Plxna3 Variant Search Result - Rat Genome Database

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753 records found for search term Plxna3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405282794	CV3191115	single nucleotide variant	NM_017514.5(PLXNA3):c.-4G>A	PLXNA3-related disorder [RCV003921530]	likely benign	X	154460180	154460180	Human		name , trait , alternate_id
405285816	CV3221566	single nucleotide variant	NM_017514.5(PLXNA3):c.-5C>T	PLXNA3-related disorder [RCV003981291]	likely benign	X	154460179	154460179	Human		name , trait , alternate_id
408373370	CV3515024	single nucleotide variant	NM_017514.5(PLXNA3):c.-7G>A	PLXNA3-related disorder [RCV004744844]	likely benign	X	154460177	154460177	Human		name , trait , alternate_id
401921539	CV2797984	single nucleotide variant	NM_017514.5(PLXNA3):c.3441+8C>T	PLXNA3-related disorder [RCV003402877]	uncertain significance	X	154467479	154467479	Human		name , trait , alternate_id
401921775	CV2804784	single nucleotide variant	NM_017514.5(PLXNA3):c.2043+7C>T	PLXNA3-related disorder [RCV003402982]	uncertain significance	X	154464875	154464875	Human		name , trait , alternate_id
401930181	CV2821727	single nucleotide variant	NM_017514.5(PLXNA3):c.1134+7C>T	not provided [RCV003440078]	uncertain significance	X	154461645	154461645	Human		name
401930172	CV2821731	single nucleotide variant	NM_017514.5(PLXNA3):c.2043+8G>A	PLXNA3-related disorder [RCV003901083]\|not provided [RCV003440082]	likely benign	X	154464876	154464876	Human		name , trait , alternate_id
401930037	CV2821738	single nucleotide variant	NM_017514.5(PLXNA3):c.3585+5G>A	not provided [RCV003440089]	uncertain significance	X	154467693	154467693	Human		name
401925815	CV2821742	single nucleotide variant	NM_017514.5(PLXNA3):c.4987-4A>G	not provided [RCV003436875]	likely benign	X	154470438	154470438	Human		name
405260574	CV3185818	single nucleotide variant	NM_017514.5(PLXNA3):c.2937-5T>C	PLXNA3-related disorder [RCV004741758]\|not provided [RCV003884894]	likely benign	X	154466618	154466618	Human		name , trait , alternate_id
405267935	CV3189528	single nucleotide variant	NM_017514.5(PLXNA3):c.4796-8T>C	PLXNA3-related disorder [RCV003898922]	likely benign	X	154469969	154469969	Human		name , trait , alternate_id
405284898	CV3190905	single nucleotide variant	NM_017514.5(PLXNA3):c.2678+9G>A	PLXNA3-related disorder [RCV003909468]	likely benign	X	154466089	154466089	Human		name , trait , alternate_id
405282441	CV3191011	single nucleotide variant	NM_017514.5(PLXNA3):c.5521-7C>T	PLXNA3-related disorder [RCV003921432]	likely benign	X	154472583	154472583	Human		name , trait , alternate_id
405258710	CV3194122	single nucleotide variant	NM_017514.5(PLXNA3):c.2937-4G>A	PLXNA3-related disorder [RCV003893704]	likely benign	X	154466619	154466619	Human		name , trait , alternate_id
405277499	CV3195823	single nucleotide variant	NM_017514.5(PLXNA3):c.1548-6G>A	PLXNA3-related disorder [RCV003904353]	likely benign	X	154463945	154463945	Human		name , trait , alternate_id
405277779	CV3196095	single nucleotide variant	NM_017514.5(PLXNA3):c.4287+4C>T	PLXNA3-related disorder [RCV003904613]	likely benign	X	154468733	154468733	Human		name , trait , alternate_id
405270003	CV3198032	duplication	NM_017514.5(PLXNA3):c.1929-3dup	PLXNA3-related disorder [RCV003899842]	likely benign	X	154464744	154464745	Human		name , trait , alternate_id
405269000	CV3201177	single nucleotide variant	NM_017514.5(PLXNA3):c.2678+8C>T	PLXNA3-related disorder [RCV003899283]	likely benign	X	154466088	154466088	Human		name , trait , alternate_id
405269591	CV3201739	single nucleotide variant	NM_017514.5(PLXNA3):c.1547+9G>A	PLXNA3-related disorder [RCV003899646]	likely benign	X	154463699	154463699	Human		name , trait , alternate_id
405287021	CV3205531	single nucleotide variant	NM_017514.5(PLXNA3):c.3964-7C>T	PLXNA3-related disorder [RCV003959683]	likely benign	X	154468296	154468296	Human		name , trait , alternate_id
405267425	CV3205709	deletion	NM_017514.5(PLXNA3):c.3964-5del	PLXNA3-related disorder [RCV003947409]	likely benign	X	154468295	154468295	Human		name , trait , alternate_id
405289432	CV3218214	single nucleotide variant	NM_017514.5(PLXNA3):c.3821-8C>T	PLXNA3-related disorder [RCV003983616]	likely benign	X	154468074	154468074	Human		name , trait , alternate_id
405261458	CV3219827	single nucleotide variant	NM_017514.5(PLXNA3):c.2800-4G>A	PLXNA3-related disorder [RCV003967013]	likely benign	X	154466372	154466372	Human		name , trait , alternate_id
405261431	CV3221471	single nucleotide variant	NM_017514.5(PLXNA3):c.2044-8C>T	PLXNA3-related disorder [RCV003966949]	likely benign	X	154465010	154465010	Human		name , trait , alternate_id
408372376	CV3509933	single nucleotide variant	NM_017514.5(PLXNA3):c.3821-5C>G	PLXNA3-related disorder [RCV004742974]	likely benign	X	154468077	154468077	Human		name , trait , alternate_id
408372456	CV3510355	single nucleotide variant	NM_017514.5(PLXNA3):c.1447-4C>T	PLXNA3-related disorder [RCV004743051]	likely benign	X	154463586	154463586	Human		name , trait , alternate_id
408372638	CV3511484	single nucleotide variant	NM_017514.5(PLXNA3):c.5521-3C>T	PLXNA3-related disorder [RCV004743733]	likely benign	X	154472587	154472587	Human		name , trait , alternate_id
408372750	CV3512255	single nucleotide variant	NM_017514.5(PLXNA3):c.3442-4C>G	PLXNA3-related disorder [RCV004743833]	uncertain significance	X	154467541	154467541	Human		name , trait , alternate_id
408372816	CV3512655	single nucleotide variant	NM_017514.5(PLXNA3):c.1548-7C>T	PLXNA3-related disorder [RCV004743896]	likely benign	X	154463944	154463944	Human		name , trait , alternate_id
408372765	CV3512665	single nucleotide variant	NM_017514.5(PLXNA3):c.4795+7G>T	PLXNA3-related disorder [RCV004743901]	likely benign	X	154469791	154469791	Human		name , trait , alternate_id
408372852	CV3512755	single nucleotide variant	NM_017514.5(PLXNA3):c.2244+9C>T	PLXNA3-related disorder [RCV004743911]	likely benign	X	154465227	154465227	Human		name , trait , alternate_id
408372792	CV3512828	single nucleotide variant	NM_017514.5(PLXNA3):c.5521-7C>A	PLXNA3-related disorder [RCV004743927]	uncertain significance	X	154472583	154472583	Human		name , trait , alternate_id
408373023	CV3513648	single nucleotide variant	NM_017514.5(PLXNA3):c.1929-7C>T	PLXNA3-related disorder [RCV004744092]	likely benign	X	154464747	154464747	Human		name , trait , alternate_id
408373051	CV3513829	single nucleotide variant	NM_017514.5(PLXNA3):c.2800-5C>T	PLXNA3-related disorder [RCV004744126]	likely benign	X	154466371	154466371	Human		name , trait , alternate_id
408373161	CV3514004	single nucleotide variant	NM_017514.5(PLXNA3):c.1828+9G>A	PLXNA3-related disorder [RCV004744649]	likely benign	X	154464322	154464322	Human		name , trait , alternate_id
408373156	CV3514220	single nucleotide variant	NM_017514.5(PLXNA3):c.1135-4C>T	PLXNA3-related disorder [RCV004744694]	likely benign	X	154462124	154462124	Human		name , trait , alternate_id
408373203	CV3514248	single nucleotide variant	NM_017514.5(PLXNA3):c.5520+3G>A	PLXNA3-related disorder [RCV004744702]	likely benign	X	154471641	154471641	Human		name , trait , alternate_id
408373244	CV3514428	single nucleotide variant	NM_017514.5(PLXNA3):c.4435-5C>G	PLXNA3-related disorder [RCV004744731]	likely benign	X	154469051	154469051	Human		name , trait , alternate_id
408373340	CV3514900	single nucleotide variant	NM_017514.5(PLXNA3):c.1548-6G>T	PLXNA3-related disorder [RCV004744820]	likely benign	X	154463945	154463945	Human		name , trait , alternate_id
408373354	CV3514962	single nucleotide variant	NM_017514.5(PLXNA3):c.3585+9G>C	PLXNA3-related disorder [RCV004744832]	likely benign	X	154467697	154467697	Human		name , trait , alternate_id
408373400	CV3515225	single nucleotide variant	NM_017514.5(PLXNA3):c.3963+6C>T	PLXNA3-related disorder [RCV004744874]	likely benign	X	154468230	154468230	Human		name , trait , alternate_id
408373462	CV3515535	single nucleotide variant	NM_017514.5(PLXNA3):c.5157-8G>A	PLXNA3-related disorder [RCV004744925]	likely benign	X	154471097	154471097	Human		name , trait , alternate_id
408373529	CV3516170	single nucleotide variant	NM_017514.5(PLXNA3):c.1447-8G>T	PLXNA3-related disorder [RCV004745032]	likely benign	X	154463582	154463582	Human		name , trait , alternate_id
408372088	CV3518064	single nucleotide variant	NM_017514.5(PLXNA3):c.2936+7C>T	PLXNA3-related disorder [RCV004742204]	likely benign	X	154466519	154466519	Human		name , trait , alternate_id
598129267	CV3888561	single nucleotide variant	NM_017514.5(PLXNA3):c.5157-7T>C	not provided [RCV005244735]	uncertain significance	X	154471098	154471098	Human		name
13446088	CV438477	single nucleotide variant	NM_017514.5(PLXNA3):c.2936+8G>A	PLXNA3-related disorder [RCV003960207]\|not provided [RCV000513259]	likely benign\|uncertain significance	X	154466520	154466520	Human		name , trait , alternate_id
15177864	CV731460	single nucleotide variant	NM_017514.5(PLXNA3):c.2342-8G>A	PLXNA3-related disorder [RCV003910457]\|not provided [RCV000884927]	benign	X	154465649	154465649	Human		name , trait , alternate_id
15131028	CV745180	single nucleotide variant	NM_017514.5(PLXNA3):c.2044-4G>A	PLXNA3-related disorder [RCV003950498]\|not provided [RCV000897702]	benign	X	154465014	154465014	Human		name , trait , alternate_id
15165623	CV745462	single nucleotide variant	NM_017514.5(PLXNA3):c.2245-7C>T	PLXNA3-related disorder [RCV003968292]\|not provided [RCV000904264]	likely benign	X	154465417	154465417	Human		name , trait , alternate_id
15169068	CV760845	single nucleotide variant	NM_017514.5(PLXNA3):c.3441+5G>A	PLXNA3-related disorder [RCV003942877]\|not provided [RCV000927423]	likely benign	X	154467476	154467476	Human		name , trait , alternate_id
152042038	CV1669950	single nucleotide variant	NM_017514.5(PLXNA3):c.3202-10G>A	not provided [RCV002224852]	uncertain significance	X	154467222	154467222	Human		name
405268194	CV3189668	single nucleotide variant	NM_017514.5(PLXNA3):c.2342-10G>C	PLXNA3-related disorder [RCV003899060]	likely benign	X	154465647	154465647	Human		name , trait , alternate_id
405259577	CV3194853	single nucleotide variant	NM_017514.5(PLXNA3):c.4795+10C>T	PLXNA3-related disorder [RCV003894241]	likely benign	X	154469794	154469794	Human		name , trait , alternate_id
408372727	CV3512509	single nucleotide variant	NM_017514.5(PLXNA3):c.2936+10G>A	PLXNA3-related disorder [RCV004743861]	likely benign	X	154466522	154466522	Human		name , trait , alternate_id
408372817	CV3512656	single nucleotide variant	NM_017514.5(PLXNA3):c.4288-10C>T	PLXNA3-related disorder [RCV004743897]	likely benign	X	154468813	154468813	Human		name , trait , alternate_id
408373264	CV3514491	single nucleotide variant	NM_017514.5(PLXNA3):c.5370-10G>T	PLXNA3-related disorder [RCV004744743]	likely benign	X	154471478	154471478	Human		name , trait , alternate_id
408371971	CV3517327	single nucleotide variant	NM_017514.5(PLXNA3):c.4287+10G>A	PLXNA3-related disorder [RCV004742074]	likely benign	X	154468739	154468739	Human		name , trait , alternate_id
405265677	CV3215592	single nucleotide variant	NM_017514.5(PLXNA3):c.18C>T (p.Leu6=)	PLXNA3-related disorder [RCV003946779]	likely benign	X	154460201	154460201	Human		name , trait , alternate_id
15097715	CV706166	single nucleotide variant	NM_017514.5(PLXNA3):c.12C>G (p.Val4=)	PLXNA3-related disorder [RCV003915970]\|not provided [RCV000958377]	benign	X	154460195	154460195	Human		name , trait , alternate_id
405273442	CV3197771	single nucleotide variant	NM_017514.5(PLXNA3):c.42G>C (p.Val14=)	PLXNA3-related disorder [RCV003901737]	likely benign	X	154460225	154460225	Human		name , trait , alternate_id
405266900	CV3211962	single nucleotide variant	NM_017514.5(PLXNA3):c.78C>T (p.Phe26=)	PLXNA3-related disorder [RCV003947228]	likely benign	X	154460261	154460261	Human		name , trait , alternate_id
405267505	CV3219316	single nucleotide variant	NM_017514.5(PLXNA3):c.39C>T (p.Ala13=)	PLXNA3-related disorder [RCV003969574]	likely benign	X	154460222	154460222	Human		name , trait , alternate_id
408372439	CV3510486	single nucleotide variant	NM_017514.5(PLXNA3):c.48G>T (p.Gly16=)	PLXNA3-related disorder [RCV004743077]	likely benign	X	154460231	154460231	Human		name , trait , alternate_id
408373321	CV3514872	single nucleotide variant	NM_017514.5(PLXNA3):c.45G>A (p.Gly15=)	PLXNA3-related disorder [RCV004744811]	likely benign	X	154460228	154460228	Human		name , trait , alternate_id
401933325	CV2797629	single nucleotide variant	NM_017514.5(PLXNA3):c.252C>G (p.Arg84=)	PLXNA3-related disorder [RCV003392797]	uncertain significance	X	154460435	154460435	Human		name , trait , alternate_id
401929951	CV2821716	single nucleotide variant	NM_017514.5(PLXNA3):c.144C>T (p.Gly48=)	PLXNA3-related disorder [RCV003908972]\|not provided [RCV003440067]	likely benign	X	154460327	154460327	Human		name , trait , alternate_id
401930200	CV2821718	single nucleotide variant	NM_017514.5(PLXNA3):c.252C>T (p.Arg84=)	PLXNA3-related disorder [RCV003919237]\|not provided [RCV003440069]	likely benign	X	154460435	154460435	Human		name , trait , alternate_id
405274106	CV3194947	single nucleotide variant	NM_017514.5(PLXNA3):c.237G>A (p.Pro79=)	PLXNA3-related disorder [RCV003902189]	likely benign	X	154460420	154460420	Human		name , trait , alternate_id
405271911	CV3202995	single nucleotide variant	NM_017514.5(PLXNA3):c.213C>T (p.Val71=)	PLXNA3-related disorder [RCV003914050]	likely benign	X	154460396	154460396	Human		name , trait , alternate_id
405289382	CV3205142	duplication	NM_017514.5(PLXNA3):c.49dup (p.Ala17fs)	PLXNA3-related disorder [RCV003961745]	uncertain significance	X	154460224	154460225	Human		name , trait , alternate_id
405267247	CV3205290	single nucleotide variant	NM_017514.5(PLXNA3):c.222C>T (p.Asn74=)	PLXNA3-related disorder [RCV003947322]	likely benign	X	154460405	154460405	Human		name , trait , alternate_id
405287667	CV3207895	single nucleotide variant	NM_017514.5(PLXNA3):c.276C>T (p.Pro92=)	PLXNA3-related disorder [RCV003924541]	likely benign	X	154460459	154460459	Human		name , trait , alternate_id
405261068	CV3216088	single nucleotide variant	NM_017514.5(PLXNA3):c.210C>T (p.Pro70=)	PLXNA3-related disorder [RCV003944310]	likely benign	X	154460393	154460393	Human		name , trait , alternate_id
408372611	CV3511273	single nucleotide variant	NM_017514.5(PLXNA3):c.267C>G (p.Arg89=)	PLXNA3-related disorder [RCV004743694]	likely benign	X	154460450	154460450	Human		name , trait , alternate_id
408373042	CV3513759	single nucleotide variant	NM_017514.5(PLXNA3):c.270G>A (p.Leu90=)	PLXNA3-related disorder [RCV004744113]	likely benign	X	154460453	154460453	Human		name , trait , alternate_id
408373251	CV3514466	single nucleotide variant	NM_017514.5(PLXNA3):c.19C>T (p.Leu7Phe)	PLXNA3-related disorder [RCV004744738]	uncertain significance	X	154460202	154460202	Human		name , trait , alternate_id
408371941	CV3517087	single nucleotide variant	NM_017514.5(PLXNA3):c.10G>C (p.Val4Leu)	PLXNA3-related disorder [RCV004742037]	uncertain significance	X	154460193	154460193	Human		name , trait , alternate_id
598127948	CV3888389	single nucleotide variant	NM_017514.5(PLXNA3):c.22C>G (p.Leu8Val)	not provided [RCV005243075]	uncertain significance	X	154460205	154460205	Human		name
15162811	CV758394	single nucleotide variant	NM_017514.5(PLXNA3):c.138C>T (p.Phe46=)	PLXNA3-related disorder [RCV003960443]\|not provided [RCV000925975]	likely benign	X	154460321	154460321	Human		name , trait , alternate_id
156369579	CV2194027	single nucleotide variant	NM_017514.5(PLXNA3):c.95C>T (p.Thr32Met)	PLXNA3-related disorder [RCV004744635]\|not specified [RCV004076793]	uncertain significance	X	154460278	154460278	Human		name , trait , alternate_id
155926692	CV2345237	single nucleotide variant	NM_017514.5(PLXNA3):c.55G>A (p.Gly19Ser)	PLXNA3-related disorder [RCV003427647]\|not specified [RCV004195976]	uncertain significance	X	154460238	154460238	Human		name , trait , alternate_id
156113646	CV2397078	single nucleotide variant	NM_017514.5(PLXNA3):c.79G>A (p.Val27Met)	PLXNA3-related disorder [RCV003928938]\|not specified [RCV004236588]	likely benign\|uncertain significance	X	154460262	154460262	Human		name , trait , alternate_id
401718536	CV2704640	single nucleotide variant	NM_017514.5(PLXNA3):c.40G>A (p.Val14Met)	not specified [RCV004313672]	uncertain significance	X	154460223	154460223	Human		name
401930196	CV2821720	single nucleotide variant	NM_017514.5(PLXNA3):c.447C>T (p.Asp149=)	PLXNA3-related disorder [RCV003966441]\|not provided [RCV003440071]	likely benign	X	154460630	154460630	Human		name , trait , alternate_id
401930194	CV2821721	single nucleotide variant	NM_017514.5(PLXNA3):c.516C>T (p.Asp172=)	PLXNA3-related disorder [RCV003919238]\|not provided [RCV003440072]	likely benign	X	154460699	154460699	Human		name , trait , alternate_id
401930192	CV2821722	single nucleotide variant	NM_017514.5(PLXNA3):c.759G>A (p.Ala253=)	PLXNA3-related disorder [RCV003908973]\|not provided [RCV003440073]	likely benign	X	154461263	154461263	Human		name , trait , alternate_id
401930187	CV2821724	single nucleotide variant	NM_017514.5(PLXNA3):c.855C>T (p.Arg285=)	PLXNA3-related disorder [RCV003966442]\|not provided [RCV003440075]	likely benign	X	154461359	154461359	Human		name , trait , alternate_id
401930185	CV2821725	single nucleotide variant	NM_017514.5(PLXNA3):c.945C>T (p.Asp315=)	PLXNA3-related disorder [RCV003901082]\|not provided [RCV003440076]	likely benign	X	154461449	154461449	Human		name , trait , alternate_id
405263383	CV3189478	single nucleotide variant	NM_017514.5(PLXNA3):c.600C>T (p.Tyr200=)	PLXNA3-related disorder [RCV003896712]	likely benign	X	154461104	154461104	Human		name , trait , alternate_id
405264184	CV3189893	single nucleotide variant	NM_017514.5(PLXNA3):c.627C>A (p.Ile209=)	PLXNA3-related disorder [RCV003896941]	likely benign	X	154461131	154461131	Human		name , trait , alternate_id
405264971	CV3190097	single nucleotide variant	NM_017514.5(PLXNA3):c.963C>T (p.Phe321=)	PLXNA3-related disorder [RCV003897136]	likely benign	X	154461467	154461467	Human		name , trait , alternate_id
405277574	CV3195895	single nucleotide variant	NM_017514.5(PLXNA3):c.657C>T (p.Tyr219=)	PLXNA3-related disorder [RCV003904421]	likely benign	X	154461161	154461161	Human		name , trait , alternate_id
405273583	CV3197848	single nucleotide variant	NM_017514.5(PLXNA3):c.798C>T (p.Cys266=)	PLXNA3-related disorder [RCV003901811]	likely benign	X	154461302	154461302	Human		name , trait , alternate_id
405270056	CV3198037	single nucleotide variant	NM_017514.5(PLXNA3):c.513C>T (p.Val171=)	PLXNA3-related disorder [RCV003899847]\|not specified [RCV005392730]	likely benign	X	154460696	154460696	Human		name , trait , alternate_id
405268154	CV3198795	single nucleotide variant	NM_017514.5(PLXNA3):c.684C>T (p.Tyr228=)	PLXNA3-related disorder [RCV003911918]	likely benign	X	154461188	154461188	Human		name , trait , alternate_id
405269008	CV3201184	single nucleotide variant	NM_017514.5(PLXNA3):c.435C>T (p.Ala145=)	PLXNA3-related disorder [RCV003899290]	likely benign	X	154460618	154460618	Human		name , trait , alternate_id
405271615	CV3202879	single nucleotide variant	NM_017514.5(PLXNA3):c.336C>T (p.Cys112=)	PLXNA3-related disorder [RCV003913941]	likely benign	X	154460519	154460519	Human		name , trait , alternate_id
405272028	CV3203003	single nucleotide variant	NM_017514.5(PLXNA3):c.720G>A (p.Thr240=)	PLXNA3-related disorder [RCV003914056]	likely benign	X	154461224	154461224	Human		name , trait , alternate_id
405274939	CV3204486	single nucleotide variant	NM_017514.5(PLXNA3):c.594C>T (p.Leu198=)	PLXNA3-related disorder [RCV003951918]	likely benign	X	154460777	154460777	Human		name , trait , alternate_id
405275031	CV3204556	single nucleotide variant	NM_017514.5(PLXNA3):c.444C>T (p.Pro148=)	PLXNA3-related disorder [RCV003951975]	likely benign	X	154460627	154460627	Human		name , trait , alternate_id
405286500	CV3205302	single nucleotide variant	NM_017514.5(PLXNA3):c.696C>T (p.Ser232=)	PLXNA3-related disorder [RCV003959505]	likely benign	X	154461200	154461200	Human		name , trait , alternate_id
405271910	CV3206247	single nucleotide variant	NM_017514.5(PLXNA3):c.645G>A (p.Thr215=)	PLXNA3-related disorder [RCV003971892]	likely benign	X	154461149	154461149	Human		name , trait , alternate_id
405291953	CV3207802	single nucleotide variant	NM_017514.5(PLXNA3):c.315G>A (p.Ala105=)	PLXNA3-related disorder [RCV003929484]	likely benign	X	154460498	154460498	Human		name , trait , alternate_id
405286021	CV3209831	single nucleotide variant	NM_017514.5(PLXNA3):c.705C>T (p.Phe235=)	PLXNA3-related disorder [RCV003959371]	likely benign	X	154461209	154461209	Human		name , trait , alternate_id
405274244	CV3211658	single nucleotide variant	NM_017514.5(PLXNA3):c.312T>C (p.Tyr104=)	PLXNA3-related disorder [RCV003951473]	likely benign	X	154460495	154460495	Human		name , trait , alternate_id
405266908	CV3211965	single nucleotide variant	NM_017514.5(PLXNA3):c.858C>T (p.Gly286=)	PLXNA3-related disorder [RCV003947231]	likely benign	X	154461362	154461362	Human		name , trait , alternate_id
405284034	CV3213490	single nucleotide variant	NM_017514.5(PLXNA3):c.576C>T (p.Ser192=)	PLXNA3-related disorder [RCV003922071]	likely benign	X	154460759	154460759	Human		name , trait , alternate_id
405291232	CV3215168	single nucleotide variant	NM_017514.5(PLXNA3):c.927C>T (p.Gly309=)	PLXNA3-related disorder [RCV003927390]	likely benign	X	154461431	154461431	Human		name , trait , alternate_id
405294368	CV3215304	single nucleotide variant	NM_017514.5(PLXNA3):c.690C>T (p.Phe230=)	PLXNA3-related disorder [RCV003934304]	likely benign	X	154461194	154461194	Human		name , trait , alternate_id
405265953	CV3215768	single nucleotide variant	NM_017514.5(PLXNA3):c.714C>T (p.Phe238=)	PLXNA3-related disorder [RCV003946924]	likely benign	X	154461218	154461218	Human		name , trait , alternate_id
405289257	CV3218115	single nucleotide variant	NM_017514.5(PLXNA3):c.549C>A (p.Ser183=)	PLXNA3-related disorder [RCV003983517]	likely benign	X	154460732	154460732	Human		name , trait , alternate_id
405289325	CV3218153	single nucleotide variant	NM_017514.5(PLXNA3):c.735C>G (p.Thr245=)	PLXNA3-related disorder [RCV003983555]	likely benign	X	154461239	154461239	Human		name , trait , alternate_id
405283527	CV3218551	single nucleotide variant	NM_017514.5(PLXNA3):c.459T>C (p.Gly153=)	PLXNA3-related disorder [RCV003957336]	likely benign	X	154460642	154460642	Human		name , trait , alternate_id
405286301	CV3218735	single nucleotide variant	NM_017514.5(PLXNA3):c.840C>T (p.Ile280=)	PLXNA3-related disorder [RCV003959453]	likely benign	X	154461344	154461344	Human		name , trait , alternate_id
405261795	CV3219899	single nucleotide variant	NM_017514.5(PLXNA3):c.801G>A (p.Ala267=)	PLXNA3-related disorder [RCV003967073]	likely benign	X	154461305	154461305	Human		name , trait , alternate_id
405267134	CV3220201	single nucleotide variant	NM_017514.5(PLXNA3):c.729G>A (p.Leu243=)	PLXNA3-related disorder [RCV003969456]	likely benign	X	154461233	154461233	Human		name , trait , alternate_id
405278911	CV3220472	single nucleotide variant	NM_017514.5(PLXNA3):c.391C>T (p.Leu131=)	PLXNA3-related disorder [RCV003976664]	likely benign	X	154460574	154460574	Human		name , trait , alternate_id
407519349	CV3467529	single nucleotide variant	NM_017514.5(PLXNA3):c.70C>T (p.Arg24Cys)	PLXNA3-related disorder [RCV004741789]\|not specified [RCV004651450]	uncertain significance	X	154460253	154460253	Human		name , trait , alternate_id
408371870	CV3507925	single nucleotide variant	NM_017514.5(PLXNA3):c.663C>T (p.Ala221=)	PLXNA3-related disorder [RCV004741942]	likely benign	X	154461167	154461167	Human		name , trait , alternate_id
408371899	CV3508194	single nucleotide variant	NM_017514.5(PLXNA3):c.702C>T (p.Ser234=)	PLXNA3-related disorder [RCV004741992]	likely benign	X	154461206	154461206	Human		name , trait , alternate_id
408372229	CV3508943	single nucleotide variant	NM_017514.5(PLXNA3):c.540C>G (p.Thr180=)	PLXNA3-related disorder [RCV004742825]	likely benign	X	154460723	154460723	Human		name , trait , alternate_id
408372249	CV3509021	single nucleotide variant	NM_017514.5(PLXNA3):c.861G>A (p.Val287=)	PLXNA3-related disorder [RCV004742839]	likely benign	X	154461365	154461365	Human		name , trait , alternate_id
408372267	CV3509127	single nucleotide variant	NM_017514.5(PLXNA3):c.43G>C (p.Gly15Arg)	PLXNA3-related disorder [RCV004742858]	uncertain significance	X	154460226	154460226	Human		name , trait , alternate_id
408372459	CV3510374	single nucleotide variant	NM_017514.5(PLXNA3):c.579G>A (p.Ala193=)	PLXNA3-related disorder [RCV004743055]	likely benign	X	154460762	154460762	Human		name , trait , alternate_id
408373020	CV3513630	single nucleotide variant	NM_017514.5(PLXNA3):c.780C>G (p.Ser260=)	PLXNA3-related disorder [RCV004744087]	likely benign	X	154461284	154461284	Human		name , trait , alternate_id
408373230	CV3514378	single nucleotide variant	NM_017514.5(PLXNA3):c.300G>A (p.Leu100=)	PLXNA3-related disorder [RCV004744723]	likely benign	X	154460483	154460483	Human		name , trait , alternate_id
408373289	CV3514692	single nucleotide variant	NM_017514.5(PLXNA3):c.552C>G (p.Arg184=)	PLXNA3-related disorder [RCV004744780]	likely benign	X	154460735	154460735	Human		name , trait , alternate_id
408373290	CV3514703	single nucleotide variant	NM_017514.5(PLXNA3):c.891G>C (p.Leu297=)	PLXNA3-related disorder [RCV004744781]	likely benign	X	154461395	154461395	Human		name , trait , alternate_id
408373267	CV3514806	single nucleotide variant	NM_017514.5(PLXNA3):c.876G>A (p.Val292=)	PLXNA3-related disorder [RCV004744797]	likely benign	X	154461380	154461380	Human		name , trait , alternate_id
408373307	CV3514838	single nucleotide variant	NM_017514.5(PLXNA3):c.651C>G (p.Ser217=)	PLXNA3-related disorder [RCV004744802]	likely benign	X	154461155	154461155	Human		name , trait , alternate_id
408373339	CV3514899	single nucleotide variant	NM_017514.5(PLXNA3):c.849C>T (p.Ser283=)	PLXNA3-related disorder [RCV004744819]	likely benign	X	154461353	154461353	Human		name , trait , alternate_id
408373445	CV3515458	single nucleotide variant	NM_017514.5(PLXNA3):c.384C>T (p.Leu128=)	PLXNA3-related disorder [RCV004744910]	likely benign	X	154460567	154460567	Human		name , trait , alternate_id
408373513	CV3515892	single nucleotide variant	NM_017514.5(PLXNA3):c.915C>T (p.Ala305=)	PLXNA3-related disorder [RCV004744984]	likely benign	X	154461419	154461419	Human		name , trait , alternate_id
408373607	CV3516293	single nucleotide variant	NM_017514.5(PLXNA3):c.594C>G (p.Leu198=)	PLXNA3-related disorder [RCV004745053]	likely benign	X	154460777	154460777	Human		name , trait , alternate_id
14350087	CV590930	single nucleotide variant	NM_017514.5(PLXNA3):c.56G>A (p.Gly19Asp)	PLXNA3-related disorder [RCV003392576]\|Short stature [RCV000736201]\|not specified [RCV002249451]	likely pathogenic\|benign\|conflicting interpretations of pathogenicity\|uncertain significance	X	154460239	154460239	Human	2	name , trait , alternate_id
15172217	CV717723	single nucleotide variant	NM_017514.5(PLXNA3):c.744G>A (p.Thr248=)	PLXNA3-related disorder [RCV003972933]\|not provided [RCV000972357]	benign	X	154461248	154461248	Human		name , trait , alternate_id
15180105	CV717724	single nucleotide variant	NM_017514.5(PLXNA3):c.786C>T (p.Ile262=)	PLXNA3-related disorder [RCV003962910]\|not provided [RCV000974070]	benign	X	154461290	154461290	Human		name , trait , alternate_id
15166093	CV717725	single nucleotide variant	NM_017514.5(PLXNA3):c.882C>T (p.Ser294=)	PLXNA3-related disorder [RCV003960832]\|not provided [RCV000971096]\|not specified [RCV005392600]	benign\|likely benign	X	154461386	154461386	Human		name , trait , alternate_id
15112039	CV729511	single nucleotide variant	NM_017514.5(PLXNA3):c.71G>A (p.Arg24His)	PLXNA3-related disorder [RCV003910650]\|not provided [RCV000894389]	benign	X	154460254	154460254	Human		name , trait , alternate_id
15184147	CV729512	single nucleotide variant	NM_017514.5(PLXNA3):c.933G>A (p.Pro311=)	PLXNA3-related disorder [RCV003968053]\|not provided [RCV000886382]	benign	X	154461437	154461437	Human		name , trait , alternate_id
15115012	CV758395	single nucleotide variant	NM_017514.5(PLXNA3):c.402G>A (p.Pro134=)	PLXNA3-related disorder [RCV003970446]\|not provided [RCV000917381]	likely benign	X	154460585	154460585	Human		name , trait , alternate_id
15179031	CV773919	single nucleotide variant	NM_017514.5(PLXNA3):c.825C>T (p.Tyr275=)	PLXNA3-related disorder [RCV003933158]\|not provided [RCV000929542]	benign\|likely benign	X	154461329	154461329	Human		name , trait , alternate_id
156030753	CV2364554	single nucleotide variant	NM_017514.5(PLXNA3):c.226C>T (p.Arg76Cys)	PLXNA3-related disorder [RCV003936683]\|not specified [RCV004217411]	likely benign\|uncertain significance	X	154460409	154460409	Human		name , trait , alternate_id
401936146	CV2796316	single nucleotide variant	NM_017514.5(PLXNA3):c.166C>G (p.Leu56Val)	PLXNA3-related disorder [RCV003414117]	uncertain significance	X	154460349	154460349	Human		name , trait , alternate_id
401920370	CV2797502	single nucleotide variant	NM_017514.5(PLXNA3):c.241C>G (p.Pro81Ala)	PLXNA3-related disorder [RCV003402614]	uncertain significance	X	154460424	154460424	Human		name , trait , alternate_id
401937582	CV2798765	single nucleotide variant	NM_017514.5(PLXNA3):c.119G>A (p.Arg40Gln)	PLXNA3-related disorder [RCV003416646]	uncertain significance	X	154460302	154460302	Human		name , trait , alternate_id
401933956	CV2802469	single nucleotide variant	NM_017514.5(PLXNA3):c.262C>T (p.His88Tyr)	PLXNA3-related disorder [RCV003410838]	uncertain significance	X	154460445	154460445	Human		name , trait , alternate_id
401936298	CV2802927	single nucleotide variant	NM_017514.5(PLXNA3):c.2655G>A (p.Pro885=)	PLXNA3-related disorder [RCV003414214]	uncertain significance	X	154466057	154466057	Human		name , trait , alternate_id
401929953	CV2821717	single nucleotide variant	NM_017514.5(PLXNA3):c.196C>T (p.His66Tyr)	not provided [RCV003440068]	likely benign	X	154460379	154460379	Human		name
401930179	CV2821728	single nucleotide variant	NM_017514.5(PLXNA3):c.1284C>T (p.Val428=)	PLXNA3-related disorder [RCV003946628]\|not provided [RCV003440079]	likely benign	X	154462277	154462277	Human		name , trait , alternate_id
401930177	CV2821729	single nucleotide variant	NM_017514.5(PLXNA3):c.1512G>C (p.Gly504=)	not provided [RCV003440080]	likely benign	X	154463655	154463655	Human		name
401930175	CV2821730	single nucleotide variant	NM_017514.5(PLXNA3):c.1596T>C (p.Phe532=)	not provided [RCV003440081]	likely benign	X	154463999	154463999	Human		name
401930170	CV2821732	single nucleotide variant	NM_017514.5(PLXNA3):c.2059C>T (p.Leu687=)	not provided [RCV003440083]	likely benign	X	154465033	154465033	Human		name
405259561	CV3186323	single nucleotide variant	NM_017514.5(PLXNA3):c.2772G>A (p.Thr924=)	not provided [RCV003884082]	likely benign	X	154466243	154466243	Human		name
405262604	CV3189306	single nucleotide variant	NM_017514.5(PLXNA3):c.295C>G (p.Leu99Val)	PLXNA3-related disorder [RCV003896539]	uncertain significance	X	154460478	154460478	Human		name , trait , alternate_id
405264626	CV3190050	single nucleotide variant	NM_017514.5(PLXNA3):c.2760C>T (p.Ala920=)	PLXNA3-related disorder [RCV003897089]	likely benign	X	154466231	154466231	Human		name , trait , alternate_id
405280911	CV3190642	single nucleotide variant	NM_017514.5(PLXNA3):c.1098C>T (p.Pro366=)	PLXNA3-related disorder [RCV003907080]	likely benign	X	154461602	154461602	Human		name , trait , alternate_id
405280208	CV3191681	single nucleotide variant	NM_017514.5(PLXNA3):c.1518G>A (p.Pro506=)	PLXNA3-related disorder [RCV003919819]	likely benign	X	154463661	154463661	Human		name , trait , alternate_id
405276998	CV3192457	single nucleotide variant	NM_017514.5(PLXNA3):c.2529G>A (p.Thr843=)	PLXNA3-related disorder [RCV003917298]	benign	X	154465844	154465844	Human		name , trait , alternate_id
405286711	CV3192915	single nucleotide variant	NM_017514.5(PLXNA3):c.1020C>T (p.Phe340=)	PLXNA3-related disorder [RCV003981619]	likely benign	X	154461524	154461524	Human		name , trait , alternate_id
405289184	CV3193965	single nucleotide variant	NM_017514.5(PLXNA3):c.2145C>T (p.Gly715=)	PLXNA3-related disorder [RCV003983468]	likely benign	X	154465119	154465119	Human		name , trait , alternate_id
405262298	CV3194394	single nucleotide variant	NM_017514.5(PLXNA3):c.1662T>C (p.Pro554=)	PLXNA3-related disorder [RCV003896424]	likely benign	X	154464065	154464065	Human		name , trait , alternate_id
405262406	CV3194411	single nucleotide variant	NM_017514.5(PLXNA3):c.2085C>T (p.Pro695=)	PLXNA3-related disorder [RCV003896440]	likely benign	X	154465059	154465059	Human		name , trait , alternate_id
405259113	CV3194535	single nucleotide variant	NM_017514.5(PLXNA3):c.2778G>A (p.Ser926=)	PLXNA3-related disorder [RCV003893930]	likely benign	X	154466249	154466249	Human		name , trait , alternate_id
405274092	CV3194982	single nucleotide variant	NM_017514.5(PLXNA3):c.2598C>T (p.Gly866=)	PLXNA3-related disorder [RCV003902224]	likely benign	X	154466000	154466000	Human		name , trait , alternate_id
405280506	CV3195560	single nucleotide variant	NM_017514.5(PLXNA3):c.2620C>T (p.Leu874=)	PLXNA3-related disorder [RCV003906804]	likely benign	X	154466022	154466022	Human		name , trait , alternate_id
405265431	CV3195764	single nucleotide variant	NM_017514.5(PLXNA3):c.1734G>A (p.Ala578=)	PLXNA3-related disorder [RCV003897407]	likely benign	X	154464219	154464219	Human		name , trait , alternate_id
405269147	CV3195765	single nucleotide variant	NM_017514.5(PLXNA3):c.2724G>A (p.Pro908=)	PLXNA3-related disorder [RCV003912329]	likely benign	X	154466195	154466195	Human		name , trait , alternate_id
405277693	CV3196018	single nucleotide variant	NM_017514.5(PLXNA3):c.1752G>A (p.Ala584=)	PLXNA3-related disorder [RCV003904539]	likely benign	X	154464237	154464237	Human		name , trait , alternate_id
405272950	CV3197514	single nucleotide variant	NM_017514.5(PLXNA3):c.272C>T (p.Ala91Val)	PLXNA3-related disorder [RCV003901483]	likely benign	X	154460455	154460455	Human		name , trait , alternate_id
405273500	CV3197802	single nucleotide variant	NM_017514.5(PLXNA3):c.2682C>T (p.Ile894=)	PLXNA3-related disorder [RCV003901766]	likely benign	X	154466153	154466153	Human		name , trait , alternate_id
405273575	CV3197841	single nucleotide variant	NM_017514.5(PLXNA3):c.1500C>T (p.Cys500=)	PLXNA3-related disorder [RCV003901804]	likely benign	X	154463643	154463643	Human		name , trait , alternate_id
405273848	CV3198237	single nucleotide variant	NM_017514.5(PLXNA3):c.1887C>T (p.Ala629=)	PLXNA3-related disorder [RCV003902006]	likely benign	X	154464460	154464460	Human		name , trait , alternate_id
405277193	CV3198786	single nucleotide variant	NM_017514.5(PLXNA3):c.1746C>T (p.Asn582=)	PLXNA3-related disorder [RCV003904109]	likely benign	X	154464231	154464231	Human		name , trait , alternate_id
405279980	CV3200166	single nucleotide variant	NM_017514.5(PLXNA3):c.2217C>T (p.Ser739=)	PLXNA3-related disorder [RCV003977094]	likely benign	X	154465191	154465191	Human		name , trait , alternate_id
405268412	CV3201012	single nucleotide variant	NM_017514.5(PLXNA3):c.2331C>T (p.Pro777=)	PLXNA3-related disorder [RCV003899124]	likely benign	X	154465510	154465510	Human		name , trait , alternate_id
405269263	CV3201497	single nucleotide variant	NM_017514.5(PLXNA3):c.2181G>A (p.Gly727=)	PLXNA3-related disorder [RCV003899413]	likely benign	X	154465155	154465155	Human		name , trait , alternate_id
405269392	CV3201573	single nucleotide variant	NM_017514.5(PLXNA3):c.1767C>T (p.Ser589=)	PLXNA3-related disorder [RCV003899486]	likely benign	X	154464252	154464252	Human		name , trait , alternate_id
405269608	CV3201749	single nucleotide variant	NM_017514.5(PLXNA3):c.1056C>T (p.Arg352=)	PLXNA3-related disorder [RCV003899656]	likely benign	X	154461560	154461560	Human		name , trait , alternate_id
405271148	CV3202758	single nucleotide variant	NM_017514.5(PLXNA3):c.1461G>A (p.Pro487=)	PLXNA3-related disorder [RCV003913829]	likely benign	X	154463604	154463604	Human		name , trait , alternate_id
405271494	CV3202827	single nucleotide variant	NM_017514.5(PLXNA3):c.1695G>A (p.Val565=)	PLXNA3-related disorder [RCV003913891]	likely benign	X	154464180	154464180	Human		name , trait , alternate_id
405271612	CV3202878	single nucleotide variant	NM_017514.5(PLXNA3):c.1791C>T (p.Pro597=)	PLXNA3-related disorder [RCV003913940]	likely benign	X	154464276	154464276	Human		name , trait , alternate_id
405275517	CV3204809	single nucleotide variant	NM_017514.5(PLXNA3):c.2580C>T (p.Ile860=)	PLXNA3-related disorder [RCV003952183]	likely benign	X	154465982	154465982	Human		name , trait , alternate_id
405289650	CV3205248	single nucleotide variant	NM_017514.5(PLXNA3):c.1692C>T (p.Asn564=)	PLXNA3-related disorder [RCV003961830]	likely benign	X	154464177	154464177	Human		name , trait , alternate_id
405268598	CV3206157	single nucleotide variant	NM_017514.5(PLXNA3):c.1134C>T (p.Thr378=)	PLXNA3-related disorder [RCV003969853]	likely benign	X	154461638	154461638	Human		name , trait , alternate_id
405292959	CV3207068	single nucleotide variant	NM_017514.5(PLXNA3):c.1254C>T (p.Ala418=)	PLXNA3-related disorder [RCV003931481]	likely benign	X	154462247	154462247	Human		name , trait , alternate_id
405288951	CV3210017	single nucleotide variant	NM_017514.5(PLXNA3):c.1845G>T (p.Val615=)	PLXNA3-related disorder [RCV003961490]	likely benign	X	154464418	154464418	Human		name , trait , alternate_id
405270754	CV3212123	single nucleotide variant	NM_017514.5(PLXNA3):c.1956C>T (p.Tyr652=)	PLXNA3-related disorder [RCV003949492]	likely benign	X	154464781	154464781	Human		name , trait , alternate_id
405282709	CV3213001	single nucleotide variant	NM_017514.5(PLXNA3):c.1656G>A (p.Thr552=)	PLXNA3-related disorder [RCV003957104]	likely benign	X	154464059	154464059	Human		name , trait , alternate_id
405293570	CV3214254	single nucleotide variant	NM_017514.5(PLXNA3):c.1167G>A (p.Leu389=)	PLXNA3-related disorder [RCV003931957]	likely benign	X	154462160	154462160	Human		name , trait , alternate_id
405266549	CV3215934	single nucleotide variant	NM_017514.5(PLXNA3):c.187C>G (p.Leu63Val)	PLXNA3-related disorder [RCV003947059]	likely benign	X	154460370	154460370	Human		name , trait , alternate_id
405282268	CV3216336	single nucleotide variant	NM_017514.5(PLXNA3):c.190C>T (p.Arg64Trp)	PLXNA3-related disorder [RCV003956840]	likely benign	X	154460373	154460373	Human		name , trait , alternate_id
405283184	CV3216968	single nucleotide variant	NM_017514.5(PLXNA3):c.2901A>G (p.Thr967=)	PLXNA3-related disorder [RCV003979119]	benign	X	154466477	154466477	Human		name , trait , alternate_id
405287396	CV3217727	single nucleotide variant	NM_017514.5(PLXNA3):c.2142G>A (p.Ser714=)	PLXNA3-related disorder [RCV003981850]	likely benign	X	154465116	154465116	Human		name , trait , alternate_id
405267472	CV3219303	single nucleotide variant	NM_017514.5(PLXNA3):c.2808G>A (p.Thr936=)	PLXNA3-related disorder [RCV003969562]	likely benign	X	154466384	154466384	Human		name , trait , alternate_id
405267770	CV3219432	single nucleotide variant	NM_017514.5(PLXNA3):c.1302C>T (p.Ser434=)	PLXNA3-related disorder [RCV003969661]	likely benign	X	154462295	154462295	Human		name , trait , alternate_id
405268245	CV3219587	single nucleotide variant	NM_017514.5(PLXNA3):c.1920C>T (p.Val640=)	PLXNA3-related disorder [RCV003969792]	likely benign	X	154464493	154464493	Human		name , trait , alternate_id
405266972	CV3220145	single nucleotide variant	NM_017514.5(PLXNA3):c.2721G>A (p.Pro907=)	PLXNA3-related disorder [RCV003969412]	likely benign	X	154466192	154466192	Human		name , trait , alternate_id
405266996	CV3220153	single nucleotide variant	NM_017514.5(PLXNA3):c.2448G>A (p.Leu816=)	PLXNA3-related disorder [RCV003969418]	likely benign	X	154465763	154465763	Human		name , trait , alternate_id
405651605	CV3366009	single nucleotide variant	NM_017514.5(PLXNA3):c.238C>G (p.Pro80Ala)	not specified [RCV004509352]	uncertain significance	X	154460421	154460421	Human		name
405651610	CV3366011	single nucleotide variant	NM_017514.5(PLXNA3):c.277G>A (p.Val93Met)	PLXNA3-related disorder [RCV004723597]\|not specified [RCV004509354]	uncertain significance	X	154460460	154460460	Human		name , trait , alternate_id
408378956	CV3504168	single nucleotide variant	NM_017514.5(PLXNA3):c.2364G>T (p.Ala788=)	PLXNA3-related disorder [RCV004728116]	likely benign	X	154465679	154465679	Human		name , trait , alternate_id
408382288	CV3504402	single nucleotide variant	NM_017514.5(PLXNA3):c.154C>G (p.Arg52Gly)	PLXNA3-related disorder [RCV004729742]	uncertain significance	X	154460337	154460337	Human		name , trait , alternate_id
408371696	CV3507208	single nucleotide variant	NM_017514.5(PLXNA3):c.145G>A (p.Ala49Thr)	PLXNA3-related disorder [RCV004741804]	uncertain significance	X	154460328	154460328	Human		name , trait , alternate_id
408371761	CV3507437	single nucleotide variant	NM_017514.5(PLXNA3):c.2775G>A (p.Gln925=)	PLXNA3-related disorder [RCV004741847]	likely benign	X	154466246	154466246	Human		name , trait , alternate_id
408371749	CV3507602	single nucleotide variant	NM_017514.5(PLXNA3):c.170C>A (p.Ala57Asp)	PLXNA3-related disorder [RCV004741880]	uncertain significance	X	154460353	154460353	Human		name , trait , alternate_id
408371764	CV3507688	single nucleotide variant	NM_017514.5(PLXNA3):c.242C>G (p.Pro81Arg)	PLXNA3-related disorder [RCV004741896]	uncertain significance	X	154460425	154460425	Human		name , trait , alternate_id
408371826	CV3507771	single nucleotide variant	NM_017514.5(PLXNA3):c.182C>G (p.Thr61Ser)	PLXNA3-related disorder [RCV004741913]	uncertain significance	X	154460365	154460365	Human		name , trait , alternate_id
408371783	CV3507783	single nucleotide variant	NM_017514.5(PLXNA3):c.124A>T (p.Thr42Ser)	PLXNA3-related disorder [RCV004741916]	uncertain significance	X	154460307	154460307	Human		name , trait , alternate_id
408371920	CV3508002	single nucleotide variant	NM_017514.5(PLXNA3):c.2856G>A (p.Arg952=)	PLXNA3-related disorder [RCV004741956]	likely benign	X	154466432	154466432	Human		name , trait , alternate_id
408371853	CV3508181	single nucleotide variant	NM_017514.5(PLXNA3):c.105C>G (p.His35Gln)	PLXNA3-related disorder [RCV004741986]	uncertain significance	X	154460288	154460288	Human		name , trait , alternate_id
408372195	CV3508655	single nucleotide variant	NM_017514.5(PLXNA3):c.2547G>A (p.Val849=)	PLXNA3-related disorder [RCV004742768]	uncertain significance	X	154465949	154465949	Human		name , trait , alternate_id
408372272	CV3509163	single nucleotide variant	NM_017514.5(PLXNA3):c.2910G>C (p.Val970=)	PLXNA3-related disorder [RCV004742867]	likely benign	X	154466486	154466486	Human		name , trait , alternate_id
408372298	CV3509633	single nucleotide variant	NM_017514.5(PLXNA3):c.1677C>T (p.Thr559=)	PLXNA3-related disorder [RCV004742932]	likely benign	X	154464162	154464162	Human		name , trait , alternate_id
408372341	CV3509644	single nucleotide variant	NM_017514.5(PLXNA3):c.1509C>T (p.Ser503=)	PLXNA3-related disorder [RCV004742933]	likely benign	X	154463652	154463652	Human		name , trait , alternate_id
408372352	CV3509756	single nucleotide variant	NM_017514.5(PLXNA3):c.2544C>T (p.Leu848=)	PLXNA3-related disorder [RCV004742947]	likely benign	X	154465946	154465946	Human		name , trait , alternate_id
408372415	CV3510130	single nucleotide variant	NM_017514.5(PLXNA3):c.1575C>T (p.Gly525=)	PLXNA3-related disorder [RCV004743007]	likely benign	X	154463978	154463978	Human		name , trait , alternate_id
408372421	CV3510156	single nucleotide variant	NM_017514.5(PLXNA3):c.2730C>T (p.Pro910=)	PLXNA3-related disorder [RCV004743012]	likely benign	X	154466201	154466201	Human		name , trait , alternate_id
408372381	CV3510197	single nucleotide variant	NM_017514.5(PLXNA3):c.1668G>A (p.Val556=)	PLXNA3-related disorder [RCV004743018]	likely benign	X	154464071	154464071	Human		name , trait , alternate_id
408372431	CV3510455	single nucleotide variant	NM_017514.5(PLXNA3):c.133G>A (p.Val45Met)	PLXNA3-related disorder [RCV004743069]	likely benign	X	154460316	154460316	Human		name , trait , alternate_id
408372773	CV3512561	single nucleotide variant	NM_017514.5(PLXNA3):c.2634C>T (p.Gly878=)	PLXNA3-related disorder [RCV004743872]	likely benign	X	154466036	154466036	Human		name , trait , alternate_id
408372867	CV3512893	single nucleotide variant	NM_017514.5(PLXNA3):c.1065C>G (p.Ser355=)	PLXNA3-related disorder [RCV004743942]	likely benign	X	154461569	154461569	Human		name , trait , alternate_id
408372921	CV3513099	single nucleotide variant	NM_017514.5(PLXNA3):c.2529G>T (p.Thr843=)	PLXNA3-related disorder [RCV004743993]	likely benign	X	154465844	154465844	Human		name , trait , alternate_id
408372948	CV3513291	single nucleotide variant	NM_017514.5(PLXNA3):c.1443G>A (p.Lys481=)	PLXNA3-related disorder [RCV004744027]	likely benign	X	154463516	154463516	Human		name , trait , alternate_id
408373063	CV3513908	single nucleotide variant	NM_017514.5(PLXNA3):c.1491C>T (p.Cys497=)	PLXNA3-related disorder [RCV004744141]	likely benign	X	154463634	154463634	Human		name , trait , alternate_id
408373272	CV3514590	single nucleotide variant	NM_017514.5(PLXNA3):c.2592C>T (p.Asn864=)	PLXNA3-related disorder [RCV004744761]	likely benign	X	154465994	154465994	Human		name , trait , alternate_id
408373283	CV3514666	single nucleotide variant	NM_017514.5(PLXNA3):c.170C>T (p.Ala57Val)	PLXNA3-related disorder [RCV004744777]	uncertain significance	X	154460353	154460353	Human		name , trait , alternate_id
408373291	CV3514708	single nucleotide variant	NM_017514.5(PLXNA3):c.1104G>A (p.Leu368=)	PLXNA3-related disorder [RCV004744782]	likely benign	X	154461608	154461608	Human		name , trait , alternate_id
408373292	CV3514711	single nucleotide variant	NM_017514.5(PLXNA3):c.1203C>T (p.Ile401=)	PLXNA3-related disorder [RCV004744783]	likely benign	X	154462196	154462196	Human		name , trait , alternate_id
408373308	CV3514841	single nucleotide variant	NM_017514.5(PLXNA3):c.1029C>T (p.Ser343=)	PLXNA3-related disorder [RCV004744803]	likely benign	X	154461533	154461533	Human		name , trait , alternate_id
408373355	CV3514968	single nucleotide variant	NM_017514.5(PLXNA3):c.2646C>T (p.Asn882=)	PLXNA3-related disorder [RCV004744833]	likely benign	X	154466048	154466048	Human		name , trait , alternate_id
408373362	CV3514998	single nucleotide variant	NM_017514.5(PLXNA3):c.2292C>T (p.Ser764=)	PLXNA3-related disorder [RCV004744839]	likely benign	X	154465471	154465471	Human		name , trait , alternate_id
408373416	CV3515303	single nucleotide variant	NM_017514.5(PLXNA3):c.2238C>T (p.Asn746=)	PLXNA3-related disorder [RCV004744887]	likely benign	X	154465212	154465212	Human		name , trait , alternate_id
408373474	CV3515663	single nucleotide variant	NM_017514.5(PLXNA3):c.1728C>T (p.Phe576=)	PLXNA3-related disorder [RCV004744939]	likely benign	X	154464213	154464213	Human		name , trait , alternate_id
408373446	CV3515769	single nucleotide variant	NM_017514.5(PLXNA3):c.118C>T (p.Arg40Trp)	PLXNA3-related disorder [RCV004744958]	uncertain significance	X	154460301	154460301	Human		name , trait , alternate_id
408373449	CV3515787	single nucleotide variant	NM_017514.5(PLXNA3):c.253G>A (p.Val85Met)	PLXNA3-related disorder [RCV004744960]\|not specified [RCV005392877]	uncertain significance	X	154460436	154460436	Human		name , trait , alternate_id
408373554	CV3516092	single nucleotide variant	NM_017514.5(PLXNA3):c.1248C>T (p.Ser416=)	PLXNA3-related disorder [RCV004745015]	likely benign	X	154462241	154462241	Human		name , trait , alternate_id
408373597	CV3516249	single nucleotide variant	NM_017514.5(PLXNA3):c.1215C>G (p.Pro405=)	PLXNA3-related disorder [RCV004745043]	likely benign	X	154462208	154462208	Human		name , trait , alternate_id
408373660	CV3516575	single nucleotide variant	NM_017514.5(PLXNA3):c.2349G>A (p.Leu783=)	PLXNA3-related disorder [RCV004745102]	likely benign	X	154465664	154465664	Human		name , trait , alternate_id
408373611	CV3516580	single nucleotide variant	NM_017514.5(PLXNA3):c.2919C>T (p.Ser973=)	PLXNA3-related disorder [RCV004745103]	uncertain significance	X	154466495	154466495	Human		name , trait , alternate_id
408371928	CV3517272	single nucleotide variant	NM_017514.5(PLXNA3):c.202A>G (p.Thr68Ala)	PLXNA3-related disorder [RCV004742064]	uncertain significance	X	154460385	154460385	Human		name , trait , alternate_id
408371985	CV3517357	single nucleotide variant	NM_017514.5(PLXNA3):c.1209G>T (p.Gly403=)	PLXNA3-related disorder [RCV004742078]	likely benign	X	154462202	154462202	Human		name , trait , alternate_id
408372007	CV3517489	single nucleotide variant	NM_017514.5(PLXNA3):c.2568C>T (p.Thr856=)	PLXNA3-related disorder [RCV004742100]	likely benign	X	154465970	154465970	Human		name , trait , alternate_id
408372017	CV3517765	single nucleotide variant	NM_017514.5(PLXNA3):c.203C>T (p.Thr68Met)	PLXNA3-related disorder [RCV004742155]	uncertain significance	X	154460386	154460386	Human		name , trait , alternate_id
408372066	CV3517819	single nucleotide variant	NM_017514.5(PLXNA3):c.1590C>T (p.His530=)	PLXNA3-related disorder [RCV004742164]	likely benign	X	154463993	154463993	Human		name , trait , alternate_id
408372086	CV3518054	single nucleotide variant	NM_017514.5(PLXNA3):c.1326C>T (p.Val442=)	PLXNA3-related disorder [RCV004742202]	likely benign	X	154463399	154463399	Human		name , trait , alternate_id
408372087	CV3518061	single nucleotide variant	NM_017514.5(PLXNA3):c.1986G>A (p.Thr662=)	PLXNA3-related disorder [RCV004742203]	likely benign	X	154464811	154464811	Human		name , trait , alternate_id
597741769	CV3573267	single nucleotide variant	NM_017514.5(PLXNA3):c.227G>A (p.Arg76His)	not specified [RCV004844787]	uncertain significance	X	154460410	154460410	Human		name
597741849	CV3573282	single nucleotide variant	NM_017514.5(PLXNA3):c.269T>A (p.Leu90Gln)	not specified [RCV004844802]	uncertain significance	X	154460452	154460452	Human		name
597741880	CV3573288	single nucleotide variant	NM_017514.5(PLXNA3):c.284A>G (p.Asn95Ser)	not specified [RCV004844808]	uncertain significance	X	154460467	154460467	Human		name
598185500	CV4007133	single nucleotide variant	NM_017514.5(PLXNA3):c.236C>T (p.Pro79Leu)	not specified [RCV005395624]	uncertain significance	X	154460419	154460419	Human		name
12892791	CV404850	single nucleotide variant	NM_017514.5(PLXNA3):c.214G>A (p.Glu72Lys)	Autism [RCV000477925]\|not specified [RCV004837765]	uncertain significance	X	154460397	154460397	Human	2	name
15186855	CV706167	single nucleotide variant	NM_017514.5(PLXNA3):c.172C>T (p.Pro58Ser)	PLXNA3-related disorder [RCV003960647]\|not provided [RCV000953409]\|not specified [RCV004029846]	likely benign\|uncertain significance	X	154460355	154460355	Human		name , trait , alternate_id
15163762	CV706168	single nucleotide variant	NM_017514.5(PLXNA3):c.2289T>C (p.Phe763=)	not provided [RCV000948168]	benign	X	154465468	154465468	Human		name
15198509	CV729513	single nucleotide variant	NM_017514.5(PLXNA3):c.1296G>A (p.Thr432=)	PLXNA3-related disorder [RCV003957937]\|not provided [RCV000890377]	benign\|likely benign	X	154462289	154462289	Human		name , trait , alternate_id
15154047	CV743244	single nucleotide variant	NM_017514.5(PLXNA3):c.266G>A (p.Arg89His)	PLXNA3-related disorder [RCV003958152]\|not provided [RCV000901880]	benign	X	154460449	154460449	Human		name , trait , alternate_id
15182830	CV743251	single nucleotide variant	NM_017514.5(PLXNA3):c.1737G>A (p.Ala579=)	PLXNA3-related disorder [RCV003932928]\|not provided [RCV000907920]\|not specified [RCV004837780]	benign\|likely benign	X	154464222	154464222	Human		name , trait , alternate_id
15192127	CV743252	single nucleotide variant	NM_017514.5(PLXNA3):c.1896C>T (p.Asp632=)	PLXNA3-related disorder [RCV003968392]\|not provided [RCV000910447]	likely benign	X	154464469	154464469	Human		name , trait , alternate_id
15185945	CV743253	single nucleotide variant	NM_017514.5(PLXNA3):c.2469G>A (p.Pro823=)	PLXNA3-related disorder [RCV003968359]\|not provided [RCV000908669]	benign\|likely benign	X	154465784	154465784	Human		name , trait , alternate_id
15147900	CV743254	single nucleotide variant	NM_017514.5(PLXNA3):c.2721G>C (p.Pro907=)	PLXNA3-related disorder [RCV003922956]\|not provided [RCV000900614]	likely benign	X	154466192	154466192	Human		name , trait , alternate_id
15111958	CV758397	single nucleotide variant	NM_017514.5(PLXNA3):c.1878G>A (p.Val626=)	PLXNA3-related disorder [RCV004743194]\|not provided [RCV000916826]	likely benign	X	154464451	154464451	Human		name , trait , alternate_id
15159656	CV758398	single nucleotide variant	NM_017514.5(PLXNA3):c.2202C>T (p.Ala734=)	PLXNA3-related disorder [RCV003960440]\|not provided [RCV000925325]	likely benign	X	154465176	154465176	Human		name , trait , alternate_id
15122497	CV773920	single nucleotide variant	NM_017514.5(PLXNA3):c.1740G>A (p.Ala580=)	PLXNA3-related disorder [RCV003913186]\|not provided [RCV000940694]	likely benign	X	154464225	154464225	Human		name , trait , alternate_id
8637804	CV93030	single nucleotide variant	NM_017514.4(PLXNA3):c.1383C>T (p.Pro461=)	Malignant melanoma [RCV000073128]	not provided	X	154463456	154463456	Human		name
155265276	CV1695487	single nucleotide variant	NM_017514.5(PLXNA3):c.589A>C (p.Ser197Arg)	not provided [RCV002280219]	uncertain significance	X	154460772	154460772	Human		name
156154794	CV2209558	single nucleotide variant	NM_017514.5(PLXNA3):c.431G>T (p.Gly144Val)	PLXNA3-related disorder [RCV003963731]\|not specified [RCV004093667]	uncertain significance	X	154460614	154460614	Human		name , trait , alternate_id
156133983	CV2216935	single nucleotide variant	NM_017514.5(PLXNA3):c.727C>G (p.Leu243Val)	not specified [RCV004083346]	uncertain significance	X	154461231	154461231	Human		name
156089070	CV2295559	single nucleotide variant	NM_017514.5(PLXNA3):c.627C>G (p.Ile209Met)	not specified [RCV004160653]	uncertain significance	X	154461131	154461131	Human		name
156196241	CV2297322	single nucleotide variant	NM_017514.5(PLXNA3):c.719C>T (p.Thr240Met)	PLXNA3-related disorder [RCV003420458]\|not specified [RCV004152981]	uncertain significance	X	154461223	154461223	Human		name , trait , alternate_id
156273494	CV2344136	single nucleotide variant	NM_017514.5(PLXNA3):c.662C>T (p.Ala221Val)	PLXNA3-related disorder [RCV004741535]\|not specified [RCV004195735]	uncertain significance	X	154461166	154461166	Human		name , trait , alternate_id
156089645	CV2344464	single nucleotide variant	NM_017514.5(PLXNA3):c.524C>T (p.Ser175Leu)	PLXNA3-related disorder [RCV003420488]\|not specified [RCV004195208]	uncertain significance	X	154460707	154460707	Human		name , trait , alternate_id
155990178	CV2352367	single nucleotide variant	NM_017514.5(PLXNA3):c.341G>C (p.Ser114Thr)	PLXNA3-related disorder [RCV003963764]\|not specified [RCV004200835]	likely benign\|uncertain significance	X	154460524	154460524	Human		name , trait , alternate_id
156049879	CV2367399	single nucleotide variant	NM_017514.5(PLXNA3):c.868C>T (p.Arg290Cys)	PLXNA3-related disorder [RCV004741541]\|not specified [RCV004209301]	uncertain significance	X	154461372	154461372	Human		name , trait , alternate_id
156059284	CV2383522	single nucleotide variant	NM_017514.5(PLXNA3):c.983G>A (p.Arg328Gln)	PLXNA3-related disorder [RCV004741543]\|not specified [RCV004222529]	uncertain significance	X	154461487	154461487	Human		name , trait , alternate_id
155998811	CV2396307	single nucleotide variant	NM_017514.5(PLXNA3):c.941A>C (p.Glu314Ala)	not specified [RCV004242039]	uncertain significance	X	154461445	154461445	Human		name
329372829	CV2428670	single nucleotide variant	NM_017514.5(PLXNA3):c.371G>A (p.Arg124His)	PLXNA3-related disorder [RCV003919025]\|not specified [RCV004255467]	likely benign\|uncertain significance	X	154460554	154460554	Human		name , trait , alternate_id
329359790	CV2446412	single nucleotide variant	NM_017514.5(PLXNA3):c.578C>A (p.Ala193Glu)	PLXNA3-related disorder [RCV004741563]\|not specified [RCV004249531]	uncertain significance	X	154460761	154460761	Human		name , trait , alternate_id
401740044	CV2683243	single nucleotide variant	NM_017514.5(PLXNA3):c.514G>A (p.Asp172Asn)	PLXNA3-related disorder [RCV004741579]\|not specified [RCV004286239]	uncertain significance	X	154460697	154460697	Human		name , trait , alternate_id
401751226	CV2712474	single nucleotide variant	NM_017514.5(PLXNA3):c.832T>C (p.Phe278Leu)	PLXNA3-related disorder [RCV004741583]\|not specified [RCV004313936]	uncertain significance	X	154461336	154461336	Human		name , trait , alternate_id
401770786	CV2726260	single nucleotide variant	NM_017514.5(PLXNA3):c.434C>A (p.Ala145Asp)	not specified [RCV004326712]	uncertain significance	X	154460617	154460617	Human		name
401829987	CV2744108	single nucleotide variant	NM_017514.5(PLXNA3):c.653T>C (p.Leu218Ser)	not provided [RCV003327250]	uncertain significance	X	154461157	154461157	Human		name
401932188	CV2797209	single nucleotide variant	NM_017514.5(PLXNA3):c.946G>A (p.Val316Ile)	PLXNA3-related disorder [RCV003408631]\|not specified [RCV004661644]	likely benign\|uncertain significance	X	154461450	154461450	Human		name , trait , alternate_id
401913387	CV2797271	single nucleotide variant	NM_017514.5(PLXNA3):c.928G>A (p.Val310Met)	PLXNA3-related disorder [RCV003427840]	uncertain significance	X	154461432	154461432	Human		name , trait , alternate_id
401913464	CV2797338	single nucleotide variant	NM_017514.5(PLXNA3):c.4698G>A (p.Gln1566=)	PLXNA3-related disorder [RCV003427858]	likely benign\|uncertain significance	X	154469482	154469482	Human		name , trait , alternate_id
401932458	CV2797420	single nucleotide variant	NM_017514.5(PLXNA3):c.997C>T (p.Arg333Trp)	PLXNA3-related disorder [RCV003408688]\|not specified [RCV004837889]	uncertain significance	X	154461501	154461501	Human		name , trait , alternate_id
401903050	CV2797796	single nucleotide variant	NM_017514.5(PLXNA3):c.685G>A (p.Gly229Ser)	PLXNA3-related disorder [RCV003419237]\|not specified [RCV004362895]	likely benign\|uncertain significance	X	154461189	154461189	Human		name , trait , alternate_id
401903072	CV2797819	single nucleotide variant	NM_017514.5(PLXNA3):c.409C>T (p.Arg137Cys)	PLXNA3-related disorder [RCV003419248]\|not specified [RCV004362898]	uncertain significance	X	154460592	154460592	Human		name , trait , alternate_id
401902865	CV2799736	single nucleotide variant	NM_017514.5(PLXNA3):c.776C>T (p.Thr259Met)	PLXNA3-related disorder [RCV003419115]	uncertain significance	X	154461280	154461280	Human		name , trait , alternate_id
401933545	CV2801890	single nucleotide variant	NM_017514.5(PLXNA3):c.314C>T (p.Ala105Val)	PLXNA3-related disorder [RCV003410417]\|not specified [RCV004362886]	uncertain significance	X	154460497	154460497	Human		name , trait , alternate_id
401933581	CV2802089	single nucleotide variant	NM_017514.5(PLXNA3):c.827T>C (p.Val276Ala)	PLXNA3-related disorder [RCV003410455]	uncertain significance	X	154461331	154461331	Human		name , trait , alternate_id
401921597	CV2802356	single nucleotide variant	NM_017514.5(PLXNA3):c.935C>G (p.Ala312Gly)	PLXNA3-related disorder [RCV003403000]	uncertain significance	X	154461439	154461439	Human		name , trait , alternate_id
401912657	CV2802862	single nucleotide variant	NM_017514.5(PLXNA3):c.3657G>A (p.Pro1219=)	PLXNA3-related disorder [RCV003399841]	uncertain significance	X	154467838	154467838	Human		name , trait , alternate_id
401933328	CV2804021	single nucleotide variant	NM_017514.5(PLXNA3):c.799G>A (p.Ala267Thr)	PLXNA3-related disorder [RCV003392801]	likely benign\|uncertain significance	X	154461303	154461303	Human		name , trait , alternate_id
401920639	CV2804260	single nucleotide variant	NM_017514.5(PLXNA3):c.998G>A (p.Arg333Gln)	PLXNA3-related disorder [RCV003402697]	likely benign\|uncertain significance	X	154461502	154461502	Human		name , trait , alternate_id
401930198	CV2821719	single nucleotide variant	NM_017514.5(PLXNA3):c.370C>T (p.Arg124Cys)	PLXNA3-related disorder [RCV003901081]\|not provided [RCV003440070]	likely benign\|uncertain significance	X	154460553	154460553	Human		name , trait , alternate_id
401930190	CV2821723	single nucleotide variant	NM_017514.5(PLXNA3):c.841G>A (p.Gly281Ser)	PLXNA3-related disorder [RCV004741607]\|not provided [RCV003440074]	likely benign\|uncertain significance	X	154461345	154461345	Human		name , trait , alternate_id
401930183	CV2821726	single nucleotide variant	NM_017514.5(PLXNA3):c.974A>C (p.Gln325Pro)	not provided [RCV003440077]\|not specified [RCV004847968]	likely benign\|uncertain significance	X	154461478	154461478	Human		name
401930103	CV2821733	single nucleotide variant	NM_017514.5(PLXNA3):c.3309C>T (p.Phe1103=)	PLXNA3-related disorder [RCV003946629]\|not provided [RCV003440084]	likely benign	X	154467339	154467339	Human		name , trait , alternate_id
401930094	CV2821734	single nucleotide variant	NM_017514.5(PLXNA3):c.3411C>T (p.Asp1137=)	PLXNA3-related disorder [RCV003980953]\|not provided [RCV003440085]	likely benign	X	154467441	154467441	Human		name , trait , alternate_id
401930092	CV2821735	single nucleotide variant	NM_017514.5(PLXNA3):c.3459C>T (p.Pro1153=)	PLXNA3-related disorder [RCV004741608]\|not provided [RCV003440086]	likely benign	X	154467562	154467562	Human		name , trait , alternate_id
401930049	CV2821737	single nucleotide variant	NM_017514.5(PLXNA3):c.3571C>A (p.Arg1191=)	PLXNA3-related disorder [RCV003901084]\|not provided [RCV003440088]	likely benign	X	154467674	154467674	Human		name , trait , alternate_id
401925812	CV2821739	single nucleotide variant	NM_017514.5(PLXNA3):c.4089C>T (p.Thr1363=)	PLXNA3-related disorder [RCV003939043]\|not provided [RCV003436872]	likely benign	X	154468428	154468428	Human		name , trait , alternate_id
401925813	CV2821740	single nucleotide variant	NM_017514.5(PLXNA3):c.4290G>A (p.Glu1430=)	PLXNA3-related disorder [RCV004741610]\|not provided [RCV003436873]	likely benign	X	154468825	154468825	Human		name , trait , alternate_id
401925816	CV2821743	single nucleotide variant	NM_017514.5(PLXNA3):c.5103G>A (p.Ala1701=)	PLXNA3-related disorder [RCV003966443]\|not provided [RCV003436876]	likely benign	X	154470558	154470558	Human		name , trait , alternate_id
405263603	CV3189762	single nucleotide variant	NM_017514.5(PLXNA3):c.697G>A (p.Ala233Thr)	PLXNA3-related disorder [RCV003896811]\|not specified [RCV004369740]	likely benign\|uncertain significance	X	154461201	154461201	Human		name , trait , alternate_id
405260102	CV3190166	single nucleotide variant	NM_017514.5(PLXNA3):c.4185C>T (p.Leu1395=)	PLXNA3-related disorder [RCV003894569]	likely benign	X	154468524	154468524	Human		name , trait , alternate_id
405260186	CV3190253	single nucleotide variant	NM_017514.5(PLXNA3):c.4089C>G (p.Thr1363=)	PLXNA3-related disorder [RCV003894652]	likely benign	X	154468428	154468428	Human		name , trait , alternate_id
405260195	CV3190263	single nucleotide variant	NM_017514.5(PLXNA3):c.3279G>A (p.Ala1093=)	PLXNA3-related disorder [RCV003894662]	likely benign	X	154467309	154467309	Human		name , trait , alternate_id
405282449	CV3191017	single nucleotide variant	NM_017514.5(PLXNA3):c.3840G>A (p.Thr1280=)	PLXNA3-related disorder [RCV003921436]	likely benign	X	154468101	154468101	Human		name , trait , alternate_id
405282464	CV3191024	single nucleotide variant	NM_017514.5(PLXNA3):c.5202C>T (p.Phe1734=)	PLXNA3-related disorder [RCV003921443]	likely benign	X	154471150	154471150	Human		name , trait , alternate_id
405285889	CV3191873	single nucleotide variant	NM_017514.5(PLXNA3):c.3183C>T (p.Arg1061=)	PLXNA3-related disorder [RCV003923821]	likely benign	X	154467132	154467132	Human		name , trait , alternate_id
405292609	CV3192538	single nucleotide variant	NM_017514.5(PLXNA3):c.4123C>A (p.Arg1375=)	PLXNA3-related disorder [RCV003929790]	likely benign	X	154468462	154468462	Human		name , trait , alternate_id
405258734	CV3194068	single nucleotide variant	NM_017514.5(PLXNA3):c.5232G>A (p.Thr1744=)	PLXNA3-related disorder [RCV003893650]	likely benign	X	154471180	154471180	Human		name , trait , alternate_id
405258902	CV3194174	single nucleotide variant	NM_017514.5(PLXNA3):c.3675G>A (p.Ala1225=)	PLXNA3-related disorder [RCV003893755]	likely benign	X	154467856	154467856	Human		name , trait , alternate_id
405259270	CV3194628	single nucleotide variant	NM_017514.5(PLXNA3):c.4350C>A (p.Gly1450=)	PLXNA3-related disorder [RCV003894022]	likely benign	X	154468885	154468885	Human		name , trait , alternate_id
405274044	CV3194894	single nucleotide variant	NM_017514.5(PLXNA3):c.5616A>G (p.Ter1872=)	PLXNA3-related disorder [RCV003902136]	likely benign	X	154472685	154472685	Human		name , trait , alternate_id
405257606	CV3195095	single nucleotide variant	NM_017514.5(PLXNA3):c.3549C>T (p.Cys1183=)	PLXNA3-related disorder [RCV003892317]	likely benign	X	154467652	154467652	Human		name , trait , alternate_id
405277446	CV3195784	single nucleotide variant	NM_017514.5(PLXNA3):c.4557G>A (p.Pro1519=)	PLXNA3-related disorder [RCV003904316]	likely benign	X	154469178	154469178	Human		name , trait , alternate_id
405277458	CV3195788	single nucleotide variant	NM_017514.5(PLXNA3):c.3975C>T (p.Asn1325=)	PLXNA3-related disorder [RCV003904320]	likely benign	X	154468314	154468314	Human		name , trait , alternate_id
405290936	CV3197191	single nucleotide variant	NM_017514.5(PLXNA3):c.4023G>A (p.Ala1341=)	PLXNA3-related disorder [RCV003984754]	likely benign	X	154468362	154468362	Human		name , trait , alternate_id
405290951	CV3197208	single nucleotide variant	NM_017514.5(PLXNA3):c.4047G>A (p.Thr1349=)	PLXNA3-related disorder [RCV003984771]	likely benign	X	154468386	154468386	Human		name , trait , alternate_id
405269863	CV3197943	single nucleotide variant	NM_017514.5(PLXNA3):c.4953C>T (p.Ser1651=)	PLXNA3-related disorder [RCV003899756]	likely benign	X	154470134	154470134	Human		name , trait , alternate_id
405273839	CV3198209	single nucleotide variant	NM_017514.5(PLXNA3):c.4723T>C (p.Leu1575=)	PLXNA3-related disorder [RCV003901978]	likely benign	X	154469712	154469712	Human		name , trait , alternate_id
405267698	CV3198438	single nucleotide variant	NM_017514.5(PLXNA3):c.4368G>A (p.Thr1456=)	PLXNA3-related disorder [RCV003911806]	likely benign	X	154468903	154468903	Human		name , trait , alternate_id
405276428	CV3198493	single nucleotide variant	NM_017514.5(PLXNA3):c.3420G>A (p.Pro1140=)	PLXNA3-related disorder [RCV003903825]	likely benign	X	154467450	154467450	Human		name , trait , alternate_id
405268812	CV3201106	single nucleotide variant	NM_017514.5(PLXNA3):c.3216C>T (p.Ile1072=)	PLXNA3-related disorder [RCV003899214]	likely benign	X	154467246	154467246	Human		name , trait , alternate_id
405266851	CV3202114	single nucleotide variant	NM_017514.5(PLXNA3):c.949C>G (p.Leu317Val)	PLXNA3-related disorder [RCV003911590]	uncertain significance	X	154461453	154461453	Human		name , trait , alternate_id
405271201	CV3202783	single nucleotide variant	NM_017514.5(PLXNA3):c.3321C>T (p.His1107=)	PLXNA3-related disorder [RCV003913852]	likely benign	X	154467351	154467351	Human		name , trait , alternate_id
405271401	CV3202797	single nucleotide variant	NM_017514.5(PLXNA3):c.5028G>A (p.Val1676=)	PLXNA3-related disorder [RCV003913864]	likely benign	X	154470483	154470483	Human		name , trait , alternate_id
405271620	CV3202880	single nucleotide variant	NM_017514.5(PLXNA3):c.3246C>T (p.Pro1082=)	PLXNA3-related disorder [RCV003913942]	likely benign	X	154467276	154467276	Human		name , trait , alternate_id
405260438	CV3204055	single nucleotide variant	NM_017514.5(PLXNA3):c.3999C>T (p.Phe1333=)	PLXNA3-related disorder [RCV003943932]	likely benign	X	154468338	154468338	Human		name , trait , alternate_id
405260591	CV3204152	single nucleotide variant	NM_017514.5(PLXNA3):c.5451C>T (p.His1817=)	PLXNA3-related disorder [RCV003944017]	likely benign	X	154471569	154471569	Human		name , trait , alternate_id
405289320	CV3205061	single nucleotide variant	NM_017514.5(PLXNA3):c.4812G>A (p.Thr1604=)	PLXNA3-related disorder [RCV003961673]	likely benign	X	154469993	154469993	Human		name , trait , alternate_id
405290063	CV3205958	single nucleotide variant	NM_017514.5(PLXNA3):c.5331C>T (p.Tyr1777=)	PLXNA3-related disorder [RCV003962122]	likely benign	X	154471279	154471279	Human		name , trait , alternate_id
405279361	CV3206183	single nucleotide variant	NM_017514.5(PLXNA3):c.4173C>T (p.Ile1391=)	PLXNA3-related disorder [RCV003954900]	likely benign	X	154468512	154468512	Human		name , trait , alternate_id
405270998	CV3209180	single nucleotide variant	NM_017514.5(PLXNA3):c.3072C>T (p.Thr1024=)	PLXNA3-related disorder [RCV003949557]	likely benign	X	154466758	154466758	Human		name , trait , alternate_id
405285672	CV3209660	single nucleotide variant	NM_017514.5(PLXNA3):c.5121C>T (p.Ser1707=)	PLXNA3-related disorder [RCV003959237]	likely benign	X	154470576	154470576	Human		name , trait , alternate_id
405261467	CV3209856	single nucleotide variant	NM_017514.5(PLXNA3):c.5373T>C (p.Tyr1791=)	PLXNA3-related disorder [RCV003944500]	likely benign	X	154471491	154471491	Human		name , trait , alternate_id
405270469	CV3211399	single nucleotide variant	NM_017514.5(PLXNA3):c.319C>T (p.Arg107Cys)	PLXNA3-related disorder [RCV003949294]	likely benign\|uncertain significance	X	154460502	154460502	Human		name , trait , alternate_id
405266396	CV3211777	single nucleotide variant	NM_017514.5(PLXNA3):c.578C>T (p.Ala193Val)	PLXNA3-related disorder [RCV003947069]	likely benign	X	154460761	154460761	Human		name , trait , alternate_id
405285299	CV3212289	single nucleotide variant	NM_017514.5(PLXNA3):c.4470C>T (p.Ser1490=)	PLXNA3-related disorder [RCV003958913]	likely benign	X	154469091	154469091	Human		name , trait , alternate_id
405282604	CV3212915	single nucleotide variant	NM_017514.5(PLXNA3):c.4989C>T (p.Gly1663=)	PLXNA3-related disorder [RCV003957034]	likely benign	X	154470444	154470444	Human		name , trait , alternate_id
405275902	CV3216041	single nucleotide variant	NM_017514.5(PLXNA3):c.3232C>T (p.Leu1078=)	PLXNA3-related disorder [RCV003952302]	likely benign	X	154467262	154467262	Human		name , trait , alternate_id
405283676	CV3218607	single nucleotide variant	NM_017514.5(PLXNA3):c.3468C>T (p.Ala1156=)	PLXNA3-related disorder [RCV003957382]	likely benign	X	154467571	154467571	Human		name , trait , alternate_id
405286403	CV3218764	single nucleotide variant	NM_017514.5(PLXNA3):c.4083C>T (p.Arg1361=)	PLXNA3-related disorder [RCV003959476]	likely benign	X	154468422	154468422	Human		name , trait , alternate_id
405279124	CV3219276	single nucleotide variant	NM_017514.5(PLXNA3):c.4794C>T (p.Tyr1598=)	PLXNA3-related disorder [RCV003954823]	likely benign	X	154469783	154469783	Human		name , trait , alternate_id
405267457	CV3219301	single nucleotide variant	NM_017514.5(PLXNA3):c.3966G>A (p.Thr1322=)	PLXNA3-related disorder [RCV003969560]	likely benign	X	154468305	154468305	Human		name , trait , alternate_id
405267544	CV3219336	single nucleotide variant	NM_017514.5(PLXNA3):c.4893G>A (p.Leu1631=)	PLXNA3-related disorder [RCV003969589]	likely benign	X	154470074	154470074	Human		name , trait , alternate_id
405267820	CV3219462	single nucleotide variant	NM_017514.5(PLXNA3):c.3906C>T (p.Tyr1302=)	PLXNA3-related disorder [RCV003969683]	likely benign	X	154468167	154468167	Human		name , trait , alternate_id
405279259	CV3219510	single nucleotide variant	NM_017514.5(PLXNA3):c.3633G>A (p.Ser1211=)	PLXNA3-related disorder [RCV003954872]	likely benign	X	154467814	154467814	Human		name , trait , alternate_id
405262075	CV3220007	single nucleotide variant	NM_017514.5(PLXNA3):c.4020C>T (p.Arg1340=)	PLXNA3-related disorder [RCV003967155]	likely benign	X	154468359	154468359	Human		name , trait , alternate_id
405262078	CV3220008	single nucleotide variant	NM_017514.5(PLXNA3):c.5607C>T (p.Ser1869=)	PLXNA3-related disorder [RCV003967156]	likely benign	X	154472676	154472676	Human		name , trait , alternate_id
405262344	CV3220086	single nucleotide variant	NM_017514.5(PLXNA3):c.4707C>T (p.Asp1569=)	PLXNA3-related disorder [RCV003967219]	likely benign	X	154469696	154469696	Human		name , trait , alternate_id
405278596	CV3220266	single nucleotide variant	NM_017514.5(PLXNA3):c.958A>G (p.Ile320Val)	PLXNA3-related disorder [RCV003976518]	likely benign	X	154461462	154461462	Human		name , trait , alternate_id
405293357	CV3221366	single nucleotide variant	NM_017514.5(PLXNA3):c.5565G>A (p.Lys1855=)	PLXNA3-related disorder [RCV003966868]	likely benign	X	154472634	154472634	Human		name , trait , alternate_id
405261243	CV3221393	single nucleotide variant	NM_017514.5(PLXNA3):c.758C>T (p.Ala253Val)	PLXNA3-related disorder [RCV003966885]	likely benign	X	154461262	154461262	Human		name , trait , alternate_id
405272629	CV3221944	single nucleotide variant	NM_017514.5(PLXNA3):c.3039C>T (p.Pro1013=)	PLXNA3-related disorder [RCV003972204]	benign	X	154466725	154466725	Human		name , trait , alternate_id
405651618	CV3366015	single nucleotide variant	NM_017514.5(PLXNA3):c.304A>G (p.Ile102Val)	PLXNA3-related disorder [RCV004723598]\|not specified [RCV004509358]	uncertain significance	X	154460487	154460487	Human		name , trait , alternate_id
405651620	CV3366016	single nucleotide variant	NM_017514.5(PLXNA3):c.357C>G (p.Ile119Met)	not specified [RCV004509359]	uncertain significance	X	154460540	154460540	Human		name
405651635	CV3366024	single nucleotide variant	NM_017514.5(PLXNA3):c.673T>C (p.Tyr225His)	not specified [RCV004509367]	uncertain significance	X	154461177	154461177	Human		name
405651637	CV3366025	single nucleotide variant	NM_017514.5(PLXNA3):c.691G>A (p.Val231Ile)	PLXNA3-related disorder [RCV004741779]\|not specified [RCV004509368]	uncertain significance	X	154461195	154461195	Human		name , trait , alternate_id
405651639	CV3366026	single nucleotide variant	NM_017514.5(PLXNA3):c.692T>G (p.Val231Gly)	PLXNA3-related disorder [RCV004741780]\|not specified [RCV004509369]	uncertain significance	X	154461196	154461196	Human		name , trait , alternate_id
405651641	CV3366027	single nucleotide variant	NM_017514.5(PLXNA3):c.743C>T (p.Thr248Met)	PLXNA3-related disorder [RCV004741781]\|not specified [RCV004509370]	uncertain significance	X	154461247	154461247	Human		name , trait , alternate_id
405651643	CV3366028	single nucleotide variant	NM_017514.5(PLXNA3):c.853C>T (p.Arg285Cys)	not specified [RCV004509371]	uncertain significance	X	154461357	154461357	Human		name
405651645	CV3366029	single nucleotide variant	NM_017514.5(PLXNA3):c.859G>A (p.Val287Met)	PLXNA3-related disorder [RCV004741782]\|not specified [RCV004509372]	uncertain significance	X	154461363	154461363	Human		name , trait , alternate_id
405651647	CV3366030	single nucleotide variant	NM_017514.5(PLXNA3):c.982C>T (p.Arg328Trp)	not specified [RCV004509373]	uncertain significance	X	154461486	154461486	Human		name
408382399	CV3503257	single nucleotide variant	NM_017514.5(PLXNA3):c.803G>A (p.Gly268Glu)	PLXNA3-related disorder [RCV004729857]	uncertain significance	X	154461307	154461307	Human		name , trait , alternate_id
408376275	CV3505749	single nucleotide variant	NM_017514.5(PLXNA3):c.696C>A (p.Ser232Arg)	PLXNA3-related disorder [RCV004726684]	uncertain significance	X	154461200	154461200	Human		name , trait , alternate_id
408375811	CV3506616	single nucleotide variant	NM_017514.5(PLXNA3):c.572A>G (p.Asp191Gly)	PLXNA3-related disorder [RCV004726402]	uncertain significance	X	154460755	154460755	Human		name , trait , alternate_id
408379512	CV3506973	single nucleotide variant	NM_017514.5(PLXNA3):c.823T>A (p.Tyr275Asn)	PLXNA3-related disorder [RCV004728458]	uncertain significance	X	154461327	154461327	Human		name , trait , alternate_id
408371725	CV3507259	single nucleotide variant	NM_017514.5(PLXNA3):c.5337G>A (p.Lys1779=)	PLXNA3-related disorder [RCV004741812]	likely benign	X	154471285	154471285	Human		name , trait , alternate_id
408371729	CV3507273	single nucleotide variant	NM_017514.5(PLXNA3):c.4077C>G (p.Arg1359=)	PLXNA3-related disorder [RCV004741816]	likely benign	X	154468416	154468416	Human		name , trait , alternate_id
408371720	CV3507447	single nucleotide variant	NM_017514.5(PLXNA3):c.575G>T (p.Ser192Ile)	PLXNA3-related disorder [RCV004741849]	uncertain significance	X	154460758	154460758	Human		name , trait , alternate_id
408371798	CV3507590	single nucleotide variant	NM_017514.5(PLXNA3):c.3324G>C (p.Val1108=)	PLXNA3-related disorder [RCV004741878]	likely benign	X	154467354	154467354	Human		name , trait , alternate_id
408371751	CV3507606	single nucleotide variant	NM_017514.5(PLXNA3):c.779C>G (p.Ser260Cys)	PLXNA3-related disorder [RCV004741882]	uncertain significance	X	154461283	154461283	Human		name , trait , alternate_id
408372132	CV3508527	single nucleotide variant	NM_017514.5(PLXNA3):c.437A>G (p.Gln146Arg)	PLXNA3-related disorder [RCV004742746]	uncertain significance	X	154460620	154460620	Human		name , trait , alternate_id
408372203	CV3508730	single nucleotide variant	NM_017514.5(PLXNA3):c.3276G>C (p.Arg1092=)	PLXNA3-related disorder [RCV004742782]	likely benign	X	154467306	154467306	Human		name , trait , alternate_id
408372371	CV3509897	single nucleotide variant	NM_017514.5(PLXNA3):c.4086C>T (p.Gly1362=)	PLXNA3-related disorder [RCV004742966]	likely benign	X	154468425	154468425	Human		name , trait , alternate_id
408372340	CV3509949	single nucleotide variant	NM_017514.5(PLXNA3):c.854G>A (p.Arg285His)	PLXNA3-related disorder [RCV004742976]	uncertain significance	X	154461358	154461358	Human		name , trait , alternate_id
408372405	CV3510072	single nucleotide variant	NM_017514.5(PLXNA3):c.3681G>A (p.Gly1227=)	PLXNA3-related disorder [RCV004742995]	likely benign	X	154467862	154467862	Human		name , trait , alternate_id
408372422	CV3510157	single nucleotide variant	NM_017514.5(PLXNA3):c.3531G>A (p.Ser1177=)	PLXNA3-related disorder [RCV004743013]	likely benign	X	154467634	154467634	Human		name , trait , alternate_id
408372427	CV3510215	single nucleotide variant	NM_017514.5(PLXNA3):c.3018C>T (p.Asp1006=)	PLXNA3-related disorder [RCV004743023]	likely benign	X	154466704	154466704	Human		name , trait , alternate_id
408372434	CV3510266	single nucleotide variant	NM_017514.5(PLXNA3):c.410G>A (p.Arg137His)	PLXNA3-related disorder [RCV004743033]	uncertain significance	X	154460593	154460593	Human		name , trait , alternate_id
408372467	CV3510427	single nucleotide variant	NM_017514.5(PLXNA3):c.4986G>A (p.Lys1662=)	PLXNA3-related disorder [RCV004743064]	likely benign	X	154470167	154470167	Human		name , trait , alternate_id
408372471	CV3510444	single nucleotide variant	NM_017514.5(PLXNA3):c.856G>A (p.Gly286Ser)	PLXNA3-related disorder [RCV004743067]	uncertain significance	X	154461360	154461360	Human		name , trait , alternate_id
408372499	CV3510634	single nucleotide variant	NM_017514.5(PLXNA3):c.3909C>T (p.Ala1303=)	PLXNA3-related disorder [RCV004743101]	likely benign	X	154468170	154468170	Human		name , trait , alternate_id
408372500	CV3510638	single nucleotide variant	NM_017514.5(PLXNA3):c.3915C>T (p.Arg1305=)	PLXNA3-related disorder [RCV004743102]	likely benign	X	154468176	154468176	Human		name , trait , alternate_id
408372556	CV3511115	single nucleotide variant	NM_017514.5(PLXNA3):c.869G>A (p.Arg290His)	PLXNA3-related disorder [RCV004743167]	likely benign	X	154461373	154461373	Human		name , trait , alternate_id
408372621	CV3511339	single nucleotide variant	NM_017514.5(PLXNA3):c.4656C>T (p.Ile1552=)	PLXNA3-related disorder [RCV004743708]	likely benign	X	154469440	154469440	Human		name , trait , alternate_id
408372655	CV3511549	single nucleotide variant	NM_017514.5(PLXNA3):c.889C>G (p.Leu297Val)	PLXNA3-related disorder [RCV004743746]	uncertain significance	X	154461393	154461393	Human		name , trait , alternate_id
408372670	CV3511676	single nucleotide variant	NM_017514.5(PLXNA3):c.3711C>T (p.Ala1237=)	PLXNA3-related disorder [RCV004743762]	likely benign	X	154467892	154467892	Human		name , trait , alternate_id
408372689	CV3511875	single nucleotide variant	NM_017514.5(PLXNA3):c.3075C>T (p.Val1025=)	PLXNA3-related disorder [RCV004743792]	likely benign	X	154466761	154466761	Human		name , trait , alternate_id
408372759	CV3512456	single nucleotide variant	NM_017514.5(PLXNA3):c.4497C>T (p.Asn1499=)	PLXNA3-related disorder [RCV004743854]	likely benign	X	154469118	154469118	Human		name , trait , alternate_id
408372768	CV3512512	single nucleotide variant	NM_017514.5(PLXNA3):c.5097G>A (p.Glu1699=)	PLXNA3-related disorder [RCV004743863]	likely benign	X	154470552	154470552	Human		name , trait , alternate_id
408372833	CV3512699	single nucleotide variant	NM_017514.5(PLXNA3):c.646C>G (p.Leu216Val)	PLXNA3-related disorder [RCV004743905]	uncertain significance	X	154461150	154461150	Human		name , trait , alternate_id
408372914	CV3513073	single nucleotide variant	NM_017514.5(PLXNA3):c.5406C>T (p.Ser1802=)	PLXNA3-related disorder [RCV004743985]	likely benign	X	154471524	154471524	Human		name , trait , alternate_id
408372920	CV3513097	single nucleotide variant	NM_017514.5(PLXNA3):c.5016C>T (p.Leu1672=)	PLXNA3-related disorder [RCV004743992]	likely benign	X	154470471	154470471	Human		name , trait , alternate_id
408372873	CV3513141	single nucleotide variant	NM_017514.5(PLXNA3):c.4857G>A (p.Thr1619=)	PLXNA3-related disorder [RCV004743998]	likely benign	X	154470038	154470038	Human		name , trait , alternate_id
408372932	CV3513152	single nucleotide variant	NM_017514.5(PLXNA3):c.448T>G (p.Ser150Ala)	PLXNA3-related disorder [RCV004744000]	uncertain significance	X	154460631	154460631	Human		name , trait , alternate_id
408372934	CV3513167	single nucleotide variant	NM_017514.5(PLXNA3):c.5445C>T (p.Arg1815=)	PLXNA3-related disorder [RCV004744004]	likely benign	X	154471563	154471563	Human		name , trait , alternate_id
408372959	CV3513347	single nucleotide variant	NM_017514.5(PLXNA3):c.4677C>T (p.Leu1559=)	PLXNA3-related disorder [RCV004744036]	likely benign	X	154469461	154469461	Human		name , trait , alternate_id
408372960	CV3513348	single nucleotide variant	NM_017514.5(PLXNA3):c.5457C>T (p.Ser1819=)	PLXNA3-related disorder [RCV004744037]	likely benign	X	154471575	154471575	Human		name , trait , alternate_id
408373082	CV3513991	single nucleotide variant	NM_017514.5(PLXNA3):c.3135G>C (p.Gly1045=)	PLXNA3-related disorder [RCV004744157]	likely benign	X	154467084	154467084	Human		name , trait , alternate_id
408373132	CV3514053	single nucleotide variant	NM_017514.5(PLXNA3):c.4488G>A (p.Lys1496=)	PLXNA3-related disorder [RCV004744660]	likely benign	X	154469109	154469109	Human		name , trait , alternate_id
408373201	CV3514246	single nucleotide variant	NM_017514.5(PLXNA3):c.4533G>A (p.Leu1511=)	PLXNA3-related disorder [RCV004744701]	likely benign	X	154469154	154469154	Human		name , trait , alternate_id
408373205	CV3514289	single nucleotide variant	NM_017514.5(PLXNA3):c.445G>A (p.Asp149Asn)	PLXNA3-related disorder [RCV004744707]	uncertain significance	X	154460628	154460628	Human		name , trait , alternate_id
408373207	CV3514299	single nucleotide variant	NM_017514.5(PLXNA3):c.3678G>A (p.Ala1226=)	PLXNA3-related disorder [RCV004744711]	likely benign	X	154467859	154467859	Human		name , trait , alternate_id
408373246	CV3514439	single nucleotide variant	NM_017514.5(PLXNA3):c.3402C>T (p.Gly1134=)	PLXNA3-related disorder [RCV004744734]	likely benign	X	154467432	154467432	Human		name , trait , alternate_id
408373270	CV3514825	single nucleotide variant	NM_017514.5(PLXNA3):c.4455G>A (p.Pro1485=)	PLXNA3-related disorder [RCV004744799]	uncertain significance	X	154469076	154469076	Human		name , trait , alternate_id
408373313	CV3514848	single nucleotide variant	NM_017514.5(PLXNA3):c.5208C>T (p.Phe1736=)	PLXNA3-related disorder [RCV004744805]	likely benign	X	154471156	154471156	Human		name , trait , alternate_id
408373396	CV3515215	single nucleotide variant	NM_017514.5(PLXNA3):c.4656C>A (p.Ile1552=)	PLXNA3-related disorder [RCV004744871]	likely benign	X	154469440	154469440	Human		name , trait , alternate_id
408373412	CV3515547	single nucleotide variant	NM_017514.5(PLXNA3):c.3807G>A (p.Leu1269=)	PLXNA3-related disorder [RCV004744928]	likely benign	X	154467988	154467988	Human		name , trait , alternate_id
408373526	CV3515944	single nucleotide variant	NM_017514.5(PLXNA3):c.5061C>T (p.Pro1687=)	PLXNA3-related disorder [RCV004744995]	likely benign	X	154470516	154470516	Human		name , trait , alternate_id
408373541	CV3515987	single nucleotide variant	NM_017514.5(PLXNA3):c.4647C>T (p.Thr1549=)	PLXNA3-related disorder [RCV004745006]	likely benign	X	154469431	154469431	Human		name , trait , alternate_id
408373594	CV3516223	single nucleotide variant	NM_017514.5(PLXNA3):c.4905C>T (p.His1635=)	PLXNA3-related disorder [RCV004745038]	likely benign	X	154470086	154470086	Human		name , trait , alternate_id
408373602	CV3516279	single nucleotide variant	NM_017514.5(PLXNA3):c.5436G>A (p.Glu1812=)	PLXNA3-related disorder [RCV004745048]	likely benign	X	154471554	154471554	Human		name , trait , alternate_id
408373627	CV3516402	single nucleotide variant	NM_017514.5(PLXNA3):c.5190G>A (p.Lys1730=)	PLXNA3-related disorder [RCV004745073]	likely benign	X	154471138	154471138	Human		name , trait , alternate_id
408373715	CV3516813	single nucleotide variant	NM_017514.5(PLXNA3):c.421T>C (p.Tyr141His)	PLXNA3-related disorder [RCV004745131]	uncertain significance	X	154460604	154460604	Human		name , trait , alternate_id
408371874	CV3516868	single nucleotide variant	NM_017514.5(PLXNA3):c.3027C>T (p.Asn1009=)	PLXNA3-related disorder [RCV004742007]	likely benign	X	154466713	154466713	Human		name , trait , alternate_id
408371915	CV3516891	single nucleotide variant	NM_017514.5(PLXNA3):c.4380A>G (p.Arg1460=)	PLXNA3-related disorder [RCV004742009]	likely benign	X	154468915	154468915	Human		name , trait , alternate_id
408371923	CV3516958	single nucleotide variant	NM_017514.5(PLXNA3):c.4803G>A (p.Leu1601=)	PLXNA3-related disorder [RCV004742016]	likely benign	X	154469984	154469984	Human		name , trait , alternate_id
408371926	CV3516978	single nucleotide variant	NM_017514.5(PLXNA3):c.4362C>T (p.Ala1454=)	PLXNA3-related disorder [RCV004742021]	likely benign	X	154468897	154468897	Human		name , trait , alternate_id
408371931	CV3517017	single nucleotide variant	NM_017514.5(PLXNA3):c.3492T>G (p.Thr1164=)	PLXNA3-related disorder [RCV004742026]	likely benign	X	154467595	154467595	Human		name , trait , alternate_id
408371961	CV3517481	single nucleotide variant	NM_017514.5(PLXNA3):c.919G>A (p.Ala307Thr)	PLXNA3-related disorder [RCV004742097]	uncertain significance	X	154461423	154461423	Human		name , trait , alternate_id
408372008	CV3517495	single nucleotide variant	NM_017514.5(PLXNA3):c.3693G>C (p.Leu1231=)	PLXNA3-related disorder [RCV004742102]	likely benign	X	154467874	154467874	Human		name , trait , alternate_id
408372048	CV3517685	single nucleotide variant	NM_017514.5(PLXNA3):c.4722A>C (p.Ala1574=)	PLXNA3-related disorder [RCV004742141]	likely benign	X	154469711	154469711	Human		name , trait , alternate_id
408372065	CV3517813	single nucleotide variant	NM_017514.5(PLXNA3):c.517G>A (p.Gly173Ser)	PLXNA3-related disorder [RCV004742163]	uncertain significance	X	154460700	154460700	Human		name , trait , alternate_id
408372074	CV3517947	single nucleotide variant	NM_017514.5(PLXNA3):c.3927G>A (p.Pro1309=)	PLXNA3-related disorder [RCV004742180]	likely benign	X	154468188	154468188	Human		name , trait , alternate_id
597741800	CV3573273	single nucleotide variant	NM_017514.5(PLXNA3):c.488G>A (p.Ser163Asn)	not specified [RCV004844793]	uncertain significance	X	154460671	154460671	Human		name
597741822	CV3573277	single nucleotide variant	NM_017514.5(PLXNA3):c.847T>C (p.Ser283Pro)	not specified [RCV004844797]	uncertain significance	X	154461351	154461351	Human		name
597741827	CV3573278	single nucleotide variant	NM_017514.5(PLXNA3):c.848C>T (p.Ser283Phe)	not specified [RCV004844798]	uncertain significance	X	154461352	154461352	Human		name
598185422	CV4007120	single nucleotide variant	NM_017514.5(PLXNA3):c.793A>G (p.Met265Val)	not specified [RCV005395611]	uncertain significance	X	154461297	154461297	Human		name
598185429	CV4007121	single nucleotide variant	NM_017514.5(PLXNA3):c.734C>T (p.Thr245Ile)	not specified [RCV005395612]	uncertain significance	X	154461238	154461238	Human		name
598185456	CV4007126	single nucleotide variant	NM_017514.5(PLXNA3):c.736C>G (p.Gln246Glu)	not specified [RCV005395617]	uncertain significance	X	154461240	154461240	Human		name
598185487	CV4007131	single nucleotide variant	NM_017514.5(PLXNA3):c.685G>T (p.Gly229Cys)	not specified [RCV005395622]	uncertain significance	X	154461189	154461189	Human		name
15163837	CV706170	single nucleotide variant	NM_017514.5(PLXNA3):c.3462T>G (p.Ala1154=)	not provided [RCV000948188]	benign	X	154467565	154467565	Human		name
15163841	CV706171	single nucleotide variant	NM_017514.5(PLXNA3):c.3723C>G (p.Ala1241=)	not provided [RCV000948189]	benign	X	154467904	154467904	Human		name
15179932	CV717728	single nucleotide variant	NM_017514.5(PLXNA3):c.3219C>T (p.Asn1073=)	PLXNA3-related disorder [RCV003906075]\|not provided [RCV000974030]	benign	X	154467249	154467249	Human		name , trait , alternate_id
15175932	CV717729	single nucleotide variant	NM_017514.5(PLXNA3):c.4077C>T (p.Arg1359=)	PLXNA3-related disorder [RCV003936157]\|not provided [RCV000973067]	benign	X	154468416	154468416	Human		name , trait , alternate_id
15101285	CV729514	single nucleotide variant	NM_017514.5(PLXNA3):c.3513G>A (p.Pro1171=)	PLXNA3-related disorder [RCV003983251]\|not provided [RCV000892257]	benign\|likely benign	X	154467616	154467616	Human		name , trait , alternate_id
15152049	CV743245	single nucleotide variant	NM_017514.5(PLXNA3):c.320G>A (p.Arg107His)	PLXNA3-related disorder [RCV003932831]\|not provided [RCV000901485]	benign\|likely benign	X	154460503	154460503	Human		name , trait , alternate_id
15125221	CV743255	single nucleotide variant	NM_017514.5(PLXNA3):c.5478G>A (p.Ala1826=)	PLXNA3-related disorder [RCV004742683]\|not provided [RCV000896724]	likely benign	X	154471596	154471596	Human		name , trait , alternate_id
15203442	CV758399	single nucleotide variant	NM_017514.5(PLXNA3):c.3405G>A (p.Val1135=)	PLXNA3-related disorder [RCV003923198]\|not provided [RCV000913996]	benign\|likely benign	X	154467435	154467435	Human		name , trait , alternate_id
15108428	CV773921	single nucleotide variant	NM_017514.5(PLXNA3):c.5301G>A (p.Gly1767=)	PLXNA3-related disorder [RCV003960529]\|not provided [RCV000938153]	likely benign	X	154471249	154471249	Human		name , trait , alternate_id
15181569	CV773922	single nucleotide variant	NM_017514.5(PLXNA3):c.5598C>T (p.Leu1866=)	PLXNA3-related disorder [RCV003960475]\|not provided [RCV000930158]	likely benign	X	154472667	154472667	Human		name , trait , alternate_id
126909297	CV970362	single nucleotide variant	NM_017514.5(PLXNA3):c.322C>T (p.Arg108Cys)	Hypogonadotropic hypogonadism [RCV001374685]	uncertain significance	X	154460505	154460505	Human	3	name
150410494	CV1196339	single nucleotide variant	NM_017514.5(PLXNA3):c.1322G>A (p.Arg441Gln)	PLXNA3-related disorder [RCV003900808]\|not provided [RCV001573132]	uncertain significance	X	154463395	154463395	Human		name , trait , alternate_id
150476867	CV1279346	single nucleotide variant	NM_017514.5(PLXNA3):c.1049G>A (p.Arg350Gln)	PLXNA3-related disorder [RCV003976066]\|not provided [RCV001714051]	benign	X	154461553	154461553	Human		name , trait , alternate_id
10448548	CV204629	single nucleotide variant	NM_017514.5(PLXNA3):c.1847G>A (p.Arg616Gln)	Childhood-onset schizophrenia [RCV000202331]\|PLXNA3-related disorder [RCV003977502]	benign\|likely benign	X	154464420	154464420	Human	1	name , trait , alternate_id
156315055	CV2104010	single nucleotide variant	NM_017514.5(PLXNA3):c.1585C>G (p.Pro529Ala)	not provided [RCV002937393]	uncertain significance	X	154463988	154463988	Human		name
155915766	CV2200503	single nucleotide variant	NM_017514.5(PLXNA3):c.2717C>T (p.Pro906Leu)	not specified [RCV004078857]	uncertain significance	X	154466188	154466188	Human		name
156237382	CV2206860	single nucleotide variant	NM_017514.5(PLXNA3):c.2702C>T (p.Ser901Leu)	PLXNA3-related disorder [RCV003918953]\|not specified [RCV004083532]	uncertain significance	X	154466173	154466173	Human		name , trait , alternate_id
156112912	CV2212627	single nucleotide variant	NM_017514.5(PLXNA3):c.1460C>T (p.Pro487Leu)	not specified [RCV004085162]	uncertain significance	X	154463603	154463603	Human		name
156134912	CV2213253	single nucleotide variant	NM_017514.5(PLXNA3):c.1468A>T (p.Thr490Ser)	PLXNA3-related disorder [RCV004744642]\|not specified [RCV004085472]	uncertain significance	X	154463611	154463611	Human		name , trait , alternate_id
156383832	CV2220218	single nucleotide variant	NM_017514.5(PLXNA3):c.1492G>A (p.Ala498Thr)	not specified [RCV004095669]	likely benign	X	154463635	154463635	Human		name
156073684	CV2230004	single nucleotide variant	NM_017514.5(PLXNA3):c.1114G>C (p.Glu372Gln)	not specified [RCV004105809]	uncertain significance	X	154461618	154461618	Human		name
155920653	CV2240395	single nucleotide variant	NM_017514.5(PLXNA3):c.1143G>T (p.Gln381His)	not specified [RCV004117293]	uncertain significance	X	154462136	154462136	Human		name
155922985	CV2251823	single nucleotide variant	NM_017514.5(PLXNA3):c.1274A>G (p.His425Arg)	not specified [RCV004119812]	uncertain significance	X	154462267	154462267	Human		name
156310588	CV2260062	single nucleotide variant	NM_017514.5(PLXNA3):c.1268G>A (p.Arg423His)	PLXNA3-related disorder [RCV003918963]\|not specified [RCV004119069]	likely benign	X	154462261	154462261	Human		name , trait , alternate_id
156364769	CV2271988	single nucleotide variant	NM_017514.5(PLXNA3):c.2450G>A (p.Arg817Gln)	not specified [RCV004124798]	uncertain significance	X	154465765	154465765	Human		name
156275375	CV2279973	single nucleotide variant	NM_017514.5(PLXNA3):c.1015C>G (p.Leu339Val)	PLXNA3-related disorder [RCV003420451]\|not specified [RCV004146342]	uncertain significance	X	154461519	154461519	Human		name , trait , alternate_id
156261977	CV2282444	single nucleotide variant	NM_017514.5(PLXNA3):c.2053G>A (p.Glu685Lys)	not specified [RCV004133252]	uncertain significance	X	154465027	154465027	Human		name
156276395	CV2287728	single nucleotide variant	NM_017514.5(PLXNA3):c.2462C>T (p.Pro821Leu)	PLXNA3-related disorder [RCV003420455]\|not specified [RCV004141145]	uncertain significance	X	154465777	154465777	Human		name , trait , alternate_id
156005161	CV2290295	single nucleotide variant	NM_017514.5(PLXNA3):c.1560A>C (p.Glu520Asp)	not specified [RCV004154730]	uncertain significance	X	154463963	154463963	Human		name
156274133	CV2344199	single nucleotide variant	NM_017514.5(PLXNA3):c.1918G>A (p.Val640Ile)	PLXNA3-related disorder [RCV003954016]\|not specified [RCV004197839]	likely benign\|uncertain significance	X	154464491	154464491	Human		name , trait , alternate_id
156089980	CV2344585	single nucleotide variant	NM_017514.5(PLXNA3):c.1213C>G (p.Pro405Ala)	not specified [RCV004197358]	uncertain significance	X	154462206	154462206	Human		name
155902095	CV2345928	single nucleotide variant	NM_017514.5(PLXNA3):c.2012C>T (p.Ser671Phe)	PLXNA3-related disorder [RCV004741537]\|not specified [RCV004198965]	uncertain significance	X	154464837	154464837	Human		name , trait , alternate_id
155991600	CV2355482	single nucleotide variant	NM_017514.5(PLXNA3):c.1423A>G (p.Ile475Val)	not specified [RCV004205332]	uncertain significance	X	154463496	154463496	Human		name
155926857	CV2365831	single nucleotide variant	NM_017514.5(PLXNA3):c.2239G>A (p.Ala747Thr)	PLXNA3-related disorder [RCV003420499]\|not specified [RCV004214366]	uncertain significance	X	154465213	154465213	Human		name , trait , alternate_id
156308830	CV2366479	single nucleotide variant	NM_017514.5(PLXNA3):c.1733C>T (p.Ala578Val)	PLXNA3-related disorder [RCV003954026]\|not specified [RCV004208456]	likely benign\|uncertain significance	X	154464218	154464218	Human		name , trait , alternate_id
156257144	CV2369313	single nucleotide variant	NM_017514.5(PLXNA3):c.1225G>A (p.Asp409Asn)	PLXNA3-related disorder [RCV003420502]\|not specified [RCV004208222]	uncertain significance	X	154462218	154462218	Human		name , trait , alternate_id
156156590	CV2388874	single nucleotide variant	NM_017514.5(PLXNA3):c.2654C>T (p.Pro885Leu)	PLXNA3-related disorder [RCV003395689]\|not specified [RCV004239715]	uncertain significance	X	154466056	154466056	Human		name , trait , alternate_id
155930085	CV2389305	single nucleotide variant	NM_017514.5(PLXNA3):c.2942A>C (p.Asp981Ala)	PLXNA3-related disorder [RCV003420534]\|not specified [RCV004235617]	uncertain significance	X	154466628	154466628	Human		name , trait , alternate_id
155955464	CV2389956	single nucleotide variant	NM_017514.5(PLXNA3):c.2038C>T (p.Pro680Ser)	PLXNA3-related disorder [RCV003427681]\|not specified [RCV004238208]	uncertain significance	X	154464863	154464863	Human		name , trait , alternate_id
329358656	CV2425302	single nucleotide variant	NM_017514.5(PLXNA3):c.1048C>T (p.Arg350Trp)	PLXNA3-related disorder [RCV003396940]\|not specified [RCV004250969]	likely benign\|uncertain significance	X	154461552	154461552	Human		name , trait , alternate_id
329374879	CV2440101	single nucleotide variant	NM_017514.5(PLXNA3):c.1627C>T (p.Arg543Trp)	PLXNA3-related disorder [RCV004741565]\|not specified [RCV004260566]	uncertain significance	X	154464030	154464030	Human		name , trait , alternate_id
329367020	CV2442045	single nucleotide variant	NM_017514.5(PLXNA3):c.2099A>G (p.Gln700Arg)	PLXNA3-related disorder [RCV003395716]\|not specified [RCV004262202]	uncertain significance	X	154465073	154465073	Human		name , trait , alternate_id
329398616	CV2471108	single nucleotide variant	NM_017514.5(PLXNA3):c.1555C>T (p.Arg519Cys)	PLXNA3-related disorder [RCV004741572]\|not specified [RCV004278363]	uncertain significance	X	154463958	154463958	Human		name , trait , alternate_id
401744855	CV2681138	single nucleotide variant	NM_017514.5(PLXNA3):c.1576G>A (p.Ala526Thr)	PLXNA3-related disorder [RCV003900996]\|not specified [RCV004296192]	uncertain significance	X	154463979	154463979	Human		name , trait , alternate_id
401725190	CV2697306	single nucleotide variant	NM_017514.5(PLXNA3):c.2521C>T (p.Arg841Cys)	not specified [RCV004304064]	uncertain significance	X	154465836	154465836	Human		name
401740395	CV2706103	single nucleotide variant	NM_017514.5(PLXNA3):c.2282T>C (p.Leu761Pro)	PLXNA3-related disorder [RCV003396980]\|not specified [RCV004314793]	uncertain significance	X	154465461	154465461	Human		name , trait , alternate_id
401861720	CV2756448	single nucleotide variant	NM_017514.5(PLXNA3):c.1768G>A (p.Gly590Ser)	PLXNA3-related disorder [RCV004741597]\|not specified [RCV004342983]	uncertain significance	X	154464253	154464253	Human		name , trait , alternate_id
401882804	CV2788599	single nucleotide variant	NM_017514.5(PLXNA3):c.1586C>T (p.Pro529Leu)	not specified [RCV004361093]	uncertain significance	X	154463989	154463989	Human		name
401875345	CV2789024	single nucleotide variant	NM_017514.5(PLXNA3):c.2545G>T (p.Val849Leu)	not specified [RCV004363331]	uncertain significance	X	154465947	154465947	Human		name
401934673	CV2795987	single nucleotide variant	NM_017514.5(PLXNA3):c.1354G>C (p.Glu452Gln)	PLXNA3-related disorder [RCV003412017]	uncertain significance	X	154463427	154463427	Human		name , trait , alternate_id
401912138	CV2796066	single nucleotide variant	NM_017514.5(PLXNA3):c.1808G>A (p.Arg603Gln)	PLXNA3-related disorder [RCV003399762]\|not specified [RCV004362787]	likely benign\|uncertain significance	X	154464293	154464293	Human		name , trait , alternate_id
401925898	CV2796322	single nucleotide variant	NM_017514.5(PLXNA3):c.2570G>A (p.Arg857Gln)	PLXNA3-related disorder [RCV003405785]\|not specified [RCV004362815]	uncertain significance	X	154465972	154465972	Human		name , trait , alternate_id
401913381	CV2797269	single nucleotide variant	NM_017514.5(PLXNA3):c.1888G>A (p.Gly630Ser)	PLXNA3-related disorder [RCV003427839]	uncertain significance	X	154464461	154464461	Human		name , trait , alternate_id
401913498	CV2797363	single nucleotide variant	NM_017514.5(PLXNA3):c.1057A>G (p.Ile353Val)	PLXNA3-related disorder [RCV003427867]\|not specified [RCV004362845]	uncertain significance	X	154461561	154461561	Human		name , trait , alternate_id
401913593	CV2797575	single nucleotide variant	NM_017514.5(PLXNA3):c.1204G>A (p.Glu402Lys)	PLXNA3-related disorder [RCV003427891]\|not specified [RCV004362860]	uncertain significance	X	154462197	154462197	Human		name , trait , alternate_id
401936504	CV2798615	single nucleotide variant	NM_017514.5(PLXNA3):c.2761G>A (p.Asp921Asn)	PLXNA3-related disorder [RCV003414517]\|not specified [RCV004654206]	uncertain significance	X	154466232	154466232	Human		name , trait , alternate_id
401913186	CV2798620	single nucleotide variant	NM_017514.5(PLXNA3):c.1556G>T (p.Arg519Leu)	PLXNA3-related disorder [RCV003427794]\|not specified [RCV004837886]	uncertain significance	X	154463959	154463959	Human		name , trait , alternate_id
401907393	CV2800212	single nucleotide variant	NM_017514.5(PLXNA3):c.1928C>T (p.Ser643Leu)	PLXNA3-related disorder [RCV003397347]	uncertain significance	X	154464501	154464501	Human		name , trait , alternate_id
401902048	CV2804037	single nucleotide variant	NM_017514.5(PLXNA3):c.1558G>A (p.Glu520Lys)	PLXNA3-related disorder [RCV003418753]\|not specified [RCV005399372]	uncertain significance	X	154463961	154463961	Human		name , trait , alternate_id
401920500	CV2804065	single nucleotide variant	NM_017514.5(PLXNA3):c.1997G>A (p.Arg666His)	PLXNA3-related disorder [RCV003402654]	uncertain significance	X	154464822	154464822	Human		name , trait , alternate_id
401920591	CV2804149	single nucleotide variant	NM_017514.5(PLXNA3):c.2087T>C (p.Val696Ala)	PLXNA3-related disorder [RCV003402682]	uncertain significance	X	154465061	154465061	Human		name , trait , alternate_id
401913618	CV2804168	single nucleotide variant	NM_017514.5(PLXNA3):c.2723C>T (p.Pro908Leu)	PLXNA3-related disorder [RCV003427898]	uncertain significance	X	154466194	154466194	Human		name , trait , alternate_id
401941827	CV2839695	single nucleotide variant	NM_017514.5(PLXNA3):c.1691A>G (p.Asn564Ser)	Autism [RCV003455874]	uncertain significance	X	154464176	154464176	Human	2	name
404991365	CV2852621	single nucleotide variant	NM_017514.5(PLXNA3):c.1540C>T (p.Arg514Ter)	not specified [RCV003490805]	uncertain significance	X	154463683	154463683	Human		name
405262550	CV3189278	single nucleotide variant	NM_017514.5(PLXNA3):c.2171G>A (p.Arg724Gln)	PLXNA3-related disorder [RCV003896512]	likely benign	X	154465145	154465145	Human		name , trait , alternate_id
405259028	CV3194469	single nucleotide variant	NM_017514.5(PLXNA3):c.1366G>A (p.Val456Met)	PLXNA3-related disorder [RCV003893866]	uncertain significance	X	154463439	154463439	Human		name , trait , alternate_id
405277535	CV3195869	single nucleotide variant	NM_017514.5(PLXNA3):c.1493C>T (p.Ala498Val)	PLXNA3-related disorder [RCV003904396]\|not specified [RCV004369769]	likely benign\|uncertain significance	X	154463636	154463636	Human		name , trait , alternate_id
405277702	CV3196032	single nucleotide variant	NM_017514.5(PLXNA3):c.1678G>A (p.Val560Ile)	PLXNA3-related disorder [RCV003904552]\|not specified [RCV004661818]	uncertain significance	X	154464163	154464163	Human		name , trait , alternate_id
405277883	CV3196138	single nucleotide variant	NM_017514.5(PLXNA3):c.1838G>A (p.Arg613His)	PLXNA3-related disorder [RCV003904655]\|not specified [RCV004837935]	uncertain significance	X	154464411	154464411	Human		name , trait , alternate_id
405275470	CV3196349	single nucleotide variant	NM_017514.5(PLXNA3):c.1295C>T (p.Thr432Met)	PLXNA3-related disorder [RCV003974198]	uncertain significance	X	154462288	154462288	Human		name , trait , alternate_id
405268766	CV3201143	single nucleotide variant	NM_017514.5(PLXNA3):c.2164G>A (p.Val722Met)	PLXNA3-related disorder [RCV003899250]\|not specified [RCV004369735]	uncertain significance	X	154465138	154465138	Human		name , trait , alternate_id
405274758	CV3204440	single nucleotide variant	NM_017514.5(PLXNA3):c.2768G>A (p.Arg923His)	PLXNA3-related disorder [RCV003951882]	uncertain significance	X	154466239	154466239	Human		name , trait , alternate_id
405291787	CV3206089	single nucleotide variant	NM_017514.5(PLXNA3):c.1234G>A (p.Asp412Asn)	PLXNA3-related disorder [RCV003964169]	likely benign	X	154462227	154462227	Human		name , trait , alternate_id
405271897	CV3206325	single nucleotide variant	NM_017514.5(PLXNA3):c.1934T>C (p.Met645Thr)	PLXNA3-related disorder [RCV003971951]\|not specified [RCV005392754]	uncertain significance	X	154464759	154464759	Human		name , trait , alternate_id
405270677	CV3212076	single nucleotide variant	NM_017514.5(PLXNA3):c.2830C>T (p.Arg944Cys)	PLXNA3-related disorder [RCV003949453]	uncertain significance	X	154466406	154466406	Human		name , trait , alternate_id
405259000	CV3215211	single nucleotide variant	NM_017514.5(PLXNA3):c.1249G>A (p.Val417Met)	PLXNA3-related disorder [RCV003942251]	uncertain significance	X	154462242	154462242	Human		name , trait , alternate_id
405270294	CV3215477	single nucleotide variant	NM_017514.5(PLXNA3):c.1634G>A (p.Arg545Gln)	PLXNA3-related disorder [RCV003949217]\|not specified [RCV004369817]	likely benign\|uncertain significance	X	154464037	154464037	Human		name , trait , alternate_id
405266036	CV3215860	single nucleotide variant	NM_017514.5(PLXNA3):c.1327G>A (p.Asp443Asn)	PLXNA3-related disorder [RCV003947005]	uncertain significance	X	154463400	154463400	Human		name , trait , alternate_id
405267374	CV3219264	single nucleotide variant	NM_017514.5(PLXNA3):c.2720C>T (p.Pro907Leu)	PLXNA3-related disorder [RCV003969529]	likely benign	X	154466191	154466191	Human		name , trait , alternate_id
405267988	CV3219512	single nucleotide variant	NM_017514.5(PLXNA3):c.2522G>A (p.Arg841His)	PLXNA3-related disorder [RCV003969726]\|not specified [RCV004654378]	likely benign\|uncertain significance	X	154465837	154465837	Human		name , trait , alternate_id
405261806	CV3219913	single nucleotide variant	NM_017514.5(PLXNA3):c.2806A>G (p.Thr936Ala)	PLXNA3-related disorder [RCV003967082]	likely benign	X	154466382	154466382	Human		name , trait , alternate_id
405265800	CV3220899	single nucleotide variant	NM_017514.5(PLXNA3):c.1314G>C (p.Lys438Asn)	PLXNA3-related disorder [RCV003969062]	likely benign	X	154462307	154462307	Human		name , trait , alternate_id
405261323	CV3221440	single nucleotide variant	NM_017514.5(PLXNA3):c.2268T>G (p.His756Gln)	PLXNA3-related disorder [RCV003966922]\|not specified [RCV004369881]	likely benign\|uncertain significance	X	154465447	154465447	Human		name , trait , alternate_id
405651542	CV3366003	single nucleotide variant	NM_017514.5(PLXNA3):c.1391G>A (p.Arg464Gln)	not specified [RCV004509346]	uncertain significance	X	154463464	154463464	Human		name
405651596	CV3366004	single nucleotide variant	NM_017514.5(PLXNA3):c.1433T>C (p.Leu478Pro)	not specified [RCV004509347]	uncertain significance	X	154463506	154463506	Human		name
405651598	CV3366005	single nucleotide variant	NM_017514.5(PLXNA3):c.1588C>T (p.His530Tyr)	not specified [RCV004509348]	uncertain significance	X	154463991	154463991	Human		name
405651600	CV3366006	single nucleotide variant	NM_017514.5(PLXNA3):c.1990A>G (p.Thr664Ala)	PLXNA3-related disorder [RCV004741777]\|not specified [RCV004509349]	uncertain significance	X	154464815	154464815	Human		name , trait , alternate_id
405651604	CV3366008	single nucleotide variant	NM_017514.5(PLXNA3):c.2183G>A (p.Arg728Gln)	not specified [RCV004509351]	uncertain significance	X	154465157	154465157	Human		name
405651612	CV3366012	single nucleotide variant	NM_017514.5(PLXNA3):c.2823T>A (p.Ser941Arg)	not specified [RCV004509355]	uncertain significance	X	154466399	154466399	Human		name
405651614	CV3366013	single nucleotide variant	NM_017514.5(PLXNA3):c.2855G>A (p.Arg952Gln)	PLXNA3-related disorder [RCV004741778]\|not specified [RCV004509356]	uncertain significance	X	154466431	154466431	Human		name , trait , alternate_id
405651616	CV3366014	single nucleotide variant	NM_017514.5(PLXNA3):c.2920G>A (p.Glu974Lys)	not specified [RCV004509357]	uncertain significance	X	154466496	154466496	Human		name
405854862	CV3394978	single nucleotide variant	NM_017514.5(PLXNA3):c.1080G>C (p.Glu360Asp)	PLXNA3-related disorder [RCV004741785]\|not provided [RCV004555119]	uncertain significance	X	154461584	154461584	Human		name , trait , alternate_id
407471454	CV3467526	single nucleotide variant	NM_017514.5(PLXNA3):c.2971C>G (p.Leu991Val)	not specified [RCV004662285]	likely benign	X	154466657	154466657	Human		name
407471465	CV3467531	single nucleotide variant	NM_017514.5(PLXNA3):c.1055G>A (p.Arg352His)	not specified [RCV004662288]	uncertain significance	X	154461559	154461559	Human		name
407519354	CV3467535	single nucleotide variant	NM_017514.5(PLXNA3):c.1736C>T (p.Ala579Val)	not specified [RCV004651452]	likely benign	X	154464221	154464221	Human		name
407519355	CV3467536	single nucleotide variant	NM_017514.5(PLXNA3):c.2962A>G (p.Ile988Val)	not specified [RCV004651453]	uncertain significance	X	154466648	154466648	Human		name
407471487	CV3467541	single nucleotide variant	NM_017514.5(PLXNA3):c.2784G>C (p.Gln928His)	PLXNA3-related disorder [RCV004741792]\|not specified [RCV004662294]	uncertain significance	X	154466255	154466255	Human		name , trait , alternate_id
408382683	CV3503593	single nucleotide variant	NM_017514.5(PLXNA3):c.1372G>T (p.Asp458Tyr)	PLXNA3-related disorder [RCV004730080]	uncertain significance	X	154463445	154463445	Human		name , trait , alternate_id
408371479	CV3503927	single nucleotide variant	NM_017514.5(PLXNA3):c.2086G>A (p.Val696Ile)	PLXNA3-related disorder [RCV004724723]	uncertain significance	X	154465060	154465060	Human		name , trait , alternate_id
408382366	CV3504499	single nucleotide variant	NM_017514.5(PLXNA3):c.2767C>T (p.Arg923Cys)	PLXNA3-related disorder [RCV004729808]	uncertain significance	X	154466238	154466238	Human		name , trait , alternate_id
408378684	CV3505281	single nucleotide variant	NM_017514.5(PLXNA3):c.2039C>T (p.Pro680Leu)	PLXNA3-related disorder [RCV004727988]	uncertain significance	X	154464864	154464864	Human		name , trait , alternate_id
408375927	CV3506702	single nucleotide variant	NM_017514.5(PLXNA3):c.2296G>T (p.Val766Phe)	PLXNA3-related disorder [RCV004726459]	uncertain significance	X	154465475	154465475	Human		name , trait , alternate_id
408379353	CV3506885	single nucleotide variant	NM_017514.5(PLXNA3):c.1996C>T (p.Arg666Cys)	PLXNA3-related disorder [RCV004728393]	uncertain significance	X	154464821	154464821	Human		name , trait , alternate_id
408379629	CV3507045	single nucleotide variant	NM_017514.5(PLXNA3):c.1402T>C (p.Phe468Leu)	PLXNA3-related disorder [RCV004728503]	uncertain significance	X	154463475	154463475	Human		name , trait , alternate_id
408371701	CV3507269	single nucleotide variant	NM_017514.5(PLXNA3):c.1757T>C (p.Leu586Pro)	PLXNA3-related disorder [RCV004741813]	uncertain significance	X	154464242	154464242	Human		name , trait , alternate_id
408371737	CV3507290	single nucleotide variant	NM_017514.5(PLXNA3):c.1837C>T (p.Arg613Cys)	PLXNA3-related disorder [RCV004741821]	uncertain significance	X	154464410	154464410	Human		name , trait , alternate_id
408371732	CV3507523	single nucleotide variant	NM_017514.5(PLXNA3):c.2659G>A (p.Glu887Lys)	PLXNA3-related disorder [RCV004741863]	uncertain significance	X	154466061	154466061	Human		name , trait , alternate_id
408371757	CV3507624	single nucleotide variant	NM_017514.5(PLXNA3):c.2108C>T (p.Thr703Ile)	PLXNA3-related disorder [RCV004741888]	uncertain significance	X	154465082	154465082	Human		name , trait , alternate_id
408371859	CV3507871	single nucleotide variant	NM_017514.5(PLXNA3):c.1835C>T (p.Thr612Ile)	PLXNA3-related disorder [RCV004741932]	uncertain significance	X	154464408	154464408	Human		name , trait , alternate_id
408371873	CV3507937	single nucleotide variant	NM_017514.5(PLXNA3):c.1055G>T (p.Arg352Leu)	PLXNA3-related disorder [RCV004741945]	uncertain significance	X	154461559	154461559	Human		name , trait , alternate_id
408371876	CV3507967	single nucleotide variant	NM_017514.5(PLXNA3):c.2797G>A (p.Val933Met)	PLXNA3-related disorder [RCV004741952]	uncertain significance	X	154466268	154466268	Human		name , trait , alternate_id
408371893	CV3508183	single nucleotide variant	NM_017514.5(PLXNA3):c.2791A>C (p.Ser931Arg)	PLXNA3-related disorder [RCV004741987]	uncertain significance	X	154466262	154466262	Human		name , trait , alternate_id
408372172	CV3508432	single nucleotide variant	NM_017514.5(PLXNA3):c.1591G>A (p.Gly531Ser)	PLXNA3-related disorder [RCV004742728]	uncertain significance	X	154463994	154463994	Human		name , trait , alternate_id
408372147	CV3508711	single nucleotide variant	NM_017514.5(PLXNA3):c.1862C>T (p.Ser621Phe)	PLXNA3-related disorder [RCV004742778]	uncertain significance	X	154464435	154464435	Human		name , trait , alternate_id
408372251	CV3509256	single nucleotide variant	NM_017514.5(PLXNA3):c.1832C>A (p.Ala611Asp)	PLXNA3-related disorder [RCV004742885]	uncertain significance	X	154464405	154464405	Human		name , trait , alternate_id
408372255	CV3509284	single nucleotide variant	NM_017514.5(PLXNA3):c.1930T>C (p.Cys644Arg)	PLXNA3-related disorder [RCV004742889]	uncertain significance	X	154464755	154464755	Human		name , trait , alternate_id
408372348	CV3509370	single nucleotide variant	NM_017514.5(PLXNA3):c.1820G>C (p.Arg607Thr)	PLXNA3-related disorder [RCV004742899]	uncertain significance	X	154464305	154464305	Human		name , trait , alternate_id
408372393	CV3510260	single nucleotide variant	NM_017514.5(PLXNA3):c.2624G>A (p.Arg875Gln)	PLXNA3-related disorder [RCV004743030]	uncertain significance	X	154466026	154466026	Human		name , trait , alternate_id
408372402	CV3510295	single nucleotide variant	NM_017514.5(PLXNA3):c.1742A>C (p.Glu581Ala)	PLXNA3-related disorder [RCV004743040]	uncertain significance	X	154464227	154464227	Human		name , trait , alternate_id
408372409	CV3510325	single nucleotide variant	NM_017514.5(PLXNA3):c.1600G>A (p.Glu534Lys)	PLXNA3-related disorder [RCV004743047]	uncertain significance	X	154464003	154464003	Human		name , trait , alternate_id
408372440	CV3510494	single nucleotide variant	NM_017514.5(PLXNA3):c.1633C>T (p.Arg545Trp)	PLXNA3-related disorder [RCV004743078]	uncertain significance	X	154464036	154464036	Human		name , trait , alternate_id
408372515	CV3510718	single nucleotide variant	NM_017514.5(PLXNA3):c.1303G>A (p.Gly435Ser)	PLXNA3-related disorder [RCV004743116]	uncertain significance	X	154462296	154462296	Human		name , trait , alternate_id
408372565	CV3511159	single nucleotide variant	NM_017514.5(PLXNA3):c.2207G>A (p.Arg736His)	PLXNA3-related disorder [RCV004743180]	uncertain significance	X	154465181	154465181	Human		name , trait , alternate_id
408372615	CV3511279	single nucleotide variant	NM_017514.5(PLXNA3):c.1418G>A (p.Arg473Gln)	PLXNA3-related disorder [RCV004743695]	uncertain significance	X	154463491	154463491	Human		name , trait , alternate_id
408372575	CV3511283	single nucleotide variant	NM_017514.5(PLXNA3):c.1747G>A (p.Glu583Lys)	PLXNA3-related disorder [RCV004743697]	uncertain significance	X	154464232	154464232	Human		name , trait , alternate_id
408372620	CV3511593	single nucleotide variant	NM_017514.5(PLXNA3):c.1297C>T (p.Arg433Cys)	PLXNA3-related disorder [RCV004743751]	uncertain significance	X	154462290	154462290	Human		name , trait , alternate_id
408372683	CV3511785	single nucleotide variant	NM_017514.5(PLXNA3):c.1556G>A (p.Arg519His)	PLXNA3-related disorder [RCV004743779]	uncertain significance	X	154463959	154463959	Human		name , trait , alternate_id
408372890	CV3513220	single nucleotide variant	NM_017514.5(PLXNA3):c.1900G>A (p.Val634Ile)	PLXNA3-related disorder [RCV004744013]	uncertain significance	X	154464473	154464473	Human		name , trait , alternate_id
408372950	CV3513512	single nucleotide variant	NM_017514.5(PLXNA3):c.2885C>T (p.Ala962Val)	PLXNA3-related disorder [RCV004744069]	uncertain significance	X	154466461	154466461	Human		name , trait , alternate_id
408373029	CV3513669	single nucleotide variant	NM_017514.5(PLXNA3):c.2639G>A (p.Arg880His)	PLXNA3-related disorder [RCV004744098]	uncertain significance	X	154466041	154466041	Human		name , trait , alternate_id
408373017	CV3513833	single nucleotide variant	NM_017514.5(PLXNA3):c.2672C>G (p.Ala891Gly)	PLXNA3-related disorder [RCV004744127]	uncertain significance	X	154466074	154466074	Human		name , trait , alternate_id
408373028	CV3513888	single nucleotide variant	NM_017514.5(PLXNA3):c.1073G>A (p.Arg358His)	PLXNA3-related disorder [RCV004744137]	uncertain significance	X	154461577	154461577	Human		name , trait , alternate_id
408373129	CV3514041	single nucleotide variant	NM_017514.5(PLXNA3):c.2656G>T (p.Ala886Ser)	PLXNA3-related disorder [RCV004744657]	uncertain significance	X	154466058	154466058	Human		name , trait , alternate_id
408373274	CV3514327	single nucleotide variant	NM_017514.5(PLXNA3):c.1645G>A (p.Val549Met)	PLXNA3-related disorder [RCV004744715]	uncertain significance	X	154464048	154464048	Human		name , trait , alternate_id
408373177	CV3514338	single nucleotide variant	NM_017514.5(PLXNA3):c.1709C>T (p.Ala570Val)	PLXNA3-related disorder [RCV004744717]	likely benign	X	154464194	154464194	Human		name , trait , alternate_id
408373338	CV3514888	single nucleotide variant	NM_017514.5(PLXNA3):c.1954T>A (p.Tyr652Asn)	PLXNA3-related disorder [RCV004744817]	uncertain significance	X	154464779	154464779	Human		name , trait , alternate_id
408373391	CV3515204	single nucleotide variant	NM_017514.5(PLXNA3):c.2635G>A (p.Val879Met)	PLXNA3-related disorder [RCV004744867]	uncertain significance	X	154466037	154466037	Human		name , trait , alternate_id
408373465	CV3515537	single nucleotide variant	NM_017514.5(PLXNA3):c.1954T>C (p.Tyr652His)	PLXNA3-related disorder [RCV004744926]	uncertain significance	X	154464779	154464779	Human		name , trait , alternate_id
408373414	CV3515561	single nucleotide variant	NM_017514.5(PLXNA3):c.2327C>G (p.Pro776Arg)	PLXNA3-related disorder [RCV004744930]	uncertain significance	X	154465506	154465506	Human		name , trait , alternate_id
408373523	CV3516141	single nucleotide variant	NM_017514.5(PLXNA3):c.1729G>A (p.Glu577Lys)	PLXNA3-related disorder [RCV004745026]	uncertain significance	X	154464214	154464214	Human		name , trait , alternate_id
408373592	CV3516480	single nucleotide variant	NM_017514.5(PLXNA3):c.1214C>T (p.Pro405Leu)	PLXNA3-related disorder [RCV004745086]	uncertain significance	X	154462207	154462207	Human		name , trait , alternate_id
408373637	CV3516487	single nucleotide variant	NM_017514.5(PLXNA3):c.2278G>A (p.Glu760Lys)	PLXNA3-related disorder [RCV004745089]	uncertain significance	X	154465457	154465457	Human		name , trait , alternate_id
408373651	CV3516542	single nucleotide variant	NM_017514.5(PLXNA3):c.2317A>G (p.Ile773Val)	PLXNA3-related disorder [RCV004745096]	uncertain significance	X	154465496	154465496	Human		name , trait , alternate_id
408371906	CV3517094	single nucleotide variant	NM_017514.5(PLXNA3):c.2854C>T (p.Arg952Trp)	PLXNA3-related disorder [RCV004742041]\|not specified [RCV004848016]	uncertain significance	X	154466430	154466430	Human		name , trait , alternate_id
408371968	CV3517298	single nucleotide variant	NM_017514.5(PLXNA3):c.2604G>C (p.Leu868Phe)	PLXNA3-related disorder [RCV004742067]	uncertain significance	X	154466006	154466006	Human		name , trait , alternate_id
408371994	CV3517462	single nucleotide variant	NM_017514.5(PLXNA3):c.2641T>C (p.Cys881Arg)	PLXNA3-related disorder [RCV004742090]	uncertain significance	X	154466043	154466043	Human		name , trait , alternate_id
408371999	CV3517667	single nucleotide variant	NM_017514.5(PLXNA3):c.1807C>G (p.Arg603Gly)	PLXNA3-related disorder [RCV004742136]	uncertain significance	X	154464292	154464292	Human		name , trait , alternate_id
408372012	CV3517744	single nucleotide variant	NM_017514.5(PLXNA3):c.1723G>A (p.Ala575Thr)	PLXNA3-related disorder [RCV004742150]	uncertain significance	X	154464208	154464208	Human		name , trait , alternate_id
408372035	CV3517882	single nucleotide variant	NM_017514.5(PLXNA3):c.2044G>A (p.Gly682Ser)	PLXNA3-related disorder [RCV004742174]	uncertain significance	X	154465018	154465018	Human		name , trait , alternate_id
408372073	CV3517935	single nucleotide variant	NM_017514.5(PLXNA3):c.2170C>T (p.Arg724Trp)	PLXNA3-related disorder [RCV004742179]	uncertain significance	X	154465144	154465144	Human		name , trait , alternate_id
597741784	CV3573270	single nucleotide variant	NM_017514.5(PLXNA3):c.2545G>A (p.Val849Met)	not specified [RCV004844790]	likely benign	X	154465947	154465947	Human		name
597741789	CV3573271	single nucleotide variant	NM_017514.5(PLXNA3):c.1360G>C (p.Val454Leu)	not specified [RCV004844791]	uncertain significance	X	154463433	154463433	Human		name
597741839	CV3573280	single nucleotide variant	NM_017514.5(PLXNA3):c.1999C>T (p.Pro667Ser)	not specified [RCV004844800]	uncertain significance	X	154464824	154464824	Human		name
597741854	CV3573283	single nucleotide variant	NM_017514.5(PLXNA3):c.1642A>C (p.Asn548His)	not specified [RCV004844803]	uncertain significance	X	154464045	154464045	Human		name
597741866	CV3573285	single nucleotide variant	NM_017514.5(PLXNA3):c.2243C>T (p.Ser748Leu)	not specified [RCV004844805]	uncertain significance	X	154465217	154465217	Human		name
597714559	CV3733121	single nucleotide variant	NM_017514.5(PLXNA3):c.2683G>A (p.Val895Met)	PLXNA3-related neurodevelopmental disorder [RCV005052310]	uncertain significance	X	154466154	154466154	Human		name , trait
597888088	CV3787682	single nucleotide variant	NM_017514.5(PLXNA3):c.1301G>A (p.Ser434Asn)	not provided [RCV005125248]	uncertain significance	X	154462294	154462294	Human		name
598127896	CV3888368	single nucleotide variant	NM_017514.5(PLXNA3):c.1940G>C (p.Cys647Ser)	not provided [RCV005243054]	uncertain significance	X	154464765	154464765	Human		name
598185403	CV4007117	single nucleotide variant	NM_017514.5(PLXNA3):c.1409C>T (p.Pro470Leu)	not specified [RCV005395608]	uncertain significance	X	154463482	154463482	Human		name
598185435	CV4007122	single nucleotide variant	NM_017514.5(PLXNA3):c.2624G>T (p.Arg875Leu)	not specified [RCV005395613]	uncertain significance	X	154466026	154466026	Human		name
598185440	CV4007123	single nucleotide variant	NM_017514.5(PLXNA3):c.2203G>A (p.Val735Met)	not specified [RCV005395614]	uncertain significance	X	154465177	154465177	Human		name
598185452	CV4007125	single nucleotide variant	NM_017514.5(PLXNA3):c.2258G>A (p.Gly753Asp)	not specified [RCV005395616]	uncertain significance	X	154465437	154465437	Human		name
598185462	CV4007127	single nucleotide variant	NM_017514.5(PLXNA3):c.1024C>G (p.Leu342Val)	not specified [RCV005395618]	uncertain significance	X	154461528	154461528	Human		name
13820834	CV576194	single nucleotide variant	NM_017514.5(PLXNA3):c.1985C>T (p.Thr662Met)	not provided [RCV000709913]\|not specified [RCV005392322]	uncertain significance\|not provided	X	154464810	154464810	Human		name
14350143	CV590931	single nucleotide variant	NM_017514.5(PLXNA3):c.1623G>C (p.Gln541His)	Short stature [RCV000736200]\|not specified [RCV004027117]	likely pathogenic\|uncertain significance	X	154464026	154464026	Human	2	name
15163765	CV706169	single nucleotide variant	NM_017514.5(PLXNA3):c.2589G>C (p.Glu863Asp)	not provided [RCV000948169]\|not specified [RCV002249582]	benign	X	154465991	154465991	Human		name
15124408	CV717726	single nucleotide variant	NM_017514.5(PLXNA3):c.1298G>A (p.Arg433His)	PLXNA3-related disorder [RCV003926207]\|not provided [RCV000963411]	benign	X	154462291	154462291	Human		name , trait , alternate_id
15175926	CV717727	single nucleotide variant	NM_017514.5(PLXNA3):c.1958C>T (p.Pro653Leu)	PLXNA3-related disorder [RCV003928547]\|not provided [RCV000973066]	benign	X	154464783	154464783	Human		name , trait , alternate_id
15135707	CV743246	single nucleotide variant	NM_017514.5(PLXNA3):c.1237G>A (p.Gly413Ser)	PLXNA3-related disorder [RCV003958098]\|not provided [RCV000898505]	likely benign	X	154462230	154462230	Human		name , trait , alternate_id
15161636	CV743247	single nucleotide variant	NM_017514.5(PLXNA3):c.1255G>A (p.Ala419Thr)	PLXNA3-related disorder [RCV003958178]\|not provided [RCV000903387]	benign\|likely benign	X	154462248	154462248	Human		name , trait , alternate_id
15134592	CV743248	single nucleotide variant	NM_017514.5(PLXNA3):c.1510G>A (p.Gly504Arg)	not provided [RCV000898317]	benign	X	154463653	154463653	Human		name
15170689	CV743249	single nucleotide variant	NM_017514.5(PLXNA3):c.1628G>A (p.Arg543Gln)	not provided [RCV000905315]	benign	X	154464031	154464031	Human		name
15154051	CV743250	single nucleotide variant	NM_017514.5(PLXNA3):c.1639A>G (p.Asn547Asp)	PLXNA3-related disorder [RCV003958153]\|not provided [RCV000901881]	likely benign	X	154464042	154464042	Human		name , trait , alternate_id
15116877	CV758396	single nucleotide variant	NM_017514.5(PLXNA3):c.1150G>A (p.Gly384Ser)	PLXNA3-related disorder [RCV003933068]\|not provided [RCV000917701]	benign	X	154462143	154462143	Human		name , trait , alternate_id
21075234	CV798228	single nucleotide variant	NM_017514.5(PLXNA3):c.1121C>T (p.Pro374Leu)	not provided [RCV000996074]	uncertain significance	X	154461625	154461625	Human		name
126909292	CV970161	single nucleotide variant	NM_017514.5(PLXNA3):c.1936T>C (p.Ser646Pro)	Hypogonadotropic hypogonadism [RCV001374681]	uncertain significance	X	154464761	154464761	Human	3	name
40815515	CV971193	single nucleotide variant	NM_017514.5(PLXNA3):c.2002C>G (p.His668Asp)	Neurodevelopmental disorder [RCV001262953]	uncertain significance	X	154464827	154464827	Human	1	name
150336900	CV1166437	single nucleotide variant	NM_017514.5(PLXNA3):c.5512C>T (p.Arg1838Cys)	not provided [RCV001532225]	uncertain significance	X	154471630	154471630	Human		name
150412236	CV1196340	single nucleotide variant	NM_017514.5(PLXNA3):c.4454C>T (p.Pro1485Leu)	not provided [RCV001574015]\|not specified [RCV004039423]	uncertain significance	X	154469075	154469075	Human		name
150516287	CV1287284	single nucleotide variant	NM_017514.5(PLXNA3):c.3550G>C (p.Asp1184His)	PLXNA3-related disorder [RCV004743563]\|not provided [RCV001723276]	uncertain significance	X	154467653	154467653	Human		name , trait , alternate_id
151663684	CV1334150	single nucleotide variant	NM_017514.5(PLXNA3):c.3628A>T (p.Ile1210Phe)	not provided [RCV001839324]	uncertain significance	X	154467809	154467809	Human		name
152981739	CV1677038	single nucleotide variant	NM_017514.5(PLXNA3):c.3280C>T (p.Gln1094Ter)	not specified [RCV002248106]	uncertain significance	X	154467310	154467310	Human		name
156399052	CV2194955	single nucleotide variant	NM_017514.5(PLXNA3):c.4112C>T (p.Ala1371Val)	PLXNA3-related disorder [RCV003946349]\|not specified [RCV004075477]	likely benign\|uncertain significance	X	154468451	154468451	Human		name , trait , alternate_id
156376514	CV2206732	single nucleotide variant	NM_017514.5(PLXNA3):c.3572G>A (p.Arg1191Gln)	not specified [RCV004083423]	uncertain significance	X	154467675	154467675	Human		name
156229054	CV2209281	single nucleotide variant	NM_017514.5(PLXNA3):c.3263G>A (p.Arg1088Gln)	not specified [RCV004091682]	likely benign	X	154467293	154467293	Human		name
156154339	CV2209516	single nucleotide variant	NM_017514.5(PLXNA3):c.3080G>A (p.Arg1027His)	not specified [RCV004093635]	uncertain significance	X	154466766	154466766	Human		name
156191491	CV2223108	single nucleotide variant	NM_017514.5(PLXNA3):c.3035G>A (p.Ser1012Asn)	not specified [RCV004103957]	uncertain significance	X	154466721	154466721	Human		name
156105903	CV2257239	single nucleotide variant	NM_017514.5(PLXNA3):c.5570G>A (p.Arg1857Gln)	PLXNA3-related disorder [RCV003963741]\|not specified [RCV004123441]	uncertain significance	X	154472639	154472639	Human		name , trait , alternate_id
156043332	CV2268443	single nucleotide variant	NM_017514.5(PLXNA3):c.4266C>G (p.Phe1422Leu)	not specified [RCV004130145]	uncertain significance	X	154468708	154468708	Human		name
155986102	CV2282495	single nucleotide variant	NM_017514.5(PLXNA3):c.3469G>A (p.Gly1157Ser)	not specified [RCV004133287]	uncertain significance	X	154467572	154467572	Human		name
156069715	CV2292816	single nucleotide variant	NM_017514.5(PLXNA3):c.3746C>T (p.Ala1249Val)	not specified [RCV004154471]	uncertain significance	X	154467927	154467927	Human		name
156204656	CV2297811	single nucleotide variant	NM_017514.5(PLXNA3):c.4834C>T (p.Arg1612Cys)	not specified [RCV004157761]	uncertain significance	X	154470015	154470015	Human		name
155938774	CV2365089	single nucleotide variant	NM_017514.5(PLXNA3):c.3026A>C (p.Asn1009Thr)	PLXNA3-related disorder [RCV003420509]\|not specified [RCV004224245]	uncertain significance	X	154466712	154466712	Human		name , trait , alternate_id
156392164	CV2378335	single nucleotide variant	NM_017514.5(PLXNA3):c.3976G>A (p.Val1326Met)	PLXNA3-related disorder [RCV003395685]\|not specified [RCV004226362]	likely benign\|uncertain significance	X	154468315	154468315	Human		name , trait , alternate_id
156082668	CV2384879	single nucleotide variant	NM_017514.5(PLXNA3):c.3571C>T (p.Arg1191Trp)	not specified [RCV004225755]	uncertain significance	X	154467674	154467674	Human		name
156200020	CV2392331	single nucleotide variant	NM_017514.5(PLXNA3):c.5467G>A (p.Val1823Ile)	PLXNA3-related disorder [RCV003900925]\|not specified [RCV004243929]	uncertain significance	X	154471585	154471585	Human		name , trait , alternate_id
329367804	CV2457107	single nucleotide variant	NM_017514.5(PLXNA3):c.4495A>G (p.Asn1499Asp)	not specified [RCV004264886]	uncertain significance	X	154469116	154469116	Human		name
329352598	CV2463784	single nucleotide variant	NM_017514.5(PLXNA3):c.4926G>C (p.Glu1642Asp)	not specified [RCV004279614]	uncertain significance	X	154470107	154470107	Human		name
401768447	CV2675344	single nucleotide variant	NM_017514.5(PLXNA3):c.4811C>T (p.Thr1604Met)	not specified [RCV004292152]	uncertain significance	X	154469992	154469992	Human		name
401770725	CV2707373	single nucleotide variant	NM_017514.5(PLXNA3):c.3764G>T (p.Arg1255Leu)	not specified [RCV004312766]	uncertain significance	X	154467945	154467945	Human		name
401778628	CV2709374	single nucleotide variant	NM_017514.5(PLXNA3):c.4856C>T (p.Thr1619Met)	not specified [RCV004316515]	uncertain significance	X	154470037	154470037	Human		name
401771770	CV2722940	single nucleotide variant	NM_017514.5(PLXNA3):c.4708G>A (p.Gly1570Ser)	PLXNA3-related disorder [RCV004741585]\|not specified [RCV004327122]	uncertain significance	X	154469697	154469697	Human		name , trait , alternate_id
401897765	CV2776573	single nucleotide variant	NM_017514.5(PLXNA3):c.4027G>A (p.Val1343Met)	not provided [RCV003436034]\|not specified [RCV004355668]	likely benign\|uncertain significance	X	154468366	154468366	Human		name
401923230	CV2796743	single nucleotide variant	NM_017514.5(PLXNA3):c.3488A>G (p.Tyr1163Cys)	PLXNA3-related disorder [RCV003404362]	uncertain significance	X	154467591	154467591	Human		name , trait , alternate_id
401933090	CV2797195	single nucleotide variant	NM_017514.5(PLXNA3):c.3710C>T (p.Ala1237Val)	PLXNA3-related disorder [RCV003392736]	uncertain significance	X	154467891	154467891	Human		name , trait , alternate_id
401933109	CV2797202	single nucleotide variant	NM_017514.5(PLXNA3):c.4915G>A (p.Asp1639Asn)	PLXNA3-related disorder [RCV003392740]	uncertain significance	X	154470096	154470096	Human		name , trait , alternate_id
401919113	CV2798177	single nucleotide variant	NM_017514.5(PLXNA3):c.4621A>G (p.Ile1541Val)	PLXNA3-related disorder [RCV003402203]	uncertain significance	X	154469405	154469405	Human		name , trait , alternate_id
401926586	CV2798665	single nucleotide variant	NM_017514.5(PLXNA3):c.3419C>T (p.Pro1140Leu)	PLXNA3-related disorder [RCV003405983]	uncertain significance	X	154467449	154467449	Human		name , trait , alternate_id
401936573	CV2798760	single nucleotide variant	NM_017514.5(PLXNA3):c.4754T>C (p.Met1585Thr)	PLXNA3-related disorder [RCV003414591]	uncertain significance	X	154469743	154469743	Human		name , trait , alternate_id
401933788	CV2799812	single nucleotide variant	NM_017514.5(PLXNA3):c.3182G>A (p.Arg1061His)	PLXNA3-related disorder [RCV003410664]	uncertain significance	X	154467131	154467131	Human		name , trait , alternate_id
401931245	CV2800676	single nucleotide variant	NM_017514.5(PLXNA3):c.3164G>A (p.Arg1055Gln)	PLXNA3-related disorder [RCV003391273]	uncertain significance	X	154467113	154467113	Human		name , trait , alternate_id
401933897	CV2802368	single nucleotide variant	NM_017514.5(PLXNA3):c.4808G>A (p.Arg1603His)	PLXNA3-related disorder [RCV003410777]\|not specified [RCV004837893]	likely benign\|uncertain significance	X	154469989	154469989	Human		name , trait , alternate_id
401905980	CV2804854	single nucleotide variant	NM_017514.5(PLXNA3):c.4657G>A (p.Glu1553Lys)	PLXNA3-related disorder [RCV003420963]	uncertain significance	X	154469441	154469441	Human		name , trait , alternate_id
401930053	CV2821736	single nucleotide variant	NM_017514.5(PLXNA3):c.3518C>T (p.Ser1173Leu)	PLXNA3-related disorder [RCV004741609]\|not provided [RCV003440087]\|not specified [RCV005399398]	likely benign\|uncertain significance	X	154467621	154467621	Human		name , trait , alternate_id
401925814	CV2821741	single nucleotide variant	NM_017514.5(PLXNA3):c.4910A>G (p.His1637Arg)	not provided [RCV003436874]	uncertain significance	X	154470091	154470091	Human		name
405269508	CV3187323	single nucleotide variant	NM_017514.5(PLXNA3):c.3323T>C (p.Val1108Ala)	not provided [RCV003887407]	uncertain significance	X	154467353	154467353	Human		name
405263527	CV3189721	single nucleotide variant	NM_017514.5(PLXNA3):c.4612A>G (p.Met1538Val)	PLXNA3-related disorder [RCV003896770]	uncertain significance	X	154469396	154469396	Human		name , trait , alternate_id
405264978	CV3190103	single nucleotide variant	NM_017514.5(PLXNA3):c.4777C>T (p.Arg1593Cys)	PLXNA3-related disorder [RCV003897142]	uncertain significance	X	154469766	154469766	Human		name , trait , alternate_id
405283149	CV3191263	single nucleotide variant	NM_017514.5(PLXNA3):c.5293C>T (p.Arg1765Cys)	PLXNA3-related disorder [RCV003921668]\|not specified [RCV005392736]	uncertain significance	X	154471241	154471241	Human		name , trait , alternate_id
405259098	CV3194477	single nucleotide variant	NM_017514.5(PLXNA3):c.3080G>T (p.Arg1027Leu)	PLXNA3-related disorder [RCV003893874]	uncertain significance	X	154466766	154466766	Human		name , trait , alternate_id
405277341	CV3195363	single nucleotide variant	NM_017514.5(PLXNA3):c.3712G>A (p.Val1238Met)	PLXNA3-related disorder [RCV003904153]	likely benign	X	154467893	154467893	Human		name , trait , alternate_id
405277508	CV3195833	single nucleotide variant	NM_017514.5(PLXNA3):c.3415A>C (p.Lys1139Gln)	PLXNA3-related disorder [RCV003904362]\|not specified [RCV004369768]	likely benign\|uncertain significance	X	154467445	154467445	Human		name , trait , alternate_id
405277694	CV3196020	single nucleotide variant	NM_017514.5(PLXNA3):c.5423C>T (p.Ala1808Val)	PLXNA3-related disorder [RCV003904541]	uncertain significance	X	154471541	154471541	Human		name , trait , alternate_id
405268549	CV3201009	single nucleotide variant	NM_017514.5(PLXNA3):c.3914G>A (p.Arg1305His)	PLXNA3-related disorder [RCV003899121]\|not specified [RCV004837929]	uncertain significance	X	154468175	154468175	Human		name , trait , alternate_id
405269096	CV3201238	single nucleotide variant	NM_017514.5(PLXNA3):c.4687G>A (p.Ala1563Thr)	PLXNA3-related disorder [RCV003899344]	likely benign	X	154469471	154469471	Human		name , trait , alternate_id
405257473	CV3201298	single nucleotide variant	NM_017514.5(PLXNA3):c.2999C>T (p.Pro1000Leu)	PLXNA3-related disorder [RCV003892260]	likely benign	X	154466685	154466685	Human		name , trait , alternate_id
405269332	CV3201550	single nucleotide variant	NM_017514.5(PLXNA3):c.3479G>A (p.Arg1160His)	PLXNA3-related disorder [RCV003899464]	likely benign	X	154467582	154467582	Human		name , trait , alternate_id
405291684	CV3206014	single nucleotide variant	NM_017514.5(PLXNA3):c.3910G>A (p.Val1304Met)	PLXNA3-related disorder [RCV003964105]	uncertain significance	X	154468171	154468171	Human		name , trait , alternate_id
405651621	CV3366017	single nucleotide variant	NM_017514.5(PLXNA3):c.3641G>A (p.Arg1214Gln)	not specified [RCV004509360]	uncertain significance	X	154467822	154467822	Human		name
405651623	CV3366018	single nucleotide variant	NM_017514.5(PLXNA3):c.4321T>C (p.Cys1441Arg)	not specified [RCV004509361]	uncertain significance	X	154468856	154468856	Human		name
405651628	CV3366020	single nucleotide variant	NM_017514.5(PLXNA3):c.4799G>A (p.Ser1600Asn)	PLXNA3-related disorder [RCV004723599]\|not specified [RCV004509363]	uncertain significance	X	154469980	154469980	Human		name , trait , alternate_id
405651629	CV3366021	single nucleotide variant	NM_017514.5(PLXNA3):c.5024C>T (p.Thr1675Ile)	not specified [RCV004509364]	uncertain significance	X	154470479	154470479	Human		name
405651631	CV3366022	single nucleotide variant	NM_017514.5(PLXNA3):c.5467G>T (p.Val1823Phe)	not specified [RCV004509365]	uncertain significance	X	154471585	154471585	Human		name
405651633	CV3366023	single nucleotide variant	NM_017514.5(PLXNA3):c.5548T>C (p.Ser1850Pro)	not specified [RCV004509366]	uncertain significance	X	154472617	154472617	Human		name
407487398	CV3414945	single nucleotide variant	NM_017514.5(PLXNA3):c.4078G>A (p.Asp1360Asn)	not specified [RCV004597280]	uncertain significance	X	154468417	154468417	Human		name
407471457	CV3467527	single nucleotide variant	NM_017514.5(PLXNA3):c.5599G>A (p.Val1867Met)	PLXNA3-related disorder [RCV004741788]\|not specified [RCV004662286]	likely benign\|uncertain significance	X	154472668	154472668	Human		name , trait , alternate_id
407519351	CV3467530	single nucleotide variant	NM_017514.5(PLXNA3):c.4656C>G (p.Ile1552Met)	PLXNA3-related disorder [RCV004741790]\|not specified [RCV004651451]	uncertain significance	X	154469440	154469440	Human		name , trait , alternate_id
407471469	CV3467532	single nucleotide variant	NM_017514.5(PLXNA3):c.3278C>T (p.Ala1093Val)	not specified [RCV004662289]	uncertain significance	X	154467308	154467308	Human		name
407471473	CV3467533	single nucleotide variant	NM_017514.5(PLXNA3):c.3674C>T (p.Ala1225Val)	PLXNA3-related disorder [RCV004741791]\|not specified [RCV004662290]	uncertain significance	X	154467855	154467855	Human		name , trait , alternate_id
407471477	CV3467534	single nucleotide variant	NM_017514.5(PLXNA3):c.4775C>T (p.Thr1592Ile)	not specified [RCV004662291]	uncertain significance	X	154469764	154469764	Human		name
407471480	CV3467539	single nucleotide variant	NM_017514.5(PLXNA3):c.5610C>G (p.Asp1870Glu)	not specified [RCV004662292]	uncertain significance	X	154472679	154472679	Human		name
407471483	CV3467540	single nucleotide variant	NM_017514.5(PLXNA3):c.4507A>G (p.Ile1503Val)	not specified [RCV004662293]	uncertain significance	X	154469128	154469128	Human		name
407519360	CV3467542	single nucleotide variant	NM_017514.5(PLXNA3):c.4541T>C (p.Val1514Ala)	not specified [RCV004651456]	uncertain significance	X	154469162	154469162	Human		name
407519362	CV3467543	single nucleotide variant	NM_017514.5(PLXNA3):c.3460G>A (p.Ala1154Thr)	not specified [RCV004651457]	uncertain significance	X	154467563	154467563	Human		name
407471491	CV3467544	single nucleotide variant	NM_017514.5(PLXNA3):c.4931A>C (p.Asp1644Ala)	not specified [RCV004662295]	uncertain significance	X	154470112	154470112	Human		name
407471495	CV3467545	single nucleotide variant	NM_017514.5(PLXNA3):c.3458C>A (p.Pro1153His)	not specified [RCV004662296]	uncertain significance	X	154467561	154467561	Human		name
407471499	CV3467546	single nucleotide variant	NM_017514.5(PLXNA3):c.3032C>T (p.Ser1011Phe)	not specified [RCV004662297]	uncertain significance	X	154466718	154466718	Human		name
408382643	CV3503552	single nucleotide variant	NM_017514.5(PLXNA3):c.3707C>T (p.Thr1236Ile)	PLXNA3-related disorder [RCV004730051]	uncertain significance	X	154467888	154467888	Human		name , trait , alternate_id
408382697	CV3503608	single nucleotide variant	NM_017514.5(PLXNA3):c.4880A>C (p.Lys1627Thr)	PLXNA3-related disorder [RCV004730091]	uncertain significance	X	154470061	154470061	Human		name , trait , alternate_id
408382735	CV3503653	single nucleotide variant	NM_017514.5(PLXNA3):c.3668G>C (p.Gly1223Ala)	PLXNA3-related disorder [RCV004730121]	uncertain significance	X	154467849	154467849	Human		name , trait , alternate_id
408379000	CV3503995	single nucleotide variant	NM_017514.5(PLXNA3):c.3971C>G (p.Pro1324Arg)	PLXNA3-related disorder [RCV004728219]	uncertain significance	X	154468310	154468310	Human		name , trait , alternate_id
408370973	CV3504577	single nucleotide variant	NM_017514.5(PLXNA3):c.5008G>A (p.Asp1670Asn)	PLXNA3-related disorder [RCV004724320]	uncertain significance	X	154470463	154470463	Human		name , trait , alternate_id
408371017	CV3504686	single nucleotide variant	NM_017514.5(PLXNA3):c.3755C>T (p.Thr1252Ile)	PLXNA3-related disorder [RCV004724388]	uncertain significance	X	154467936	154467936	Human		name , trait , alternate_id
408378240	CV3505017	single nucleotide variant	NM_017514.5(PLXNA3):c.3466G>A (p.Ala1156Thr)	PLXNA3-related disorder [RCV004727817]	uncertain significance	X	154467569	154467569	Human		name , trait , alternate_id
408378482	CV3505276	single nucleotide variant	NM_017514.5(PLXNA3):c.5384T>G (p.Ile1795Ser)	PLXNA3-related disorder [RCV004727985]	uncertain significance	X	154471502	154471502	Human		name , trait , alternate_id
408376284	CV3505755	single nucleotide variant	NM_017514.5(PLXNA3):c.4150A>G (p.Lys1384Glu)	PLXNA3-related disorder [RCV004726689]	uncertain significance	X	154468489	154468489	Human		name , trait , alternate_id
408382895	CV3506115	single nucleotide variant	NM_017514.5(PLXNA3):c.4465G>T (p.Gly1489Cys)	PLXNA3-related disorder [RCV004730225]	uncertain significance	X	154469086	154469086	Human		name , trait , alternate_id
408375752	CV3506570	single nucleotide variant	NM_017514.5(PLXNA3):c.3040G>T (p.Gly1014Trp)	PLXNA3-related disorder [RCV004726373]	uncertain significance	X	154466726	154466726	Human		name , trait , alternate_id
408379224	CV3506790	single nucleotide variant	NM_017514.5(PLXNA3):c.3163C>T (p.Arg1055Trp)	PLXNA3-related disorder [RCV004728320]	uncertain significance	X	154467112	154467112	Human		name , trait , alternate_id
408379525	CV3506985	single nucleotide variant	NM_017514.5(PLXNA3):c.4190G>A (p.Ser1397Asn)	PLXNA3-related disorder [RCV004728467]	uncertain significance	X	154468529	154468529	Human		name , trait , alternate_id
408371694	CV3507205	single nucleotide variant	NM_017514.5(PLXNA3):c.4174G>A (p.Glu1392Lys)	PLXNA3-related disorder [RCV004741802]	uncertain significance	X	154468513	154468513	Human		name , trait , alternate_id
408371706	CV3507295	single nucleotide variant	NM_017514.5(PLXNA3):c.5159T>C (p.Leu1720Pro)	PLXNA3-related disorder [RCV004741823]	uncertain significance	X	154471107	154471107	Human		name , trait , alternate_id
408371775	CV3507754	single nucleotide variant	NM_017514.5(PLXNA3):c.3157G>A (p.Glu1053Lys)	PLXNA3-related disorder [RCV004741908]	uncertain significance	X	154467106	154467106	Human		name , trait , alternate_id
408371903	CV3508232	single nucleotide variant	NM_017514.5(PLXNA3):c.3992G>A (p.Arg1331His)	PLXNA3-related disorder [RCV004742001]	uncertain significance	X	154468331	154468331	Human		name , trait , alternate_id
408372106	CV3508338	single nucleotide variant	NM_017514.5(PLXNA3):c.3184G>A (p.Gly1062Ser)	PLXNA3-related disorder [RCV004742710]	uncertain significance	X	154467133	154467133	Human		name , trait , alternate_id
408372115	CV3508389	single nucleotide variant	NM_017514.5(PLXNA3):c.5570G>C (p.Arg1857Pro)	PLXNA3-related disorder [RCV004742719]	uncertain significance	X	154472639	154472639	Human		name , trait , alternate_id
408372129	CV3508599	single nucleotide variant	NM_017514.5(PLXNA3):c.4930G>T (p.Asp1644Tyr)	PLXNA3-related disorder [RCV004742760]	uncertain significance	X	154470111	154470111	Human		name , trait , alternate_id
408372144	CV3508701	single nucleotide variant	NM_017514.5(PLXNA3):c.5068A>G (p.Ile1690Val)	PLXNA3-related disorder [RCV004742775]	uncertain significance	X	154470523	154470523	Human		name , trait , alternate_id
408372219	CV3508822	single nucleotide variant	NM_017514.5(PLXNA3):c.3034A>T (p.Ser1012Cys)	PLXNA3-related disorder [RCV004742798]	likely benign	X	154466720	154466720	Human		name , trait , alternate_id
408372184	CV3508895	single nucleotide variant	NM_017514.5(PLXNA3):c.3727A>G (p.Lys1243Glu)	PLXNA3-related disorder [RCV004742815]	uncertain significance	X	154467908	154467908	Human		name , trait , alternate_id
408372189	CV3508914	single nucleotide variant	NM_017514.5(PLXNA3):c.3984G>T (p.Lys1328Asn)	PLXNA3-related disorder [RCV004742820]	uncertain significance	X	154468323	154468323	Human		name , trait , alternate_id
408372287	CV3509506	single nucleotide variant	NM_017514.5(PLXNA3):c.4618C>T (p.Arg1540Cys)	PLXNA3-related disorder [RCV004742921]	uncertain significance	X	154469402	154469402	Human		name , trait , alternate_id
408372322	CV3509843	single nucleotide variant	NM_017514.5(PLXNA3):c.4657G>C (p.Glu1553Gln)	PLXNA3-related disorder [RCV004742958]	uncertain significance	X	154469441	154469441	Human		name , trait , alternate_id
408372517	CV3510480	single nucleotide variant	NM_017514.5(PLXNA3):c.3700G>A (p.Ala1234Thr)	PLXNA3-related disorder [RCV004743075]	uncertain significance	X	154467881	154467881	Human		name , trait , alternate_id
408372482	CV3510755	single nucleotide variant	NM_017514.5(PLXNA3):c.5483A>G (p.Asn1828Ser)	PLXNA3-related disorder [RCV004743121]	uncertain significance	X	154471601	154471601	Human		name , trait , alternate_id
408372597	CV3511206	single nucleotide variant	NM_017514.5(PLXNA3):c.5287G>A (p.Glu1763Lys)	PLXNA3-related disorder [RCV004743682]	uncertain significance	X	154471235	154471235	Human		name , trait , alternate_id
408372619	CV3511338	single nucleotide variant	NM_017514.5(PLXNA3):c.3612G>T (p.Trp1204Cys)	PLXNA3-related disorder [RCV004743707]	uncertain significance	X	154467793	154467793	Human		name , trait , alternate_id
408372647	CV3511787	single nucleotide variant	NM_017514.5(PLXNA3):c.3583A>T (p.Met1195Leu)	PLXNA3-related disorder [RCV004743780]	uncertain significance	X	154467686	154467686	Human		name , trait , alternate_id
408372747	CV3512607	single nucleotide variant	NM_017514.5(PLXNA3):c.5477C>T (p.Ala1826Val)	PLXNA3-related disorder [RCV004743882]	uncertain significance	X	154471595	154471595	Human		name , trait , alternate_id
408372764	CV3512663	single nucleotide variant	NM_017514.5(PLXNA3):c.4420G>A (p.Asp1474Asn)	PLXNA3-related disorder [RCV004743900]\|not specified [RCV004837946]	uncertain significance	X	154468955	154468955	Human		name , trait , alternate_id
408372776	CV3512758	single nucleotide variant	NM_017514.5(PLXNA3):c.3722C>A (p.Ala1241Asp)	PLXNA3-related disorder [RCV004743912]	uncertain significance	X	154467903	154467903	Human		name , trait , alternate_id
408372980	CV3513659	single nucleotide variant	NM_017514.5(PLXNA3):c.3262C>T (p.Arg1088Trp)	PLXNA3-related disorder [RCV004744095]\|not specified [RCV004837949]	uncertain significance	X	154467292	154467292	Human		name , trait , alternate_id
408373249	CV3514451	single nucleotide variant	NM_017514.5(PLXNA3):c.5294G>T (p.Arg1765Leu)	PLXNA3-related disorder [RCV004744736]	uncertain significance	X	154471242	154471242	Human		name , trait , alternate_id
408373221	CV3514565	single nucleotide variant	NM_017514.5(PLXNA3):c.3346C>T (p.Arg1116Cys)	PLXNA3-related disorder [RCV004744756]	uncertain significance	X	154467376	154467376	Human		name , trait , alternate_id
408373229	CV3514602	single nucleotide variant	NM_017514.5(PLXNA3):c.5555G>A (p.Arg1852Gln)	PLXNA3-related disorder [RCV004744764]	uncertain significance	X	154472624	154472624	Human		name , trait , alternate_id
408373377	CV3515092	single nucleotide variant	NM_017514.5(PLXNA3):c.4013A>T (p.His1338Leu)	PLXNA3-related disorder [RCV004744852]\|not specified [RCV004837951]	uncertain significance	X	154468352	154468352	Human		name , trait , alternate_id
408373452	CV3515470	single nucleotide variant	NM_017514.5(PLXNA3):c.4372G>A (p.Glu1458Lys)	PLXNA3-related disorder [RCV004744915]	uncertain significance	X	154468907	154468907	Human		name , trait , alternate_id
408373422	CV3515624	single nucleotide variant	NM_017514.5(PLXNA3):c.5023A>G (p.Thr1675Ala)	PLXNA3-related disorder [RCV004744937]	uncertain significance	X	154470478	154470478	Human		name , trait , alternate_id
408373487	CV3515755	single nucleotide variant	NM_017514.5(PLXNA3):c.4021G>A (p.Ala1341Thr)	PLXNA3-related disorder [RCV004744955]	uncertain significance	X	154468360	154468360	Human		name , trait , alternate_id
408373613	CV3516339	single nucleotide variant	NM_017514.5(PLXNA3):c.3898C>T (p.Arg1300Trp)	PLXNA3-related disorder [RCV004745058]	uncertain significance	X	154468159	154468159	Human		name , trait , alternate_id
408373621	CV3516341	single nucleotide variant	NM_017514.5(PLXNA3):c.5111G>A (p.Arg1704His)	PLXNA3-related disorder [RCV004745060]	uncertain significance	X	154470566	154470566	Human		name , trait , alternate_id
408373646	CV3516816	single nucleotide variant	NM_017514.5(PLXNA3):c.3974A>C (p.Asn1325Thr)	PLXNA3-related disorder [RCV004745133]	uncertain significance	X	154468313	154468313	Human		name , trait , alternate_id
408371896	CV3517046	single nucleotide variant	NM_017514.5(PLXNA3):c.3871G>A (p.Glu1291Lys)	PLXNA3-related disorder [RCV004742029]	uncertain significance	X	154468132	154468132	Human		name , trait , alternate_id
408371909	CV3517109	single nucleotide variant	NM_017514.5(PLXNA3):c.3275G>C (p.Arg1092Pro)	PLXNA3-related disorder [RCV004742044]	uncertain significance	X	154467305	154467305	Human		name , trait , alternate_id
597741779	CV3573269	single nucleotide variant	NM_017514.5(PLXNA3):c.3632C>T (p.Ser1211Leu)	not specified [RCV004844789]	uncertain significance	X	154467813	154467813	Human		name
597741794	CV3573272	single nucleotide variant	NM_017514.5(PLXNA3):c.3058A>G (p.Thr1020Ala)	not specified [RCV004844792]	uncertain significance	X	154466744	154466744	Human		name
597741806	CV3573274	single nucleotide variant	NM_017514.5(PLXNA3):c.3994C>T (p.Leu1332Phe)	not specified [RCV004844794]	uncertain significance	X	154468333	154468333	Human		name
597741811	CV3573275	single nucleotide variant	NM_017514.5(PLXNA3):c.3797G>A (p.Arg1266His)	not specified [RCV004844795]	uncertain significance	X	154467978	154467978	Human		name
597741816	CV3573276	single nucleotide variant	NM_017514.5(PLXNA3):c.3255T>G (p.Phe1085Leu)	not specified [RCV004844796]	uncertain significance	X	154467285	154467285	Human		name
597741844	CV3573281	single nucleotide variant	NM_017514.5(PLXNA3):c.3870C>G (p.Asp1290Glu)	not specified [RCV004844801]	uncertain significance	X	154468131	154468131	Human		name
597741859	CV3573284	single nucleotide variant	NM_017514.5(PLXNA3):c.3680G>A (p.Gly1227Glu)	not specified [RCV004844804]	uncertain significance	X	154467861	154467861	Human		name
597741871	CV3573286	single nucleotide variant	NM_017514.5(PLXNA3):c.3871G>C (p.Glu1291Gln)	not specified [RCV004844806]	uncertain significance	X	154468132	154468132	Human		name
597741876	CV3573287	single nucleotide variant	NM_017514.5(PLXNA3):c.3554C>T (p.Ser1185Leu)	not specified [RCV004844807]	uncertain significance	X	154467657	154467657	Human		name
598129135	CV3888428	single nucleotide variant	NM_017514.5(PLXNA3):c.3124A>G (p.Thr1042Ala)	not provided [RCV005244602]	uncertain significance	X	154467073	154467073	Human		name
598185410	CV4007118	single nucleotide variant	NM_017514.5(PLXNA3):c.3058A>T (p.Thr1020Ser)	not specified [RCV005395609]	uncertain significance	X	154466744	154466744	Human		name
598185446	CV4007124	single nucleotide variant	NM_017514.5(PLXNA3):c.4459A>G (p.Asn1487Asp)	not specified [RCV005395615]	uncertain significance	X	154469080	154469080	Human		name
598185475	CV4007129	single nucleotide variant	NM_017514.5(PLXNA3):c.4616C>T (p.Thr1539Ile)	not specified [RCV005395620]	uncertain significance	X	154469400	154469400	Human		name
598185482	CV4007130	single nucleotide variant	NM_017514.5(PLXNA3):c.3403G>A (p.Val1135Met)	not specified [RCV005395621]	uncertain significance	X	154467433	154467433	Human		name
598185494	CV4007132	single nucleotide variant	NM_017514.5(PLXNA3):c.3893A>C (p.Asp1298Ala)	not specified [RCV005395623]	uncertain significance	X	154468154	154468154	Human		name
15163770	CV706172	single nucleotide variant	NM_017514.5(PLXNA3):c.4001G>A (p.Gly1334Glu)	PLXNA3-related disorder [RCV003933266]\|not provided [RCV000948170]	benign	X	154468340	154468340	Human		name , trait , alternate_id
126909293	CV970162	single nucleotide variant	NM_017514.5(PLXNA3):c.3256C>G (p.Leu1086Val)	Hypogonadotropic hypogonadism [RCV001374682]	uncertain significance	X	154467286	154467286	Human	3	name
126909294	CV970163	single nucleotide variant	NM_017514.5(PLXNA3):c.4075C>T (p.Arg1359Cys)	Hypogonadotropic hypogonadism [RCV001374683]	uncertain significance	X	154468414	154468414	Human	3	name
150416172	CV1192600	deletion	NM_017514.5(PLXNA3):c.788_797del (p.Val263fs)	Disorder of sexual differentiation [RCV001568329]	uncertain significance	X	154461291	154461300	Human	1	name
408373126	CV3514030	inversion	NM_017514.5(PLXNA3):c.2900_2901inv (p.Thr967Met)	PLXNA3-related disorder [RCV004744653]	uncertain significance	X	154466476	154466477	Human		name , trait , alternate_id
151663387	CV1331097	insertion	NM_017514.5(PLXNA3):c.1008_1009insAGAG (p.Leu337fs)	not provided [RCV001825270]	not provided	X	154461512	154461513	Human		name
28886239	CV860813	deletion	NM_017514.5(PLXNA3):c.720_734del (p.Leu241_Thr245del)	not provided [RCV001091836]	uncertain significance	X	154461222	154461236	Human		name
408379195	CV3506763	indel	NM_017514.5(PLXNA3):c.4501_4502delinsTG (p.Asp1501Cys)	PLXNA3-related disorder [RCV004728306]	uncertain significance	X	154469122	154469123	Human		name , trait , alternate_id
151663417	CV1333939	indel	NM_017514.5(PLXNA3):c.746_795delinsCCCAGACACAGCGGGCGAGAAATTTTCACGTCCAAAAT (p.Leu249_Met265delinsProGlnThrGlnArgAlaArgAsnPheHisValGlnAsn)	PLXNA3-associated seizure disorder [RCV001839114]	uncertain significance	X	154461250	154461299	Human		name , trait

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