Nckap5l Variant Search Result - Rat Genome Database

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154 records found for search term Nckap5l

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405797785	CV3347374	single nucleotide variant	NM_001037806.4(NCKAP5L):c.21G>C (p.Gln7His)	not specified [RCV004476299]	uncertain significance	12	49804024	49804024	Human		name
598217274	CV4003722	single nucleotide variant	NM_001037806.4(NCKAP5L):c.16G>A (p.Asp6Asn)	not specified [RCV005379035]	uncertain significance	12	49804029	49804029	Human		name
156087096	CV2299090	single nucleotide variant	NM_001037806.4(NCKAP5L):c.28G>A (p.Gly10Arg)	not specified [RCV004152451]	uncertain significance	12	49804017	49804017	Human		name
407488524	CV3458400	single nucleotide variant	NM_001037806.4(NCKAP5L):c.95A>G (p.Glu32Gly)	not specified [RCV004641315]	uncertain significance	12	49803950	49803950	Human		name
156055433	CV2320539	single nucleotide variant	NM_001037806.4(NCKAP5L):c.295A>C (p.Met99Leu)	not specified [RCV004172164]	uncertain significance	12	49801904	49801904	Human		name
329373053	CV2439261	single nucleotide variant	NM_001037806.4(NCKAP5L):c.132C>G (p.Asn44Lys)	not specified [RCV004255543]	uncertain significance	12	49803157	49803157	Human		name
401761182	CV2689055	single nucleotide variant	NM_001037806.4(NCKAP5L):c.283C>T (p.Arg95Trp)	not specified [RCV004305827]	uncertain significance	12	49801916	49801916	Human		name
405797623	CV3347320	single nucleotide variant	NM_001037806.4(NCKAP5L):c.112C>T (p.Arg38Trp)	not specified [RCV004476245]	uncertain significance	12	49803933	49803933	Human		name
597649450	CV3558603	single nucleotide variant	NM_001037806.4(NCKAP5L):c.181T>A (p.Cys61Ser)	not specified [RCV004826665]	uncertain significance	12	49803108	49803108	Human		name
597649485	CV3558607	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2649C>T (p.Ile883=)	not specified [RCV004826669]	likely benign	12	49795211	49795211	Human		name
598253237	CV4003724	single nucleotide variant	NM_001037806.4(NCKAP5L):c.209T>C (p.Val70Ala)	not specified [RCV005385305]	uncertain significance	12	49802980	49802980	Human		name
15193503	CV725134	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2244G>A (p.Gly748=)	not provided [RCV000888965]	benign	12	49795616	49795616	Human		name
15179142	CV725135	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1482C>T (p.Asp494=)	not provided [RCV000885224]	benign	12	49796378	49796378	Human		name
8634704	CV89924	single nucleotide variant	NM_001037806.3(NCKAP5L):c.2850C>T (p.Leu950=)	Malignant melanoma [RCV000070021]	not provided	12	49795010	49795010	Human		name
155960722	CV2204330	single nucleotide variant	NM_001037806.4(NCKAP5L):c.442G>A (p.Gly148Arg)	not specified [RCV004079154]	uncertain significance	12	49798373	49798373	Human		name
155931402	CV2221025	single nucleotide variant	NM_001037806.4(NCKAP5L):c.721G>C (p.Ala241Pro)	not specified [RCV004092704]	uncertain significance	12	49797139	49797139	Human		name
155977567	CV2246872	single nucleotide variant	NM_001037806.4(NCKAP5L):c.655C>T (p.Pro219Ser)	not specified [RCV004112679]	uncertain significance	12	49797205	49797205	Human		name
156362398	CV2265520	single nucleotide variant	NM_001037806.4(NCKAP5L):c.400T>G (p.Ser134Ala)	not specified [RCV004124272]	uncertain significance	12	49798415	49798415	Human		name
156293644	CV2321332	single nucleotide variant	NM_001037806.4(NCKAP5L):c.530T>C (p.Leu177Pro)	not specified [RCV004177337]	uncertain significance	12	49797330	49797330	Human		name
155933944	CV2372366	single nucleotide variant	NM_001037806.4(NCKAP5L):c.347C>G (p.Pro116Arg)	not specified [RCV004217133]	uncertain significance	12	49801852	49801852	Human		name
156143432	CV2393574	single nucleotide variant	NM_001037806.4(NCKAP5L):c.422C>T (p.Pro141Leu)	not specified [RCV004231390]	uncertain significance	12	49798393	49798393	Human		name
329395613	CV2452399	single nucleotide variant	NM_001037806.4(NCKAP5L):c.545C>T (p.Pro182Leu)	not specified [RCV004272716]	uncertain significance	12	49797315	49797315	Human		name
401763520	CV2714581	single nucleotide variant	NM_001037806.4(NCKAP5L):c.739G>T (p.Gly247Cys)	not specified [RCV004318090]	uncertain significance	12	49797121	49797121	Human		name
405759592	CV3347473	single nucleotide variant	NM_001037806.4(NCKAP5L):c.332C>T (p.Thr111Met)	not specified [RCV004468382]	uncertain significance	12	49801867	49801867	Human		name
405759733	CV3347497	single nucleotide variant	NM_001037806.4(NCKAP5L):c.350A>T (p.Gln117Leu)	not specified [RCV004468406]	uncertain significance	12	49801849	49801849	Human		name
405760014	CV3347545	single nucleotide variant	NM_001037806.4(NCKAP5L):c.542C>G (p.Ser181Cys)	not specified [RCV004468454]	uncertain significance	12	49797318	49797318	Human		name
405760037	CV3347549	single nucleotide variant	NM_001037806.4(NCKAP5L):c.695C>T (p.Pro232Leu)	not specified [RCV004468458]	uncertain significance	12	49797165	49797165	Human		name
407488508	CV3458391	single nucleotide variant	NM_001037806.4(NCKAP5L):c.926A>G (p.Asn309Ser)	not specified [RCV004641311]	uncertain significance	12	49796934	49796934	Human		name
407521399	CV3458394	single nucleotide variant	NM_001037806.4(NCKAP5L):c.986G>A (p.Gly329Asp)	not specified [RCV004652515]	uncertain significance	12	49796874	49796874	Human		name
407488520	CV3458398	single nucleotide variant	NM_001037806.4(NCKAP5L):c.554G>A (p.Arg185Gln)	not specified [RCV004641314]	uncertain significance	12	49797306	49797306	Human		name
597649422	CV3558600	single nucleotide variant	NM_001037806.4(NCKAP5L):c.505C>T (p.Pro169Ser)	not specified [RCV004826662]	uncertain significance	12	49797355	49797355	Human		name
597649402	CV3562489	single nucleotide variant	NM_001037806.4(NCKAP5L):c.967C>T (p.Arg323Cys)	not specified [RCV004826660]	uncertain significance	12	49796893	49796893	Human		name
598253221	CV4003709	single nucleotide variant	NM_001037806.4(NCKAP5L):c.814C>T (p.Arg272Trp)	not specified [RCV005385302]	uncertain significance	12	49797046	49797046	Human		name
598217219	CV4003711	single nucleotide variant	NM_001037806.4(NCKAP5L):c.437C>A (p.Pro146His)	not specified [RCV005379026]	uncertain significance	12	49798378	49798378	Human		name
156035564	CV2208189	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2752G>A (p.Ala918Thr)	not specified [RCV004088653]	uncertain significance	12	49795108	49795108	Human		name
156122712	CV2227158	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2584C>T (p.Pro862Ser)	not specified [RCV004091769]	likely benign	12	49795276	49795276	Human		name
156157034	CV2266259	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1675A>G (p.Ile559Val)	not specified [RCV004128820]	uncertain significance	12	49796185	49796185	Human		name
156114744	CV2268641	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2748C>G (p.Ser916Arg)	not specified [RCV004124046]	uncertain significance	12	49795112	49795112	Human		name
156066286	CV2270767	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2540G>A (p.Gly847Asp)	not specified [RCV004131825]	uncertain significance	12	49795320	49795320	Human		name
156062319	CV2277190	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2545C>T (p.Pro849Ser)	not specified [RCV004142827]	uncertain significance	12	49795315	49795315	Human		name
155996941	CV2277463	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1904G>A (p.Arg635His)	not specified [RCV004144865]	uncertain significance	12	49795956	49795956	Human		name
155989189	CV2285641	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2380C>G (p.Pro794Ala)	not specified [RCV004141503]	uncertain significance	12	49795480	49795480	Human		name
156271697	CV2290380	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2407A>G (p.Ser803Gly)	not specified [RCV004154804]	uncertain significance	12	49795453	49795453	Human		name
156070702	CV2295831	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2488C>A (p.Pro830Thr)	not specified [RCV004151746]	uncertain significance	12	49795372	49795372	Human		name
155904089	CV2298741	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1772T>C (p.Val591Ala)	not specified [RCV004156306]	uncertain significance	12	49796088	49796088	Human		name
156087069	CV2299089	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2582C>T (p.Thr861Ile)	not specified [RCV004152450]	uncertain significance	12	49795278	49795278	Human		name
155955705	CV2303941	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2124G>A (p.Met708Ile)	not specified [RCV004168214]	uncertain significance	12	49795736	49795736	Human		name
155957713	CV2304189	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2863A>G (p.Lys955Glu)	not specified [RCV004170213]	uncertain significance	12	49794997	49794997	Human		name
156020197	CV2309477	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1390A>G (p.Thr464Ala)	not specified [RCV004158881]	likely benign	12	49796470	49796470	Human		name
156262549	CV2319795	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2402C>T (p.Ala801Val)	not specified [RCV004187323]	uncertain significance	12	49795458	49795458	Human		name
156355926	CV2320687	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2980C>T (p.Arg994Trp)	not specified [RCV004179046]	uncertain significance	12	49794880	49794880	Human		name
156360330	CV2325003	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2401G>T (p.Ala801Ser)	not specified [RCV004175553]	uncertain significance	12	49795459	49795459	Human		name
156082149	CV2333943	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1628C>T (p.Ser543Phe)	not specified [RCV004183475]	uncertain significance	12	49796232	49796232	Human		name
155922800	CV2347384	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2617G>A (p.Gly873Ser)	not specified [RCV004207224]	uncertain significance	12	49795243	49795243	Human		name
156077021	CV2350999	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1253G>A (p.Gly418Asp)	not specified [RCV004211824]	uncertain significance	12	49796607	49796607	Human		name
155984155	CV2367870	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2986C>T (p.Arg996Trp)	not specified [RCV004222973]	uncertain significance	12	49794874	49794874	Human		name
156390717	CV2383342	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2612G>A (p.Ser871Asn)	not specified [RCV004222378]	uncertain significance	12	49795248	49795248	Human		name
155961462	CV2388042	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2938C>T (p.Arg980Trp)	not specified [RCV004241173]	uncertain significance	12	49794922	49794922	Human		name
155960383	CV2390676	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2618G>A (p.Gly873Asp)	not specified [RCV004239192]	uncertain significance	12	49795242	49795242	Human		name
329367807	CV2427569	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1677T>G (p.Ile559Met)	not specified [RCV004250205]	uncertain significance	12	49796183	49796183	Human		name
329398968	CV2428607	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2077G>A (p.Glu693Lys)	not specified [RCV004255413]	uncertain significance	12	49795783	49795783	Human		name
329373021	CV2434076	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2032G>A (p.Ala678Thr)	not specified [RCV004249976]	uncertain significance	12	49795828	49795828	Human		name
329377601	CV2435973	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2798G>A (p.Arg933His)	not specified [RCV004255195]	uncertain significance	12	49795062	49795062	Human		name
329366539	CV2445809	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2719G>A (p.Ala907Thr)	not specified [RCV004259864]	likely benign	12	49795141	49795141	Human		name
329373851	CV2447440	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2167G>C (p.Gly723Arg)	not specified [RCV004262714]	uncertain significance	12	49795693	49795693	Human		name
329373376	CV2456069	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1547C>T (p.Ala516Val)	not specified [RCV004272966]	uncertain significance	12	49796313	49796313	Human		name
401752010	CV2703198	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1438C>T (p.Leu480Phe)	not specified [RCV004315260]	uncertain significance	12	49796422	49796422	Human		name
401721584	CV2710045	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1613C>A (p.Pro538Gln)	not specified [RCV004315106]	uncertain significance	12	49796247	49796247	Human		name
401762869	CV2720110	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2375G>A (p.Arg792His)	not specified [RCV004323674]	uncertain significance	12	49795485	49795485	Human		name
401743676	CV2726142	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1588C>G (p.Pro530Ala)	not specified [RCV004326622]	uncertain significance	12	49796272	49796272	Human		name
401751680	CV2727101	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2915T>C (p.Met972Thr)	not specified [RCV004325467]	uncertain significance	12	49794945	49794945	Human		name
401757819	CV2731473	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1853C>G (p.Pro618Arg)	not specified [RCV004330827]	uncertain significance	12	49796007	49796007	Human		name
401867819	CV2767091	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2249G>A (p.Arg750Gln)	not specified [RCV004347493]	uncertain significance	12	49795611	49795611	Human		name
405797608	CV3347314	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1097C>T (p.Ala366Val)	not specified [RCV004476239]	uncertain significance	12	49796763	49796763	Human		name
405797621	CV3347319	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1112C>T (p.Ser371Phe)	not specified [RCV004476244]	uncertain significance	12	49796748	49796748	Human		name
405797632	CV3347323	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1133A>C (p.Lys378Thr)	not specified [RCV004476248]	uncertain significance	12	49796727	49796727	Human		name
405797675	CV3347337	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1451C>T (p.Ser484Leu)	not specified [RCV004476262]	uncertain significance	12	49796409	49796409	Human		name
405797678	CV3347338	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1454G>A (p.Arg485Gln)	not specified [RCV004476263]	uncertain significance	12	49796406	49796406	Human		name
405797694	CV3347343	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1613C>T (p.Pro538Leu)	not specified [RCV004476268]	uncertain significance	12	49796247	49796247	Human		name
405797739	CV3347358	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1800C>G (p.Ser600Arg)	not specified [RCV004476283]	uncertain significance	12	49796060	49796060	Human		name
405797748	CV3347361	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2086C>T (p.Arg696Trp)	not specified [RCV004476286]	uncertain significance	12	49795774	49795774	Human		name
405797767	CV3347368	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2176C>T (p.Arg726Trp)	not specified [RCV004476293]	uncertain significance	12	49795684	49795684	Human		name
405797776	CV3347371	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2179G>T (p.Gly727Trp)	not specified [RCV004476296]	uncertain significance	12	49795681	49795681	Human		name
405797799	CV3347379	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2261C>G (p.Ser754Cys)	not specified [RCV004476304]	uncertain significance	12	49795599	49795599	Human		name
405797805	CV3347381	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2264A>G (p.His755Arg)	not specified [RCV004476306]	uncertain significance	12	49795596	49795596	Human		name
405797899	CV3347412	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2788G>T (p.Ala930Ser)	not specified [RCV004476337]	uncertain significance	12	49795072	49795072	Human		name
405798239	CV3347419	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2803A>G (p.Thr935Ala)	not specified [RCV004476344]	uncertain significance	12	49795057	49795057	Human		name
405798216	CV3347427	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2852G>A (p.Arg951Gln)	not specified [RCV004476352]	uncertain significance	12	49795008	49795008	Human		name
405798207	CV3347430	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2855G>A (p.Arg952Lys)	not specified [RCV004476355]	likely benign	12	49795005	49795005	Human		name
407488503	CV3458389	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2492G>T (p.Gly831Val)	not specified [RCV004641310]	likely benign	12	49795368	49795368	Human		name
407521392	CV3458390	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2996G>A (p.Gly999Asp)	not specified [RCV004652513]	uncertain significance	12	49794864	49794864	Human		name
407488515	CV3458395	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1048C>T (p.Leu350Phe)	not specified [RCV004641313]	uncertain significance	12	49796812	49796812	Human		name
407521402	CV3458396	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2366A>C (p.Gln789Pro)	not specified [RCV004652516]	uncertain significance	12	49795494	49795494	Human		name
407521408	CV3458399	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2111G>A (p.Ser704Asn)	not specified [RCV004652518]	uncertain significance	12	49795749	49795749	Human		name
407521411	CV3458401	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2432C>T (p.Pro811Leu)	not specified [RCV004652519]	uncertain significance	12	49795428	49795428	Human		name
407521418	CV3458403	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1678C>A (p.Leu560Met)	not specified [RCV004652521]	uncertain significance	12	49796182	49796182	Human		name
407521423	CV3458404	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1036G>A (p.Ala346Thr)	not specified [RCV004652522]	uncertain significance	12	49796824	49796824	Human		name
597649432	CV3558601	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2222C>T (p.Pro741Leu)	not specified [RCV004826663]	uncertain significance	12	49795638	49795638	Human		name
597649460	CV3558604	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2708G>A (p.Arg903Gln)	not specified [RCV004826666]	uncertain significance	12	49795152	49795152	Human		name
597649467	CV3558605	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1335G>C (p.Gln445His)	not specified [RCV004826667]	uncertain significance	12	49796525	49796525	Human		name
597649122	CV3562480	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1844A>G (p.Tyr615Cys)	not specified [RCV004826651]	uncertain significance	12	49796016	49796016	Human		name
597649131	CV3562481	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2482C>T (p.Pro828Ser)	not specified [RCV004826652]	uncertain significance	12	49795378	49795378	Human		name
597649139	CV3562482	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1421C>T (p.Pro474Leu)	not specified [RCV004826653]	uncertain significance	12	49796439	49796439	Human		name
597649155	CV3562484	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1513G>A (p.Gly505Ser)	not specified [RCV004826655]	uncertain significance	12	49796347	49796347	Human		name
598217215	CV4003710	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2842T>A (p.Ser948Thr)	not specified [RCV005379025]	uncertain significance	12	49795018	49795018	Human		name
598217225	CV4003712	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1900G>A (p.Gly634Ser)	not specified [RCV005379027]	uncertain significance	12	49795960	49795960	Human		name
598217239	CV4003714	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1852C>T (p.Pro618Ser)	not specified [RCV005379029]	uncertain significance	12	49796008	49796008	Human		name
598217244	CV4003715	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1394C>T (p.Ser465Leu)	not specified [RCV005379030]	uncertain significance	12	49796466	49796466	Human		name
598217251	CV4003716	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2279G>A (p.Arg760Gln)	not specified [RCV005379031]	uncertain significance	12	49795581	49795581	Human		name
598217255	CV4003717	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2801G>A (p.Arg934His)	not specified [RCV005379032]	uncertain significance	12	49795059	49795059	Human		name
598253227	CV4003718	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2771A>G (p.Lys924Arg)	not specified [RCV005385303]	uncertain significance	12	49795089	49795089	Human		name
598217268	CV4003720	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1810C>T (p.Pro604Ser)	not specified [RCV005379034]	uncertain significance	12	49796050	49796050	Human		name
598253231	CV4003721	single nucleotide variant	NM_001037806.4(NCKAP5L):c.1699T>C (p.Phe567Leu)	not specified [RCV005385304]	uncertain significance	12	49796161	49796161	Human		name
598253242	CV4003725	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2963A>G (p.Tyr988Cys)	not specified [RCV005385306]	uncertain significance	12	49794897	49794897	Human		name
598217287	CV4003726	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2851C>T (p.Arg951Trp)	not specified [RCV005379037]	uncertain significance	12	49795009	49795009	Human		name
15139006	CV713561	single nucleotide variant	NM_001037806.4(NCKAP5L):c.2075C>T (p.Thr692Ile)	not provided [RCV000965890]	benign	12	49795785	49795785	Human		name
156129598	CV2209830	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3841C>T (p.Pro1281Ser)	not specified [RCV004076294]	uncertain significance	12	49792003	49792003	Human		name
156086790	CV2258936	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3164C>T (p.Pro1055Leu)	not specified [RCV004120216]	uncertain significance	12	49793828	49793828	Human		name
155904672	CV2276070	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3901G>A (p.Glu1301Lys)	not specified [RCV004141742]	uncertain significance	12	49791943	49791943	Human		name
156293224	CV2306303	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3038G>C (p.Gly1013Ala)	not specified [RCV004163018]	uncertain significance	12	49794822	49794822	Human		name
156168995	CV2320132	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3532C>T (p.Arg1178Trp)	not specified [RCV004167974]	uncertain significance	12	49792795	49792795	Human		name
156354582	CV2324307	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3722C>A (p.Ala1241Glu)	not specified [RCV004177031]	uncertain significance	12	49792516	49792516	Human		name
156066821	CV2346874	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3292C>G (p.Pro1098Ala)	not specified [RCV004199868]	uncertain significance	12	49793400	49793400	Human		name
155907568	CV2354450	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3487C>T (p.Pro1163Ser)	not specified [RCV004202443]	uncertain significance	12	49792840	49792840	Human		name
156205397	CV2385203	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3757C>A (p.Pro1253Thr)	not specified [RCV004228452]	uncertain significance	12	49792481	49792481	Human		name
155908256	CV2387264	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3281G>A (p.Arg1094Gln)	not specified [RCV004238356]	likely benign	12	49793411	49793411	Human		name
401731229	CV2674303	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3932C>T (p.Pro1311Leu)	not specified [RCV004289181]	uncertain significance	12	49791912	49791912	Human		name
401722425	CV2676980	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3512G>A (p.Arg1171His)	not specified [RCV004293582]	uncertain significance	12	49792815	49792815	Human		name
401741035	CV2680533	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3596C>T (p.Pro1199Leu)	not specified [RCV004291167]	uncertain significance	12	49792731	49792731	Human		name
401861732	CV2756460	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3142C>T (p.Pro1048Ser)	not specified [RCV004342993]	uncertain significance	12	49793850	49793850	Human		name
405759492	CV3347456	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3008G>C (p.Gly1003Ala)	not specified [RCV004468365]	uncertain significance	12	49794852	49794852	Human		name
405759503	CV3347458	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3031G>A (p.Val1011Met)	not specified [RCV004468367]	uncertain significance	12	49794829	49794829	Human		name
405759543	CV3347465	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3241G>A (p.Gly1081Arg)	not specified [RCV004468374]	uncertain significance	12	49793751	49793751	Human		name
405759560	CV3347468	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3271C>T (p.Pro1091Ser)	not specified [RCV004468377]	uncertain significance	12	49793421	49793421	Human		name
405759613	CV3347477	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3442A>C (p.Lys1148Gln)	not specified [RCV004468386]	uncertain significance	12	49792885	49792885	Human		name
405759630	CV3347480	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3452G>A (p.Arg1151Gln)	not specified [RCV004468389]	uncertain significance	12	49792875	49792875	Human		name
405759647	CV3347483	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3464C>G (p.Pro1155Arg)	not specified [RCV004468392]	uncertain significance	12	49792863	49792863	Human		name
405759666	CV3347486	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3464C>T (p.Pro1155Leu)	not specified [RCV004468395]	uncertain significance	12	49792863	49792863	Human		name
405759865	CV3347520	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3772G>A (p.Gly1258Arg)	not specified [RCV004468429]	uncertain significance	12	49792466	49792466	Human		name
407521395	CV3458393	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3449C>T (p.Pro1150Leu)	not specified [RCV004652514]	uncertain significance	12	49792878	49792878	Human		name
407521405	CV3458397	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3592T>C (p.Phe1198Leu)	not specified [RCV004652517]	uncertain significance	12	49792735	49792735	Human		name
407488528	CV3458405	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3035A>C (p.Gln1012Pro)	not specified [RCV004641316]	uncertain significance	12	49794825	49794825	Human		name
597649440	CV3558602	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3907G>A (p.Gly1303Ser)	not specified [RCV004826664]	uncertain significance	12	49791937	49791937	Human		name
597649103	CV3562478	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3017C>T (p.Thr1006Met)	not specified [RCV004826649]	uncertain significance	12	49794843	49794843	Human		name
597649112	CV3562479	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3037G>A (p.Gly1013Ser)	not specified [RCV004826650]	uncertain significance	12	49794823	49794823	Human		name
597649146	CV3562483	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3808C>T (p.Arg1270Trp)	not specified [RCV004826654]	uncertain significance	12	49792036	49792036	Human		name
597649372	CV3562485	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3208C>T (p.Arg1070Trp)	not specified [RCV004826656]	uncertain significance	12	49793784	49793784	Human		name
597649382	CV3562486	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3625C>T (p.Arg1209Trp)	not specified [RCV004826657]	uncertain significance	12	49792702	49792702	Human		name
597649397	CV3562488	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3572G>A (p.Arg1191Gln)	not specified [RCV004826659]	uncertain significance	12	49792755	49792755	Human		name
597649412	CV3562490	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3737C>T (p.Ser1246Leu)	not specified [RCV004826661]	uncertain significance	12	49792501	49792501	Human		name
598217263	CV4003719	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3761G>A (p.Arg1254Gln)	not specified [RCV005379033]	uncertain significance	12	49792477	49792477	Human		name
598217293	CV4003727	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3126C>G (p.Ser1042Arg)	not specified [RCV005379038]	uncertain significance	12	49793866	49793866	Human		name
598253248	CV4003728	single nucleotide variant	NM_001037806.4(NCKAP5L):c.3975C>A (p.Asp1325Glu)	not specified [RCV005385307]	uncertain significance	12	49791869	49791869	Human		name
8634703	CV89923	single nucleotide variant	NM_001037806.3(NCKAP5L):c.3247C>T (p.Pro1083Ser)	Malignant melanoma [RCV000070020]	not provided	12	49793745	49793745	Human		name

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