Afap1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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275 records found for search term Afap1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329362171	CV2466082	single nucleotide variant	NM_001134647.2(AFAP1):c.26G>C (p.Arg9Pro)	not specified [RCV004277968]	uncertain significance	4	7872053	7872053	Human		name
401881886	CV2783992	single nucleotide variant	NM_001134647.2(AFAP1):c.51T>G (p.His17Gln)	not specified [RCV004362404]	uncertain significance	4	7872028	7872028	Human		name
15151667	CV721079	single nucleotide variant	NM_001134647.2(AFAP1):c.645C>T (p.His215=)	not provided [RCV000879645]	benign	4	7838605	7838605	Human		name
329362597	CV2444779	single nucleotide variant	NM_001134647.2(AFAP1):c.253C>G (p.Pro85Ala)	not specified [RCV004259023]	uncertain significance	4	7855547	7855547	Human		name
401890279	CV2767987	single nucleotide variant	NM_001134647.2(AFAP1):c.2058C>T (p.Asn686=)	not provided [RCV004711955]\|not specified [RCV004348232]	likely benign	4	7774743	7774743	Human		name
401928051	CV2822404	single nucleotide variant	NM_001134647.2(AFAP1):c.2436C>T (p.Asn812=)	not provided [RCV003439242]	likely benign	4	7763774	7763774	Human		name
401927907	CV2822405	single nucleotide variant	NM_001134647.2(AFAP1):c.2349C>T (p.Ala783=)	not provided [RCV003439243]	likely benign	4	7768913	7768913	Human		name
405724607	CV3249649	single nucleotide variant	NM_001134647.2(AFAP1):c.136G>A (p.Val46Met)	not specified [RCV004378469]	uncertain significance	4	7868711	7868711	Human		name
405724864	CV3249679	single nucleotide variant	NM_001134647.2(AFAP1):c.173G>C (p.Ser58Thr)	not specified [RCV004378499]	uncertain significance	4	7868674	7868674	Human		name
405725713	CV3249751	single nucleotide variant	NM_001134647.2(AFAP1):c.268C>T (p.Pro90Ser)	not specified [RCV004378571]	uncertain significance	4	7855532	7855532	Human		name
405725738	CV3249754	single nucleotide variant	NM_001134647.2(AFAP1):c.283G>C (p.Glu95Gln)	not specified [RCV004378574]	uncertain significance	4	7855517	7855517	Human		name
405725782	CV3249759	single nucleotide variant	NM_001134647.2(AFAP1):c.296C>T (p.Pro99Leu)	not specified [RCV004378579]	uncertain significance	4	7855504	7855504	Human		name
597712786	CV3656095	single nucleotide variant	NM_001134647.2(AFAP1):c.242C>T (p.Pro81Leu)	not specified [RCV004917971]	uncertain significance	4	7855558	7855558	Human		name
597713008	CV3663189	single nucleotide variant	NM_001134647.2(AFAP1):c.233A>G (p.Asp78Gly)	not specified [RCV004917991]	uncertain significance	4	7855567	7855567	Human		name
598161376	CV3952927	single nucleotide variant	NM_001134647.2(AFAP1):c.172A>G (p.Ser58Gly)	not specified [RCV005328962]	uncertain significance	4	7868675	7868675	Human		name
15171648	CV734722	single nucleotide variant	NM_001134647.2(AFAP1):c.2115G>A (p.Glu705=)	not provided [RCV000905509]	benign	4	7772958	7772958	Human		name
155968557	CV2244265	single nucleotide variant	NM_001134647.2(AFAP1):c.499G>C (p.Gly167Arg)	not specified [RCV004100261]	uncertain significance	4	7843186	7843186	Human		name
155910671	CV2303645	single nucleotide variant	NM_001134647.2(AFAP1):c.716A>G (p.Gln239Arg)	not specified [RCV004161726]	uncertain significance	4	7838534	7838534	Human		name
156229779	CV2353017	single nucleotide variant	NM_001134647.2(AFAP1):c.863T>C (p.Val288Ala)	not provided [RCV004695637]\|not specified [RCV004201046]	uncertain significance	4	7816059	7816059	Human		name
156115156	CV2392256	single nucleotide variant	NM_001134647.2(AFAP1):c.691G>A (p.Val231Ile)	not specified [RCV004243865]	uncertain significance	4	7838559	7838559	Human		name
156152762	CV2394893	single nucleotide variant	NM_001134647.2(AFAP1):c.317C>T (p.Pro106Leu)	not specified [RCV004234549]	uncertain significance	4	7855483	7855483	Human		name
329370786	CV2435686	single nucleotide variant	NM_001134647.2(AFAP1):c.989T>G (p.Leu330Arg)	not specified [RCV004254921]	uncertain significance	4	7809679	7809679	Human		name
401772433	CV2687526	single nucleotide variant	NM_001134647.2(AFAP1):c.865G>C (p.Val289Leu)	not specified [RCV004300756]	uncertain significance	4	7816057	7816057	Human		name
401875595	CV2766106	single nucleotide variant	NM_001134647.2(AFAP1):c.523G>A (p.Val175Ile)	not specified [RCV004340561]	uncertain significance	4	7843162	7843162	Human		name
401870393	CV2792361	single nucleotide variant	NM_001134647.2(AFAP1):c.384G>C (p.Glu128Asp)	not specified [RCV004361529]	uncertain significance	4	7843301	7843301	Human		name
405725808	CV3249762	single nucleotide variant	NM_001134647.2(AFAP1):c.342T>G (p.Asp114Glu)	not specified [RCV004378582]	uncertain significance	4	7843343	7843343	Human		name
405725868	CV3249768	single nucleotide variant	NM_001134647.2(AFAP1):c.398A>G (p.Lys133Arg)	not specified [RCV004378588]	uncertain significance	4	7843287	7843287	Human		name
405725923	CV3249775	single nucleotide variant	NM_001134647.2(AFAP1):c.468C>G (p.Ile156Met)	not specified [RCV004378595]	uncertain significance	4	7843217	7843217	Human		name
405725973	CV3249780	single nucleotide variant	NM_001134647.2(AFAP1):c.484C>T (p.Arg162Trp)	not specified [RCV004378600]	uncertain significance	4	7843201	7843201	Human		name
405726153	CV3249800	single nucleotide variant	NM_001134647.2(AFAP1):c.965A>C (p.Lys322Thr)	not specified [RCV004378620]	uncertain significance	4	7809703	7809703	Human		name
405726195	CV3249804	single nucleotide variant	NM_001134647.2(AFAP1):c.991G>A (p.Gly331Arg)	not specified [RCV004378624]	uncertain significance	4	7809677	7809677	Human		name
597641553	CV3656102	single nucleotide variant	NM_001134647.2(AFAP1):c.632A>G (p.Lys211Arg)	not specified [RCV004909196]	uncertain significance	4	7838618	7838618	Human		name
597641836	CV3656141	single nucleotide variant	NM_001134647.2(AFAP1):c.926A>T (p.Lys309Ile)	not specified [RCV004909223]	uncertain significance	4	7809742	7809742	Human		name
598161278	CV3952910	single nucleotide variant	NM_001134647.2(AFAP1):c.752G>A (p.Cys251Tyr)	not specified [RCV005328945]	uncertain significance	4	7819146	7819146	Human		name
598161428	CV3952937	single nucleotide variant	NM_001134647.2(AFAP1):c.599G>T (p.Gly200Val)	not specified [RCV005328972]	uncertain significance	4	7838651	7838651	Human		name
598161669	CV3952985	single nucleotide variant	NM_001134647.2(AFAP1):c.335A>G (p.Asn112Ser)	not specified [RCV005329020]	uncertain significance	4	7843350	7843350	Human		name
598161859	CV3953024	single nucleotide variant	NM_001134647.2(AFAP1):c.307G>A (p.Gly103Arg)	not specified [RCV005329059]	uncertain significance	4	7855493	7855493	Human		name
156279378	CV2206263	single nucleotide variant	NM_001134647.2(AFAP1):c.1423A>G (p.Arg475Gly)	not specified [RCV004078613]	uncertain significance	4	7786301	7786301	Human		name
155967627	CV2216881	single nucleotide variant	NM_001134647.2(AFAP1):c.1214A>G (p.His405Arg)	not specified [RCV004083297]	uncertain significance	4	7800494	7800494	Human		name
156342329	CV2222207	single nucleotide variant	NM_001134647.2(AFAP1):c.2093A>G (p.Lys698Arg)	not specified [RCV004105238]	uncertain significance	4	7772980	7772980	Human		name
156277500	CV2230750	single nucleotide variant	NM_001134647.2(AFAP1):c.2345C>T (p.Ala782Val)	not specified [RCV004091975]	uncertain significance	4	7768917	7768917	Human		name
155988978	CV2234267	single nucleotide variant	NM_001134647.2(AFAP1):c.2218G>T (p.Ala740Ser)	not specified [RCV004106340]	uncertain significance	4	7772855	7772855	Human		name
156207423	CV2250039	single nucleotide variant	NM_001134647.2(AFAP1):c.1730C>A (p.Ser577Tyr)	not specified [RCV004116868]	uncertain significance	4	7781428	7781428	Human		name
156246284	CV2276732	single nucleotide variant	NM_001134647.2(AFAP1):c.1871C>T (p.Ala624Val)	not specified [RCV004146518]	uncertain significance	4	7778788	7778788	Human		name
155945405	CV2292087	single nucleotide variant	NM_001134647.2(AFAP1):c.2047A>G (p.Ile683Val)	not specified [RCV004160356]	uncertain significance	4	7774754	7774754	Human		name
156353819	CV2324149	single nucleotide variant	NM_001134647.2(AFAP1):c.1094G>A (p.Arg365His)	not specified [RCV004176899]	uncertain significance	4	7800614	7800614	Human		name
156079549	CV2351195	single nucleotide variant	NM_001134647.2(AFAP1):c.2389T>A (p.Cys797Ser)	not specified [RCV004214043]	uncertain significance	4	7768873	7768873	Human		name
155988755	CV2371858	single nucleotide variant	NM_001134647.2(AFAP1):c.1643G>T (p.Arg548Leu)	not specified [RCV004221551]	uncertain significance	4	7781515	7781515	Human		name
156041890	CV2381407	single nucleotide variant	NM_001134647.2(AFAP1):c.2119C>T (p.Arg707Trp)	not specified [RCV004229896]	uncertain significance	4	7772954	7772954	Human		name
329386683	CV2428381	single nucleotide variant	NM_001134647.2(AFAP1):c.2350G>A (p.Val784Ile)	not specified [RCV004253187]	uncertain significance	4	7768912	7768912	Human		name
329399230	CV2436435	single nucleotide variant	NM_001134647.2(AFAP1):c.1514C>T (p.Pro505Leu)	not specified [RCV004251818]	uncertain significance	4	7786210	7786210	Human		name
329397193	CV2460002	single nucleotide variant	NM_001134647.2(AFAP1):c.1633A>G (p.Ile545Val)	not specified [RCV004279477]	uncertain significance	4	7781525	7781525	Human		name
401767757	CV2677806	single nucleotide variant	NM_001134647.2(AFAP1):c.1172C>T (p.Pro391Leu)	not specified [RCV004294304]	uncertain significance	4	7800536	7800536	Human		name
401758193	CV2678266	single nucleotide variant	NM_001134647.2(AFAP1):c.1738A>G (p.Asn580Asp)	not specified [RCV004290265]	uncertain significance	4	7781420	7781420	Human		name
401740106	CV2683260	single nucleotide variant	NM_001134647.2(AFAP1):c.1487G>A (p.Gly496Glu)	not specified [RCV004288045]	uncertain significance	4	7786237	7786237	Human		name
401769673	CV2689883	single nucleotide variant	NM_001134647.2(AFAP1):c.2102A>G (p.Gln701Arg)	not specified [RCV004297780]	likely benign	4	7772971	7772971	Human		name
401757832	CV2707987	single nucleotide variant	NM_001134647.2(AFAP1):c.2200G>C (p.Gly734Arg)	not specified [RCV004309239]	uncertain significance	4	7772873	7772873	Human		name
401860295	CV2762384	single nucleotide variant	NM_001134647.2(AFAP1):c.1178G>T (p.Arg393Leu)	not specified [RCV004335493]	uncertain significance	4	7800530	7800530	Human		name
401859145	CV2771417	single nucleotide variant	NM_001134647.2(AFAP1):c.2372C>T (p.Ala791Val)	not specified [RCV004348470]	uncertain significance	4	7768890	7768890	Human		name
401872511	CV2793032	single nucleotide variant	NM_001134647.2(AFAP1):c.2432A>G (p.Lys811Arg)	not specified [RCV004360365]	uncertain significance	4	7763778	7763778	Human		name
401927909	CV2822406	single nucleotide variant	NM_001134647.2(AFAP1):c.1546G>A (p.Gly516Ser)	not provided [RCV003439244]\|not specified [RCV004917847]	likely benign\|uncertain significance	4	7781612	7781612	Human		name
405724567	CV3249645	single nucleotide variant	NM_001134647.2(AFAP1):c.1312G>T (p.Ala438Ser)	not specified [RCV004378465]	uncertain significance	4	7793781	7793781	Human		name
405724682	CV3249658	single nucleotide variant	NM_001134647.2(AFAP1):c.1502A>G (p.Tyr501Cys)	not specified [RCV004378478]	uncertain significance	4	7786222	7786222	Human		name
405724729	CV3249664	single nucleotide variant	NM_001134647.2(AFAP1):c.1610A>C (p.Tyr537Ser)	not specified [RCV004378484]	uncertain significance	4	7781548	7781548	Human		name
405725107	CV3249683	single nucleotide variant	NM_001134647.2(AFAP1):c.1765C>A (p.Leu589Ile)	not specified [RCV004378503]	uncertain significance	4	7781393	7781393	Human		name
405725164	CV3249689	single nucleotide variant	NM_001134647.2(AFAP1):c.1838C>A (p.Thr613Asn)	not specified [RCV004378509]	uncertain significance	4	7778821	7778821	Human		name
405725225	CV3249695	single nucleotide variant	NM_001134647.2(AFAP1):c.2039G>A (p.Arg680Gln)	not specified [RCV004378515]	uncertain significance	4	7774762	7774762	Human		name
405725291	CV3249702	single nucleotide variant	NM_001134647.2(AFAP1):c.2091G>C (p.Glu697Asp)	not specified [RCV004378522]	likely benign	4	7772982	7772982	Human		name
405725384	CV3249713	single nucleotide variant	NM_001134647.2(AFAP1):c.2132C>T (p.Ala711Val)	not specified [RCV004378533]	uncertain significance	4	7772941	7772941	Human		name
405725463	CV3249722	single nucleotide variant	NM_001134647.2(AFAP1):c.2232G>C (p.Lys744Asn)	not specified [RCV004378542]	uncertain significance	4	7772841	7772841	Human		name
405725585	CV3249736	single nucleotide variant	NM_001134647.2(AFAP1):c.2374C>T (p.Pro792Ser)	not specified [RCV004378556]	uncertain significance	4	7768888	7768888	Human		name
405725628	CV3249741	single nucleotide variant	NM_001134647.2(AFAP1):c.2396G>A (p.Gly799Glu)	not specified [RCV004378561]	uncertain significance	4	7768866	7768866	Human		name
407477294	CV3431229	single nucleotide variant	NM_001134647.2(AFAP1):c.1562G>A (p.Cys521Tyr)	not specified [RCV004617300]	uncertain significance	4	7781596	7781596	Human		name
407477341	CV3431240	single nucleotide variant	NM_001134647.2(AFAP1):c.1460C>T (p.Thr487Ile)	not specified [RCV004617311]	uncertain significance	4	7786264	7786264	Human		name
407477366	CV3431246	single nucleotide variant	NM_001134647.2(AFAP1):c.2162C>T (p.Thr721Met)	not specified [RCV004617317]	uncertain significance	4	7772911	7772911	Human		name
407477389	CV3431252	single nucleotide variant	NM_001134647.2(AFAP1):c.1081C>T (p.Arg361Cys)	not specified [RCV004617323]	uncertain significance	4	7800627	7800627	Human		name
407477445	CV3431263	single nucleotide variant	NM_001134647.2(AFAP1):c.1433T>C (p.Ile478Thr)	not specified [RCV004617334]	uncertain significance	4	7786291	7786291	Human		name
407477506	CV3431273	single nucleotide variant	NM_001134647.2(AFAP1):c.1763C>G (p.Ser588Cys)	not specified [RCV004617344]	uncertain significance	4	7781395	7781395	Human		name
407477560	CV3431282	single nucleotide variant	NM_001134647.2(AFAP1):c.2177G>A (p.Ser726Asn)	not specified [RCV004617353]	uncertain significance	4	7772896	7772896	Human		name
407477601	CV3431288	single nucleotide variant	NM_001134647.2(AFAP1):c.1391A>G (p.Gln464Arg)	not specified [RCV004617359]	uncertain significance	4	7793702	7793702	Human		name
407477632	CV3431293	single nucleotide variant	NM_001134647.2(AFAP1):c.1169T>C (p.Ile390Thr)	not specified [RCV004617364]	uncertain significance	4	7800539	7800539	Human		name
597641348	CV3656055	single nucleotide variant	NM_001134647.2(AFAP1):c.1721C>T (p.Ser574Phe)	not specified [RCV004909159]	uncertain significance	4	7781437	7781437	Human		name
597641407	CV3656066	single nucleotide variant	NM_001134647.2(AFAP1):c.2189C>T (p.Ala730Val)	not specified [RCV004909170]	uncertain significance	4	7772884	7772884	Human		name
597641462	CV3656077	single nucleotide variant	NM_001134647.2(AFAP1):c.1778C>T (p.Ser593Leu)	not specified [RCV004909180]	uncertain significance	4	7781380	7781380	Human		name
597641508	CV3656088	single nucleotide variant	NM_001134647.2(AFAP1):c.1622C>T (p.Pro541Leu)	not specified [RCV004909188]	uncertain significance	4	7781536	7781536	Human		name
597641585	CV3656111	single nucleotide variant	NM_001134647.2(AFAP1):c.2078C>T (p.Ala693Val)	not specified [RCV004909202]	likely benign	4	7772995	7772995	Human		name
597641625	CV3656120	single nucleotide variant	NM_001134647.2(AFAP1):c.1538C>T (p.Pro513Leu)	not specified [RCV004909210]	uncertain significance	4	7781620	7781620	Human		name
597641794	CV3656130	single nucleotide variant	NM_001134647.2(AFAP1):c.2218G>A (p.Ala740Thr)	not specified [RCV004909215]	uncertain significance	4	7772855	7772855	Human		name
597641895	CV3656151	single nucleotide variant	NM_001134647.2(AFAP1):c.1996C>T (p.Arg666Trp)	not specified [RCV004909232]	uncertain significance	4	7774805	7774805	Human		name
597712976	CV3663171	single nucleotide variant	NM_001134647.2(AFAP1):c.1739A>G (p.Asn580Ser)	not specified [RCV004917988]	uncertain significance	4	7781419	7781419	Human		name
597712988	CV3663182	single nucleotide variant	NM_001134647.2(AFAP1):c.2167G>A (p.Val723Ile)	not specified [RCV004917989]	uncertain significance	4	7772906	7772906	Human		name
597713018	CV3663196	single nucleotide variant	NM_001134647.2(AFAP1):c.2386C>T (p.Pro796Ser)	not specified [RCV004917992]	uncertain significance	4	7768876	7768876	Human		name
598161342	CV3952920	single nucleotide variant	NM_001134647.2(AFAP1):c.2384C>T (p.Ser795Phe)	not specified [RCV005328955]	uncertain significance	4	7768878	7768878	Human		name
598161466	CV3952945	single nucleotide variant	NM_001134647.2(AFAP1):c.2227C>T (p.Pro743Ser)	not specified [RCV005328980]	uncertain significance	4	7772846	7772846	Human		name
598161505	CV3952953	single nucleotide variant	NM_001134647.2(AFAP1):c.1760C>T (p.Ala587Val)	not specified [RCV005328988]	uncertain significance	4	7781398	7781398	Human		name
598161559	CV3952963	single nucleotide variant	NM_001134647.2(AFAP1):c.1534G>A (p.Glu512Lys)	not specified [RCV005328998]	uncertain significance	4	7781624	7781624	Human		name
598161619	CV3952975	single nucleotide variant	NM_001134647.2(AFAP1):c.1549T>C (p.Phe517Leu)	not specified [RCV005329010]	uncertain significance	4	7781609	7781609	Human		name
598161701	CV3952991	single nucleotide variant	NM_001134647.2(AFAP1):c.1387A>T (p.Ile463Phe)	not specified [RCV005329026]	uncertain significance	4	7793706	7793706	Human		name
598161759	CV3953002	single nucleotide variant	NM_001134647.2(AFAP1):c.2070G>C (p.Lys690Asn)	not specified [RCV005329037]	uncertain significance	4	7773003	7773003	Human		name
598161794	CV3953010	single nucleotide variant	NM_001134647.2(AFAP1):c.1186G>A (p.Glu396Lys)	not specified [RCV005329045]	uncertain significance	4	7800522	7800522	Human		name
598161822	CV3953016	single nucleotide variant	NM_001134647.2(AFAP1):c.2039G>T (p.Arg680Leu)	not specified [RCV005329051]	uncertain significance	4	7774762	7774762	Human		name
598162440	CV3953137	single nucleotide variant	NM_152406.4(AFAP1L1):c.4G>T (p.Asp2Tyr)	not specified [RCV005329172]	uncertain significance	5	149271972	149271972	Human		name
405727427	CV3259846	single nucleotide variant	NM_152406.4(AFAP1L1):c.68A>G (p.His23Arg)	not specified [RCV004378726]	uncertain significance	5	149299560	149299560	Human		name
405727005	CV3259858	single nucleotide variant	NM_152406.4(AFAP1L1):c.86C>T (p.Thr29Ile)	not specified [RCV004378739]	uncertain significance	5	149299578	149299578	Human		name
155929083	CV2389055	single nucleotide variant	NM_152406.4(AFAP1L1):c.104T>C (p.Met35Thr)	not specified [RCV004235393]	uncertain significance	5	149299596	149299596	Human		name
401730628	CV2711423	single nucleotide variant	NM_152406.4(AFAP1L1):c.248T>A (p.Leu83His)	not specified [RCV004313173]	uncertain significance	5	149301151	149301151	Human		name
401718102	CV2725313	single nucleotide variant	NM_152406.4(AFAP1L1):c.286G>A (p.Gly96Arg)	not specified [RCV004319975]	uncertain significance	5	149301189	149301189	Human		name
407477983	CV3431356	single nucleotide variant	NM_152406.4(AFAP1L1):c.175A>C (p.Thr59Pro)	not specified [RCV004617426]	uncertain significance	5	149300300	149300300	Human		name
597642026	CV3663210	single nucleotide variant	NM_152406.4(AFAP1L1):c.244G>A (p.Asp82Asn)	not specified [RCV004909254]	uncertain significance	5	149301147	149301147	Human		name
598162180	CV3953084	single nucleotide variant	NM_152406.4(AFAP1L1):c.185T>G (p.Leu62Arg)	not specified [RCV005329119]	uncertain significance	5	149300310	149300310	Human		name
155974571	CV2211186	single nucleotide variant	NM_152406.4(AFAP1L1):c.458C>T (p.Ser153Leu)	not specified [RCV004088347]	uncertain significance	5	149306327	149306327	Human		name
156060754	CV2236032	single nucleotide variant	NM_152406.4(AFAP1L1):c.620A>C (p.Gln207Pro)	not specified [RCV004114200]	uncertain significance	5	149307486	149307486	Human		name
156246049	CV2310499	single nucleotide variant	NM_152406.4(AFAP1L1):c.913G>A (p.Glu305Lys)	not specified [RCV004163523]	uncertain significance	5	149310121	149310121	Human		name
156353198	CV2324120	single nucleotide variant	NM_152406.4(AFAP1L1):c.418G>A (p.Glu140Lys)	not specified [RCV004178406]	uncertain significance	5	149302508	149302508	Human		name
155920805	CV2350567	single nucleotide variant	NM_152406.4(AFAP1L1):c.406G>A (p.Gly136Ser)	not specified [RCV004204920]	uncertain significance	5	149302496	149302496	Human		name
401781306	CV2681960	single nucleotide variant	NM_152406.4(AFAP1L1):c.347C>T (p.Pro116Leu)	not specified [RCV004296944]	uncertain significance	5	149302437	149302437	Human		name
401762735	CV2710296	single nucleotide variant	NM_152406.4(AFAP1L1):c.994C>T (p.Leu332Phe)	not specified [RCV004317479]	uncertain significance	5	149312178	149312178	Human		name
405726916	CV3259825	single nucleotide variant	NM_152406.4(AFAP1L1):c.317G>T (p.Arg106Leu)	not specified [RCV004378705]	uncertain significance	5	149301220	149301220	Human		name
405727543	CV3259834	single nucleotide variant	NM_152406.4(AFAP1L1):c.424A>G (p.Ile142Val)	not specified [RCV004378714]	uncertain significance	5	149302514	149302514	Human		name
405727478	CV3259841	single nucleotide variant	NM_152406.4(AFAP1L1):c.520G>A (p.Glu174Lys)	not specified [RCV004378721]	uncertain significance	5	149306389	149306389	Human		name
405726933	CV3259851	single nucleotide variant	NM_152406.4(AFAP1L1):c.695G>A (p.Arg232His)	not specified [RCV004378731]	uncertain significance	5	149307561	149307561	Human		name
405726972	CV3259854	single nucleotide variant	NM_152406.4(AFAP1L1):c.746T>C (p.Leu249Pro)	not specified [RCV004378735]	uncertain significance	5	149307612	149307612	Human		name
405727066	CV3259866	single nucleotide variant	NM_152406.4(AFAP1L1):c.935G>A (p.Arg312Gln)	not specified [RCV004378747]	uncertain significance	5	149312119	149312119	Human		name
405727116	CV3259872	single nucleotide variant	NM_152406.4(AFAP1L1):c.989C>T (p.Pro330Leu)	not specified [RCV004378753]	uncertain significance	5	149312173	149312173	Human		name
407477771	CV3431314	single nucleotide variant	NM_152406.4(AFAP1L1):c.511G>A (p.Val171Met)	not specified [RCV004617385]	likely benign	5	149306380	149306380	Human		name
407477837	CV3431326	single nucleotide variant	NM_152406.4(AFAP1L1):c.367C>T (p.Pro123Ser)	not specified [RCV004617397]	uncertain significance	5	149302457	149302457	Human		name
407477934	CV3431346	single nucleotide variant	NM_152406.4(AFAP1L1):c.362C>T (p.Pro121Leu)	not specified [RCV004617416]	uncertain significance	5	149302452	149302452	Human		name
596941396	CV3542497	single nucleotide variant	NM_152406.4(AFAP1L1):c.685C>T (p.Arg229Trp)	Neuromuscular disease [RCV004797743]	uncertain significance	5	149307551	149307551	Human	1	name
597642020	CV3663204	single nucleotide variant	NM_152406.4(AFAP1L1):c.770G>A (p.Arg257Gln)	not specified [RCV004909253]	uncertain significance	5	149309978	149309978	Human		name
597713029	CV3663219	single nucleotide variant	NM_152406.4(AFAP1L1):c.817G>A (p.Val273Met)	not specified [RCV004917993]	uncertain significance	5	149310025	149310025	Human		name
597713041	CV3663237	single nucleotide variant	NM_152406.4(AFAP1L1):c.769C>T (p.Arg257Trp)	not specified [RCV004917994]	uncertain significance	5	149309977	149309977	Human		name
597642039	CV3663248	single nucleotide variant	NM_152406.4(AFAP1L1):c.832C>T (p.Arg278Trp)	not specified [RCV004909256]	uncertain significance	5	149310040	149310040	Human		name
597713052	CV3663259	single nucleotide variant	NM_152406.4(AFAP1L1):c.607C>A (p.Gln203Lys)	not specified [RCV004917995]	uncertain significance	5	149307473	149307473	Human		name
597642062	CV3663298	single nucleotide variant	NM_152406.4(AFAP1L1):c.389C>G (p.Ala130Gly)	not specified [RCV004909260]	uncertain significance	5	149302479	149302479	Human		name
597642075	CV3663329	single nucleotide variant	NM_152406.4(AFAP1L1):c.613C>G (p.Arg205Gly)	not specified [RCV004909262]	uncertain significance	5	149307479	149307479	Human		name
597642081	CV3663340	single nucleotide variant	NM_152406.4(AFAP1L1):c.367C>A (p.Pro123Thr)	not specified [RCV004909263]	uncertain significance	5	149302457	149302457	Human		name
597642128	CV3663362	single nucleotide variant	NM_152406.4(AFAP1L1):c.368C>G (p.Pro123Arg)	not specified [RCV004909271]	uncertain significance	5	149302458	149302458	Human		name
597642527	CV3663378	single nucleotide variant	NM_152406.4(AFAP1L1):c.461T>C (p.Ile154Thr)	not specified [RCV004909282]	uncertain significance	5	149306330	149306330	Human		name
597642361	CV3663485	single nucleotide variant	NM_001001936.3(AFAP1L2):c.20T>C (p.Leu7Pro)	not specified [RCV004909335]	uncertain significance	10	114340728	114340728	Human		name
598162073	CV3953066	single nucleotide variant	NM_152406.4(AFAP1L1):c.554T>C (p.Met185Thr)	not specified [RCV005329101]	uncertain significance	5	149307420	149307420	Human		name
598162204	CV3953088	single nucleotide variant	NM_152406.4(AFAP1L1):c.686G>A (p.Arg229Gln)	not specified [RCV005329123]	uncertain significance	5	149307552	149307552	Human		name
156228851	CV2213107	single nucleotide variant	NM_152406.4(AFAP1L1):c.2001A>C (p.Glu667Asp)	not specified [RCV004091658]	uncertain significance	5	149332720	149332720	Human		name
156302884	CV2258746	single nucleotide variant	NM_152406.4(AFAP1L1):c.2123G>A (p.Gly708Glu)	not specified [RCV004117981]	uncertain significance	5	149332842	149332842	Human		name
156273037	CV2277647	single nucleotide variant	NM_152406.4(AFAP1L1):c.1785G>C (p.Gln595His)	not specified [RCV004147109]	uncertain significance	5	149322692	149322692	Human		name
156272298	CV2283560	single nucleotide variant	NM_152406.4(AFAP1L1):c.1781C>T (p.Pro594Leu)	not specified [RCV004140074]	uncertain significance	5	149322688	149322688	Human		name
156161385	CV2311736	single nucleotide variant	NM_152406.4(AFAP1L1):c.1909C>T (p.Arg637Trp)	not specified [RCV004170603]	uncertain significance	5	149329764	149329764	Human		name
156056281	CV2326651	single nucleotide variant	NM_152406.4(AFAP1L1):c.1675G>A (p.Asp559Asn)	not specified [RCV004185231]	uncertain significance	5	149320440	149320440	Human		name
156050414	CV2336592	single nucleotide variant	NM_152406.4(AFAP1L1):c.1771C>T (p.Arg591Cys)	not specified [RCV004196840]	uncertain significance	5	149322678	149322678	Human		name
155985093	CV2344488	single nucleotide variant	NM_152406.4(AFAP1L1):c.1565A>G (p.Tyr522Cys)	not specified [RCV004195231]	uncertain significance	5	149319667	149319667	Human		name
155988838	CV2355167	single nucleotide variant	NM_152406.4(AFAP1L1):c.1738C>T (p.Arg580Cys)	not specified [RCV004198553]	uncertain significance	5	149322645	149322645	Human		name
156207433	CV2360420	single nucleotide variant	NM_152406.4(AFAP1L1):c.1874A>G (p.Glu625Gly)	not specified [RCV004208745]	uncertain significance	5	149329729	149329729	Human		name
156084523	CV2381993	single nucleotide variant	NM_152406.4(AFAP1L1):c.2245G>A (p.Val749Ile)	not specified [RCV004225921]	uncertain significance	5	149335684	149335684	Human		name
156228343	CV2392952	single nucleotide variant	NM_152406.4(AFAP1L1):c.1904C>T (p.Thr635Met)	not specified [RCV004242807]	uncertain significance	5	149329759	149329759	Human		name
329388631	CV2447712	single nucleotide variant	NM_152406.4(AFAP1L1):c.2048G>A (p.Arg683Gln)	not specified [RCV004258502]	uncertain significance	5	149332767	149332767	Human		name
329395405	CV2458334	single nucleotide variant	NM_152406.4(AFAP1L1):c.2077G>A (p.Val693Met)	not specified [RCV004265976]	uncertain significance	5	149332796	149332796	Human		name
401893255	CV2755379	single nucleotide variant	NM_152406.4(AFAP1L1):c.1841G>A (p.Arg614Gln)	not specified [RCV004337544]	uncertain significance	5	149329696	149329696	Human		name
401889604	CV2758320	single nucleotide variant	NM_152406.4(AFAP1L1):c.1424G>A (p.Arg475Gln)	not specified [RCV004341672]	uncertain significance	5	149317885	149317885	Human		name
401861863	CV2766456	single nucleotide variant	NM_152406.4(AFAP1L1):c.1550C>T (p.Pro517Leu)	not specified [RCV004347082]	uncertain significance	5	149319652	149319652	Human		name
401868338	CV2767207	single nucleotide variant	NM_152406.4(AFAP1L1):c.1187G>A (p.Arg396His)	not specified [RCV004349386]	uncertain significance	5	149316223	149316223	Human		name
405726228	CV3249808	single nucleotide variant	NM_152406.4(AFAP1L1):c.1096C>T (p.Arg366Trp)	not specified [RCV004378628]	uncertain significance	5	149315896	149315896	Human		name
405726261	CV3249812	single nucleotide variant	NM_152406.4(AFAP1L1):c.1201T>C (p.Ser401Pro)	not specified [RCV004378632]	uncertain significance	5	149316237	149316237	Human		name
405726380	CV3259765	single nucleotide variant	NM_152406.4(AFAP1L1):c.1723G>A (p.Gly575Arg)	not specified [RCV004378645]	uncertain significance	5	149322630	149322630	Human		name
405726472	CV3259775	single nucleotide variant	NM_152406.4(AFAP1L1):c.1744G>A (p.Ala582Thr)	not specified [RCV004378655]	uncertain significance	5	149322651	149322651	Human		name
405726723	CV3259802	single nucleotide variant	NM_152406.4(AFAP1L1):c.2021C>T (p.Ala674Val)	not specified [RCV004378682]	uncertain significance	5	149332740	149332740	Human		name
405726824	CV3259814	single nucleotide variant	NM_152406.4(AFAP1L1):c.2144C>T (p.Pro715Leu)	not specified [RCV004378694]	uncertain significance	5	149332863	149332863	Human		name
407477704	CV3431303	single nucleotide variant	NM_152406.4(AFAP1L1):c.1702G>A (p.Glu568Lys)	not specified [RCV004617374]	uncertain significance	5	149322609	149322609	Human		name
407477886	CV3431336	single nucleotide variant	NM_152406.4(AFAP1L1):c.1319T>C (p.Leu440Pro)	not specified [RCV004617407]	uncertain significance	5	149317780	149317780	Human		name
596941199	CV3542443	single nucleotide variant	NM_152406.4(AFAP1L1):c.1513G>A (p.Gly505Arg)	Neuromuscular disease [RCV004797689]	uncertain significance	5	149319615	149319615	Human	1	name
597642032	CV3663227	single nucleotide variant	NM_152406.4(AFAP1L1):c.2008G>T (p.Ala670Ser)	not specified [RCV004909255]	uncertain significance	5	149332727	149332727	Human		name
597642045	CV3663270	single nucleotide variant	NM_152406.4(AFAP1L1):c.1754G>T (p.Cys585Phe)	not specified [RCV004909257]	uncertain significance	5	149322661	149322661	Human		name
597642050	CV3663281	single nucleotide variant	NM_152406.4(AFAP1L1):c.1532T>C (p.Met511Thr)	not specified [RCV004909258]	uncertain significance	5	149319634	149319634	Human		name
597642056	CV3663290	single nucleotide variant	NM_152406.4(AFAP1L1):c.1060G>A (p.Val354Met)	not specified [RCV004909259]	uncertain significance	5	149315860	149315860	Human		name
597642069	CV3663309	single nucleotide variant	NM_152406.4(AFAP1L1):c.2045G>A (p.Arg682His)	not specified [RCV004909261]	uncertain significance	5	149332764	149332764	Human		name
597642087	CV3663351	single nucleotide variant	NM_152406.4(AFAP1L1):c.1426C>T (p.His476Tyr)	not specified [RCV004909264]	uncertain significance	5	149317887	149317887	Human		name
597642559	CV3663371	single nucleotide variant	NM_152406.4(AFAP1L1):c.1681C>G (p.Pro561Ala)	not specified [RCV004909277]	uncertain significance	5	149320446	149320446	Human		name
597642466	CV3663389	single nucleotide variant	NM_152406.4(AFAP1L1):c.1306C>T (p.Arg436Cys)	not specified [RCV004909292]	uncertain significance	5	149317767	149317767	Human		name
597642430	CV3663400	single nucleotide variant	NM_152406.4(AFAP1L1):c.1535G>A (p.Gly512Asp)	not specified [RCV004909299]	uncertain significance	5	149319637	149319637	Human		name
598161909	CV3953034	single nucleotide variant	NM_152406.4(AFAP1L1):c.2005G>A (p.Val669Met)	not specified [RCV005329069]	uncertain significance	5	149332724	149332724	Human		name
598162009	CV3953054	single nucleotide variant	NM_152406.4(AFAP1L1):c.2126T>G (p.Leu709Arg)	not specified [RCV005329089]	uncertain significance	5	149332845	149332845	Human		name
598162122	CV3953074	single nucleotide variant	NM_152406.4(AFAP1L1):c.1798C>T (p.Arg600Cys)	not specified [RCV005329109]	uncertain significance	5	149322705	149322705	Human		name
598162240	CV3953095	single nucleotide variant	NM_152406.4(AFAP1L1):c.1175G>A (p.Arg392His)	not specified [RCV005329130]	uncertain significance	5	149316211	149316211	Human		name
598162286	CV3953105	single nucleotide variant	NM_152406.4(AFAP1L1):c.2233A>T (p.Ser745Cys)	not specified [RCV005329140]	uncertain significance	5	149335672	149335672	Human		name
598162345	CV3953116	single nucleotide variant	NM_152406.4(AFAP1L1):c.1880A>G (p.Glu627Gly)	not specified [RCV005329151]	uncertain significance	5	149329735	149329735	Human		name
598162402	CV3953127	single nucleotide variant	NM_152406.4(AFAP1L1):c.1093C>T (p.Arg365Cys)	not specified [RCV005329162]	uncertain significance	5	149315893	149315893	Human		name
156233993	CV2197165	single nucleotide variant	NM_001001936.3(AFAP1L2):c.112G>A (p.Ala38Thr)	not specified [RCV004071586]	uncertain significance	10	114340636	114340636	Human		name
155948496	CV2245938	single nucleotide variant	NM_001001936.3(AFAP1L2):c.277C>T (p.Pro93Ser)	not specified [RCV004113563]	uncertain significance	10	114331841	114331841	Human		name
156250624	CV2359144	single nucleotide variant	NM_001001936.3(AFAP1L2):c.178G>A (p.Val60Met)	not specified [RCV004214502]	uncertain significance	10	114333263	114333263	Human		name
329382506	CV2424409	single nucleotide variant	NM_001001936.3(AFAP1L2):c.124C>T (p.Arg42Trp)	not specified [RCV004252305]	uncertain significance	10	114340624	114340624	Human		name
401907793	CV2809648	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2286C>T (p.His762=)	not provided [RCV003422909]	likely benign	10	114297241	114297241	Human		name
401907794	CV2809649	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1905C>G (p.Thr635=)	not provided [RCV003422910]	likely benign	10	114300246	114300246	Human		name
401907796	CV2809650	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1056G>A (p.Arg352=)	not provided [RCV003422911]	likely benign	10	114307821	114307821	Human		name
405727395	CV3259905	single nucleotide variant	NM_001001936.3(AFAP1L2):c.125G>A (p.Arg42Gln)	not specified [RCV004378786]	uncertain significance	10	114340623	114340623	Human		name
405727738	CV3259920	single nucleotide variant	NM_001001936.3(AFAP1L2):c.156G>C (p.Glu52Asp)	not specified [RCV004378801]	uncertain significance	10	114333285	114333285	Human		name
405728092	CV3259959	single nucleotide variant	NM_001001936.3(AFAP1L2):c.217A>G (p.Lys73Glu)	not specified [RCV004378840]	uncertain significance	10	114333224	114333224	Human		name
405743707	CV3260010	single nucleotide variant	NM_001001936.3(AFAP1L2):c.292C>G (p.Pro98Ala)	not specified [RCV004380965]	uncertain significance	10	114331826	114331826	Human		name
597642272	CV3663422	single nucleotide variant	NM_001001936.3(AFAP1L2):c.272C>T (p.Ser91Leu)	not specified [RCV004909320]	uncertain significance	10	114331846	114331846	Human		name
15186525	CV701192	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2190C>T (p.Arg730=)	not provided [RCV000953309]	benign\|likely benign	10	114297337	114297337	Human		name
15183394	CV723787	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1590G>A (p.Glu530=)	not provided [RCV000886216]	benign	10	114300643	114300643	Human		name
156270857	CV2195195	single nucleotide variant	NM_001001936.3(AFAP1L2):c.886G>A (p.Asp296Asn)	not specified [RCV004080137]	uncertain significance	10	114308514	114308514	Human		name
155931210	CV2220995	single nucleotide variant	NM_001001936.3(AFAP1L2):c.489G>T (p.Trp163Cys)	not specified [RCV004092679]	uncertain significance	10	114315683	114315683	Human		name
156241673	CV2265802	single nucleotide variant	NM_001001936.3(AFAP1L2):c.890T>C (p.Ile297Thr)	not specified [RCV004126418]	uncertain significance	10	114308510	114308510	Human		name
156029334	CV2278617	single nucleotide variant	NM_001001936.3(AFAP1L2):c.326G>A (p.Arg109Gln)	not specified [RCV004134830]	uncertain significance	10	114323251	114323251	Human		name
155940791	CV2294141	single nucleotide variant	NM_001001936.3(AFAP1L2):c.731T>C (p.Met244Thr)	not specified [RCV004149510]	uncertain significance	10	114313932	114313932	Human		name
156207144	CV2307874	single nucleotide variant	NM_001001936.3(AFAP1L2):c.382G>A (p.Glu128Lys)	not specified [RCV004170334]	uncertain significance	10	114323195	114323195	Human		name
156202584	CV2334726	single nucleotide variant	NM_001001936.3(AFAP1L2):c.526G>A (p.Ala176Thr)	not specified [RCV004188705]	uncertain significance	10	114315646	114315646	Human		name
155908405	CV2387313	single nucleotide variant	NM_001001936.3(AFAP1L2):c.454G>A (p.Asp152Asn)	not specified [RCV004238401]	uncertain significance	10	114315718	114315718	Human		name
156256228	CV2397745	single nucleotide variant	NM_001001936.3(AFAP1L2):c.529C>T (p.Arg177Cys)	not specified [RCV004239223]	uncertain significance	10	114315643	114315643	Human		name
329375467	CV2468627	single nucleotide variant	NM_001001936.3(AFAP1L2):c.958A>G (p.Thr320Ala)	not specified [RCV004278182]	uncertain significance	10	114308442	114308442	Human		name
329353161	CV2471510	single nucleotide variant	NM_001001936.3(AFAP1L2):c.392A>G (p.Asp131Gly)	not specified [RCV004280502]	uncertain significance	10	114323185	114323185	Human		name
401760751	CV2715921	single nucleotide variant	NM_001001936.3(AFAP1L2):c.830C>T (p.Ala277Val)	not specified [RCV004329027]	uncertain significance	10	114310406	114310406	Human		name
401871063	CV2766759	single nucleotide variant	NM_001001936.3(AFAP1L2):c.475G>A (p.Ala159Thr)	not specified [RCV004349149]	uncertain significance	10	114315697	114315697	Human		name
401862430	CV2775297	single nucleotide variant	NM_001001936.3(AFAP1L2):c.530G>A (p.Arg177His)	not specified [RCV004348414]	uncertain significance	10	114315642	114315642	Human		name
405743831	CV3260028	single nucleotide variant	NM_001001936.3(AFAP1L2):c.457G>A (p.Gly153Ser)	not specified [RCV004380983]	likely benign	10	114315715	114315715	Human		name
405744143	CV3260051	single nucleotide variant	NM_001001936.3(AFAP1L2):c.538G>A (p.Ala180Thr)	not specified [RCV004381006]	uncertain significance	10	114315634	114315634	Human		name
405744240	CV3260065	single nucleotide variant	NM_001001936.3(AFAP1L2):c.866G>A (p.Arg289His)	not specified [RCV004381020]	uncertain significance	10	114310370	114310370	Human		name
407478081	CV3431378	single nucleotide variant	NM_001001936.3(AFAP1L2):c.346A>G (p.Lys116Glu)	not specified [RCV004617448]	uncertain significance	10	114323231	114323231	Human		name
597642344	CV3663452	single nucleotide variant	NM_001001936.3(AFAP1L2):c.514C>G (p.Leu172Val)	not specified [RCV004909332]	uncertain significance	10	114315658	114315658	Human		name
597642356	CV3663469	single nucleotide variant	NM_001001936.3(AFAP1L2):c.694G>A (p.Val232Met)	not specified [RCV004909334]	uncertain significance	10	114313969	114313969	Human		name
598171558	CV3953195	single nucleotide variant	NM_001001936.3(AFAP1L2):c.318T>G (p.Ile106Met)	not specified [RCV005331204]	uncertain significance	10	114323259	114323259	Human		name
598171596	CV3953202	single nucleotide variant	NM_001001936.3(AFAP1L2):c.535T>C (p.Cys179Arg)	not specified [RCV005331211]	uncertain significance	10	114315637	114315637	Human		name
8633500	CV88715	single nucleotide variant	NM_001001936.3(AFAP1L2):c.490C>T (p.Pro164Ser)	not specified [RCV004092680]	uncertain significance\|not provided	10	114315682	114315682	Human		name
155963848	CV2194156	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1297G>A (p.Glu433Lys)	not specified [RCV004077246]	uncertain significance	10	114302472	114302472	Human		name
155960883	CV2204383	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2176G>A (p.Glu726Lys)	not specified [RCV004079200]	uncertain significance	10	114297351	114297351	Human		name
156329243	CV2216363	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2338G>T (p.Asp780Tyr)	not specified [RCV004097231]	uncertain significance	10	114297070	114297070	Human		name
155967991	CV2216949	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1387G>A (p.Asp463Asn)	not specified [RCV004085320]	uncertain significance	10	114302382	114302382	Human		name
156289498	CV2229918	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2447G>A (p.Gly816Glu)	not specified [RCV004105464]	uncertain significance	10	114296052	114296052	Human		name
156138555	CV2236706	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1487A>T (p.Gln496Leu)	not specified [RCV004110661]	uncertain significance	10	114301409	114301409	Human		name
155962781	CV2285695	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2252C>T (p.Pro751Leu)	not specified [RCV004141543]	uncertain significance	10	114297275	114297275	Human		name
156092001	CV2300103	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2387C>T (p.Ser796Leu)	not specified [RCV004151301]	uncertain significance	10	114297021	114297021	Human		name
155967640	CV2329944	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1655G>A (p.Ser552Asn)	not specified [RCV004183398]	uncertain significance	10	114300578	114300578	Human		name
156082229	CV2333957	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1627G>A (p.Val543Ile)	not specified [RCV004183489]	uncertain significance	10	114300606	114300606	Human		name
156135036	CV2347176	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2129C>T (p.Ala710Val)	not specified [RCV004204650]	uncertain significance	10	114297398	114297398	Human		name
156077396	CV2351032	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1943G>A (p.Arg648His)	not provided [RCV004695682]\|not specified [RCV004211856]	uncertain significance	10	114300208	114300208	Human		name
156082202	CV2368885	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1063G>A (p.Glu355Lys)	not specified [RCV004207842]	uncertain significance	10	114307814	114307814	Human		name
155991599	CV2384301	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1493G>A (p.Arg498His)	not specified [RCV004227685]	uncertain significance	10	114301403	114301403	Human		name
156053018	CV2385427	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1492C>T (p.Arg498Cys)	not specified [RCV004233081]	uncertain significance	10	114301404	114301404	Human		name
156152344	CV2394849	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2161G>A (p.Glu721Lys)	not specified [RCV004234509]	uncertain significance	10	114297366	114297366	Human		name
329381844	CV2424239	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1682C>G (p.Thr561Arg)	not specified [RCV004250360]	uncertain significance	10	114300551	114300551	Human		name
329360572	CV2439509	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1795G>A (p.Glu599Lys)	not specified [RCV004262448]	uncertain significance	10	114300356	114300356	Human		name
329387839	CV2440155	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2284C>A (p.His762Asn)	not specified [RCV004260611]	uncertain significance	10	114297243	114297243	Human		name
401766462	CV2679700	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2237A>G (p.Lys746Arg)	not specified [RCV004282170]	uncertain significance	10	114297290	114297290	Human		name
401744266	CV2680928	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1837G>A (p.Val613Ile)	not specified [RCV004296000]	uncertain significance	10	114300314	114300314	Human		name
401755398	CV2682472	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1678C>T (p.Pro560Ser)	not specified [RCV004290497]	uncertain significance	10	114300555	114300555	Human		name
401773365	CV2698187	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1481C>T (p.Pro494Leu)	not specified [RCV004304756]	uncertain significance	10	114301415	114301415	Human		name
401747947	CV2698892	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1005C>A (p.Asn335Lys)	not specified [RCV004301649]	uncertain significance	10	114307872	114307872	Human		name
401763039	CV2707456	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2238G>C (p.Lys746Asn)	not specified [RCV004312837]	uncertain significance	10	114297289	114297289	Human		name
401757907	CV2731531	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2372A>G (p.Lys791Arg)	not specified [RCV004330880]	uncertain significance	10	114297036	114297036	Human		name
401894719	CV2785224	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2269A>G (p.Thr757Ala)	not specified [RCV004356998]	uncertain significance	10	114297258	114297258	Human		name
401876981	CV2793305	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2138A>G (p.Glu713Gly)	not specified [RCV004362125]	uncertain significance	10	114297389	114297389	Human		name
401882189	CV2793398	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1156C>T (p.Arg386Trp)	not specified [RCV004362497]	uncertain significance	10	114304847	114304847	Human		name
405727192	CV3259881	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1010T>A (p.Met337Lys)	not specified [RCV004378762]	uncertain significance	10	114307867	114307867	Human		name
405727289	CV3259893	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1195G>A (p.Val399Met)	not specified [RCV004378774]	uncertain significance	10	114304808	114304808	Human		name
405727334	CV3259898	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1206G>T (p.Glu402Asp)	not specified [RCV004378779]	uncertain significance	10	114304797	114304797	Human		name
405727669	CV3259912	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1446G>T (p.Lys482Asn)	not specified [RCV004378793]	uncertain significance	10	114301450	114301450	Human		name
405727747	CV3259921	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1586A>C (p.Asn529Thr)	not specified [RCV004378802]	uncertain significance	10	114300647	114300647	Human		name
405728055	CV3259954	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2170C>T (p.Arg724Trp)	not specified [RCV004378835]	uncertain significance	10	114297357	114297357	Human		name
405743919	CV3259964	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2188C>T (p.Arg730Cys)	not specified [RCV004380919]	uncertain significance	10	114297339	114297339	Human		name
405743612	CV3259996	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2392G>A (p.Val798Met)	not specified [RCV004380951]	likely benign	10	114297016	114297016	Human		name
407478031	CV3431367	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1129G>A (p.Asp377Asn)	not specified [RCV004617437]	uncertain significance	10	114304874	114304874	Human		name
407478127	CV3441410	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1123G>C (p.Val375Leu)	not specified [RCV004617458]	uncertain significance	10	114304880	114304880	Human		name
597642213	CV3663411	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1412C>A (p.Ala471Glu)	not specified [RCV004909310]	uncertain significance	10	114302357	114302357	Human		name
597642317	CV3663431	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1426C>A (p.Leu476Ile)	not specified [RCV004909328]	uncertain significance	10	114302343	114302343	Human		name
597642323	CV3663433	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1894G>A (p.Val632Met)	not specified [RCV004909329]	uncertain significance	10	114300257	114300257	Human		name
597713191	CV3663440	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1925C>T (p.Pro642Leu)	not specified [RCV004918008]	uncertain significance	10	114300226	114300226	Human		name
597642335	CV3663445	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2313A>C (p.Lys771Asn)	not specified [RCV004909331]	uncertain significance	10	114297095	114297095	Human		name
597642350	CV3663461	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1259A>G (p.Lys420Arg)	not specified [RCV004909333]	uncertain significance	10	114304744	114304744	Human		name
597713204	CV3663477	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1111C>T (p.Arg371Cys)	not specified [RCV004918009]	uncertain significance	10	114304892	114304892	Human		name
597713215	CV3663492	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1826G>C (p.Arg609Thr)	not specified [RCV004918010]	uncertain significance	10	114300325	114300325	Human		name
597642419	CV3663503	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1363T>C (p.Phe455Leu)	not specified [RCV004909345]	uncertain significance	10	114302406	114302406	Human		name
598162513	CV3953149	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1604G>A (p.Arg535Gln)	not specified [RCV005329184]	uncertain significance	10	114300629	114300629	Human		name
598171450	CV3953176	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1679C>T (p.Pro560Leu)	not specified [RCV005331185]	uncertain significance	10	114300554	114300554	Human		name
598171493	CV3953182	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1945G>A (p.Val649Met)	not specified [RCV005331191]	uncertain significance	10	114300206	114300206	Human		name
598171516	CV3953187	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1133A>G (p.Asn378Ser)	not specified [RCV005331196]	likely benign	10	114304870	114304870	Human		name
598171642	CV3953211	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1999C>T (p.Arg667Trp)	not specified [RCV005331220]	uncertain significance	10	114299374	114299374	Human		name
598171692	CV3953222	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1151A>G (p.Gln384Arg)	not specified [RCV005331231]	uncertain significance	10	114304852	114304852	Human		name

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