Ankrd50 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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102 records found for search term Ankrd50

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329373427	CV2434246	single nucleotide variant	NM_020337.3(ANKRD50):c.11C>T (p.Pro4Leu)	not specified [RCV004251922]	uncertain significance	4	124710501	124710501	Human		name
329363828	CV2469405	single nucleotide variant	NM_020337.3(ANKRD50):c.26T>C (p.Val9Ala)	not specified [RCV004281034]	uncertain significance	4	124710486	124710486	Human		name
597635634	CV3554493	single nucleotide variant	NM_020337.3(ANKRD50):c.19G>C (p.Glu7Gln)	not specified [RCV004831227]	uncertain significance	4	124710493	124710493	Human		name
156029681	CV2238333	single nucleotide variant	NM_020337.3(ANKRD50):c.161T>C (p.Val54Ala)	not specified [RCV004113407]	uncertain significance	4	124710351	124710351	Human		name
156272946	CV2277627	single nucleotide variant	NM_020337.3(ANKRD50):c.103C>T (p.His35Tyr)	not specified [RCV004147092]	uncertain significance	4	124710409	124710409	Human		name
401720200	CV2675806	single nucleotide variant	NM_020337.3(ANKRD50):c.256C>G (p.Leu86Val)	not specified [RCV004281821]	uncertain significance	4	124710256	124710256	Human		name
401771926	CV2689655	single nucleotide variant	NM_020337.3(ANKRD50):c.294T>A (p.Ser98Arg)	not specified [RCV004297582]	uncertain significance	4	124710218	124710218	Human		name
401923494	CV2820158	single nucleotide variant	NM_020337.3(ANKRD50):c.1701G>A (p.Arg567=)	not provided [RCV003435154]	likely benign	4	124671576	124671576	Human		name
401928457	CV2820159	single nucleotide variant	NM_020337.3(ANKRD50):c.1563C>T (p.Ala521=)	not provided [RCV003439490]	likely benign	4	124671714	124671714	Human		name
405683587	CV3282250	single nucleotide variant	NM_020337.3(ANKRD50):c.196G>A (p.Gly66Arg)	not specified [RCV004422229]	uncertain significance	4	124710316	124710316	Human		name
156092685	CV2256692	single nucleotide variant	NM_020337.3(ANKRD50):c.640G>A (p.Val214Ile)	not specified [RCV004118866]	uncertain significance	4	124678778	124678778	Human		name
156264343	CV2364286	single nucleotide variant	NM_020337.3(ANKRD50):c.598A>T (p.Ile200Phe)	not specified [RCV004223511]	uncertain significance	4	124678820	124678820	Human		name
401889419	CV2756505	single nucleotide variant	NM_020337.3(ANKRD50):c.787G>A (p.Val263Ile)	not specified [RCV004345038]	uncertain significance	4	124672490	124672490	Human		name
401928455	CV2820157	single nucleotide variant	NM_020337.3(ANKRD50):c.3588A>G (p.Ser1196=)	not provided [RCV003439489]	likely benign	4	124669689	124669689	Human		name
405683641	CV3282264	single nucleotide variant	NM_020337.3(ANKRD50):c.957G>T (p.Met319Ile)	not specified [RCV004422243]	uncertain significance	4	124672320	124672320	Human		name
407504597	CV3450734	single nucleotide variant	NM_020337.3(ANKRD50):c.754A>G (p.Ile252Val)	not specified [RCV004645875]	uncertain significance	4	124672523	124672523	Human		name
407504660	CV3450766	single nucleotide variant	NM_020337.3(ANKRD50):c.407G>A (p.Arg136His)	not specified [RCV004645887]	uncertain significance	4	124710105	124710105	Human		name
597638577	CV3554500	single nucleotide variant	NM_020337.3(ANKRD50):c.379A>C (p.Ile127Leu)	not specified [RCV004824954]	uncertain significance	4	124710133	124710133	Human		name
597638587	CV3554527	single nucleotide variant	NM_020337.3(ANKRD50):c.617C>T (p.Thr206Met)	not specified [RCV004824956]	uncertain significance	4	124678801	124678801	Human		name
598167070	CV3989543	single nucleotide variant	NM_020337.3(ANKRD50):c.659G>C (p.Gly220Ala)	not specified [RCV005369450]	uncertain significance	4	124678759	124678759	Human		name
156387656	CV2221570	single nucleotide variant	NM_020337.3(ANKRD50):c.2752C>T (p.Arg918Trp)	not specified [RCV004096832]	uncertain significance	4	124670525	124670525	Human		name
155912615	CV2245595	single nucleotide variant	NM_020337.3(ANKRD50):c.2960G>C (p.Cys987Ser)	not specified [RCV004109670]	uncertain significance	4	124670317	124670317	Human		name
156033335	CV2256399	single nucleotide variant	NM_020337.3(ANKRD50):c.1358A>G (p.Gln453Arg)	not specified [RCV004116839]	uncertain significance	4	124671919	124671919	Human		name
156360244	CV2269005	single nucleotide variant	NM_020337.3(ANKRD50):c.2636A>G (p.Asp879Gly)	not specified [RCV004128402]	uncertain significance	4	124670641	124670641	Human		name
156132310	CV2280048	single nucleotide variant	NM_020337.3(ANKRD50):c.2218G>A (p.Glu740Lys)	not specified [RCV004146406]	uncertain significance	4	124671059	124671059	Human		name
155990812	CV2281002	single nucleotide variant	NM_020337.3(ANKRD50):c.1573G>A (p.Glu525Lys)	not specified [RCV004145499]	uncertain significance	4	124671704	124671704	Human		name
156059274	CV2305316	single nucleotide variant	NM_020337.3(ANKRD50):c.2882T>A (p.Met961Lys)	not specified [RCV004171229]	uncertain significance	4	124670395	124670395	Human		name
155979292	CV2335354	single nucleotide variant	NM_020337.3(ANKRD50):c.1588A>G (p.Thr530Ala)	not specified [RCV004186912]	uncertain significance	4	124671689	124671689	Human		name
156337943	CV2343123	single nucleotide variant	NM_020337.3(ANKRD50):c.1586G>A (p.Arg529Gln)	not specified [RCV004192715]	uncertain significance	4	124671691	124671691	Human		name
156108487	CV2355405	single nucleotide variant	NM_020337.3(ANKRD50):c.1406C>T (p.Ala469Val)	not specified [RCV004205261]	uncertain significance	4	124671871	124671871	Human		name
156217768	CV2386182	single nucleotide variant	NM_020337.3(ANKRD50):c.2213G>A (p.Gly738Asp)	not specified [RCV004229225]	uncertain significance	4	124671064	124671064	Human		name
329395775	CV2454556	single nucleotide variant	NM_020337.3(ANKRD50):c.1651A>G (p.Asn551Asp)	not specified [RCV004268038]	uncertain significance	4	124671626	124671626	Human		name
401768168	CV2675076	single nucleotide variant	NM_020337.3(ANKRD50):c.1112A>G (p.His371Arg)	not specified [RCV004289857]	uncertain significance	4	124672165	124672165	Human		name
401723999	CV2684935	single nucleotide variant	NM_020337.3(ANKRD50):c.1537C>T (p.Arg513Cys)	not specified [RCV004296438]	uncertain significance	4	124671740	124671740	Human		name
401783005	CV2703710	single nucleotide variant	NM_020337.3(ANKRD50):c.1310C>T (p.Ala437Val)	not specified [RCV004306599]	uncertain significance	4	124671967	124671967	Human		name
401743407	CV2715473	single nucleotide variant	NM_020337.3(ANKRD50):c.1186C>T (p.Leu396Phe)	not specified [RCV004326574]	uncertain significance	4	124672091	124672091	Human		name
405683579	CV3282248	single nucleotide variant	NM_020337.3(ANKRD50):c.1063A>C (p.Asn355His)	not specified [RCV004422227]	uncertain significance	4	124672214	124672214	Human		name
405683583	CV3282249	single nucleotide variant	NM_020337.3(ANKRD50):c.1603G>A (p.Gly535Arg)	not specified [RCV004422228]	uncertain significance	4	124671674	124671674	Human		name
405683591	CV3282251	single nucleotide variant	NM_020337.3(ANKRD50):c.2059A>G (p.Met687Val)	not specified [RCV004422230]	uncertain significance	4	124671218	124671218	Human		name
405683595	CV3282252	single nucleotide variant	NM_020337.3(ANKRD50):c.2086C>G (p.Leu696Val)	not specified [RCV004422231]	uncertain significance	4	124671191	124671191	Human		name
405683598	CV3282253	single nucleotide variant	NM_020337.3(ANKRD50):c.2291T>C (p.Val764Ala)	not specified [RCV004422232]	uncertain significance	4	124670986	124670986	Human		name
405683603	CV3282254	single nucleotide variant	NM_020337.3(ANKRD50):c.2344C>T (p.Arg782Cys)	not specified [RCV004422233]	uncertain significance	4	124670933	124670933	Human		name
405683606	CV3282255	single nucleotide variant	NM_020337.3(ANKRD50):c.2350C>T (p.Pro784Ser)	not specified [RCV004422234]	uncertain significance	4	124670927	124670927	Human		name
405683610	CV3282256	single nucleotide variant	NM_020337.3(ANKRD50):c.2642G>A (p.Arg881Gln)	not specified [RCV004422235]	uncertain significance	4	124670635	124670635	Human		name
405683614	CV3282257	single nucleotide variant	NM_020337.3(ANKRD50):c.2672G>A (p.Gly891Asp)	not specified [RCV004422236]	uncertain significance	4	124670605	124670605	Human		name
405683617	CV3282258	single nucleotide variant	NM_020337.3(ANKRD50):c.2944G>A (p.Ala982Thr)	not specified [RCV004422237]	uncertain significance	4	124670333	124670333	Human		name
407515389	CV3450723	single nucleotide variant	NM_020337.3(ANKRD50):c.1399G>C (p.Glu467Gln)	not specified [RCV004649878]	uncertain significance	4	124671878	124671878	Human		name
407515433	CV3450745	single nucleotide variant	NM_020337.3(ANKRD50):c.1387A>G (p.Asn463Asp)	not specified [RCV004649892]	uncertain significance	4	124671890	124671890	Human		name
407515454	CV3450756	single nucleotide variant	NM_020337.3(ANKRD50):c.2000G>A (p.Gly667Asp)	not specified [RCV004649899]	uncertain significance	4	124671277	124671277	Human		name
597635623	CV3554486	single nucleotide variant	NM_020337.3(ANKRD50):c.2207A>G (p.Asp736Gly)	not specified [RCV004831225]	uncertain significance	4	124671070	124671070	Human		name
597638582	CV3554505	single nucleotide variant	NM_020337.3(ANKRD50):c.1654G>A (p.Ala552Thr)	not specified [RCV004824955]	uncertain significance	4	124671623	124671623	Human		name
597635645	CV3554514	single nucleotide variant	NM_020337.3(ANKRD50):c.2492G>A (p.Arg831His)	not specified [RCV004831229]	uncertain significance	4	124670785	124670785	Human		name
597635661	CV3554540	single nucleotide variant	NM_020337.3(ANKRD50):c.1363T>A (p.Phe455Ile)	not specified [RCV004831232]	uncertain significance	4	124671914	124671914	Human		name
597635672	CV3554549	single nucleotide variant	NM_020337.3(ANKRD50):c.2368T>A (p.Ser790Thr)	not specified [RCV004831234]	uncertain significance	4	124670909	124670909	Human		name
597635677	CV3554559	single nucleotide variant	NM_020337.3(ANKRD50):c.2611G>A (p.Ala871Thr)	not specified [RCV004831235]	uncertain significance	4	124670666	124670666	Human		name
598166831	CV3989435	single nucleotide variant	NM_020337.3(ANKRD50):c.1114G>A (p.Ala372Thr)	not specified [RCV005369404]	uncertain significance	4	124672163	124672163	Human		name
598166887	CV3989458	single nucleotide variant	NM_020337.3(ANKRD50):c.2692A>T (p.Ile898Leu)	not specified [RCV005369415]	uncertain significance	4	124670585	124670585	Human		name
598166914	CV3989467	single nucleotide variant	NM_020337.3(ANKRD50):c.1165T>G (p.Leu389Val)	not specified [RCV005369420]	uncertain significance	4	124672112	124672112	Human		name
598188212	CV3989494	single nucleotide variant	NM_020337.3(ANKRD50):c.2968G>A (p.Gly990Ser)	not specified [RCV005373683]	uncertain significance	4	124670309	124670309	Human		name
598167004	CV3989503	single nucleotide variant	NM_020337.3(ANKRD50):c.2609G>A (p.Gly870Asp)	not specified [RCV005369436]	uncertain significance	4	124670668	124670668	Human		name
598188298	CV3989514	single nucleotide variant	NM_020337.3(ANKRD50):c.2888A>T (p.Glu963Val)	not specified [RCV005373695]	uncertain significance	4	124670389	124670389	Human		name
598199862	CV3989559	single nucleotide variant	NM_020337.3(ANKRD50):c.1817A>C (p.His606Pro)	not specified [RCV005375761]	uncertain significance	4	124671460	124671460	Human		name
598167100	CV3989568	single nucleotide variant	NM_020337.3(ANKRD50):c.1670G>A (p.Ser557Asn)	not specified [RCV005369457]	likely benign	4	124671607	124671607	Human		name
598199912	CV3989574	single nucleotide variant	NM_020337.3(ANKRD50):c.2428A>G (p.Ile810Val)	not specified [RCV005375771]	uncertain significance	4	124670849	124670849	Human		name
598199936	CV3989582	single nucleotide variant	NM_020337.3(ANKRD50):c.1525A>G (p.Ser509Gly)	not specified [RCV005375775]	uncertain significance	4	124671752	124671752	Human		name
598199973	CV3989592	single nucleotide variant	NM_020337.3(ANKRD50):c.1301G>A (p.Arg434Lys)	not specified [RCV005375781]	uncertain significance	4	124671976	124671976	Human		name
156136918	CV2196212	single nucleotide variant	NM_020337.3(ANKRD50):c.3943A>G (p.Thr1315Ala)	not specified [RCV004073567]	uncertain significance	4	124669334	124669334	Human		name
156256414	CV2219760	single nucleotide variant	NM_020337.3(ANKRD50):c.3520C>T (p.Arg1174Trp)	not specified [RCV004095453]	uncertain significance	4	124669757	124669757	Human		name
156122251	CV2227110	single nucleotide variant	NM_020337.3(ANKRD50):c.3848G>A (p.Gly1283Glu)	not specified [RCV004091737]	uncertain significance	4	124669429	124669429	Human		name
156135559	CV2256917	single nucleotide variant	NM_020337.3(ANKRD50):c.3694A>G (p.Ile1232Val)	not specified [RCV004121117]	uncertain significance	4	124669583	124669583	Human		name
156385058	CV2371687	single nucleotide variant	NM_020337.3(ANKRD50):c.4121T>C (p.Val1374Ala)	not specified [RCV004218971]	uncertain significance	4	124669156	124669156	Human		name
156265429	CV2372220	single nucleotide variant	NM_020337.3(ANKRD50):c.4100A>G (p.Tyr1367Cys)	not specified [RCV004216999]	uncertain significance	4	124669177	124669177	Human		name
329400249	CV2437498	single nucleotide variant	NM_020337.3(ANKRD50):c.3436A>T (p.Met1146Leu)	not specified [RCV004258785]	uncertain significance	4	124669841	124669841	Human		name
329383160	CV2441931	single nucleotide variant	NM_020337.3(ANKRD50):c.4148G>T (p.Arg1383Leu)	not specified [RCV004262108]	uncertain significance	4	124669129	124669129	Human		name
401744103	CV2680891	single nucleotide variant	NM_020337.3(ANKRD50):c.3524A>G (p.Gln1175Arg)	not specified [RCV004295967]	uncertain significance	4	124669753	124669753	Human		name
401720842	CV2702148	single nucleotide variant	NM_020337.3(ANKRD50):c.3973G>A (p.Glu1325Lys)	not specified [RCV004314500]	uncertain significance	4	124669304	124669304	Human		name
401749363	CV2706628	single nucleotide variant	NM_020337.3(ANKRD50):c.3418A>G (p.Ser1140Gly)	not specified [RCV004319208]	uncertain significance	4	124669859	124669859	Human		name
401783919	CV2720859	single nucleotide variant	NM_020337.3(ANKRD50):c.3925C>T (p.Pro1309Ser)	not specified [RCV004328233]	uncertain significance	4	124669352	124669352	Human		name
401783605	CV2723757	single nucleotide variant	NM_020337.3(ANKRD50):c.3334C>G (p.Pro1112Ala)	not specified [RCV004325917]	uncertain significance	4	124669943	124669943	Human		name
401857721	CV2765996	single nucleotide variant	NM_020337.3(ANKRD50):c.3109G>A (p.Val1037Ile)	not specified [RCV004340464]	likely benign	4	124670168	124670168	Human		name
401881823	CV2784842	single nucleotide variant	NM_020337.3(ANKRD50):c.3442C>T (p.Pro1148Ser)	not specified [RCV004352625]	uncertain significance	4	124669835	124669835	Human		name
405683621	CV3282259	single nucleotide variant	NM_020337.3(ANKRD50):c.3103G>C (p.Gly1035Arg)	not specified [RCV004422238]	uncertain significance	4	124670174	124670174	Human		name
405683625	CV3282260	single nucleotide variant	NM_020337.3(ANKRD50):c.3326C>G (p.Ser1109Cys)	not specified [RCV004422239]	uncertain significance	4	124669951	124669951	Human		name
405683629	CV3282261	single nucleotide variant	NM_020337.3(ANKRD50):c.3515T>G (p.Val1172Gly)	not specified [RCV004422240]	uncertain significance	4	124669762	124669762	Human		name
405683633	CV3282262	single nucleotide variant	NM_020337.3(ANKRD50):c.3598A>G (p.Thr1200Ala)	not specified [RCV004422241]	uncertain significance	4	124669679	124669679	Human		name
405683637	CV3282263	single nucleotide variant	NM_020337.3(ANKRD50):c.3808G>T (p.Gly1270Trp)	not specified [RCV004422242]	uncertain significance	4	124669469	124669469	Human		name
407504565	CV3450714	single nucleotide variant	NM_020337.3(ANKRD50):c.3446C>T (p.Ser1149Leu)	not specified [RCV004645866]	uncertain significance	4	124669831	124669831	Human		name
407515459	CV3450760	single nucleotide variant	NM_020337.3(ANKRD50):c.4058G>C (p.Gly1353Ala)	not specified [RCV004649901]	uncertain significance	4	124669219	124669219	Human		name
407515486	CV3450777	single nucleotide variant	NM_020337.3(ANKRD50):c.3614C>T (p.Pro1205Leu)	not specified [RCV004649914]	uncertain significance	4	124669663	124669663	Human		name
597635628	CV3554489	single nucleotide variant	NM_020337.3(ANKRD50):c.3242C>G (p.Ala1081Gly)	not specified [RCV004831226]	uncertain significance	4	124670035	124670035	Human		name
597635639	CV3554509	single nucleotide variant	NM_020337.3(ANKRD50):c.4265A>T (p.Asn1422Ile)	not specified [RCV004831228]	uncertain significance	4	124669012	124669012	Human		name
597635651	CV3554519	single nucleotide variant	NM_020337.3(ANKRD50):c.3643A>G (p.Thr1215Ala)	not specified [RCV004831230]	uncertain significance	4	124669634	124669634	Human		name
597635656	CV3554534	single nucleotide variant	NM_020337.3(ANKRD50):c.3359C>T (p.Pro1120Leu)	not specified [RCV004831231]	uncertain significance	4	124669918	124669918	Human		name
597635667	CV3554545	single nucleotide variant	NM_020337.3(ANKRD50):c.3716C>T (p.Thr1239Ile)	not specified [RCV004831233]	uncertain significance	4	124669561	124669561	Human		name
597638598	CV3554564	single nucleotide variant	NM_020337.3(ANKRD50):c.3446C>G (p.Ser1149Trp)	not specified [RCV004824958]	uncertain significance	4	124669831	124669831	Human		name
598187963	CV3989424	single nucleotide variant	NM_020337.3(ANKRD50):c.3440A>G (p.Gln1147Arg)	not specified [RCV005373645]	uncertain significance	4	124669837	124669837	Human		name
598166865	CV3989446	single nucleotide variant	NM_020337.3(ANKRD50):c.3686G>A (p.Arg1229Gln)	not specified [RCV005369410]	uncertain significance	4	124669591	124669591	Human		name
598166941	CV3989477	single nucleotide variant	NM_020337.3(ANKRD50):c.3601G>T (p.Ala1201Ser)	not specified [RCV005369425]	uncertain significance	4	124669676	124669676	Human		name
598188194	CV3989487	single nucleotide variant	NM_020337.3(ANKRD50):c.3158C>T (p.Ala1053Val)	not specified [RCV005373680]	uncertain significance	4	124670119	124670119	Human		name
598188341	CV3989522	single nucleotide variant	NM_020337.3(ANKRD50):c.3953C>A (p.Pro1318Gln)	not specified [RCV005373702]	uncertain significance	4	124669324	124669324	Human		name
598167060	CV3989532	single nucleotide variant	NM_020337.3(ANKRD50):c.3469C>T (p.Pro1157Ser)	not specified [RCV005369448]	uncertain significance	4	124669808	124669808	Human		name
598199832	CV3989553	single nucleotide variant	NM_020337.3(ANKRD50):c.3767G>A (p.Ser1256Asn)	not specified [RCV005375756]	uncertain significance	4	124669510	124669510	Human		name

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