Gas6 Variant Search Result - Rat Genome Database

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93 records found for search term Gas6

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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

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