Micall2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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201 records found for search term Micall2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8632438	CV87646	single nucleotide variant	NM_182924.3(MICALL2):c.*28G>A	Malignant melanoma [RCV000067738]	not provided	7	1434568	1434568	Human		name
15195662	CV759515	single nucleotide variant	NM_182924.4(MICALL2):c.525+9C>G	not provided [RCV000911478]	benign	7	1447566	1447566	Human		name
15176810	CV744311	single nucleotide variant	NM_182924.4(MICALL2):c.2592-8C>T	not provided [RCV000906512]	benign	7	1435155	1435155	Human		name
15127301	CV710851	single nucleotide variant	NM_182924.4(MICALL2):c.90C>T (p.Phe30=)	not provided [RCV000963878]	benign	7	1459237	1459237	Human		name
401749327	CV2706505	single nucleotide variant	NM_182924.4(MICALL2):c.10A>G (p.Ile4Val)	not specified [RCV004317318]	uncertain significance	7	1459317	1459317	Human		name
598186022	CV3993088	single nucleotide variant	NM_182924.4(MICALL2):c.23A>G (p.Gln8Arg)	not specified [RCV005373350]	uncertain significance	7	1459304	1459304	Human		name
15157970	CV699919	single nucleotide variant	NM_182924.4(MICALL2):c.273C>T (p.Asp91=)	not provided [RCV000946985]	benign	7	1448681	1448681	Human		name
401780852	CV2681791	single nucleotide variant	NM_182924.4(MICALL2):c.58G>A (p.Asp20Asn)	not specified [RCV004296793]	uncertain significance	7	1459269	1459269	Human		name
401889899	CV2763532	single nucleotide variant	NM_182924.4(MICALL2):c.34C>T (p.Arg12Trp)	not specified [RCV004343053]	uncertain significance	7	1459293	1459293	Human		name
405671848	CV3289475	single nucleotide variant	NM_182924.4(MICALL2):c.60C>G (p.Asp20Glu)	not specified [RCV004419666]	uncertain significance	7	1459267	1459267	Human		name
15117367	CV710848	single nucleotide variant	NM_182924.4(MICALL2):c.852G>A (p.Pro284=)	not provided [RCV000962192]	benign	7	1445218	1445218	Human		name
15125726	CV710850	single nucleotide variant	NM_182924.4(MICALL2):c.510C>T (p.Gly170=)	not provided [RCV000963627]	benign	7	1447590	1447590	Human		name
15155521	CV722382	single nucleotide variant	NM_182924.4(MICALL2):c.855G>A (p.Ser285=)	not provided [RCV000880434]	likely benign	7	1445215	1445215	Human		name
15190462	CV722383	single nucleotide variant	NM_182924.4(MICALL2):c.609C>T (p.Ala203=)	not provided [RCV000888105]	benign	7	1446745	1446745	Human		name
15169300	CV722385	single nucleotide variant	NM_182924.4(MICALL2):c.321C>T (p.His107=)	not provided [RCV000883239]	likely benign	7	1448633	1448633	Human		name
15199117	CV750476	single nucleotide variant	NM_182924.4(MICALL2):c.672G>A (p.Ser224=)	not provided [RCV000912452]	benign	7	1445398	1445398	Human		name
156093539	CV2309939	single nucleotide variant	NM_182924.4(MICALL2):c.166G>C (p.Glu56Gln)	not specified [RCV004163096]	uncertain significance	7	1450266	1450266	Human		name
156390665	CV2383301	single nucleotide variant	NM_182924.4(MICALL2):c.138C>G (p.Asp46Glu)	not specified [RCV004222346]	uncertain significance	7	1459189	1459189	Human		name
401780925	CV2681821	single nucleotide variant	NM_182924.4(MICALL2):c.200G>A (p.Arg67His)	not specified [RCV004296822]	uncertain significance	7	1448754	1448754	Human		name
401921107	CV2828177	single nucleotide variant	NM_182924.4(MICALL2):c.2316C>T (p.Asp772=)	not provided [RCV003432197]	likely benign	7	1437976	1437976	Human		name
405671747	CV3289455	single nucleotide variant	NM_182924.4(MICALL2):c.142A>C (p.Ile48Leu)	not specified [RCV004419646]	uncertain significance	7	1459185	1459185	Human		name
407485373	CV3446939	single nucleotide variant	NM_182924.4(MICALL2):c.199C>T (p.Arg67Cys)	not specified [RCV004640708]	uncertain significance	7	1448755	1448755	Human		name
407518468	CV3446945	single nucleotide variant	NM_182924.4(MICALL2):c.173T>C (p.Ile58Thr)	not specified [RCV004628884]	uncertain significance	7	1450259	1450259	Human		name
597646011	CV3563673	single nucleotide variant	NM_182924.4(MICALL2):c.2256C>T (p.Asp752=)	not specified [RCV004832996]	likely benign	7	1438152	1438152	Human		name
598254152	CV3993086	single nucleotide variant	NM_182924.4(MICALL2):c.1635C>T (p.Val545=)	not specified [RCV005367155]	likely benign	7	1442268	1442268	Human		name
15187923	CV699914	single nucleotide variant	NM_182924.4(MICALL2):c.1914C>T (p.Pro638=)	not provided [RCV000953732]	benign	7	1439977	1439977	Human		name
15130682	CV710840	single nucleotide variant	NM_182924.4(MICALL2):c.2572C>T (p.Leu858=)	not provided [RCV000964475]	benign\|likely benign	7	1436761	1436761	Human		name
15180803	CV722378	single nucleotide variant	NM_182924.4(MICALL2):c.2022C>T (p.Asp674=)	not provided [RCV000885614]	benign	7	1438940	1438940	Human		name
15154661	CV722379	single nucleotide variant	NM_182924.4(MICALL2):c.1605C>A (p.Gly535=)	not provided [RCV000880262]	likely benign	7	1442298	1442298	Human		name
15180806	CV722380	single nucleotide variant	NM_182924.4(MICALL2):c.1350G>A (p.Glu450=)	not provided [RCV000885615]	benign	7	1444720	1444720	Human		name
15149396	CV722381	single nucleotide variant	NM_182924.4(MICALL2):c.1023C>A (p.Thr341=)	not provided [RCV000879156]	benign	7	1445047	1445047	Human		name
15119042	CV736008	single nucleotide variant	NM_182924.4(MICALL2):c.1999C>T (p.Leu667=)	not provided [RCV000895654]	benign	7	1438963	1438963	Human		name
15192279	CV736011	single nucleotide variant	NM_182924.4(MICALL2):c.1290C>G (p.Thr430=)	not provided [RCV000910492]	likely benign	7	1444780	1444780	Human		name
15117418	CV750472	single nucleotide variant	NM_182924.4(MICALL2):c.2667C>G (p.Arg889=)	not provided [RCV000917791]	likely benign	7	1434644	1434644	Human		name
15117032	CV750473	single nucleotide variant	NM_182924.4(MICALL2):c.2547C>T (p.Asn849=)	not provided [RCV000917730]	likely benign	7	1436786	1436786	Human		name
8632439	CV87647	single nucleotide variant	NM_182924.3(MICALL2):c.1947C>T (p.Ser649=)	Malignant melanoma [RCV000067739]	not provided	7	1439944	1439944	Human		name
156379896	CV2211650	single nucleotide variant	NM_182924.4(MICALL2):c.791G>T (p.Gly264Val)	not specified [RCV004084542]	uncertain significance	7	1445279	1445279	Human		name
156169778	CV2247338	single nucleotide variant	NM_182924.4(MICALL2):c.425C>A (p.Pro142His)	not specified [RCV004108682]	uncertain significance	7	1447675	1447675	Human		name
156104031	CV2260544	single nucleotide variant	NM_182924.4(MICALL2):c.782G>A (p.Gly261Glu)	not specified [RCV004123323]	uncertain significance	7	1445288	1445288	Human		name
156104534	CV2291739	single nucleotide variant	NM_182924.4(MICALL2):c.481G>A (p.Val161Ile)	not specified [RCV004158018]	uncertain significance	7	1447619	1447619	Human		name
155942962	CV2298370	single nucleotide variant	NM_182924.4(MICALL2):c.701G>A (p.Gly234Asp)	not specified [RCV004160262]	uncertain significance	7	1445369	1445369	Human		name
156042841	CV2381493	single nucleotide variant	NM_182924.4(MICALL2):c.976C>T (p.Arg326Cys)	not specified [RCV004229971]	likely benign	7	1445094	1445094	Human		name
329391264	CV2452194	single nucleotide variant	NM_182924.4(MICALL2):c.934A>C (p.Thr312Pro)	not specified [RCV004278900]	uncertain significance	7	1445136	1445136	Human		name
329398019	CV2466550	single nucleotide variant	NM_182924.4(MICALL2):c.898G>T (p.Val300Phe)	not specified [RCV004274087]	uncertain significance	7	1445172	1445172	Human		name
401723580	CV2675005	single nucleotide variant	NM_182924.4(MICALL2):c.686C>T (p.Ala229Val)	not specified [RCV004296309]	uncertain significance	7	1445384	1445384	Human		name
401781910	CV2722331	single nucleotide variant	NM_182924.4(MICALL2):c.322G>A (p.Gly108Ser)	not specified [RCV004322745]	uncertain significance	7	1448632	1448632	Human		name
401859788	CV2768340	single nucleotide variant	NM_182924.4(MICALL2):c.781G>A (p.Gly261Arg)	not specified [RCV004350604]	uncertain significance	7	1445289	1445289	Human		name
401866800	CV2792509	single nucleotide variant	NM_182924.4(MICALL2):c.698C>A (p.Pro233Gln)	not specified [RCV004363555]	uncertain significance	7	1445372	1445372	Human		name
401921109	CV2828178	single nucleotide variant	NM_182924.4(MICALL2):c.872C>T (p.Ala291Val)	not provided [RCV003432198]	likely benign	7	1445198	1445198	Human		name
405671833	CV3289472	single nucleotide variant	NM_182924.4(MICALL2):c.299C>T (p.Ser100Phe)	not specified [RCV004419663]	uncertain significance	7	1448655	1448655	Human		name
405671838	CV3289473	single nucleotide variant	NM_182924.4(MICALL2):c.335T>C (p.Ile112Thr)	not specified [RCV004419664]	uncertain significance	7	1447765	1447765	Human		name
405671843	CV3289474	single nucleotide variant	NM_182924.4(MICALL2):c.413C>T (p.Ala138Val)	not specified [RCV004419665]	uncertain significance	7	1447687	1447687	Human		name
405671853	CV3289476	single nucleotide variant	NM_182924.4(MICALL2):c.610G>A (p.Asp204Asn)	not specified [RCV004419667]	uncertain significance	7	1446744	1446744	Human		name
405671857	CV3289477	single nucleotide variant	NM_182924.4(MICALL2):c.626A>G (p.His209Arg)	not specified [RCV004419668]	uncertain significance	7	1446728	1446728	Human		name
405671862	CV3289478	single nucleotide variant	NM_182924.4(MICALL2):c.716C>G (p.Thr239Ser)	not specified [RCV004419669]	uncertain significance	7	1445354	1445354	Human		name
405671867	CV3289479	single nucleotide variant	NM_182924.4(MICALL2):c.752A>G (p.Lys251Arg)	not specified [RCV004419670]	uncertain significance	7	1445318	1445318	Human		name
405671870	CV3289480	single nucleotide variant	NM_182924.4(MICALL2):c.815C>T (p.Ser272Phe)	not specified [RCV004419671]	uncertain significance	7	1445255	1445255	Human		name
405671873	CV3289481	single nucleotide variant	NM_182924.4(MICALL2):c.830A>G (p.Gln277Arg)	not specified [RCV004419672]	uncertain significance	7	1445240	1445240	Human		name
405671878	CV3289482	single nucleotide variant	NM_182924.4(MICALL2):c.967T>C (p.Ser323Pro)	not specified [RCV004419673]	likely benign	7	1445103	1445103	Human		name
407485404	CV3446944	single nucleotide variant	NM_182924.4(MICALL2):c.914A>G (p.Asn305Ser)	not specified [RCV004640713]	uncertain significance	7	1445156	1445156	Human		name
407485411	CV3446946	single nucleotide variant	NM_182924.4(MICALL2):c.565G>C (p.Gly189Arg)	not specified [RCV004640714]	uncertain significance	7	1446789	1446789	Human		name
597645983	CV3563668	single nucleotide variant	NM_182924.4(MICALL2):c.682A>G (p.Lys228Glu)	not specified [RCV004832992]	uncertain significance	7	1445388	1445388	Human		name
597645997	CV3563671	single nucleotide variant	NM_182924.4(MICALL2):c.946G>T (p.Val316Leu)	not specified [RCV004832994]	uncertain significance	7	1445124	1445124	Human		name
597646025	CV3563677	single nucleotide variant	NM_182924.4(MICALL2):c.964C>T (p.Pro322Ser)	not specified [RCV004832998]	uncertain significance	7	1445106	1445106	Human		name
12791685	CV362148	single nucleotide variant	NM_182924.4(MICALL2):c.851C>G (p.Pro284Arg)	Joubert syndrome 1 [RCV000416431]	pathogenic	7	1445219	1445219	Human	1	name
598185971	CV3993073	single nucleotide variant	NM_182924.4(MICALL2):c.512C>T (p.Pro171Leu)	not specified [RCV005373342]	uncertain significance	7	1447588	1447588	Human		name
598185986	CV3993076	single nucleotide variant	NM_182924.4(MICALL2):c.671C>T (p.Ser224Leu)	not specified [RCV005373344]	uncertain significance	7	1445399	1445399	Human		name
598186036	CV3993091	single nucleotide variant	NM_182924.4(MICALL2):c.838A>C (p.Asn280His)	not specified [RCV005373352]	uncertain significance	7	1445232	1445232	Human		name
15192799	CV699918	single nucleotide variant	NM_182924.4(MICALL2):c.325C>T (p.Arg109Cys)	not provided [RCV000955179]	benign	7	1448629	1448629	Human		name
15132432	CV736012	single nucleotide variant	NM_182924.4(MICALL2):c.821A>G (p.Gln274Arg)	not provided [RCV000897955]	likely benign	7	1445249	1445249	Human		name
15174960	CV736013	single nucleotide variant	NM_182924.4(MICALL2):c.352G>T (p.Val118Leu)	not provided [RCV000906098]	benign	7	1447748	1447748	Human		name
15203266	CV750475	single nucleotide variant	NM_182924.4(MICALL2):c.784G>A (p.Ala262Thr)	not provided [RCV000913817]	benign	7	1445286	1445286	Human		name
156165286	CV2196065	single nucleotide variant	NM_182924.4(MICALL2):c.1016G>A (p.Arg339His)	not specified [RCV004072305]	uncertain significance	7	1445054	1445054	Human		name
155963319	CV2197852	single nucleotide variant	NM_182924.4(MICALL2):c.1715T>G (p.Met572Arg)	not specified [RCV004077087]	likely benign	7	1440681	1440681	Human		name
156324055	CV2198534	single nucleotide variant	NM_182924.4(MICALL2):c.1409C>T (p.Ala470Val)	not specified [RCV004075561]	uncertain significance	7	1444661	1444661	Human		name
156167663	CV2201033	single nucleotide variant	NM_182924.4(MICALL2):c.2248C>T (p.Arg750Trp)	not specified [RCV004074797]	uncertain significance	7	1438160	1438160	Human		name
155915087	CV2203977	single nucleotide variant	NM_182924.4(MICALL2):c.1559T>C (p.Leu520Pro)	not specified [RCV004070020]	uncertain significance	7	1442344	1442344	Human		name
156083200	CV2205498	single nucleotide variant	NM_182924.4(MICALL2):c.1709A>G (p.Gln570Arg)	not specified [RCV004082433]	uncertain significance	7	1442194	1442194	Human		name
155964530	CV2209993	single nucleotide variant	NM_182924.4(MICALL2):c.2117A>G (p.Lys706Arg)	not specified [RCV004076431]	uncertain significance	7	1438845	1438845	Human		name
156248305	CV2215416	single nucleotide variant	NM_182924.4(MICALL2):c.1184C>T (p.Ser395Phe)	not specified [RCV004089219]	uncertain significance	7	1444886	1444886	Human		name
156381612	CV2215650	single nucleotide variant	NM_182924.4(MICALL2):c.2033A>G (p.Asn678Ser)	not specified [RCV004089396]	uncertain significance	7	1438929	1438929	Human		name
156018404	CV2233123	single nucleotide variant	NM_182924.4(MICALL2):c.1951G>A (p.Gly651Arg)	not specified [RCV004103739]	uncertain significance	7	1439940	1439940	Human		name
155986665	CV2234017	single nucleotide variant	NM_182924.4(MICALL2):c.2368C>T (p.Leu790Phe)	not specified [RCV004106138]	uncertain significance	7	1437924	1437924	Human		name
156033837	CV2236395	single nucleotide variant	NM_182924.4(MICALL2):c.1387C>G (p.Leu463Val)	not specified [RCV004108073]	uncertain significance	7	1444683	1444683	Human		name
156174094	CV2247649	single nucleotide variant	NM_182924.4(MICALL2):c.2455C>T (p.Arg819Cys)	not specified [RCV004110981]	uncertain significance	7	1437556	1437556	Human		name
156349281	CV2309375	single nucleotide variant	NM_182924.4(MICALL2):c.2395A>G (p.Met799Val)	not specified [RCV004165524]	uncertain significance	7	1437897	1437897	Human		name
156266022	CV2312291	single nucleotide variant	NM_182924.4(MICALL2):c.2332A>G (p.Met778Val)	not specified [RCV004167002]	uncertain significance	7	1437960	1437960	Human		name
156274564	CV2316386	single nucleotide variant	NM_182924.4(MICALL2):c.1294C>T (p.Leu432Phe)	not specified [RCV004169886]	uncertain significance	7	1444776	1444776	Human		name
156068419	CV2317987	single nucleotide variant	NM_182924.4(MICALL2):c.2138C>T (p.Pro713Leu)	not specified [RCV004177104]	uncertain significance	7	1438338	1438338	Human		name
155974570	CV2317988	single nucleotide variant	NM_182924.4(MICALL2):c.2610G>C (p.Gln870His)	not specified [RCV004177105]	uncertain significance	7	1435129	1435129	Human		name
156359597	CV2328244	single nucleotide variant	NM_182924.4(MICALL2):c.2128C>G (p.Pro710Ala)	not specified [RCV004173331]	uncertain significance	7	1438348	1438348	Human		name
156084874	CV2330986	single nucleotide variant	NM_182924.4(MICALL2):c.1135G>A (p.Gly379Arg)	not specified [RCV004188028]	likely benign	7	1444935	1444935	Human		name
155982633	CV2337182	single nucleotide variant	NM_182924.4(MICALL2):c.2575G>A (p.Asp859Asn)	not specified [RCV004192939]	uncertain significance	7	1436758	1436758	Human		name
156182387	CV2338197	single nucleotide variant	NM_182924.4(MICALL2):c.1058C>T (p.Pro353Leu)	not specified [RCV004186266]	uncertain significance	7	1445012	1445012	Human		name
155927744	CV2349739	single nucleotide variant	NM_182924.4(MICALL2):c.1661C>T (p.Pro554Leu)	not specified [RCV004204153]	likely benign	7	1442242	1442242	Human		name
156125111	CV2350160	single nucleotide variant	NM_182924.4(MICALL2):c.2417G>A (p.Arg806His)	not specified [RCV004200077]	uncertain significance	7	1437594	1437594	Human		name
156336921	CV2360843	single nucleotide variant	NM_182924.4(MICALL2):c.2135C>T (p.Ser712Phe)	not specified [RCV004603368]	uncertain significance	7	1438341	1438341	Human		name
156008328	CV2365257	single nucleotide variant	NM_182924.4(MICALL2):c.1829G>A (p.Arg610Gln)	not specified [RCV004209355]	uncertain significance	7	1440062	1440062	Human		name
155925837	CV2365652	single nucleotide variant	NM_182924.4(MICALL2):c.1588G>A (p.Ala530Thr)	not specified [RCV004214208]	uncertain significance	7	1442315	1442315	Human		name
156101515	CV2367657	single nucleotide variant	NM_182924.4(MICALL2):c.1714A>G (p.Met572Val)	not specified [RCV004211576]	uncertain significance	7	1440682	1440682	Human		name
156341000	CV2368348	single nucleotide variant	NM_182924.4(MICALL2):c.1357C>T (p.Arg453Trp)	not specified [RCV004219125]	uncertain significance	7	1444713	1444713	Human		name
156186863	CV2378016	single nucleotide variant	NM_182924.4(MICALL2):c.1118C>T (p.Pro373Leu)	not specified [RCV004232581]	uncertain significance	7	1444952	1444952	Human		name
156172247	CV2380797	single nucleotide variant	NM_182924.4(MICALL2):c.1636G>A (p.Gly546Ser)	not specified [RCV004218358]	likely benign	7	1442267	1442267	Human		name
156213959	CV2385884	single nucleotide variant	NM_182924.4(MICALL2):c.2665C>T (p.Arg889Cys)	not specified [RCV004226924]	uncertain significance	7	1434646	1434646	Human		name
156039766	CV2390363	single nucleotide variant	NM_182924.4(MICALL2):c.2144A>G (p.Asn715Ser)	not specified [RCV004240723]	uncertain significance	7	1438332	1438332	Human		name
155928113	CV2391651	single nucleotide variant	NM_182924.4(MICALL2):c.1455G>C (p.Gln485His)	not specified [RCV004241812]	likely benign	7	1442448	1442448	Human		name
156199986	CV2392329	single nucleotide variant	NM_182924.4(MICALL2):c.1555C>A (p.Pro519Thr)	not specified [RCV004243928]	uncertain significance	7	1442348	1442348	Human		name
155996064	CV2393139	single nucleotide variant	NM_182924.4(MICALL2):c.2548G>A (p.Asp850Asn)	not specified [RCV004226617]	uncertain significance	7	1436785	1436785	Human		name
156165601	CV2398841	single nucleotide variant	NM_182924.4(MICALL2):c.1913C>T (p.Pro638Leu)	not specified [RCV004245164]	uncertain significance	7	1439978	1439978	Human		name
156222186	CV2399686	single nucleotide variant	NM_182924.4(MICALL2):c.1483C>A (p.Pro495Thr)	not specified [RCV004245505]	uncertain significance	7	1442420	1442420	Human		name
156103181	CV2400193	single nucleotide variant	NM_182924.4(MICALL2):c.1606A>G (p.Arg536Gly)	not specified [RCV004242988]	uncertain significance	7	1442297	1442297	Human		name
156003870	CV2400926	single nucleotide variant	NM_182924.4(MICALL2):c.2042G>A (p.Arg681Gln)	not specified [RCV004244216]	likely benign	7	1438920	1438920	Human		name
329359552	CV2446320	single nucleotide variant	NM_182924.4(MICALL2):c.1517G>A (p.Arg506Gln)	not specified [RCV004249452]	likely benign	7	1442386	1442386	Human		name
329393054	CV2449469	single nucleotide variant	NM_182924.4(MICALL2):c.1070C>T (p.Ala357Val)	not specified [RCV004268412]	likely benign	7	1445000	1445000	Human		name
329402661	CV2451198	single nucleotide variant	NM_182924.4(MICALL2):c.2464A>G (p.Met822Val)	not specified [RCV004270118]	uncertain significance	7	1437547	1437547	Human		name
329376888	CV2451553	single nucleotide variant	NM_182924.4(MICALL2):c.1183T>G (p.Ser395Ala)	not specified [RCV004274492]	uncertain significance	7	1444887	1444887	Human		name
329376364	CV2471999	single nucleotide variant	NM_182924.4(MICALL2):c.1301G>T (p.Gly434Val)	not specified [RCV004283154]	uncertain significance	7	1444769	1444769	Human		name
401755094	CV2682378	single nucleotide variant	NM_182924.4(MICALL2):c.1686G>T (p.Lys562Asn)	not specified [RCV004290408]	uncertain significance	7	1442217	1442217	Human		name
401756329	CV2687093	single nucleotide variant	NM_182924.4(MICALL2):c.2511G>C (p.Glu837Asp)	not specified [RCV004304407]	uncertain significance	7	1436822	1436822	Human		name
401750584	CV2689462	single nucleotide variant	NM_182924.4(MICALL2):c.1003A>G (p.Lys335Glu)	not specified [RCV004308309]	uncertain significance	7	1445067	1445067	Human		name
401782709	CV2697174	single nucleotide variant	NM_182924.4(MICALL2):c.2617C>T (p.Arg873Trp)	not specified [RCV004302158]	uncertain significance	7	1435122	1435122	Human		name
401773284	CV2698159	single nucleotide variant	NM_182924.4(MICALL2):c.2012C>G (p.Ala671Gly)	not specified [RCV004304730]	uncertain significance	7	1438950	1438950	Human		name
401758040	CV2704141	single nucleotide variant	NM_182924.4(MICALL2):c.1267A>G (p.Thr423Ala)	not specified [RCV004311158]	uncertain significance	7	1444803	1444803	Human		name
401746504	CV2731826	single nucleotide variant	NM_182924.4(MICALL2):c.1943C>T (p.Ala648Val)	not specified [RCV004333079]	uncertain significance	7	1439948	1439948	Human		name
401768302	CV2735256	single nucleotide variant	NM_182924.4(MICALL2):c.2563G>T (p.Val855Leu)	not specified [RCV004333930]	uncertain significance	7	1436770	1436770	Human		name
401778685	CV2735454	single nucleotide variant	NM_182924.4(MICALL2):c.1788G>T (p.Arg596Ser)	not specified [RCV004331013]	uncertain significance	7	1440608	1440608	Human		name
401857336	CV2759043	single nucleotide variant	NM_182924.4(MICALL2):c.1964C>T (p.Pro655Leu)	not specified [RCV004342350]	uncertain significance	7	1439927	1439927	Human		name
401888981	CV2761626	single nucleotide variant	NM_182924.4(MICALL2):c.1850C>T (p.Ala617Val)	not specified [RCV004337250]	uncertain significance	7	1440041	1440041	Human		name
401860267	CV2768531	single nucleotide variant	NM_182924.4(MICALL2):c.1022C>T (p.Thr341Ile)	not specified [RCV004344406]	uncertain significance	7	1445048	1445048	Human		name
401875867	CV2777563	single nucleotide variant	NM_182924.4(MICALL2):c.2266C>T (p.Leu756Phe)	not specified [RCV004343419]	uncertain significance	7	1438142	1438142	Human		name
401864701	CV2777983	single nucleotide variant	NM_182924.4(MICALL2):c.1990C>T (p.Arg664Cys)	not specified [RCV004347942]	uncertain significance	7	1438972	1438972	Human		name
401881116	CV2788023	single nucleotide variant	NM_182924.4(MICALL2):c.2299G>T (p.Ala767Ser)	not specified [RCV004358675]	uncertain significance	7	1438109	1438109	Human		name
405671727	CV3289451	single nucleotide variant	NM_182924.4(MICALL2):c.1010G>A (p.Arg337His)	not specified [RCV004419642]	uncertain significance	7	1445060	1445060	Human		name
405671733	CV3289452	single nucleotide variant	NM_182924.4(MICALL2):c.1199C>T (p.Thr400Met)	not specified [RCV004419643]	uncertain significance	7	1444871	1444871	Human		name
405671737	CV3289453	single nucleotide variant	NM_182924.4(MICALL2):c.1268C>T (p.Thr423Ile)	not specified [RCV004419644]	uncertain significance	7	1444802	1444802	Human		name
405671742	CV3289454	single nucleotide variant	NM_182924.4(MICALL2):c.1358G>A (p.Arg453Gln)	not specified [RCV004419645]	uncertain significance	7	1444712	1444712	Human		name
405671752	CV3289456	single nucleotide variant	NM_182924.4(MICALL2):c.1463C>T (p.Thr488Ile)	not specified [RCV004419647]	uncertain significance	7	1442440	1442440	Human		name
405671757	CV3289457	single nucleotide variant	NM_182924.4(MICALL2):c.1526G>T (p.Gly509Val)	not specified [RCV004419648]	uncertain significance	7	1442377	1442377	Human		name
405671763	CV3289458	single nucleotide variant	NM_182924.4(MICALL2):c.1562G>A (p.Ser521Asn)	not specified [RCV004419649]	uncertain significance	7	1442341	1442341	Human		name
405671781	CV3289461	single nucleotide variant	NM_182924.4(MICALL2):c.1858G>A (p.Ala620Thr)	not specified [RCV004419652]	uncertain significance	7	1440033	1440033	Human		name
405671784	CV3289462	single nucleotide variant	NM_182924.4(MICALL2):c.1936C>T (p.Arg646Cys)	not specified [RCV004419653]	uncertain significance	7	1439955	1439955	Human		name
405671789	CV3289463	single nucleotide variant	NM_182924.4(MICALL2):c.2023G>A (p.Val675Ile)	not specified [RCV004419654]	uncertain significance	7	1438939	1438939	Human		name
405671793	CV3289464	single nucleotide variant	NM_182924.4(MICALL2):c.2038C>T (p.Leu680Phe)	not specified [RCV004419655]	uncertain significance	7	1438924	1438924	Human		name
405671799	CV3289465	single nucleotide variant	NM_182924.4(MICALL2):c.2113G>A (p.Gly705Ser)	not specified [RCV004419656]	uncertain significance	7	1438849	1438849	Human		name
405671804	CV3289466	single nucleotide variant	NM_182924.4(MICALL2):c.2302G>T (p.Ala768Ser)	not specified [RCV004419657]	uncertain significance	7	1438106	1438106	Human		name
405671811	CV3289467	single nucleotide variant	NM_182924.4(MICALL2):c.2317G>A (p.Ala773Thr)	not specified [RCV004419658]	uncertain significance	7	1437975	1437975	Human		name
405671814	CV3289468	single nucleotide variant	NM_182924.4(MICALL2):c.2434C>G (p.Leu812Val)	not specified [RCV004419659]	uncertain significance	7	1437577	1437577	Human		name
405671819	CV3289469	single nucleotide variant	NM_182924.4(MICALL2):c.2435T>G (p.Leu812Arg)	not specified [RCV004419660]	uncertain significance	7	1437576	1437576	Human		name
405671825	CV3289470	single nucleotide variant	NM_182924.4(MICALL2):c.2542G>A (p.Val848Met)	not specified [RCV004419661]	uncertain significance	7	1436791	1436791	Human		name
405671830	CV3289471	single nucleotide variant	NM_182924.4(MICALL2):c.2675A>G (p.Lys892Arg)	not specified [RCV004419662]	uncertain significance	7	1434636	1434636	Human		name
407485366	CV3446937	single nucleotide variant	NM_182924.4(MICALL2):c.1710G>C (p.Gln570His)	not specified [RCV004640706]	uncertain significance	7	1442193	1442193	Human		name
407485367	CV3446938	single nucleotide variant	NM_182924.4(MICALL2):c.1316C>T (p.Pro439Leu)	not specified [RCV004640707]	uncertain significance	7	1444754	1444754	Human		name
407485380	CV3446940	single nucleotide variant	NM_182924.4(MICALL2):c.1402G>A (p.Ala468Thr)	not specified [RCV004640709]	uncertain significance	7	1444668	1444668	Human		name
407485384	CV3446941	single nucleotide variant	NM_182924.4(MICALL2):c.1336G>A (p.Asp446Asn)	not specified [RCV004640710]	uncertain significance	7	1444734	1444734	Human		name
407485390	CV3446942	single nucleotide variant	NM_182924.4(MICALL2):c.1741G>A (p.Glu581Lys)	not specified [RCV004640711]	uncertain significance	7	1440655	1440655	Human		name
407485397	CV3446943	single nucleotide variant	NM_182924.4(MICALL2):c.1704A>C (p.Leu568Phe)	not specified [RCV004640712]	uncertain significance	7	1442199	1442199	Human		name
407485416	CV3446947	single nucleotide variant	NM_182924.4(MICALL2):c.2260C>A (p.Leu754Met)	not specified [RCV004640715]	uncertain significance	7	1438148	1438148	Human		name
597645949	CV3563661	single nucleotide variant	NM_182924.4(MICALL2):c.1676C>T (p.Pro559Leu)	not specified [RCV004832987]	uncertain significance	7	1442227	1442227	Human		name
597645955	CV3563662	single nucleotide variant	NM_182924.4(MICALL2):c.1246G>T (p.Ala416Ser)	not specified [RCV004832988]	uncertain significance	7	1444824	1444824	Human		name
597635673	CV3563663	single nucleotide variant	NM_182924.4(MICALL2):c.2269C>T (p.Arg757Cys)	not specified [RCV004824414]	uncertain significance	7	1438139	1438139	Human		name
597645962	CV3563664	single nucleotide variant	NM_182924.4(MICALL2):c.2459G>A (p.Arg820Gln)	not specified [RCV004832989]	uncertain significance	7	1437552	1437552	Human		name
597645969	CV3563665	single nucleotide variant	NM_182924.4(MICALL2):c.1777C>T (p.Pro593Ser)	not specified [RCV004832990]	uncertain significance	7	1440619	1440619	Human		name
597635678	CV3563666	single nucleotide variant	NM_182924.4(MICALL2):c.1949C>G (p.Pro650Arg)	not specified [RCV004824415]	uncertain significance	7	1439942	1439942	Human		name
597645975	CV3563667	single nucleotide variant	NM_182924.4(MICALL2):c.2141C>T (p.Ala714Val)	not specified [RCV004832991]	uncertain significance	7	1438335	1438335	Human		name
597645990	CV3563669	single nucleotide variant	NM_182924.4(MICALL2):c.1921C>G (p.Pro641Ala)	not specified [RCV004832993]	uncertain significance	7	1439970	1439970	Human		name
597635684	CV3563670	single nucleotide variant	NM_182924.4(MICALL2):c.1187C>T (p.Thr396Ile)	not specified [RCV004824416]	uncertain significance	7	1444883	1444883	Human		name
597646004	CV3563672	single nucleotide variant	NM_182924.4(MICALL2):c.1929G>T (p.Arg643Ser)	not specified [RCV004832995]	uncertain significance	7	1439962	1439962	Human		name
597635689	CV3563674	single nucleotide variant	NM_182924.4(MICALL2):c.1001G>C (p.Gly334Ala)	not specified [RCV004824417]	uncertain significance	7	1445069	1445069	Human		name
597635694	CV3563675	single nucleotide variant	NM_182924.4(MICALL2):c.2159C>T (p.Pro720Leu)	not specified [RCV004824418]	uncertain significance	7	1438317	1438317	Human		name
597646018	CV3563676	single nucleotide variant	NM_182924.4(MICALL2):c.2119C>T (p.Pro707Ser)	not specified [RCV004832997]	uncertain significance	7	1438843	1438843	Human		name
597635700	CV3563678	single nucleotide variant	NM_182924.4(MICALL2):c.1211C>G (p.Pro404Arg)	not specified [RCV004824419]	uncertain significance	7	1444859	1444859	Human		name
597646031	CV3563679	single nucleotide variant	NM_182924.4(MICALL2):c.2554A>G (p.Ser852Gly)	not specified [RCV004832999]	uncertain significance	7	1436779	1436779	Human		name
597646038	CV3563680	single nucleotide variant	NM_182924.4(MICALL2):c.1148G>A (p.Arg383Gln)	not specified [RCV004833000]	uncertain significance	7	1444922	1444922	Human		name
597646045	CV3563681	single nucleotide variant	NM_182924.4(MICALL2):c.1586C>G (p.Ser529Cys)	not specified [RCV004833001]	uncertain significance	7	1442317	1442317	Human		name
598185964	CV3993071	single nucleotide variant	NM_182924.4(MICALL2):c.1628C>T (p.Ser543Leu)	not specified [RCV005373341]	uncertain significance	7	1442275	1442275	Human		name
598254110	CV3993072	single nucleotide variant	NM_182924.4(MICALL2):c.1306G>A (p.Gly436Ser)	not specified [RCV005367149]	uncertain significance	7	1444764	1444764	Human		name
598185980	CV3993074	single nucleotide variant	NM_182924.4(MICALL2):c.2533G>A (p.Val845Met)	not specified [RCV005373343]	uncertain significance	7	1436800	1436800	Human		name
598254116	CV3993075	single nucleotide variant	NM_182924.4(MICALL2):c.1516C>T (p.Arg506Trp)	not specified [RCV005367150]	uncertain significance	7	1442387	1442387	Human		name
598185992	CV3993077	single nucleotide variant	NM_182924.4(MICALL2):c.1897C>T (p.His633Tyr)	not specified [RCV005373345]	uncertain significance	7	1439994	1439994	Human		name
598254125	CV3993079	single nucleotide variant	NM_182924.4(MICALL2):c.1067C>T (p.Ala356Val)	not specified [RCV005367151]	uncertain significance	7	1445003	1445003	Human		name
598254131	CV3993080	single nucleotide variant	NM_182924.4(MICALL2):c.1444C>G (p.Pro482Ala)	not specified [RCV005367152]	uncertain significance	7	1442459	1442459	Human		name
598186005	CV3993081	single nucleotide variant	NM_182924.4(MICALL2):c.1159C>T (p.Pro387Ser)	not specified [RCV005373347]	uncertain significance	7	1444911	1444911	Human		name
598254137	CV3993082	single nucleotide variant	NM_182924.4(MICALL2):c.2456G>A (p.Arg819His)	not specified [RCV005367153]	uncertain significance	7	1437555	1437555	Human		name
598186009	CV3993083	single nucleotide variant	NM_182924.4(MICALL2):c.1001G>A (p.Gly334Glu)	not specified [RCV005373348]	uncertain significance	7	1445069	1445069	Human		name
598254146	CV3993084	single nucleotide variant	NM_182924.4(MICALL2):c.1435G>T (p.Ala479Ser)	not specified [RCV005367154]	likely benign	7	1442468	1442468	Human		name
598186017	CV3993085	single nucleotide variant	NM_182924.4(MICALL2):c.1460A>G (p.Lys487Arg)	not specified [RCV005373349]	likely benign	7	1442443	1442443	Human		name
598254170	CV3993089	single nucleotide variant	NM_182924.4(MICALL2):c.2050C>A (p.Pro684Thr)	not specified [RCV005367157]	uncertain significance	7	1438912	1438912	Human		name
598186029	CV3993090	single nucleotide variant	NM_182924.4(MICALL2):c.2468C>T (p.Ala823Val)	not specified [RCV005373351]	uncertain significance	7	1437543	1437543	Human		name
598186044	CV3993092	single nucleotide variant	NM_182924.4(MICALL2):c.1110C>A (p.Asp370Glu)	not specified [RCV005373353]	uncertain significance	7	1444960	1444960	Human		name
598254177	CV3993093	single nucleotide variant	NM_182924.4(MICALL2):c.1972T>C (p.Ser658Pro)	not specified [RCV005367158]	uncertain significance	7	1438990	1438990	Human		name
15168670	CV699912	single nucleotide variant	NM_182924.4(MICALL2):c.2143A>C (p.Asn715His)	not provided [RCV000949306]	benign	7	1438333	1438333	Human		name
15166117	CV699913	single nucleotide variant	NM_182924.4(MICALL2):c.1988G>A (p.Arg663His)	not provided [RCV000948757]	benign	7	1438974	1438974	Human		name
15157965	CV699915	single nucleotide variant	NM_182924.4(MICALL2):c.1556C>T (p.Pro519Leu)	not provided [RCV000946984]	benign	7	1442347	1442347	Human		name
15164963	CV710838	single nucleotide variant	NM_182924.4(MICALL2):c.2687C>T (p.Pro896Leu)	not provided [RCV000970847]	benign	7	1434624	1434624	Human		name
15123181	CV710839	single nucleotide variant	NM_182924.4(MICALL2):c.2660A>C (p.Lys887Thr)	not provided [RCV000963195]	benign	7	1434651	1434651	Human		name
15125715	CV710841	single nucleotide variant	NM_182924.4(MICALL2):c.2270G>A (p.Arg757His)	not provided [RCV000963625]	benign	7	1438138	1438138	Human		name
15145672	CV710845	single nucleotide variant	NM_182924.4(MICALL2):c.1420C>T (p.Pro474Ser)	not provided [RCV000967037]	benign	7	1442483	1442483	Human		name
15125720	CV710847	single nucleotide variant	NM_182924.4(MICALL2):c.1097C>T (p.Pro366Leu)	not provided [RCV000963626]	benign	7	1444973	1444973	Human		name
15195726	CV722377	single nucleotide variant	NM_182924.4(MICALL2):c.2257G>T (p.Ala753Ser)	not provided [RCV000889584]	benign	7	1438151	1438151	Human		name
15140652	CV736006	single nucleotide variant	NM_182924.4(MICALL2):c.2458C>T (p.Arg820Trp)	not provided [RCV000899355]\|not specified [RCV004028491]	likely benign\|uncertain significance	7	1437553	1437553	Human		name
15181073	CV736007	single nucleotide variant	NM_182924.4(MICALL2):c.2150C>T (p.Pro717Leu)	not provided [RCV000907502]	benign	7	1438326	1438326	Human		name

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