Cd68 Variant Search Result - Rat Genome Database

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47 records found for search term Cd68

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15163865	CV760658	single nucleotide variant	NM_001251.3(CD68):c.931+9T>C	not provided [RCV000926236]	likely benign	17	7581075	7581075	Human		name
15192896	CV771838	single nucleotide variant	NM_001251.3(CD68):c.27G>C (p.Gly9=)	not provided [RCV000933211]	likely benign	17	7579704	7579704	Human		name
15186827	CV727446	single nucleotide variant	NM_001251.3(CD68):c.54G>A (p.Gln18=)	not provided [RCV000887083]	benign	17	7579814	7579814	Human		name
597778666	CV3648472	single nucleotide variant	NM_001251.3(CD68):c.23C>T (p.Ser8Leu)	not specified [RCV004899080]	likely benign	17	7579700	7579700	Human		name
156361983	CV2322970	single nucleotide variant	NM_001251.3(CD68):c.29C>T (p.Ala10Val)	not specified [RCV004185411]	uncertain significance	17	7579706	7579706	Human		name
597738832	CV3648469	single nucleotide variant	NM_001251.3(CD68):c.37G>T (p.Gly13Trp)	not specified [RCV004890201]	uncertain significance	17	7579714	7579714	Human		name
597778664	CV3648471	single nucleotide variant	NM_001251.3(CD68):c.79A>G (p.Lys27Glu)	not specified [RCV004899079]	uncertain significance	17	7579839	7579839	Human		name
597738837	CV3648473	single nucleotide variant	NM_001251.3(CD68):c.71G>A (p.Cys24Tyr)	not specified [RCV004890202]	uncertain significance	17	7579831	7579831	Human		name
15108879	CV756132	single nucleotide variant	NM_001251.3(CD68):c.549A>G (p.Thr183=)	not provided [RCV000916223]	likely benign	17	7580309	7580309	Human		name
15107153	CV756133	single nucleotide variant	NM_001251.3(CD68):c.640C>T (p.Leu214=)	not provided [RCV000915898]	likely benign	17	7580538	7580538	Human		name
156141663	CV2208436	single nucleotide variant	NM_001251.3(CD68):c.202G>A (p.Gly68Ser)	not specified [RCV004090977]	uncertain significance	17	7579962	7579962	Human		name
156242927	CV2210809	single nucleotide variant	NM_001251.3(CD68):c.224C>T (p.Thr75Met)	not specified [RCV004085901]	uncertain significance	17	7579984	7579984	Human		name
156124775	CV2350131	single nucleotide variant	NM_001251.3(CD68):c.118C>T (p.Pro40Ser)	not specified [RCV004200051]	uncertain significance	17	7579878	7579878	Human		name
155934945	CV2372578	single nucleotide variant	NM_001251.3(CD68):c.290G>A (p.Ser97Asn)	not specified [RCV004219370]	uncertain significance	17	7580050	7580050	Human		name
401754265	CV2726870	single nucleotide variant	NM_001251.3(CD68):c.176C>G (p.Thr59Ser)	not specified [RCV004323164]	uncertain significance	17	7579936	7579936	Human		name
405772418	CV3299847	single nucleotide variant	NM_001251.3(CD68):c.248C>T (p.Thr83Ile)	not specified [RCV004435519]	uncertain significance	17	7580008	7580008	Human		name
405772423	CV3299848	single nucleotide variant	NM_001251.3(CD68):c.253A>C (p.Ser85Arg)	not specified [RCV004435520]	uncertain significance	17	7580013	7580013	Human		name
407498861	CV3425004	single nucleotide variant	NM_001251.3(CD68):c.176C>T (p.Thr59Ile)	not specified [RCV004606586]	uncertain significance	17	7579936	7579936	Human		name
407498857	CV3425005	single nucleotide variant	NM_001251.3(CD68):c.220C>G (p.Pro74Ala)	not specified [RCV004606587]	uncertain significance	17	7579980	7579980	Human		name
598207673	CV3950815	single nucleotide variant	NM_001251.3(CD68):c.205A>G (p.Thr69Ala)	not specified [RCV005315326]	uncertain significance	17	7579965	7579965	Human		name
15197980	CV727447	single nucleotide variant	NM_001251.3(CD68):c.122C>T (p.Thr41Met)	not provided [RCV000890222]	benign	17	7579882	7579882	Human		name
156192769	CV2202422	single nucleotide variant	NM_001251.3(CD68):c.470T>C (p.Ile157Thr)	not specified [RCV004080731]	uncertain significance	17	7580230	7580230	Human		name
155927278	CV2230761	single nucleotide variant	NM_001251.3(CD68):c.652T>C (p.Phe218Leu)	not specified [RCV004091981]	uncertain significance	17	7580550	7580550	Human		name
156032110	CV2259504	single nucleotide variant	NM_001251.3(CD68):c.867C>A (p.His289Gln)	not specified [RCV004122700]	uncertain significance	17	7581002	7581002	Human		name
155993487	CV2286304	single nucleotide variant	NM_001251.3(CD68):c.842G>A (p.Ser281Asn)	not specified [RCV004146255]	uncertain significance	17	7580977	7580977	Human		name
156075853	CV2377087	single nucleotide variant	NM_001251.3(CD68):c.883C>G (p.Leu295Val)	not specified [RCV004229760]	uncertain significance	17	7581018	7581018	Human		name
156348477	CV2383120	single nucleotide variant	NM_001251.3(CD68):c.721A>G (p.Met241Val)	not specified [RCV004217690]	uncertain significance	17	7580744	7580744	Human		name
401731099	CV2674260	single nucleotide variant	NM_001251.3(CD68):c.551C>T (p.Thr184Ile)	not specified [RCV004289145]	uncertain significance	17	7580311	7580311	Human		name
401881800	CV2783962	single nucleotide variant	NM_001251.3(CD68):c.635C>T (p.Pro212Leu)	not specified [RCV004362381]	uncertain significance	17	7580533	7580533	Human		name
405772437	CV3299850	single nucleotide variant	NM_001251.3(CD68):c.659A>G (p.Tyr220Cys)	not specified [RCV004435522]	uncertain significance	17	7580557	7580557	Human		name
405772444	CV3299851	single nucleotide variant	NM_001251.3(CD68):c.773C>T (p.Ser258Leu)	not specified [RCV004435523]	uncertain significance	17	7580908	7580908	Human		name
405772448	CV3299852	single nucleotide variant	NM_001251.3(CD68):c.896C>A (p.Ala299Asp)	not specified [RCV004435524]	uncertain significance	17	7581031	7581031	Human		name
407498864	CV3425003	single nucleotide variant	NM_001251.3(CD68):c.448A>G (p.Ser150Gly)	not specified [RCV004606585]	uncertain significance	17	7580208	7580208	Human		name
407498853	CV3425006	single nucleotide variant	NM_001251.3(CD68):c.361G>A (p.Val121Ile)	not specified [RCV004606588]	uncertain significance	17	7580121	7580121	Human		name
597778656	CV3648468	single nucleotide variant	NM_001251.3(CD68):c.341C>T (p.Thr114Ile)	not specified [RCV004899077]	uncertain significance	17	7580101	7580101	Human		name
597778671	CV3648474	single nucleotide variant	NM_001251.3(CD68):c.709T>A (p.Tyr237Asn)	not specified [RCV004899081]	uncertain significance	17	7580732	7580732	Human		name
597778675	CV3648475	single nucleotide variant	NM_001251.3(CD68):c.718T>G (p.Tyr240Asp)	not specified [RCV004899082]	uncertain significance	17	7580741	7580741	Human		name
597738842	CV3648476	single nucleotide variant	NM_001251.3(CD68):c.887G>A (p.Arg296Lys)	not specified [RCV004890203]	likely benign	17	7581022	7581022	Human		name
597778679	CV3648477	single nucleotide variant	NM_001251.3(CD68):c.299C>G (p.Thr100Ser)	not specified [RCV004899083]	uncertain significance	17	7580059	7580059	Human		name
597778682	CV3648478	single nucleotide variant	NM_001251.3(CD68):c.784G>A (p.Ala262Thr)	not specified [RCV004899084]	uncertain significance	17	7580919	7580919	Human		name
597778691	CV3648480	single nucleotide variant	NM_001251.3(CD68):c.482C>A (p.Thr161Lys)	not specified [RCV004899086]	uncertain significance	17	7580242	7580242	Human		name
598207687	CV3950817	single nucleotide variant	NM_001251.3(CD68):c.550A>G (p.Thr184Ala)	not specified [RCV005315328]	uncertain significance	17	7580310	7580310	Human		name
15135925	CV715711	single nucleotide variant	NM_001251.3(CD68):c.986T>C (p.Ile329Thr)	not provided [RCV000965366]	benign	17	7581432	7581432	Human		name
329371272	CV2458058	single nucleotide variant	NM_001251.3(CD68):c.1036A>G (p.Arg346Gly)	not specified [RCV004271891]	uncertain significance	17	7581482	7581482	Human		name
405772411	CV3299846	single nucleotide variant	NM_001251.3(CD68):c.1033C>T (p.Arg345Trp)	not specified [RCV004435518]	uncertain significance	17	7581479	7581479	Human		name
597778686	CV3648479	single nucleotide variant	NM_001251.3(CD68):c.1034G>C (p.Arg345Pro)	not specified [RCV004899085]	uncertain significance	17	7581480	7581480	Human		name
598207680	CV3950816	single nucleotide variant	NM_001251.3(CD68):c.1039C>T (p.Arg347Cys)	not specified [RCV005315327]	uncertain significance	17	7581485	7581485	Human		name

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