Cdc5l Variant Search Result - Rat Genome Database

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86 records found for search term Cdc5l

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405273132	CV3190876	single nucleotide variant	NM_001253.4(CDC5L):c.-7C>T	CDC5L-related disorder [RCV003909442]	likely benign	6	44387817	44387817	Human		name , trait , alternate_id
405273677	CV3214093	single nucleotide variant	NM_001253.4(CDC5L):c.-2A>G	CDC5L-related disorder [RCV003914756]	likely benign	6	44387822	44387822	Human		name , trait , alternate_id
150451967	CV1254896	single nucleotide variant	NM_001253.3(CDC5L):c.-138C>T	not provided [RCV001667955]	benign	6	44387686	44387686	Human		name
150448581	CV1270482	single nucleotide variant	NM_001253.3(CDC5L):c.-162G>T	not provided [RCV001691620]	benign	6	44387662	44387662	Human		name
150432991	CV1231625	single nucleotide variant	NM_001253.4(CDC5L):c.45+77G>A	not provided [RCV001643287]	benign	6	44387945	44387945	Human		name
150474258	CV1263332	single nucleotide variant	NM_001253.4(CDC5L):c.45+94T>C	not provided [RCV001684854]	benign	6	44387962	44387962	Human		name
401750020	CV2736204	single nucleotide variant	NM_001253.4(CDC5L):c.759-4A>G	not provided [RCV003312652]	benign	6	44406319	44406319	Human		name
150511254	CV1229404	single nucleotide variant	NM_001253.4(CDC5L):c.46-121T>G	not provided [RCV001637333]	benign	6	44390147	44390147	Human		name
405273613	CV3199286	single nucleotide variant	NM_001253.4(CDC5L):c.904-10G>A	CDC5L-related disorder [RCV003914236]	likely benign	6	44408434	44408434	Human		name , trait , alternate_id
150336574	CV1171594	single nucleotide variant	NM_001253.4(CDC5L):c.903+263A>G	not provided [RCV001541051]	benign	6	44406730	44406730	Human		name
150460891	CV1231406	single nucleotide variant	NM_001253.4(CDC5L):c.903+304G>A	not provided [RCV001640971]	benign	6	44406771	44406771	Human		name
150475512	CV1263513	single nucleotide variant	NM_001253.4(CDC5L):c.150-249T>A	not provided [RCV001685036]	benign	6	44392418	44392418	Human		name
150462613	CV1264762	single nucleotide variant	NM_001253.4(CDC5L):c.149+336T>G	not provided [RCV001682386]	benign	6	44390707	44390707	Human		name
150446039	CV1271808	single nucleotide variant	NM_001253.4(CDC5L):c.311+115A>G	not provided [RCV001691222]	benign	6	44392943	44392943	Human		name
150454930	CV1277095	single nucleotide variant	NM_001253.4(CDC5L):c.904-262T>C	not provided [RCV001708887]	benign	6	44408182	44408182	Human		name
150506927	CV1211046	single nucleotide variant	NM_001253.4(CDC5L):c.1569+194G>A	not provided [RCV001596164]	benign	6	44424777	44424777	Human		name
150505671	CV1213584	single nucleotide variant	NM_001253.4(CDC5L):c.2091+235T>C	not provided [RCV001595840]	benign	6	44430145	44430145	Human		name
150469674	CV1219113	single nucleotide variant	NM_001253.4(CDC5L):c.2304+132A>G	not provided [RCV001614865]	benign	6	44445999	44445999	Human		name
150455645	CV1220490	single nucleotide variant	NM_001253.4(CDC5L):c.1241+256C>A	not provided [RCV001612583]	benign	6	44419853	44419853	Human		name
150480197	CV1221922	single nucleotide variant	NM_001253.4(CDC5L):c.1405-140A>C	not provided [RCV001616718]	benign	6	44424279	44424279	Human		name
150454411	CV1232266	single nucleotide variant	NM_001253.4(CDC5L):c.1404+218G>T	not provided [RCV001648279]	benign	6	44423027	44423027	Human		name
150449944	CV1232615	single nucleotide variant	NM_001253.4(CDC5L):c.1894-169G>C	not provided [RCV001647690]	benign	6	44429544	44429544	Human		name
150470285	CV1247962	single nucleotide variant	NM_001253.4(CDC5L):c.1241+183C>G	not provided [RCV001670998]	benign	6	44419780	44419780	Human		name
150445166	CV1269391	single nucleotide variant	NM_001253.4(CDC5L):c.1570-205G>A	not provided [RCV001691078]	benign	6	44425898	44425898	Human		name
405275430	CV3211149	single nucleotide variant	NM_001253.4(CDC5L):c.66G>A (p.Ala22=)	CDC5L-related disorder [RCV003937137]	likely benign	6	44390288	44390288	Human		name , trait , alternate_id
150476260	CV1271309	single nucleotide variant	NM_001253.4(CDC5L):c.279G>A (p.Ala93=)	not provided [RCV001696132]	benign	6	44392796	44392796	Human		name
401904659	CV2802803	single nucleotide variant	NM_001253.4(CDC5L):c.147A>G (p.Arg49=)	CDC5L-related disorder [RCV003427763]	uncertain significance	6	44390369	44390369	Human		name , trait , alternate_id
405271335	CV3190052	single nucleotide variant	NM_001253.4(CDC5L):c.237A>G (p.Pro79=)	CDC5L-related disorder [RCV003897091]	likely benign	6	44392754	44392754	Human		name , trait , alternate_id
150466098	CV1218132	single nucleotide variant	NM_001253.4(CDC5L):c.708C>T (p.Asp236=)	not provided [RCV001614258]	benign	6	44403977	44403977	Human		name
401750012	CV2736203	single nucleotide variant	NM_001253.4(CDC5L):c.438G>A (p.Glu146=)	not provided [RCV003312651]	benign	6	44393572	44393572	Human		name
405275439	CV3204547	single nucleotide variant	NM_001253.4(CDC5L):c.526T>C (p.Leu176=)	CDC5L-related disorder [RCV003937324]	likely benign	6	44396427	44396427	Human		name , trait , alternate_id
405274433	CV3213920	single nucleotide variant	NM_001253.4(CDC5L):c.915A>G (p.Ala305=)	CDC5L-related disorder [RCV003926774]	benign	6	44408455	44408455	Human		name , trait , alternate_id
408378488	CV3512298	single nucleotide variant	NM_001253.4(CDC5L):c.396A>G (p.Pro132=)	CDC5L-related disorder [RCV004752230]	likely benign	6	44393530	44393530	Human		name , trait , alternate_id
150500993	CV1213264	single nucleotide variant	NM_001253.4(CDC5L):c.2163T>A (p.Leu721=)	not provided [RCV001594676]	benign	6	44445726	44445726	Human		name
155959870	CV2390597	single nucleotide variant	NM_001253.4(CDC5L):c.211C>G (p.Leu71Val)	not specified [RCV004239123]	uncertain significance	6	44392728	44392728	Human		name
405271289	CV3189716	single nucleotide variant	NM_001253.4(CDC5L):c.1548T>C (p.Ala516=)	CDC5L-related disorder [RCV003896765]	likely benign	6	44424562	44424562	Human		name , trait , alternate_id
405275074	CV3214852	single nucleotide variant	NM_001253.4(CDC5L):c.1500G>A (p.Lys500=)	CDC5L-related disorder [RCV003934262]	likely benign	6	44424514	44424514	Human		name , trait , alternate_id
405277739	CV3216260	single nucleotide variant	NM_001253.4(CDC5L):c.1140A>G (p.Lys380=)	CDC5L-related disorder [RCV003956772]	likely benign	6	44419496	44419496	Human		name , trait , alternate_id
598167724	CV3947130	single nucleotide variant	NM_001253.4(CDC5L):c.1494C>T (p.Ala498=)	not specified [RCV005308113]	likely benign	6	44424508	44424508	Human		name
15161747	CV710543	single nucleotide variant	NM_001253.4(CDC5L):c.1854T>C (p.His618=)	not provided [RCV000970145]	benign	6	44426685	44426685	Human		name
8626221	CV81365	single nucleotide variant	NM_001253.3(CDC5L):c.1416C>T (p.Ser472=)	Malignant melanoma [RCV000061443]	not provided	6	44424430	44424430	Human		name
156226387	CV2226433	single nucleotide variant	NM_001253.4(CDC5L):c.605G>A (p.Arg202Lys)	not specified [RCV004099646]	uncertain significance	6	44403874	44403874	Human		name
156251286	CV2232286	single nucleotide variant	NM_001253.4(CDC5L):c.445C>T (p.Leu149Phe)	not specified [RCV004105066]	uncertain significance	6	44396346	44396346	Human		name
156088167	CV2290662	single nucleotide variant	NM_001253.4(CDC5L):c.775G>A (p.Asp259Asn)	not specified [RCV004149193]	uncertain significance	6	44406339	44406339	Human		name
155961950	CV2311975	single nucleotide variant	NM_001253.4(CDC5L):c.605G>C (p.Arg202Thr)	not specified [RCV004170792]	uncertain significance	6	44403874	44403874	Human		name
329349463	CV2435756	single nucleotide variant	NM_001253.4(CDC5L):c.424A>G (p.Ile142Val)	not specified [RCV004253385]	uncertain significance	6	44393558	44393558	Human		name
329349536	CV2437818	single nucleotide variant	NM_001253.4(CDC5L):c.650A>C (p.Glu217Ala)	not specified [RCV004261114]	uncertain significance	6	44403919	44403919	Human		name
401743939	CV2679372	single nucleotide variant	NM_001253.4(CDC5L):c.586A>T (p.Ile196Leu)	not specified [RCV004285903]	uncertain significance	6	44403855	44403855	Human		name
597788189	CV3644933	single nucleotide variant	NM_001253.4(CDC5L):c.713A>G (p.Asp238Gly)	not specified [RCV004901416]	uncertain significance	6	44403982	44403982	Human		name
598167712	CV3947128	single nucleotide variant	NM_001253.4(CDC5L):c.299A>G (p.Tyr100Cys)	not specified [RCV005308111]	uncertain significance	6	44392816	44392816	Human		name
598167729	CV3947131	single nucleotide variant	NM_001253.4(CDC5L):c.802A>G (p.Lys268Glu)	not specified [RCV005308114]	uncertain significance	6	44406366	44406366	Human		name
13798388	CV551297	single nucleotide variant	NM_001253.4(CDC5L):c.698A>G (p.Gln233Arg)	not provided [RCV000678307]	uncertain significance	6	44403967	44403967	Human		name
15121336	CV750107	single nucleotide variant	NM_001253.4(CDC5L):c.929T>C (p.Val310Ala)	CDC5L-related disorder [RCV003923257]\|not provided [RCV000918466]	likely benign	6	44408469	44408469	Human		name , trait , alternate_id
156307425	CV2252848	single nucleotide variant	NM_001253.4(CDC5L):c.1946A>T (p.His649Leu)	not specified [RCV004120459]	uncertain significance	6	44429765	44429765	Human		name
12791318	CV226085	single nucleotide variant	NM_001253.4(CDC5L):c.1802A>G (p.Lys601Arg)	Congenital anomaly of kidney and urinary tract [RCV000416577]	uncertain significance	6	44426633	44426633	Human	1	name
156144963	CV2292358	single nucleotide variant	NM_001253.4(CDC5L):c.1334G>C (p.Arg445Pro)	not specified [RCV004150166]	uncertain significance	6	44422739	44422739	Human		name
155908815	CV2307153	single nucleotide variant	NM_001253.4(CDC5L):c.2180G>A (p.Arg727His)	not specified [RCV004159629]	uncertain significance	6	44445743	44445743	Human		name
156382925	CV2363041	single nucleotide variant	NM_001253.4(CDC5L):c.2225T>C (p.Ile742Thr)	not specified [RCV004211175]	uncertain significance	6	44445788	44445788	Human		name
156385516	CV2364491	single nucleotide variant	NM_001253.4(CDC5L):c.1025A>G (p.Asn342Ser)	not specified [RCV004217361]	uncertain significance	6	44408565	44408565	Human		name
155995508	CV2375824	single nucleotide variant	NM_001253.4(CDC5L):c.2249G>A (p.Arg750His)	not specified [RCV004224404]	uncertain significance	6	44445812	44445812	Human		name
156042609	CV2387856	single nucleotide variant	NM_001253.4(CDC5L):c.2236C>T (p.His746Tyr)	not specified [RCV004236412]	likely benign	6	44445799	44445799	Human		name
156223925	CV2395047	single nucleotide variant	NM_001253.4(CDC5L):c.1316C>T (p.Pro439Leu)	not specified [RCV004236733]	uncertain significance	6	44422721	44422721	Human		name
329349574	CV2427549	single nucleotide variant	NM_001253.4(CDC5L):c.1562G>A (p.Arg521Gln)	not specified [RCV004250187]	uncertain significance	6	44424576	44424576	Human		name
401747697	CV2691100	single nucleotide variant	NM_001253.4(CDC5L):c.1587G>T (p.Glu529Asp)	not specified [RCV004301097]	uncertain significance	6	44426120	44426120	Human		name
401745408	CV2712024	single nucleotide variant	NM_001253.4(CDC5L):c.2248C>T (p.Arg750Cys)	not specified [RCV004311445]	uncertain significance	6	44445811	44445811	Human		name
401902685	CV2801323	single nucleotide variant	NM_001253.4(CDC5L):c.1745T>G (p.Met582Arg)	CDC5L-related disorder [RCV003397564]	uncertain significance	6	44426576	44426576	Human		name , trait , alternate_id
401903406	CV2802967	single nucleotide variant	NM_001253.4(CDC5L):c.1277G>A (p.Arg426Gln)	CDC5L-related disorder [RCV003412222]	uncertain significance	6	44422682	44422682	Human		name , trait , alternate_id
405274477	CV3203752	single nucleotide variant	NM_001253.4(CDC5L):c.1376A>G (p.Tyr459Cys)	CDC5L-related disorder [RCV003927338]	benign	6	44422781	44422781	Human		name , trait , alternate_id
405276167	CV3203966	single nucleotide variant	NM_001253.4(CDC5L):c.2160G>C (p.Leu720Phe)	CDC5L-related disorder [RCV003942120]	benign	6	44445723	44445723	Human		name , trait , alternate_id
405774351	CV3296276	single nucleotide variant	NM_001253.4(CDC5L):c.1374C>G (p.Asp458Glu)	not specified [RCV004435841]	uncertain significance	6	44422779	44422779	Human		name
405774356	CV3296277	single nucleotide variant	NM_001253.4(CDC5L):c.1853A>C (p.His618Pro)	not specified [RCV004435842]	uncertain significance	6	44426684	44426684	Human		name
407482031	CV3425168	single nucleotide variant	NM_001253.4(CDC5L):c.1688C>T (p.Pro563Leu)	CDC5L-related disorder [RCV004750971]\|not specified [RCV004609967]	uncertain significance	6	44426519	44426519	Human		name , trait , alternate_id
407481783	CV3425169	single nucleotide variant	NM_001253.4(CDC5L):c.2110A>G (p.Thr704Ala)	not specified [RCV004606729]	uncertain significance	6	44445673	44445673	Human		name
407481789	CV3425170	single nucleotide variant	NM_001253.4(CDC5L):c.2042A>G (p.Asn681Ser)	not specified [RCV004606730]	uncertain significance	6	44429861	44429861	Human		name
407481795	CV3425171	single nucleotide variant	NM_001253.4(CDC5L):c.1588C>G (p.Arg530Gly)	not specified [RCV004606731]	uncertain significance	6	44426121	44426121	Human		name
407481802	CV3425172	single nucleotide variant	NM_001253.4(CDC5L):c.2026C>T (p.Arg676Cys)	not specified [RCV004606732]	uncertain significance	6	44429845	44429845	Human		name
597788154	CV3644924	single nucleotide variant	NM_001253.4(CDC5L):c.2050A>G (p.Ser684Gly)	not specified [RCV004901407]	uncertain significance	6	44429869	44429869	Human		name
597788158	CV3644925	single nucleotide variant	NM_001253.4(CDC5L):c.1369G>A (p.Ala457Thr)	not specified [RCV004901408]	uncertain significance	6	44422774	44422774	Human		name
597788162	CV3644926	single nucleotide variant	NM_001253.4(CDC5L):c.1607G>A (p.Arg536Gln)	not specified [RCV004901409]	uncertain significance	6	44426140	44426140	Human		name
597788166	CV3644927	single nucleotide variant	NM_001253.4(CDC5L):c.1535T>C (p.Ile512Thr)	not specified [RCV004901410]	uncertain significance	6	44424549	44424549	Human		name
597788171	CV3644928	single nucleotide variant	NM_001253.4(CDC5L):c.2185A>G (p.Met729Val)	not specified [RCV004901411]	uncertain significance	6	44445748	44445748	Human		name
597788174	CV3644929	single nucleotide variant	NM_001253.4(CDC5L):c.1189C>T (p.Pro397Ser)	not specified [RCV004901412]	uncertain significance	6	44419545	44419545	Human		name
597788185	CV3644932	single nucleotide variant	NM_001253.4(CDC5L):c.2066T>C (p.Ile689Thr)	not specified [RCV004901415]	uncertain significance	6	44429885	44429885	Human		name
598167733	CV3947132	single nucleotide variant	NM_001253.4(CDC5L):c.1109T>C (p.Met370Thr)	not specified [RCV005308115]	uncertain significance	6	44419465	44419465	Human		name
14696510	CV622104	single nucleotide variant	NM_001253.4(CDC5L):c.2014C>T (p.Pro672Ser)	not provided [RCV000782186]	uncertain significance	6	44429833	44429833	Human		name
8632089	CV87295	single nucleotide variant	NM_001253.3(CDC5L):c.1321A>G (p.Arg441Gly)	Malignant melanoma [RCV000067386]	not provided	6	44422726	44422726	Human		name

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