Efna4 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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43 records found for search term Efna4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156211379	CV2314536	single nucleotide variant	NM_005227.3(EFNA4):c.*77G>C	not specified [RCV004168628]	uncertain significance	1	155069066	155069066	Human		name
15181169	CV729923	single nucleotide variant	NM_005227.3(EFNA4):c.*24C>G	not provided [RCV000885701]	likely benign	1	155069013	155069013	Human		name
401781224	CV2681934	single nucleotide variant	NM_005227.3(EFNA4):c.*105G>A	not specified [RCV004296922]	uncertain significance	1	155069094	155069094	Human		name
407478882	CV3441770	single nucleotide variant	NM_005227.3(EFNA4):c.*150C>T	not specified [RCV004622317]	uncertain significance	1	155069139	155069139	Human		name
597926233	CV3748878	single nucleotide variant	NM_005227.3(EFNA4):c.113+7G>A	not provided [RCV005075334]	likely benign	1	155063943	155063943	Human		name
152117713	CV1633695	single nucleotide variant	NM_005227.3(EFNA4):c.113+19G>A	not provided [RCV002117422]	benign	1	155063955	155063955	Human		name
156048217	CV1978143	single nucleotide variant	NM_005227.3(EFNA4):c.113+18G>A	not provided [RCV002590572]	likely benign	1	155063954	155063954	Human		name
405195146	CV3128654	single nucleotide variant	NM_005227.3(EFNA4):c.400+14G>A	not provided [RCV003821392]	likely benign	1	155067030	155067030	Human		name
597837003	CV3736497	single nucleotide variant	NM_005227.3(EFNA4):c.114-13G>A	not provided [RCV005064170]	likely benign	1	155066717	155066717	Human		name
597868004	CV3742847	single nucleotide variant	NM_005227.3(EFNA4):c.114-18C>G	not provided [RCV005068270]	likely benign	1	155066712	155066712	Human		name
405083320	CV2865050	single nucleotide variant	NM_005227.3(EFNA4):c.216G>A (p.Thr72=)	not provided [RCV003549394]	likely benign	1	155066832	155066832	Human		name
402495038	CV3183052	single nucleotide variant	NM_005227.3(EFNA4):c.297C>T (p.Cys99=)	not provided [RCV003877360]	likely benign	1	155066913	155066913	Human		name
156033082	CV2126825	single nucleotide variant	NM_005227.3(EFNA4):c.402G>A (p.Ser134=)	not provided [RCV002949314]	likely benign	1	155067373	155067373	Human		name
405045463	CV2859915	single nucleotide variant	NM_005227.3(EFNA4):c.360C>T (p.Leu120=)	not provided [RCV003579416]	likely benign	1	155066976	155066976	Human		name
597950638	CV3768692	single nucleotide variant	NM_005227.3(EFNA4):c.336T>C (p.Ile112=)	not provided [RCV005120878]	likely benign	1	155066952	155066952	Human		name
15162919	CV718255	single nucleotide variant	NM_005227.3(EFNA4):c.372C>T (p.Phe124=)	not provided [RCV000881856]	benign\|likely benign	1	155066988	155066988	Human	1	name
15162919	CV718255	single nucleotide variant	NM_005227.3(EFNA4):c.372C>T (p.Phe124=)	not provided [RCV000881856]	benign\|likely benign	1	155066988	155066989	Human	1	name
152077418	CV1564679	single nucleotide variant	NM_005227.3(EFNA4):c.178C>T (p.His60Tyr)	not provided [RCV002192598]	likely benign	1	155066794	155066794	Human	1	name
152077418	CV1564679	single nucleotide variant	NM_005227.3(EFNA4):c.178C>T (p.His60Tyr)	not provided [RCV002192598]	likely benign	1	155066794	155066795	Human	1	name
156227138	CV2006099	duplication	NM_005227.3(EFNA4):c.535dup (p.Asp179fs)	not provided [RCV002667445]	uncertain significance	1	155068911	155068912	Human		name
156019138	CV2141102	single nucleotide variant	NM_005227.3(EFNA4):c.275G>A (p.Arg92Gln)	not provided [RCV002976062]\|not specified [RCV005333406]	uncertain significance	1	155066891	155066891	Human		name
156111964	CV2267353	single nucleotide variant	NM_005227.3(EFNA4):c.133G>C (p.Val45Leu)	not provided [RCV003561106]\|not specified [RCV004134011]	uncertain significance	1	155066749	155066749	Human		name
156254101	CV2325597	single nucleotide variant	NM_005227.3(EFNA4):c.105T>A (p.Ser35Arg)	not specified [RCV004180017]	uncertain significance	1	155063928	155063928	Human		name
401781743	CV2682166	single nucleotide variant	NM_005227.3(EFNA4):c.229A>G (p.Met77Val)	not specified [RCV004290212]	uncertain significance	1	155066845	155066845	Human		name
401735609	CV2695357	single nucleotide variant	NM_005227.3(EFNA4):c.280T>G (p.Tyr94Asp)	not specified [RCV004305568]	uncertain significance	1	155066896	155066896	Human		name
405047697	CV3141720	single nucleotide variant	NM_005227.3(EFNA4):c.108C>A (p.Asn36Lys)	not provided [RCV003831821]	uncertain significance	1	155063931	155063931	Human		name
407478876	CV3441769	single nucleotide variant	NM_005227.3(EFNA4):c.185A>G (p.Glu62Gly)	not specified [RCV004622316]	uncertain significance	1	155066801	155066801	Human		name
597887777	CV3839108	single nucleotide variant	NM_005227.3(EFNA4):c.211G>A (p.Glu71Lys)	not provided [RCV005179193]	uncertain significance	1	155066827	155066827	Human		name
597967764	CV3853257	single nucleotide variant	NM_005227.3(EFNA4):c.278C>A (p.Ala93Asp)	not provided [RCV005194899]	uncertain significance	1	155066894	155066894	Human		name
151824985	CV1373376	single nucleotide variant	NM_005227.3(EFNA4):c.425G>T (p.Gly142Val)	not provided [RCV001934508]	uncertain significance	1	155067396	155067396	Human		name
156243698	CV1956828	single nucleotide variant	NM_005227.3(EFNA4):c.471G>T (p.Lys157Asn)	not provided [RCV002576308]	uncertain significance	1	155068854	155068854	Human		name
156018973	CV2019231	single nucleotide variant	NM_005227.3(EFNA4):c.325T>C (p.Ser109Pro)	not provided [RCV002690905]	uncertain significance	1	155066941	155066941	Human		name
155904838	CV2048026	single nucleotide variant	NM_005227.3(EFNA4):c.500C>T (p.Pro167Leu)	not provided [RCV002771202]	uncertain significance	1	155068883	155068883	Human		name
156106983	CV2120944	single nucleotide variant	NM_005227.3(EFNA4):c.349C>A (p.Pro117Thr)	not provided [RCV002952950]	likely benign	1	155066965	155066965	Human		name
156233752	CV2153335	single nucleotide variant	NM_005227.3(EFNA4):c.347C>T (p.Thr116Ile)	not provided [RCV003025744]	uncertain significance	1	155066963	155066963	Human		name
156328451	CV2180742	single nucleotide variant	NM_005227.3(EFNA4):c.472T>A (p.Ser158Thr)	not provided [RCV003047069]	uncertain significance	1	155068855	155068855	Human		name
329379091	CV2443291	single nucleotide variant	NM_005227.3(EFNA4):c.386C>G (p.Thr129Ser)	not specified [RCV004260093]	uncertain significance	1	155067002	155067002	Human		name
402471001	CV3171462	single nucleotide variant	NM_005227.3(EFNA4):c.429G>C (p.Gln143His)	not provided [RCV003874246]	uncertain significance	1	155067400	155067400	Human		name
404996280	CV3172870	single nucleotide variant	NM_005227.3(EFNA4):c.590T>G (p.Leu197Arg)	not provided [RCV003882152]	likely benign	1	155068973	155068973	Human		name
597645954	CV3664333	single nucleotide variant	NM_005227.3(EFNA4):c.401C>T (p.Ser134Leu)	not specified [RCV004909894]	uncertain significance	1	155067372	155067372	Human		name
597919520	CV3811660	single nucleotide variant	NM_005227.3(EFNA4):c.586C>T (p.Arg196Cys)	not provided [RCV005155491]	uncertain significance	1	155068969	155068969	Human		name
597929016	CV3816216	single nucleotide variant	NM_005227.3(EFNA4):c.451G>C (p.Val151Leu)	not provided [RCV005156797]	uncertain significance	1	155067422	155067422	Human		name
598167492	CV3964881	single nucleotide variant	NM_005227.3(EFNA4):c.374T>C (p.Leu125Ser)	not specified [RCV005330057]	uncertain significance	1	155066990	155066990	Human		name

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