Gprasp1 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

103 records found for search term Gprasp1

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405740324	CV3252154	single nucleotide variant	NM_001184727.2(GPRASP1):c.11C>A (p.Ala4Glu)	not specified [RCV004391238]	uncertain significance	X	102653924	102653924	Human		name
405740398	CV3252165	single nucleotide variant	NM_001184727.2(GPRASP1):c.21G>C (p.Glu7Asp)	not specified [RCV004391249]	uncertain significance	X	102653934	102653934	Human		name
401921193	CV2826669	single nucleotide variant	NM_001184727.2(GPRASP1):c.783C>G (p.Pro261=)	not provided [RCV003432256]	likely benign	X	102654696	102654696	Human		name
401921194	CV2826670	single nucleotide variant	NM_001184727.2(GPRASP1):c.972G>A (p.Gly324=)	not provided [RCV003432257]	likely benign	X	102654885	102654885	Human		name
597745616	CV3681682	single nucleotide variant	NM_001184727.2(GPRASP1):c.55G>T (p.Gly19Trp)	not specified [RCV004922513]	uncertain significance	X	102653968	102653968	Human		name
598274739	CV3967419	single nucleotide variant	NM_001184727.2(GPRASP1):c.64G>A (p.Val22Ile)	not specified [RCV005351559]	uncertain significance	X	102653977	102653977	Human		name
150529685	CV1289382	single nucleotide variant	NM_001184727.2(GPRASP1):c.197T>A (p.Val66Asp)	not provided [RCV001728133]	uncertain significance	X	102654110	102654110	Human		name
401738926	CV2676403	single nucleotide variant	NM_001184727.2(GPRASP1):c.223C>T (p.Arg75Cys)	not specified [RCV004286424]	uncertain significance	X	102654136	102654136	Human		name
401747921	CV2699956	single nucleotide variant	NM_001184727.2(GPRASP1):c.286G>A (p.Ala96Thr)	not specified [RCV004310396]	uncertain significance	X	102654199	102654199	Human		name
401921195	CV2826671	single nucleotide variant	NM_001184727.2(GPRASP1):c.1698C>T (p.Ile566=)	not provided [RCV003432258]	likely benign	X	102655611	102655611	Human		name
401921197	CV2826672	single nucleotide variant	NM_001184727.2(GPRASP1):c.2064C>T (p.Ala688=)	not provided [RCV003432259]	likely benign	X	102655977	102655977	Human		name
407479964	CV3436830	single nucleotide variant	NM_001184727.2(GPRASP1):c.260G>A (p.Arg87Gln)	not specified [RCV004632574]	likely benign	X	102654173	102654173	Human		name
156015491	CV2360285	single nucleotide variant	NM_001184727.2(GPRASP1):c.379G>C (p.Val127Leu)	not specified [RCV004208626]	uncertain significance	X	102654292	102654292	Human		name
329400425	CV2441652	single nucleotide variant	NM_001184727.2(GPRASP1):c.816G>T (p.Trp272Cys)	not specified [RCV004259475]	uncertain significance	X	102654729	102654729	Human		name
329378195	CV2457214	single nucleotide variant	NM_001184727.2(GPRASP1):c.368G>T (p.Ser123Ile)	not specified [RCV004265288]	uncertain significance	X	102654281	102654281	Human		name
401743139	CV2677777	single nucleotide variant	NM_001184727.2(GPRASP1):c.655G>A (p.Val219Ile)	not specified [RCV004291849]	uncertain significance	X	102654568	102654568	Human		name
401749300	CV2694611	single nucleotide variant	NM_001184727.2(GPRASP1):c.857G>A (p.Arg286Lys)	not specified [RCV004298729]	uncertain significance	X	102654770	102654770	Human		name
401771757	CV2722936	single nucleotide variant	NM_001184727.2(GPRASP1):c.931G>A (p.Ala311Thr)	not specified [RCV004327118]	uncertain significance	X	102654844	102654844	Human		name
405740429	CV3252169	single nucleotide variant	NM_001184727.2(GPRASP1):c.371C>T (p.Thr124Ile)	not specified [RCV004391253]	uncertain significance	X	102654284	102654284	Human		name
405740467	CV3252175	single nucleotide variant	NM_001184727.2(GPRASP1):c.622G>A (p.Glu208Lys)	not specified [RCV004391259]	uncertain significance	X	102654535	102654535	Human		name
405740476	CV3252176	single nucleotide variant	NM_001184727.2(GPRASP1):c.737A>G (p.Tyr246Cys)	not specified [RCV004391260]	uncertain significance	X	102654650	102654650	Human		name
407479947	CV3436826	single nucleotide variant	NM_001184727.2(GPRASP1):c.389C>T (p.Ala130Val)	not specified [RCV004632570]	uncertain significance	X	102654302	102654302	Human		name
407479954	CV3436828	single nucleotide variant	NM_001184727.2(GPRASP1):c.431C>G (p.Thr144Arg)	not specified [RCV004632572]	uncertain significance	X	102654344	102654344	Human		name
598274748	CV3967423	single nucleotide variant	NM_001184727.2(GPRASP1):c.860C>G (p.Ser287Cys)	not specified [RCV005351563]	uncertain significance	X	102654773	102654773	Human		name
598274755	CV3967427	single nucleotide variant	NM_001184727.2(GPRASP1):c.812C>T (p.Thr271Ile)	not specified [RCV005351566]	uncertain significance	X	102654725	102654725	Human		name
15170362	CV706036	single nucleotide variant	NM_001184727.2(GPRASP1):c.3840G>A (p.Gly1280=)	not provided [RCV000949636]	benign	X	102657753	102657753	Human		name
8637694	CV92920	single nucleotide variant	NM_001184727.1(GPRASP1):c.3333C>T (p.Phe1111=)	Malignant melanoma [RCV000073018]	not provided	X	102657246	102657246	Human		name
150411758	CV1196268	single nucleotide variant	NM_001184727.2(GPRASP1):c.1783A>G (p.Arg595Gly)	not provided [RCV001573823]	likely benign	X	102655696	102655696	Human		name
156249411	CV2199483	single nucleotide variant	NM_001184727.2(GPRASP1):c.1679T>C (p.Val560Ala)	not specified [RCV004071039]	uncertain significance	X	102655592	102655592	Human		name
156144079	CV2200134	single nucleotide variant	NM_001184727.2(GPRASP1):c.1156A>C (p.Lys386Gln)	not specified [RCV004069705]	uncertain significance	X	102655069	102655069	Human		name
156279813	CV2224010	single nucleotide variant	NM_001184727.2(GPRASP1):c.2162G>A (p.Gly721Glu)	not specified [RCV004094257]	uncertain significance	X	102656075	102656075	Human		name
156388530	CV2231875	single nucleotide variant	NM_001184727.2(GPRASP1):c.1691C>G (p.Ala564Gly)	not specified [RCV004098673]	uncertain significance	X	102655604	102655604	Human		name
156185579	CV2251691	single nucleotide variant	NM_001184727.2(GPRASP1):c.1652G>T (p.Gly551Val)	not specified [RCV004119703]	uncertain significance	X	102655565	102655565	Human		name
155956433	CV2281920	single nucleotide variant	NM_001184727.2(GPRASP1):c.2666C>T (p.Ala889Val)	not specified [RCV004138695]	uncertain significance	X	102656579	102656579	Human		name
156185540	CV2292328	single nucleotide variant	NM_001184727.2(GPRASP1):c.2897G>A (p.Gly966Glu)	not specified [RCV004150144]	uncertain significance	X	102656810	102656810	Human		name
156187749	CV2292487	single nucleotide variant	NM_001184727.2(GPRASP1):c.1754G>C (p.Trp585Ser)	not specified [RCV004150274]	uncertain significance	X	102655667	102655667	Human		name
155918526	CV2333020	single nucleotide variant	NM_001184727.2(GPRASP1):c.2446G>T (p.Gly816Trp)	not specified [RCV004194319]	likely benign	X	102656359	102656359	Human		name
156047358	CV2336364	single nucleotide variant	NM_001184727.2(GPRASP1):c.1108A>T (p.Met370Leu)	not specified [RCV004194585]	uncertain significance	X	102655021	102655021	Human		name
156149588	CV2359521	single nucleotide variant	NM_001184727.2(GPRASP1):c.1547C>G (p.Thr516Ser)	not provided [RCV003434668]\|not specified [RCV004214830]	likely benign\|uncertain significance	X	102655460	102655460	Human		name
156344824	CV2372825	single nucleotide variant	NM_001184727.2(GPRASP1):c.1808T>C (p.Met603Thr)	not specified [RCV004222008]	uncertain significance	X	102655721	102655721	Human		name
401864802	CV2778055	single nucleotide variant	NM_001184727.2(GPRASP1):c.1682A>G (p.Asp561Gly)	not specified [RCV004348005]	uncertain significance	X	102655595	102655595	Human		name
401880917	CV2789428	single nucleotide variant	NM_001184727.2(GPRASP1):c.2405G>A (p.Arg802Lys)	not specified [RCV004360066]	uncertain significance	X	102656318	102656318	Human		name
401921198	CV2826673	single nucleotide variant	NM_001184727.2(GPRASP1):c.2204C>T (p.Thr735Ile)	GPRASP1-related disorder [RCV003954214]\|not provided [RCV003432260]\|not specified [RCV004364655]	likely benign\|uncertain significance	X	102656117	102656117	Human		name , trait , alternate_id
405294231	CV3214728	single nucleotide variant	NM_001184727.2(GPRASP1):c.1800T>G (p.Cys600Trp)	GPRASP1-related disorder [RCV003934158]	uncertain significance	X	102655713	102655713	Human		name , trait , alternate_id
405740310	CV3252152	single nucleotide variant	NM_001184727.2(GPRASP1):c.1057A>G (p.Lys353Glu)	not specified [RCV004391236]	uncertain significance	X	102654970	102654970	Human		name
405740330	CV3252155	single nucleotide variant	NM_001184727.2(GPRASP1):c.1300A>G (p.Ile434Val)	not specified [RCV004391239]	uncertain significance	X	102655213	102655213	Human		name
405740338	CV3252156	single nucleotide variant	NM_001184727.2(GPRASP1):c.1358G>C (p.Ser453Thr)	not specified [RCV004391240]	uncertain significance	X	102655271	102655271	Human		name
405740345	CV3252157	single nucleotide variant	NM_001184727.2(GPRASP1):c.1543G>A (p.Glu515Lys)	not specified [RCV004391241]	uncertain significance	X	102655456	102655456	Human		name
405740352	CV3252158	single nucleotide variant	NM_001184727.2(GPRASP1):c.1617G>T (p.Glu539Asp)	not specified [RCV004391242]	uncertain significance	X	102655530	102655530	Human		name
405740358	CV3252159	single nucleotide variant	NM_001184727.2(GPRASP1):c.1652G>A (p.Gly551Asp)	not specified [RCV004391243]	uncertain significance	X	102655565	102655565	Human		name
405740370	CV3252161	single nucleotide variant	NM_001184727.2(GPRASP1):c.1943C>T (p.Ala648Val)	not specified [RCV004391245]	uncertain significance	X	102655856	102655856	Human		name
405740376	CV3252162	single nucleotide variant	NM_001184727.2(GPRASP1):c.1958G>A (p.Ser653Asn)	not specified [RCV004391246]	uncertain significance	X	102655871	102655871	Human		name
405740382	CV3252163	single nucleotide variant	NM_001184727.2(GPRASP1):c.2176G>C (p.Ala726Pro)	not specified [RCV004391247]	uncertain significance	X	102656089	102656089	Human		name
405740390	CV3252164	single nucleotide variant	NM_001184727.2(GPRASP1):c.2180C>T (p.Thr727Ile)	not specified [RCV004391248]	uncertain significance	X	102656093	102656093	Human		name
405740405	CV3252166	single nucleotide variant	NM_001184727.2(GPRASP1):c.2551G>A (p.Glu851Lys)	not specified [RCV004391250]	uncertain significance	X	102656464	102656464	Human		name
407479951	CV3436827	single nucleotide variant	NM_001184727.2(GPRASP1):c.1388G>A (p.Arg463His)	not specified [RCV004632571]	uncertain significance	X	102655301	102655301	Human		name
407479968	CV3436831	single nucleotide variant	NM_001184727.2(GPRASP1):c.1750T>C (p.Phe584Leu)	not specified [RCV004632575]	uncertain significance	X	102655663	102655663	Human		name
407479974	CV3436832	single nucleotide variant	NM_001184727.2(GPRASP1):c.2055G>T (p.Met685Ile)	not specified [RCV004632576]	uncertain significance	X	102655968	102655968	Human		name
407479978	CV3436833	single nucleotide variant	NM_001184727.2(GPRASP1):c.2984C>T (p.Ala995Val)	not specified [RCV004632577]	uncertain significance	X	102656897	102656897	Human		name
597745592	CV3681676	single nucleotide variant	NM_001184727.2(GPRASP1):c.1741G>A (p.Gly581Arg)	not specified [RCV004922508]	uncertain significance	X	102655654	102655654	Human		name
597745607	CV3681679	single nucleotide variant	NM_001184727.2(GPRASP1):c.1982G>A (p.Arg661Lys)	not specified [RCV004922511]	uncertain significance	X	102655895	102655895	Human		name
597769862	CV3681683	single nucleotide variant	NM_001184727.2(GPRASP1):c.2245A>G (p.Ile749Val)	not specified [RCV004928184]	uncertain significance	X	102656158	102656158	Human		name
597745620	CV3681684	single nucleotide variant	NM_001184727.2(GPRASP1):c.1969G>A (p.Gly657Arg)	not specified [RCV004922514]	uncertain significance	X	102655882	102655882	Human		name
597745625	CV3681686	single nucleotide variant	NM_001184727.2(GPRASP1):c.2968G>A (p.Gly990Arg)	not specified [RCV004922515]	uncertain significance	X	102656881	102656881	Human		name
598274733	CV3967416	single nucleotide variant	NM_001184727.2(GPRASP1):c.2663A>C (p.Gln888Pro)	not specified [RCV005351556]	uncertain significance	X	102656576	102656576	Human		name
598274735	CV3967417	single nucleotide variant	NM_001184727.2(GPRASP1):c.2661A>G (p.Ile887Met)	not specified [RCV005351557]	uncertain significance	X	102656574	102656574	Human		name
598274742	CV3967420	single nucleotide variant	NM_001184727.2(GPRASP1):c.1852T>C (p.Trp618Arg)	not specified [RCV005351560]	uncertain significance	X	102655765	102655765	Human		name
598274744	CV3967421	single nucleotide variant	NM_001184727.2(GPRASP1):c.2936T>C (p.Val979Ala)	not specified [RCV005351561]	uncertain significance	X	102656849	102656849	Human		name
598274746	CV3967422	single nucleotide variant	NM_001184727.2(GPRASP1):c.2374G>A (p.Glu792Lys)	not specified [RCV005351562]	uncertain significance	X	102656287	102656287	Human		name
598274753	CV3967425	single nucleotide variant	NM_001184727.2(GPRASP1):c.1841G>A (p.Gly614Glu)	not specified [RCV005351565]	uncertain significance	X	102655754	102655754	Human		name
598234164	CV3967426	single nucleotide variant	NM_001184727.2(GPRASP1):c.1306G>A (p.Gly436Arg)	not specified [RCV005342867]	uncertain significance	X	102655219	102655219	Human		name
598274762	CV3967430	single nucleotide variant	NM_001184727.2(GPRASP1):c.1015G>A (p.Ala339Thr)	not specified [RCV005351569]	uncertain significance	X	102654928	102654928	Human		name
15158099	CV758209	single nucleotide variant	NM_001184727.2(GPRASP1):c.2372T>C (p.Leu791Pro)	not provided [RCV000925000]	likely benign	X	102656285	102656285	Human		name
156229788	CV2209454	single nucleotide variant	NM_001184727.2(GPRASP1):c.3722G>T (p.Cys1241Phe)	not specified [RCV004093601]	uncertain significance	X	102657635	102657635	Human		name
156179199	CV2327643	single nucleotide variant	NM_001184727.2(GPRASP1):c.3665G>A (p.Arg1222His)	not specified [RCV004177225]	uncertain significance	X	102657578	102657578	Human		name
329376090	CV2437967	single nucleotide variant	NM_001184727.2(GPRASP1):c.3334C>A (p.Pro1112Thr)	not specified [RCV004263684]	uncertain significance	X	102657247	102657247	Human		name
329389804	CV2441344	single nucleotide variant	NM_001184727.2(GPRASP1):c.3086C>G (p.Thr1029Arg)	Inborn genetic diseases [RCV003191322]	likely benign	X	102656999	102656999	Human	1	name
329391961	CV2445220	single nucleotide variant	NM_001184727.2(GPRASP1):c.3896T>C (p.Met1299Thr)	not specified [RCV004263854]	uncertain significance	X	102657809	102657809	Human		name
401769876	CV2693105	single nucleotide variant	NM_001184727.2(GPRASP1):c.4162G>A (p.Asp1388Asn)	not specified [RCV004308641]	uncertain significance	X	102658075	102658075	Human		name
401717734	CV2703991	single nucleotide variant	NM_001184727.2(GPRASP1):c.3806A>T (p.Asp1269Val)	not specified [RCV004308885]	uncertain significance	X	102657719	102657719	Human		name
401894753	CV2785266	single nucleotide variant	NM_001184727.2(GPRASP1):c.3623C>T (p.Pro1208Leu)	not specified [RCV004357032]	uncertain significance	X	102657536	102657536	Human		name
405740413	CV3252167	single nucleotide variant	NM_001184727.2(GPRASP1):c.3031G>A (p.Glu1011Lys)	not specified [RCV004391251]	uncertain significance	X	102656944	102656944	Human		name
405740420	CV3252168	single nucleotide variant	NM_001184727.2(GPRASP1):c.3256C>T (p.Pro1086Ser)	not specified [RCV004391252]	uncertain significance	X	102657169	102657169	Human		name
405740433	CV3252170	single nucleotide variant	NM_001184727.2(GPRASP1):c.3755C>T (p.Pro1252Leu)	not specified [RCV004391254]	uncertain significance	X	102657668	102657668	Human		name
405740440	CV3252171	single nucleotide variant	NM_001184727.2(GPRASP1):c.4029G>C (p.Glu1343Asp)	not specified [RCV004391255]	uncertain significance	X	102657942	102657942	Human		name
405740448	CV3252172	single nucleotide variant	NM_001184727.2(GPRASP1):c.4067C>T (p.Ser1356Phe)	not specified [RCV004391256]	uncertain significance	X	102657980	102657980	Human		name
405740454	CV3252173	single nucleotide variant	NM_001184727.2(GPRASP1):c.4138C>A (p.Gln1380Lys)	not specified [RCV004391257]	uncertain significance	X	102658051	102658051	Human		name
405740460	CV3252174	single nucleotide variant	NM_001184727.2(GPRASP1):c.4153A>C (p.Asn1385His)	not specified [RCV004391258]	uncertain significance	X	102658066	102658066	Human		name
407479958	CV3436829	single nucleotide variant	NM_001184727.2(GPRASP1):c.3535A>G (p.Met1179Val)	not specified [RCV004632573]	uncertain significance	X	102657448	102657448	Human		name
407479982	CV3436834	single nucleotide variant	NM_001184727.2(GPRASP1):c.3851T>C (p.Leu1284Ser)	not specified [RCV004632578]	uncertain significance	X	102657764	102657764	Human		name
12741806	CV361077	single nucleotide variant	NM_001184727.2(GPRASP1):c.3379G>C (p.Glu1127Gln)	Intellectual disability [RCV000415157]	uncertain significance	X	102657292	102657292	Human	2	name
597745597	CV3681677	single nucleotide variant	NM_001184727.2(GPRASP1):c.3061G>A (p.Val1021Met)	not specified [RCV004922509]	uncertain significance	X	102656974	102656974	Human		name
597745602	CV3681678	single nucleotide variant	NM_001184727.2(GPRASP1):c.3433A>C (p.Ile1145Leu)	not specified [RCV004922510]	uncertain significance	X	102657346	102657346	Human		name
597745612	CV3681680	single nucleotide variant	NM_001184727.2(GPRASP1):c.3785G>A (p.Arg1262Lys)	not specified [RCV004922512]	uncertain significance	X	102657698	102657698	Human		name
597769858	CV3681681	single nucleotide variant	NM_001184727.2(GPRASP1):c.3516T>A (p.His1172Gln)	not specified [RCV004928183]	uncertain significance	X	102657429	102657429	Human		name
597769867	CV3681685	single nucleotide variant	NM_001184727.2(GPRASP1):c.4041C>A (p.Asn1347Lys)	not specified [RCV004928185]	uncertain significance	X	102657954	102657954	Human		name
598274737	CV3967418	single nucleotide variant	NM_001184727.2(GPRASP1):c.3715A>C (p.Lys1239Gln)	not specified [RCV005351558]	likely benign	X	102657628	102657628	Human		name
598274751	CV3967424	single nucleotide variant	NM_001184727.2(GPRASP1):c.3086C>T (p.Thr1029Met)	not specified [RCV005351564]	uncertain significance	X	102656999	102656999	Human		name
598274757	CV3967428	single nucleotide variant	NM_001184727.2(GPRASP1):c.3554C>T (p.Ser1185Phe)	not specified [RCV005351567]	uncertain significance	X	102657467	102657467	Human		name
598274759	CV3967429	single nucleotide variant	NM_001184727.2(GPRASP1):c.3434T>C (p.Ile1145Thr)	not specified [RCV005351568]	uncertain significance	X	102657347	102657347	Human		name
14395673	CV611438	single nucleotide variant	NM_001184727.2(GPRASP1):c.3106C>T (p.Pro1036Ser)	Intellectual disability [RCV000760242]	uncertain significance	X	102657019	102657019	Human	2	name
14395639	CV611439	single nucleotide variant	NM_001184727.2(GPRASP1):c.3754C>A (p.Pro1252Thr)	Intellectual disability [RCV000760203]	uncertain significance	X	102657667	102657667	Human	2	name
405854854	CV3394970	microsatellite	NM_001184727.2(GPRASP1):c.327_330del (p.Arg110fs)	not provided [RCV004555111]	uncertain significance	X	102654237	102654240	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message