Egfl6 Variant Search Result - Rat Genome Database

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57 records found for search term Egfl6

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401931046	CV2823895	single nucleotide variant	NM_015507.4(EGFL6):c.60C>T (p.Phe20=)	not provided [RCV003441013]	likely benign	X	13569921	13569921	Human		name
155965224	CV2261755	single nucleotide variant	NM_015507.4(EGFL6):c.86A>G (p.His29Arg)	not specified [RCV004126045]	uncertain significance	X	13589567	13589567	Human		name
401931047	CV2823896	single nucleotide variant	NM_015507.4(EGFL6):c.393G>A (p.Thr131=)	not provided [RCV003441014]	likely benign	X	13600087	13600087	Human		name
401931048	CV2823897	single nucleotide variant	NM_015507.4(EGFL6):c.624G>T (p.Leu208=)	not provided [RCV003441015]	likely benign	X	13606482	13606482	Human		name
15203254	CV706109	single nucleotide variant	NM_015507.4(EGFL6):c.348C>T (p.Tyr116=)	not provided [RCV000958310]	benign	X	13600042	13600042	Human		name
15115067	CV717655	single nucleotide variant	NM_015507.4(EGFL6):c.324A>G (p.Arg108=)	not provided [RCV000961785]	benign	X	13600018	13600018	Human		name
15115073	CV717656	single nucleotide variant	NM_015507.4(EGFL6):c.351G>A (p.Lys117=)	not provided [RCV000961786]	benign	X	13600045	13600045	Human		name
156376152	CV2210466	single nucleotide variant	NM_015507.4(EGFL6):c.262G>A (p.Gly88Arg)	not specified [RCV004089599]	uncertain significance	X	13594910	13594910	Human		name
405716505	CV3241718	single nucleotide variant	NM_015507.4(EGFL6):c.134C>T (p.Thr45Ile)	not specified [RCV004377455]	uncertain significance	X	13589615	13589615	Human		name
405716522	CV3241720	single nucleotide variant	NM_015507.4(EGFL6):c.143C>T (p.Ala48Val)	not specified [RCV004377457]	uncertain significance	X	13589624	13589624	Human		name
405716533	CV3241722	single nucleotide variant	NM_015507.4(EGFL6):c.232A>G (p.Asn78Asp)	not specified [RCV004377459]	uncertain significance	X	13594880	13594880	Human		name
598167677	CV3964914	single nucleotide variant	NM_015507.4(EGFL6):c.136A>G (p.Lys46Glu)	not specified [RCV005330090]	uncertain significance	X	13589617	13589617	Human		name
598167694	CV3964917	single nucleotide variant	NM_015507.4(EGFL6):c.115G>T (p.Gly39Trp)	not specified [RCV005330093]	uncertain significance	X	13589596	13589596	Human		name
598167699	CV3964918	single nucleotide variant	NM_015507.4(EGFL6):c.116G>C (p.Gly39Ala)	not specified [RCV005330094]	uncertain significance	X	13589597	13589597	Human		name
15171423	CV717654	single nucleotide variant	NM_015507.4(EGFL6):c.223G>A (p.Val75Met)	not provided [RCV000972197]	likely benign	X	13594871	13594871	Human		name
15174752	CV729422	single nucleotide variant	NM_015507.4(EGFL6):c.196G>A (p.Glu66Lys)	not provided [RCV000884199]	benign	X	13594844	13594844	Human		name
156295026	CV2239558	single nucleotide variant	NM_015507.4(EGFL6):c.803A>G (p.Glu268Gly)	not specified [RCV004114554]	uncertain significance	X	13617754	13617754	Human		name
156288011	CV2301298	single nucleotide variant	NM_015507.4(EGFL6):c.298A>C (p.Met100Leu)	not specified [RCV004160471]	uncertain significance	X	13599992	13599992	Human		name
156354464	CV2324284	single nucleotide variant	NM_015507.4(EGFL6):c.524T>C (p.Ile175Thr)	not specified [RCV004177012]	uncertain significance	X	13606382	13606382	Human		name
405716542	CV3241723	single nucleotide variant	NM_015507.4(EGFL6):c.337C>T (p.His113Tyr)	not specified [RCV004377460]	uncertain significance	X	13600031	13600031	Human		name
405716550	CV3241724	single nucleotide variant	NM_015507.4(EGFL6):c.431A>G (p.Gln144Arg)	not specified [RCV004377461]	uncertain significance	X	13603347	13603347	Human		name
405716557	CV3241725	single nucleotide variant	NM_015507.4(EGFL6):c.441T>G (p.Cys147Trp)	not specified [RCV004377462]	uncertain significance	X	13603357	13603357	Human		name
405716568	CV3241727	single nucleotide variant	NM_015507.4(EGFL6):c.487C>T (p.Leu163Phe)	not specified [RCV004377464]	uncertain significance	X	13603403	13603403	Human		name
405716576	CV3241728	single nucleotide variant	NM_015507.4(EGFL6):c.674T>C (p.Met225Thr)	not specified [RCV004377465]	uncertain significance	X	13608342	13608342	Human		name
405716584	CV3241729	single nucleotide variant	NM_015507.4(EGFL6):c.773G>A (p.Cys258Tyr)	not specified [RCV004377466]	uncertain significance	X	13608441	13608441	Human		name
405716592	CV3241730	single nucleotide variant	NM_015507.4(EGFL6):c.872A>G (p.Lys291Arg)	not specified [RCV004377467]	uncertain significance	X	13617823	13617823	Human		name
407497971	CV3441800	single nucleotide variant	NM_015507.4(EGFL6):c.635G>A (p.Ser212Asn)	not specified [RCV004622347]	uncertain significance	X	13606493	13606493	Human		name
407497975	CV3441801	single nucleotide variant	NM_015507.4(EGFL6):c.440G>A (p.Cys147Tyr)	not specified [RCV004622348]	uncertain significance	X	13603356	13603356	Human		name
597646468	CV3664409	single nucleotide variant	NM_015507.4(EGFL6):c.928A>G (p.Lys310Glu)	not specified [RCV004909944]	uncertain significance	X	13617879	13617879	Human		name
597646480	CV3664411	single nucleotide variant	NM_015507.4(EGFL6):c.619G>A (p.Glu207Lys)	not specified [RCV004909946]	uncertain significance	X	13606477	13606477	Human		name
597646501	CV3664415	single nucleotide variant	NM_015507.4(EGFL6):c.385G>A (p.Asp129Asn)	not specified [RCV004909949]	uncertain significance	X	13600079	13600079	Human		name
597646508	CV3664416	single nucleotide variant	NM_015507.4(EGFL6):c.719A>G (p.Gln240Arg)	not specified [RCV004909950]	uncertain significance	X	13608387	13608387	Human		name
598167659	CV3964910	single nucleotide variant	NM_015507.4(EGFL6):c.566G>A (p.Arg189Gln)	not specified [RCV005330086]	uncertain significance	X	13606424	13606424	Human		name
598167661	CV3964911	single nucleotide variant	NM_015507.4(EGFL6):c.653T>C (p.Ile218Thr)	not specified [RCV005330087]	uncertain significance	X	13606511	13606511	Human		name
598167666	CV3964912	single nucleotide variant	NM_015507.4(EGFL6):c.359G>C (p.Cys120Ser)	not specified [RCV005330088]	uncertain significance	X	13600053	13600053	Human		name
598167673	CV3964913	single nucleotide variant	NM_015507.4(EGFL6):c.502A>G (p.Asn168Asp)	not specified [RCV005330089]	uncertain significance	X	13603418	13603418	Human		name
598167683	CV3964915	single nucleotide variant	NM_015507.4(EGFL6):c.629A>G (p.Tyr210Cys)	not specified [RCV005330091]	uncertain significance	X	13606487	13606487	Human		name
598167706	CV3964919	single nucleotide variant	NM_015507.4(EGFL6):c.563A>G (p.Asn188Ser)	not specified [RCV005330095]	uncertain significance	X	13606421	13606421	Human		name
15171149	CV729423	single nucleotide variant	NM_015507.4(EGFL6):c.307C>T (p.Arg103Trp)	not provided [RCV000883601]	likely benign	X	13600001	13600001	Human		name
15174758	CV729424	single nucleotide variant	NM_015507.4(EGFL6):c.490C>T (p.Arg164Cys)	not provided [RCV000884200]	benign	X	13603406	13603406	Human		name
156319801	CV2200592	single nucleotide variant	NM_015507.4(EGFL6):c.1277G>A (p.Arg426Gln)	not specified [RCV004078932]	uncertain significance	X	13623917	13623917	Human		name
156365928	CV2203236	single nucleotide variant	NM_015507.4(EGFL6):c.1414G>A (p.Gly472Arg)	not specified [RCV004071274]	uncertain significance	X	13627139	13627139	Human		name
156084400	CV2205584	single nucleotide variant	NM_015507.4(EGFL6):c.1436G>C (p.Arg479Pro)	not specified [RCV004082507]	uncertain significance	X	13627161	13627161	Human		name
156245662	CV2396705	single nucleotide variant	NM_015507.4(EGFL6):c.1132G>A (p.Gly378Ser)	not specified [RCV004233861]	uncertain significance	X	13619192	13619192	Human		name
329366659	CV2441788	single nucleotide variant	NM_015507.4(EGFL6):c.1537G>A (p.Asp513Asn)	not specified [RCV004261993]	uncertain significance	X	13627262	13627262	Human		name
401727817	CV2678481	single nucleotide variant	NM_015507.4(EGFL6):c.1343G>A (p.Arg448Gln)	Exstrophy-epispadias complex [RCV003389416]\|not specified [RCV004292498]	uncertain significance	X	13627068	13627068	Human	1	name
401770102	CV2719037	single nucleotide variant	NM_015507.4(EGFL6):c.1034A>G (p.Asp345Gly)	not specified [RCV004322619]	uncertain significance	X	13617985	13617985	Human		name
405716492	CV3241716	single nucleotide variant	NM_015507.4(EGFL6):c.1033G>T (p.Asp345Tyr)	not specified [RCV004377453]	uncertain significance	X	13617984	13617984	Human		name
405716499	CV3241717	single nucleotide variant	NM_015507.4(EGFL6):c.1124G>A (p.Gly375Asp)	not specified [RCV004377454]	uncertain significance	X	13619184	13619184	Human		name
405716529	CV3241721	single nucleotide variant	NM_015507.4(EGFL6):c.1472G>C (p.Trp491Ser)	not specified [RCV004377458]	uncertain significance	X	13627197	13627197	Human		name
407497967	CV3441799	single nucleotide variant	NM_015507.4(EGFL6):c.1216C>T (p.His406Tyr)	not specified [RCV004622346]	uncertain significance	X	13623856	13623856	Human		name
597646472	CV3664410	single nucleotide variant	NM_015507.4(EGFL6):c.1350A>C (p.Lys450Asn)	not specified [RCV004909945]	uncertain significance	X	13627075	13627075	Human		name
597646487	CV3664413	single nucleotide variant	NM_015507.4(EGFL6):c.1570C>T (p.Arg524Cys)	not specified [RCV004909947]	uncertain significance	X	13633003	13633003	Human		name
597646495	CV3664414	single nucleotide variant	NM_015507.4(EGFL6):c.1591G>A (p.Glu531Lys)	not specified [RCV004909948]	uncertain significance	X	13633024	13633024	Human		name
598167689	CV3964916	single nucleotide variant	NM_015507.4(EGFL6):c.1588G>A (p.Gly530Ser)	not specified [RCV005330092]	uncertain significance	X	13633021	13633021	Human		name
598167713	CV3964920	single nucleotide variant	NM_015507.4(EGFL6):c.1495G>A (p.Glu499Lys)	not specified [RCV005330096]	uncertain significance	X	13627220	13627220	Human		name
15120784	CV717660	single nucleotide variant	NM_015507.4(EGFL6):c.1524G>T (p.Leu508Phe)	not provided [RCV000962776]	benign	X	13627249	13627249	Human		name

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