Pla2g4b Variant Search Result - Rat Genome Database

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120 records found for search term Pla2g4b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405294344	CV3214872	single nucleotide variant	NM_001114633.2(PLA2G4B):c.83-5C>T	PLA2G4B-related disorder [RCV003934278]	benign	15	41840519	41840519	Human		name , trait , alternate_id
405260231	CV3190340	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1932+4C>T	JMJD7-PLA2G4B-related disorder [RCV003894736]	likely benign	15	41845074	41845074	Human		name , trait , alternate_id
405276458	CV3193359	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2640+5G>A	JMJD7-PLA2G4B-related disorder [RCV003974526]	benign	15	41846840	41846840	Human		name , trait , alternate_id
405291543	CV3205833	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1573-4C>G	JMJD7-PLA2G4B-related disorder [RCV003963957]	likely benign	15	41844467	41844467	Human		name , trait , alternate_id
405290597	CV3207577	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1184-6T>C	JMJD7-PLA2G4B-related disorder [RCV003927150]	likely benign	15	41841813	41841813	Human		name , trait , alternate_id
405260395	CV3203988	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.702+611C>T	JMJD7-PLA2G4B-related disorder [RCV003943881]	likely benign	15	41837162	41837162	Human		name , trait , alternate_id
8635442	CV90663	single nucleotide variant	NM_005090.3(JMJD7-PLA2G4B):c.2294-18C>T	Malignant melanoma [RCV000070761]	not provided	15	41846185	41846185	Human		name
405270827	CV3219770	single nucleotide variant	NM_001114633.2(PLA2G4B):c.102C>T (p.Tyr34=)	PLA2G4B-related disorder [RCV003971509]	likely benign	15	41840543	41840543	Human		name , trait , alternate_id
401934301	CV2817441	single nucleotide variant	NM_001114633.2(PLA2G4B):c.414C>T (p.Leu138=)	not provided [RCV003411164]	likely benign	15	41841252	41841252	Human		name
401934302	CV2817442	single nucleotide variant	NM_001114633.2(PLA2G4B):c.699G>A (p.Thr233=)	not provided [RCV003411165]	likely benign	15	41842270	41842270	Human		name
405275034	CV3204605	single nucleotide variant	NM_001114633.2(PLA2G4B):c.459C>T (p.His153=)	PLA2G4B-related disorder [RCV003952017]	benign	15	41841540	41841540	Human		name , trait , alternate_id
405291673	CV3205938	single nucleotide variant	NM_001114633.2(PLA2G4B):c.382C>T (p.Leu128=)	PLA2G4B-related disorder [RCV003964044]	likely benign	15	41841085	41841085	Human		name , trait , alternate_id
597705126	CV3569667	single nucleotide variant	NM_001114633.2(PLA2G4B):c.73A>G (p.Lys25Glu)	not specified [RCV004840206]	uncertain significance	15	41840221	41840221	Human		name
15149243	CV739614	single nucleotide variant	NM_001114633.2(PLA2G4B):c.420C>T (p.Ser140=)	JMJD7-PLA2G4B-related disorder [RCV003940859]\|not provided [RCV000900893]	benign	15	41841258	41841258	Human		name , trait , alternate_id
405285193	CV3202560	microsatellite	NM_005090.4(JMJD7-PLA2G4B):c.1710-25TGGCTT[2]	JMJD7-PLA2G4B-related disorder [RCV003909817]	benign	15	41844823	41844828	Human		name , trait , alternate_id
405289039	CV3204881	microsatellite	NM_005090.4(JMJD7-PLA2G4B):c.1573-9_1573-7del	JMJD7-PLA2G4B-related disorder [RCV003961533]	benign	15	41844458	41844460	Human		name , trait , alternate_id
401863532	CV2770674	single nucleotide variant	NM_001114633.2(PLA2G4B):c.323G>A (p.Arg108Gln)	not specified [RCV004349722]	uncertain significance	15	41840877	41840877	Human		name
405294106	CV3203462	single nucleotide variant	NM_001114633.2(PLA2G4B):c.688G>C (p.Val230Leu)	PLA2G4B-related disorder [RCV003933996]	benign	15	41842259	41842259	Human		name , trait , alternate_id
405295051	CV3210940	single nucleotide variant	NM_001114633.2(PLA2G4B):c.982G>A (p.Val328Ile)	PLA2G4B-related disorder [RCV003936953]	likely benign	15	41844573	41844573	Human		name , trait , alternate_id
405282573	CV3220605	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.20A>G (p.Glu7Gly)	JMJD7-PLA2G4B-related disorder [RCV003978927]	benign	15	41828144	41828144	Human		name , trait , alternate_id
155925930	CV2348544	single nucleotide variant	NM_001114633.2(PLA2G4B):c.1609C>G (p.Gln537Glu)	not specified [RCV004193726]	uncertain significance	15	41846211	41846211	Human		name
405280718	CV3195669	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.997C>T (p.Leu333=)	JMJD7-PLA2G4B-related disorder [RCV003906904]	likely benign	15	41840858	41840858	Human		name , trait , alternate_id
405275041	CV3199979	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.444C>T (p.Ser148=)	JMJD7-PLA2G4B-related disorder [RCV003973992]	likely benign	15	41835195	41835195	Human		name , trait , alternate_id
405284387	CV3213750	single nucleotide variant	NM_001114633.2(PLA2G4B):c.2119G>A (p.Glu707Lys)	PLA2G4B-related disorder [RCV003922306]	likely benign	15	41847508	41847508	Human		name , trait , alternate_id
405795766	CV3275558	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.34G>C (p.Glu12Gln)	not specified [RCV004401332]	uncertain significance	15	41828158	41828158	Human		name
405656360	CV3375996	single nucleotide variant	NM_001114633.2(PLA2G4B):c.2257A>C (p.Thr753Pro)	not specified [RCV004511466]	uncertain significance	15	41847771	41847771	Human		name
407482105	CV3460670	single nucleotide variant	NM_001114633.2(PLA2G4B):c.1967G>A (p.Arg656Gln)	not specified [RCV004648553]	uncertain significance	15	41847356	41847356	Human		name
40815510	CV971015	single nucleotide variant	NM_001114633.2(PLA2G4B):c.2305C>T (p.Arg769Cys)	JMJD7-PLA2G4B-related disorder [RCV003928805]\|Neurodevelopmental disorder [RCV001262947]\|not provided [RCV004692375]	benign\|uncertain significance	15	41847819	41847819	Human	1	name , trait , alternate_id
155908652	CV2302480	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.292C>T (p.Arg98Cys)	not specified [RCV004161207]	uncertain significance	15	41835043	41835043	Human		name
155930061	CV2366518	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.253G>A (p.Val85Met)	not specified [RCV004208493]	uncertain significance	15	41835004	41835004	Human		name
405292443	CV3196514	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1887C>T (p.Phe629=)	JMJD7-PLA2G4B-related disorder [RCV003964552]	likely benign	15	41845025	41845025	Human		name , trait , alternate_id
405284201	CV3196695	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2349G>A (p.Arg783=)	JMJD7-PLA2G4B-related disorder [RCV003979594]	benign	15	41846258	41846258	Human		name , trait , alternate_id
405289438	CV3205127	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2856A>G (p.Ala952=)	JMJD7-PLA2G4B-related disorder [RCV003961732]	benign	15	41847677	41847677	Human		name , trait , alternate_id
405291762	CV3206057	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2883G>A (p.Ser961=)	JMJD7-PLA2G4B-related disorder [RCV003964144]	benign	15	41847704	41847704	Human		name , trait , alternate_id
405287707	CV3208030	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2073C>T (p.Tyr691=)	JMJD7-PLA2G4B-related disorder [RCV003924559]	likely benign	15	41845660	41845660	Human		name , trait , alternate_id
405284628	CV3213746	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2124C>G (p.Gly708=)	JMJD7-PLA2G4B-related disorder [RCV003922302]	likely benign	15	41845711	41845711	Human		name , trait , alternate_id
405288074	CV3214839	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2379G>A (p.Thr793=)	JMJD7-PLA2G4B-related disorder [RCV003924691]	benign	15	41846288	41846288	Human		name , trait , alternate_id
405294900	CV3214919	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1608G>C (p.Gly536=)	JMJD7-PLA2G4B-related disorder [RCV003936783]	likely benign	15	41844506	41844506	Human		name , trait , alternate_id
405277028	CV3217675	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1551C>T (p.Asp517=)	JMJD7-PLA2G4B-related disorder [RCV003974740]	benign	15	41843790	41843790	Human		name , trait , alternate_id
405276907	CV3217679	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2748C>T (p.Ser916=)	JMJD7-PLA2G4B-related disorder [RCV003974744]	benign	15	41847444	41847444	Human		name , trait , alternate_id
405289598	CV3220806	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2994T>C (p.Ala998=)	JMJD7-PLA2G4B-related disorder [RCV003961842]	likely benign	15	41847815	41847815	Human		name , trait , alternate_id
405278371	CV3221903	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2466A>C (p.Thr822=)	JMJD7-PLA2G4B-related disorder [RCV003976455]	benign	15	41846375	41846375	Human		name , trait , alternate_id
405260992	CV3215519	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.3000C>G (p.Arg1000=)	JMJD7-PLA2G4B-related disorder [RCV003944258]	likely benign	15	41847821	41847821	Human		name , trait , alternate_id
405795769	CV3275559	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.751C>G (p.His251Asp)	not specified [RCV004401333]	uncertain significance	15	41840206	41840206	Human		name
405795772	CV3275560	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.779C>T (p.Thr260Ile)	not specified [RCV004401334]	uncertain significance	15	41840527	41840527	Human		name
405795775	CV3275561	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.794A>G (p.Tyr265Cys)	not specified [RCV004401335]	uncertain significance	15	41840542	41840542	Human		name
405795778	CV3275562	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.824G>A (p.Ser275Asn)	not specified [RCV004401336]	uncertain significance	15	41840572	41840572	Human		name
405795781	CV3275563	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.841C>T (p.Arg281Cys)	not specified [RCV004401337]	uncertain significance	15	41840589	41840589	Human		name
405795784	CV3275564	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.845C>T (p.Thr282Met)	not specified [RCV004401338]	uncertain significance	15	41840593	41840593	Human		name
405795787	CV3275565	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.892A>G (p.Arg298Gly)	not specified [RCV004401339]	uncertain significance	15	41840640	41840640	Human		name
405795790	CV3275566	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.914A>G (p.Asn305Ser)	not specified [RCV004401340]	uncertain significance	15	41840775	41840775	Human		name
405795792	CV3275567	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.920T>C (p.Met307Thr)	not specified [RCV004401341]	uncertain significance	15	41840781	41840781	Human		name
405795795	CV3275568	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.976G>A (p.Val326Ile)	not specified [RCV004401342]	uncertain significance	15	41840837	41840837	Human		name
401866525	CV2775577	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1663C>T (p.Leu555Phe)	not specified [RCV004350740]	uncertain significance	15	41844561	41844561	Human		name
405276306	CV3193371	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1264C>T (p.Arg422Cys)	JMJD7-PLA2G4B-related disorder [RCV003974538]	benign	15	41841899	41841899	Human		name , trait , alternate_id
405268021	CV3198811	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2048G>T (p.Gly683Val)	JMJD7-PLA2G4B-related disorder [RCV003911934]	likely benign	15	41845318	41845318	Human		name , trait , alternate_id
405291005	CV3203910	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2710G>A (p.Glu904Lys)	JMJD7-PLA2G4B-related disorder [RCV003927359]	likely benign	15	41847406	41847406	Human		name , trait , alternate_id
405289380	CV3205089	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2465C>T (p.Thr822Ile)	JMJD7-PLA2G4B-related disorder [RCV003961699]	benign	15	41846374	41846374	Human		name , trait , alternate_id
405258123	CV3208162	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1376G>T (p.Arg459Met)	JMJD7-PLA2G4B-related disorder [RCV003941603]\|not specified [RCV004369802]	likely benign\|uncertain significance	15	41842254	41842254	Human		name , trait , alternate_id
405260369	CV3209149	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2315T>G (p.Leu772Arg)	JMJD7-PLA2G4B-related disorder [RCV003943853]	likely benign	15	41846224	41846224	Human		name , trait , alternate_id
405274129	CV3211573	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1153G>A (p.Val385Ile)	JMJD7-PLA2G4B-related disorder [RCV003951405]	benign	15	41841541	41841541	Human		name , trait , alternate_id
405270925	CV3212149	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1816G>T (p.Ala606Ser)	JMJD7-PLA2G4B-related disorder [RCV003949515]	likely benign	15	41844954	41844954	Human		name , trait , alternate_id
405266094	CV3215893	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1410G>A (p.Met470Ile)	JMJD7-PLA2G4B-related disorder [RCV003947029]	likely benign	15	41842565	41842565	Human		name , trait , alternate_id
405278062	CV3216424	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1865G>A (p.Arg622His)	JMJD7-PLA2G4B-related disorder [RCV003954365]	benign	15	41845003	41845003	Human		name , trait , alternate_id
405278291	CV3216558	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2740A>C (p.Thr914Pro)	JMJD7-PLA2G4B-related disorder [RCV003954470]	benign	15	41847436	41847436	Human		name , trait , alternate_id
405795539	CV3275506	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1007G>C (p.Gly336Ala)	not specified [RCV004401280]	uncertain significance	15	41840868	41840868	Human		name
405795542	CV3275507	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1019G>A (p.Arg340His)	not specified [RCV004401281]	likely benign	15	41840880	41840880	Human		name
405795545	CV3275508	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1097G>T (p.Gly366Val)	not specified [RCV004401282]	uncertain significance	15	41841242	41841242	Human		name
405795619	CV3275509	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1108G>A (p.Val370Ile)	not specified [RCV004401283]	uncertain significance	15	41841253	41841253	Human		name
405795622	CV3275510	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1120G>A (p.Val374Ile)	not specified [RCV004401284]	likely benign	15	41841265	41841265	Human		name
405795625	CV3275511	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1133G>A (p.Arg378Gln)	not specified [RCV004401285]	uncertain significance	15	41841521	41841521	Human		name
405795628	CV3275512	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1150C>T (p.His384Tyr)	not specified [RCV004401286]	uncertain significance	15	41841538	41841538	Human		name
405795631	CV3275513	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1171G>A (p.Gly391Arg)	not specified [RCV004401287]	uncertain significance	15	41841559	41841559	Human		name
405795634	CV3275514	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1252A>C (p.Thr418Pro)	not specified [RCV004401288]	uncertain significance	15	41841887	41841887	Human		name
405795637	CV3275515	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1253C>G (p.Thr418Ser)	not specified [RCV004401289]	uncertain significance	15	41841888	41841888	Human		name
405795640	CV3275516	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1284C>G (p.Cys428Trp)	not specified [RCV004401290]	uncertain significance	15	41841919	41841919	Human		name
405795643	CV3275517	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1324G>A (p.Glu442Lys)	not specified [RCV004401291]	likely benign	15	41842202	41842202	Human		name
405795650	CV3275519	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1463G>A (p.Gly488Asp)	not specified [RCV004401293]	uncertain significance	15	41843702	41843702	Human		name
405795653	CV3275520	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1490C>A (p.Ala497Asp)	not specified [RCV004401294]	uncertain significance	15	41843729	41843729	Human		name
405795656	CV3275521	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1535A>G (p.Gln512Arg)	not specified [RCV004401295]	uncertain significance	15	41843774	41843774	Human		name
405795659	CV3275522	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1612C>T (p.Arg538Trp)	not specified [RCV004401296]	uncertain significance	15	41844510	41844510	Human		name
405795662	CV3275523	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1661G>A (p.Gly554Asp)	not specified [RCV004401297]	uncertain significance	15	41844559	41844559	Human		name
405795665	CV3275524	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1686C>G (p.Ile562Met)	not specified [RCV004401298]	uncertain significance	15	41844584	41844584	Human		name
405795668	CV3275525	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1690G>A (p.Gly564Arg)	not specified [RCV004401299]	uncertain significance	15	41844588	41844588	Human		name
405795671	CV3275526	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1772A>C (p.Glu591Ala)	not specified [RCV004401300]	uncertain significance	15	41844910	41844910	Human		name
405795674	CV3275527	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1807G>A (p.Gly603Ser)	not specified [RCV004401301]	uncertain significance	15	41844945	41844945	Human		name
405795677	CV3275528	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1813C>G (p.Leu605Val)	not specified [RCV004401302]	uncertain significance	15	41844951	41844951	Human		name
405795680	CV3275529	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1834C>T (p.Arg612Trp)	not specified [RCV004401303]	uncertain significance	15	41844972	41844972	Human		name
405795683	CV3275530	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1835G>A (p.Arg612Gln)	not specified [RCV004401304]	uncertain significance	15	41844973	41844973	Human		name
405795686	CV3275531	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1910A>G (p.Asn637Ser)	not specified [RCV004401305]	uncertain significance	15	41845048	41845048	Human		name
405795690	CV3275532	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1948C>G (p.Leu650Val)	not specified [RCV004401306]	uncertain significance	15	41845218	41845218	Human		name
405795693	CV3275533	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2008C>G (p.Leu670Val)	not specified [RCV004401307]	uncertain significance	15	41845278	41845278	Human		name
405795696	CV3275534	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2008C>T (p.Leu670Phe)	not specified [RCV004401308]	uncertain significance	15	41845278	41845278	Human		name
405795699	CV3275535	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2057G>A (p.Cys686Tyr)	not specified [RCV004401309]	uncertain significance	15	41845644	41845644	Human		name
405795702	CV3275536	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2059G>A (p.Glu687Lys)	not specified [RCV004401310]	uncertain significance	15	41845646	41845646	Human		name
405795706	CV3275537	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2260T>A (p.Trp754Arg)	not specified [RCV004401311]	uncertain significance	15	41846014	41846014	Human		name
405795709	CV3275538	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2266C>T (p.Arg756Cys)	not specified [RCV004401312]	uncertain significance	15	41846020	41846020	Human		name
405795712	CV3275539	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2322A>G (p.Ile774Met)	not specified [RCV004401313]	uncertain significance	15	41846231	41846231	Human		name
405795715	CV3275540	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2368G>A (p.Asp790Asn)	not specified [RCV004401314]	uncertain significance	15	41846277	41846277	Human		name
405795718	CV3275541	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2368G>C (p.Asp790His)	not specified [RCV004401315]	uncertain significance	15	41846277	41846277	Human		name
405795721	CV3275542	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2414T>C (p.Leu805Pro)	not specified [RCV004401316]	uncertain significance	15	41846323	41846323	Human		name
405795724	CV3275543	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2513C>T (p.Ser838Leu)	not specified [RCV004401317]	uncertain significance	15	41846708	41846708	Human		name
405795727	CV3275544	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2581C>A (p.Pro861Thr)	not specified [RCV004401318]	uncertain significance	15	41846776	41846776	Human		name
405795731	CV3275545	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2592C>G (p.Asp864Glu)	not specified [RCV004401319]	uncertain significance	15	41846787	41846787	Human		name
405795734	CV3275546	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2659C>T (p.Arg887Trp)	not specified [RCV004401320]	uncertain significance	15	41847355	41847355	Human		name
405795737	CV3275547	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2684C>T (p.Pro895Leu)	not specified [RCV004401321]	uncertain significance	15	41847380	41847380	Human		name
405795740	CV3275548	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2688C>G (p.Phe896Leu)	not specified [RCV004401322]	uncertain significance	15	41847384	41847384	Human		name
405795743	CV3275549	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2728C>T (p.Arg910Trp)	not specified [RCV004401323]	uncertain significance	15	41847424	41847424	Human		name
405795745	CV3275550	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2774C>T (p.Ala925Val)	not specified [RCV004401324]	uncertain significance	15	41847470	41847470	Human		name
405795747	CV3275551	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2848G>A (p.Glu950Lys)	not specified [RCV004401325]	uncertain significance	15	41847669	41847669	Human		name
405795749	CV3275552	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2852C>T (p.Ala951Val)	not specified [RCV004401326]	uncertain significance	15	41847673	41847673	Human		name
405795751	CV3275553	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2888C>G (p.Ser963Cys)	not specified [RCV004401327]	uncertain significance	15	41847709	41847709	Human		name
405795755	CV3275554	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2912C>A (p.Thr971Asn)	not specified [RCV004401328]	uncertain significance	15	41847733	41847733	Human		name
405795758	CV3275555	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2929G>A (p.Val977Met)	not specified [RCV004401329]	uncertain significance	15	41847750	41847750	Human		name
407480444	CV3448132	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.1841G>A (p.Arg614Gln)	not specified [RCV004635770]	likely benign	15	41844979	41844979	Human		name
597777629	CV3691340	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2588G>A (p.Arg863Gln)	not specified [RCV004929935]	uncertain significance	15	41846783	41846783	Human		name
597777635	CV3691341	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2519C>T (p.Pro840Leu)	not specified [RCV004929936]	uncertain significance	15	41846714	41846714	Human		name
598212144	CV3969418	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.2788C>T (p.Pro930Ser)	not specified [RCV005358785]	uncertain significance	15	41847484	41847484	Human		name
405795760	CV3275556	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.3008T>G (p.Val1003Gly)	not specified [RCV004401330]	uncertain significance	15	41847829	41847829	Human		name
405795763	CV3275557	single nucleotide variant	NM_005090.4(JMJD7-PLA2G4B):c.3013C>T (p.Arg1005Trp)	not specified [RCV004401331]	uncertain significance	15	41847834	41847834	Human		name

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