Lrrc4c Variant Search Result - Rat Genome Database

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62 records found for search term Lrrc4c

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8652977	CV129552	single nucleotide variant	NM_001258419.1(LRRC4C):c.-42-10102C>A	Lung cancer [RCV000110039]	uncertain significance	11	40126436	40126436	Human		name
8652978	CV129553	single nucleotide variant	NM_001258419.1(LRRC4C):c.-43+11694C>T	Lung cancer [RCV000110040]	uncertain significance	11	40129107	40129107	Human		name
8652979	CV129554	single nucleotide variant	NM_001258419.1(LRRC4C):c.-95-29316C>T	Lung cancer [RCV000110041]	uncertain significance	11	40170169	40170169	Human		name
8652980	CV129555	single nucleotide variant	NM_001258419.1(LRRC4C):c.-96+44944A>G	Lung cancer [RCV000110042]	uncertain significance	11	40196575	40196575	Human		name
8652981	CV129556	single nucleotide variant	NM_001258419.1(LRRC4C):c.-96+31864C>G	Lung cancer [RCV000110043]	uncertain significance	11	40209655	40209655	Human		name
8652986	CV129561	single nucleotide variant	NM_001258419.1(LRRC4C):c.-270+6068A>T	Lung cancer [RCV000110048]	uncertain significance	11	40642074	40642074	Human		name
8652982	CV129557	single nucleotide variant	NM_001258419.1(LRRC4C):c.-175-38971A>T	Lung cancer [RCV000110044]	uncertain significance	11	40280569	40280569	Human		name
8652983	CV129558	single nucleotide variant	NM_001258419.1(LRRC4C):c.-176+21081C>A	Lung cancer [RCV000110045]	uncertain significance	11	40298547	40298547	Human		name
8652984	CV129559	single nucleotide variant	NM_001258419.1(LRRC4C):c.-269-68724T>A	Lung cancer [RCV000110046]	uncertain significance	11	40388445	40388445	Human		name
8652985	CV129560	single nucleotide variant	NM_001258419.1(LRRC4C):c.-270+34603G>T	Lung cancer [RCV000110047]	uncertain significance	11	40613539	40613539	Human		name
8652987	CV129562	single nucleotide variant	NM_001258419.1(LRRC4C):c.-495-77251A>G	Lung cancer [RCV000110049]	uncertain significance	11	41010974	41010974	Human		name
8652988	CV129563	single nucleotide variant	NM_001258419.1(LRRC4C):c.-495-99891G>A	Lung cancer [RCV000110050]	uncertain significance	11	41033614	41033614	Human		name
8652995	CV129570	single nucleotide variant	NM_001258419.1(LRRC4C):c.-496+88435C>T	Lung cancer [RCV000110057]	uncertain significance	11	41370996	41370996	Human		name
8652996	CV129571	single nucleotide variant	NM_001258419.1(LRRC4C):c.-496+13519A>G	Lung cancer [RCV000110058]	uncertain significance	11	41445912	41445912	Human		name
8652989	CV129564	single nucleotide variant	NM_001258419.1(LRRC4C):c.-495-169079G>A	Lung cancer [RCV000110051]	uncertain significance	11	41102802	41102802	Human		name
8652990	CV129565	single nucleotide variant	NM_001258419.1(LRRC4C):c.-495-189501T>A	Lung cancer [RCV000110052]	uncertain significance	11	41123224	41123224	Human		name
8652991	CV129566	single nucleotide variant	NM_001258419.1(LRRC4C):c.-495-209486A>C	Lung cancer [RCV000110053]	uncertain significance	11	41143209	41143209	Human		name
8652992	CV129567	single nucleotide variant	NM_001258419.1(LRRC4C):c.-495-226256G>T	Lung cancer [RCV000110054]	uncertain significance	11	41159979	41159979	Human		name
8652993	CV129568	single nucleotide variant	NM_001258419.1(LRRC4C):c.-495-228777C>G	Lung cancer [RCV000110055]	uncertain significance	11	41162500	41162500	Human		name
8652994	CV129569	single nucleotide variant	NM_001258419.1(LRRC4C):c.-496+224792T>G	Lung cancer [RCV000110056]	uncertain significance	11	41234639	41234639	Human		name
405278918	CV3212752	single nucleotide variant	NM_001258419.2(LRRC4C):c.8A>C (p.Asn3Thr)	LRRC4C-related disorder [RCV003954769]	likely benign	11	40116285	40116285	Human		name , trait , alternate_id
8626985	CV82129	single nucleotide variant	NM_020929.2(LRRC4C):c.1713G>A (p.Val571=)	Malignant melanoma [RCV000062208]	not provided	11	40114580	40114580	Human		name
8634034	CV89252	single nucleotide variant	NM_020929.2(LRRC4C):c.1842A>T (p.Ile614=)	Malignant melanoma [RCV000069349]	not provided	11	40114451	40114451	Human		name
8634035	CV89253	single nucleotide variant	NM_020929.2(LRRC4C):c.169T>C (p.Phe57Leu)	Malignant melanoma [RCV000069350]	not provided	11	40116124	40116124	Human		name
8626986	CV82130	single nucleotide variant	NM_020929.2(LRRC4C):c.945G>A (p.Trp315Ter)	Malignant melanoma [RCV000062209]	not provided	11	40115348	40115348	Human		name
8626987	CV82131	single nucleotide variant	NM_020929.2(LRRC4C):c.623A>G (p.Asn208Ser)	Malignant melanoma [RCV000062210]	not provided	11	40115670	40115670	Human		name
329401574	CV2461073	single nucleotide variant	NM_001258419.2(LRRC4C):c.220A>G (p.Ile74Val)	not specified [RCV004265218]	uncertain significance	11	40116073	40116073	Human		name
401928841	CV2816572	single nucleotide variant	NM_001258419.2(LRRC4C):c.1680C>T (p.His560=)	not provided [RCV003390036]	likely benign	11	40114613	40114613	Human		name
405656036	CV3287881	single nucleotide variant	NM_001258419.2(LRRC4C):c.102A>T (p.Gln34His)	not specified [RCV004415669]	uncertain significance	11	40116191	40116191	Human		name
597633153	CV3693494	single nucleotide variant	NM_001258419.2(LRRC4C):c.107T>C (p.Leu36Pro)	not specified [RCV004940134]	uncertain significance	11	40116186	40116186	Human		name
156070511	CV2204016	single nucleotide variant	NM_001258419.2(LRRC4C):c.766C>A (p.Gln256Lys)	not specified [RCV004070054]	uncertain significance	11	40115527	40115527	Human		name
155968523	CV2244259	single nucleotide variant	NM_001258419.2(LRRC4C):c.698C>T (p.Ala233Val)	not specified [RCV004599467]	uncertain significance	11	40115595	40115595	Human		name
155906652	CV2303351	single nucleotide variant	NM_001258419.2(LRRC4C):c.698C>A (p.Ala233Asp)	not specified [RCV004159087]	uncertain significance	11	40115595	40115595	Human		name
156304618	CV2369173	single nucleotide variant	NM_001258419.2(LRRC4C):c.404G>A (p.Arg135His)	not specified [RCV004208096]	uncertain significance	11	40115889	40115889	Human		name
329392080	CV2445293	single nucleotide variant	NM_001258419.2(LRRC4C):c.730C>T (p.His244Tyr)	not specified [RCV004263920]	uncertain significance	11	40115563	40115563	Human		name
329401043	CV2446070	single nucleotide variant	NM_001258419.2(LRRC4C):c.676C>A (p.Leu226Ile)	not specified [RCV004270632]	uncertain significance	11	40115617	40115617	Human		name
401931777	CV2803795	single nucleotide variant	NM_001258419.2(LRRC4C):c.873T>A (p.His291Gln)	LRRC4C-related disorder [RCV003408391]	uncertain significance	11	40115420	40115420	Human		name , trait , alternate_id
405656047	CV3287887	single nucleotide variant	NM_001258419.2(LRRC4C):c.415A>G (p.Ile139Val)	not specified [RCV004415675]	uncertain significance	11	40115878	40115878	Human		name
405656049	CV3287888	single nucleotide variant	NM_001258419.2(LRRC4C):c.474C>A (p.Asn158Lys)	not specified [RCV004415676]	uncertain significance	11	40115819	40115819	Human		name
405656051	CV3287889	single nucleotide variant	NM_001258419.2(LRRC4C):c.494C>T (p.Ser165Phe)	not specified [RCV004415677]	uncertain significance	11	40115799	40115799	Human		name
405656052	CV3287890	single nucleotide variant	NM_001258419.2(LRRC4C):c.779G>A (p.Arg260Gln)	not specified [RCV004415678]	uncertain significance	11	40115514	40115514	Human		name
405656054	CV3287891	single nucleotide variant	NM_001258419.2(LRRC4C):c.823G>A (p.Ala275Thr)	not specified [RCV004415679]	uncertain significance	11	40115470	40115470	Human		name
405656056	CV3287892	single nucleotide variant	NM_001258419.2(LRRC4C):c.863C>T (p.Thr288Ile)	not specified [RCV004415680]	uncertain significance	11	40115430	40115430	Human		name
405656058	CV3287893	single nucleotide variant	NM_001258419.2(LRRC4C):c.965C>T (p.Ser322Leu)	not specified [RCV004415681]	uncertain significance	11	40115328	40115328	Human		name
156352043	CV2323884	single nucleotide variant	NM_001258419.2(LRRC4C):c.1732G>A (p.Asp578Asn)	not specified [RCV004599537]	uncertain significance	11	40114561	40114561	Human		name
155972564	CV2335813	single nucleotide variant	NM_001258419.2(LRRC4C):c.1727C>T (p.Thr576Met)	not specified [RCV004196048]	uncertain significance	11	40114566	40114566	Human		name
155932074	CV2371093	single nucleotide variant	NM_001258419.2(LRRC4C):c.1193C>T (p.Ala398Val)	not specified [RCV004220846]	uncertain significance	11	40115100	40115100	Human		name
329381422	CV2437481	single nucleotide variant	NM_001258419.2(LRRC4C):c.1229C>T (p.Thr410Met)	not specified [RCV004258772]	uncertain significance	11	40115064	40115064	Human		name
329376283	CV2438075	single nucleotide variant	NM_001258419.2(LRRC4C):c.1091A>G (p.Asn364Ser)	not specified [RCV004256863]	uncertain significance	11	40115202	40115202	Human		name
329377873	CV2460791	single nucleotide variant	NM_001258419.2(LRRC4C):c.1438C>T (p.Pro480Ser)	not specified [RCV004271111]	uncertain significance	11	40114855	40114855	Human		name
401728084	CV2675946	single nucleotide variant	NM_001258419.2(LRRC4C):c.1337C>T (p.Ala446Val)	not specified [RCV004281942]	uncertain significance	11	40114956	40114956	Human		name
405656038	CV3287882	single nucleotide variant	NM_001258419.2(LRRC4C):c.1205G>A (p.Arg402Gln)	not specified [RCV004415670]	uncertain significance	11	40115088	40115088	Human		name
405656040	CV3287883	single nucleotide variant	NM_001258419.2(LRRC4C):c.1418A>T (p.Asp473Val)	not specified [RCV004415671]	uncertain significance	11	40114875	40114875	Human		name
405656042	CV3287884	single nucleotide variant	NM_001258419.2(LRRC4C):c.1447G>A (p.Asp483Asn)	not specified [RCV004415672]	uncertain significance	11	40114846	40114846	Human		name
405656043	CV3287885	single nucleotide variant	NM_001258419.2(LRRC4C):c.1771G>A (p.Glu591Lys)	not specified [RCV004415673]	uncertain significance	11	40114522	40114522	Human		name
405656045	CV3287886	single nucleotide variant	NM_001258419.2(LRRC4C):c.1810C>T (p.Pro604Ser)	not specified [RCV004415674]	uncertain significance	11	40114483	40114483	Human		name
407501078	CV3456556	single nucleotide variant	NM_001258419.2(LRRC4C):c.1393T>C (p.Ser465Pro)	not specified [RCV004644780]	uncertain significance	11	40114900	40114900	Human		name
407501084	CV3456558	single nucleotide variant	NM_001258419.2(LRRC4C):c.1093G>A (p.Val365Ile)	not specified [RCV004644782]	uncertain significance	11	40115200	40115200	Human		name
598222576	CV3984752	single nucleotide variant	NM_001258419.2(LRRC4C):c.1082C>A (p.Ala361Glu)	not specified [RCV005379910]	uncertain significance	11	40115211	40115211	Human		name
598251164	CV3984753	single nucleotide variant	NM_001258419.2(LRRC4C):c.1429G>A (p.Gly477Ser)	not specified [RCV005366634]	uncertain significance	11	40114864	40114864	Human		name
598251169	CV3984754	single nucleotide variant	NM_001258419.2(LRRC4C):c.1517C>G (p.Thr506Ser)	not specified [RCV005366635]	uncertain significance	11	40114776	40114776	Human		name
598251174	CV3984755	single nucleotide variant	NM_001258419.2(LRRC4C):c.1564G>T (p.Val522Phe)	not specified [RCV005366636]	uncertain significance	11	40114729	40114729	Human		name

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