Gas6 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

93 records found for search term Gas6

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15123381	CV744685	single nucleotide variant	NM_000820.4(GAS6):c.835-8C>T	not provided [RCV000896402]	benign	13	113832760	113832760	Human		name
15178551	CV730906	single nucleotide variant	NM_000820.4(GAS6):c.1883-3C>T	not provided [RCV000885087]	likely benign	13	113821021	113821021	Human		name
156151737	CV2318818	single nucleotide variant	NM_000820.4(GAS6):c.40C>A (p.Arg14Ser)	not specified [RCV004175730]	uncertain significance	13	113863881	113863881	Human		name
597754812	CV3681042	single nucleotide variant	NM_000820.4(GAS6):c.41G>A (p.Arg14His)	not specified [RCV004924465]	uncertain significance	13	113863880	113863880	Human		name
15117800	CV753736	single nucleotide variant	NM_000820.4(GAS6):c.816G>A (p.Gln272=)	not provided [RCV000917861]	likely benign	13	113834569	113834569	Human		name
155970436	CV2338063	single nucleotide variant	NM_000820.4(GAS6):c.215G>A (p.Arg72His)	not specified [RCV004186102]	uncertain significance	13	113863615	113863615	Human		name
407462439	CV3436487	single nucleotide variant	NM_000820.4(GAS6):c.295T>C (p.Tyr99His)	not specified [RCV004634553]	likely benign	13	113846575	113846575	Human		name
15160763	CV702613	single nucleotide variant	NM_000820.4(GAS6):c.1497C>T (p.Val499=)	not provided [RCV000947550]	benign	13	113823531	113823531	Human		name
15180982	CV713858	single nucleotide variant	NM_000820.4(GAS6):c.1321C>T (p.Leu441=)	not provided [RCV000974282]	benign	13	113827152	113827152	Human		name
15175891	CV738978	single nucleotide variant	NM_000820.4(GAS6):c.1791C>T (p.Ser597=)	not provided [RCV000906314]	benign	13	113822049	113822049	Human		name
15106802	CV769413	single nucleotide variant	NM_000820.4(GAS6):c.1902G>A (p.Ala634=)	not provided [RCV000937848]	likely benign	13	113820999	113820999	Human		name
155943926	CV2241798	single nucleotide variant	NM_000820.4(GAS6):c.731A>C (p.Gln244Pro)	not specified [RCV004106732]	uncertain significance	13	113834654	113834654	Human		name
156244818	CV2243213	single nucleotide variant	NM_000820.4(GAS6):c.827C>T (p.Thr276Ile)	not specified [RCV004110104]	uncertain significance	13	113834558	113834558	Human		name
156078876	CV2248518	single nucleotide variant	NM_000820.4(GAS6):c.794G>T (p.Arg265Leu)	not specified [RCV004119647]	uncertain significance	13	113834591	113834591	Human		name
156198161	CV2259328	single nucleotide variant	NM_000820.4(GAS6):c.460G>A (p.Asp154Asn)	not specified [RCV004122338]	uncertain significance	13	113839734	113839734	Human		name
155968748	CV2262029	single nucleotide variant	NM_000820.4(GAS6):c.790G>A (p.Gly264Arg)	not specified [RCV004126512]	uncertain significance	13	113834595	113834595	Human		name
156169434	CV2276744	single nucleotide variant	NM_000820.4(GAS6):c.797G>A (p.Gly266Glu)	not specified [RCV004146530]	uncertain significance	13	113834588	113834588	Human		name
156204753	CV2311197	single nucleotide variant	NM_000820.4(GAS6):c.362C>T (p.Thr121Met)	not specified [RCV004166291]	uncertain significance	13	113839832	113839832	Human		name
155919932	CV2343259	single nucleotide variant	NM_000820.4(GAS6):c.850G>A (p.Val284Met)	not specified [RCV004194882]	uncertain significance	13	113832737	113832737	Human		name
156147691	CV2358030	single nucleotide variant	NM_000820.4(GAS6):c.410T>C (p.Met137Thr)	not specified [RCV004209802]	uncertain significance	13	113839784	113839784	Human		name
156073015	CV2365427	single nucleotide variant	NM_000820.4(GAS6):c.997A>G (p.Ile333Val)	not specified [RCV004209506]	likely benign	13	113832445	113832445	Human		name
401746349	CV2678820	single nucleotide variant	NM_000820.4(GAS6):c.305C>T (p.Pro102Leu)	not specified [RCV004292801]	uncertain significance	13	113846565	113846565	Human		name
401745826	CV2695448	single nucleotide variant	NM_000820.4(GAS6):c.497G>A (p.Gly166Asp)	not specified [RCV004305644]	uncertain significance	13	113838161	113838161	Human		name
401720039	CV2705625	single nucleotide variant	NM_000820.4(GAS6):c.672C>G (p.Asp224Glu)	not specified [RCV004318485]	uncertain significance	13	113835553	113835553	Human		name
405765631	CV3251513	single nucleotide variant	NM_000820.4(GAS6):c.395C>T (p.Ala132Val)	not specified [RCV004395030]	likely benign	13	113839799	113839799	Human		name
405765636	CV3251514	single nucleotide variant	NM_000820.4(GAS6):c.460G>C (p.Asp154His)	not specified [RCV004395031]	uncertain significance	13	113839734	113839734	Human		name
405765642	CV3251515	single nucleotide variant	NM_000820.4(GAS6):c.559G>A (p.Glu187Lys)	not specified [RCV004395032]	uncertain significance	13	113838099	113838099	Human		name
405765648	CV3251516	single nucleotide variant	NM_000820.4(GAS6):c.617C>T (p.Ala206Val)	not specified [RCV004395033]	uncertain significance	13	113835608	113835608	Human		name
405765656	CV3251517	single nucleotide variant	NM_000820.4(GAS6):c.692C>A (p.Ser231Tyr)	not specified [RCV004395034]	uncertain significance	13	113835533	113835533	Human		name
405765662	CV3251518	single nucleotide variant	NM_000820.4(GAS6):c.710G>C (p.Arg237Pro)	not specified [RCV004395035]	uncertain significance	13	113835515	113835515	Human		name
405765667	CV3251519	single nucleotide variant	NM_000820.4(GAS6):c.718G>A (p.Asp240Asn)	not specified [RCV004395036]	uncertain significance	13	113834667	113834667	Human		name
405765672	CV3251520	single nucleotide variant	NM_000820.4(GAS6):c.789C>G (p.Asp263Glu)	not specified [RCV004395037]	uncertain significance	13	113834596	113834596	Human		name
405765685	CV3251522	single nucleotide variant	NM_000820.4(GAS6):c.946C>G (p.Pro316Ala)	not specified [RCV004395039]	uncertain significance	13	113832641	113832641	Human		name
407462435	CV3436485	single nucleotide variant	NM_000820.4(GAS6):c.428T>C (p.Leu143Pro)	not specified [RCV004634552]	uncertain significance	13	113839766	113839766	Human		name
407503687	CV3436486	single nucleotide variant	NM_000820.4(GAS6):c.823G>A (p.Asp275Asn)	not specified [RCV004623828]	likely benign	13	113834562	113834562	Human		name
597754820	CV3681044	single nucleotide variant	NM_000820.4(GAS6):c.946C>T (p.Pro316Ser)	not specified [RCV004924467]	uncertain significance	13	113832641	113832641	Human		name
597780320	CV3681047	single nucleotide variant	NM_000820.4(GAS6):c.600G>T (p.Glu200Asp)	not specified [RCV004930629]	uncertain significance	13	113835625	113835625	Human		name
597780324	CV3681050	single nucleotide variant	NM_000820.4(GAS6):c.558C>G (p.Phe186Leu)	not specified [RCV004930630]	uncertain significance	13	113838100	113838100	Human		name
597780328	CV3681051	single nucleotide variant	NM_000820.4(GAS6):c.419T>A (p.Phe140Tyr)	not specified [RCV004930631]	uncertain significance	13	113839775	113839775	Human		name
598204557	CV3974154	single nucleotide variant	NM_000820.4(GAS6):c.492C>A (p.Asn164Lys)	not specified [RCV005337445]	uncertain significance	13	113838166	113838166	Human		name
598204568	CV3974156	single nucleotide variant	NM_000820.4(GAS6):c.952A>G (p.Arg318Gly)	not specified [RCV005337447]	uncertain significance	13	113832635	113832635	Human		name
15178556	CV725403	single nucleotide variant	NM_000820.4(GAS6):c.683C>T (p.Ala228Val)	not provided [RCV000885088]	benign	13	113835542	113835542	Human		name
156325250	CV2195260	single nucleotide variant	NM_000820.4(GAS6):c.1870G>A (p.Gly624Ser)	not specified [RCV004080194]	uncertain significance	13	113821970	113821970	Human		name
156274820	CV2202670	single nucleotide variant	NM_000820.4(GAS6):c.1792G>A (p.Glu598Lys)	not specified [RCV004082920]	uncertain significance	13	113822048	113822048	Human		name
156113937	CV2224992	single nucleotide variant	NM_000820.4(GAS6):c.1592G>A (p.Arg531His)	not specified [RCV004094833]	likely benign	13	113823436	113823436	Human		name
156388391	CV2231810	single nucleotide variant	NM_000820.4(GAS6):c.1427G>A (p.Arg476Lys)	not specified [RCV004098619]	likely benign	13	113827046	113827046	Human		name
155948560	CV2245958	single nucleotide variant	NM_000820.4(GAS6):c.1457C>T (p.Ala486Val)	not specified [RCV004113580]	uncertain significance	13	113827016	113827016	Human		name
156358259	CV2250979	single nucleotide variant	NM_000820.4(GAS6):c.1720G>A (p.Glu574Lys)	not specified [RCV004123549]	uncertain significance	13	113822120	113822120	Human		name
156161984	CV2272645	single nucleotide variant	NM_000820.4(GAS6):c.1625A>G (p.Tyr542Cys)	not specified [RCV004133524]	uncertain significance	13	113823403	113823403	Human		name
156278762	CV2284983	single nucleotide variant	NM_000820.4(GAS6):c.1690C>A (p.Leu564Ile)	not specified [RCV004143418]	uncertain significance	13	113822150	113822150	Human		name
156149416	CV2307407	single nucleotide variant	NM_000820.4(GAS6):c.1322T>C (p.Leu441Pro)	not specified [RCV004166084]	uncertain significance	13	113827151	113827151	Human		name
155967384	CV2329912	single nucleotide variant	NM_000820.4(GAS6):c.1828G>A (p.Val610Met)	not specified [RCV004183367]	uncertain significance	13	113822012	113822012	Human		name
156149570	CV2359519	single nucleotide variant	NM_000820.4(GAS6):c.1421C>T (p.Thr474Met)	not specified [RCV004214828]	uncertain significance	13	113827052	113827052	Human		name
156401995	CV2367799	single nucleotide variant	NM_000820.4(GAS6):c.1168A>G (p.Asn390Asp)	not specified [RCV004222914]	uncertain significance	13	113828687	113828687	Human		name
156113082	CV2387987	single nucleotide variant	NM_000820.4(GAS6):c.1111G>A (p.Gly371Ser)	not specified [RCV004236521]	uncertain significance	13	113832331	113832331	Human		name
401752480	CV2682834	single nucleotide variant	NM_000820.4(GAS6):c.1591C>T (p.Arg531Cys)	not specified [RCV004281802]	uncertain significance	13	113823437	113823437	Human		name
401770857	CV2686048	single nucleotide variant	NM_000820.4(GAS6):c.1432T>G (p.Ser478Ala)	not specified [RCV004297061]	uncertain significance	13	113827041	113827041	Human		name
401734410	CV2688500	single nucleotide variant	NM_000820.4(GAS6):c.2015C>T (p.Pro672Leu)	not specified [RCV004301473]	uncertain significance	13	113820886	113820886	Human		name
401742626	CV2715278	single nucleotide variant	NM_000820.4(GAS6):c.1384G>A (p.Val462Met)	not specified [RCV004324617]	uncertain significance	13	113827089	113827089	Human		name
401899753	CV2762160	single nucleotide variant	NM_000820.4(GAS6):c.1912G>A (p.Ala638Thr)	not specified [RCV004341974]	uncertain significance	13	113820989	113820989	Human		name
401886948	CV2777037	single nucleotide variant	NM_000820.4(GAS6):c.1640A>C (p.Lys547Thr)	not specified [RCV004351833]	uncertain significance	13	113823388	113823388	Human		name
405765554	CV3251501	single nucleotide variant	NM_000820.4(GAS6):c.1078C>T (p.Arg360Cys)	not specified [RCV004395018]	uncertain significance	13	113832364	113832364	Human		name
405765560	CV3251502	single nucleotide variant	NM_000820.4(GAS6):c.1093G>A (p.Gly365Ser)	not specified [RCV004395019]	uncertain significance	13	113832349	113832349	Human		name
405765566	CV3251503	single nucleotide variant	NM_000820.4(GAS6):c.1153G>A (p.Glu385Lys)	not specified [RCV004395020]	uncertain significance	13	113828702	113828702	Human		name
405765572	CV3251504	single nucleotide variant	NM_000820.4(GAS6):c.1166G>A (p.Arg389Gln)	not specified [RCV004395021]	uncertain significance	13	113828689	113828689	Human		name
405765578	CV3251505	single nucleotide variant	NM_000820.4(GAS6):c.1213G>A (p.Val405Met)	not specified [RCV004395022]	uncertain significance	13	113828642	113828642	Human		name
405765586	CV3251506	single nucleotide variant	NM_000820.4(GAS6):c.1216G>A (p.Ala406Thr)	not specified [RCV004395023]	uncertain significance	13	113828639	113828639	Human		name
405765592	CV3251507	single nucleotide variant	NM_000820.4(GAS6):c.1415C>T (p.Ser472Leu)	not specified [RCV004395024]	uncertain significance	13	113827058	113827058	Human		name
405765598	CV3251508	single nucleotide variant	NM_000820.4(GAS6):c.1495G>A (p.Val499Ile)	not specified [RCV004395025]	likely benign	13	113823533	113823533	Human		name
405765605	CV3251509	single nucleotide variant	NM_000820.4(GAS6):c.1715G>A (p.Gly572Asp)	not specified [RCV004395026]	uncertain significance	13	113822125	113822125	Human		name
405765611	CV3251510	single nucleotide variant	NM_000820.4(GAS6):c.1765G>C (p.Glu589Gln)	not specified [RCV004395027]	uncertain significance	13	113822075	113822075	Human		name
405765618	CV3251511	single nucleotide variant	NM_000820.4(GAS6):c.1769T>C (p.Val590Ala)	not specified [RCV004395028]	uncertain significance	13	113822071	113822071	Human		name
405765625	CV3251512	single nucleotide variant	NM_000820.4(GAS6):c.1943T>G (p.Val648Gly)	not specified [RCV004395029]	uncertain significance	13	113820958	113820958	Human		name
407503684	CV3436482	single nucleotide variant	NM_000820.4(GAS6):c.1750G>T (p.Gly584Cys)	not specified [RCV004623827]	uncertain significance	13	113822090	113822090	Human		name
407462433	CV3436483	single nucleotide variant	NM_000820.4(GAS6):c.1168A>C (p.Asn390His)	not specified [RCV004634550]	uncertain significance	13	113828687	113828687	Human		name
597754800	CV3681037	single nucleotide variant	NM_000820.4(GAS6):c.1804G>A (p.Ala602Thr)	not specified [RCV004924462]	likely benign	13	113822036	113822036	Human		name
597754804	CV3681038	single nucleotide variant	NM_000820.4(GAS6):c.1115C>T (p.Pro372Leu)	not specified [RCV004924463]	uncertain significance	13	113832327	113832327	Human		name
597754808	CV3681039	single nucleotide variant	NM_000820.4(GAS6):c.1976C>T (p.Ala659Val)	not specified [RCV004924464]	uncertain significance	13	113820925	113820925	Human		name
597780313	CV3681040	single nucleotide variant	NM_000820.4(GAS6):c.1397C>T (p.Thr466Met)	not specified [RCV004930627]	uncertain significance	13	113827076	113827076	Human		name
597780317	CV3681041	single nucleotide variant	NM_000820.4(GAS6):c.1003C>T (p.Leu335Phe)	not specified [RCV004930628]	likely benign	13	113832439	113832439	Human		name
597754816	CV3681043	single nucleotide variant	NM_000820.4(GAS6):c.1675C>G (p.His559Asp)	not specified [RCV004924466]	uncertain significance	13	113822165	113822165	Human		name
597754824	CV3681045	single nucleotide variant	NM_000820.4(GAS6):c.1504G>C (p.Glu502Gln)	not specified [RCV004924468]	uncertain significance	13	113823524	113823524	Human		name
597754828	CV3681046	single nucleotide variant	NM_000820.4(GAS6):c.1852C>G (p.Pro618Ala)	not specified [RCV004924469]	uncertain significance	13	113821988	113821988	Human		name
597754832	CV3681048	single nucleotide variant	NM_000820.4(GAS6):c.1780A>T (p.Arg594Trp)	not specified [RCV004924470]	uncertain significance	13	113822060	113822060	Human		name
597754836	CV3681049	single nucleotide variant	NM_000820.4(GAS6):c.1730T>C (p.Val577Ala)	not specified [RCV004924471]	uncertain significance	13	113822110	113822110	Human		name
598204562	CV3974155	single nucleotide variant	NM_000820.4(GAS6):c.1801G>A (p.Ala601Thr)	not specified [RCV005337446]	uncertain significance	13	113822039	113822039	Human		name
598158948	CV3974157	single nucleotide variant	NM_000820.4(GAS6):c.1124A>G (p.Asn375Ser)	not specified [RCV005328165]	uncertain significance	13	113832318	113832318	Human		name
598204575	CV3974158	single nucleotide variant	NM_000820.4(GAS6):c.1267G>A (p.Val423Met)	not specified [RCV005337448]	uncertain significance	13	113828588	113828588	Human		name
598204582	CV3974159	single nucleotide variant	NM_000820.4(GAS6):c.1672G>C (p.Glu558Gln)	not specified [RCV005337449]	uncertain significance	13	113822168	113822168	Human		name
15159092	CV713854	single nucleotide variant	NM_000820.4(GAS6):c.1847G>A (p.Arg616Gln)	not provided [RCV000969645]	benign	13	113821993	113821993	Human		name
15152048	CV713855	single nucleotide variant	NM_000820.4(GAS6):c.1834G>A (p.Glu612Lys)	not provided [RCV000968271]	benign	13	113822006	113822006	Human		name
15118116	CV713856	single nucleotide variant	NM_000820.4(GAS6):c.1739C>T (p.Ser580Leu)	not provided [RCV000962318]	benign	13	113822101	113822101	Human		name
15180978	CV713857	single nucleotide variant	NM_000820.4(GAS6):c.1498G>A (p.Gly500Arg)	not provided [RCV000974281]	benign	13	113823530	113823530	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