Pla2r1 Variant Search Result - Rat Genome Database

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130 records found for search term Pla2r1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155645612	CV1710947	deletion	NM_007366.5(PLA2R1):c.-127del	Kidney disorder [RCV002294728]	likely benign	2	160062530	160062530	Human	2	name
407518598	CV3470763	single nucleotide variant	NM_007366.5(PLA2R1):c.14C>G (p.Pro5Arg)	not specified [RCV004651056]	uncertain significance	2	160062390	160062390	Human		name
155645382	CV1710825	single nucleotide variant	NM_007366.5(PLA2R1):c.86C>G (p.Pro29Arg)	Kidney disorder [RCV002294606]\|not specified [RCV004047632]	uncertain significance	2	160062318	160062318	Human	2	name
155645392	CV1710830	single nucleotide variant	NM_007366.5(PLA2R1):c.816T>C (p.Asp272=)	Kidney disorder [RCV002294611]	likely benign	2	160032984	160032984	Human	2	name
401772768	CV2719753	single nucleotide variant	NM_007366.5(PLA2R1):c.50G>C (p.Arg17Pro)	not specified [RCV004329188]	uncertain significance	2	160062354	160062354	Human		name
15170700	CV732860	single nucleotide variant	NM_007366.5(PLA2R1):c.882C>T (p.Leu294=)	not provided [RCV000905317]	likely benign	2	160028923	160028923	Human		name
401916993	CV2819139	single nucleotide variant	NM_007366.5(PLA2R1):c.1110G>A (p.Ala370=)	not provided [RCV003429329]	likely benign	2	160022849	160022849	Human		name
405656773	CV3376100	single nucleotide variant	NM_007366.5(PLA2R1):c.139A>T (p.Ser47Cys)	not specified [RCV004511571]	uncertain significance	2	160045128	160045128	Human		name
155645394	CV1710831	single nucleotide variant	NM_007366.5(PLA2R1):c.425G>A (p.Arg142Gln)	Kidney disorder [RCV002294612]	likely benign	2	160044842	160044842	Human	2	name
155645563	CV1710912	single nucleotide variant	NM_007366.5(PLA2R1):c.898C>G (p.His300Asp)	Atypical hemolytic-uremic syndrome [RCV002294693]	benign	2	160028907	160028907	Human	2	name
155645563	CV1710912	single nucleotide variant	NM_007366.5(PLA2R1):c.898C>G (p.His300Asp)	Atypical hemolytic-uremic syndrome [RCV002294693]	benign	2	160028907	160028908	Human	2	name
155645564	CV1710913	single nucleotide variant	NM_007366.5(PLA2R1):c.874A>G (p.Met292Val)	Atypical hemolytic-uremic syndrome [RCV002294694]	benign	2	160028931	160028931	Human	4	name
155645591	CV1710932	deletion	NM_007366.5(PLA2R1):c.1957del (p.Ala653fs)	Kidney disorder [RCV002294713]	benign	2	159987236	159987236	Human	2	name
155645620	CV1710953	single nucleotide variant	NM_007366.5(PLA2R1):c.3570C>T (p.Gly1190=)	Kidney disorder [RCV002294734]	uncertain significance	2	159949747	159949747	Human	2	name
156374168	CV2198276	single nucleotide variant	NM_007366.5(PLA2R1):c.901G>A (p.Ala301Thr)	not specified [RCV004081832]	uncertain significance	2	160028904	160028904	Human		name
156250532	CV2273298	single nucleotide variant	NM_007366.5(PLA2R1):c.439A>G (p.Lys147Glu)	not specified [RCV004132090]	uncertain significance	2	160044828	160044828	Human		name
156222147	CV2399679	single nucleotide variant	NM_007366.5(PLA2R1):c.523G>A (p.Gly175Arg)	not specified [RCV004245498]	uncertain significance	2	160042169	160042169	Human		name
329372749	CV2451635	single nucleotide variant	NM_007366.5(PLA2R1):c.893A>C (p.Asp298Ala)	not specified [RCV004274555]	uncertain significance	2	160028912	160028912	Human		name
401740725	CV2679790	single nucleotide variant	NM_007366.5(PLA2R1):c.448T>C (p.Ser150Pro)	not specified [RCV004282253]	uncertain significance	2	160044819	160044819	Human		name
401877786	CV2786789	single nucleotide variant	NM_007366.5(PLA2R1):c.875T>C (p.Met292Thr)	not specified [RCV004365958]	uncertain significance	2	160028930	160028930	Human		name
401916991	CV2819138	single nucleotide variant	NM_007366.5(PLA2R1):c.3645C>T (p.Asn1215=)	not provided [RCV003429328]	likely benign	2	159949672	159949672	Human		name
405656831	CV3376118	single nucleotide variant	NM_007366.5(PLA2R1):c.566A>G (p.His189Arg)	not specified [RCV004511589]	uncertain significance	2	160042126	160042126	Human		name
405656834	CV3376119	single nucleotide variant	NM_007366.5(PLA2R1):c.580C>T (p.Arg194Cys)	not specified [RCV004511590]	uncertain significance	2	160042112	160042112	Human		name
405656837	CV3376120	single nucleotide variant	NM_007366.5(PLA2R1):c.581G>A (p.Arg194His)	not specified [RCV004511591]	uncertain significance	2	160042111	160042111	Human		name
405656841	CV3376121	single nucleotide variant	NM_007366.5(PLA2R1):c.694A>G (p.Ile232Val)	not specified [RCV004511592]	likely benign	2	160033106	160033106	Human		name
405656844	CV3376122	single nucleotide variant	NM_007366.5(PLA2R1):c.725G>A (p.Cys242Tyr)	not specified [RCV004511593]	uncertain significance	2	160033075	160033075	Human		name
405656847	CV3376123	single nucleotide variant	NM_007366.5(PLA2R1):c.884A>G (p.Asn295Ser)	not specified [RCV004511594]	uncertain significance	2	160028921	160028921	Human		name
407518606	CV3470766	single nucleotide variant	NM_007366.5(PLA2R1):c.331G>A (p.Val111Ile)	not specified [RCV004651059]	likely benign	2	160044936	160044936	Human		name
407518609	CV3470768	single nucleotide variant	NM_007366.5(PLA2R1):c.361A>G (p.Met121Val)	not specified [RCV004651060]	uncertain significance	2	160044906	160044906	Human		name
407518617	CV3470772	single nucleotide variant	NM_007366.5(PLA2R1):c.400C>T (p.His134Tyr)	not specified [RCV004651063]	uncertain significance	2	160044867	160044867	Human		name
407470238	CV3470774	single nucleotide variant	NM_007366.5(PLA2R1):c.507C>G (p.Ile169Met)	not specified [RCV004661992]	uncertain significance	2	160042185	160042185	Human		name
597725693	CV3569753	single nucleotide variant	NM_007366.5(PLA2R1):c.578C>T (p.Thr193Ile)	not specified [RCV004842332]	uncertain significance	2	160042114	160042114	Human		name
597725709	CV3569755	single nucleotide variant	NM_007366.5(PLA2R1):c.596A>T (p.Asp199Val)	not specified [RCV004842334]	uncertain significance	2	160042096	160042096	Human		name
598262656	CV4000304	single nucleotide variant	NM_007366.5(PLA2R1):c.398C>T (p.Ala133Val)	not specified [RCV005387137]	uncertain significance	2	160044869	160044869	Human		name
598262681	CV4000309	single nucleotide variant	NM_007366.5(PLA2R1):c.746C>T (p.Ser249Leu)	not specified [RCV005387142]	uncertain significance	2	160033054	160033054	Human		name
155645485	CV1710864	single nucleotide variant	NM_007366.5(PLA2R1):c.1956A>C (p.Lys652Asn)	Kidney disorder [RCV002294645]	benign	2	159987237	159987237	Human	3	name
155645485	CV1710864	single nucleotide variant	NM_007366.5(PLA2R1):c.1956A>C (p.Lys652Asn)	Kidney disorder [RCV002294645]	benign	2	159987237	159987238	Human	3	name
155645616	CV1710950	single nucleotide variant	NM_007366.5(PLA2R1):c.2096G>A (p.Cys699Tyr)	Kidney disorder [RCV002294731]	uncertain significance	2	159984015	159984015	Human	2	name
156398016	CV2194126	single nucleotide variant	NM_007366.5(PLA2R1):c.1903C>T (p.Arg635Trp)	not specified [RCV004076880]	uncertain significance	2	159987290	159987290	Human		name
156186520	CV2195678	single nucleotide variant	NM_007366.5(PLA2R1):c.2404G>A (p.Val802Met)	not specified [RCV004076041]	uncertain significance	2	159976718	159976718	Human		name
156078429	CV2198309	single nucleotide variant	NM_007366.5(PLA2R1):c.1031G>A (p.Arg344Gln)	not specified [RCV004081862]	uncertain significance	2	160028286	160028286	Human		name
156318393	CV2200309	single nucleotide variant	NM_007366.5(PLA2R1):c.1883G>T (p.Arg628Leu)	not specified [RCV004076644]	uncertain significance	2	159987310	159987310	Human		name
156250503	CV2215674	single nucleotide variant	NM_007366.5(PLA2R1):c.2954C>A (p.Thr985Lys)	not specified [RCV004091206]	uncertain significance	2	159956578	159956578	Human		name
155995816	CV2250388	single nucleotide variant	NM_007366.5(PLA2R1):c.1012C>G (p.Pro338Ala)	not specified [RCV004127271]	uncertain significance	2	160028305	160028305	Human		name
156276038	CV2287684	single nucleotide variant	NM_007366.5(PLA2R1):c.1316T>C (p.Ile439Thr)	not specified [RCV004141109]	uncertain significance	2	160020242	160020242	Human		name
156086631	CV2295349	single nucleotide variant	NM_007366.5(PLA2R1):c.1476T>G (p.Asn492Lys)	not specified [RCV004158705]	uncertain significance	2	160016689	160016689	Human		name
156327541	CV2332119	single nucleotide variant	NM_007366.5(PLA2R1):c.1464G>C (p.Trp488Cys)	not specified [RCV004189159]	uncertain significance	2	160016701	160016701	Human		name
156185142	CV2335785	single nucleotide variant	NM_007366.5(PLA2R1):c.1799C>T (p.Pro600Leu)	not specified [RCV004193976]	uncertain significance	2	160005687	160005687	Human		name
156222092	CV2343916	single nucleotide variant	NM_007366.5(PLA2R1):c.2465C>G (p.Ala822Gly)	not specified [RCV004195538]	uncertain significance	2	159976198	159976198	Human		name
156188063	CV2346783	single nucleotide variant	NM_007366.5(PLA2R1):c.2492C>T (p.Ser831Leu)	not specified [RCV004199792]	uncertain significance	2	159976171	159976171	Human		name
155920515	CV2350521	single nucleotide variant	NM_007366.5(PLA2R1):c.1394C>T (p.Thr465Ile)	not specified [RCV004204880]	uncertain significance	2	160020164	160020164	Human		name
156224719	CV2352604	single nucleotide variant	NM_007366.5(PLA2R1):c.2645C>T (p.Ala882Val)	not specified [RCV004198638]	uncertain significance	2	159970163	159970163	Human		name
156106046	CV2400416	single nucleotide variant	NM_007366.5(PLA2R1):c.1957G>T (p.Ala653Ser)	not specified [RCV004244464]	uncertain significance	2	159987236	159987236	Human		name
329356317	CV2430688	single nucleotide variant	NM_007366.5(PLA2R1):c.1397T>C (p.Leu466Pro)	not specified [RCV004253876]	uncertain significance	2	160020161	160020161	Human		name
329356392	CV2460302	single nucleotide variant	NM_007366.5(PLA2R1):c.2984G>C (p.Gly995Ala)	not specified [RCV004266843]	likely benign	2	159956548	159956548	Human		name
401768762	CV2686363	single nucleotide variant	NM_007366.5(PLA2R1):c.1420A>G (p.Arg474Gly)	not specified [RCV004297437]	uncertain significance	2	160020138	160020138	Human		name
401773245	CV2716502	single nucleotide variant	NM_007366.5(PLA2R1):c.2064G>A (p.Met688Ile)	not specified [RCV004327589]	uncertain significance	2	159984047	159984047	Human		name
401779608	CV2731921	single nucleotide variant	NM_007366.5(PLA2R1):c.2651A>G (p.Asp884Gly)	not specified [RCV004333162]	uncertain significance	2	159970157	159970157	Human		name
401887784	CV2770440	single nucleotide variant	NM_007366.5(PLA2R1):c.2176T>A (p.Phe726Ile)	not specified [RCV004358080]	uncertain significance	2	159983935	159983935	Human		name
401894519	CV2788311	single nucleotide variant	NM_007366.5(PLA2R1):c.1406A>G (p.His469Arg)	not specified [RCV004352895]	uncertain significance	2	160020152	160020152	Human		name
405656769	CV3376099	single nucleotide variant	NM_007366.5(PLA2R1):c.1372G>C (p.Val458Leu)	not specified [RCV004511570]	uncertain significance	2	160020186	160020186	Human		name
405656777	CV3376101	single nucleotide variant	NM_007366.5(PLA2R1):c.1498A>G (p.Ile500Val)	not specified [RCV004511572]	uncertain significance	2	160016667	160016667	Human		name
405656779	CV3376102	single nucleotide variant	NM_007366.5(PLA2R1):c.1882C>T (p.Arg628Cys)	not specified [RCV004511573]	uncertain significance	2	159987311	159987311	Human		name
405656785	CV3376104	single nucleotide variant	NM_007366.5(PLA2R1):c.2168A>G (p.His723Arg)	not specified [RCV004511575]	uncertain significance	2	159983943	159983943	Human		name
405656789	CV3376105	single nucleotide variant	NM_007366.5(PLA2R1):c.2606A>G (p.Tyr869Cys)	not specified [RCV004511576]	uncertain significance	2	159970202	159970202	Human		name
405656791	CV3376106	single nucleotide variant	NM_007366.5(PLA2R1):c.2777G>C (p.Ser926Thr)	not specified [RCV004511577]	uncertain significance	2	159967666	159967666	Human		name
405656800	CV3376108	single nucleotide variant	NM_007366.5(PLA2R1):c.2818A>G (p.Lys940Glu)	not specified [RCV004511579]	uncertain significance	2	159967625	159967625	Human		name
407470362	CV3470767	single nucleotide variant	NM_007366.5(PLA2R1):c.2438A>G (p.Asp813Gly)	not specified [RCV004661989]	uncertain significance	2	159976225	159976225	Human		name
407470280	CV3470770	single nucleotide variant	NM_007366.5(PLA2R1):c.1751A>G (p.Asn584Ser)	not specified [RCV004661990]	uncertain significance	2	160005735	160005735	Human		name
407518614	CV3470771	single nucleotide variant	NM_007366.5(PLA2R1):c.2819A>G (p.Lys940Arg)	not specified [RCV004651062]	uncertain significance	2	159967624	159967624	Human		name
597725646	CV3569748	single nucleotide variant	NM_007366.5(PLA2R1):c.2743G>A (p.Gly915Ser)	not specified [RCV004842327]	uncertain significance	2	159969277	159969277	Human		name
597725658	CV3569749	single nucleotide variant	NM_007366.5(PLA2R1):c.2870C>T (p.Thr957Met)	not specified [RCV004842328]	uncertain significance	2	159967573	159967573	Human		name
597725676	CV3569751	single nucleotide variant	NM_007366.5(PLA2R1):c.1019C>T (p.Ala340Val)	not specified [RCV004842330]	uncertain significance	2	160028298	160028298	Human		name
597725701	CV3569754	single nucleotide variant	NM_007366.5(PLA2R1):c.1234G>A (p.Ala412Thr)	not specified [RCV004842333]	likely benign	2	160022725	160022725	Human		name
597725717	CV3569756	single nucleotide variant	NM_007366.5(PLA2R1):c.2767C>T (p.Leu923Phe)	not specified [RCV004842335]	uncertain significance	2	159967676	159967676	Human		name
597725726	CV3569757	single nucleotide variant	NM_007366.5(PLA2R1):c.1984C>T (p.His662Tyr)	not specified [RCV004842336]	uncertain significance	2	159987209	159987209	Human		name
597725735	CV3569758	single nucleotide variant	NM_007366.5(PLA2R1):c.2861A>G (p.Gln954Arg)	not specified [RCV004842337]	uncertain significance	2	159967582	159967582	Human		name
597725743	CV3569759	single nucleotide variant	NM_007366.5(PLA2R1):c.2279C>T (p.Ser760Leu)	not specified [RCV004842338]	uncertain significance	2	159977406	159977406	Human		name
597725752	CV3569760	single nucleotide variant	NM_007366.5(PLA2R1):c.1945A>T (p.Asn649Tyr)	not specified [RCV004842339]	uncertain significance	2	159987248	159987248	Human		name
597725759	CV3569761	single nucleotide variant	NM_007366.5(PLA2R1):c.2072C>T (p.Thr691Ile)	not specified [RCV004842340]	uncertain significance	2	159984039	159984039	Human		name
598262642	CV4000301	single nucleotide variant	NM_007366.5(PLA2R1):c.1333A>G (p.Lys445Glu)	not specified [RCV005387134]	uncertain significance	2	160020225	160020225	Human		name
598262670	CV4000307	single nucleotide variant	NM_007366.5(PLA2R1):c.2797A>G (p.Met933Val)	not specified [RCV005387140]	uncertain significance	2	159967646	159967646	Human		name
598262686	CV4000310	single nucleotide variant	NM_007366.5(PLA2R1):c.1820A>G (p.Asn607Ser)	not specified [RCV005387143]	uncertain significance	2	160005666	160005666	Human		name
598205956	CV4000311	single nucleotide variant	NM_007366.5(PLA2R1):c.1988C>G (p.Pro663Arg)	not specified [RCV005399548]	uncertain significance	2	159987205	159987205	Human		name
598262690	CV4000312	single nucleotide variant	NM_007366.5(PLA2R1):c.1030C>T (p.Arg344Trp)	not specified [RCV005387144]	uncertain significance	2	160028287	160028287	Human		name
598262694	CV4000313	single nucleotide variant	NM_007366.5(PLA2R1):c.1558G>A (p.Glu520Lys)	not specified [RCV005387145]	uncertain significance	2	160013369	160013369	Human		name
598262698	CV4000314	single nucleotide variant	NM_007366.5(PLA2R1):c.2981A>C (p.Glu994Ala)	not specified [RCV005387146]	uncertain significance	2	159956551	159956551	Human		name
15129650	CV732859	single nucleotide variant	NM_007366.5(PLA2R1):c.1814A>C (p.His605Pro)	not provided [RCV000897475]	likely benign	2	160005672	160005672	Human		name
8629903	CV85050	single nucleotide variant	NM_001007267.2(PLA2R1):c.426G>A (p.Arg142=)	Malignant melanoma [RCV000065132]	not provided	2	160044841	160044841	Human		name
155645561	CV1710911	single nucleotide variant	NM_007366.5(PLA2R1):c.3316G>A (p.Gly1106Ser)	Atypical hemolytic-uremic syndrome [RCV002294692]	benign	2	159951564	159951564	Human	1	name
156191403	CV2206154	single nucleotide variant	NM_007366.5(PLA2R1):c.4036A>G (p.Thr1346Ala)	not specified [RCV004078555]	uncertain significance	2	159945014	159945014	Human		name
156239566	CV2221266	single nucleotide variant	NM_007366.5(PLA2R1):c.3628G>A (p.Val1210Ile)	not specified [RCV004094699]	uncertain significance	2	159949689	159949689	Human		name
156359447	CV2257701	single nucleotide variant	NM_007366.5(PLA2R1):c.3611C>G (p.Ser1204Cys)	not specified [RCV004127782]	uncertain significance	2	159949706	159949706	Human		name
155952036	CV2264171	single nucleotide variant	NM_007366.5(PLA2R1):c.3611C>T (p.Ser1204Phe)	not specified [RCV004136323]	uncertain significance	2	159949706	159949706	Human		name
156252947	CV2264539	single nucleotide variant	NM_007366.5(PLA2R1):c.3976A>C (p.Ile1326Leu)	not specified [RCV004132558]	uncertain significance	2	159945074	159945074	Human		name
156296302	CV2318131	single nucleotide variant	NM_007366.5(PLA2R1):c.3314A>G (p.His1105Arg)	not specified [RCV004177544]	likely benign	2	159951566	159951566	Human		name
156202838	CV2334782	single nucleotide variant	NM_007366.5(PLA2R1):c.3977T>C (p.Ile1326Thr)	not specified [RCV004188756]	uncertain significance	2	159945073	159945073	Human		name
156278896	CV2348280	single nucleotide variant	NM_007366.5(PLA2R1):c.3008G>A (p.Ser1003Asn)	not specified [RCV004191316]	likely benign	2	159956524	159956524	Human		name
156089116	CV2359332	single nucleotide variant	NM_007366.5(PLA2R1):c.4103C>T (p.Pro1368Leu)	not specified [RCV004212613]	uncertain significance	2	159944947	159944947	Human		name
401720944	CV2673545	single nucleotide variant	NM_007366.5(PLA2R1):c.4019G>T (p.Gly1340Val)	not specified [RCV004288510]	uncertain significance	2	159945031	159945031	Human		name
401744919	CV2697100	single nucleotide variant	NM_007366.5(PLA2R1):c.3272G>A (p.Gly1091Asp)	not specified [RCV004293078]	uncertain significance	2	159955228	159955228	Human		name
401770673	CV2726224	single nucleotide variant	NM_007366.5(PLA2R1):c.3401C>G (p.Thr1134Ser)	not specified [RCV004326688]	uncertain significance	2	159951479	159951479	Human		name
401863031	CV2755800	single nucleotide variant	NM_007366.5(PLA2R1):c.3067A>G (p.Ile1023Val)	not specified [RCV004342173]	uncertain significance	2	159955784	159955784	Human		name
401890858	CV2772239	single nucleotide variant	NM_007366.5(PLA2R1):c.3436A>G (p.Lys1146Glu)	not specified [RCV004346877]	uncertain significance	2	159951444	159951444	Human		name
405656804	CV3376109	single nucleotide variant	NM_007366.5(PLA2R1):c.2998G>T (p.Ala1000Ser)	not specified [RCV004511580]	likely benign	2	159956534	159956534	Human		name
405656807	CV3376110	single nucleotide variant	NM_007366.5(PLA2R1):c.3002T>C (p.Ile1001Thr)	not specified [RCV004511581]	uncertain significance	2	159956530	159956530	Human		name
405656809	CV3376111	single nucleotide variant	NM_007366.5(PLA2R1):c.3037A>T (p.Asn1013Tyr)	not specified [RCV004511582]	uncertain significance	2	159955814	159955814	Human		name
405656811	CV3376112	single nucleotide variant	NM_007366.5(PLA2R1):c.3265A>G (p.Lys1089Glu)	not specified [RCV004511583]	uncertain significance	2	159955235	159955235	Human		name
405656814	CV3376113	single nucleotide variant	NM_007366.5(PLA2R1):c.3670G>A (p.Glu1224Lys)	not specified [RCV004511584]	uncertain significance	2	159949647	159949647	Human		name
405656823	CV3376115	single nucleotide variant	NM_007366.5(PLA2R1):c.4054C>T (p.His1352Tyr)	not specified [RCV004511586]	uncertain significance	2	159944996	159944996	Human		name
405656825	CV3376116	single nucleotide variant	NM_007366.5(PLA2R1):c.4148T>G (p.Ile1383Ser)	not specified [RCV004511587]	uncertain significance	2	159942156	159942156	Human		name
405656829	CV3376117	single nucleotide variant	NM_007366.5(PLA2R1):c.4382G>C (p.Ser1461Thr)	not specified [RCV004511588]	uncertain significance	2	159941788	159941788	Human		name
407518600	CV3470764	single nucleotide variant	NM_007366.5(PLA2R1):c.3603G>T (p.Glu1201Asp)	not specified [RCV004651057]	likely benign	2	159949714	159949714	Human		name
407518603	CV3470765	single nucleotide variant	NM_007366.5(PLA2R1):c.2998G>A (p.Ala1000Thr)	not specified [RCV004651058]	uncertain significance	2	159956534	159956534	Human		name
407518612	CV3470769	single nucleotide variant	NM_007366.5(PLA2R1):c.4304G>A (p.Arg1435Gln)	not specified [RCV004651061]	likely benign	2	159941866	159941866	Human		name
407470234	CV3470773	single nucleotide variant	NM_007366.5(PLA2R1):c.4369G>A (p.Asp1457Asn)	not specified [RCV004661991]	uncertain significance	2	159941801	159941801	Human		name
597725618	CV3569745	single nucleotide variant	NM_007366.5(PLA2R1):c.3619G>A (p.Gly1207Ser)	not specified [RCV004842324]	uncertain significance	2	159949698	159949698	Human		name
597725627	CV3569746	single nucleotide variant	NM_007366.5(PLA2R1):c.3500G>A (p.Arg1167Gln)	not specified [RCV004842325]	uncertain significance	2	159951380	159951380	Human		name
597725638	CV3569747	single nucleotide variant	NM_007366.5(PLA2R1):c.3111G>C (p.Lys1037Asn)	not specified [RCV004842326]	uncertain significance	2	159955740	159955740	Human		name
597725668	CV3569750	single nucleotide variant	NM_007366.5(PLA2R1):c.4318C>A (p.Pro1440Thr)	not specified [RCV004842329]	uncertain significance	2	159941852	159941852	Human		name
597725684	CV3569752	single nucleotide variant	NM_007366.5(PLA2R1):c.3161G>A (p.Ser1054Asn)	not specified [RCV004842331]	likely benign	2	159955339	159955339	Human		name
597767818	CV3569762	single nucleotide variant	NM_007366.5(PLA2R1):c.4240T>G (p.Cys1414Gly)	not specified [RCV004850561]	uncertain significance	2	159941930	159941930	Human		name
598262646	CV4000302	single nucleotide variant	NM_007366.5(PLA2R1):c.3202G>A (p.Ala1068Thr)	not specified [RCV005387135]	uncertain significance	2	159955298	159955298	Human		name
598262652	CV4000303	single nucleotide variant	NM_007366.5(PLA2R1):c.3947A>G (p.Asn1316Ser)	not specified [RCV005387136]	uncertain significance	2	159946821	159946821	Human		name
598262661	CV4000305	single nucleotide variant	NM_007366.5(PLA2R1):c.3383T>C (p.Ile1128Thr)	not specified [RCV005387138]	uncertain significance	2	159951497	159951497	Human		name
598262676	CV4000308	single nucleotide variant	NM_007366.5(PLA2R1):c.3797C>T (p.Thr1266Ile)	not specified [RCV005387141]	uncertain significance	2	159947472	159947472	Human		name
598205963	CV4000315	single nucleotide variant	NM_007366.5(PLA2R1):c.3725A>G (p.Glu1242Gly)	not specified [RCV005399549]	likely benign	2	159947544	159947544	Human		name
8625169	CV80288	single nucleotide variant	NM_001007267.2(PLA2R1):c.2652T>C (p.Asp884=)	Malignant melanoma [RCV000060364]	not provided	2	159970156	159970156	Human		name
8625170	CV80289	single nucleotide variant	NM_001007267.2(PLA2R1):c.1207C>T (p.Leu403=)	Malignant melanoma [RCV000060365]	not provided	2	160022752	160022752	Human		name
155645529	CV1710888	deletion	NM_007366.5(PLA2R1):c.3857_3861del (p.Asn1286fs)	Kidney disorder [RCV002294669]	uncertain significance	2	159946907	159946911	Human	2	name

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