Arhgap26 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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72 records found for search term Arhgap26

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8591594	CV20092	insertion	ARHGAP26, 52-BP INS	Juvenile myelomonocytic leukemia [RCV000005356]	pathogenic\|other				Human	2	name
8591595	CV20093	insertion	ARHGAP26, 74-BP INS	Juvenile myelomonocytic leukemia [RCV000005357]	pathogenic\|other				Human	2	name
150479629	CV1239418	single nucleotide variant	NM_001135608.3(ARHGAP26):c.*3558C>T	not provided [RCV001652581]	benign	5	143226004	143226004	Human		name
408367470	CV3514227	single nucleotide variant	NM_001135608.3(ARHGAP26):c.486+7G>A	ARHGAP26-related disorder [RCV004758512]	likely benign	5	142885406	142885406	Human		name , trait , alternate_id
15108044	CV730336	single nucleotide variant	NM_001135608.3(ARHGAP26):c.598-7A>G	not provided [RCV000893595]	benign	5	142901928	142901928	Human		name
405266128	CV3201896	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1285+9C>T	ARHGAP26-related disorder [RCV003911385]	likely benign	5	143041899	143041899	Human		name , trait , alternate_id
8580404	CV114834	single nucleotide variant	NM_015071.4(ARHGAP26):c.1539-28723G>T	Lung cancer [RCV000095357]	uncertain significance	5	143092265	143092265	Human		name
8686863	CV137285	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2099+69A>G	not specified [RCV000120059]	not provided	5	143207377	143207377	Human		name
401747204	CV2692094	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2099+93A>G	not specified [RCV004301806]	uncertain significance	5	143207401	143207401	Human		name
405265452	CV3202559	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1838-10T>C	ARHGAP26-related disorder [RCV003897373]	likely benign	5	143147221	143147221	Human		name , trait , alternate_id
405272295	CV3221621	single nucleotide variant	NM_001135608.3(ARHGAP26):c.154+462T>C	ARHGAP26-related disorder [RCV003972126]	benign	5	142771377	142771377	Human		name , trait , alternate_id
598174393	CV4006820	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2099+38G>C	not specified [RCV005393334]	uncertain significance	5	143207346	143207346	Human		name
597745649	CV3587456	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2099+149G>A	not specified [RCV004845459]	uncertain significance	5	143207457	143207457	Human		name
405284515	CV3196929	single nucleotide variant	NM_001135608.3(ARHGAP26):c.255A>G (p.Arg85=)	ARHGAP26-related disorder [RCV003979781]	benign	5	142875114	142875114	Human		name , trait , alternate_id
156235169	CV2271314	single nucleotide variant	NM_001135608.3(ARHGAP26):c.59A>G (p.Glu20Gly)	not specified [RCV004136434]	uncertain significance	5	142770820	142770820	Human		name
598174321	CV4006810	single nucleotide variant	NM_001135608.3(ARHGAP26):c.43A>G (p.Ser15Gly)	not specified [RCV005393324]	uncertain significance	5	142770804	142770804	Human		name
15123911	CV709695	single nucleotide variant	NM_001135608.3(ARHGAP26):c.327C>T (p.Ser109=)	not provided [RCV000963326]	benign	5	142879388	142879388	Human		name
8686857	CV137279	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1107T>C (p.Pro369=)	not specified [RCV000120053]	not provided	5	142932125	142932125	Human		name
401771348	CV2711626	single nucleotide variant	NM_001135608.3(ARHGAP26):c.173G>T (p.Arg58Leu)	not specified [RCV004307267]	uncertain significance	5	142873418	142873418	Human		name
405276158	CV3193299	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2190C>T (p.Asn730=)	ARHGAP26-related disorder [RCV003974466]	benign	5	143214087	143214087	Human		name , trait , alternate_id
405277257	CV3195423	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1947C>T (p.Asp649=)	ARHGAP26-related disorder [RCV003904209]	likely benign	5	143147340	143147340	Human		name , trait , alternate_id
405262437	CV3200293	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1692C>T (p.His564=)	ARHGAP26-related disorder [RCV003967304]	likely benign	5	143121141	143121141	Human		name , trait , alternate_id
405280447	CV3200784	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1245T>G (p.Gly415=)	ARHGAP26-related disorder [RCV003977409]	benign	5	143041850	143041850	Human		name , trait , alternate_id
405287622	CV3210712	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1710C>T (p.Thr570=)	ARHGAP26-related disorder [RCV003924471]	likely benign	5	143133978	143133978	Human		name , trait , alternate_id
405685499	CV3282756	single nucleotide variant	NM_001135608.3(ARHGAP26):c.223G>A (p.Ala75Thr)	not specified [RCV004422567]	uncertain significance	5	142873468	142873468	Human		name
597745566	CV3587441	single nucleotide variant	NM_001135608.3(ARHGAP26):c.123G>C (p.Lys41Asn)	not specified [RCV004845444]	uncertain significance	5	142770884	142770884	Human		name
598174209	CV4006795	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1989C>T (p.Leu663=)	not specified [RCV005393309]	likely benign	5	143207198	143207198	Human		name
598174269	CV4006803	single nucleotide variant	NM_001135608.3(ARHGAP26):c.140T>C (p.Ile47Thr)	not specified [RCV005393317]	uncertain significance	5	142770901	142770901	Human		name
598174603	CV4006850	single nucleotide variant	NM_001135608.3(ARHGAP26):c.173G>A (p.Arg58Gln)	not specified [RCV005393364]	uncertain significance	5	142873418	142873418	Human		name
15182174	CV709696	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2163G>A (p.Ser721=)	not provided [RCV000974568]	benign	5	143214060	143214060	Human		name
8686862	CV137284	single nucleotide variant	NM_001135608.3(ARHGAP26):c.307C>T (p.Arg103Trp)	not specified [RCV000120058]	not provided	5	142875166	142875166	Human		name
156362973	CV2330466	single nucleotide variant	NM_001135608.3(ARHGAP26):c.430A>G (p.Ile144Val)	not specified [RCV004181036]	uncertain significance	5	142885343	142885343	Human		name
156091546	CV2389476	single nucleotide variant	NM_001135608.3(ARHGAP26):c.692G>A (p.Ser231Asn)	not specified [RCV004238194]	uncertain significance	5	142902029	142902029	Human		name
401770068	CV2719021	single nucleotide variant	NM_001135608.3(ARHGAP26):c.328G>A (p.Glu110Lys)	not specified [RCV004322607]	uncertain significance	5	142879389	142879389	Human		name
405685495	CV3282757	single nucleotide variant	NM_001135608.3(ARHGAP26):c.681G>C (p.Gln227His)	not specified [RCV004422568]	uncertain significance	5	142902018	142902018	Human		name
405685491	CV3282758	single nucleotide variant	NM_001135608.3(ARHGAP26):c.932G>A (p.Gly311Glu)	not specified [RCV004422569]	uncertain significance	5	142907803	142907803	Human		name
597745544	CV3587437	single nucleotide variant	NM_001135608.3(ARHGAP26):c.818A>G (p.Tyr273Cys)	not specified [RCV004845440]	uncertain significance	5	142903655	142903655	Human		name
8686859	CV137281	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1775A>G (p.Lys592Arg)	not specified [RCV000120055]	not provided	5	143134043	143134043	Human		name
8686860	CV137282	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1829C>T (p.Thr610Ile)	not specified [RCV000120056]	not provided	5	143134097	143134097	Human		name
8686861	CV137283	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2185G>A (p.Asp729Asn)	not specified [RCV000120057]	not provided	5	143214082	143214082	Human		name
8591593	CV20091	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1250A>G (p.Asn417Ser)	Juvenile myelomonocytic leukemia [RCV000005355]	pathogenic\|other	5	143041855	143041855	Human	2	name
156111291	CV2207894	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1735G>C (p.Ala579Pro)	not specified [RCV004084320]	uncertain significance	5	143134003	143134003	Human		name
156282534	CV2220824	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1816A>G (p.Thr606Ala)	not specified [RCV004092260]	likely benign	5	143134084	143134084	Human		name
156327616	CV2332128	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1970C>A (p.Pro657His)	not specified [RCV004189167]	uncertain significance	5	143147363	143147363	Human		name
155969383	CV2337948	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1754G>A (p.Arg585Gln)	not specified [RCV004185997]	uncertain significance	5	143134022	143134022	Human		name
155908198	CV2354587	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2095G>A (p.Val699Ile)	not specified [RCV004202559]	likely benign	5	143207304	143207304	Human		name
156008263	CV2365252	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2054G>A (p.Ser685Asn)	not specified [RCV004209351]	uncertain significance	5	143207263	143207263	Human		name
156132628	CV2365829	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1726C>T (p.Leu576Phe)	not specified [RCV004214364]	uncertain significance	5	143133994	143133994	Human		name
155929249	CV2389103	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1160G>A (p.Ser387Asn)	not specified [RCV004235438]	uncertain significance	5	143037211	143037211	Human		name
329370878	CV2431797	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1015G>A (p.Glu339Lys)	not specified [RCV004254946]	uncertain significance	5	142913280	142913280	Human		name
329386459	CV2456027	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1687A>C (p.Asn563His)	not specified [RCV004272931]	uncertain significance	5	143121136	143121136	Human		name
401755460	CV2682492	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2266G>A (p.Val756Met)	not specified [RCV004290514]	uncertain significance	5	143222432	143222432	Human		name
401888512	CV2757627	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2023C>A (p.Pro675Thr)	not specified [RCV004334746]	uncertain significance	5	143207232	143207232	Human		name
405261514	CV3209995	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1669A>G (p.Ile557Val)	ARHGAP26-related disorder [RCV003944524]	likely benign	5	143121118	143121118	Human		name , trait , alternate_id
405685522	CV3282751	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1316A>G (p.Asp439Gly)	not specified [RCV004422562]	uncertain significance	5	143054469	143054469	Human		name
405685519	CV3282752	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1711G>A (p.Val571Met)	not specified [RCV004422563]	uncertain significance	5	143133979	143133979	Human		name
405685513	CV3282753	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1843C>A (p.Gln615Lys)	not specified [RCV004422564]	uncertain significance	5	143147236	143147236	Human		name
405685508	CV3282754	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1919G>A (p.Ser640Asn)	not specified [RCV004422565]	uncertain significance	5	143147312	143147312	Human		name
405685504	CV3282755	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1990C>A (p.Pro664Thr)	not specified [RCV004422566]	uncertain significance	5	143207199	143207199	Human		name
407472320	CV3468334	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1556A>G (p.Lys519Arg)	not specified [RCV004662483]	uncertain significance	5	143121005	143121005	Human		name
407472361	CV3468345	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1805C>T (p.Thr602Met)	not specified [RCV004662491]	uncertain significance	5	143134073	143134073	Human		name
407472398	CV3468355	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1975C>T (p.Arg659Trp)	not specified [RCV004662497]	uncertain significance	5	143147368	143147368	Human		name
407472431	CV3468363	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1025A>G (p.Asp342Gly)	not specified [RCV004662503]	uncertain significance	5	142913290	142913290	Human		name
407472452	CV3468368	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1442A>G (p.Asn481Ser)	not specified [RCV004662508]	uncertain significance	5	143057651	143057651	Human		name
597745501	CV3587429	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2084A>T (p.Asp695Val)	not specified [RCV004845432]	uncertain significance	5	143207293	143207293	Human		name
597745518	CV3587432	single nucleotide variant	NM_001135608.3(ARHGAP26):c.2042C>T (p.Ser681Leu)	not specified [RCV004845435]	uncertain significance	5	143207251	143207251	Human		name
597745590	CV3587445	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1945G>A (p.Asp649Asn)	not specified [RCV004845448]	uncertain significance	5	143147338	143147338	Human		name
597745632	CV3587453	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1030C>T (p.Pro344Ser)	not specified [RCV004845456]	uncertain significance	5	142932048	142932048	Human		name
598174452	CV4006828	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1417T>C (p.Phe473Leu)	not specified [RCV005393342]	uncertain significance	5	143056071	143056071	Human		name
598174529	CV4006839	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1247T>A (p.Val416Asp)	not specified [RCV005393353]	uncertain significance	5	143041852	143041852	Human		name
598174566	CV4006844	single nucleotide variant	NM_001135608.3(ARHGAP26):c.1588G>A (p.Val530Met)	not specified [RCV005393358]	uncertain significance	5	143121037	143121037	Human		name
8686858	CV137280	indel	NM_001135608.3(ARHGAP26):c.1245delinsGTGGGG (p.Val416fs)	not specified [RCV000120054]	pathogenic\|not provided	5	143041850	143041850	Human		name

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