Unc5c Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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157 records found for search term Unc5c

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405280938	CV3190665	single nucleotide variant	NM_003728.4(UNC5C):c.124+6G>A	UNC5C-related disorder [RCV003907101]	likely benign	4	95548728	95548728	Human		name , trait , alternate_id
408380287	CV3512778	single nucleotide variant	NM_003728.4(UNC5C):c.490+8A>G	UNC5C-related disorder [RCV004754057]	likely benign	4	95301598	95301598	Human		name , trait , alternate_id
8580158	CV114584	single nucleotide variant	NM_003728.3(UNC5C):c.125-49125C>A	Lung cancer [RCV000095107]	uncertain significance	4	95384756	95384756	Human		name
8580159	CV114585	single nucleotide variant	NM_003728.3(UNC5C):c.125-61844A>G	Lung cancer [RCV000095108]	uncertain significance	4	95397475	95397475	Human		name
156279961	CV2206335	single nucleotide variant	NM_003728.4(UNC5C):c.26C>A (p.Ala9Glu)	not specified [RCV004078672]	uncertain significance	4	95548832	95548832	Human		name
329386839	CV2439436	single nucleotide variant	NM_003728.4(UNC5C):c.10G>T (p.Gly4Cys)	not specified [RCV004249726]	uncertain significance	4	95548848	95548848	Human		name
405275949	CV3193160	single nucleotide variant	NM_003728.4(UNC5C):c.291T>C (p.Ser97=)	UNC5C-related disorder [RCV003974326]	benign	4	95335465	95335465	Human		name , trait , alternate_id
401928353	CV2820042	single nucleotide variant	NM_003728.4(UNC5C):c.933G>A (p.Thr311=)	UNC5C-related disorder [RCV003919192]\|not provided [RCV003439421]	likely benign	4	95244987	95244987	Human		name , trait , alternate_id
405274748	CV3199803	single nucleotide variant	NM_003728.4(UNC5C):c.801G>A (p.Thr267=)	UNC5C-related disorder [RCV003973856]	benign	4	95245119	95245119	Human		name , trait , alternate_id
405809928	CV3345043	single nucleotide variant	NM_003728.4(UNC5C):c.38G>A (p.Gly13Glu)	not specified [RCV004482003]	uncertain significance	4	95548820	95548820	Human		name
597721155	CV3632886	single nucleotide variant	NM_003728.4(UNC5C):c.66G>T (p.Met22Ile)	not specified [RCV004887893]	uncertain significance	4	95548792	95548792	Human		name
598191234	CV3925640	single nucleotide variant	NM_003728.4(UNC5C):c.70G>C (p.Val24Leu)	not specified [RCV005288324]	uncertain significance	4	95548788	95548788	Human		name
150456846	CV1248708	single nucleotide variant	NM_003728.4(UNC5C):c.1614G>A (p.Ser538=)	UNC5C-related disorder [RCV003975856]\|not provided [RCV001668884]	benign	4	95219000	95219000	Human		name , trait , alternate_id
401928348	CV2820040	single nucleotide variant	NM_003728.4(UNC5C):c.2514G>A (p.Gly838=)	UNC5C-related disorder [RCV003938999]\|not provided [RCV003439419]	likely benign	4	95170270	95170270	Human		name , trait , alternate_id
401928350	CV2820041	single nucleotide variant	NM_003728.4(UNC5C):c.1524G>A (p.Ser508=)	UNC5C-related disorder [RCV003966407]\|not provided [RCV003439420]	likely benign	4	95219090	95219090	Human		name , trait , alternate_id
405286154	CV3192009	single nucleotide variant	NM_003728.4(UNC5C):c.2709T>C (p.Asp903=)	UNC5C-related disorder [RCV003923939]	benign	4	95169321	95169321	Human		name , trait , alternate_id
405276520	CV3193381	single nucleotide variant	NM_003728.4(UNC5C):c.1812A>C (p.Pro604=)	UNC5C-related disorder [RCV003974548]	benign	4	95206718	95206718	Human		name , trait , alternate_id
405275544	CV3196335	single nucleotide variant	NM_003728.4(UNC5C):c.2221C>T (p.Leu741=)	UNC5C-related disorder [RCV003974185]	likely benign	4	95185112	95185112	Human		name , trait , alternate_id
405275819	CV3196440	single nucleotide variant	NM_003728.4(UNC5C):c.1494G>A (p.Thr498=)	UNC5C-related disorder [RCV003974272]	likely benign	4	95219120	95219120	Human		name , trait , alternate_id
405290733	CV3197125	single nucleotide variant	NM_003728.4(UNC5C):c.2037G>A (p.Ala679=)	UNC5C-related disorder [RCV003984687]	benign	4	95202830	95202830	Human		name , trait , alternate_id
405275804	CV3199438	single nucleotide variant	NM_003728.4(UNC5C):c.2442C>T (p.Thr814=)	UNC5C-related disorder [RCV003916845]	likely benign	4	95182906	95182906	Human		name , trait , alternate_id
405291095	CV3203960	single nucleotide variant	NM_003728.4(UNC5C):c.2448A>G (p.Ser816=)	UNC5C-related disorder [RCV003927364]	likely benign	4	95182900	95182900	Human		name , trait , alternate_id
405281874	CV3216148	single nucleotide variant	NM_003728.4(UNC5C):c.2772C>T (p.Ser924=)	UNC5C-related disorder [RCV003956682]	likely benign	4	95169258	95169258	Human		name , trait , alternate_id
597790628	CV3632887	single nucleotide variant	NM_003728.4(UNC5C):c.103G>A (p.Gly35Ser)	not specified [RCV004876398]	uncertain significance	4	95548755	95548755	Human		name
598191248	CV3925643	single nucleotide variant	NM_003728.4(UNC5C):c.132C>A (p.Asp44Glu)	not specified [RCV005288326]	uncertain significance	4	95335624	95335624	Human		name
616939535	CV4014030	single nucleotide variant	NM_003728.4(UNC5C):c.1374C>T (p.Asp458=)	not provided [RCV005413522]	likely benign	4	95219240	95219240	Human		name
15150927	CV709534	single nucleotide variant	NM_003728.4(UNC5C):c.2670C>T (p.Gly890=)	not provided [RCV000968036]	benign	4	95169360	95169360	Human		name
8631333	CV86494	single nucleotide variant	NM_003728.3(UNC5C):c.2176C>T (p.Leu726=)	Malignant melanoma [RCV000066585]	not provided	4	95185157	95185157	Human		name
156123062	CV2227195	single nucleotide variant	NM_003728.4(UNC5C):c.857C>A (p.Thr286Asn)	not specified [RCV004091804]	uncertain significance	4	95245063	95245063	Human		name
156335997	CV2228475	single nucleotide variant	NM_003728.4(UNC5C):c.686C>T (p.Ala229Val)	not specified [RCV004098441]	uncertain significance	4	95250576	95250576	Human		name
156052949	CV2246363	single nucleotide variant	NM_003728.4(UNC5C):c.631G>C (p.Val211Leu)	not specified [RCV004107802]	uncertain significance	4	95250631	95250631	Human		name
156141832	CV2288592	single nucleotide variant	NM_003728.4(UNC5C):c.340A>T (p.Thr114Ser)	not specified [RCV004152111]	uncertain significance	4	95335416	95335416	Human		name
156263321	CV2329363	single nucleotide variant	NM_003728.4(UNC5C):c.800C>T (p.Thr267Met)	not specified [RCV004187381]	uncertain significance	4	95245120	95245120	Human		name
401773795	CV2691410	single nucleotide variant	NM_003728.4(UNC5C):c.541G>A (p.Glu181Lys)	not specified [RCV004305272]	uncertain significance	4	95278312	95278312	Human		name
405284753	CV3201851	single nucleotide variant	NM_003728.4(UNC5C):c.319G>C (p.Val107Leu)	UNC5C-related disorder [RCV003909374]	benign	4	95335437	95335437	Human		name , trait , alternate_id
405809929	CV3345044	single nucleotide variant	NM_003728.4(UNC5C):c.848G>A (p.Arg283His)	not specified [RCV004482004]	uncertain significance	4	95245072	95245072	Human		name
407462501	CV3489341	single nucleotide variant	NM_003728.4(UNC5C):c.354T>G (p.Ile118Met)	not specified [RCV004687983]	uncertain significance	4	95301742	95301742	Human		name
407462505	CV3489342	single nucleotide variant	NM_003728.4(UNC5C):c.751A>G (p.Thr251Ala)	not specified [RCV004687984]	uncertain significance	4	95250511	95250511	Human		name
407454715	CV3489343	single nucleotide variant	NM_003728.4(UNC5C):c.884G>C (p.Gly295Ala)	not specified [RCV004685194]	uncertain significance	4	95245036	95245036	Human		name
597721142	CV3632883	single nucleotide variant	NM_003728.4(UNC5C):c.382C>T (p.Arg128Cys)	not specified [RCV004887892]	uncertain significance	4	95301714	95301714	Human		name
597721169	CV3632889	single nucleotide variant	NM_003728.4(UNC5C):c.449C>T (p.Ala150Val)	not specified [RCV004887894]	uncertain significance	4	95301647	95301647	Human		name
598274637	CV3925639	single nucleotide variant	NM_003728.4(UNC5C):c.388C>A (p.Gln130Lys)	not specified [RCV005304035]	uncertain significance	4	95301708	95301708	Human		name
598191242	CV3925641	single nucleotide variant	NM_003728.4(UNC5C):c.463A>G (p.Ser155Gly)	not specified [RCV005288325]	uncertain significance	4	95301633	95301633	Human		name
155916475	CV2197446	single nucleotide variant	NM_003728.4(UNC5C):c.2443G>A (p.Val815Met)	not specified [RCV004081181]	uncertain significance	4	95182905	95182905	Human		name
155915066	CV2242904	single nucleotide variant	NM_003728.4(UNC5C):c.2688G>C (p.Trp896Cys)	not specified [RCV004107493]	uncertain significance	4	95169342	95169342	Human		name
156077642	CV2248125	single nucleotide variant	NM_003728.4(UNC5C):c.2587G>A (p.Gly863Ser)	not specified [RCV004117529]	uncertain significance	4	95170197	95170197	Human		name
155922877	CV2251795	single nucleotide variant	NM_003728.4(UNC5C):c.2265C>G (p.Ser755Arg)	not specified [RCV004119786]	uncertain significance	4	95185068	95185068	Human		name
155990028	CV2259761	single nucleotide variant	NM_003728.4(UNC5C):c.1738C>A (p.Pro580Thr)	not specified [RCV004116771]	uncertain significance	4	95206792	95206792	Human		name
156158215	CV2262463	single nucleotide variant	NM_003728.4(UNC5C):c.2389C>T (p.Leu797Phe)	not specified [RCV004128901]	uncertain significance	4	95182959	95182959	Human		name
155977497	CV2266417	single nucleotide variant	NM_003728.4(UNC5C):c.2434A>C (p.Asn812His)	not specified [RCV004131008]	uncertain significance	4	95182914	95182914	Human		name
156122065	CV2276063	single nucleotide variant	NM_003728.4(UNC5C):c.2312G>A (p.Ser771Asn)	not specified [RCV004141737]	uncertain significance	4	95183036	95183036	Human		name
156065512	CV2287371	single nucleotide variant	NM_003728.4(UNC5C):c.2789A>G (p.Gln930Arg)	not specified [RCV004146984]	uncertain significance	4	95169241	95169241	Human		name
156094537	CV2300306	single nucleotide variant	NM_003728.4(UNC5C):c.1025C>T (p.Ala342Val)	not specified [RCV004153258]	uncertain significance	4	95242512	95242512	Human		name
156019041	CV2301731	single nucleotide variant	NM_003728.4(UNC5C):c.2163G>A (p.Met721Ile)	not specified [RCV004156548]	uncertain significance	4	95185170	95185170	Human		name
155911479	CV2303827	single nucleotide variant	NM_003728.4(UNC5C):c.2534C>T (p.Pro845Leu)	not specified [RCV004163664]	uncertain significance	4	95170250	95170250	Human		name
156241454	CV2310205	single nucleotide variant	NM_003728.4(UNC5C):c.1315C>A (p.Pro439Thr)	not specified [RCV004163310]	uncertain significance	4	95219299	95219299	Human		name
156115648	CV2349318	single nucleotide variant	NM_003728.4(UNC5C):c.1154T>C (p.Ile385Thr)	not specified [RCV004199262]	uncertain significance	4	95220131	95220131	Human		name
156126708	CV2351022	single nucleotide variant	NM_003728.4(UNC5C):c.2388A>T (p.Lys796Asn)	not specified [RCV004211846]	uncertain significance	4	95182960	95182960	Human		name
156011696	CV2358764	single nucleotide variant	NM_003728.4(UNC5C):c.1400A>G (p.Asn467Ser)	not specified [RCV004210072]	uncertain significance	4	95219214	95219214	Human		name
156249630	CV2358932	single nucleotide variant	NM_003728.4(UNC5C):c.2401C>G (p.Gln801Glu)	not specified [RCV004212267]	uncertain significance	4	95182947	95182947	Human		name
155910590	CV2366508	single nucleotide variant	NM_003728.4(UNC5C):c.2791T>C (p.Tyr931His)	not specified [RCV004208484]	uncertain significance	4	95169239	95169239	Human		name
156265603	CV2372268	single nucleotide variant	NM_003728.4(UNC5C):c.1666G>A (p.Ala556Thr)	not specified [RCV004217045]	uncertain significance	4	95216191	95216191	Human		name
156219338	CV2393579	single nucleotide variant	NM_003728.4(UNC5C):c.2707G>A (p.Asp903Asn)	not specified [RCV004231395]	uncertain significance	4	95169323	95169323	Human		name
156225289	CV2399613	single nucleotide variant	NM_003728.4(UNC5C):c.2416G>A (p.Gly806Arg)	not specified [RCV004244132]	uncertain significance	4	95182932	95182932	Human		name
329382745	CV2424541	single nucleotide variant	NM_003728.4(UNC5C):c.2225G>A (p.Arg742His)	not specified [RCV004254042]	uncertain significance	4	95185108	95185108	Human		name
329374788	CV2431046	single nucleotide variant	NM_003728.4(UNC5C):c.2582C>T (p.Thr861Met)	not specified [RCV004250416]	uncertain significance	4	95170202	95170202	Human		name
329396759	CV2459014	single nucleotide variant	NM_003728.4(UNC5C):c.2156G>C (p.Arg719Thr)	not specified [RCV004272493]	uncertain significance	4	95185177	95185177	Human		name
401751723	CV2672555	single nucleotide variant	NM_003728.4(UNC5C):c.2452G>C (p.Glu818Gln)	not specified [RCV004287589]	uncertain significance	4	95170332	95170332	Human		name
401734174	CV2694461	single nucleotide variant	NM_003728.4(UNC5C):c.1375G>C (p.Val459Leu)	not specified [RCV004304625]	uncertain significance	4	95219239	95219239	Human		name
401750793	CV2715764	single nucleotide variant	NM_003728.4(UNC5C):c.1318C>G (p.Pro440Ala)	not specified [RCV004328901]	uncertain significance	4	95219296	95219296	Human		name
401728590	CV2729678	single nucleotide variant	NM_003728.4(UNC5C):c.2467G>A (p.Asp823Asn)	not specified [RCV004331938]	uncertain significance	4	95170317	95170317	Human		name
401920057	CV2796394	single nucleotide variant	NM_003728.4(UNC5C):c.2537T>C (p.Leu846Pro)	UNC5C-related disorder [RCV003402449]	uncertain significance	4	95170247	95170247	Human		name , trait , alternate_id
401928346	CV2820039	single nucleotide variant	NM_003728.4(UNC5C):c.2521G>A (p.Ala841Thr)	UNC5C-related disorder [RCV003980923]\|not provided [RCV003439418]	benign	4	95170263	95170263	Human		name , trait , alternate_id
401944157	CV2840515	single nucleotide variant	NM_003728.4(UNC5C):c.1807C>T (p.Arg603Cys)	not provided [RCV003457123]	likely benign	4	95206723	95206723	Human		name
404996683	CV2851465	single nucleotide variant	NM_003728.4(UNC5C):c.2676C>G (p.Ile892Met)	not provided [RCV003491841]	uncertain significance	4	95169354	95169354	Human		name
404996690	CV2851466	single nucleotide variant	NM_003728.4(UNC5C):c.2578C>A (p.Gln860Lys)	not provided [RCV003491842]	uncertain significance	4	95170206	95170206	Human		name
405277034	CV3192571	single nucleotide variant	NM_003728.4(UNC5C):c.1882G>A (p.Ala628Thr)	UNC5C-related disorder [RCV003917311]	benign	4	95206648	95206648	Human		name , trait , alternate_id
405292170	CV3199792	single nucleotide variant	NM_003728.4(UNC5C):c.2065C>G (p.Pro689Ala)	UNC5C-related disorder [RCV003964414]	benign	4	95202802	95202802	Human		name , trait , alternate_id
405255973	CV3208510	single nucleotide variant	NM_003728.4(UNC5C):c.2036C>T (p.Ala679Val)	UNC5C-related disorder [RCV003939597]	likely benign	4	95202831	95202831	Human		name , trait , alternate_id
405293911	CV3210506	single nucleotide variant	NM_003728.4(UNC5C):c.1883C>A (p.Ala628Glu)	UNC5C-related disorder [RCV003932325]	benign	4	95206647	95206647	Human		name , trait , alternate_id
405288027	CV3218088	single nucleotide variant	NM_003728.4(UNC5C):c.2162T>C (p.Met721Thr)	UNC5C-related disorder [RCV003982213]	benign	4	95185171	95185171	Human		name , trait , alternate_id
405809914	CV3345035	single nucleotide variant	NM_003728.4(UNC5C):c.1237A>G (p.Ile413Val)	not specified [RCV004481995]	uncertain significance	4	95220048	95220048	Human		name
405809916	CV3345036	single nucleotide variant	NM_003728.4(UNC5C):c.1450A>C (p.Thr484Pro)	not specified [RCV004481996]	uncertain significance	4	95219164	95219164	Human		name
405809917	CV3345037	single nucleotide variant	NM_003728.4(UNC5C):c.1599T>G (p.Phe533Leu)	not specified [RCV004481997]	uncertain significance	4	95219015	95219015	Human		name
405809919	CV3345038	single nucleotide variant	NM_003728.4(UNC5C):c.1837G>A (p.Ala613Thr)	not specified [RCV004481998]	uncertain significance	4	95206693	95206693	Human		name
405809921	CV3345039	single nucleotide variant	NM_003728.4(UNC5C):c.1918G>A (p.Gly640Arg)	not specified [RCV004481999]	uncertain significance	4	95202949	95202949	Human		name
405809923	CV3345040	single nucleotide variant	NM_003728.4(UNC5C):c.2210G>C (p.Ser737Thr)	not specified [RCV004482000]	uncertain significance	4	95185123	95185123	Human		name
405809924	CV3345041	single nucleotide variant	NM_003728.4(UNC5C):c.2239G>A (p.Asp747Asn)	not specified [RCV004482001]	uncertain significance	4	95185094	95185094	Human		name
405809926	CV3345042	single nucleotide variant	NM_003728.4(UNC5C):c.2462G>A (p.Gly821Asp)	not specified [RCV004482002]	uncertain significance	4	95170322	95170322	Human		name
407462498	CV3489337	single nucleotide variant	NM_003728.4(UNC5C):c.1328C>T (p.Thr443Met)	not specified [RCV004687982]	uncertain significance	4	95219286	95219286	Human		name
407454708	CV3489338	single nucleotide variant	NM_003728.4(UNC5C):c.1559A>G (p.Gln520Arg)	not specified [RCV004685191]	uncertain significance	4	95219055	95219055	Human		name
407454710	CV3489339	single nucleotide variant	NM_003728.4(UNC5C):c.1462G>A (p.Val488Ile)	not specified [RCV004685192]	uncertain significance	4	95219152	95219152	Human		name
407454713	CV3489340	single nucleotide variant	NM_003728.4(UNC5C):c.2542A>C (p.Ile848Leu)	not specified [RCV004685193]	uncertain significance	4	95170242	95170242	Human		name
407454716	CV3489344	single nucleotide variant	NM_003728.4(UNC5C):c.2695C>G (p.Gln899Glu)	not specified [RCV004685195]	uncertain significance	4	95169335	95169335	Human		name
407454720	CV3489346	single nucleotide variant	NM_003728.4(UNC5C):c.2207G>A (p.Gly736Asp)	not specified [RCV004685197]	uncertain significance	4	95185126	95185126	Human		name
407462509	CV3489347	single nucleotide variant	NM_003728.4(UNC5C):c.1310C>T (p.Ala437Val)	not specified [RCV004687985]	uncertain significance	4	95219304	95219304	Human		name
597790624	CV3632885	single nucleotide variant	NM_003728.4(UNC5C):c.1590T>G (p.Cys530Trp)	not specified [RCV004876397]	uncertain significance	4	95219024	95219024	Human		name
597790632	CV3632888	single nucleotide variant	NM_003728.4(UNC5C):c.2780C>G (p.Ala927Gly)	not specified [RCV004876399]	uncertain significance	4	95169250	95169250	Human		name
597790636	CV3632890	single nucleotide variant	NM_003728.4(UNC5C):c.1364C>T (p.Ala455Val)	not specified [RCV004876400]	uncertain significance	4	95219250	95219250	Human		name
597790640	CV3632891	single nucleotide variant	NM_003728.4(UNC5C):c.2671G>A (p.Val891Ile)	not specified [RCV004876401]	uncertain significance	4	95169359	95169359	Human		name
597790642	CV3632892	single nucleotide variant	NM_003728.4(UNC5C):c.2288A>C (p.Glu763Ala)	not specified [RCV004876402]	uncertain significance	4	95183060	95183060	Human		name
597790646	CV3632893	single nucleotide variant	NM_003728.4(UNC5C):c.1465A>C (p.Thr489Pro)	not specified [RCV004876403]	uncertain significance	4	95219149	95219149	Human		name
598274635	CV3925638	single nucleotide variant	NM_003728.4(UNC5C):c.2405T>G (p.Val802Gly)	not specified [RCV005304034]	uncertain significance	4	95182943	95182943	Human		name
598274639	CV3925642	single nucleotide variant	NM_003728.4(UNC5C):c.2545C>T (p.Arg849Trp)	not specified [RCV005304036]	uncertain significance	4	95170239	95170239	Human		name
156369924	CV2263442	single nucleotide variant	NM_173561.3(UNC5CL):c.70G>T (p.Val24Phe)	not specified [RCV004133688]	uncertain significance	6	41035005	41035005	Human		name
401866082	CV2762517	single nucleotide variant	NM_173561.3(UNC5CL):c.40C>G (p.Leu14Val)	not specified [RCV004338052]	uncertain significance	6	41035035	41035035	Human		name
405809936	CV3345048	single nucleotide variant	NM_173561.3(UNC5CL):c.38T>C (p.Phe13Ser)	not specified [RCV004482008]	uncertain significance	6	41035037	41035037	Human		name
156277859	CV2209966	single nucleotide variant	NM_173561.3(UNC5CL):c.143G>T (p.Gly48Val)	not specified [RCV004076408]	uncertain significance	6	41034932	41034932	Human		name
156173638	CV2326864	single nucleotide variant	NM_173561.3(UNC5CL):c.229G>C (p.Val77Leu)	not specified [RCV004176690]	uncertain significance	6	41034846	41034846	Human		name
329372181	CV2443010	single nucleotide variant	NM_173561.3(UNC5CL):c.124G>T (p.Ala42Ser)	not specified [RCV004253601]	uncertain significance	6	41034951	41034951	Human		name
401867521	CV2780487	single nucleotide variant	NM_173561.3(UNC5CL):c.274A>G (p.Met92Val)	not specified [RCV004358182]	likely benign	6	41034801	41034801	Human		name
407454724	CV3489350	single nucleotide variant	NM_173561.3(UNC5CL):c.157G>A (p.Val53Met)	not specified [RCV004685199]	uncertain significance	6	41034918	41034918	Human		name
598191258	CV3925644	single nucleotide variant	NM_173561.3(UNC5CL):c.212C>A (p.Ala71Asp)	not specified [RCV005288327]	uncertain significance	6	41034863	41034863	Human		name
156316146	CV2193013	single nucleotide variant	NM_173561.3(UNC5CL):c.730C>T (p.Arg244Cys)	not specified [RCV004069564]	uncertain significance	6	41033103	41033103	Human		name
156028583	CV2238242	single nucleotide variant	NM_173561.3(UNC5CL):c.784C>G (p.His262Asp)	not specified [RCV004113331]	uncertain significance	6	41033049	41033049	Human		name
156201614	CV2313157	single nucleotide variant	NM_173561.3(UNC5CL):c.653G>A (p.Arg218Gln)	not specified [RCV004161417]	uncertain significance	6	41033914	41033914	Human		name
156075605	CV2331748	single nucleotide variant	NM_173561.3(UNC5CL):c.869G>A (p.Arg290His)	not specified [RCV004184373]	uncertain significance	6	41032964	41032964	Human		name
155978685	CV2335139	single nucleotide variant	NM_173561.3(UNC5CL):c.493G>T (p.Ala165Ser)	not specified [RCV004184670]	uncertain significance	6	41034074	41034074	Human		name
156383563	CV2361601	single nucleotide variant	NM_173561.3(UNC5CL):c.575G>A (p.Arg192His)	not specified [RCV004221227]	uncertain significance	6	41033992	41033992	Human		name
155910682	CV2366586	single nucleotide variant	NM_173561.3(UNC5CL):c.797G>A (p.Arg266His)	not specified [RCV004210604]	uncertain significance	6	41033036	41033036	Human		name
329372723	CV2433995	single nucleotide variant	NM_173561.3(UNC5CL):c.578C>A (p.Thr193Asn)	not specified [RCV004249901]	uncertain significance	6	41033989	41033989	Human		name
329357777	CV2453783	single nucleotide variant	NM_173561.3(UNC5CL):c.515C>G (p.Ser172Cys)	not specified [RCV004269404]	uncertain significance	6	41034052	41034052	Human		name
405809938	CV3345049	single nucleotide variant	NM_173561.3(UNC5CL):c.662G>C (p.Cys221Ser)	not specified [RCV004482009]	uncertain significance	6	41033905	41033905	Human		name
405810046	CV3345050	single nucleotide variant	NM_173561.3(UNC5CL):c.818C>T (p.Thr273Met)	not specified [RCV004482010]	uncertain significance	6	41033015	41033015	Human		name
405809942	CV3345051	single nucleotide variant	NM_173561.3(UNC5CL):c.826G>A (p.Ala276Thr)	not specified [RCV004482011]	uncertain significance	6	41033007	41033007	Human		name
407454722	CV3489348	single nucleotide variant	NM_173561.3(UNC5CL):c.391G>A (p.Val131Met)	not specified [RCV004685198]	uncertain significance	6	41034176	41034176	Human		name
597790650	CV3632896	single nucleotide variant	NM_173561.3(UNC5CL):c.572C>A (p.Ala191Asp)	not specified [RCV004876404]	uncertain significance	6	41033995	41033995	Human		name
597790654	CV3632897	single nucleotide variant	NM_173561.3(UNC5CL):c.764C>T (p.Pro255Leu)	not specified [RCV004876405]	uncertain significance	6	41033069	41033069	Human		name
597721194	CV3632898	single nucleotide variant	NM_173561.3(UNC5CL):c.844A>G (p.Thr282Ala)	not specified [RCV004887896]	uncertain significance	6	41032989	41032989	Human		name
597721206	CV3632899	single nucleotide variant	NM_173561.3(UNC5CL):c.332G>A (p.Arg111His)	not specified [RCV004887897]	uncertain significance	6	41034743	41034743	Human		name
597790658	CV3632901	single nucleotide variant	NM_173561.3(UNC5CL):c.650C>T (p.Ser217Phe)	not specified [RCV004876406]	uncertain significance	6	41033917	41033917	Human		name
597790662	CV3632902	single nucleotide variant	NM_173561.3(UNC5CL):c.304G>A (p.Val102Met)	not specified [RCV004876407]	uncertain significance	6	41034771	41034771	Human		name
597790666	CV3632903	single nucleotide variant	NM_173561.3(UNC5CL):c.665G>A (p.Arg222His)	not specified [RCV004876408]	uncertain significance	6	41033902	41033902	Human		name
597790668	CV3632904	single nucleotide variant	NM_173561.3(UNC5CL):c.922T>C (p.Cys308Arg)	not specified [RCV004876409]	uncertain significance	6	41032911	41032911	Human		name
598274641	CV3925645	single nucleotide variant	NM_173561.3(UNC5CL):c.799A>G (p.Ile267Val)	not specified [RCV005304037]	likely benign	6	41033034	41033034	Human		name
598274645	CV3925647	single nucleotide variant	NM_173561.3(UNC5CL):c.413G>A (p.Arg138Gln)	not specified [RCV005304039]	uncertain significance	6	41034154	41034154	Human		name
598274649	CV3925649	single nucleotide variant	NM_173561.3(UNC5CL):c.695C>T (p.Thr232Ile)	not specified [RCV005304041]	uncertain significance	6	41033138	41033138	Human		name
156379291	CV2207934	single nucleotide variant	NM_173561.3(UNC5CL):c.1485C>G (p.His495Gln)	not specified [RCV004084353]	likely benign	6	41028445	41028445	Human		name
155957551	CV2282084	single nucleotide variant	NM_173561.3(UNC5CL):c.1025G>T (p.Arg342Leu)	not specified [RCV004138830]	uncertain significance	6	41032062	41032062	Human		name
156278460	CV2316688	single nucleotide variant	NM_173561.3(UNC5CL):c.1249C>T (p.Arg417Trp)	not specified [RCV004171918]	uncertain significance	6	41030473	41030473	Human		name
156062568	CV2321008	single nucleotide variant	NM_173561.3(UNC5CL):c.1205C>A (p.Pro402Gln)	not specified [RCV004172801]	uncertain significance	6	41030670	41030670	Human		name
156337584	CV2343072	single nucleotide variant	NM_173561.3(UNC5CL):c.1304C>T (p.Ser435Phe)	not specified [RCV004192669]	uncertain significance	6	41030418	41030418	Human		name
156195033	CV2347408	single nucleotide variant	NM_173561.3(UNC5CL):c.1039C>T (p.Arg347Trp)	not specified [RCV004207246]	uncertain significance	6	41032048	41032048	Human		name
155917518	CV2362326	single nucleotide variant	NM_173561.3(UNC5CL):c.1448G>A (p.Cys483Tyr)	not specified [RCV004212960]	uncertain significance	6	41028482	41028482	Human		name
156043870	CV2381582	single nucleotide variant	NM_173561.3(UNC5CL):c.1024C>T (p.Arg342Cys)	not specified [RCV004232060]	uncertain significance	6	41032063	41032063	Human		name
156390946	CV2384966	single nucleotide variant	NM_173561.3(UNC5CL):c.1184C>T (p.Ala395Val)	not specified [RCV004226194]	uncertain significance	6	41030691	41030691	Human		name
401865309	CV2791602	single nucleotide variant	NM_173561.3(UNC5CL):c.1502C>A (p.Pro501His)	not specified [RCV004358968]	uncertain significance	6	41028428	41028428	Human		name
405809931	CV3345045	single nucleotide variant	NM_173561.3(UNC5CL):c.1238T>C (p.Phe413Ser)	not specified [RCV004482005]	uncertain significance	6	41030484	41030484	Human		name
405809933	CV3345046	single nucleotide variant	NM_173561.3(UNC5CL):c.1333C>T (p.Arg445Trp)	not specified [RCV004482006]	uncertain significance	6	41030389	41030389	Human		name
405809934	CV3345047	single nucleotide variant	NM_173561.3(UNC5CL):c.1442T>C (p.Leu481Pro)	not specified [RCV004482007]	uncertain significance	6	41028488	41028488	Human		name
407462513	CV3489349	single nucleotide variant	NM_173561.3(UNC5CL):c.1250G>A (p.Arg417Gln)	not specified [RCV004687986]	likely benign	6	41030472	41030472	Human		name
407454726	CV3489351	single nucleotide variant	NM_173561.3(UNC5CL):c.1031T>C (p.Phe344Ser)	not specified [RCV004685200]	uncertain significance	6	41032056	41032056	Human		name
597721183	CV3632895	single nucleotide variant	NM_173561.3(UNC5CL):c.1391A>G (p.Gln464Arg)	not specified [RCV004887895]	uncertain significance	6	41028539	41028539	Human		name
597721218	CV3632900	single nucleotide variant	NM_173561.3(UNC5CL):c.1070G>A (p.Cys357Tyr)	not specified [RCV004887898]	uncertain significance	6	41031730	41031730	Human		name
597790672	CV3632905	single nucleotide variant	NM_173561.3(UNC5CL):c.1094T>C (p.Ile365Thr)	not specified [RCV004876410]	uncertain significance	6	41031706	41031706	Human		name
598274643	CV3925646	single nucleotide variant	NM_173561.3(UNC5CL):c.1534C>G (p.Leu512Val)	not specified [RCV005304038]	uncertain significance	6	41028396	41028396	Human		name
598274647	CV3925648	single nucleotide variant	NM_173561.3(UNC5CL):c.1025G>A (p.Arg342His)	not specified [RCV005304040]	uncertain significance	6	41032062	41032062	Human		name

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