Iqch Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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106 records found for search term Iqch

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15121840	CV744875	single nucleotide variant	NM_001031715.3(IQCH):c.1906-6T>G	not provided [RCV000896137]	benign	15	67400108	67400108	Human		name
8584536	CV119109	single nucleotide variant	NM_001031715.2(IQCH):c.1632+2740G>A	Lung cancer [RCV000099629]	uncertain significance	15	67391746	67391746	Human		name
8584537	CV119110	single nucleotide variant	NM_001031715.2(IQCH):c.2097+2301T>C	Lung cancer [RCV000099630]	uncertain significance	15	67402606	67402606	Human		name
617152874	CV4020915	single nucleotide variant	NM_001031715.3(IQCH):c.387+24827C>T	not provided [RCV005428668]	benign	15	67304339	67304339	Human		name
15146211	CV739748	single nucleotide variant	NM_001031715.3(IQCH):c.21C>T (p.Asn7=)	not provided [RCV000900287]	benign	15	67254917	67254917	Human		name
8627686	CV82830	single nucleotide variant	NM_001031715.2(IQCH):c.63C>T (p.Asp21=)	Malignant melanoma [RCV000062910]	not provided	15	67261283	67261283	Human		name
156299867	CV2326179	single nucleotide variant	NM_001031715.3(IQCH):c.24C>G (p.His8Gln)	not specified [RCV004180447]	uncertain significance	15	67254920	67254920	Human		name
156173260	CV2380896	single nucleotide variant	NM_001031715.3(IQCH):c.28C>T (p.Pro10Ser)	not specified [RCV004218442]	uncertain significance	15	67254924	67254924	Human		name
597785900	CV3680469	single nucleotide variant	NM_001031715.3(IQCH):c.55C>T (p.His19Tyr)	not specified [RCV004932081]	uncertain significance	15	67261275	67261275	Human		name
15124346	CV739749	single nucleotide variant	NM_001031715.3(IQCH):c.915C>T (p.Val305=)	not provided [RCV000896572]	benign	15	67372272	67372272	Human		name
8635546	CV90767	single nucleotide variant	NM_001031715.2(IQCH):c.309C>T (p.Phe103=)	Malignant melanoma [RCV000070865]	not provided	15	67279434	67279434	Human		name
156067692	CV2221887	single nucleotide variant	NM_001031715.3(IQCH):c.181A>G (p.Ile61Val)	not specified [RCV004102905]	uncertain significance	15	67263128	67263128	Human		name
155989788	CV2276384	single nucleotide variant	NM_001031715.3(IQCH):c.112G>A (p.Gly38Arg)	not specified [RCV004144119]	likely benign	15	67261332	67261332	Human		name
329355895	CV2442384	single nucleotide variant	NM_001031715.3(IQCH):c.125A>G (p.Asp42Gly)	not specified [RCV004266637]	uncertain significance	15	67261345	67261345	Human		name
401904425	CV2814264	single nucleotide variant	NM_001031715.3(IQCH):c.1824C>T (p.Thr608=)	not provided [RCV003394952]	likely benign	15	67395482	67395482	Human		name
405794475	CV3274917	single nucleotide variant	NM_001031715.3(IQCH):c.179A>G (p.His60Arg)	not specified [RCV004400881]	uncertain significance	15	67263126	67263126	Human		name
405794496	CV3274924	single nucleotide variant	NM_001031715.3(IQCH):c.274C>T (p.Leu92Phe)	not specified [RCV004400888]	uncertain significance	15	67279399	67279399	Human		name
596938985	CV3547584	single nucleotide variant	NM_001031715.3(IQCH):c.2241A>C (p.Pro747=)	not provided [RCV004811888]	likely benign	15	67421313	67421313	Human		name
8635547	CV90768	single nucleotide variant	NM_001031715.2(IQCH):c.1002G>A (p.Thr334=)	Malignant melanoma [RCV000070866]	not provided	15	67372359	67372359	Human		name
156031866	CV2218151	single nucleotide variant	NM_001031715.3(IQCH):c.388A>G (p.Ile130Val)	not specified [RCV004086575]	likely benign	15	67336975	67336975	Human		name
156078960	CV2230395	single nucleotide variant	NM_001031715.3(IQCH):c.619C>T (p.Arg207Cys)	not specified [RCV004101775]	uncertain significance	15	67344173	67344173	Human		name
156290226	CV2309802	single nucleotide variant	NM_001031715.3(IQCH):c.481C>T (p.Pro161Ser)	not specified [RCV004160921]	uncertain significance	15	67337068	67337068	Human		name
156274018	CV2319928	single nucleotide variant	NM_001031715.3(IQCH):c.554G>A (p.Arg185Lys)	not specified [RCV004167806]	likely benign	15	67344108	67344108	Human		name
156285896	CV2327184	single nucleotide variant	NM_001031715.3(IQCH):c.879A>T (p.Leu293Phe)	not specified [RCV004174651]	uncertain significance	15	67372236	67372236	Human		name
329349984	CV2454055	single nucleotide variant	NM_001031715.3(IQCH):c.725G>A (p.Arg242Lys)	not specified [RCV004271702]	likely benign	15	67359857	67359857	Human		name
401856725	CV2756367	single nucleotide variant	NM_001031715.3(IQCH):c.631A>G (p.Thr211Ala)	not specified [RCV004342911]	likely benign	15	67344185	67344185	Human		name
401858806	CV2773935	single nucleotide variant	NM_001031715.3(IQCH):c.767A>G (p.Lys256Arg)	not specified [RCV004358357]	uncertain significance	15	67372124	67372124	Human		name
401857696	CV2781743	single nucleotide variant	NM_001031715.3(IQCH):c.773C>T (p.Pro258Leu)	not specified [RCV004356714]	uncertain significance	15	67372130	67372130	Human		name
405794499	CV3274925	single nucleotide variant	NM_001031715.3(IQCH):c.367C>T (p.Pro123Ser)	not specified [RCV004400889]	uncertain significance	15	67279492	67279492	Human		name
405794502	CV3274926	single nucleotide variant	NM_001031715.3(IQCH):c.716G>A (p.Gly239Glu)	not specified [RCV004400890]	uncertain significance	15	67359848	67359848	Human		name
405794505	CV3274927	single nucleotide variant	NM_001031715.3(IQCH):c.820G>T (p.Asp274Tyr)	not specified [RCV004400891]	uncertain significance	15	67372177	67372177	Human		name
407484469	CV3455191	single nucleotide variant	NM_001031715.3(IQCH):c.821A>G (p.Asp274Gly)	not specified [RCV004630981]	uncertain significance	15	67372178	67372178	Human		name
407523184	CV3455193	single nucleotide variant	NM_001031715.3(IQCH):c.437T>C (p.Val146Ala)	not specified [RCV004630983]	uncertain significance	15	67337024	67337024	Human		name
407484454	CV3455195	single nucleotide variant	NM_001031715.3(IQCH):c.910C>G (p.His304Asp)	not specified [RCV004630984]	uncertain significance	15	67372267	67372267	Human		name
597785896	CV3680466	single nucleotide variant	NM_001031715.3(IQCH):c.410A>G (p.Lys137Arg)	not specified [RCV004932078]	uncertain significance	15	67336997	67336997	Human		name
597696270	CV3680468	single nucleotide variant	NM_001031715.3(IQCH):c.708A>T (p.Arg236Ser)	not specified [RCV004932080]	likely benign	15	67357415	67357415	Human		name
597696303	CV3680472	single nucleotide variant	NM_001031715.3(IQCH):c.929G>A (p.Arg310Lys)	not specified [RCV004932084]	likely benign	15	67372286	67372286	Human		name
597696310	CV3680473	single nucleotide variant	NM_001031715.3(IQCH):c.620G>A (p.Arg207His)	not specified [RCV004932085]	likely benign	15	67344174	67344174	Human		name
597696326	CV3680475	single nucleotide variant	NM_001031715.3(IQCH):c.611A>T (p.Asp204Val)	not specified [RCV004932087]	uncertain significance	15	67344165	67344165	Human		name
597696334	CV3680476	single nucleotide variant	NM_001031715.3(IQCH):c.839C>T (p.Thr280Ile)	not specified [RCV004932088]	uncertain significance	15	67372196	67372196	Human		name
597785902	CV3680485	single nucleotide variant	NM_001031715.3(IQCH):c.453T>A (p.His151Gln)	not specified [RCV004932097]	uncertain significance	15	67337040	67337040	Human		name
598160631	CV3979419	single nucleotide variant	NM_001031715.3(IQCH):c.605G>A (p.Ser202Asn)	not specified [RCV005368281]	uncertain significance	15	67344159	67344159	Human		name
598160656	CV3979426	single nucleotide variant	NM_001031715.3(IQCH):c.850T>A (p.Phe284Ile)	not specified [RCV005368285]	uncertain significance	15	67372207	67372207	Human		name
598160667	CV3979428	single nucleotide variant	NM_001031715.3(IQCH):c.737G>A (p.Gly246Glu)	not specified [RCV005368287]	uncertain significance	15	67359869	67359869	Human		name
8627687	CV82831	single nucleotide variant	NM_001031715.2(IQCH):c.430C>T (p.Leu144Phe)	Malignant melanoma [RCV000062911]	not provided	15	67337017	67337017	Human		name
156378449	CV2207727	single nucleotide variant	NM_001031715.3(IQCH):c.1504G>A (p.Glu502Lys)	not specified [RCV004084170]	uncertain significance	15	67388878	67388878	Human		name
155923160	CV2215483	single nucleotide variant	NM_001031715.3(IQCH):c.1664T>G (p.Met555Arg)	not specified [RCV004089273]	uncertain significance	15	67395322	67395322	Human		name
155981489	CV2233084	single nucleotide variant	NM_001031715.3(IQCH):c.1997C>T (p.Thr666Ile)	not specified [RCV004103712]	uncertain significance	15	67400205	67400205	Human		name
156208533	CV2250127	single nucleotide variant	NM_001031715.3(IQCH):c.2660G>A (p.Ser887Asn)	not specified [RCV004116938]	likely benign	15	67465281	67465281	Human		name
156160891	CV2272547	single nucleotide variant	NM_001031715.3(IQCH):c.1010T>C (p.Leu337Pro)	not specified [RCV004133444]	uncertain significance	15	67372367	67372367	Human		name
155920629	CV2279626	single nucleotide variant	NM_001031715.3(IQCH):c.2467C>G (p.Leu823Val)	not specified [RCV004142125]	uncertain significance	15	67421539	67421539	Human		name
156044046	CV2305881	single nucleotide variant	NM_001031715.3(IQCH):c.1453T>G (p.Leu485Val)	not specified [RCV004167671]	uncertain significance	15	67385016	67385016	Human		name
156396658	CV2330196	single nucleotide variant	NM_001031715.3(IQCH):c.2183C>T (p.Thr728Met)	not specified [RCV004187658]	uncertain significance	15	67417016	67417016	Human		name
156289878	CV2333246	single nucleotide variant	NM_001031715.3(IQCH):c.2293G>A (p.Gly765Arg)	not specified [RCV004196576]	uncertain significance	15	67421365	67421365	Human		name
155979169	CV2335304	single nucleotide variant	NM_001031715.3(IQCH):c.2305G>A (p.Val769Met)	not specified [RCV004186868]	uncertain significance	15	67421377	67421377	Human		name
155916562	CV2336167	single nucleotide variant	NM_001031715.3(IQCH):c.1726G>A (p.Val576Ile)	not specified [RCV004189759]	uncertain significance	15	67395384	67395384	Human		name
156220469	CV2345039	single nucleotide variant	NM_001031715.3(IQCH):c.1018T>G (p.Tyr340Asp)	not specified [RCV004193322]	uncertain significance	15	67372375	67372375	Human		name
156282729	CV2348880	single nucleotide variant	NM_001031715.3(IQCH):c.1694A>T (p.Lys565Ile)	not specified [RCV004203317]	uncertain significance	15	67395352	67395352	Human		name
155922244	CV2350795	single nucleotide variant	NM_001031715.3(IQCH):c.2727C>G (p.Ser909Arg)	not specified [RCV004207129]	uncertain significance	15	67475746	67475746	Human		name
155928435	CV2360031	single nucleotide variant	NM_001031715.3(IQCH):c.2224G>A (p.Val742Met)	not specified [RCV004212866]	uncertain significance	15	67421296	67421296	Human		name
155916492	CV2366676	single nucleotide variant	NM_001031715.3(IQCH):c.2835C>A (p.His945Gln)	not specified [RCV004210681]	uncertain significance	15	67490038	67490038	Human		name
156288324	CV2370634	single nucleotide variant	NM_001031715.3(IQCH):c.2679G>A (p.Met893Ile)	not specified [RCV004215955]	uncertain significance	15	67475698	67475698	Human		name
156198854	CV2392208	single nucleotide variant	NM_001031715.3(IQCH):c.2693G>A (p.Arg898His)	not specified [RCV004243822]	uncertain significance	15	67475712	67475712	Human		name
156100098	CV2392919	single nucleotide variant	NM_001031715.3(IQCH):c.2720G>A (p.Arg907Lys)	not specified [RCV004247268]	likely benign	15	67475739	67475739	Human		name
329395948	CV2451807	single nucleotide variant	NM_001031715.3(IQCH):c.1762G>A (p.Ala588Thr)	not specified [RCV004276490]	uncertain significance	15	67395420	67395420	Human		name
401744847	CV2682404	single nucleotide variant	NM_001031715.3(IQCH):c.1184A>G (p.Gln395Arg)	not specified [RCV004290433]	uncertain significance	15	67372541	67372541	Human		name
401746401	CV2725165	single nucleotide variant	NM_001031715.3(IQCH):c.1010T>G (p.Leu337Arg)	not specified [RCV004319905]	uncertain significance	15	67372367	67372367	Human		name
401857349	CV2766213	single nucleotide variant	NM_001031715.3(IQCH):c.2260A>C (p.Asn754His)	not specified [RCV004340653]	uncertain significance	15	67421332	67421332	Human		name
401857316	CV2774711	single nucleotide variant	NM_001031715.3(IQCH):c.2426C>G (p.Ala809Gly)	not specified [RCV004343816]	uncertain significance	15	67421498	67421498	Human		name
401858917	CV2780124	single nucleotide variant	NM_001031715.3(IQCH):c.2456T>G (p.Phe819Cys)	not specified [RCV004355782]	uncertain significance	15	67421528	67421528	Human		name
401902607	CV2814265	single nucleotide variant	NM_001031715.3(IQCH):c.2020T>C (p.Tyr674His)	not provided [RCV003394953]	likely benign	15	67400228	67400228	Human		name
405794469	CV3274915	single nucleotide variant	NM_001031715.3(IQCH):c.1140G>C (p.Trp380Cys)	not specified [RCV004400879]	uncertain significance	15	67372497	67372497	Human		name
405794472	CV3274916	single nucleotide variant	NM_001031715.3(IQCH):c.1283A>G (p.Glu428Gly)	not specified [RCV004400880]	uncertain significance	15	67372640	67372640	Human		name
405794478	CV3274918	single nucleotide variant	NM_001031715.3(IQCH):c.1817A>G (p.Tyr606Cys)	not specified [RCV004400882]	uncertain significance	15	67395475	67395475	Human		name
405794481	CV3274919	single nucleotide variant	NM_001031715.3(IQCH):c.1955G>A (p.Arg652His)	not specified [RCV004400883]	uncertain significance	15	67400163	67400163	Human		name
405794484	CV3274920	single nucleotide variant	NM_001031715.3(IQCH):c.2291A>G (p.Asn764Ser)	not specified [RCV004400884]	uncertain significance	15	67421363	67421363	Human		name
405794488	CV3274921	single nucleotide variant	NM_001031715.3(IQCH):c.2340C>A (p.Ser780Arg)	not specified [RCV004400885]	uncertain significance	15	67421412	67421412	Human		name
405794490	CV3274922	single nucleotide variant	NM_001031715.3(IQCH):c.2393T>G (p.Val798Gly)	not specified [RCV004400886]	uncertain significance	15	67421465	67421465	Human		name
405794493	CV3274923	single nucleotide variant	NM_001031715.3(IQCH):c.2620C>T (p.Arg874Cys)	not specified [RCV004400887]	uncertain significance	15	67465241	67465241	Human		name
407484461	CV3455192	single nucleotide variant	NM_001031715.3(IQCH):c.1178G>A (p.Arg393His)	not specified [RCV004630982]	uncertain significance	15	67372535	67372535	Human		name
407511367	CV3455194	single nucleotide variant	NM_001031715.3(IQCH):c.1841G>A (p.Arg614His)	not specified [RCV004626441]	uncertain significance	15	67395499	67395499	Human		name
597696236	CV3680463	single nucleotide variant	NM_001031715.3(IQCH):c.1615G>A (p.Ala539Thr)	not specified [RCV004932075]	uncertain significance	15	67388989	67388989	Human		name
597696244	CV3680464	single nucleotide variant	NM_001031715.3(IQCH):c.2986A>G (p.Ile996Val)	not specified [RCV004932076]	uncertain significance	15	67500648	67500648	Human		name
597696252	CV3680465	single nucleotide variant	NM_001031715.3(IQCH):c.1549G>A (p.Val517Ile)	not specified [RCV004932077]	uncertain significance	15	67388923	67388923	Human		name
597696261	CV3680467	single nucleotide variant	NM_001031715.3(IQCH):c.2365G>A (p.Val789Met)	not specified [RCV004932079]	likely benign	15	67421437	67421437	Human		name
597696282	CV3680470	single nucleotide variant	NM_001031715.3(IQCH):c.2417T>C (p.Ile806Thr)	not specified [RCV004932082]	uncertain significance	15	67421489	67421489	Human		name
597696317	CV3680474	single nucleotide variant	NM_001031715.3(IQCH):c.2646A>T (p.Lys882Asn)	not specified [RCV004932086]	uncertain significance	15	67465267	67465267	Human		name
597696344	CV3680477	single nucleotide variant	NM_001031715.3(IQCH):c.2252A>G (p.Asn751Ser)	not specified [RCV004932089]	likely benign	15	67421324	67421324	Human		name
597696353	CV3680478	single nucleotide variant	NM_001031715.3(IQCH):c.1395A>C (p.Glu465Asp)	not specified [RCV004932090]	uncertain significance	15	67384958	67384958	Human		name
597696363	CV3680479	single nucleotide variant	NM_001031715.3(IQCH):c.1121T>C (p.Met374Thr)	not specified [RCV004932091]	uncertain significance	15	67372478	67372478	Human		name
597696371	CV3680480	single nucleotide variant	NM_001031715.3(IQCH):c.2463A>G (p.Ile821Met)	not specified [RCV004932092]	uncertain significance	15	67421535	67421535	Human		name
597696380	CV3680481	single nucleotide variant	NM_001031715.3(IQCH):c.2222G>T (p.Gly741Val)	not specified [RCV004932093]	uncertain significance	15	67421294	67421294	Human		name
597696398	CV3680483	single nucleotide variant	NM_001031715.3(IQCH):c.1376A>G (p.Tyr459Cys)	not specified [RCV004932095]	uncertain significance	15	67384939	67384939	Human		name
597696406	CV3680484	single nucleotide variant	NM_001031715.3(IQCH):c.2621G>T (p.Arg874Leu)	not specified [RCV004932096]	uncertain significance	15	67465242	67465242	Human		name
598160625	CV3979418	single nucleotide variant	NM_001031715.3(IQCH):c.1268G>A (p.Arg423His)	not specified [RCV005368280]	uncertain significance	15	67372625	67372625	Human		name
598160638	CV3979420	single nucleotide variant	NM_001031715.3(IQCH):c.1397A>G (p.His466Arg)	not specified [RCV005368282]	uncertain significance	15	67384960	67384960	Human		name
598160649	CV3979423	single nucleotide variant	NM_001031715.3(IQCH):c.2933T>C (p.Ile978Thr)	not specified [RCV005368284]	uncertain significance	15	67494329	67494329	Human		name
598210686	CV3979424	single nucleotide variant	NM_001031715.3(IQCH):c.2385T>G (p.Asp795Glu)	not specified [RCV005358570]	uncertain significance	15	67421457	67421457	Human		name
598194422	CV3979425	single nucleotide variant	NM_001031715.3(IQCH):c.2152G>A (p.Ala718Thr)	not specified [RCV005354825]	uncertain significance	15	67416985	67416985	Human		name
598160662	CV3979427	single nucleotide variant	NM_001031715.3(IQCH):c.2206T>C (p.Phe736Leu)	not specified [RCV005368286]	uncertain significance	15	67417039	67417039	Human		name
598194430	CV3979429	single nucleotide variant	NM_001031715.3(IQCH):c.1474A>G (p.Ile492Val)	not specified [RCV005354826]	uncertain significance	15	67388848	67388848	Human		name
15155390	CV739750	single nucleotide variant	NM_001031715.3(IQCH):c.1496T>C (p.Met499Thr)	not provided [RCV000902132]	likely benign	15	67388870	67388870	Human		name
8627688	CV82832	single nucleotide variant	NM_001031715.2(IQCH):c.2929G>A (p.Glu977Lys)	Malignant melanoma [RCV000062912]	not provided	15	67494325	67494325	Human		name
155924178	CV2248721	single nucleotide variant	NM_001031715.3(IQCH):c.3065T>C (p.Leu1022Pro)	not specified [RCV004121885]	uncertain significance	15	67500727	67500727	Human		name
597696293	CV3680471	single nucleotide variant	NM_001031715.3(IQCH):c.3010A>G (p.Lys1004Glu)	not specified [RCV004932083]	likely benign	15	67500672	67500672	Human		name
597696390	CV3680482	single nucleotide variant	NM_001031715.3(IQCH):c.3064C>A (p.Leu1022Ile)	not specified [RCV004932094]	uncertain significance	15	67500726	67500726	Human		name

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