Nos2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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162 records found for search term Nos2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15146780	CV760389	single nucleotide variant	NM_000625.4(NOS2):c.196-9C>G	not provided [RCV000922778]	likely benign	17	27788940	27788940	Human		name
404982214	CV2848993	single nucleotide variant	NM_000625.4(NOS2):c.2428+6C>T	NOS2-related disorder [RCV003984371]\|not specified [RCV003488865]	benign	17	27765529	27765529	Human	1	name , trait , alternate_id
404982261	CV2848997	single nucleotide variant	NM_000625.4(NOS2):c.864+22A>G	not specified [RCV003488869]	benign	17	27781014	27781014	Human		name
404982265	CV2848998	single nucleotide variant	NM_000625.4(NOS2):c.722+11A>G	not specified [RCV003488870]	benign	17	27782004	27782004	Human		name
404982912	CV2849157	single nucleotide variant	NM_000625.4(NOS2):c.-73-10C>T	not specified [RCV003489029]	benign	17	27798892	27798892	Human	3	name
404982912	CV2849157	single nucleotide variant	NM_000625.4(NOS2):c.-73-10C>T	not specified [RCV003489029]	benign	17	27798892	27798893	Human	3	name
15157177	CV744922	single nucleotide variant	NM_000625.4(NOS2):c.2429-8C>T	not provided [RCV000902474]	likely benign	17	27764152	27764152	Human		name
15188183	CV744924	single nucleotide variant	NM_000625.4(NOS2):c.1860-7C>T	not provided [RCV000909297]	likely benign	17	27769158	27769158	Human		name
15189863	CV778335	single nucleotide variant	NM_000625.4(NOS2):c.2428+9C>T	not provided [RCV000954305]	benign	17	27765526	27765526	Human		name
404982270	CV2848999	single nucleotide variant	NM_000625.4(NOS2):c.1477-52T>C	not specified [RCV003488871]	benign	17	27773295	27773295	Human		name
404983309	CV2849131	single nucleotide variant	NM_000625.4(NOS2):c.1859+88G>T	not specified [RCV003489003]	benign	17	27769447	27769447	Human	3	name
404983309	CV2849131	single nucleotide variant	NM_000625.4(NOS2):c.1859+88G>T	not specified [RCV003489003]	benign	17	27769447	27769448	Human	3	name
404983283	CV2849182	single nucleotide variant	NM_000625.4(NOS2):c.1476+46C>T	not specified [RCV003489054]	benign	17	27774211	27774211	Human		name
15161707	CV731138	single nucleotide variant	NM_000625.4(NOS2):c.1704+10C>T	NOS2-related disorder [RCV003920550]\|not provided [RCV000881620]	benign	17	27772298	27772298	Human	1	name , trait , alternate_id
15124393	CV744925	single nucleotide variant	NM_000625.4(NOS2):c.1005-10T>C	not provided [RCV000896580]	benign	17	27779066	27779066	Human		name
15190541	CV778333	single nucleotide variant	NM_000625.4(NOS2):c.2888+10C>G	NOS2-related disorder [RCV003926005]\|not provided [RCV000954507]	likely benign	17	27761134	27761134	Human	1	name , trait , alternate_id
404983954	CV2849385	microsatellite	NM_000625.4(NOS2):c.1476+51TG[10]	not specified [RCV003489257]	benign	17	27774188	27774189	Human		name
15130015	CV715313	single nucleotide variant	NM_000625.4(NOS2):c.297A>T (p.Thr99=)	not provided [RCV000964360]	benign	17	27788830	27788830	Human		name
15106328	CV771324	single nucleotide variant	NM_000625.4(NOS2):c.117G>A (p.Val39=)	not provided [RCV000937759]	likely benign	17	27789682	27789682	Human		name
401914148	CV2811155	single nucleotide variant	NM_000625.4(NOS2):c.300T>C (p.Leu100=)	not provided [RCV003428191]	likely benign	17	27788827	27788827	Human		name
405260674	CV3204216	single nucleotide variant	NM_000625.4(NOS2):c.735C>T (p.Thr245=)	NOS2-related disorder [RCV003944071]	likely benign	17	27781165	27781165	Human		name , trait , alternate_id
405678532	CV3351889	single nucleotide variant	NM_000625.4(NOS2):c.92C>T (p.Ala31Val)	not specified [RCV004488190]	uncertain significance	17	27798718	27798718	Human		name
597673713	CV3563253	single nucleotide variant	NM_000625.4(NOS2):c.894G>A (p.Lys298=)	not specified [RCV004830091]	likely benign	17	27780877	27780877	Human		name
15178249	CV740657	single nucleotide variant	NM_000625.4(NOS2):c.957C>T (p.Phe319=)	not provided [RCV000906834]	benign	17	27780814	27780814	Human		name
15160886	CV755715	single nucleotide variant	NM_000625.4(NOS2):c.558C>T (p.Leu186=)	not provided [RCV000925575]	likely benign	17	27783016	27783016	Human		name
8627945	CV83089	single nucleotide variant	NM_000625.4(NOS2):c.487C>T (p.Leu163=)	Malignant melanoma [RCV000063169]	not provided	17	27783087	27783087	Human		name
156192811	CV2223212	single nucleotide variant	NM_000625.4(NOS2):c.145C>T (p.Leu49Phe)	not specified [RCV004104046]	uncertain significance	17	27789654	27789654	Human		name
156042221	CV2381437	single nucleotide variant	NM_000625.4(NOS2):c.202C>T (p.Pro68Ser)	not specified [RCV004229925]	uncertain significance	17	27788925	27788925	Human		name
401731711	CV2674459	single nucleotide variant	NM_000625.4(NOS2):c.188C>T (p.Thr63Met)	not specified [RCV004291363]	uncertain significance	17	27789611	27789611	Human		name
401903845	CV2811153	single nucleotide variant	NM_000625.4(NOS2):c.2740C>A (p.Arg914=)	not provided [RCV003419683]	likely benign	17	27762858	27762858	Human		name
401935716	CV2811154	single nucleotide variant	NM_000625.4(NOS2):c.1755G>C (p.Leu585=)	not provided [RCV003413176]	likely benign	17	27770967	27770967	Human		name
404981964	CV2848992	single nucleotide variant	NM_000625.4(NOS2):c.2757A>G (p.Thr919=)	NOS2-related disorder [RCV003980959]\|not specified [RCV003488864]	benign	17	27762841	27762841	Human	1	name , trait , alternate_id
404982218	CV2848994	single nucleotide variant	NM_000625.4(NOS2):c.2358T>C (p.Gly786=)	NOS2-related disorder [RCV003980960]\|not specified [RCV003488866]	benign	17	27765605	27765605	Human	1	name , trait , alternate_id
404983533	CV2849288	single nucleotide variant	NM_000625.4(NOS2):c.1155C>T (p.Asp385=)	NOS2-related disorder [RCV003980963]\|not specified [RCV003489160]	benign	17	27778906	27778906	Human	1	name , trait , alternate_id
405294650	CV3204212	single nucleotide variant	NM_000625.4(NOS2):c.1905C>T (p.Cys635=)	NOS2-related disorder [RCV003934558]	likely benign	17	27769106	27769106	Human		name , trait , alternate_id
405696674	CV3226759	single nucleotide variant	NM_000625.4(NOS2):c.1509C>T (p.Asp503=)	not provided [RCV003993152]	likely benign	17	27773211	27773211	Human		name
405678458	CV3351869	single nucleotide variant	NM_000625.4(NOS2):c.113C>G (p.Pro38Arg)	not specified [RCV004488170]	uncertain significance	17	27789686	27789686	Human		name
407509992	CV3469192	single nucleotide variant	NM_000625.4(NOS2):c.238T>A (p.Ser80Thr)	not specified [RCV004647565]	uncertain significance	17	27788889	27788889	Human		name
596947684	CV3547265	single nucleotide variant	NM_000625.4(NOS2):c.2892C>G (p.Ala964=)	not provided [RCV004811569]	likely benign	17	27760741	27760741	Human		name
15122934	CV715312	single nucleotide variant	NM_000625.4(NOS2):c.1755G>A (p.Leu585=)	not provided [RCV000963155]	benign	17	27770967	27770967	Human		name
15176614	CV727076	single nucleotide variant	NM_000625.4(NOS2):c.1080C>T (p.Gly360=)	not provided [RCV000884623]	likely benign	17	27778981	27778981	Human		name
15170349	CV755711	single nucleotide variant	NM_000625.4(NOS2):c.2322G>T (p.Gly774=)	not provided [RCV000927682]	likely benign	17	27765641	27765641	Human		name
15151943	CV755712	single nucleotide variant	NM_000625.4(NOS2):c.2046G>A (p.Glu682=)	not provided [RCV000923775]	likely benign	17	27767826	27767826	Human		name
15120846	CV755713	single nucleotide variant	NM_000625.4(NOS2):c.1626C>T (p.Leu542=)	not provided [RCV000918384]	likely benign	17	27772386	27772386	Human		name
15136823	CV755714	single nucleotide variant	NM_000625.4(NOS2):c.1461T>C (p.Pro487=)	not provided [RCV000921071]	likely benign	17	27774272	27774272	Human		name
15202163	CV771322	single nucleotide variant	NM_000625.4(NOS2):c.1878C>T (p.Leu626=)	not provided [RCV000935867]	likely benign	17	27769133	27769133	Human		name
15111339	CV771323	single nucleotide variant	NM_000625.4(NOS2):c.1449C>T (p.Tyr483=)	not provided [RCV000938729]	likely benign	17	27774284	27774284	Human		name
156047956	CV2304384	single nucleotide variant	NM_000625.4(NOS2):c.341C>A (p.Ser114Tyr)	not specified [RCV004164490]	uncertain significance	17	27787804	27787804	Human		name
156050939	CV2304619	single nucleotide variant	NM_000625.4(NOS2):c.683G>T (p.Cys228Phe)	not specified [RCV004166509]	uncertain significance	17	27782054	27782054	Human		name
156304785	CV2304893	single nucleotide variant	NM_000625.4(NOS2):c.793A>G (p.Ile265Val)	not specified [RCV004168813]	uncertain significance	17	27781107	27781107	Human		name
156217314	CV2348124	single nucleotide variant	NM_000625.4(NOS2):c.681C>G (p.Ile227Met)	not specified [RCV004197801]	uncertain significance	17	27782056	27782056	Human		name
155993906	CV2379475	single nucleotide variant	NM_000625.4(NOS2):c.503C>T (p.Ala168Val)	not specified [RCV004217194]	uncertain significance	17	27783071	27783071	Human		name
156091114	CV2384633	single nucleotide variant	NM_000625.4(NOS2):c.353C>G (p.Ser118Cys)	not specified [RCV004232415]	uncertain significance	17	27787792	27787792	Human		name
329381997	CV2424292	single nucleotide variant	NM_000625.4(NOS2):c.695G>A (p.Arg232His)	not specified [RCV004252201]	uncertain significance	17	27782042	27782042	Human		name
329360407	CV2458723	single nucleotide variant	NM_000625.4(NOS2):c.832A>G (p.Arg278Gly)	not specified [RCV004268376]	uncertain significance	17	27781068	27781068	Human		name
401732283	CV2708759	single nucleotide variant	NM_000625.4(NOS2):c.341C>T (p.Ser114Phe)	not specified [RCV004307725]	uncertain significance	17	27787804	27787804	Human		name
401878677	CV2754776	single nucleotide variant	NM_000625.4(NOS2):c.512A>T (p.Lys171Met)	not specified [RCV004341259]	uncertain significance	17	27783062	27783062	Human		name
405266349	CV3215865	single nucleotide variant	NM_000625.4(NOS2):c.3291G>A (p.Gln1097=)	NOS2-related disorder [RCV003947009]	likely benign	17	27758944	27758944	Human		name , trait , alternate_id
405262088	CV3220010	single nucleotide variant	NM_000625.4(NOS2):c.545C>T (p.Thr182Met)	NOS2-related disorder [RCV003967158]	likely benign	17	27783029	27783029	Human		name , trait , alternate_id
405678518	CV3351885	single nucleotide variant	NM_000625.4(NOS2):c.530G>A (p.Gly177Glu)	not specified [RCV004488186]	uncertain significance	17	27783044	27783044	Human		name
405678522	CV3351886	single nucleotide variant	NM_000625.4(NOS2):c.584G>A (p.Arg195His)	not specified [RCV004488187]	uncertain significance	17	27782990	27782990	Human		name
405678527	CV3351887	single nucleotide variant	NM_000625.4(NOS2):c.775G>C (p.Val259Leu)	not specified [RCV004488188]	uncertain significance	17	27781125	27781125	Human		name
405678528	CV3351888	single nucleotide variant	NM_000625.4(NOS2):c.890C>T (p.Pro297Leu)	not specified [RCV004488189]	uncertain significance	17	27780881	27780881	Human		name
597673610	CV3563242	single nucleotide variant	NM_000625.4(NOS2):c.305A>G (p.His102Arg)	not specified [RCV004830080]	uncertain significance	17	27788822	27788822	Human		name
597673639	CV3563245	single nucleotide variant	NM_000625.4(NOS2):c.509C>T (p.Thr170Ile)	not specified [RCV004830083]	uncertain significance	17	27783065	27783065	Human		name
597673647	CV3563246	single nucleotide variant	NM_000625.4(NOS2):c.813G>C (p.Gln271His)	not specified [RCV004830084]	uncertain significance	17	27781087	27781087	Human		name
597673694	CV3563251	single nucleotide variant	NM_000625.4(NOS2):c.386C>T (p.Pro129Leu)	not specified [RCV004830089]	uncertain significance	17	27787759	27787759	Human		name
598207482	CV4000752	single nucleotide variant	NM_000625.4(NOS2):c.827G>C (p.Ser276Thr)	not specified [RCV005377099]	likely benign	17	27781073	27781073	Human		name
598240459	CV4000753	single nucleotide variant	NM_000625.4(NOS2):c.796C>T (p.Arg266Cys)	not specified [RCV005383093]	uncertain significance	17	27781104	27781104	Human		name
598240452	CV4000757	single nucleotide variant	NM_000625.4(NOS2):c.851T>C (p.Val284Ala)	not specified [RCV005383094]	uncertain significance	17	27781049	27781049	Human		name
15142533	CV715309	single nucleotide variant	NM_000625.4(NOS2):c.3408G>A (p.Ala1136=)	NOS2-related disorder [RCV003943151]\|not provided [RCV000966506]	benign\|likely benign	17	27757300	27757300	Human	1	name , trait , alternate_id
15161702	CV727074	single nucleotide variant	NM_000625.4(NOS2):c.3330C>T (p.Val1110=)	NOS2-related disorder [RCV003920549]\|not provided [RCV000881619]	benign	17	27758905	27758905	Human	1	name , trait , alternate_id
15135922	CV771319	single nucleotide variant	NM_000625.4(NOS2):c.3333G>A (p.Glu1111=)	not provided [RCV000942995]	benign\|likely benign	17	27758902	27758902	Human		name
15178638	CV771320	single nucleotide variant	NM_000625.4(NOS2):c.3231C>A (p.Gly1077=)	not provided [RCV000929446]	likely benign	17	27759004	27759004	Human		name
34888824	CV904752	duplication	NM_000625.4(NOS2):c.1172dup (p.Leu392fs)	Malaria, susceptibility to [RCV002252323]	uncertain significance	17	27778888	27778889	Human	1	name
151353232	CV1326236	single nucleotide variant	NM_000625.4(NOS2):c.2269C>G (p.Leu757Val)	not provided [RCV001816197]	uncertain significance	17	27765694	27765694	Human		name
156370211	CV2204147	single nucleotide variant	NM_000625.4(NOS2):c.1135G>A (p.Gly379Arg)	not specified [RCV004076951]	uncertain significance	17	27778926	27778926	Human		name
156250254	CV2215646	single nucleotide variant	NM_000625.4(NOS2):c.1065G>C (p.Met355Ile)	not specified [RCV004089394]	uncertain significance	17	27778996	27778996	Human		name
155931568	CV2221057	single nucleotide variant	NM_000625.4(NOS2):c.1373C>T (p.Pro458Leu)	not specified [RCV004094517]	uncertain significance	17	27774360	27774360	Human		name
156300362	CV2244896	single nucleotide variant	NM_000625.4(NOS2):c.2042G>A (p.Cys681Tyr)	not specified [RCV004104648]	uncertain significance	17	27767830	27767830	Human		name
156151541	CV2245179	single nucleotide variant	NM_000625.4(NOS2):c.1243G>A (p.Val415Ile)	not specified [RCV004106960]	uncertain significance	17	27778728	27778728	Human		name
156292237	CV2246611	single nucleotide variant	NM_000625.4(NOS2):c.1360C>T (p.Arg454Cys)	not specified [RCV004110354]	uncertain significance	17	27774373	27774373	Human		name
156359395	CV2257675	single nucleotide variant	NM_000625.4(NOS2):c.1541C>T (p.Pro514Leu)	not specified [RCV004127762]	uncertain significance	17	27773179	27773179	Human		name
156059590	CV2262993	single nucleotide variant	NM_000625.4(NOS2):c.2827G>C (p.Val943Leu)	not specified [RCV004131257]	uncertain significance	17	27761205	27761205	Human		name
155968035	CV2277133	single nucleotide variant	NM_000625.4(NOS2):c.1967T>C (p.Met656Thr)	not specified [RCV004142779]	likely benign	17	27769044	27769044	Human		name
156184147	CV2292211	single nucleotide variant	NM_000625.4(NOS2):c.2048C>T (p.Thr683Met)	not specified [RCV004148255]	uncertain significance	17	27767824	27767824	Human		name
156253080	CV2325468	single nucleotide variant	NM_000625.4(NOS2):c.2669G>T (p.Arg890Leu)	not specified [RCV004179922]	uncertain significance	17	27762929	27762929	Human		name
156079272	CV2341243	single nucleotide variant	NM_000625.4(NOS2):c.1355G>A (p.Arg452Gln)	not specified [RCV004186656]	uncertain significance	17	27774378	27774378	Human		name
156160515	CV2361804	single nucleotide variant	NM_000625.4(NOS2):c.1256A>G (p.Asn419Ser)	not specified [RCV004223275]	uncertain significance	17	27778715	27778715	Human		name
156101222	CV2367626	single nucleotide variant	NM_000625.4(NOS2):c.2327G>T (p.Cys776Phe)	not specified [RCV004211549]	likely benign	17	27765636	27765636	Human		name
155957846	CV2396596	single nucleotide variant	NM_000625.4(NOS2):c.2509C>A (p.Pro837Thr)	not specified [RCV004240425]	uncertain significance	17	27764064	27764064	Human		name
329364521	CV2443648	single nucleotide variant	NM_000625.4(NOS2):c.1588C>G (p.Arg530Gly)	not specified [RCV004255954]	uncertain significance	17	27772424	27772424	Human		name
329385198	CV2454808	single nucleotide variant	NM_000625.4(NOS2):c.1273A>G (p.Ser425Gly)	not specified [RCV004270029]	uncertain significance	17	27778698	27778698	Human		name
329394811	CV2457649	single nucleotide variant	NM_000625.4(NOS2):c.1495C>G (p.His499Asp)	not specified [RCV004269502]	uncertain significance	17	27773225	27773225	Human		name
401738582	CV2676326	single nucleotide variant	NM_000625.4(NOS2):c.2249G>A (p.Arg750His)	not specified [RCV004286360]	uncertain significance	17	27765714	27765714	Human		name
401727911	CV2678577	single nucleotide variant	NM_000625.4(NOS2):c.1354C>T (p.Arg452Trp)	not specified [RCV004292585]	uncertain significance	17	27774379	27774379	Human		name
401741193	CV2680567	single nucleotide variant	NM_000625.4(NOS2):c.1205A>C (p.Glu402Ala)	not specified [RCV004291199]	uncertain significance	17	27778766	27778766	Human		name
401743595	CV2684742	single nucleotide variant	NM_000625.4(NOS2):c.2741G>A (p.Arg914Gln)	not specified [RCV004293830]	likely benign	17	27762857	27762857	Human		name
401767307	CV2718459	single nucleotide variant	NM_000625.4(NOS2):c.2218C>T (p.Arg740Trp)	not specified [RCV004318272]	uncertain significance	17	27766538	27766538	Human		name
401861719	CV2756447	single nucleotide variant	NM_000625.4(NOS2):c.1006T>C (p.Tyr336His)	not specified [RCV004342982]	uncertain significance	17	27779055	27779055	Human		name
401864358	CV2760785	single nucleotide variant	NM_000625.4(NOS2):c.2342C>T (p.Pro781Leu)	not specified [RCV004336428]	uncertain significance	17	27765621	27765621	Human		name
401862570	CV2768430	single nucleotide variant	NM_000625.4(NOS2):c.2855A>G (p.Lys952Arg)	not specified [RCV004344321]	uncertain significance	17	27761177	27761177	Human		name
404983256	CV2849265	single nucleotide variant	NM_000625.4(NOS2):c.1823C>T (p.Ser608Leu)	NOS2-related disorder [RCV003980962]\|not specified [RCV003489137]	benign	17	27769571	27769571	Human	5	name , trait , alternate_id
405678455	CV3351868	single nucleotide variant	NM_000625.4(NOS2):c.1018C>T (p.Arg340Trp)	not specified [RCV004488169]	uncertain significance	17	27779043	27779043	Human		name
405678461	CV3351870	single nucleotide variant	NM_000625.4(NOS2):c.1655C>T (p.Ala552Val)	not specified [RCV004488171]	uncertain significance	17	27772357	27772357	Human		name
405678466	CV3351871	single nucleotide variant	NM_000625.4(NOS2):c.1685G>A (p.Ser562Asn)	not specified [RCV004488172]	uncertain significance	17	27772327	27772327	Human		name
405678469	CV3351872	single nucleotide variant	NM_000625.4(NOS2):c.1889T>C (p.Met630Thr)	not specified [RCV004488173]	uncertain significance	17	27769122	27769122	Human		name
405678472	CV3351873	single nucleotide variant	NM_000625.4(NOS2):c.1943T>A (p.Leu648Gln)	not specified [RCV004488174]	uncertain significance	17	27769068	27769068	Human		name
405678477	CV3351874	single nucleotide variant	NM_000625.4(NOS2):c.2117C>T (p.Pro706Leu)	not specified [RCV004488175]	uncertain significance	17	27767755	27767755	Human		name
405678481	CV3351875	single nucleotide variant	NM_000625.4(NOS2):c.2194G>A (p.Val732Met)	not specified [RCV004488176]	uncertain significance	17	27766562	27766562	Human		name
405678483	CV3351876	single nucleotide variant	NM_000625.4(NOS2):c.2738C>G (p.Ser913Cys)	not specified [RCV004488177]	uncertain significance	17	27762860	27762860	Human		name
405678487	CV3351877	single nucleotide variant	NM_000625.4(NOS2):c.2792A>T (p.His931Leu)	not specified [RCV004488178]	uncertain significance	17	27762806	27762806	Human		name
405678492	CV3351878	single nucleotide variant	NM_000625.4(NOS2):c.2913G>C (p.Glu971Asp)	not specified [RCV004488179]	uncertain significance	17	27760720	27760720	Human		name
407509976	CV3469187	single nucleotide variant	NM_000625.4(NOS2):c.1313C>T (p.Ser438Leu)	not specified [RCV004647561]	uncertain significance	17	27774420	27774420	Human		name
407509980	CV3469188	single nucleotide variant	NM_000625.4(NOS2):c.1540C>A (p.Pro514Thr)	not specified [RCV004647562]	uncertain significance	17	27773180	27773180	Human		name
407509983	CV3469190	single nucleotide variant	NM_000625.4(NOS2):c.1450G>A (p.Val484Ile)	not specified [RCV004647563]	likely benign	17	27774283	27774283	Human		name
407509988	CV3469191	single nucleotide variant	NM_000625.4(NOS2):c.1493C>A (p.Thr498Asn)	not specified [RCV004647564]	uncertain significance	17	27773227	27773227	Human		name
407509995	CV3469193	single nucleotide variant	NM_000625.4(NOS2):c.2083C>T (p.Pro695Ser)	not specified [RCV004647566]	uncertain significance	17	27767789	27767789	Human		name
407510005	CV3469196	single nucleotide variant	NM_000625.4(NOS2):c.2280G>C (p.Glu760Asp)	not specified [RCV004647569]	uncertain significance	17	27765683	27765683	Human		name
597673617	CV3563243	single nucleotide variant	NM_000625.4(NOS2):c.2593C>T (p.Pro865Ser)	not specified [RCV004830081]	uncertain significance	17	27763005	27763005	Human		name
597673626	CV3563244	single nucleotide variant	NM_000625.4(NOS2):c.2147A>T (p.Gln716Leu)	not specified [RCV004830082]	uncertain significance	17	27767725	27767725	Human		name
597673656	CV3563247	single nucleotide variant	NM_000625.4(NOS2):c.1562C>A (p.Ala521Asp)	not specified [RCV004830085]	uncertain significance	17	27772450	27772450	Human		name
597673663	CV3563248	single nucleotide variant	NM_000625.4(NOS2):c.1249G>C (p.Glu417Gln)	not specified [RCV004830086]	uncertain significance	17	27778722	27778722	Human		name
597673684	CV3563250	single nucleotide variant	NM_000625.4(NOS2):c.2489A>C (p.Tyr830Ser)	not specified [RCV004830088]	uncertain significance	17	27764084	27764084	Human		name
597673703	CV3563252	single nucleotide variant	NM_000625.4(NOS2):c.1229G>C (p.Trp410Ser)	not specified [RCV004830090]	uncertain significance	17	27778742	27778742	Human		name
597673721	CV3563254	single nucleotide variant	NM_000625.4(NOS2):c.2875T>C (p.Cys959Arg)	not specified [RCV004830092]	uncertain significance	17	27761157	27761157	Human		name
598240472	CV4000750	single nucleotide variant	NM_000625.4(NOS2):c.2314C>G (p.His772Asp)	not specified [RCV005383091]	uncertain significance	17	27765649	27765649	Human		name
598240465	CV4000751	single nucleotide variant	NM_000625.4(NOS2):c.2894G>T (p.Ser965Ile)	not specified [RCV005383092]	uncertain significance	17	27760739	27760739	Human		name
598207475	CV4000754	single nucleotide variant	NM_000625.4(NOS2):c.2500A>G (p.Ile834Val)	not specified [RCV005377100]	uncertain significance	17	27764073	27764073	Human		name
598207469	CV4000755	single nucleotide variant	NM_000625.4(NOS2):c.2112G>C (p.Trp704Cys)	not specified [RCV005377101]	uncertain significance	17	27767760	27767760	Human		name
598240447	CV4000758	single nucleotide variant	NM_000625.4(NOS2):c.2885G>A (p.Arg962Gln)	not specified [RCV005383095]	uncertain significance	17	27761147	27761147	Human		name
598207456	CV4000759	single nucleotide variant	NM_000625.4(NOS2):c.2383C>T (p.Pro795Ser)	not specified [RCV005377103]	uncertain significance	17	27765580	27765580	Human		name
15160751	CV727075	single nucleotide variant	NM_000625.4(NOS2):c.2345C>T (p.Ala782Val)	not provided [RCV000881445]	likely benign	17	27765618	27765618	Human		name
15135926	CV771321	single nucleotide variant	NM_000625.4(NOS2):c.2102A>G (p.Asn701Ser)	not provided [RCV000942996]	likely benign	17	27767770	27767770	Human		name
156187422	CV2226683	single nucleotide variant	NM_000625.4(NOS2):c.3005A>T (p.His1002Leu)	not specified [RCV004101914]	uncertain significance	17	27760628	27760628	Human		name
156220055	CV2254116	single nucleotide variant	NM_000625.4(NOS2):c.3395T>A (p.Phe1132Tyr)	not specified [RCV004129556]	uncertain significance	17	27757313	27757313	Human		name
156248844	CV2264025	single nucleotide variant	NM_000625.4(NOS2):c.3265C>T (p.Arg1089Trp)	not specified [RCV004138045]	likely benign	17	27758970	27758970	Human		name
155969059	CV2309025	single nucleotide variant	NM_000625.4(NOS2):c.3400T>C (p.Tyr1134His)	not specified [RCV004171397]	uncertain significance	17	27757308	27757308	Human		name
156268388	CV2314753	single nucleotide variant	NM_000625.4(NOS2):c.3086T>C (p.Met1029Thr)	not specified [RCV004170890]	uncertain significance	17	27760103	27760103	Human		name
156300261	CV2322412	single nucleotide variant	NM_000625.4(NOS2):c.3134A>G (p.Tyr1045Cys)	not specified [RCV004180546]	uncertain significance	17	27760055	27760055	Human		name
156274529	CV2344246	single nucleotide variant	NM_000625.4(NOS2):c.3198C>G (p.Ser1066Arg)	not specified [RCV004197879]	uncertain significance	17	27759037	27759037	Human		name
156226160	CV2390752	single nucleotide variant	NM_000625.4(NOS2):c.3092A>C (p.Glu1031Ala)	not specified [RCV004241041]	uncertain significance	17	27760097	27760097	Human		name
401722297	CV2706459	single nucleotide variant	NM_000625.4(NOS2):c.3016C>T (p.Arg1006Trp)	not specified [RCV004317279]	uncertain significance	17	27760173	27760173	Human		name
401882728	CV2778443	single nucleotide variant	NM_000625.4(NOS2):c.3140G>A (p.Arg1047His)	not specified [RCV004344112]	uncertain significance	17	27760049	27760049	Human		name
405678494	CV3351879	single nucleotide variant	NM_000625.4(NOS2):c.3026G>A (p.Arg1009His)	not specified [RCV004488180]	uncertain significance	17	27760163	27760163	Human		name
405678497	CV3351880	single nucleotide variant	NM_000625.4(NOS2):c.3119C>T (p.Ala1040Val)	not specified [RCV004488181]	uncertain significance	17	27760070	27760070	Human		name
405678501	CV3351881	single nucleotide variant	NM_000625.4(NOS2):c.3131C>T (p.Ala1044Val)	not specified [RCV004488182]	uncertain significance	17	27760058	27760058	Human		name
405678511	CV3351883	single nucleotide variant	NM_000625.4(NOS2):c.3235C>T (p.Leu1079Phe)	not specified [RCV004488184]	uncertain significance	17	27759000	27759000	Human		name
405678515	CV3351884	single nucleotide variant	NM_000625.4(NOS2):c.3281C>T (p.Thr1094Ile)	not specified [RCV004488185]	uncertain significance	17	27758954	27758954	Human		name
407498210	CV3469185	single nucleotide variant	NM_000625.4(NOS2):c.3257G>A (p.Arg1086His)	not specified [RCV004643943]	uncertain significance	17	27758978	27758978	Human		name
407498218	CV3469189	single nucleotide variant	NM_000625.4(NOS2):c.3139C>T (p.Arg1047Cys)	not specified [RCV004643945]	uncertain significance	17	27760050	27760050	Human		name
407509998	CV3469194	single nucleotide variant	NM_000625.4(NOS2):c.3247G>A (p.Gly1083Arg)	not specified [RCV004647567]	uncertain significance	17	27758988	27758988	Human		name
407510001	CV3469195	single nucleotide variant	NM_000625.4(NOS2):c.3115C>T (p.His1039Tyr)	not specified [RCV004647568]	uncertain significance	17	27760074	27760074	Human		name
407498222	CV3469198	single nucleotide variant	NM_000625.4(NOS2):c.3458T>C (p.Leu1153Pro)	not specified [RCV004643946]	uncertain significance	17	27757250	27757250	Human		name
597673673	CV3563249	single nucleotide variant	NM_000625.4(NOS2):c.3017G>C (p.Arg1006Pro)	not specified [RCV004830087]	uncertain significance	17	27760172	27760172	Human		name
598207490	CV4000748	single nucleotide variant	NM_000625.4(NOS2):c.3407C>T (p.Ala1136Val)	not specified [RCV005377098]	likely benign	17	27757301	27757301	Human		name
598240478	CV4000749	single nucleotide variant	NM_000625.4(NOS2):c.3116A>G (p.His1039Arg)	not specified [RCV005383090]	uncertain significance	17	27760073	27760073	Human		name
598207463	CV4000756	single nucleotide variant	NM_000625.4(NOS2):c.3372C>G (p.His1124Gln)	not specified [RCV005377102]	uncertain significance	17	27757336	27757336	Human		name
15152421	CV715310	single nucleotide variant	NM_000625.4(NOS2):c.3256C>T (p.Arg1086Cys)	not provided [RCV000968347]	likely benign	17	27758979	27758979	Human		name
15152426	CV715311	single nucleotide variant	NM_000625.4(NOS2):c.3052C>A (p.Arg1018Ser)	not provided [RCV000968348]	likely benign	17	27760137	27760137	Human		name
8627944	CV83088	single nucleotide variant	NM_000625.4(NOS2):c.3160G>A (p.Val1054Ile)	Malignant melanoma [RCV000063168]	not provided	17	27759075	27759075	Human		name
9684241	CV132016	single nucleotide variant	NC_000017.11:g.27803092=	repeat number of microsatellite [RCV000115028]	association	17	27803092	27803092	Human		alternate_id

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