Nrp2 Variant Search Result - Rat Genome Database

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345 records found for search term Nrp2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405269943	CV3197992	single nucleotide variant	NM_003872.3(NRP2):c.*2G>A	NRP2-related disorder [RCV003899803]	likely benign	2	205795060	205795060	Human		name , trait , alternate_id
408376762	CV3516246	single nucleotide variant	NM_003872.3(NRP2):c.*3G>T	NRP2-related disorder [RCV004749444]	likely benign	2	205795061	205795061	Human		name , trait , alternate_id
405264892	CV3201390	single nucleotide variant	NM_003872.3(NRP2):c.433+9G>T	NRP2-related disorder [RCV003897149]	likely benign	2	205716383	205716383	Human		name , trait , alternate_id
405270126	CV3215364	single nucleotide variant	NM_003872.3(NRP2):c.251+9C>T	NRP2-related disorder [RCV003949123]	likely benign	2	205697730	205697730	Human		name , trait , alternate_id
405289795	CV3218898	single nucleotide variant	NM_003872.3(NRP2):c.991-9A>C	NRP2-related disorder [RCV003962013]	likely benign	2	205727882	205727882	Human		name , trait , alternate_id
408377285	CV3507939	single nucleotide variant	NM_003872.3(NRP2):c.434-4A>G	NRP2-related disorder [RCV004750599]	likely benign	2	205722474	205722474	Human		name , trait , alternate_id
408375488	CV3509813	single nucleotide variant	NM_003872.3(NRP2):c.664+7G>A	NRP2-related disorder [RCV004748137]	likely benign	2	205722715	205722715	Human		name , trait , alternate_id
408375644	CV3510180	single nucleotide variant	NM_003872.3(NRP2):c.433+8T>G	NRP2-related disorder [RCV004748179]	likely benign	2	205716382	205716382	Human		name , trait , alternate_id
408376476	CV3513818	single nucleotide variant	NM_003872.3(NRP2):c.990+4C>G	NRP2-related disorder [RCV004749143]	likely benign	2	205726086	205726086	Human		name , trait , alternate_id
408376948	CV3517201	single nucleotide variant	NM_003872.3(NRP2):c.665-8A>T	NRP2-related disorder [RCV004750087]	likely benign	2	205723777	205723777	Human		name , trait , alternate_id
329375548	CV2468680	single nucleotide variant	NM_003872.3(NRP2):c.2425+7A>C	not specified [RCV004278222]	uncertain significance	2	205766810	205766810	Human		name
405267793	CV3189550	single nucleotide variant	NM_003872.3(NRP2):c.1787-5C>T	NRP2-related disorder [RCV003898944]	likely benign	2	205749720	205749720	Human		name , trait , alternate_id
405288919	CV3193873	single nucleotide variant	NM_003872.3(NRP2):c.2477-3C>T	NRP2-related disorder [RCV003983375]	likely benign	2	205794751	205794751	Human		name , trait , alternate_id
405268303	CV3200974	single nucleotide variant	NM_003872.3(NRP2):c.2307+6G>A	NRP2-related disorder [RCV003899089]	likely benign	2	205763942	205763942	Human		name , trait , alternate_id
405271295	CV3202817	single nucleotide variant	NM_003872.3(NRP2):c.2477-5C>T	NRP2-related disorder [RCV003913881]	likely benign	2	205794749	205794749	Human		name , trait , alternate_id
405277947	CV3202984	single nucleotide variant	NM_003872.3(NRP2):c.251+10G>A	NRP2-related disorder [RCV003904764]	likely benign	2	205697731	205697731	Human		name , trait , alternate_id
405294859	CV3214913	single nucleotide variant	NM_003872.3(NRP2):c.1147-9A>G	NRP2-related disorder [RCV003936777]	likely benign	2	205740510	205740510	Human		name , trait , alternate_id
405283457	CV3218579	single nucleotide variant	NM_003872.3(NRP2):c.1147-8C>T	NRP2-related disorder [RCV003957359]	likely benign	2	205740511	205740511	Human		name , trait , alternate_id
408377330	CV3508569	single nucleotide variant	NM_003872.3(NRP2):c.1292-4G>A	NRP2-related disorder [RCV004750681]	likely benign	2	205743199	205743199	Human		name , trait , alternate_id
408375337	CV3508802	single nucleotide variant	NM_003872.3(NRP2):c.2405-2A>G	NRP2-related disorder [RCV004748016]	uncertain significance	2	205766781	205766781	Human		name , trait , alternate_id
408376315	CV3513006	single nucleotide variant	NM_003872.3(NRP2):c.1787-3C>T	NRP2-related disorder [RCV004749023]	likely benign	2	205749722	205749722	Human		name , trait , alternate_id
408376378	CV3513523	single nucleotide variant	NM_003872.3(NRP2):c.1291+6G>A	NRP2-related disorder [RCV004749093]	likely benign	2	205740669	205740669	Human		name , trait , alternate_id
408376776	CV3516412	single nucleotide variant	NM_003872.3(NRP2):c.1903+5G>A	NRP2-related disorder [RCV004749469]	likely benign	2	205749846	205749846	Human		name , trait , alternate_id
15122685	CV778896	single nucleotide variant	NM_003872.3(NRP2):c.1146+7C>T	not provided [RCV000963111]	likely benign	2	205728053	205728053	Human		name
405282430	CV3191005	single nucleotide variant	NM_003872.3(NRP2):c.1641+24G>T	NRP2-related disorder [RCV003921427]	likely benign	2	205743576	205743576	Human		name , trait , alternate_id
405277424	CV3195771	single nucleotide variant	NM_003872.3(NRP2):c.2425+22A>G	NRP2-related disorder [RCV003904304]	likely benign	2	205766825	205766825	Human		name , trait , alternate_id
405277809	CV3196174	single nucleotide variant	NM_003872.3(NRP2):c.1641+29G>A	NRP2-related disorder [RCV003904688]	likely benign	2	205743581	205743581	Human		name , trait , alternate_id
405284284	CV3213582	single nucleotide variant	NM_003872.3(NRP2):c.1641+28C>T	NRP2-related disorder [RCV003922155]	likely benign	2	205743580	205743580	Human		name , trait , alternate_id
405293316	CV3221408	single nucleotide variant	NM_003872.3(NRP2):c.2425+16G>A	NRP2-related disorder [RCV003966898]	uncertain significance	2	205766819	205766819	Human		name , trait , alternate_id
15168931	CV759082	single nucleotide variant	NM_003872.3(NRP2):c.2425+24A>T	NRP2-related disorder [RCV004749548]\|not provided [RCV000927395]	likely benign	2	205766827	205766827	Human		name , trait , alternate_id
401936111	CV2796252	single nucleotide variant	NM_003872.3(NRP2):c.2425+9584A>G	NRP2-related disorder [RCV003414082]	uncertain significance	2	205776387	205776387	Human		name , trait , alternate_id
401933353	CV2804114	single nucleotide variant	NM_003872.3(NRP2):c.2425+9476T>A	NRP2-related disorder [RCV003392852]	uncertain significance	2	205776279	205776279	Human		name , trait , alternate_id
401902077	CV2804178	single nucleotide variant	NM_003872.3(NRP2):c.2425+9707G>A	NRP2-related disorder [RCV003418765]\|not provided [RCV003883993]	likely benign\|uncertain significance	2	205776510	205776510	Human		name , trait , alternate_id
405285781	CV3191901	single nucleotide variant	NM_003872.3(NRP2):c.2425+9733C>T	NRP2-related disorder [RCV003923845]	likely benign	2	205776536	205776536	Human		name , trait , alternate_id
405276603	CV3193471	single nucleotide variant	NM_003872.3(NRP2):c.2425+9489C>A	NRP2-related disorder [RCV003974639]	likely benign	2	205776292	205776292	Human		name , trait , alternate_id
405273915	CV3194886	single nucleotide variant	NM_003872.3(NRP2):c.2425+9657G>T	NRP2-related disorder [RCV003902128]	likely benign	2	205776460	205776460	Human		name , trait , alternate_id
405265787	CV3215706	single nucleotide variant	NM_003872.3(NRP2):c.2425+9543G>A	NRP2-related disorder [RCV003946876]	likely benign	2	205776346	205776346	Human		name , trait , alternate_id
405275659	CV3216034	single nucleotide variant	NM_003872.3(NRP2):c.2425+9705C>T	NRP2-related disorder [RCV003952297]	likely benign	2	205776508	205776508	Human		name , trait , alternate_id
405282283	CV3216359	single nucleotide variant	NM_003872.3(NRP2):c.2425+9714G>A	NRP2-related disorder [RCV003956859]	likely benign	2	205776517	205776517	Human		name , trait , alternate_id
405289636	CV3220977	single nucleotide variant	NM_003872.3(NRP2):c.2425+9729G>A	NRP2-related disorder [RCV003961874]	likely benign	2	205776532	205776532	Human		name , trait , alternate_id
408382812	CV3506055	single nucleotide variant	NM_003872.3(NRP2):c.2425+9693G>C	NRP2-related disorder [RCV004730186]	uncertain significance	2	205776496	205776496	Human		name , trait , alternate_id
408377240	CV3508033	single nucleotide variant	NM_003872.3(NRP2):c.2425+9690T>G	NRP2-related disorder [RCV004750610]	uncertain significance	2	205776493	205776493	Human		name , trait , alternate_id
408377282	CV3508275	single nucleotide variant	NM_003872.3(NRP2):c.2425+9671T>C	NRP2-related disorder [RCV004750645]	uncertain significance	2	205776474	205776474	Human		name , trait , alternate_id
408375356	CV3508916	single nucleotide variant	NM_003872.3(NRP2):c.2425+9620A>G	NRP2-related disorder [RCV004748032]	uncertain significance	2	205776423	205776423	Human		name , trait , alternate_id
408375543	CV3510070	single nucleotide variant	NM_003872.3(NRP2):c.2425+9639C>A	NRP2-related disorder [RCV004748168]	likely benign	2	205776442	205776442	Human		name , trait , alternate_id
408375808	CV3510792	single nucleotide variant	NM_003872.3(NRP2):c.2425+9532G>A	NRP2-related disorder [RCV004748267]	uncertain significance	2	205776335	205776335	Human		name , trait , alternate_id
408376407	CV3513715	single nucleotide variant	NM_003872.3(NRP2):c.2425+9651C>A	NRP2-related disorder [RCV004749122]	likely benign	2	205776454	205776454	Human		name , trait , alternate_id
408376418	CV3513770	single nucleotide variant	NM_003872.3(NRP2):c.2425+9726G>A	NRP2-related disorder [RCV004749133]	likely benign	2	205776529	205776529	Human		name , trait , alternate_id
408376579	CV3514963	single nucleotide variant	NM_003872.3(NRP2):c.2425+9468G>A	NRP2-related disorder [RCV004749295]	likely benign	2	205776271	205776271	Human		name , trait , alternate_id
408376690	CV3515519	single nucleotide variant	NM_003872.3(NRP2):c.2425+9669G>A	NRP2-related disorder [RCV004749367]	likely benign	2	205776472	205776472	Human		name , trait , alternate_id
408376696	CV3515924	deletion	NM_003872.3(NRP2):c.2425+9440del	NRP2-related disorder [RCV004749413]	likely benign	2	205776242	205776242	Human		name , trait , alternate_id
408376737	CV3515986	single nucleotide variant	NM_003872.3(NRP2):c.2425+9434C>T	NRP2-related disorder [RCV004749420]	likely benign	2	205776237	205776237	Human		name , trait , alternate_id
408376883	CV3516750	single nucleotide variant	NM_003872.3(NRP2):c.2425+9557C>G	NRP2-related disorder [RCV004750011]	uncertain significance	2	205776360	205776360	Human		name , trait , alternate_id
408376831	CV3516789	single nucleotide variant	NM_003872.3(NRP2):c.2425+9654C>T	NRP2-related disorder [RCV004750015]	likely benign	2	205776457	205776457	Human		name , trait , alternate_id
408376905	CV3516902	single nucleotide variant	NM_003872.3(NRP2):c.2425+9468G>T	NRP2-related disorder [RCV004750032]	uncertain significance	2	205776271	205776271	Human		name , trait , alternate_id
408376949	CV3517504	single nucleotide variant	NM_003872.3(NRP2):c.2425+9609G>A	NRP2-related disorder [RCV004750132]	likely benign	2	205776412	205776412	Human		name , trait , alternate_id
405279297	CV3219605	single nucleotide variant	NM_003872.3(NRP2):c.81G>A (p.Pro27=)	NRP2-related disorder [RCV003954883]	likely benign	2	205697551	205697551	Human		name , trait , alternate_id
407516955	CV3465927	single nucleotide variant	NM_003872.3(NRP2):c.8T>A (p.Met3Lys)	not specified [RCV004650465]	uncertain significance	2	205683298	205683298	Human		name
408376347	CV3512788	single nucleotide variant	NM_003872.3(NRP2):c.81G>T (p.Pro27=)	NRP2-related disorder [RCV004749004]	likely benign	2	205697551	205697551	Human		name , trait , alternate_id
408376372	CV3513491	single nucleotide variant	NM_003872.3(NRP2):c.60G>A (p.Val20=)	NRP2-related disorder [RCV004749087]	likely benign	2	205683350	205683350	Human		name , trait , alternate_id
408376477	CV3514218	single nucleotide variant	NM_003872.3(NRP2):c.84C>T (p.Cys28=)	NRP2-related disorder [RCV004749192]	likely benign	2	205697554	205697554	Human		name , trait , alternate_id
408376800	CV3516479	single nucleotide variant	NM_003872.3(NRP2):c.94T>C (p.Leu32=)	NRP2-related disorder [RCV004749969]	likely benign	2	205697564	205697564	Human		name , trait , alternate_id
597706950	CV3576905	single nucleotide variant	NM_003872.3(NRP2):c.4G>C (p.Asp2His)	not specified [RCV004840395]	uncertain significance	2	205683294	205683294	Human		name
405259333	CV3194747	single nucleotide variant	NM_003872.3(NRP2):c.186C>T (p.Pro62=)	NRP2-related disorder [RCV003894136]	likely benign	2	205697656	205697656	Human		name , trait , alternate_id
405277435	CV3195776	single nucleotide variant	NM_003872.3(NRP2):c.168G>A (p.Glu56=)	NRP2-related disorder [RCV003904309]	likely benign	2	205697638	205697638	Human		name , trait , alternate_id
405268271	CV3200966	single nucleotide variant	NM_003872.3(NRP2):c.150C>G (p.Pro50=)	NRP2-related disorder [RCV003899081]	likely benign	2	205697620	205697620	Human		name , trait , alternate_id
405257468	CV3201775	single nucleotide variant	NM_003872.3(NRP2):c.129C>T (p.Pro43=)	NRP2-related disorder [RCV003892303]	likely benign	2	205697599	205697599	Human		name , trait , alternate_id
405290844	CV3208476	single nucleotide variant	NM_003872.3(NRP2):c.234C>T (p.Ile78=)	NRP2-related disorder [RCV003927266]	likely benign	2	205697704	205697704	Human		name , trait , alternate_id
408376343	CV3512780	deletion	NM_003872.3(NRP2):c.2045-17_2045-8del	NRP2-related disorder [RCV004749003]	likely benign	2	205763652	205763661	Human		name , trait , alternate_id
408376605	CV3515157	single nucleotide variant	NM_003872.3(NRP2):c.138C>G (p.Pro46=)	NRP2-related disorder [RCV004749321]	likely benign	2	205697608	205697608	Human		name , trait , alternate_id
408376892	CV3517125	single nucleotide variant	NM_003872.3(NRP2):c.243C>T (p.His81=)	NRP2-related disorder [RCV004750078]	likely benign	2	205697713	205697713	Human		name , trait , alternate_id
408376985	CV3517792	single nucleotide variant	NM_003872.3(NRP2):c.165C>T (p.Cys55=)	NRP2-related disorder [RCV004750168]	likely benign	2	205697635	205697635	Human		name , trait , alternate_id
15202834	CV697260	variation	NM_003872.3(NRP2):c.1404= (p.Val468=)	not provided [RCV000958061]	benign	2	205743315	205743315	Human		name
15174286	CV707954	single nucleotide variant	NM_003872.3(NRP2):c.123C>T (p.Thr41=)	NRP2-related disorder [RCV003918503]\|not provided [RCV000972689]	benign	2	205697593	205697593	Human		name , trait , alternate_id
15181633	CV707955	single nucleotide variant	NM_003872.3(NRP2):c.180C>T (p.Tyr60=)	NRP2-related disorder [RCV003962918]\|not provided [RCV000974438]	likely benign	2	205697650	205697650	Human		name , trait , alternate_id
156340772	CV2368317	single nucleotide variant	NM_003872.3(NRP2):c.55C>G (p.Gln19Glu)	NRP2-related disorder [RCV003906628]\|not specified [RCV004219097]	likely benign\|uncertain significance	2	205683345	205683345	Human		name , trait , alternate_id
329389104	CV2448721	single nucleotide variant	NM_003872.3(NRP2):c.41A>T (p.Tyr14Phe)	not specified [RCV004259377]	uncertain significance	2	205683331	205683331	Human		name
401743985	CV2722293	single nucleotide variant	NM_003872.3(NRP2):c.41A>G (p.Tyr14Cys)	not specified [RCV004328843]	uncertain significance	2	205683331	205683331	Human		name
401906068	CV2802302	single nucleotide variant	NM_003872.3(NRP2):c.85G>A (p.Gly29Arg)	NRP2-related disorder [RCV003421005]	uncertain significance	2	205697555	205697555	Human		name , trait , alternate_id
405262527	CV3189264	single nucleotide variant	NM_003872.3(NRP2):c.696C>T (p.Thr232=)	NRP2-related disorder [RCV003896498]	likely benign	2	205723816	205723816	Human		name , trait , alternate_id
405262693	CV3196876	single nucleotide variant	NM_003872.3(NRP2):c.870T>C (p.Asn290=)	NRP2-related disorder [RCV003967396]	benign	2	205725962	205725962	Human		name , trait , alternate_id
405271821	CV3202959	single nucleotide variant	NM_003872.3(NRP2):c.354C>T (p.Ser118=)	NRP2-related disorder [RCV003914016]	likely benign	2	205716295	205716295	Human		name , trait , alternate_id
405285403	CV3212466	single nucleotide variant	NM_003872.3(NRP2):c.618G>C (p.Gly206=)	NRP2-related disorder [RCV003959057]	likely benign	2	205722662	205722662	Human		name , trait , alternate_id
405262006	CV3220023	single nucleotide variant	NM_003872.3(NRP2):c.810G>A (p.Glu270=)	NRP2-related disorder [RCV003967170]	likely benign	2	205723930	205723930	Human		name , trait , alternate_id
405709366	CV3359267	single nucleotide variant	NM_003872.3(NRP2):c.92G>A (p.Arg31His)	NRP2-related disorder [RCV004750472]\|not specified [RCV004493614]	uncertain significance	2	205697562	205697562	Human		name , trait , alternate_id
408378310	CV3505187	single nucleotide variant	NM_003872.3(NRP2):c.753G>A (p.Thr251=)	NRP2-related disorder [RCV004727928]	likely benign	2	205723873	205723873	Human		name , trait , alternate_id
408376174	CV3505618	deletion	NM_003872.3(NRP2):c.189del (p.Glu63fs)	NRP2-related disorder [RCV004726598]	uncertain significance	2	205697658	205697658	Human		name , trait , alternate_id
408377148	CV3507412	single nucleotide variant	NM_003872.3(NRP2):c.702A>G (p.Thr234=)	NRP2-related disorder [RCV004750530]	likely benign	2	205723822	205723822	Human		name , trait , alternate_id
408377260	CV3507728	single nucleotide variant	NM_003872.3(NRP2):c.585C>T (p.Asp195=)	NRP2-related disorder [RCV004750572]	likely benign	2	205722629	205722629	Human		name , trait , alternate_id
408377383	CV3508427	single nucleotide variant	NM_003872.3(NRP2):c.601T>C (p.Leu201=)	NRP2-related disorder [RCV004750661]	likely benign	2	205722645	205722645	Human		name , trait , alternate_id
408375591	CV3509894	single nucleotide variant	NM_003872.3(NRP2):c.73G>A (p.Asp25Asn)	NRP2-related disorder [RCV004748148]	uncertain significance	2	205683363	205683363	Human		name , trait , alternate_id
408375841	CV3511260	single nucleotide variant	NM_003872.3(NRP2):c.786G>A (p.Ala262=)	NRP2-related disorder [RCV004748326]	likely benign	2	205723906	205723906	Human		name , trait , alternate_id
408375951	CV3511735	single nucleotide variant	NM_003872.3(NRP2):c.471C>T (p.Asn157=)	NRP2-related disorder [RCV004748385]	likely benign	2	205722515	205722515	Human		name , trait , alternate_id
408376293	CV3512619	single nucleotide variant	NM_003872.3(NRP2):c.408T>C (p.Ser136=)	NRP2-related disorder [RCV004748984]	likely benign	2	205716349	205716349	Human		name , trait , alternate_id
408376453	CV3514017	single nucleotide variant	NM_003872.3(NRP2):c.330G>A (p.Pro110=)	NRP2-related disorder [RCV004749168]	likely benign	2	205716271	205716271	Human		name , trait , alternate_id
597706934	CV3576903	single nucleotide variant	NM_003872.3(NRP2):c.80C>T (p.Pro27Leu)	not specified [RCV004840393]	uncertain significance	2	205697550	205697550	Human		name
15195816	CV697259	single nucleotide variant	NM_003872.3(NRP2):c.726G>A (p.Thr242=)	not provided [RCV000956028]	benign	2	205723846	205723846	Human		name
15133816	CV747176	single nucleotide variant	NM_003872.3(NRP2):c.420G>A (p.Glu140=)	NRP2-related disorder [RCV003895599]\|not provided [RCV000920580]	likely benign	2	205716361	205716361	Human		name , trait , alternate_id
15112849	CV762794	single nucleotide variant	NM_003872.3(NRP2):c.387C>A (p.Ala129=)	NRP2-related disorder [RCV003895707]\|not provided [RCV000939018]	benign\|likely benign	2	205716328	205716328	Human		name , trait , alternate_id
15193972	CV762795	single nucleotide variant	NM_003872.3(NRP2):c.996C>T (p.Asp332=)	not provided [RCV000933510]	likely benign	2	205727896	205727896	Human		name
15103743	CV781116	single nucleotide variant	NM_003872.3(NRP2):c.762G>A (p.Ala254=)	NRP2-related disorder [RCV003953355]\|not provided [RCV000976077]	likely benign	2	205723882	205723882	Human		name , trait , alternate_id
156359925	CV2258026	single nucleotide variant	NM_003872.3(NRP2):c.187G>A (p.Glu63Lys)	not provided [RCV004695457]\|not specified [RCV004129824]	uncertain significance	2	205697657	205697657	Human		name
401857598	CV2767026	single nucleotide variant	NM_003872.3(NRP2):c.191C>T (p.Pro64Leu)	NRP2-related disorder [RCV004750371]\|not specified [RCV004347438]	uncertain significance	2	205697661	205697661	Human		name , trait , alternate_id
405262599	CV3189299	single nucleotide variant	NM_003872.3(NRP2):c.1944C>T (p.Phe648=)	NRP2-related disorder [RCV003896533]	likely benign	2	205752875	205752875	Human		name , trait , alternate_id
405262934	CV3189441	single nucleotide variant	NM_003872.3(NRP2):c.1851C>T (p.Tyr617=)	NRP2-related disorder [RCV003896675]	likely benign	2	205749789	205749789	Human		name , trait , alternate_id
405267813	CV3189555	single nucleotide variant	NM_003872.3(NRP2):c.2571G>A (p.Leu857=)	NRP2-related disorder [RCV003898949]	benign	2	205794848	205794848	Human		name , trait , alternate_id
405264931	CV3190064	single nucleotide variant	NM_003872.3(NRP2):c.1467G>A (p.Gln489=)	NRP2-related disorder [RCV003897103]	likely benign	2	205743378	205743378	Human		name , trait , alternate_id
405260164	CV3190211	single nucleotide variant	NM_003872.3(NRP2):c.1197C>T (p.His399=)	NRP2-related disorder [RCV003894612]	likely benign	2	205740569	205740569	Human		name , trait , alternate_id
405260173	CV3190277	single nucleotide variant	NM_003872.3(NRP2):c.2772C>T (p.Ser924=)	NRP2-related disorder [RCV003894676]	likely benign	2	205795049	205795049	Human		name , trait , alternate_id
405284797	CV3190850	single nucleotide variant	NM_003872.3(NRP2):c.2124C>T (p.His708=)	NRP2-related disorder [RCV003909416]\|not provided [RCV004711977]	likely benign	2	205763753	205763753	Human		name , trait , alternate_id
405282896	CV3191215	single nucleotide variant	NM_003872.3(NRP2):c.1785A>C (p.Thr595=)	NRP2-related disorder [RCV003921621]	likely benign	2	205745889	205745889	Human		name , trait , alternate_id
405283228	CV3191298	single nucleotide variant	NM_003872.3(NRP2):c.1743G>A (p.Ala581=)	NRP2-related disorder [RCV003921699]	likely benign	2	205745847	205745847	Human		name , trait , alternate_id
405276088	CV3193271	single nucleotide variant	NM_003872.3(NRP2):c.1071T>C (p.Tyr357=)	NRP2-related disorder [RCV003974437]	benign	2	205727971	205727971	Human		name , trait , alternate_id
405262036	CV3194278	single nucleotide variant	NM_003872.3(NRP2):c.1857C>T (p.Thr619=)	NRP2-related disorder [RCV003896313]	likely benign	2	205749795	205749795	Human		name , trait , alternate_id
405262060	CV3194368	single nucleotide variant	NM_003872.3(NRP2):c.2139G>A (p.Pro713=)	NRP2-related disorder [RCV003896400]	likely benign	2	205763768	205763768	Human		name , trait , alternate_id
405272796	CV3197524	single nucleotide variant	NM_003872.3(NRP2):c.2046T>C (p.Asp682=)	NRP2-related disorder [RCV003901493]	likely benign	2	205763675	205763675	Human		name , trait , alternate_id
405272838	CV3197537	single nucleotide variant	NM_003872.3(NRP2):c.2037G>A (p.Thr679=)	NRP2-related disorder [RCV003901506]	likely benign	2	205752968	205752968	Human		name , trait , alternate_id
405273610	CV3197860	single nucleotide variant	NM_003872.3(NRP2):c.2028C>T (p.Asn676=)	NRP2-related disorder [RCV003901823]	likely benign	2	205752959	205752959	Human		name , trait , alternate_id
405269890	CV3197951	single nucleotide variant	NM_003872.3(NRP2):c.1179G>A (p.Val393=)	NRP2-related disorder [RCV003899764]	likely benign	2	205740551	205740551	Human		name , trait , alternate_id
405273577	CV3198092	single nucleotide variant	NM_003872.3(NRP2):c.1725G>A (p.Pro575=)	NRP2-related disorder [RCV003901862]	likely benign	2	205745829	205745829	Human		name , trait , alternate_id
405273822	CV3198273	single nucleotide variant	NM_003872.3(NRP2):c.2508T>C (p.Ser836=)	NRP2-related disorder [RCV003902041]	likely benign	2	205794785	205794785	Human		name , trait , alternate_id
405288248	CV3200607	single nucleotide variant	NM_003872.3(NRP2):c.1674T>G (p.Pro558=)	NRP2-related disorder [RCV003982320]	benign	2	205745778	205745778	Human		name , trait , alternate_id
405271125	CV3202748	single nucleotide variant	NM_003872.3(NRP2):c.1164C>T (p.Asn388=)	NRP2-related disorder [RCV003913821]	likely benign	2	205740536	205740536	Human		name , trait , alternate_id
405260826	CV3204378	single nucleotide variant	NM_003872.3(NRP2):c.2541C>T (p.Thr847=)	NRP2-related disorder [RCV003944206]	likely benign	2	205794818	205794818	Human		name , trait , alternate_id
405295463	CV3204743	single nucleotide variant	NM_003872.3(NRP2):c.1455G>A (p.Glu485=)	NRP2-related disorder [RCV003937363]	likely benign	2	205743366	205743366	Human		name , trait , alternate_id
405255870	CV3208385	single nucleotide variant	NM_003872.3(NRP2):c.2115C>T (p.Pro705=)	NRP2-related disorder [RCV003939490]	likely benign	2	205763744	205763744	Human		name , trait , alternate_id
405270921	CV3209189	single nucleotide variant	NM_003872.3(NRP2):c.1875G>A (p.Glu625=)	NRP2-related disorder [RCV003949564]	likely benign	2	205749813	205749813	Human		name , trait , alternate_id
405294517	CV3211693	single nucleotide variant	NM_003872.3(NRP2):c.2613C>T (p.Gly871=)	NRP2-related disorder [RCV003934427]	likely benign	2	205794890	205794890	Human		name , trait , alternate_id
405270794	CV3212146	single nucleotide variant	NM_003872.3(NRP2):c.1593C>T (p.Asn531=)	NRP2-related disorder [RCV003949512]	likely benign	2	205743504	205743504	Human		name , trait , alternate_id
405275649	CV3216030	single nucleotide variant	NM_003872.3(NRP2):c.1563G>A (p.Val521=)	NRP2-related disorder [RCV003952294]	likely benign	2	205743474	205743474	Human		name , trait , alternate_id
405278103	CV3216401	single nucleotide variant	NM_003872.3(NRP2):c.1989G>A (p.Lys663=)	NRP2-related disorder [RCV003954347]	likely benign	2	205752920	205752920	Human		name , trait , alternate_id
405283338	CV3217106	single nucleotide variant	NM_003872.3(NRP2):c.1041G>A (p.Ala347=)	NRP2-related disorder [RCV003979224]	likely benign	2	205727941	205727941	Human		name , trait , alternate_id
405268248	CV3219590	single nucleotide variant	NM_003872.3(NRP2):c.2529C>T (p.Gly843=)	NRP2-related disorder [RCV003969795]	likely benign	2	205794806	205794806	Human		name , trait , alternate_id
405265744	CV3220866	single nucleotide variant	NM_003872.3(NRP2):c.2475T>C (p.Asp825=)	NRP2-related disorder [RCV003969034]	likely benign	2	205792284	205792284	Human		name , trait , alternate_id
405709330	CV3359262	single nucleotide variant	NM_003872.3(NRP2):c.166G>A (p.Glu56Lys)	not specified [RCV004493609]	uncertain significance	2	205697636	205697636	Human		name
405709343	CV3359264	single nucleotide variant	NM_003872.3(NRP2):c.262A>G (p.Ile88Val)	not specified [RCV004493611]	uncertain significance	2	205716203	205716203	Human		name
408382578	CV3503477	single nucleotide variant	NM_003872.3(NRP2):c.137C>G (p.Pro46Arg)	NRP2-related disorder [RCV004730002]	uncertain significance	2	205697607	205697607	Human		name , trait , alternate_id
408378990	CV3503987	single nucleotide variant	NM_003872.3(NRP2):c.2532C>T (p.Ala844=)	NRP2-related disorder [RCV004728214]	likely benign	2	205794809	205794809	Human		name , trait , alternate_id
408379114	CV3504087	single nucleotide variant	NM_003872.3(NRP2):c.181G>A (p.Ala61Thr)	NRP2-related disorder [RCV004728271]	uncertain significance	2	205697651	205697651	Human		name , trait , alternate_id
408382314	CV3504432	single nucleotide variant	NM_003872.3(NRP2):c.2643C>G (p.Leu881=)	NRP2-related disorder [RCV004729762]	likely benign	2	205794920	205794920	Human		name , trait , alternate_id
408379871	CV3505940	single nucleotide variant	NM_003872.3(NRP2):c.280G>C (p.Asp94His)	NRP2-related disorder [RCV004728629]	uncertain significance	2	205716221	205716221	Human		name , trait , alternate_id
408377118	CV3507253	single nucleotide variant	NM_003872.3(NRP2):c.265G>T (p.Glu89Ter)	NRP2-related disorder [RCV004750506]	uncertain significance	2	205716206	205716206	Human		name , trait , alternate_id
408377123	CV3507299	single nucleotide variant	NM_003872.3(NRP2):c.1560T>C (p.Phe520=)	NRP2-related disorder [RCV004750513]	likely benign	2	205743471	205743471	Human		name , trait , alternate_id
408377335	CV3507847	single nucleotide variant	NM_003872.3(NRP2):c.1920C>T (p.Leu640=)	NRP2-related disorder [RCV004750587]	likely benign	2	205752851	205752851	Human		name , trait , alternate_id
408377235	CV3507995	single nucleotide variant	NM_003872.3(NRP2):c.2523G>A (p.Gly841=)	NRP2-related disorder [RCV004750606]	likely benign	2	205794800	205794800	Human		name , trait , alternate_id
408377274	CV3508246	single nucleotide variant	NM_003872.3(NRP2):c.2757C>T (p.His919=)	NRP2-related disorder [RCV004750639]	likely benign	2	205795034	205795034	Human		name , trait , alternate_id
408375439	CV3508880	single nucleotide variant	NM_003872.3(NRP2):c.1203A>G (p.Pro401=)	NRP2-related disorder [RCV004748025]	likely benign	2	205740575	205740575	Human		name , trait , alternate_id
408375621	CV3510405	single nucleotide variant	NM_003872.3(NRP2):c.2595C>A (p.Ile865=)	NRP2-related disorder [RCV004748210]	likely benign	2	205794872	205794872	Human		name , trait , alternate_id
408375775	CV3510665	single nucleotide variant	NM_003872.3(NRP2):c.2272C>A (p.Arg758=)	NRP2-related disorder [RCV004748241]	likely benign	2	205763901	205763901	Human		name , trait , alternate_id
408375693	CV3510691	single nucleotide variant	NM_003872.3(NRP2):c.2172C>A (p.Gly724=)	NRP2-related disorder [RCV004748248]	likely benign	2	205763801	205763801	Human		name , trait , alternate_id
408375847	CV3511280	single nucleotide variant	NM_003872.3(NRP2):c.1353C>T (p.Ser451=)	NRP2-related disorder [RCV004748329]	likely benign	2	205743264	205743264	Human		name , trait , alternate_id
408376303	CV3512774	single nucleotide variant	NM_003872.3(NRP2):c.2196G>A (p.Val732=)	NRP2-related disorder [RCV004749001]	likely benign	2	205763825	205763825	Human		name , trait , alternate_id
408376433	CV3513854	single nucleotide variant	NM_003872.3(NRP2):c.2271G>A (p.Gly757=)	NRP2-related disorder [RCV004749148]	likely benign	2	205763900	205763900	Human		name , trait , alternate_id
408376522	CV3514097	single nucleotide variant	NM_003872.3(NRP2):c.1926G>A (p.Ser642=)	NRP2-related disorder [RCV004749179]	likely benign	2	205752857	205752857	Human		name , trait , alternate_id
408376602	CV3515152	single nucleotide variant	NM_003872.3(NRP2):c.2142G>A (p.Val714=)	NRP2-related disorder [RCV004749318]	likely benign	2	205763771	205763771	Human		name , trait , alternate_id
408376648	CV3515175	single nucleotide variant	NM_003872.3(NRP2):c.1059G>A (p.Gln353=)	NRP2-related disorder [RCV004749323]	likely benign	2	205727959	205727959	Human		name , trait , alternate_id
408376636	CV3515422	single nucleotide variant	NM_003872.3(NRP2):c.1248A>G (p.Ser416=)	NRP2-related disorder [RCV004749353]	likely benign	2	205740620	205740620	Human		name , trait , alternate_id
408376880	CV3517055	single nucleotide variant	NM_003872.3(NRP2):c.1026C>T (p.Ile342=)	NRP2-related disorder [RCV004750066]	likely benign	2	205727926	205727926	Human		name , trait , alternate_id
408376888	CV3517073	single nucleotide variant	NM_003872.3(NRP2):c.1254C>T (p.Ile418=)	NRP2-related disorder [RCV004750074]	likely benign	2	205740626	205740626	Human		name , trait , alternate_id
408376920	CV3517318	single nucleotide variant	NM_003872.3(NRP2):c.1935T>C (p.Asn645=)	NRP2-related disorder [RCV004750104]	likely benign	2	205752866	205752866	Human		name , trait , alternate_id
408376990	CV3517424	single nucleotide variant	NM_003872.3(NRP2):c.2595C>T (p.Ile865=)	NRP2-related disorder [RCV004750121]	likely benign	2	205794872	205794872	Human		name , trait , alternate_id
408376944	CV3517466	single nucleotide variant	NM_003872.3(NRP2):c.2343C>T (p.Ser781=)	NRP2-related disorder [RCV004750127]	likely benign	2	205765509	205765509	Human		name , trait , alternate_id
408376953	CV3517533	single nucleotide variant	NM_003872.3(NRP2):c.1770G>A (p.Leu590=)	NRP2-related disorder [RCV004750136]	likely benign	2	205745874	205745874	Human		name , trait , alternate_id
15126860	CV707957	single nucleotide variant	NM_003872.3(NRP2):c.1149A>G (p.Val383=)	not provided [RCV000963811]	benign	2	205740521	205740521	Human		name
15171538	CV707958	single nucleotide variant	NM_003872.3(NRP2):c.1737G>A (p.Ser579=)	NRP2-related disorder [RCV003936145]\|not provided [RCV000972219]	benign\|likely benign	2	205745841	205745841	Human		name , trait , alternate_id
15171543	CV707959	single nucleotide variant	NM_003872.3(NRP2):c.1800G>A (p.Thr600=)	NRP2-related disorder [RCV003936146]\|not provided [RCV000972220]	likely benign	2	205749738	205749738	Human		name , trait , alternate_id
15105706	CV719529	single nucleotide variant	NM_003872.3(NRP2):c.2679C>T (p.Ser893=)	not provided [RCV000893132]	benign	2	205794956	205794956	Human		name
15134036	CV733081	single nucleotide variant	NM_003872.3(NRP2):c.1449C>T (p.Pro483=)	not provided [RCV000898224]	benign	2	205743360	205743360	Human		name
15200714	CV747177	single nucleotide variant	NM_003872.3(NRP2):c.1416G>A (p.Ser472=)	NRP2-related disorder [RCV003902914]\|not provided [RCV000912924]	likely benign	2	205743327	205743327	Human		name , trait , alternate_id
15118680	CV747179	single nucleotide variant	NM_003872.3(NRP2):c.1953C>T (p.Leu651=)	NRP2-related disorder [RCV003950853]\|not provided [RCV000918020]	likely benign	2	205752884	205752884	Human		name , trait , alternate_id
15136904	CV747180	single nucleotide variant	NM_003872.3(NRP2):c.2649C>T (p.Leu883=)	NRP2-related disorder [RCV003895603]\|not provided [RCV000921083]	likely benign	2	205794926	205794926	Human		name , trait , alternate_id
15117337	CV762796	single nucleotide variant	NM_003872.3(NRP2):c.2316C>T (p.Phe772=)	NRP2-related disorder [RCV003913184]\|not provided [RCV000939816]	likely benign	2	205765482	205765482	Human		name , trait , alternate_id
15110010	CV781117	single nucleotide variant	NM_003872.3(NRP2):c.1719A>G (p.Val573=)	NRP2-related disorder [RCV004749576]\|not provided [RCV000977350]	likely benign	2	205745823	205745823	Human		name , trait , alternate_id
8625271	CV80390	single nucleotide variant	NM_003872.3(NRP2):c.2568C>T (p.Thr856=)	NRP2-related disorder [RCV003915029]\|not provided [RCV000923492]	likely benign\|not provided	2	205794845	205794845	Human		name , trait , alternate_id
156079439	CV2198384	single nucleotide variant	NM_003872.3(NRP2):c.554T>A (p.Met185Lys)	NRP2-related disorder [RCV004750311]\|not specified [RCV004081923]	uncertain significance	2	205722598	205722598	Human		name , trait , alternate_id
155916203	CV2239677	single nucleotide variant	NM_003872.3(NRP2):c.914C>A (p.Thr305Asn)	not specified [RCV004108224]	uncertain significance	2	205726006	205726006	Human		name
156343332	CV2353432	single nucleotide variant	NM_003872.3(NRP2):c.904G>A (p.Gly302Arg)	not specified [RCV004205888]	uncertain significance	2	205725996	205725996	Human		name
155958279	CV2395144	single nucleotide variant	NM_003872.3(NRP2):c.905G>A (p.Gly302Glu)	NRP2-related disorder [RCV003395687]\|not specified [RCV004236819]	uncertain significance	2	205725997	205725997	Human		name , trait , alternate_id
329351648	CV2459226	single nucleotide variant	NM_003872.3(NRP2):c.304G>A (p.Gly102Ser)	not specified [RCV004274665]	uncertain significance	2	205716245	205716245	Human		name
401781847	CV2678343	single nucleotide variant	NM_003872.3(NRP2):c.418G>C (p.Glu140Gln)	NRP2-related disorder [RCV004750362]\|not specified [RCV004290329]	uncertain significance	2	205716359	205716359	Human		name , trait , alternate_id
401933192	CV2797478	single nucleotide variant	NM_003872.3(NRP2):c.725C>T (p.Thr242Met)	NRP2-related disorder [RCV003392760]	uncertain significance	2	205723845	205723845	Human		name , trait , alternate_id
401921232	CV2797945	single nucleotide variant	NM_003872.3(NRP2):c.670C>A (p.Pro224Thr)	NRP2-related disorder [RCV003402861]\|not specified [RCV004364451]	uncertain significance	2	205723790	205723790	Human		name , trait , alternate_id
401934806	CV2803011	single nucleotide variant	NM_003872.3(NRP2):c.850G>A (p.Glu284Lys)	NRP2-related disorder [RCV003412238]	uncertain significance	2	205725942	205725942	Human		name , trait , alternate_id
401933364	CV2804095	single nucleotide variant	NM_003872.3(NRP2):c.472G>C (p.Gly158Arg)	NRP2-related disorder [RCV003392841]	uncertain significance	2	205722516	205722516	Human		name , trait , alternate_id
401932669	CV2804351	single nucleotide variant	NM_003872.3(NRP2):c.788G>A (p.Arg263His)	NRP2-related disorder [RCV003408757]	uncertain significance	2	205723908	205723908	Human		name , trait , alternate_id
405273103	CV3197658	single nucleotide variant	NM_003872.3(NRP2):c.649G>A (p.Asp217Asn)	NRP2-related disorder [RCV003901626]	uncertain significance	2	205722693	205722693	Human		name , trait , alternate_id
405273468	CV3197787	single nucleotide variant	NM_003872.3(NRP2):c.470A>T (p.Asn157Ile)	NRP2-related disorder [RCV003901751]\|not specified [RCV004837930]	uncertain significance	2	205722514	205722514	Human		name , trait , alternate_id
405271452	CV3202865	single nucleotide variant	NM_003872.3(NRP2):c.785C>T (p.Ala262Val)	NRP2-related disorder [RCV003913927]	likely benign	2	205723905	205723905	Human		name , trait , alternate_id
405284180	CV3213628	single nucleotide variant	NM_003872.3(NRP2):c.716G>A (p.Arg239His)	NRP2-related disorder [RCV003922198]	likely benign	2	205723836	205723836	Human		name , trait , alternate_id
405709351	CV3359265	single nucleotide variant	NM_003872.3(NRP2):c.337A>G (p.Ile113Val)	not specified [RCV004493612]	uncertain significance	2	205716278	205716278	Human		name
405709360	CV3359266	single nucleotide variant	NM_003872.3(NRP2):c.859C>T (p.Arg287Trp)	not specified [RCV004493613]	uncertain significance	2	205725951	205725951	Human		name
405709378	CV3359268	single nucleotide variant	NM_003872.3(NRP2):c.971C>G (p.Ser324Cys)	NRP2-related disorder [RCV004750473]\|not specified [RCV004493615]	uncertain significance	2	205726063	205726063	Human		name , trait , alternate_id
408382866	CV3506040	single nucleotide variant	NM_003872.3(NRP2):c.847A>G (p.Met283Val)	NRP2-related disorder [RCV004730174]	uncertain significance	2	205725939	205725939	Human		name , trait , alternate_id
408379208	CV3506772	single nucleotide variant	NM_003872.3(NRP2):c.484T>A (p.Ser162Thr)	NRP2-related disorder [RCV004728311]	uncertain significance	2	205722528	205722528	Human		name , trait , alternate_id
408375541	CV3510066	single nucleotide variant	NM_003872.3(NRP2):c.835G>A (p.Val279Ile)	NRP2-related disorder [RCV004748167]	uncertain significance	2	205725927	205725927	Human		name , trait , alternate_id
408376345	CV3513276	single nucleotide variant	NM_003872.3(NRP2):c.553A>T (p.Met185Leu)	NRP2-related disorder [RCV004749061]	uncertain significance	2	205722597	205722597	Human		name , trait , alternate_id
408376462	CV3513764	single nucleotide variant	NM_003872.3(NRP2):c.527C>T (p.Thr176Ile)	NRP2-related disorder [RCV004749132]	uncertain significance	2	205722571	205722571	Human		name , trait , alternate_id
408376546	CV3514704	single nucleotide variant	NM_003872.3(NRP2):c.990G>C (p.Gln330His)	NRP2-related disorder [RCV004749261]	uncertain significance	2	205726082	205726082	Human		name , trait , alternate_id
408376940	CV3517099	single nucleotide variant	NM_003872.3(NRP2):c.929G>A (p.Arg310Gln)	NRP2-related disorder [RCV004750077]	uncertain significance	2	205726021	205726021	Human		name , trait , alternate_id
597643104	CV3576900	single nucleotide variant	NM_003872.3(NRP2):c.964T>A (p.Leu322Met)	not specified [RCV004832554]	uncertain significance	2	205726056	205726056	Human		name
13532092	CV511389	deletion	NM_003872.3(NRP2):c.2118del (p.Val707fs)	Inborn genetic diseases [RCV000623908]\|NRP2-related disorder [RCV004748864]	likely pathogenic\|uncertain significance	2	205763747	205763747	Human	1	name , trait , alternate_id
15165540	CV697258	single nucleotide variant	NM_003872.3(NRP2):c.368A>G (p.Lys123Arg)	not provided [RCV000948613]\|not specified [RCV002249585]	benign	2	205716309	205716309	Human		name
15183719	CV707956	single nucleotide variant	NM_003872.3(NRP2):c.860G>A (p.Arg287Gln)	NRP2-related disorder [RCV003928595]\|not provided [RCV000974941]	benign	2	205725952	205725952	Human		name , trait , alternate_id
15199152	CV719527	single nucleotide variant	NM_003872.3(NRP2):c.838C>T (p.Pro280Ser)	NRP2-related disorder [RCV003975619]\|not provided [RCV000890555]	likely benign	2	205725930	205725930	Human		name , trait , alternate_id
15116084	CV733079	single nucleotide variant	NM_003872.3(NRP2):c.559A>G (p.Ile187Val)	NRP2-related disorder [RCV003920829]\|not provided [RCV000895139]	likely benign	2	205722603	205722603	Human		name , trait , alternate_id
15166390	CV733080	single nucleotide variant	NM_003872.3(NRP2):c.962A>T (p.Asn321Ile)	not provided [RCV000904432]	benign	2	205726054	205726054	Human		name
156027867	CV2195612	single nucleotide variant	NM_003872.3(NRP2):c.2131C>G (p.Arg711Gly)	not specified [RCV004082820]	uncertain significance	2	205763760	205763760	Human		name
156323925	CV2201921	single nucleotide variant	NM_003872.3(NRP2):c.2356A>G (p.Ile786Val)	not specified [RCV004075502]	uncertain significance	2	205765522	205765522	Human		name
156365766	CV2272171	single nucleotide variant	NM_003872.3(NRP2):c.1609T>C (p.Tyr537His)	not specified [RCV004124941]	uncertain significance	2	205743520	205743520	Human		name
156285019	CV2291951	single nucleotide variant	NM_003872.3(NRP2):c.1409G>C (p.Ser470Thr)	not specified [RCV004158463]	uncertain significance	2	205743320	205743320	Human		name
156057926	CV2316846	single nucleotide variant	NM_003872.3(NRP2):c.1411C>G (p.Arg471Gly)	not specified [RCV004172330]	uncertain significance	2	205743322	205743322	Human		name
156352383	CV2323960	single nucleotide variant	NM_003872.3(NRP2):c.1199C>G (p.Ala400Gly)	not specified [RCV004176482]	uncertain significance	2	205740571	205740571	Human		name
156076231	CV2331791	single nucleotide variant	NM_003872.3(NRP2):c.1799C>T (p.Thr600Met)	NRP2-related disorder [RCV003396838]\|not specified [RCV004184408]	uncertain significance	2	205749737	205749737	Human		name , trait , alternate_id
156069354	CV2341119	single nucleotide variant	NM_003872.3(NRP2):c.2090G>A (p.Gly697Asp)	NRP2-related disorder [RCV004750331]\|not specified [RCV004181598]	uncertain significance	2	205763719	205763719	Human		name , trait , alternate_id
329358074	CV2453882	single nucleotide variant	NM_003872.3(NRP2):c.2026A>C (p.Asn676His)	not specified [RCV004271272]	uncertain significance	2	205752957	205752957	Human		name
329386447	CV2456012	single nucleotide variant	NM_003872.3(NRP2):c.2254G>A (p.Gly752Ser)	not specified [RCV004272918]	likely benign	2	205763883	205763883	Human		name
329352848	CV2470528	single nucleotide variant	NM_003872.3(NRP2):c.1830C>G (p.Ser610Arg)	not specified [RCV004273541]	uncertain significance	2	205749768	205749768	Human		name
13437286	CV263842	single nucleotide variant	NM_003872.3(NRP2):c.1000C>T (p.Arg334Cys)	Hirschsprung disease, susceptibility to, 1 [RCV000508614]\|NRP2-related disorder [RCV003920028]\|not provided [RCV004692883]	likely benign\|uncertain significance	2	205727900	205727900	Human	2	name , trait , alternate_id
13437286	CV263842	single nucleotide variant	NM_003872.3(NRP2):c.1000C>T (p.Arg334Cys)	Hirschsprung disease, susceptibility to, 1 [RCV000508614]\|NRP2-related disorder [RCV003920028]\|not provided [RCV004692883]	likely benign\|uncertain significance	2	205727900	205727901	Human	2	name , trait , alternate_id
401718804	CV2704809	single nucleotide variant	NM_003872.3(NRP2):c.1411C>A (p.Arg471Ser)	not specified [RCV004307397]	uncertain significance	2	205743322	205743322	Human		name
401761782	CV2726905	single nucleotide variant	NM_003872.3(NRP2):c.1565G>A (p.Arg522His)	not specified [RCV004323194]	uncertain significance	2	205743476	205743476	Human		name
401726141	CV2736070	single nucleotide variant	NM_003872.3(NRP2):c.1450G>A (p.Gly484Ser)	NRP2-related disorder [RCV003966310]\|not provided [RCV003312515]	likely benign	2	205743361	205743361	Human		name , trait , alternate_id
401857601	CV2767027	single nucleotide variant	NM_003872.3(NRP2):c.2285C>A (p.Pro762His)	NRP2-related disorder [RCV004750372]\|not specified [RCV004347439]	uncertain significance	2	205763914	205763914	Human		name , trait , alternate_id
401891995	CV2780777	single nucleotide variant	NM_003872.3(NRP2):c.1808C>G (p.Thr603Arg)	not specified [RCV004352100]	uncertain significance	2	205749746	205749746	Human		name
401895333	CV2786374	single nucleotide variant	NM_003872.3(NRP2):c.1468G>C (p.Val490Leu)	not specified [RCV004361969]	uncertain significance	2	205743379	205743379	Human		name
401911842	CV2795919	single nucleotide variant	NM_003872.3(NRP2):c.1685G>A (p.Arg562Lys)	NRP2-related disorder [RCV003399657]	uncertain significance	2	205745789	205745789	Human		name , trait , alternate_id
401912098	CV2796055	single nucleotide variant	NM_003872.3(NRP2):c.1001G>A (p.Arg334His)	NRP2-related disorder [RCV003399751]\|not specified [RCV004837884]	uncertain significance	2	205727901	205727901	Human		name , trait , alternate_id
401932289	CV2797298	single nucleotide variant	NM_003872.3(NRP2):c.1282C>T (p.Arg428Trp)	NRP2-related disorder [RCV003408653]	uncertain significance	2	205740654	205740654	Human		name , trait , alternate_id
401938009	CV2797384	single nucleotide variant	NM_003872.3(NRP2):c.1019C>T (p.Thr340Met)	NRP2-related disorder [RCV003417109]\|not specified [RCV004701053]	uncertain significance	2	205727919	205727919	Human		name , trait , alternate_id
401933141	CV2797461	single nucleotide variant	NM_003872.3(NRP2):c.1059G>C (p.Gln353His)	NRP2-related disorder [RCV003392747]\|not specified [RCV004362853]	uncertain significance	2	205727959	205727959	Human		name , trait , alternate_id
401902914	CV2797664	single nucleotide variant	NM_003872.3(NRP2):c.2773G>A (p.Glu925Lys)	NRP2-related disorder [RCV003419163]	uncertain significance	2	205795050	205795050	Human		name , trait , alternate_id
401902946	CV2797728	single nucleotide variant	NM_003872.3(NRP2):c.1715G>A (p.Arg572Gln)	NRP2-related disorder [RCV003419195]	uncertain significance	2	205745819	205745819	Human		name , trait , alternate_id
401907153	CV2797780	single nucleotide variant	NM_003872.3(NRP2):c.1412G>A (p.Arg471His)	NRP2-related disorder [RCV003422431]	uncertain significance	2	205743323	205743323	Human		name , trait , alternate_id
401905472	CV2797876	single nucleotide variant	NM_003872.3(NRP2):c.2537C>T (p.Ser846Leu)	NRP2-related disorder [RCV003420847]	uncertain significance	2	205794814	205794814	Human		name , trait , alternate_id
401905479	CV2797879	single nucleotide variant	NM_003872.3(NRP2):c.2029G>T (p.Asp677Tyr)	NRP2-related disorder [RCV003420849]	uncertain significance	2	205752960	205752960	Human		name , trait , alternate_id
401921573	CV2797977	single nucleotide variant	NM_003872.3(NRP2):c.1411C>T (p.Arg471Cys)	NRP2-related disorder [RCV003402873]	uncertain significance	2	205743322	205743322	Human		name , trait , alternate_id
401916388	CV2799675	single nucleotide variant	NM_003872.3(NRP2):c.1879G>A (p.Gly627Arg)	NRP2-related disorder [RCV003429073]	uncertain significance	2	205749817	205749817	Human		name , trait , alternate_id
401902867	CV2799740	single nucleotide variant	NM_003872.3(NRP2):c.2132G>A (p.Arg711Gln)	NRP2-related disorder [RCV003419117]\|not specified [RCV005382640]	likely benign\|uncertain significance	2	205763761	205763761	Human		name , trait , alternate_id
401903052	CV2799807	single nucleotide variant	NM_003872.3(NRP2):c.1996C>T (p.Arg666Trp)	NRP2-related disorder [RCV003419144]\|not specified [RCV005377368]	uncertain significance	2	205752927	205752927	Human		name , trait , alternate_id
401932721	CV2801839	single nucleotide variant	NM_003872.3(NRP2):c.2542G>A (p.Asp848Asn)	NRP2-related disorder [RCV003408809]	uncertain significance	2	205794819	205794819	Human		name , trait , alternate_id
401906166	CV2802379	single nucleotide variant	NM_003872.3(NRP2):c.1841C>T (p.Thr614Ile)	NRP2-related disorder [RCV003421040]	uncertain significance	2	205749779	205749779	Human		name , trait , alternate_id
401934027	CV2802418	single nucleotide variant	NM_003872.3(NRP2):c.2494T>C (p.Trp832Arg)	NRP2-related disorder [RCV003410807]	uncertain significance	2	205794771	205794771	Human		name , trait , alternate_id
401934689	CV2802721	single nucleotide variant	NM_003872.3(NRP2):c.2530G>A (p.Ala844Thr)	NRP2-related disorder [RCV003412115]	uncertain significance	2	205794807	205794807	Human		name , trait , alternate_id
401931346	CV2802870	single nucleotide variant	NM_003872.3(NRP2):c.2338C>T (p.Arg780Cys)	NRP2-related disorder [RCV003391241]	uncertain significance	2	205765504	205765504	Human		name , trait , alternate_id
405267928	CV3189593	single nucleotide variant	NM_003872.3(NRP2):c.2350A>G (p.Ile784Val)	NRP2-related disorder [RCV003898985]\|not specified [RCV005377620]	uncertain significance	2	205765516	205765516	Human		name , trait , alternate_id
405264165	CV3189891	single nucleotide variant	NM_003872.3(NRP2):c.2116C>G (p.Pro706Ala)	NRP2-related disorder [RCV003896939]	uncertain significance	2	205763745	205763745	Human		name , trait , alternate_id
405260252	CV3190302	single nucleotide variant	NM_003872.3(NRP2):c.1598A>G (p.Lys533Arg)	NRP2-related disorder [RCV003894700]\|not specified [RCV004837934]	uncertain significance	2	205743509	205743509	Human		name , trait , alternate_id
405259211	CV3194623	single nucleotide variant	NM_003872.3(NRP2):c.2569C>G (p.Leu857Val)	NRP2-related disorder [RCV003894017]	uncertain significance	2	205794846	205794846	Human		name , trait , alternate_id
405259488	CV3194856	single nucleotide variant	NM_003872.3(NRP2):c.1541C>T (p.Ala514Val)	NRP2-related disorder [RCV003894244]	uncertain significance	2	205743452	205743452	Human		name , trait , alternate_id
405273776	CV3198161	single nucleotide variant	NM_003872.3(NRP2):c.2758C>A (p.Gln920Lys)	NRP2-related disorder [RCV003901931]	likely benign	2	205795035	205795035	Human		name , trait , alternate_id
405268383	CV3201002	single nucleotide variant	NM_003872.3(NRP2):c.2768G>C (p.Cys923Ser)	NRP2-related disorder [RCV003899114]	uncertain significance	2	205795045	205795045	Human		name , trait , alternate_id
405269620	CV3201756	single nucleotide variant	NM_003872.3(NRP2):c.2323G>A (p.Val775Met)	NRP2-related disorder [RCV003899663]	uncertain significance	2	205765489	205765489	Human		name , trait , alternate_id
405294530	CV3208956	single nucleotide variant	NM_003872.3(NRP2):c.1468G>A (p.Val490Ile)	NRP2-related disorder [RCV003934476]	likely benign	2	205743379	205743379	Human		name , trait , alternate_id
405274734	CV3209075	single nucleotide variant	NM_003872.3(NRP2):c.2590A>G (p.Ile864Val)	NRP2-related disorder [RCV003951827]	likely benign	2	205794867	205794867	Human		name , trait , alternate_id
405295323	CV3209441	single nucleotide variant	NM_003872.3(NRP2):c.1682G>A (p.Arg561Gln)	NRP2-related disorder [RCV003937268]	uncertain significance	2	205745786	205745786	Human		name , trait , alternate_id
405266941	CV3211975	single nucleotide variant	NM_003872.3(NRP2):c.2512G>C (p.Ala838Pro)	NRP2-related disorder [RCV003947238]	likely benign	2	205794789	205794789	Human		name , trait , alternate_id
405278822	CV3212694	single nucleotide variant	NM_003872.3(NRP2):c.1780T>C (p.Trp594Arg)	NRP2-related disorder [RCV003954720]	likely benign	2	205745884	205745884	Human		name , trait , alternate_id
405293883	CV3214621	single nucleotide variant	NM_003872.3(NRP2):c.1321C>T (p.Leu441Phe)	NRP2-related disorder [RCV003932279]	likely benign	2	205743232	205743232	Human		name , trait , alternate_id
405278558	CV3216716	single nucleotide variant	NM_003872.3(NRP2):c.2033G>A (p.Arg678Gln)	NRP2-related disorder [RCV003954602]	likely benign	2	205752964	205752964	Human		name , trait , alternate_id
405289525	CV3218327	single nucleotide variant	NM_003872.3(NRP2):c.2402T>C (p.Met801Thr)	NRP2-related disorder [RCV003983729]	uncertain significance	2	205765568	205765568	Human		name , trait , alternate_id
405286172	CV3218736	single nucleotide variant	NM_003872.3(NRP2):c.1062T>G (p.Asn354Lys)	NRP2-related disorder [RCV003959454]	likely benign	2	205727962	205727962	Human		name , trait , alternate_id
405279075	CV3219374	single nucleotide variant	NM_003872.3(NRP2):c.1522G>A (p.Gly508Arg)	NRP2-related disorder [RCV003954841]	likely benign\|uncertain significance	2	205743433	205743433	Human		name , trait , alternate_id
405265688	CV3220782	single nucleotide variant	NM_003872.3(NRP2):c.1808C>T (p.Thr603Met)	NRP2-related disorder [RCV003968963]	uncertain significance	2	205749746	205749746	Human		name , trait , alternate_id
405291832	CV3221147	single nucleotide variant	NM_003872.3(NRP2):c.2656A>T (p.Thr886Ser)	NRP2-related disorder [RCV003964246]	likely benign	2	205794933	205794933	Human		name , trait , alternate_id
405261412	CV3221526	single nucleotide variant	NM_003872.3(NRP2):c.2564A>T (p.Tyr855Phe)	NRP2-related disorder [RCV003966994]	likely benign	2	205794841	205794841	Human		name , trait , alternate_id
405709313	CV3359260	single nucleotide variant	NM_003872.3(NRP2):c.1145A>G (p.Lys382Arg)	not specified [RCV004493607]	uncertain significance	2	205728045	205728045	Human		name
405709320	CV3359261	single nucleotide variant	NM_003872.3(NRP2):c.1262G>A (p.Arg421Gln)	not specified [RCV004493608]	uncertain significance	2	205740634	205740634	Human		name
407516952	CV3465925	single nucleotide variant	NM_003872.3(NRP2):c.1925C>T (p.Ser642Leu)	not specified [RCV004650464]	uncertain significance	2	205752856	205752856	Human		name
407477221	CV3465926	single nucleotide variant	NM_003872.3(NRP2):c.1997G>A (p.Arg666Gln)	not specified [RCV004638716]	uncertain significance	2	205752928	205752928	Human		name
408382742	CV3503661	single nucleotide variant	NM_003872.3(NRP2):c.2633G>T (p.Cys878Phe)	NRP2-related disorder [RCV004730127]	uncertain significance	2	205794910	205794910	Human		name , trait , alternate_id
408371354	CV3503810	single nucleotide variant	NM_003872.3(NRP2):c.2486A>C (p.Glu829Ala)	NRP2-related disorder [RCV004724657]	uncertain significance	2	205794763	205794763	Human		name , trait , alternate_id
408371402	CV3503844	single nucleotide variant	NM_003872.3(NRP2):c.2408C>G (p.Pro803Arg)	NRP2-related disorder [RCV004724681]	uncertain significance	2	205766786	205766786	Human		name , trait , alternate_id
408370993	CV3504607	single nucleotide variant	NM_003872.3(NRP2):c.2414C>T (p.Ser805Leu)	NRP2-related disorder [RCV004724339]	uncertain significance	2	205766792	205766792	Human		name , trait , alternate_id
408378183	CV3505105	single nucleotide variant	NM_003872.3(NRP2):c.1794G>C (p.Lys598Asn)	NRP2-related disorder [RCV004727874]	uncertain significance	2	205749732	205749732	Human		name , trait , alternate_id
408378606	CV3505218	single nucleotide variant	NM_003872.3(NRP2):c.1574A>G (p.Lys525Arg)	NRP2-related disorder [RCV004727947]	uncertain significance	2	205743485	205743485	Human		name , trait , alternate_id
408376150	CV3505580	single nucleotide variant	NM_003872.3(NRP2):c.1828A>G (p.Ser610Gly)	NRP2-related disorder [RCV004726578]	uncertain significance	2	205749766	205749766	Human		name , trait , alternate_id
408382801	CV3506042	single nucleotide variant	NM_003872.3(NRP2):c.1799C>A (p.Thr600Lys)	NRP2-related disorder [RCV004730176]	uncertain significance	2	205749737	205749737	Human		name , trait , alternate_id
408382805	CV3506045	single nucleotide variant	NM_003872.3(NRP2):c.2645T>C (p.Leu882Pro)	NRP2-related disorder [RCV004730179]	uncertain significance	2	205794922	205794922	Human		name , trait , alternate_id
408377111	CV3507218	single nucleotide variant	NM_003872.3(NRP2):c.1835A>G (p.Glu612Gly)	NRP2-related disorder [RCV004750500]	uncertain significance	2	205749773	205749773	Human		name , trait , alternate_id
408377195	CV3507311	single nucleotide variant	NM_003872.3(NRP2):c.1252A>G (p.Ile418Val)	NRP2-related disorder [RCV004750515]	uncertain significance	2	205740624	205740624	Human		name , trait , alternate_id
408377218	CV3507534	single nucleotide variant	NM_003872.3(NRP2):c.1888T>G (p.Cys630Gly)	NRP2-related disorder [RCV004750549]	uncertain significance	2	205749826	205749826	Human		name , trait , alternate_id
408377267	CV3507839	single nucleotide variant	NM_003872.3(NRP2):c.1708T>C (p.Tyr570His)	NRP2-related disorder [RCV004750586]	uncertain significance	2	205745812	205745812	Human		name , trait , alternate_id
408377290	CV3508355	single nucleotide variant	NM_003872.3(NRP2):c.1010C>T (p.Thr337Ile)	NRP2-related disorder [RCV004750652]	uncertain significance	2	205727910	205727910	Human		name , trait , alternate_id
408377315	CV3508479	single nucleotide variant	NM_003872.3(NRP2):c.2471T>C (p.Ile824Thr)	NRP2-related disorder [RCV004750670]	uncertain significance	2	205792280	205792280	Human		name , trait , alternate_id
408377325	CV3508544	single nucleotide variant	NM_003872.3(NRP2):c.2533C>G (p.Pro845Ala)	NRP2-related disorder [RCV004750678]	uncertain significance	2	205794810	205794810	Human		name , trait , alternate_id
408375495	CV3509494	single nucleotide variant	NM_003872.3(NRP2):c.1858G>A (p.Glu620Lys)	NRP2-related disorder [RCV004748096]	uncertain significance	2	205749796	205749796	Human		name , trait , alternate_id
408375509	CV3509499	single nucleotide variant	NM_003872.3(NRP2):c.2317G>A (p.Glu773Lys)	NRP2-related disorder [RCV004748099]	uncertain significance	2	205765483	205765483	Human		name , trait , alternate_id
408375484	CV3509799	single nucleotide variant	NM_003872.3(NRP2):c.1810C>G (p.Leu604Val)	NRP2-related disorder [RCV004748135]	uncertain significance	2	205749748	205749748	Human		name , trait , alternate_id
408375598	CV3509979	single nucleotide variant	NM_003872.3(NRP2):c.2036C>T (p.Thr679Met)	NRP2-related disorder [RCV004748155]	uncertain significance	2	205752967	205752967	Human		name , trait , alternate_id
408375638	CV3510100	single nucleotide variant	NM_003872.3(NRP2):c.1613T>C (p.Ile538Thr)	NRP2-related disorder [RCV004748170]\|not specified [RCV004837942]	uncertain significance	2	205743524	205743524	Human		name , trait , alternate_id
408375551	CV3510123	single nucleotide variant	NM_003872.3(NRP2):c.1517C>T (p.Ala506Val)	NRP2-related disorder [RCV004748172]	uncertain significance	2	205743428	205743428	Human		name , trait , alternate_id
408375574	CV3510211	single nucleotide variant	NM_003872.3(NRP2):c.1879G>C (p.Gly627Arg)	NRP2-related disorder [RCV004748185]	uncertain significance	2	205749817	205749817	Human		name , trait , alternate_id
408375576	CV3510212	single nucleotide variant	NM_003872.3(NRP2):c.2596G>A (p.Ala866Thr)	NRP2-related disorder [RCV004748186]	uncertain significance	2	205794873	205794873	Human		name , trait , alternate_id
408375700	CV3510744	single nucleotide variant	NM_003872.3(NRP2):c.1594G>A (p.Gly532Ser)	NRP2-related disorder [RCV004748252]	likely benign	2	205743505	205743505	Human		name , trait , alternate_id
408375814	CV3511151	single nucleotide variant	NM_003872.3(NRP2):c.1736C>T (p.Ser579Leu)	NRP2-related disorder [RCV004748312]	uncertain significance	2	205745840	205745840	Human		name , trait , alternate_id
408375920	CV3511597	single nucleotide variant	NM_003872.3(NRP2):c.2312T>C (p.Val771Ala)	NRP2-related disorder [RCV004748369]	uncertain significance	2	205765478	205765478	Human		name , trait , alternate_id
408375936	CV3511651	single nucleotide variant	NM_003872.3(NRP2):c.2369G>A (p.Arg790Gln)	NRP2-related disorder [RCV004748377]	uncertain significance	2	205765535	205765535	Human		name , trait , alternate_id
408375947	CV3511722	single nucleotide variant	NM_003872.3(NRP2):c.2339G>A (p.Arg780His)	NRP2-related disorder [RCV004748383]	uncertain significance	2	205765505	205765505	Human		name , trait , alternate_id
408376263	CV3512483	single nucleotide variant	NM_003872.3(NRP2):c.1905C>A (p.Asp635Glu)	NRP2-related disorder [RCV004748478]	uncertain significance	2	205752836	205752836	Human		name , trait , alternate_id
408376141	CV3512580	single nucleotide variant	NM_003872.3(NRP2):c.1283G>A (p.Arg428Gln)	NRP2-related disorder [RCV004748486]	uncertain significance	2	205740655	205740655	Human		name , trait , alternate_id
408376295	CV3512679	single nucleotide variant	NM_003872.3(NRP2):c.1052A>T (p.Glu351Val)	NRP2-related disorder [RCV004748988]	uncertain significance	2	205727952	205727952	Human		name , trait , alternate_id
408376299	CV3512705	single nucleotide variant	NM_003872.3(NRP2):c.2029G>A (p.Asp677Asn)	NRP2-related disorder [RCV004748993]	uncertain significance	2	205752960	205752960	Human		name , trait , alternate_id
408376320	CV3513106	single nucleotide variant	NM_003872.3(NRP2):c.2327T>C (p.Ile776Thr)	NRP2-related disorder [RCV004749033]	uncertain significance	2	205765493	205765493	Human		name , trait , alternate_id
408376444	CV3513956	single nucleotide variant	NM_003872.3(NRP2):c.1000C>A (p.Arg334Ser)	NRP2-related disorder [RCV004749159]	uncertain significance	2	205727900	205727900	Human		name , trait , alternate_id
408376532	CV3514303	single nucleotide variant	NM_003872.3(NRP2):c.1903G>A (p.Asp635Asn)	NRP2-related disorder [RCV004749203]	uncertain significance	2	205749841	205749841	Human		name , trait , alternate_id
408376533	CV3514305	single nucleotide variant	NM_003872.3(NRP2):c.1631A>G (p.Gln544Arg)	NRP2-related disorder [RCV004749204]	uncertain significance	2	205743542	205743542	Human		name , trait , alternate_id
408376498	CV3514362	single nucleotide variant	NM_003872.3(NRP2):c.2716G>A (p.Glu906Lys)	NRP2-related disorder [RCV004749213]	uncertain significance	2	205794993	205794993	Human		name , trait , alternate_id
408376509	CV3514423	single nucleotide variant	NM_003872.3(NRP2):c.1433T>C (p.Ile478Thr)	NRP2-related disorder [RCV004749224]	uncertain significance	2	205743344	205743344	Human		name , trait , alternate_id
408376513	CV3514435	single nucleotide variant	NM_003872.3(NRP2):c.1276G>A (p.Gly426Ser)	NRP2-related disorder [RCV004749228]	uncertain significance	2	205740648	205740648	Human		name , trait , alternate_id
408376615	CV3514863	single nucleotide variant	NM_003872.3(NRP2):c.2497A>G (p.Ser833Gly)	NRP2-related disorder [RCV004749283]	uncertain significance	2	205794774	205794774	Human		name , trait , alternate_id
408376570	CV3514921	single nucleotide variant	NM_003872.3(NRP2):c.2279T>C (p.Ile760Thr)	NRP2-related disorder [RCV004749286]	uncertain significance	2	205763908	205763908	Human		name , trait , alternate_id
408376722	CV3516184	single nucleotide variant	NM_003872.3(NRP2):c.1421G>T (p.Trp474Leu)	NRP2-related disorder [RCV004749439]	uncertain significance	2	205743332	205743332	Human		name , trait , alternate_id
408376744	CV3516378	single nucleotide variant	NM_003872.3(NRP2):c.1691A>G (p.Asp564Gly)	NRP2-related disorder [RCV004749462]	uncertain significance	2	205745795	205745795	Human		name , trait , alternate_id
408376748	CV3516392	single nucleotide variant	NM_003872.3(NRP2):c.2278A>G (p.Ile760Val)	NRP2-related disorder [RCV004749466]	uncertain significance	2	205763907	205763907	Human		name , trait , alternate_id
408376799	CV3516449	single nucleotide variant	NM_003872.3(NRP2):c.2259G>C (p.Glu753Asp)	NRP2-related disorder [RCV004749966]	uncertain significance	2	205763888	205763888	Human		name , trait , alternate_id
408376822	CV3516692	single nucleotide variant	NM_003872.3(NRP2):c.1382G>C (p.Ser461Thr)	NRP2-related disorder [RCV004750001]	uncertain significance	2	205743293	205743293	Human		name , trait , alternate_id
408376856	CV3516928	single nucleotide variant	NM_003872.3(NRP2):c.2116C>A (p.Pro706Thr)	NRP2-related disorder [RCV004750041]	uncertain significance	2	205763745	205763745	Human		name , trait , alternate_id
408376867	CV3516985	single nucleotide variant	NM_003872.3(NRP2):c.2442A>G (p.Ile814Met)	NRP2-related disorder [RCV004750054]	uncertain significance	2	205792251	205792251	Human		name , trait , alternate_id
408376875	CV3517040	single nucleotide variant	NM_003872.3(NRP2):c.2174G>A (p.Gly725Asp)	NRP2-related disorder [RCV004750062]	uncertain significance	2	205763803	205763803	Human		name , trait , alternate_id
408376911	CV3517267	single nucleotide variant	NM_003872.3(NRP2):c.1406G>A (p.Ser469Asn)	NRP2-related disorder [RCV004750097]	uncertain significance	2	205743317	205743317	Human		name , trait , alternate_id
408376916	CV3517301	single nucleotide variant	NM_003872.3(NRP2):c.1954G>A (p.Glu652Lys)	NRP2-related disorder [RCV004750100]	uncertain significance	2	205752885	205752885	Human		name , trait , alternate_id
408376917	CV3517310	single nucleotide variant	NM_003872.3(NRP2):c.1913T>C (p.Leu638Ser)	NRP2-related disorder [RCV004750101]	uncertain significance	2	205752844	205752844	Human		name , trait , alternate_id
408376918	CV3517314	single nucleotide variant	NM_003872.3(NRP2):c.2330G>T (p.Gly777Val)	NRP2-related disorder [RCV004750102]	uncertain significance	2	205765496	205765496	Human		name , trait , alternate_id
408376986	CV3517386	single nucleotide variant	NM_003872.3(NRP2):c.2515A>G (p.Thr839Ala)	NRP2-related disorder [RCV004750115]	uncertain significance	2	205794792	205794792	Human		name , trait , alternate_id
408376988	CV3517387	single nucleotide variant	NM_003872.3(NRP2):c.1255G>A (p.Ala419Thr)	NRP2-related disorder [RCV004750116]	uncertain significance	2	205740627	205740627	Human		name , trait , alternate_id
408376967	CV3517633	single nucleotide variant	NM_003872.3(NRP2):c.2692A>G (p.Thr898Ala)	NRP2-related disorder [RCV004750150]	uncertain significance	2	205794969	205794969	Human		name , trait , alternate_id
408376983	CV3517781	single nucleotide variant	NM_003872.3(NRP2):c.1198G>A (p.Ala400Thr)	NRP2-related disorder [RCV004750166]	uncertain significance	2	205740570	205740570	Human		name , trait , alternate_id
597706875	CV3576895	single nucleotide variant	NM_003872.3(NRP2):c.2128C>T (p.Pro710Ser)	not specified [RCV004840386]	uncertain significance	2	205763757	205763757	Human		name
597706882	CV3576896	single nucleotide variant	NM_003872.3(NRP2):c.1847C>T (p.Pro616Leu)	not specified [RCV004840387]	uncertain significance	2	205749785	205749785	Human		name
597706892	CV3576897	single nucleotide variant	NM_003872.3(NRP2):c.1945G>A (p.Asp649Asn)	not specified [RCV004840388]	uncertain significance	2	205752876	205752876	Human		name
597706899	CV3576898	single nucleotide variant	NM_003872.3(NRP2):c.1647C>G (p.Phe549Leu)	not specified [RCV004840389]	uncertain significance	2	205745751	205745751	Human		name
597706907	CV3576899	single nucleotide variant	NM_003872.3(NRP2):c.1118T>C (p.Met373Thr)	not specified [RCV004840390]	uncertain significance	2	205728018	205728018	Human		name
597706917	CV3576901	single nucleotide variant	NM_003872.3(NRP2):c.1700C>T (p.Pro567Leu)	not specified [RCV004840391]	uncertain significance	2	205745804	205745804	Human		name
597706925	CV3576902	single nucleotide variant	NM_003872.3(NRP2):c.1064G>A (p.Gly355Asp)	not specified [RCV004840392]	uncertain significance	2	205727964	205727964	Human		name
597706941	CV3576904	single nucleotide variant	NM_003872.3(NRP2):c.2089G>A (p.Gly697Ser)	not specified [RCV004840394]	uncertain significance	2	205763718	205763718	Human		name
598220449	CV3998143	single nucleotide variant	NM_003872.3(NRP2):c.1067A>G (p.Tyr356Cys)	not specified [RCV005379509]	uncertain significance	2	205727967	205727967	Human		name
598220456	CV3998144	single nucleotide variant	NM_003872.3(NRP2):c.1349T>C (p.Ile450Thr)	not specified [RCV005379510]	uncertain significance	2	205743260	205743260	Human		name
598264790	CV3998145	single nucleotide variant	NM_003872.3(NRP2):c.1934A>G (p.Asn645Ser)	not specified [RCV005387827]	uncertain significance	2	205752865	205752865	Human		name
15199883	CV719528	single nucleotide variant	NM_003872.3(NRP2):c.1333A>C (p.Ile445Leu)	not provided [RCV000890758]	likely benign	2	205743244	205743244	Human		name
15099961	CV747178	single nucleotide variant	NM_003872.3(NRP2):c.1831G>A (p.Glu611Lys)	NRP2-related disorder [RCV003950805]\|not provided [RCV000914535]	likely benign	2	205749769	205749769	Human		name , trait , alternate_id
8625270	CV80389	single nucleotide variant	NM_201266.1(NRP2):c.2582C>T (p.Thr861Ile)	Malignant melanoma [RCV000060466]	not provided	2	205794844	205794844	Human		name
405292159	CV3217146	deletion	NM_003872.3(NRP2):c.2425+9714_2425+9717del	NRP2-related disorder [RCV003964356]	benign\|likely benign	2	205776516	205776519	Human		name , trait , alternate_id
598208664	CV4007748	deletion	NM_003872.3(NRP2):c.2425+9717_2425+9718del	NRP2-related disorder [RCV005400062]	uncertain significance	2	205776520	205776521	Human		name , trait , alternate_id
10449815	CV215236	insertion	NM_003872.3(NRP2):c.2425+9718_2425+9719insA	NRP2-related disorder [RCV003967545]\|not specified [RCV000202952]	benign	2	205776521	205776522	Human		name , trait , alternate_id
408375416	CV3509409	indel	NM_003872.3(NRP2):c.1673_1674delinsTG (p.Pro558Leu)	NRP2-related disorder [RCV004748087]	uncertain significance	2	205745777	205745778	Human		name , trait , alternate_id

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