Cd93 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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87 records found for search term Cd93

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
404989767	CV2849571	single nucleotide variant	NM_012072.4(CD93):c.1934+86G>A	not specified [RCV003490428]	benign	20	23084173	23084173	Human		name
156148514	CV2307348	single nucleotide variant	NM_012072.4(CD93):c.23T>C (p.Leu8Pro)	not specified [RCV004166035]	uncertain significance	20	23086170	23086170	Human		name
405258865	CV3194155	single nucleotide variant	NM_012072.4(CD93):c.123G>A (p.Ser41=)	CD93-related disorder [RCV003893736]	likely benign	20	23086070	23086070	Human		name , trait , alternate_id
407498326	CV3425036	single nucleotide variant	NM_012072.4(CD93):c.13A>G (p.Met5Val)	not specified [RCV004606613]	likely benign	20	23086180	23086180	Human		name
408366388	CV3508302	single nucleotide variant	NM_012072.4(CD93):c.102C>A (p.Thr34=)	CD93-related disorder [RCV004756621]	likely benign	20	23086091	23086091	Human		name , trait , alternate_id
156119938	CV2275875	single nucleotide variant	NM_012072.4(CD93):c.70G>C (p.Ala24Pro)	not specified [RCV004139535]	uncertain significance	20	23086123	23086123	Human		name
329388950	CV2469654	single nucleotide variant	NM_012072.4(CD93):c.50A>T (p.Gln17Leu)	not specified [RCV004283076]	uncertain significance	20	23086143	23086143	Human		name
401748626	CV2694464	single nucleotide variant	NM_012072.4(CD93):c.61G>A (p.Gly21Arg)	not specified [RCV004304954]	uncertain significance	20	23086132	23086132	Human		name
405275800	CV3199435	single nucleotide variant	NM_012072.4(CD93):c.354C>G (p.Gly118=)	CD93-related disorder [RCV003916843]	likely benign	20	23085839	23085839	Human		name , trait , alternate_id
597778869	CV3648533	single nucleotide variant	NM_012072.4(CD93):c.89T>C (p.Val30Ala)	not specified [RCV004899132]	uncertain significance	20	23086104	23086104	Human		name
404989722	CV2849475	single nucleotide variant	NM_012072.4(CD93):c.1488T>C (p.Arg496=)	not specified [RCV003490332]	benign	20	23084705	23084705	Human		name
405772780	CV3299909	single nucleotide variant	NM_012072.4(CD93):c.103G>C (p.Ala35Pro)	not specified [RCV004435581]	uncertain significance	20	23086090	23086090	Human		name
597787299	CV3648540	single nucleotide variant	NM_012072.4(CD93):c.187G>C (p.Val63Leu)	not specified [RCV004901195]	uncertain significance	20	23086006	23086006	Human		name
598229149	CV3950864	single nucleotide variant	NM_012072.4(CD93):c.206C>T (p.Ala69Val)	not specified [RCV005319174]	uncertain significance	20	23085987	23085987	Human		name
15166050	CV716882	single nucleotide variant	NM_012072.4(CD93):c.1344G>A (p.Gly448=)	not provided [RCV000971086]	benign	20	23084849	23084849	Human		name
156266281	CV2198729	single nucleotide variant	NM_012072.4(CD93):c.320C>T (p.Pro107Leu)	not specified [RCV004075736]	uncertain significance	20	23085873	23085873	Human		name
156097126	CV2253163	single nucleotide variant	NM_012072.4(CD93):c.764C>G (p.Pro255Arg)	not specified [RCV004120933]	uncertain significance	20	23085429	23085429	Human		name
156058858	CV2343652	single nucleotide variant	NM_012072.4(CD93):c.335A>G (p.Lys112Arg)	not specified [RCV004190680]	uncertain significance	20	23085858	23085858	Human		name
156139851	CV2374336	single nucleotide variant	NM_012072.4(CD93):c.833G>A (p.Gly278Glu)	not specified [RCV004229464]	uncertain significance	20	23085360	23085360	Human		name
155938276	CV2380666	single nucleotide variant	NM_012072.4(CD93):c.832G>A (p.Gly278Arg)	not specified [RCV004218252]	uncertain significance	20	23085361	23085361	Human		name
155991729	CV2384341	single nucleotide variant	NM_012072.4(CD93):c.833G>C (p.Gly278Ala)	not specified [RCV004227720]	uncertain significance	20	23085360	23085360	Human		name
329400352	CV2441555	single nucleotide variant	NM_012072.4(CD93):c.832G>T (p.Gly278Trp)	not specified [RCV004257339]	uncertain significance	20	23085361	23085361	Human		name
401771823	CV2693537	single nucleotide variant	NM_012072.4(CD93):c.549C>A (p.Ser183Arg)	not specified [RCV004297520]	uncertain significance	20	23085644	23085644	Human		name
405280955	CV3190691	single nucleotide variant	NM_012072.4(CD93):c.350T>G (p.Val117Gly)	CD93-related disorder [RCV003907127]	benign	20	23085843	23085843	Human		name , trait , alternate_id
405772820	CV3299916	single nucleotide variant	NM_012072.4(CD93):c.393G>C (p.Glu131Asp)	not specified [RCV004435588]	uncertain significance	20	23085800	23085800	Human		name
405772826	CV3299917	single nucleotide variant	NM_012072.4(CD93):c.783G>C (p.Lys261Asn)	not specified [RCV004435589]	uncertain significance	20	23085410	23085410	Human		name
407454705	CV3425030	single nucleotide variant	NM_012072.4(CD93):c.845C>T (p.Ser282Phe)	not specified [RCV004609950]	uncertain significance	20	23085348	23085348	Human		name
407498306	CV3425032	single nucleotide variant	NM_012072.4(CD93):c.998G>A (p.Gly333Glu)	not specified [RCV004606609]	uncertain significance	20	23085195	23085195	Human		name
407498316	CV3425034	single nucleotide variant	NM_012072.4(CD93):c.943G>A (p.Ala315Thr)	not specified [RCV004606611]	uncertain significance	20	23085250	23085250	Human		name
407498331	CV3425037	single nucleotide variant	NM_012072.4(CD93):c.893T>A (p.Val298Glu)	not specified [RCV004606614]	uncertain significance	20	23085300	23085300	Human		name
407498340	CV3425039	single nucleotide variant	NM_012072.4(CD93):c.719G>T (p.Cys240Phe)	not specified [RCV004606616]	uncertain significance	20	23085474	23085474	Human		name
408383262	CV3504917	single nucleotide variant	NM_012072.4(CD93):c.561G>A (p.Met187Ile)	CD93-related disorder [RCV004730481]	uncertain significance	20	23085632	23085632	Human		name , trait , alternate_id
597778867	CV3648532	single nucleotide variant	NM_012072.4(CD93):c.727A>G (p.Lys243Glu)	not specified [RCV004899131]	uncertain significance	20	23085466	23085466	Human		name
597778889	CV3648538	single nucleotide variant	NM_012072.4(CD93):c.856G>A (p.Gly286Ser)	not specified [RCV004899137]	uncertain significance	20	23085337	23085337	Human		name
597787296	CV3648539	single nucleotide variant	NM_012072.4(CD93):c.745G>A (p.Asp249Asn)	not specified [RCV004901194]	uncertain significance	20	23085448	23085448	Human		name
597787317	CV3648544	single nucleotide variant	NM_012072.4(CD93):c.817C>G (p.Gln273Glu)	not specified [RCV004901199]	uncertain significance	20	23085376	23085376	Human		name
597787320	CV3648545	single nucleotide variant	NM_012072.4(CD93):c.571C>A (p.Leu191Met)	not specified [RCV004901200]	uncertain significance	20	23085622	23085622	Human		name
598229144	CV3950862	single nucleotide variant	NM_012072.4(CD93):c.805G>A (p.Gly269Arg)	not specified [RCV005319173]	uncertain significance	20	23085388	23085388	Human		name
598166833	CV3950863	single nucleotide variant	NM_012072.4(CD93):c.689A>C (p.Lys230Thr)	not specified [RCV005307948]	uncertain significance	20	23085504	23085504	Human		name
156177926	CV2201550	single nucleotide variant	NM_012072.4(CD93):c.1301C>T (p.Pro434Leu)	CD93-related disorder [RCV003946350]\|not specified [RCV004080041]	likely benign\|uncertain significance	20	23084892	23084892	Human		name , trait , alternate_id
156066565	CV2236920	single nucleotide variant	NM_012072.4(CD93):c.1609C>T (p.Pro537Ser)	not specified [RCV004112924]	uncertain significance	20	23084584	23084584	Human		name
156129506	CV2238541	single nucleotide variant	NM_012072.4(CD93):c.1832C>G (p.Ala611Gly)	not specified [RCV004107157]	uncertain significance	20	23084361	23084361	Human		name
156014402	CV2300543	single nucleotide variant	NM_012072.4(CD93):c.1856A>C (p.Lys619Thr)	not specified [RCV004155511]	uncertain significance	20	23084337	23084337	Human		name
156307809	CV2312435	single nucleotide variant	NM_012072.4(CD93):c.1777A>G (p.Ile593Val)	not specified [RCV004167120]	uncertain significance	20	23084416	23084416	Human		name
156296158	CV2318117	single nucleotide variant	NM_012072.4(CD93):c.1264G>C (p.Gly422Arg)	not specified [RCV004177532]	uncertain significance	20	23084929	23084929	Human		name
329357999	CV2427908	single nucleotide variant	NM_012072.4(CD93):c.1937C>T (p.Pro646Leu)	not specified [RCV004254299]	uncertain significance	20	23083972	23083972	Human		name
329374769	CV2431039	single nucleotide variant	NM_012072.4(CD93):c.1901G>A (p.Arg634Gln)	not specified [RCV004250410]	uncertain significance	20	23084292	23084292	Human		name
329387760	CV2446785	single nucleotide variant	NM_012072.4(CD93):c.1409G>A (p.Gly470Glu)	not specified [RCV004257647]	uncertain significance	20	23084784	23084784	Human		name
401738054	CV2700925	single nucleotide variant	NM_012072.4(CD93):c.1135G>A (p.Gly379Arg)	not specified [RCV004307190]	uncertain significance	20	23085058	23085058	Human		name
401734349	CV2709466	single nucleotide variant	NM_012072.4(CD93):c.1547C>G (p.Thr516Arg)	not specified [RCV004318713]	uncertain significance	20	23084646	23084646	Human		name
401893380	CV2766760	single nucleotide variant	NM_012072.4(CD93):c.1751T>A (p.Phe584Tyr)	not specified [RCV004349150]	uncertain significance	20	23084442	23084442	Human		name
401921023	CV2804441	single nucleotide variant	NM_012072.4(CD93):c.1900C>T (p.Arg634Ter)	CD93-related disorder [RCV003402722]	uncertain significance	20	23084293	23084293	Human		name , trait , alternate_id
404989775	CV2849572	single nucleotide variant	NM_012072.4(CD93):c.1621C>T (p.Pro541Ser)	not specified [RCV003490429]	benign	20	23084572	23084572	Human		name
405290900	CV3197174	single nucleotide variant	NM_012072.4(CD93):c.1487G>A (p.Arg496His)	CD93-related disorder [RCV003984736]	likely benign	20	23084706	23084706	Human		name , trait , alternate_id
405266379	CV3201933	single nucleotide variant	NM_012072.4(CD93):c.1439C>G (p.Pro480Arg)	CD93-related disorder [RCV003911420]	uncertain significance	20	23084754	23084754	Human		name , trait , alternate_id
405267371	CV3205434	single nucleotide variant	NM_012072.4(CD93):c.1627G>A (p.Val543Ile)	CD93-related disorder [RCV003947355]	likely benign	20	23084566	23084566	Human		name , trait , alternate_id
405772786	CV3299910	single nucleotide variant	NM_012072.4(CD93):c.1390G>A (p.Gly464Arg)	not specified [RCV004435582]	uncertain significance	20	23084803	23084803	Human		name
405772800	CV3299912	single nucleotide variant	NM_012072.4(CD93):c.1483C>T (p.Pro495Ser)	not specified [RCV004435584]	uncertain significance	20	23084710	23084710	Human		name
405772806	CV3299913	single nucleotide variant	NM_012072.4(CD93):c.1820G>A (p.Arg607His)	not specified [RCV004435585]	uncertain significance	20	23084373	23084373	Human		name
405772811	CV3299914	single nucleotide variant	NM_012072.4(CD93):c.1838G>A (p.Arg613Lys)	not specified [RCV004435586]	uncertain significance	20	23084355	23084355	Human		name
407498302	CV3425031	single nucleotide variant	NM_012072.4(CD93):c.1926C>A (p.Asn642Lys)	not specified [RCV004606608]	uncertain significance	20	23084267	23084267	Human		name
407498322	CV3425035	single nucleotide variant	NM_012072.4(CD93):c.1501A>G (p.Ser501Gly)	not specified [RCV004606612]	uncertain significance	20	23084692	23084692	Human		name
407498336	CV3425038	single nucleotide variant	NM_012072.4(CD93):c.1825C>T (p.Arg609Trp)	not specified [RCV004606615]	uncertain significance	20	23084368	23084368	Human		name
407498890	CV3425040	single nucleotide variant	NM_012072.4(CD93):c.1379T>C (p.Leu460Pro)	not specified [RCV004606617]	uncertain significance	20	23084814	23084814	Human		name
407498348	CV3425041	single nucleotide variant	NM_012072.4(CD93):c.1084C>T (p.Pro362Ser)	not specified [RCV004606618]	uncertain significance	20	23085109	23085109	Human		name
407498356	CV3425043	single nucleotide variant	NM_012072.4(CD93):c.1235A>C (p.Glu412Ala)	not specified [RCV004606620]	uncertain significance	20	23084958	23084958	Human		name
408366451	CV3509870	single nucleotide variant	NM_012072.4(CD93):c.1486C>T (p.Arg496Cys)	CD93-related disorder [RCV004756681]	likely benign	20	23084707	23084707	Human		name , trait , alternate_id
597778872	CV3648534	single nucleotide variant	NM_012072.4(CD93):c.1459G>A (p.Gly487Arg)	not specified [RCV004899133]	uncertain significance	20	23084734	23084734	Human		name
597778877	CV3648535	single nucleotide variant	NM_012072.4(CD93):c.1579A>G (p.Ile527Val)	not specified [RCV004899134]	uncertain significance	20	23084614	23084614	Human		name
597778880	CV3648536	single nucleotide variant	NM_012072.4(CD93):c.1036G>A (p.Val346Met)	not specified [RCV004899135]	uncertain significance	20	23085157	23085157	Human		name
597787303	CV3648541	single nucleotide variant	NM_012072.4(CD93):c.1653C>G (p.His551Gln)	not specified [RCV004901196]	uncertain significance	20	23084540	23084540	Human		name
597787307	CV3648542	single nucleotide variant	NM_012072.4(CD93):c.1855A>G (p.Lys619Glu)	not specified [RCV004901197]	uncertain significance	20	23084338	23084338	Human		name
597787311	CV3648543	single nucleotide variant	NM_012072.4(CD93):c.1901G>T (p.Arg634Leu)	not specified [RCV004901198]	uncertain significance	20	23084292	23084292	Human		name
597787324	CV3648546	single nucleotide variant	NM_012072.4(CD93):c.1438C>T (p.Pro480Ser)	not specified [RCV004901201]	uncertain significance	20	23084755	23084755	Human		name
597787327	CV3648547	single nucleotide variant	NM_012072.4(CD93):c.1264G>A (p.Gly422Arg)	not specified [RCV004901202]	uncertain significance	20	23084929	23084929	Human		name
598166811	CV3950856	single nucleotide variant	NM_012072.4(CD93):c.1858A>G (p.Lys620Glu)	not specified [RCV005307944]	uncertain significance	20	23084335	23084335	Human		name
598166816	CV3950857	single nucleotide variant	NM_012072.4(CD93):c.1697C>T (p.Ser566Phe)	not specified [RCV005307945]	likely benign	20	23084496	23084496	Human		name
598229130	CV3950858	single nucleotide variant	NM_012072.4(CD93):c.1880G>A (p.Ser627Asn)	not specified [RCV005319171]	uncertain significance	20	23084313	23084313	Human		name
598166821	CV3950859	single nucleotide variant	NM_012072.4(CD93):c.1801C>G (p.Leu601Val)	not specified [RCV005307946]	uncertain significance	20	23084392	23084392	Human		name
598229137	CV3950860	single nucleotide variant	NM_012072.4(CD93):c.1955G>A (p.Cys652Tyr)	not specified [RCV005319172]	uncertain significance	20	23083954	23083954	Human		name
598166827	CV3950861	single nucleotide variant	NM_012072.4(CD93):c.1553G>A (p.Arg518Lys)	not specified [RCV005307947]	uncertain significance	20	23084640	23084640	Human		name
15169331	CV705404	single nucleotide variant	NM_012072.4(CD93):c.1559C>T (p.Ser520Leu)	not provided [RCV000949436]	benign	20	23084634	23084634	Human		name
15163234	CV705405	single nucleotide variant	NM_012072.4(CD93):c.1282G>T (p.Val428Leu)	not provided [RCV000948036]	benign	20	23084911	23084911	Human		name
15191735	CV742298	single nucleotide variant	NM_012072.4(CD93):c.1478C>T (p.Thr493Ile)	not provided [RCV000910333]	benign	20	23084715	23084715	Human		name
8637222	CV92448	single nucleotide variant	NM_012072.3(CD93):c.1055C>T (p.Ser352Phe)	Malignant melanoma [RCV000072546]	not provided	20	23085138	23085138	Human		name
8637223	CV92449	single nucleotide variant	NM_012072.3(CD93):c.1033G>A (p.Asp345Asn)	Malignant melanoma [RCV000072547]	not provided	20	23085160	23085160	Human		name
405256047	CV3208557	microsatellite	NM_012072.4(CD93):c.1449GGA[1] (p.Glu484del)	CD93-related disorder [RCV003939635]	likely benign	20	23084739	23084741	Human		name , trait , alternate_id

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