C>T (p.Ala1084Val)	not specified [RCV004251174]	uncertain significance	3	57457806	57457806	Human		name
329376677	CV2428504	single nucleotide variant	NM_001366028.2(DNAH12):c.9760C>T (p.Pro3254Ser)	not specified [RCV004253290]	uncertain significance	3	57334855	57334855	Human		name
329359139	CV2435309	single nucleotide variant	NM_001366028.2(DNAH12):c.5663T>C (p.Met1888Thr)	not specified [RCV004252972]	uncertain significance	3	57419418	57419418	Human		name
329360394	CV2442767	single nucleotide variant	NM_001366028.2(DNAH12):c.5794G>A (p.Asp1932Asn)	not specified [RCV004251599]	uncertain significance	3	57415485	57415485	Human		name
329364578	CV2443708	single nucleotide variant	NM_001366028.2(DNAH12):c.5681C>T (p.Thr1894Met)	not specified [RCV004256008]	uncertain significance	3	57419400	57419400	Human		name
329391965	CV2445224	single nucleotide variant	NM_001366028.2(DNAH12):c.3958T>G (p.Ser1320Ala)	not specified [RCV004263857]	uncertain significance	3	57446252	57446252	Human		name
329385478	CV2451474	single nucleotide variant	NM_001366028.2(DNAH12):c.6355C>T (p.Arg2119Cys)	not specified [RCV004272142]	uncertain significance	3	57405874	57405874	Human		name
329402452	CV2454273	single nucleotide variant	NM_001366028.2(DNAH12):c.9808G>C (p.Glu3270Gln)	not specified [RCV004265743]	uncertain significance	3	57334807	57334807	Human		name
329362031	CV2456660	single nucleotide variant	NM_001366028.2(DNAH12):c.3947A>G (p.Lys1316Arg)	not specified [RCV004277843]	uncertain significance	3	57446263	57446263	Human		name
329394807	CV2457613	single nucleotide variant	NM_001366028.2(DNAH12):c.4445A>G (p.Asp1482Gly)	not specified [RCV004269472]	uncertain significance	3	57444797	57444797	Human		name
329382288	CV2465158	single nucleotide variant	NM_001366028.2(DNAH12):c.4835A>G (p.His1612Arg)	not specified [RCV004287207]	uncertain significance	3	57433649	57433649	Human		name
401729187	CV2673183	single nucleotide variant	NM_001366028.2(DNAH12):c.3254G>A (p.Arg1085Gln)	not specified [RCV004285994]	uncertain significance	3	57457803	57457803	Human		name
401768380	CV2675290	single nucleotide variant	NM_001366028.2(DNAH12):c.4169A>G (p.Asp1390Gly)	not specified [RCV004290055]	uncertain significance	3	57446041	57446041	Human		name
401727924	CV2678587	single nucleotide variant	NM_001366028.2(DNAH12):c.5630A>T (p.Gln1877Leu)	not specified [RCV004292594]	uncertain significance	3	57419451	57419451	Human		name
401727156	CV2684492	single nucleotide variant	NM_001366028.2(DNAH12):c.5737A>G (p.Thr1913Ala)	not specified [RCV004291564]	uncertain significance	3	57415542	57415542	Human		name
401781923	CV2690003	single nucleotide variant	NM_001366028.2(DNAH12):c.9799C>T (p.Arg3267Trp)	not specified [RCV004299883]	uncertain significance	3	57334816	57334816	Human		name
401733328	CV2691270	single nucleotide variant	NM_001366028.2(DNAH12):c.5861T>C (p.Ile1954Thr)	not specified [RCV004303032]	uncertain significance	3	57413905	57413905	Human		name
401783201	CV2703874	single nucleotide variant	NM_001366028.2(DNAH12):c.4967A>G (p.Asp1656Gly)	not specified [RCV004306736]	uncertain significance	3	57433380	57433380	Human		name
401760547	CV2705983	single nucleotide variant	NM_001366028.2(DNAH12):c.3941T>G (p.Phe1314Cys)	not specified [RCV004320901]	uncertain significance	3	57446269	57446269	Human		name
401730411	CV2711282	single nucleotide variant	NM_001366028.2(DNAH12):c.9704T>C (p.Leu3235Pro)	not specified [RCV004313063]	uncertain significance	3	57334911	57334911	Human		name
401749162	CV2713808	single nucleotide variant	NM_001366028.2(DNAH12):c.3031A>G (p.Lys1011Glu)	not specified [RCV004321148]	uncertain significance	3	57458121	57458121	Human		name
401725630	CV2721864	single nucleotide variant	NM_001366028.2(DNAH12):c.5434C>T (p.Arg1812Cys)	not specified [RCV004326375]	uncertain significance	3	57421646	57421646	Human		name
401723644	CV2724977	single nucleotide variant	NM_001366028.2(DNAH12):c.9959G>A (p.Arg3320Gln)	not specified [RCV004319740]	uncertain significance	3	57334484	57334484	Human		name
401777118	CV2730149	single nucleotide variant	NM_001366028.2(DNAH12):c.3263T>C (p.Val1088Ala)	not specified [RCV004332433]	uncertain significance	3	57457794	57457794	Human		name
401878805	CV2754833	single nucleotide variant	NM_001366028.2(DNAH12):c.4348A>G (p.Met1450Val)	not specified [RCV004341310]	uncertain significance	3	57445251	57445251	Human		name
401866107	CV2762527	single nucleotide variant	NM_001366028.2(DNAH12):c.9538A>C (p.Lys3180Gln)	not specified [RCV004338061]	uncertain significance	3	57352221	57352221	Human		name
401866312	CV2762602	single nucleotide variant	NM_001366028.2(DNAH12):c.4858G>A (p.Ala1620Thr)	not specified [RCV004338125]	uncertain significance	3	57433489	57433489	Human		name
401864600	CV2781881	single nucleotide variant	NM_001366028.2(DNAH12):c.3341A>C (p.Tyr1114Ser)	not specified [RCV004356823]	uncertain significance	3	57454890	57454890	Human		name
401866724	CV2782926	single nucleotide variant	NM_001366028.2(DNAH12):c.3514G>A (p.Val1172Ile)	not specified [RCV004361725]	uncertain significance	3	57453346	57453346	Human		name
401885256	CV2786723	single nucleotide variant	NM_001366028.2(DNAH12):c.4732A>C (p.Asn1578His)	not specified [RCV004363840]	uncertain significance	3	57433752	57433752	Human		name
405672430	CV3237647	single nucleotide variant	NM_001366028.2(DNAH12):c.3037C>T (p.Arg1013Cys)	not specified [RCV004368966]	uncertain significance	3	57458115	57458115	Human		name
405672436	CV3237648	single nucleotide variant	NM_001366028.2(DNAH12):c.3254G>T (p.Arg1085Leu)	not specified [RCV004368967]	uncertain significance	3	57457803	57457803	Human		name
405672439	CV3237649	single nucleotide variant	NM_001366028.2(DNAH12):c.3301C>T (p.Arg1101Trp)	not specified [RCV004368968]	uncertain significance	3	57457756	57457756	Human		name
405672444	CV3237650	single nucleotide variant	NM_001366028.2(DNAH12):c.3370C>G (p.Arg1124Gly)	not specified [RCV004368969]	uncertain significance	3	57454861	57454861	Human		name
405672449	CV3237651	single nucleotide variant	NM_001366028.2(DNAH12):c.3688C>T (p.Arg1230Cys)	not specified [RCV004368970]	uncertain significance	3	57452941	57452941	Human		name
405682381	CV3237652	single nucleotide variant	NM_001366028.2(DNAH12):c.3910G>A (p.Asp1304Asn)	not specified [RCV004371421]	uncertain significance	3	57446566	57446566	Human		name
405682386	CV3237653	single nucleotide variant	NM_001366028.2(DNAH12):c.3946A>G (p.Lys1316Glu)	not specified [RCV004371422]	uncertain significance	3	57446264	57446264	Human		name
405682391	CV3237654	single nucleotide variant	NM_001366028.2(DNAH12):c.3955G>T (p.Ala1319Ser)	not specified [RCV004371423]	uncertain significance	3	57446255	57446255	Human		name
405682396	CV3237655	single nucleotide variant	NM_001366028.2(DNAH12):c.4109C>T (p.Pro1370Leu)	not specified [RCV004371424]	uncertain significance	3	57446101	57446101	Human		name
405682408	CV3237657	single nucleotide variant	NM_001366028.2(DNAH12):c.4339G>C (p.Asp1447His)	not specified [RCV004371426]	uncertain significance	3	57445260	57445260	Human		name
405682411	CV3237658	single nucleotide variant	NM_001366028.2(DNAH12):c.4433G>A (p.Arg1478Gln)	not specified [RCV004371427]	uncertain significance	3	57444809	57444809	Human		name
405682416	CV3237659	single nucleotide variant	NM_001366028.2(DNAH12):c.4712C>T (p.Ala1571Val)	not specified [RCV004371428]	uncertain significance	3	57433772	57433772	Human		name
405682420	CV3247224	single nucleotide variant	NM_001366028.2(DNAH12):c.4761G>T (p.Lys1587Asn)	not specified [RCV004371429]	uncertain significance	3	57433723	57433723	Human		name
405682425	CV3247225	single nucleotide variant	NM_001366028.2(DNAH12):c.4951A>G (p.Met1651Val)	not specified [RCV004371430]	uncertain significance	3	57433396	57433396	Human		name
405682430	CV3247226	single nucleotide variant	NM_001366028.2(DNAH12):c.5029C>T (p.Leu1677Phe)	not specified [RCV004371431]	uncertain significance	3	57429726	57429726	Human		name
405709186	CV3247227	single nucleotide variant	NM_001366028.2(DNAH12):c.5044A>G (p.Met1682Val)	not specified [RCV004376370]	uncertain significance	3	57429711	57429711	Human		name
405709192	CV3247228	single nucleotide variant	NM_001366028.2(DNAH12):c.5216T>C (p.Ile1739Thr)	not specified [RCV004376371]	uncertain significance	3	57428670	57428670	Human		name
405709205	CV3247230	single nucleotide variant	NM_001366028.2(DNAH12):c.5477A>T (p.Asp1826Val)	not specified [RCV004376373]	uncertain significance	3	57421603	57421603	Human		name
405709216	CV3247231	single nucleotide variant	NM_001366028.2(DNAH12):c.5585T>C (p.Val1862Ala)	not specified [RCV004376374]	uncertain significance	3	57419496	57419496	Human		name
405709223	CV3247232	single nucleotide variant	NM_001366028.2(DNAH12):c.5839G>A (p.Ala1947Thr)	not specified [RCV004376375]	uncertain significance	3	57415440	57415440	Human		name
405709232	CV3247233	single nucleotide variant	NM_001366028.2(DNAH12):c.6176T>C (p.Val2059Ala)	not specified [RCV004376376]	uncertain significance	3	57408380	57408380	Human		name
405709239	CV3247234	single nucleotide variant	NM_001366028.2(DNAH12):c.6364C>T (p.Arg2122Trp)	not specified [RCV004376377]	uncertain significance	3	57405865	57405865	Human		name
405709250	CV3247235	single nucleotide variant	NM_001366028.2(DNAH12):c.6418C>T (p.Arg2140Cys)	not specified [RCV004376378]	uncertain significance	3	57405811	57405811	Human		name
405709258	CV3247236	single nucleotide variant	NM_001366028.2(DNAH12):c.6523T>G (p.Phe2175Val)	not specified [RCV004376379]	uncertain significance	3	57405706	57405706	Human		name
405709280	CV3247239	single nucleotide variant	NM_001366028.2(DNAH12):c.6911A>G (p.Lys2304Arg)	not specified [RCV004376382]	uncertain significance	3	57403346	57403346	Human		name
405709285	CV3247240	single nucleotide variant	NM_001366028.2(DNAH12):c.9568T>C (p.Tyr3190His)	not specified [RCV004376383]	uncertain significance	3	57352191	57352191	Human		name
405709294	CV3247241	single nucleotide variant	NM_001366028.2(DNAH12):c.9598T>C (p.Tyr3200His)	not specified [RCV004376384]	uncertain significance	3	57352161	57352161	Human		name
405709298	CV3247242	single nucleotide variant	NM_001366028.2(DNAH12):c.9626A>G (p.Glu3209Gly)	not specified [RCV004376385]	uncertain significance	3	57352133	57352133	Human		name
405709305	CV3247243	single nucleotide variant	NM_001366028.2(DNAH12):c.9642A>T (p.Leu3214Phe)	not specified [RCV004376386]	uncertain significance	3	57352117	57352117	Human		name
405709310	CV3247244	single nucleotide variant	NM_001366028.2(DNAH12):c.9679A>G (p.Arg3227Gly)	not specified [RCV004376387]	uncertain significance	3	57334936	57334936	Human		name
405709322	CV3247246	single nucleotide variant	NM_001366028.2(DNAH12):c.9857A>G (p.Tyr3286Cys)	not specified [RCV004376389]	uncertain significance	3	57334586	57334586	Human		name
405709328	CV3247247	single nucleotide variant	NM_001366028.2(DNAH12):c.9988G>A (p.Ala3330Thr)	not specified [RCV004376390]	uncertain significance	3	57323610	57323610	Human		name
407453763	CV3416383	single nucleotide variant	NM_001366028.2(DNAH12):c.5740G>A (p.Gly1914Ser)	not provided [RCV004597641]	likely benign	3	57415539	57415539	Human		name
407453479	CV3441022	single nucleotide variant	NM_001366028.2(DNAH12):c.9614G>A (p.Arg3205Gln)	not specified [RCV004609057]	uncertain significance	3	57352145	57352145	Human		name
407453488	CV3441024	single nucleotide variant	NM_001366028.2(DNAH12):c.4196T>C (p.Val1399Ala)	not specified [RCV004609059]	uncertain significance	3	57445403	57445403	Human		name
407453493	CV3441025	single nucleotide variant	NM_001366028.2(DNAH12):c.3528G>T (p.Leu1176Phe)	not specified [RCV004609060]	uncertain significance	3	57453332	57453332	Human		name
407453497	CV3441026	single nucleotide variant	NM_001366028.2(DNAH12):c.6520C>A (p.His2174Asn)	not specified [RCV004609061]	uncertain significance	3	57405709	57405709	Human		name
407453501	CV3441028	single nucleotide variant	NM_001366028.2(DNAH12):c.3313G>A (p.Asp1105Asn)	not specified [RCV004609063]	uncertain significance	3	57457744	57457744	Human		name
407453503	CV3441029	single nucleotide variant	NM_001366028.2(DNAH12):c.3005T>C (p.Met1002Thr)	not specified [RCV004609064]	uncertain significance	3	57458147	57458147	Human		name
407453508	CV3441030	single nucleotide variant	NM_001366028.2(DNAH12):c.9692A>G (p.Glu3231Gly)	not specified [RCV004609065]	uncertain significance	3	57334923	57334923	Human		name
407453510	CV3441031	single nucleotide variant	NM_001366028.2(DNAH12):c.4321T>A (p.Ser1441Thr)	not specified [RCV004609066]	uncertain significance	3	57445278	57445278	Human		name
407453518	CV3441034	single nucleotide variant	NM_001366028.2(DNAH12):c.5428G>T (p.Gly1810Cys)	not specified [RCV004609069]	uncertain significance	3	57421652	57421652	Human		name
407453526	CV3441037	single nucleotide variant	NM_001366028.2(DNAH12):c.4391A>G (p.Lys1464Arg)	not specified [RCV004609072]	uncertain significance	3	57445208	57445208	Human		name
407453528	CV3441038	single nucleotide variant	NM_001366028.2(DNAH12):c.6356G>A (p.Arg2119His)	not specified [RCV004609073]	uncertain significance	3	57405873	57405873	Human		name
407453531	CV3441039	single nucleotide variant	NM_001366028.2(DNAH12):c.9850C>T (p.His3284Tyr)	not specified [RCV004609074]	uncertain significance	3	57334593	57334593	Human		name
407453534	CV3441040	single nucleotide variant	NM_001366028.2(DNAH12):c.4451A>T (p.Asn1484Ile)	not specified [RCV004609075]	uncertain significance	3	57444791	57444791	Human		name
407453536	CV3441041	single nucleotide variant	NM_001366028.2(DNAH12):c.5054C>T (p.Ser1685Phe)	not specified [RCV004609076]	uncertain significance	3	57429701	57429701	Human		name
407453541	CV3441043	single nucleotide variant	NM_001366028.2(DNAH12):c.4471C>T (p.His1491Tyr)	not specified [RCV004609078]	uncertain significance	3	57444771	57444771	Human		name
596947026	CV3547088	single nucleotide variant	NM_001366028.2(DNAH12):c.3160T>G (p.Leu1054Val)	not provided [RCV004810895]	benign	3	57457897	57457897	Human		name
597641295	CV3656040	single nucleotide variant	NM_001366028.2(DNAH12):c.6179G>A (p.Arg2060Gln)	not specified [RCV004909150]	uncertain significance	3	57408377	57408377	Human		name
597641301	CV3656042	single nucleotide variant	NM_001366028.2(DNAH12):c.5830C>T (p.Arg1944Trp)	not specified [RCV004909151]	uncertain significance	3	57415449	57415449	Human		name
597641307	CV3656043	single nucleotide variant	NM_001366028.2(DNAH12):c.3011G>A (p.Gly1004Asp)	not specified [RCV004909152]	uncertain significance	3	57458141	57458141	Human		name
597712641	CV3656044	single nucleotide variant	NM_001366028.2(DNAH12):c.4894C>G (p.Pro1632Ala)	not specified [RCV004917958]	uncertain significance	3	57433453	57433453	Human		name
597641313	CV3656045	single nucleotide variant	NM_001366028.2(DNAH12):c.9991A>G (p.Ile3331Val)	not specified [RCV004909153]	uncertain significance	3	57323607	57323607	Human		name
597712653	CV3656046	single nucleotide variant	NM_001366028.2(DNAH12):c.6064G>C (p.Glu2022Gln)	not specified [RCV004917959]	likely benign	3	57408492	57408492	Human		name
597641325	CV3656048	single nucleotide variant	NM_001366028.2(DNAH12):c.9560G>A (p.Arg3187His)	not specified [RCV004909155]	uncertain significance	3	57352199	57352199	Human		name
597641776	CV3656049	single nucleotide variant	NM_001366028.2(DNAH12):c.4206G>A (p.Met1402Ile)	not specified [RCV004909156]	uncertain significance	3	57445393	57445393	Human		name
597641343	CV3656052	single nucleotide variant	NM_001366028.2(DNAH12):c.5627A>G (p.Lys1876Arg)	not specified [RCV004909158]	uncertain significance	3	57419454	57419454	Human		name
597712675	CV3656053	single nucleotide variant	NM_001366028.2(DNAH12):c.5449T>C (p.Phe1817Leu)	not specified [RCV004917961]	uncertain significance	3	57421631	57421631	Human		name
597712686	CV3656054	single nucleotide variant	NM_001366028.2(DNAH12):c.5435G>A (p.Arg1812His)	not specified [RCV004917962]	likely benign	3	57421645	57421645	Human		name
597641353	CV3656056	single nucleotide variant	NM_001366028.2(DNAH12):c.5906C>A (p.Pro1969His)	not specified [RCV004909160]	uncertain significance	3	57413860	57413860	Human		name
597641365	CV3656058	single nucleotide variant	NM_001366028.2(DNAH12):c.5487C>G (p.Asn1829Lys)	not specified [RCV004909162]	uncertain significance	3	57421593	57421593	Human		name
597641380	CV3656061	single nucleotide variant	NM_001366028.2(DNAH12):c.6457C>T (p.Arg2153Cys)	not specified [RCV004909165]	uncertain significance	3	57405772	57405772	Human		name
597641391	CV3656063	single nucleotide variant	NM_001366028.2(DNAH12):c.3808C>T (p.Leu1270Phe)	not specified [RCV004909167]	uncertain significance	3	57446668	57446668	Human		name
597712697	CV3656068	single nucleotide variant	NM_001366028.2(DNAH12):c.3060C>A (p.Phe1020Leu)	not specified [RCV004917963]	uncertain significance	3	57457997	57457997	Human		name
597641424	CV3656070	single nucleotide variant	NM_001366028.2(DNAH12):c.5032A>G (p.Ile1678Val)	not specified [RCV004909173]	uncertain significance	3	57429723	57429723	Human		name
597641434	CV3656072	single nucleotide variant	NM_001366028.2(DNAH12):c.9870A>C (p.Glu3290Asp)	not specified [RCV004909175]	uncertain significance	3	57334573	57334573	Human		name
597641440	CV3656073	single nucleotide variant	NM_001366028.2(DNAH12):c.3947A>T (p.Lys1316Ile)	not specified [RCV004909176]	uncertain significance	3	57446263	57446263	Human		name
597641446	CV3656074	single nucleotide variant	NM_001366028.2(DNAH12):c.3389T>C (p.Val1130Ala)	not specified [RCV004909177]	uncertain significance	3	57454842	57454842	Human		name
597641458	CV3656076	single nucleotide variant	NM_001366028.2(DNAH12):c.3925C>G (p.Leu1309Val)	not specified [RCV004909179]	uncertain significance	3	57446551	57446551	Human		name
597641479	CV3656080	single nucleotide variant	NM_001366028.2(DNAH12):c.3554G>A (p.Gly1185Glu)	not specified [RCV004909183]	uncertain significance	3	57453306	57453306	Human		name
597641490	CV3656083	single nucleotide variant	NM_001366028.2(DNAH12):c.6536T>G (p.Phe2179Cys)	not specified [RCV004909185]	uncertain significance	3	57405693	57405693	Human		name
597712717	CV3656085	single nucleotide variant	NM_001366028.2(DNAH12):c.5824T>C (p.Ser1942Pro)	not specified [RCV004917965]	uncertain significance	3	57415455	57415455	Human		name
597712731	CV3656086	single nucleotide variant	NM_001366028.2(DNAH12):c.4106A>G (p.Asn1369Ser)	not specified [RCV004917966]	uncertain significance	3	57446104	57446104	Human		name
597641513	CV3656089	single nucleotide variant	NM_001366028.2(DNAH12):c.5852A>C (p.Gln1951Pro)	not specified [RCV004909189]	uncertain significance	3	57415427	57415427	Human		name
12896862	CV389577	single nucleotide variant	NM_001366028.2(DNAH12):c.4714G>A (p.Asp1572Asn)	not provided [RCV004717603]\|not specified [RCV000455925]	benign	3	57433770	57433770	Human		name
12896425	CV389613	single nucleotide variant	NM_001366028.2(DNAH12):c.5179T>C (p.Tyr1727His)	not provided [RCV004716475]\|not specified [RCV000455323]	benign	3	57428707	57428707	Human		name
598265073	CV3956807	single nucleotide variant	NM_001366028.2(DNAH12):c.9880A>G (p.Ser3294Gly)	not specified [RCV005326272]	uncertain significance	3	57334563	57334563	Human		name
598265093	CV3956811	single nucleotide variant	NM_001366028.2(DNAH12):c.6922A>T (p.Met2308Leu)	not specified [RCV005326276]	uncertain significance	3	57403335	57403335	Human		name
598265158	CV3956824	single nucleotide variant	NM_001366028.2(DNAH12):c.4943T>C (p.Ile1648Thr)	not specified [RCV005326289]	uncertain significance	3	57433404	57433404	Human		name
598265180	CV3956829	single nucleotide variant	NM_001366028.2(DNAH12):c.6785G>A (p.Cys2262Tyr)	not specified [RCV005326294]	uncertain significance	3	57403472	57403472	Human		name
598265185	CV3956830	single nucleotide variant	NM_001366028.2(DNAH12):c.4761G>C (p.Lys1587Asn)	not specified [RCV005326295]	uncertain significance	3	57433723	57433723	Human		name
598265190	CV3956831	single nucleotide variant	NM_001366028.2(DNAH12):c.6745G>C (p.Val2249Leu)	not specified [RCV005326296]	uncertain significance	3	57404979	57404979	Human		name
598265209	CV3956835	single nucleotide variant	NM_001366028.2(DNAH12):c.3935G>C (p.Gly1312Ala)	not specified [RCV005326300]	uncertain significance	3	57446541	57446541	Human		name
598265213	CV3956836	single nucleotide variant	NM_001366028.2(DNAH12):c.5977C>A (p.Pro1993Thr)	not specified [RCV005326301]	uncertain significance	3	57413789	57413789	Human		name
598265220	CV3956837	single nucleotide variant	NM_001366028.2(DNAH12):c.4843A>G (p.Thr1615Ala)	not specified [RCV005326302]	uncertain significance	3	57433504	57433504	Human		name
598265230	CV3956839	single nucleotide variant	NM_001366028.2(DNAH12):c.4885T>C (p.Ser1629Pro)	not specified [RCV005326304]	uncertain significance	3	57433462	57433462	Human		name
598265234	CV3956840	single nucleotide variant	NM_001366028.2(DNAH12):c.6371G>T (p.Cys2124Phe)	not specified [RCV005326305]	uncertain significance	3	57405858	57405858	Human		name
598265245	CV3956842	single nucleotide variant	NM_001366028.2(DNAH12):c.6562A>G (p.Lys2188Glu)	not specified [RCV005326307]	uncertain significance	3	57405667	57405667	Human		name
598265250	CV3956843	single nucleotide variant	NM_001366028.2(DNAH12):c.3532A>C (p.Lys1178Gln)	not specified [RCV005326308]	uncertain significance	3	57453328	57453328	Human		name
598265276	CV3956848	single nucleotide variant	NM_001366028.2(DNAH12):c.5015C>T (p.Ser1672Phe)	not specified [RCV005326313]	uncertain significance	3	57429740	57429740	Human		name
598265282	CV3956849	single nucleotide variant	NM_001366028.2(DNAH12):c.6370T>A (p.Cys2124Ser)	not specified [RCV005326314]	uncertain significance	3	57405859	57405859	Human		name
616938117	CV4015771	single nucleotide variant	NM_001366028.2(DNAH12):c.4166C>T (p.Pro1389Leu)	SPERMATOGENIC FAILURE 100 [RCV005414303]	pathogenic	3	57446044	57446044	Human	1	name
616938118	CV4015772	single nucleotide variant	NM_001366028.2(DNAH12):c.6533C>G (p.Ser2178Ter)	SPERMATOGENIC FAILURE 100 [RCV005414304]	pathogenic	3	57405696	57405696	Human	1	name
156074425	CV2201474	single nucleotide variant	NM_001366028.2(DNAH12):c.11042C>T (p.Thr3681Ile)	not specified [RCV004079624]	uncertain significance	3	57309709	57309709	Human		name
156247378	CV2202878	single nucleotide variant	NM_001366028.2(DNAH12):c.10292T>C (p.Met3431Thr)	not specified [RCV004069154]	uncertain significance	3	57323098	57323098	Human		name
156275884	CV2209715	single nucleotide variant	NM_001366028.2(DNAH12):c.10334C>G (p.Thr3445Ser)	not specified [RCV004083040]	uncertain significance	3	57323056	57323056	Human		name
155919902	CV2209769	single nucleotide variant	NM_001366028.2(DNAH12):c.10112G>A (p.Gly3371Glu)	not specified [RCV004083083]	uncertain significance	3	57323486	57323486	Human		name
155973274	CV2224593	single nucleotide variant	NM_001366028.2(DNAH12):c.10883T>C (p.Ile3628Thr)	not specified [RCV004098162]	uncertain significance	3	57310730	57310730	Human		name
156246134	CV2263701	single nucleotide variant	NM_001366028.2(DNAH12):c.10639C>T (p.Arg3547Cys)	not specified [RCV004135994]	uncertain significance	3	57314517	57314517	Human		name
156140232	CV2280816	single nucleotide variant	NM_001366028.2(DNAH12):c.10336T>A (p.Cys3446Ser)	not specified [RCV004145077]	uncertain significance	3	57323054	57323054	Human		name
156007040	CV2299648	single nucleotide variant	NM_001366028.2(DNAH12):c.11755C>T (p.Arg3919Cys)	not specified [RCV004154964]	uncertain significance	3	57293909	57293909	Human		name
155957038	CV2304104	single nucleotide variant	NM_001366028.2(DNAH12):c.11453A>G (p.Gln3818Arg)	not specified [RCV004170143]	uncertain significance	3	57296926	57296926	Human		name
156151276	CV2307545	single nucleotide variant	NM_001366028.2(DNAH12):c.10211T>C (p.Ile3404Thr)	not specified [RCV004166185]	uncertain significance	3	57323179	57323179	Human		name
156171825	CV2312604	single nucleotide variant	NM_001366028.2(DNAH12):c.11355T>A (p.Ser3785Arg)	not specified [RCV004169342]	uncertain significance	3	57301774	57301774	Human		name
156274994	CV2330642	single nucleotide variant	NM_001366028.2(DNAH12):c.10006A>G (p.Thr3336Ala)	not specified [RCV004183671]	uncertain significance	3	57323592	57323592	Human		name
155919562	CV2333219	single nucleotide variant	NM_001366028.2(DNAH12):c.11717C>T (p.Ser3906Leu)	not specified [RCV004194505]	uncertain significance	3	57293947	57293947	Human		name
156217554	CV2348155	single nucleotide variant	NM_001366028.2(DNAH12):c.11587G>A (p.Gly3863Arg)	not specified [RCV004197827]	uncertain significance	3	57296381	57296381	Human		name
156194567	CV2398308	single nucleotide variant	NM_001366028.2(DNAH12):c.11756G>A (p.Arg3919His)	not specified [RCV004235213]	uncertain significance	3	57293908	57293908	Human		name
329355909	CV2430531	single nucleotide variant	NM_001366028.2(DNAH12):c.10628A>C (p.Glu3543Ala)	not specified [RCV004252117]	uncertain significance	3	57314528	57314528	Human		name
329375813	CV2431629	single nucleotide variant	NM_001366028.2(DNAH12):c.11877T>A (p.Asp3959Glu)	not specified [RCV004254774]	uncertain significance	3	57293787	57293787	Human		name
329378410	CV2447001	single nucleotide variant	NM_001366028.2(DNAH12):c.10099G>A (p.Val3367Ile)	not specified [RCV004257838]	uncertain significance	3	57323499	57323499	Human		name
401780593	CV2674095	single nucleotide variant	NM_001366028.2(DNAH12):c.11833C>T (p.Arg3945Trp)	not specified [RCV004295501]	uncertain significance	3	57293831	57293831	Human		name
401732192	CV2678026	single nucleotide variant	NM_001366028.2(DNAH12):c.10115C>T (p.Ala3372Val)	not specified [RCV004296551]	uncertain significance	3	57323483	57323483	Human		name
401756084	CV2686286	single nucleotide variant	NM_001366028.2(DNAH12):c.11365G>A (p.Asp3789Asn)	not specified [RCV004297370]	uncertain significance	3	57301764	57301764	Human		name
401781623	CV2722192	single nucleotide variant	NM_001366028.2(DNAH12):c.11072A>G (p.Asp3691Gly)	not specified [RCV004328759]	uncertain significance	3	57309679	57309679	Human		name
401780121	CV2725884	single nucleotide variant	NM_001366028.2(DNAH12):c.10973C>G (p.Thr3658Arg)	not specified [RCV004324263]	uncertain significance	3	57309778	57309778	Human		name
401779783	CV2732017	single nucleotide variant	NM_001366028.2(DNAH12):c.11101G>A (p.Asp3701Asn)	not specified [RCV004333250]	uncertain significance	3	57309239	57309239	Human		name
401876675	CV2767676	single nucleotide variant	NM_001366028.2(DNAH12):c.10183A>G (p.Ile3395Val)	not specified [RCV004345812]	uncertain significance	3	57323207	57323207	Human		name
401893874	CV2774118	single nucleotide variant	NM_001366028.2(DNAH12):c.11834G>A (p.Arg3945Gln)	not specified [RCV004345711]	likely benign	3	57293830	57293830	Human		name
405709335	CV3247248	single nucleotide variant	NM_001366028.2(DNAH12):c.10247G>A (p.Gly3416Glu)	not specified [RCV004376391]	uncertain significance	3	57323143	57323143	Human		name
405709339	CV3247249	single nucleotide variant	NM_001366028.2(DNAH12):c.10254G>T (p.Trp3418Cys)	not specified [RCV004376392]	uncertain significance	3	57323136	57323136	Human		name
405709345	CV3247250	single nucleotide variant	NM_001366028.2(DNAH12):c.10372C>T (p.Pro3458Ser)	not specified [RCV004376393]	uncertain significance	3	57323018	57323018	Human		name
405709354	CV3247251	single nucleotide variant	NM_001366028.2(DNAH12):c.10409G>C (p.Gly3470Ala)	not specified [RCV004376394]	uncertain significance	3	57322458	57322458	Human		name
405709361	CV3247252	single nucleotide variant	NM_001366028.2(DNAH12):c.10436C>T (p.Thr3479Met)	not specified [RCV004376395]	uncertain significance	3	57322431	57322431	Human		name
405709369	CV3247253	single nucleotide variant	NM_001366028.2(DNAH12):c.10481T>G (p.Val3494Gly)	not specified [RCV004376396]	uncertain significance	3	57322386	57322386	Human		name
405709376	CV3247254	single nucleotide variant	NM_001366028.2(DNAH12):c.10762C>T (p.Arg3588Cys)	not specified [RCV004376397]	uncertain significance	3	57310851	57310851	Human		name
405709380	CV3247255	single nucleotide variant	NM_001366028.2(DNAH12):c.11120G>A (p.Arg3707Gln)	not specified [RCV004376398]	likely benign	3	57309220	57309220	Human		name
405709389	CV3247256	single nucleotide variant	NM_001366028.2(DNAH12):c.11183T>C (p.Phe3728Ser)	not specified [RCV004376399]	uncertain significance	3	57309157	57309157	Human		name
405709397	CV3247257	single nucleotide variant	NM_001366028.2(DNAH12):c.11248G>A (p.Val3750Ile)	not specified [RCV004376400]	uncertain significance	3	57301881	57301881	Human		name
405709409	CV3247259	single nucleotide variant	NM_001366028.2(DNAH12):c.11506A>G (p.Ile3836Val)	not specified [RCV004376402]	uncertain significance	3	57296873	57296873	Human		name
405709418	CV3247260	single nucleotide variant	NM_001366028.2(DNAH12):c.11507T>C (p.Ile3836Thr)	not specified [RCV004376403]	uncertain significance	3	57296872	57296872	Human		name
405709425	CV3247261	single nucleotide variant	NM_001366028.2(DNAH12):c.11705G>A (p.Arg3902Gln)	not specified [RCV004376404]	likely benign	3	57293959	57293959	Human		name
405709432	CV3247262	single nucleotide variant	NM_001366028.2(DNAH12):c.11830A>G (p.Thr3944Ala)	not specified [RCV004376405]	uncertain significance	3	57293834	57293834	Human		name
405709439	CV3247263	single nucleotide variant	NM_001366028.2(DNAH12):c.11845A>G (p.Lys3949Glu)	not specified [RCV004376406]	uncertain significance	3	57293819	57293819	Human		name
597712662	CV3656050	single nucleotide variant	NM_001366028.2(DNAH12):c.11518G>A (p.Gly3840Arg)	not specified [RCV004917960]	uncertain significance	3	57296861	57296861	Human		name
597641339	CV3656051	single nucleotide variant	NM_001366028.2(DNAH12):c.11680T>C (p.Trp3894Arg)	not specified [RCV004909157]	uncertain significance	3	57295537	57295537	Human		name
597641371	CV3656059	single nucleotide variant	NM_001366028.2(DNAH12):c.10844A>G (p.Asn3615Ser)	not specified [RCV004909163]	uncertain significance	3	57310769	57310769	Human		name
597641376	CV3656060	single nucleotide variant	NM_001366028.2(DNAH12):c.10510C>G (p.Arg3504Gly)	not specified [RCV004909164]	uncertain significance	3	57322357	57322357	Human		name
597641386	CV3656062	single nucleotide variant	NM_001366028.2(DNAH12):c.11158G>T (p.Val3720Leu)	not specified [RCV004909166]	uncertain significance	3	57309182	57309182	Human		name
597641783	CV3656078	single nucleotide variant	NM_001366028.2(DNAH12):c.11516T>G (p.Leu3839Arg)	not specified [RCV004909181]	uncertain significance	3	57296863	57296863	Human		name
597712707	CV3656081	single nucleotide variant	NM_001366028.2(DNAH12):c.10421C>G (p.Thr3474Ser)	not specified [RCV004917964]	uncertain significance	3	57322446	57322446	Human		name
597641501	CV3656087	single nucleotide variant	NM_001366028.2(DNAH12):c.10640G>A (p.Arg3547His)	not specified [RCV004909187]	uncertain significance	3	57314516	57314516	Human		name
12896751	CV389587	single nucleotide variant	NM_001366028.2(DNAH12):c.11281G>A (p.Gly3761Ser)	not provided [RCV004717601]\|not specified [RCV000455776]	benign	3	57301848	57301848	Human		name
598265055	CV3956804	single nucleotide variant	NM_001366028.2(DNAH12):c.11044G>A (p.Asp3682Asn)	not specified [RCV005326269]	uncertain significance	3	57309707	57309707	Human		name
598265129	CV3956818	single nucleotide variant	NM_001366028.2(DNAH12):c.11378G>T (p.Arg3793Leu)	not specified [RCV005326283]	uncertain significance	3	57301751	57301751	Human		name
598265134	CV3956819	single nucleotide variant	NM_001366028.2(DNAH12):c.11554G>A (p.Asp3852Asn)	not specified [RCV005326284]	uncertain significance	3	57296414	57296414	Human		name
598265139	CV3956820	single nucleotide variant	NM_001366028.2(DNAH12):c.10778T>C (p.Met3593Thr)	not specified [RCV005326285]	uncertain significance	3	57310835	57310835	Human		name
598265143	CV3956821	single nucleotide variant	NM_001366028.2(DNAH12):c.11090C>T (p.Pro3697Leu)	not specified [RCV005326286]	uncertain significance	3	57309250	57309250	Human		name
598265148	CV3956822	single nucleotide variant	NM_001366028.2(DNAH12):c.10021A>G (p.Lys3341Glu)	not specified [RCV005326287]	uncertain significance	3	57323577	57323577	Human		name
598265172	CV3956827	single nucleotide variant	NM_001366028.2(DNAH12):c.10820A>G (p.His3607Arg)	not specified [RCV005326292]	uncertain significance	3	57310793	57310793	Human		name
598265175	CV3956828	single nucleotide variant	NM_001366028.2(DNAH12):c.10940A>C (p.Glu3647Ala)	not specified [RCV005326293]	uncertain significance	3	57309811	57309811	Human		name
598265200	CV3956833	single nucleotide variant	NM_001366028.2(DNAH12):c.10472C>T (p.Thr3491Ile)	not specified [RCV005326298]	uncertain significance	3	57322395	57322395	Human		name
598265240	CV3956841	single nucleotide variant	NM_001366028.2(DNAH12):c.10436C>G (p.Thr3479Arg)	not specified [RCV005326306]	uncertain significance	3	57322431	57322431	Human		name
598265255	CV3956844	single nucleotide variant	NM_001366028.2(DNAH12):c.10154A>C (p.Lys3385Thr)	not specified [RCV005326309]	uncertain significance	3	57323236	57323236	Human		name

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