Sycp2 Variant Search Result - Rat Genome Database

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224 records found for search term Sycp2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405718554	CV2852001	single nucleotide variant	NM_014258.4(SYCP2):c.600-1G>A	Male infertility with azoospermia or oligozoospermia due to single gene mutation [RCV003991629]	likely pathogenic	20	59915200	59915200	Human	1	name
405271886	CV3202986	duplication	NM_014258.4(SYCP2):c.298-3dup	SYCP2-related disorder [RCV003914040]	likely benign	20	59919599	59919600	Human		name , trait , alternate_id
405706147	CV3224809	single nucleotide variant	NM_014258.4(SYCP2):c.513+1G>T	Oligosynaptic infertility [RCV003990189]	likely pathogenic	20	59916485	59916485	Human	1	name
9686989	CV171660	single nucleotide variant	NM_014258.4(SYCP2):c.2365-8T>C	Prostate cancer [RCV000149208]	uncertain significance	20	59886842	59886842	Human	2	name
617153101	CV4021073	single nucleotide variant	NM_014258.4(SYCP2):c.1505-6T>C	not provided [RCV005428826]	uncertain significance	20	59895603	59895603	Human		name
156151478	CV2268957	single nucleotide variant	NM_014258.4(SYCP2):c.13C>A (p.Pro5Thr)	not specified [RCV004128359]	uncertain significance	20	59922401	59922401	Human		name
408377874	CV3500856	single nucleotide variant	NM_014258.4(SYCP2):c.276A>T (p.Ile92=)	not provided [RCV004722506]	likely benign	20	59920380	59920380	Human		name
15202899	CV705580	single nucleotide variant	NM_014258.4(SYCP2):c.95T>C (p.Ile32Thr)	not provided [RCV000958098]	benign	20	59921383	59921383	Human		name
156297839	CV2297719	single nucleotide variant	NM_014258.4(SYCP2):c.162A>G (p.Ile54Met)	not specified [RCV004155398]	likely benign	20	59921316	59921316	Human		name
401735459	CV2672658	single nucleotide variant	NM_014258.4(SYCP2):c.212T>C (p.Val71Ala)	not specified [RCV004287679]	uncertain significance	20	59920444	59920444	Human		name
401776880	CV2721509	single nucleotide variant	NM_014258.4(SYCP2):c.249G>C (p.Leu83Phe)	not specified [RCV004316025]	uncertain significance	20	59920407	59920407	Human		name
401930497	CV2824545	single nucleotide variant	NM_014258.4(SYCP2):c.2262C>T (p.Cys754=)	not provided [RCV003440470]	likely benign	20	59892092	59892092	Human		name
405723604	CV3324078	single nucleotide variant	NM_014258.4(SYCP2):c.242G>A (p.Ser81Asn)	not specified [RCV004463489]	uncertain significance	20	59920414	59920414	Human		name
407505385	CV3482112	single nucleotide variant	NM_014258.4(SYCP2):c.143A>G (p.His48Arg)	not specified [RCV004670823]	uncertain significance	20	59921335	59921335	Human		name
597770748	CV3609048	single nucleotide variant	NM_014258.4(SYCP2):c.250G>A (p.Gly84Arg)	not specified [RCV004871507]	uncertain significance	20	59920406	59920406	Human		name
598223117	CV3912784	single nucleotide variant	NM_014258.4(SYCP2):c.2871G>A (p.Pro957=)	not specified [RCV005293903]	likely benign	20	59880373	59880373	Human		name
15163316	CV705579	single nucleotide variant	NM_014258.4(SYCP2):c.2016T>C (p.Tyr672=)	not provided [RCV000948057]	benign	20	59892338	59892338	Human		name
156025168	CV2242207	single nucleotide variant	NM_014258.4(SYCP2):c.985G>C (p.Glu329Gln)	not specified [RCV004111240]	uncertain significance	20	59907412	59907412	Human		name
155967500	CV2312731	single nucleotide variant	NM_014258.4(SYCP2):c.955A>G (p.Ile319Val)	not specified [RCV004169453]	uncertain significance	20	59911767	59911767	Human		name
156162765	CV2323557	single nucleotide variant	NM_014258.4(SYCP2):c.563G>A (p.Arg188Gln)	not specified [RCV004165754]	uncertain significance	20	59915501	59915501	Human		name
156353765	CV2324140	single nucleotide variant	NM_014258.4(SYCP2):c.926A>G (p.Asn309Ser)	not specified [RCV004176891]	uncertain significance	20	59911796	59911796	Human		name
329395453	CV2458386	single nucleotide variant	NM_014258.4(SYCP2):c.531T>G (p.Asn177Lys)	not specified [RCV004266021]	uncertain significance	20	59915533	59915533	Human		name
329360872	CV2463070	single nucleotide variant	NM_014258.4(SYCP2):c.757A>G (p.Lys253Glu)	not specified [RCV004272881]	uncertain significance	20	59914129	59914129	Human		name
329352647	CV2476866	single nucleotide variant	NM_014258.4(SYCP2):c.4368C>T (p.Ser1456=)	SYCP2-related disorder [RCV003919036]\|not provided [RCV003223098]	likely benign	20	59865818	59865818	Human	1	name , trait , alternate_id
329352650	CV2476867	single nucleotide variant	NM_014258.4(SYCP2):c.3456C>T (p.Asn1152=)	not provided [RCV003223099]	likely benign	20	59873955	59873955	Human		name
401731605	CV2693903	single nucleotide variant	NM_014258.4(SYCP2):c.305C>A (p.Ala102Asp)	not specified [RCV004300203]	uncertain significance	20	59919590	59919590	Human		name
401783407	CV2723539	single nucleotide variant	NM_014258.4(SYCP2):c.461G>A (p.Arg154His)	not specified [RCV004323942]	uncertain significance	20	59916538	59916538	Human		name
401919840	CV2824544	single nucleotide variant	NM_014258.4(SYCP2):c.4248C>T (p.Phe1416=)	not provided [RCV003431387]	likely benign	20	59866365	59866365	Human		name
407505374	CV3482108	single nucleotide variant	NM_014258.4(SYCP2):c.616A>G (p.Arg206Gly)	not specified [RCV004670820]	uncertain significance	20	59915183	59915183	Human		name
597770711	CV3609040	single nucleotide variant	NM_014258.4(SYCP2):c.541G>A (p.Asp181Asn)	not specified [RCV004871500]	uncertain significance	20	59915523	59915523	Human		name
597770805	CV3609062	single nucleotide variant	NM_014258.4(SYCP2):c.326A>G (p.Asp109Gly)	not specified [RCV004871518]	uncertain significance	20	59919569	59919569	Human		name
598223084	CV3912778	single nucleotide variant	NM_014258.4(SYCP2):c.824A>G (p.Lys275Arg)	not specified [RCV005293898]	uncertain significance	20	59913981	59913981	Human		name
598223105	CV3912782	single nucleotide variant	NM_014258.4(SYCP2):c.797A>G (p.Asn266Ser)	not specified [RCV005293901]	uncertain significance	20	59914008	59914008	Human		name
15202897	CV705577	single nucleotide variant	NM_014258.4(SYCP2):c.4158G>A (p.Thr1386=)	not provided [RCV000958097]	benign	20	59866557	59866557	Human		name
15121026	CV717089	single nucleotide variant	NM_014258.4(SYCP2):c.305C>T (p.Ala102Val)	not provided [RCV000962818]	benign	20	59919590	59919590	Human		name
15117847	CV742489	single nucleotide variant	NM_014258.4(SYCP2):c.4023C>T (p.Asp1341=)	not provided [RCV000895447]	benign	20	59867813	59867813	Human		name
156180435	CV2201737	single nucleotide variant	NM_014258.4(SYCP2):c.1037G>A (p.Arg346Lys)	not specified [RCV004082181]	uncertain significance	20	59901807	59901807	Human		name
156180450	CV2201738	single nucleotide variant	NM_014258.4(SYCP2):c.2848G>A (p.Asp950Asn)	not specified [RCV004082182]	uncertain significance	20	59880396	59880396	Human		name
156042047	CV2215732	single nucleotide variant	NM_014258.4(SYCP2):c.2377A>G (p.Lys793Glu)	not specified [RCV004095342]	uncertain significance	20	59886822	59886822	Human		name
156031027	CV2243355	single nucleotide variant	NM_014258.4(SYCP2):c.1123G>A (p.Asp375Asn)	not specified [RCV004112049]	uncertain significance	20	59901721	59901721	Human		name
156357588	CV2254067	single nucleotide variant	NM_014258.4(SYCP2):c.1171A>G (p.Thr391Ala)	not specified [RCV004129515]	uncertain significance	20	59901673	59901673	Human		name
155980236	CV2263632	single nucleotide variant	NM_014258.4(SYCP2):c.1373A>G (p.Asp458Gly)	not specified [RCV004135634]	uncertain significance	20	59900169	59900169	Human		name
156361738	CV2265410	single nucleotide variant	NM_014258.4(SYCP2):c.2216A>G (p.Tyr739Cys)	not specified [RCV004130444]	uncertain significance	20	59892138	59892138	Human		name
156046047	CV2268652	single nucleotide variant	NM_014258.4(SYCP2):c.2786A>G (p.His929Arg)	not specified [RCV004124057]	uncertain significance	20	59880458	59880458	Human		name
156077775	CV2291677	single nucleotide variant	NM_014258.4(SYCP2):c.1065T>G (p.Ile355Met)	not specified [RCV004155960]	uncertain significance	20	59901779	59901779	Human		name
156173579	CV2326859	single nucleotide variant	NM_014258.4(SYCP2):c.1147G>C (p.Val383Leu)	not specified [RCV004176686]	uncertain significance	20	59901697	59901697	Human		name
156277945	CV2328375	single nucleotide variant	NM_014258.4(SYCP2):c.2262C>G (p.Cys754Trp)	not specified [RCV004175488]	uncertain significance	20	59892092	59892092	Human		name
155926964	CV2365853	single nucleotide variant	NM_014258.4(SYCP2):c.1834C>G (p.His612Asp)	not specified [RCV004214384]	uncertain significance	20	59892661	59892661	Human		name
156224636	CV2399457	single nucleotide variant	NM_014258.4(SYCP2):c.2870C>T (p.Pro957Leu)	not specified [RCV004242726]	uncertain significance	20	59880374	59880374	Human		name
329387489	CV2436500	single nucleotide variant	NM_014258.4(SYCP2):c.1887C>G (p.Asn629Lys)	not specified [RCV004251876]	uncertain significance	20	59892608	59892608	Human		name
329400843	CV2449754	single nucleotide variant	NM_014258.4(SYCP2):c.1418G>A (p.Ser473Asn)	not specified [RCV004270433]	uncertain significance	20	59896515	59896515	Human		name
329359393	CV2450993	single nucleotide variant	NM_014258.4(SYCP2):c.2461A>G (p.Thr821Ala)	not specified [RCV004267874]	uncertain significance	20	59886738	59886738	Human		name
329382584	CV2465273	single nucleotide variant	NM_014258.4(SYCP2):c.1009A>G (p.Lys337Glu)	not specified [RCV004281073]	uncertain significance	20	59907388	59907388	Human		name
329352654	CV2476868	single nucleotide variant	NM_014258.4(SYCP2):c.2312A>C (p.Glu771Ala)	not provided [RCV003223100]	likely benign	20	59892042	59892042	Human		name
401728551	CV2672968	single nucleotide variant	NM_014258.4(SYCP2):c.1439C>T (p.Ala480Val)	not specified [RCV004283969]	uncertain significance	20	59896494	59896494	Human		name
401736750	CV2679139	single nucleotide variant	NM_014258.4(SYCP2):c.1781G>T (p.Arg594Ile)	not specified [RCV004283872]	likely benign	20	59893154	59893154	Human		name
401718806	CV2679314	single nucleotide variant	NM_014258.4(SYCP2):c.1211T>C (p.Val404Ala)	not specified [RCV004285854]	uncertain significance	20	59900790	59900790	Human		name
401735198	CV2699196	single nucleotide variant	NM_014258.4(SYCP2):c.2806A>G (p.Ser936Gly)	not specified [RCV004303690]	uncertain significance	20	59880438	59880438	Human		name
401770642	CV2707326	single nucleotide variant	NM_014258.4(SYCP2):c.1570A>T (p.Ser524Cys)	not specified [RCV004312729]	uncertain significance	20	59895532	59895532	Human		name
401737294	CV2718062	single nucleotide variant	NM_014258.4(SYCP2):c.2768A>G (p.Lys923Arg)	not specified [RCV004315784]	uncertain significance	20	59880970	59880970	Human		name
401761837	CV2726926	single nucleotide variant	NM_014258.4(SYCP2):c.1792A>T (p.Ile598Leu)	not specified [RCV004323209]	uncertain significance	20	59893143	59893143	Human		name
401869238	CV2776050	single nucleotide variant	NM_014258.4(SYCP2):c.2215T>C (p.Tyr739His)	not specified [RCV004353156]	uncertain significance	20	59892139	59892139	Human		name
405723523	CV3324068	single nucleotide variant	NM_014258.4(SYCP2):c.1012G>A (p.Val338Ile)	not specified [RCV004463479]	uncertain significance	20	59907385	59907385	Human		name
405723537	CV3324070	single nucleotide variant	NM_014258.4(SYCP2):c.1158A>C (p.Lys386Asn)	not specified [RCV004463481]	uncertain significance	20	59901686	59901686	Human		name
405723548	CV3324071	single nucleotide variant	NM_014258.4(SYCP2):c.1247G>A (p.Ser416Asn)	not specified [RCV004463482]	uncertain significance	20	59900754	59900754	Human		name
405723556	CV3324072	single nucleotide variant	NM_014258.4(SYCP2):c.1643A>G (p.His548Arg)	not specified [RCV004463483]	uncertain significance	20	59895459	59895459	Human		name
405723563	CV3324073	single nucleotide variant	NM_014258.4(SYCP2):c.1913A>G (p.Asp638Gly)	not specified [RCV004463484]	uncertain significance	20	59892582	59892582	Human		name
405723573	CV3324074	single nucleotide variant	NM_014258.4(SYCP2):c.1931T>C (p.Ile644Thr)	not specified [RCV004463485]	uncertain significance	20	59892423	59892423	Human		name
405723580	CV3324075	single nucleotide variant	NM_014258.4(SYCP2):c.2212A>G (p.Ile738Val)	not specified [RCV004463486]	uncertain significance	20	59892142	59892142	Human		name
405723588	CV3324076	single nucleotide variant	NM_014258.4(SYCP2):c.2239A>G (p.Lys747Glu)	not specified [RCV004463487]	uncertain significance	20	59892115	59892115	Human		name
405723596	CV3324077	single nucleotide variant	NM_014258.4(SYCP2):c.2399T>C (p.Val800Ala)	not specified [RCV004463488]	likely benign	20	59886800	59886800	Human		name
405723617	CV3324080	single nucleotide variant	NM_014258.4(SYCP2):c.2465G>A (p.Arg822Lys)	not specified [RCV004463491]	uncertain significance	20	59886734	59886734	Human		name
405723624	CV3324081	single nucleotide variant	NM_014258.4(SYCP2):c.2579A>G (p.Asn860Ser)	not specified [RCV004463492]	uncertain significance	20	59882116	59882116	Human		name
405723632	CV3324082	single nucleotide variant	NM_014258.4(SYCP2):c.2996T>C (p.Ile999Thr)	not specified [RCV004463493]	uncertain significance	20	59877539	59877539	Human		name
407530254	CV3482102	single nucleotide variant	NM_014258.4(SYCP2):c.2866G>A (p.Glu956Lys)	not specified [RCV004681802]	uncertain significance	20	59880378	59880378	Human		name
407505366	CV3482104	single nucleotide variant	NM_014258.4(SYCP2):c.2882C>A (p.Pro961Gln)	not specified [RCV004670818]	uncertain significance	20	59880362	59880362	Human		name
407530256	CV3482106	single nucleotide variant	NM_014258.4(SYCP2):c.1446G>A (p.Met482Ile)	not specified [RCV004681804]	uncertain significance	20	59896487	59896487	Human		name
407530257	CV3482109	single nucleotide variant	NM_014258.4(SYCP2):c.1228C>T (p.His410Tyr)	not specified [RCV004681805]	uncertain significance	20	59900773	59900773	Human		name
407505390	CV3482113	single nucleotide variant	NM_014258.4(SYCP2):c.2792A>G (p.Lys931Arg)	not specified [RCV004670824]	uncertain significance	20	59880452	59880452	Human		name
407530258	CV3482115	single nucleotide variant	NM_014258.4(SYCP2):c.2050A>G (p.Lys684Glu)	not specified [RCV004681806]	uncertain significance	20	59892304	59892304	Human		name
407505401	CV3482117	single nucleotide variant	NM_014258.4(SYCP2):c.1189A>G (p.Ile397Val)	not specified [RCV004670827]	uncertain significance	20	59900812	59900812	Human		name
407530259	CV3482118	single nucleotide variant	NM_014258.4(SYCP2):c.1763C>T (p.Ser588Leu)	not specified [RCV004681807]	uncertain significance	20	59893172	59893172	Human		name
597770716	CV3609041	single nucleotide variant	NM_014258.4(SYCP2):c.2717T>C (p.Val906Ala)	not specified [RCV004871501]	uncertain significance	20	59881021	59881021	Human		name
597770721	CV3609042	single nucleotide variant	NM_014258.4(SYCP2):c.1060A>G (p.Ile354Val)	not specified [RCV004871502]	uncertain significance	20	59901784	59901784	Human		name
597770732	CV3609044	single nucleotide variant	NM_014258.4(SYCP2):c.2035C>T (p.His679Tyr)	not specified [RCV004871504]	uncertain significance	20	59892319	59892319	Human		name
597770738	CV3609045	single nucleotide variant	NM_014258.4(SYCP2):c.2624T>C (p.Leu875Ser)	not specified [RCV004871505]	uncertain significance	20	59881979	59881979	Human		name
597794607	CV3609047	single nucleotide variant	NM_014258.4(SYCP2):c.2897A>G (p.Tyr966Cys)	not specified [RCV004877912]	uncertain significance	20	59880347	59880347	Human		name
597770753	CV3609049	single nucleotide variant	NM_014258.4(SYCP2):c.1001C>T (p.Pro334Leu)	not specified [RCV004871508]	uncertain significance	20	59907396	59907396	Human		name
597770758	CV3609050	single nucleotide variant	NM_014258.4(SYCP2):c.2441C>T (p.Thr814Ile)	not specified [RCV004871509]	uncertain significance	20	59886758	59886758	Human		name
597794609	CV3609051	single nucleotide variant	NM_014258.4(SYCP2):c.2698G>A (p.Asp900Asn)	not specified [RCV004877913]	uncertain significance	20	59881453	59881453	Human		name
597770768	CV3609053	single nucleotide variant	NM_014258.4(SYCP2):c.1687G>A (p.Val563Ile)	not specified [RCV004871511]	uncertain significance	20	59893572	59893572	Human		name
597794612	CV3609054	single nucleotide variant	NM_014258.4(SYCP2):c.2228A>G (p.Tyr743Cys)	not specified [RCV004877914]	uncertain significance	20	59892126	59892126	Human		name
597794616	CV3609058	single nucleotide variant	NM_014258.4(SYCP2):c.1043C>T (p.Ser348Leu)	not specified [RCV004877915]	uncertain significance	20	59901801	59901801	Human		name
597770789	CV3609059	single nucleotide variant	NM_014258.4(SYCP2):c.2484G>T (p.Leu828Phe)	not specified [RCV004871515]	uncertain significance	20	59886715	59886715	Human		name
597770800	CV3609061	single nucleotide variant	NM_014258.4(SYCP2):c.2044A>G (p.Ile682Val)	not specified [RCV004871517]	uncertain significance	20	59892310	59892310	Human		name
598223071	CV3912775	single nucleotide variant	NM_014258.4(SYCP2):c.2564A>C (p.Lys855Thr)	not specified [RCV005293896]	uncertain significance	20	59882131	59882131	Human		name
598263811	CV3912779	single nucleotide variant	NM_014258.4(SYCP2):c.1720C>A (p.Pro574Thr)	not specified [RCV005280619]	uncertain significance	20	59893539	59893539	Human		name
15186805	CV705578	single nucleotide variant	NM_014258.4(SYCP2):c.2452A>G (p.Ile818Val)	not provided [RCV000953395]	benign	20	59886747	59886747	Human		name
15168814	CV717088	single nucleotide variant	NM_014258.4(SYCP2):c.2885A>G (p.Gln962Arg)	not provided [RCV000971691]	benign	20	59880359	59880359	Human		name
15164751	CV742490	single nucleotide variant	NM_014258.4(SYCP2):c.2852T>C (p.Ile951Thr)	not provided [RCV000904072]	benign	20	59880392	59880392	Human		name
8637409	CV92635	single nucleotide variant	NM_014258.2(SYCP2):c.1644T>A (p.His548Gln)	Malignant melanoma [RCV000072733]	not provided	20	59895458	59895458	Human		name
156125620	CV2237632	single nucleotide variant	NM_014258.4(SYCP2):c.3055A>T (p.Thr1019Ser)	not specified [RCV004106563]	uncertain significance	20	59877480	59877480	Human		name
156168619	CV2270574	single nucleotide variant	NM_014258.4(SYCP2):c.3863T>G (p.Ile1288Arg)	not specified [RCV004137523]	uncertain significance	20	59868538	59868538	Human		name
156019406	CV2272601	single nucleotide variant	NM_014258.4(SYCP2):c.4568C>T (p.Ser1523Phe)	not specified [RCV004133484]	uncertain significance	20	59864336	59864336	Human		name
156069496	CV2295741	single nucleotide variant	NM_014258.4(SYCP2):c.3460G>A (p.Gly1154Arg)	not specified [RCV004151673]	uncertain significance	20	59873951	59873951	Human		name
155914350	CV2341977	single nucleotide variant	NM_014258.4(SYCP2):c.3407C>G (p.Ser1136Cys)	not specified [RCV004184919]	uncertain significance	20	59874004	59874004	Human		name
156084365	CV2343226	single nucleotide variant	NM_014258.4(SYCP2):c.3644A>G (p.Asn1215Ser)	not specified [RCV004194853]	uncertain significance	20	59869895	59869895	Human		name
156343265	CV2353404	single nucleotide variant	NM_014258.4(SYCP2):c.4048C>A (p.Gln1350Lys)	not specified [RCV004205863]	uncertain significance	20	59867788	59867788	Human		name
156382976	CV2363085	single nucleotide variant	NM_014258.4(SYCP2):c.4206A>C (p.Gln1402His)	not specified [RCV004211211]	uncertain significance	20	59866509	59866509	Human		name
156072139	CV2365365	single nucleotide variant	NM_014258.4(SYCP2):c.3491A>G (p.Asn1164Ser)	not specified [RCV004209449]	uncertain significance	20	59873920	59873920	Human		name
156307123	CV2369600	single nucleotide variant	NM_014258.4(SYCP2):c.4441A>G (p.Thr1481Ala)	not specified [RCV004215012]	uncertain significance	20	59865590	59865590	Human		name
155983233	CV2371247	single nucleotide variant	NM_014258.4(SYCP2):c.4564A>G (p.Met1522Val)	not specified [RCV004220985]	uncertain significance	20	59864340	59864340	Human		name
155995301	CV2375805	single nucleotide variant	NM_014258.4(SYCP2):c.3596G>A (p.Arg1199Lys)	not specified [RCV004224388]	uncertain significance	20	59869943	59869943	Human		name
401722821	CV2677110	single nucleotide variant	NM_014258.4(SYCP2):c.3854G>A (p.Arg1285His)	not specified [RCV004295747]	uncertain significance	20	59868547	59868547	Human		name
401725368	CV2721740	single nucleotide variant	NM_014258.4(SYCP2):c.3071A>T (p.Asn1024Ile)	not specified [RCV004324481]	uncertain significance	20	59877464	59877464	Human		name
401889609	CV2766754	single nucleotide variant	NM_014258.4(SYCP2):c.3970G>C (p.Asp1324His)	not specified [RCV004349144]	uncertain significance	20	59868431	59868431	Human		name
405723642	CV3324083	single nucleotide variant	NM_014258.4(SYCP2):c.3062C>A (p.Thr1021Lys)	not specified [RCV004463494]	uncertain significance	20	59877473	59877473	Human		name
405723650	CV3324084	single nucleotide variant	NM_014258.4(SYCP2):c.3161T>G (p.Ile1054Ser)	not specified [RCV004463495]	uncertain significance	20	59875459	59875459	Human		name
405723657	CV3324085	single nucleotide variant	NM_014258.4(SYCP2):c.3556C>T (p.Pro1186Ser)	not specified [RCV004463496]	uncertain significance	20	59869983	59869983	Human		name
405723668	CV3324086	single nucleotide variant	NM_014258.4(SYCP2):c.3598A>G (p.Lys1200Glu)	not specified [RCV004463497]	uncertain significance	20	59869941	59869941	Human		name
405723676	CV3324087	single nucleotide variant	NM_014258.4(SYCP2):c.3611C>A (p.Ser1204Tyr)	not specified [RCV004463498]	uncertain significance	20	59869928	59869928	Human		name
405723686	CV3324088	single nucleotide variant	NM_014258.4(SYCP2):c.3635A>G (p.Gln1212Arg)	not specified [RCV004463499]	uncertain significance	20	59869904	59869904	Human		name
405723694	CV3324089	single nucleotide variant	NM_014258.4(SYCP2):c.4003T>C (p.Ser1335Pro)	not specified [RCV004463500]	uncertain significance	20	59867833	59867833	Human		name
405723700	CV3324090	single nucleotide variant	NM_014258.4(SYCP2):c.4249A>T (p.Ile1417Phe)	not specified [RCV004463501]	uncertain significance	20	59866364	59866364	Human		name
405723707	CV3324091	single nucleotide variant	NM_014258.4(SYCP2):c.4405G>A (p.Ala1469Thr)	not specified [RCV004463502]	uncertain significance	20	59865626	59865626	Human		name
405723714	CV3324092	single nucleotide variant	NM_014258.4(SYCP2):c.4462T>C (p.Cys1488Arg)	not specified [RCV004463503]	uncertain significance	20	59865441	59865441	Human		name
407530255	CV3482105	single nucleotide variant	NM_014258.4(SYCP2):c.3186G>C (p.Lys1062Asn)	not specified [RCV004681803]	uncertain significance	20	59875434	59875434	Human		name
407505368	CV3482107	single nucleotide variant	NM_014258.4(SYCP2):c.3269A>G (p.Lys1090Arg)	not specified [RCV004670819]	uncertain significance	20	59875351	59875351	Human		name
407505378	CV3482110	single nucleotide variant	NM_014258.4(SYCP2):c.4574A>T (p.Glu1525Val)	not specified [RCV004670821]	uncertain significance	20	59864330	59864330	Human		name
407505382	CV3482111	single nucleotide variant	NM_014258.4(SYCP2):c.3842A>T (p.Gln1281Leu)	not specified [RCV004670822]	uncertain significance	20	59868559	59868559	Human		name
407505394	CV3482114	single nucleotide variant	NM_014258.4(SYCP2):c.3777T>G (p.Ser1259Arg)	not specified [RCV004670825]	uncertain significance	20	59868890	59868890	Human		name
407505398	CV3482116	single nucleotide variant	NM_014258.4(SYCP2):c.4010T>C (p.Leu1337Ser)	not specified [RCV004670826]	uncertain significance	20	59867826	59867826	Human		name
597770727	CV3609043	single nucleotide variant	NM_014258.4(SYCP2):c.3941C>T (p.Pro1314Leu)	not specified [RCV004871503]	uncertain significance	20	59868460	59868460	Human		name
597770744	CV3609046	single nucleotide variant	NM_014258.4(SYCP2):c.3878A>G (p.Asn1293Ser)	not specified [RCV004871506]	uncertain significance	20	59868523	59868523	Human		name
597770763	CV3609052	single nucleotide variant	NM_014258.4(SYCP2):c.4118G>A (p.Arg1373Lys)	not specified [RCV004871510]	likely benign	20	59867718	59867718	Human		name
597770774	CV3609055	single nucleotide variant	NM_014258.4(SYCP2):c.4296A>T (p.Leu1432Phe)	not specified [RCV004871512]	uncertain significance	20	59866317	59866317	Human		name
597770779	CV3609056	single nucleotide variant	NM_014258.4(SYCP2):c.3163C>T (p.His1055Tyr)	not specified [RCV004871513]	uncertain significance	20	59875457	59875457	Human		name
597770794	CV3609060	single nucleotide variant	NM_014258.4(SYCP2):c.3455A>G (p.Asn1152Ser)	not specified [RCV004871516]	uncertain significance	20	59873956	59873956	Human		name
598223078	CV3912776	single nucleotide variant	NM_014258.4(SYCP2):c.3324T>A (p.Ser1108Arg)	not specified [RCV005293897]	uncertain significance	20	59875296	59875296	Human		name
598263808	CV3912777	single nucleotide variant	NM_014258.4(SYCP2):c.3457A>G (p.Ser1153Gly)	not specified [RCV005280618]	uncertain significance	20	59873954	59873954	Human		name
598223091	CV3912780	single nucleotide variant	NM_014258.4(SYCP2):c.3012C>G (p.Asp1004Glu)	not specified [RCV005293899]	uncertain significance	20	59877523	59877523	Human		name
598223110	CV3912783	single nucleotide variant	NM_014258.4(SYCP2):c.4540C>T (p.Arg1514Cys)	not specified [RCV005293902]	uncertain significance	20	59864364	59864364	Human		name
15121021	CV717087	single nucleotide variant	NM_014258.4(SYCP2):c.3023C>T (p.Pro1008Leu)	not provided [RCV000962817]	benign	20	59877512	59877512	Human		name
407469836	CV3415389	deletion	NM_014258.4(SYCP2):c.1593_1594del (p.Asn531fs)	Oligosynaptic infertility [RCV004598348]	likely pathogenic	20	59895508	59895509	Human	1	name
15040558	CV622044	deletion	NM_014258.4(SYCP2):c.2793_2797del (p.Lys932fs)	Cryptozoospermia [RCV000855716]\|Non-obstructive azoospermia [RCV001644818]\|Oligosynaptic infertility [RCV001005041]	pathogenic\|likely pathogenic	20	59880447	59880451	Human	5	name
15040559	CV622045	microsatellite	NM_014258.4(SYCP2):c.2022_2025del (p.Lys674fs)	Cryptozoospermia [RCV000855717]\|Non-obstructive azoospermia [RCV001644819]\|Oligosynaptic infertility [RCV001005042]	pathogenic\|likely pathogenic	20	59892329	59892332	Human		name
15040560	CV622046	deletion	NM_014258.4(SYCP2):c.3067_3071del (p.Lys1023fs)	Non-obstructive azoospermia [RCV001644820]\|Oligosynaptic infertility [RCV001005040]\|Spermatocyte maturation arrest [RCV000855718]	pathogenic\|likely pathogenic	20	59877464	59877468	Human	5	name
8581463	CV115902	single nucleotide variant	NM_001040274.2(SYCP2L):c.2163+170G>C	Lung cancer [RCV000096425]	uncertain significance	6	10956412	10956412	Human		name
155902357	CV2274674	single nucleotide variant	NM_001040274.3(SYCP2L):c.22G>T (p.Ala8Ser)	not specified [RCV004139046]	uncertain significance	6	10891525	10891525	Human		name
401768738	CV2686355	single nucleotide variant	NM_001040274.3(SYCP2L):c.47G>A (p.Arg16Lys)	not specified [RCV004297430]	uncertain significance	6	10891550	10891550	Human		name
401725838	CV2687297	single nucleotide variant	NM_001040274.3(SYCP2L):c.95C>T (p.Thr32Met)	not specified [RCV004298231]	likely benign	6	10893883	10893883	Human		name
597770810	CV3609063	single nucleotide variant	NM_001040274.3(SYCP2L):c.34A>C (p.Ile12Leu)	not specified [RCV004871519]	uncertain significance	6	10891537	10891537	Human		name
156164342	CV2270261	single nucleotide variant	NM_001040274.3(SYCP2L):c.287G>A (p.Gly96Asp)	not specified [RCV004135480]	likely benign	6	10894155	10894155	Human		name
401925428	CV2822698	single nucleotide variant	NM_001040274.3(SYCP2L):c.1380T>C (p.Thr460=)	not provided [RCV003436495]	likely benign	6	10927307	10927307	Human		name
597770816	CV3609064	single nucleotide variant	NM_001040274.3(SYCP2L):c.101C>A (p.Ala34Glu)	not specified [RCV004871520]	uncertain significance	6	10893889	10893889	Human		name
597770848	CV3609071	single nucleotide variant	NM_001040274.3(SYCP2L):c.133G>A (p.Glu45Lys)	not specified [RCV004871526]	uncertain significance	6	10893921	10893921	Human		name
598223134	CV3912788	single nucleotide variant	NM_001040274.3(SYCP2L):c.286G>A (p.Gly96Ser)	not specified [RCV005293906]	uncertain significance	6	10894154	10894154	Human		name
8626072	CV81216	single nucleotide variant	NM_001040274.2(SYCP2L):c.1236G>A (p.Thr412=)	Malignant melanoma [RCV000061294]	not provided	6	10926356	10926356	Human		name
8631769	CV86975	single nucleotide variant	NM_001040274.2(SYCP2L):c.116G>A (p.Gly39Glu)	Malignant melanoma [RCV000067066]	not provided	6	10893904	10893904	Human		name
156225254	CV2226139	single nucleotide variant	NM_001040274.3(SYCP2L):c.829C>T (p.Arg277Cys)	not specified [RCV004105545]	uncertain significance	6	10910157	10910157	Human		name
156303380	CV2258845	single nucleotide variant	NM_001040274.3(SYCP2L):c.707C>G (p.Ala236Gly)	not specified [RCV004118058]	uncertain significance	6	10907572	10907572	Human		name
155945802	CV2265870	single nucleotide variant	NM_001040274.3(SYCP2L):c.563C>T (p.Thr188Ile)	not specified [RCV004126730]	uncertain significance	6	10902885	10902885	Human		name
155991082	CV2372126	single nucleotide variant	NM_001040274.3(SYCP2L):c.721A>G (p.Thr241Ala)	not specified [RCV004223653]	uncertain significance	6	10907586	10907586	Human		name
329367158	CV2427248	single nucleotide variant	NM_001040274.3(SYCP2L):c.377C>T (p.Ser126Leu)	not specified [RCV004248115]	likely benign	6	10898051	10898051	Human		name
401726505	CV2674163	single nucleotide variant	NM_001040274.3(SYCP2L):c.782A>C (p.Glu261Ala)	not specified [RCV004295564]	uncertain significance	6	10907647	10907647	Human		name
401866324	CV2782828	single nucleotide variant	NM_001040274.3(SYCP2L):c.629T>C (p.Met210Thr)	not specified [RCV004361640]	uncertain significance	6	10902951	10902951	Human		name
405723964	CV3324100	single nucleotide variant	NM_001040274.3(SYCP2L):c.352G>A (p.Glu118Lys)	not specified [RCV004463511]	uncertain significance	6	10898026	10898026	Human		name
405723972	CV3324101	single nucleotide variant	NM_001040274.3(SYCP2L):c.583G>A (p.Ala195Thr)	not specified [RCV004463512]	uncertain significance	6	10902905	10902905	Human		name
405723980	CV3324102	single nucleotide variant	NM_001040274.3(SYCP2L):c.658A>G (p.Thr220Ala)	not specified [RCV004463513]	uncertain significance	6	10906036	10906036	Human		name
405723987	CV3324103	single nucleotide variant	NM_001040274.3(SYCP2L):c.773T>C (p.Val258Ala)	not specified [RCV004463514]	uncertain significance	6	10907638	10907638	Human		name
405723993	CV3324104	single nucleotide variant	NM_001040274.3(SYCP2L):c.859G>C (p.Gly287Arg)	not specified [RCV004463515]	uncertain significance	6	10910187	10910187	Human		name
405852609	CV3396276	single nucleotide variant	NM_001040274.3(SYCP2L):c.999A>G (p.Ile333Met)	Premature ovarian failure 24 [RCV004557229]	pathogenic	6	10912753	10912753	Human	1	name
407505405	CV3482119	single nucleotide variant	NM_001040274.3(SYCP2L):c.977G>A (p.Ser326Asn)	not specified [RCV004670828]	uncertain significance	6	10912731	10912731	Human		name
598223123	CV3912786	single nucleotide variant	NM_001040274.3(SYCP2L):c.722C>T (p.Thr241Met)	not specified [RCV005293904]	uncertain significance	6	10907587	10907587	Human		name
156380572	CV2218820	single nucleotide variant	NM_001040274.3(SYCP2L):c.1805A>G (p.Gln602Arg)	not specified [RCV004085065]	uncertain significance	6	10935179	10935179	Human		name
156233301	CV2227751	single nucleotide variant	NM_001040274.3(SYCP2L):c.1084A>T (p.Ile362Leu)	not specified [RCV004094137]	uncertain significance	6	10924507	10924507	Human		name
156037857	CV2239577	single nucleotide variant	NM_001040274.3(SYCP2L):c.1435A>G (p.Ser479Gly)	not specified [RCV004108145]	uncertain significance	6	10927362	10927362	Human		name
155920882	CV2240435	single nucleotide variant	NM_001040274.3(SYCP2L):c.2432C>T (p.Thr811Ile)	not specified [RCV004117324]	uncertain significance	6	10963799	10963799	Human		name
156075770	CV2248272	single nucleotide variant	NM_001040274.3(SYCP2L):c.1850C>T (p.Ser617Phe)	not specified [RCV004119440]	uncertain significance	6	10942495	10942495	Human		name
156217882	CV2253899	single nucleotide variant	NM_001040274.3(SYCP2L):c.1723C>A (p.Gln575Lys)	not specified [RCV004127579]	uncertain significance	6	10935097	10935097	Human		name
155946719	CV2262407	single nucleotide variant	NM_001040274.3(SYCP2L):c.1006G>A (p.Ala336Thr)	not specified [RCV004128854]	likely benign	6	10912760	10912760	Human		name
156022341	CV2273635	single nucleotide variant	NM_001040274.3(SYCP2L):c.2238C>G (p.Asn746Lys)	not specified [RCV004132305]	uncertain significance	6	10958858	10958858	Human		name
155994224	CV2286389	single nucleotide variant	NM_001040274.3(SYCP2L):c.1093T>C (p.Phe365Leu)	not specified [RCV004139914]	likely benign	6	10924516	10924516	Human		name
156068225	CV2289493	single nucleotide variant	NM_001040274.3(SYCP2L):c.1436G>A (p.Ser479Asn)	not specified [RCV004154223]	uncertain significance	6	10927363	10927363	Human		name
156299416	CV2310730	single nucleotide variant	NM_001040274.3(SYCP2L):c.1314G>C (p.Glu438Asp)	not specified [RCV004157379]	likely benign	6	10927241	10927241	Human		name
156274043	CV2334077	single nucleotide variant	NM_001040274.3(SYCP2L):c.2102A>T (p.Asn701Ile)	not specified [RCV004183592]	uncertain significance	6	10956181	10956181	Human		name
156332796	CV2339839	single nucleotide variant	NM_001040274.3(SYCP2L):c.1379C>G (p.Thr460Ser)	not specified [RCV004196523]	uncertain significance	6	10927306	10927306	Human		name
155983086	CV2347899	single nucleotide variant	NM_001040274.3(SYCP2L):c.1934T>G (p.Leu645Arg)	not specified [RCV004197593]	uncertain significance	6	10942726	10942726	Human		name
156340152	CV2351722	single nucleotide variant	NM_001040274.3(SYCP2L):c.2104G>A (p.Gly702Ser)	not specified [RCV004195426]	uncertain significance	6	10956183	10956183	Human		name
155908394	CV2354629	single nucleotide variant	NM_001040274.3(SYCP2L):c.1724A>G (p.Gln575Arg)	not specified [RCV004202596]	uncertain significance	6	10935098	10935098	Human		name
156256597	CV2374117	single nucleotide variant	NM_001040274.3(SYCP2L):c.1957A>G (p.Ile653Val)	not specified [RCV004227228]	uncertain significance	6	10955118	10955118	Human		name
156149336	CV2377400	single nucleotide variant	NM_001040274.3(SYCP2L):c.1924A>G (p.Lys642Glu)	not specified [RCV004225577]	uncertain significance	6	10942716	10942716	Human		name
329387947	CV2440266	single nucleotide variant	NM_001040274.3(SYCP2L):c.1478C>T (p.Pro493Leu)	not specified [RCV004262751]	uncertain significance	6	10928440	10928440	Human		name
329354840	CV2449005	single nucleotide variant	NM_001040274.3(SYCP2L):c.2137A>G (p.Thr713Ala)	not specified [RCV004264084]	uncertain significance	6	10956216	10956216	Human		name
329355052	CV2449244	single nucleotide variant	NM_001040274.3(SYCP2L):c.1367G>A (p.Arg456His)	not specified [RCV004257383]	uncertain significance	6	10927294	10927294	Human		name
401739511	CV2683091	single nucleotide variant	NM_001040274.3(SYCP2L):c.1366C>T (p.Arg456Cys)	not specified [RCV004286098]	uncertain significance	6	10927293	10927293	Human		name
401731861	CV2690175	single nucleotide variant	NM_001040274.3(SYCP2L):c.1658G>A (p.Ser553Asn)	not specified [RCV004302188]	uncertain significance	6	10931464	10931464	Human		name
401783175	CV2703853	single nucleotide variant	NM_001040274.3(SYCP2L):c.1901C>T (p.Ser634Leu)	not specified [RCV004306718]	uncertain significance	6	10942693	10942693	Human		name
401741604	CV2713758	single nucleotide variant	NM_001040274.3(SYCP2L):c.2155A>G (p.Lys719Glu)	not specified [RCV004321104]	uncertain significance	6	10956234	10956234	Human		name
401887741	CV2772134	single nucleotide variant	NM_001040274.3(SYCP2L):c.1909G>C (p.Glu637Gln)	not specified [RCV004344785]	uncertain significance	6	10942701	10942701	Human		name
405874766	CV2842191	single nucleotide variant	NM_001040274.3(SYCP2L):c.1528C>T (p.Gln510Ter)	See cases [RCV004579611]	likely pathogenic	6	10930409	10930409	Human		name
405723721	CV3324093	single nucleotide variant	NM_001040274.3(SYCP2L):c.1049C>T (p.Ala350Val)	not specified [RCV004463504]	uncertain significance	6	10912904	10912904	Human		name
405723728	CV3324094	single nucleotide variant	NM_001040274.3(SYCP2L):c.1389A>C (p.Leu463Phe)	not specified [RCV004463505]	uncertain significance	6	10927316	10927316	Human		name
405723736	CV3324095	single nucleotide variant	NM_001040274.3(SYCP2L):c.1466T>C (p.Val489Ala)	not specified [RCV004463506]	uncertain significance	6	10928428	10928428	Human		name
405723930	CV3324096	single nucleotide variant	NM_001040274.3(SYCP2L):c.1838G>A (p.Ser613Asn)	not specified [RCV004463507]	uncertain significance	6	10942483	10942483	Human		name
405723937	CV3324097	single nucleotide variant	NM_001040274.3(SYCP2L):c.1880C>T (p.Pro627Leu)	not specified [RCV004463508]	uncertain significance	6	10942525	10942525	Human		name
405723946	CV3324098	single nucleotide variant	NM_001040274.3(SYCP2L):c.1886T>C (p.Ile629Thr)	not specified [RCV004463509]	likely benign	6	10942678	10942678	Human		name
405723953	CV3324099	single nucleotide variant	NM_001040274.3(SYCP2L):c.2374T>A (p.Ser792Thr)	not specified [RCV004463510]	uncertain significance	6	10961518	10961518	Human		name
407530260	CV3482120	single nucleotide variant	NM_001040274.3(SYCP2L):c.2272C>T (p.Arg758Cys)	not specified [RCV004681808]	uncertain significance	6	10961321	10961321	Human		name
596947069	CV3547133	single nucleotide variant	NM_001040274.3(SYCP2L):c.1432G>A (p.Asp478Asn)	not provided [RCV004810941]	likely benign	6	10927359	10927359	Human		name
597770821	CV3609065	single nucleotide variant	NM_001040274.3(SYCP2L):c.1570A>C (p.Lys524Gln)	not specified [RCV004871521]	uncertain significance	6	10930451	10930451	Human		name
597770827	CV3609067	single nucleotide variant	NM_001040274.3(SYCP2L):c.1309A>G (p.Thr437Ala)	not specified [RCV004871522]	uncertain significance	6	10926429	10926429	Human		name
597770833	CV3609068	single nucleotide variant	NM_001040274.3(SYCP2L):c.1502G>A (p.Arg501Lys)	not specified [RCV004871523]	uncertain significance	6	10930383	10930383	Human		name
597770838	CV3609069	single nucleotide variant	NM_001040274.3(SYCP2L):c.2057A>G (p.Glu686Gly)	not specified [RCV004871524]	uncertain significance	6	10956136	10956136	Human		name
597770842	CV3609070	single nucleotide variant	NM_001040274.3(SYCP2L):c.1408C>T (p.Pro470Ser)	not specified [RCV004871525]	uncertain significance	6	10927335	10927335	Human		name
597770853	CV3609072	single nucleotide variant	NM_001040274.3(SYCP2L):c.2286G>T (p.Leu762Phe)	not specified [RCV004871527]	likely benign	6	10961335	10961335	Human		name
597770858	CV3609073	single nucleotide variant	NM_001040274.3(SYCP2L):c.1328C>A (p.Ser443Tyr)	not specified [RCV004871528]	uncertain significance	6	10927255	10927255	Human		name
597770863	CV3609074	single nucleotide variant	NM_001040274.3(SYCP2L):c.2075C>G (p.Ser692Cys)	not specified [RCV004871529]	uncertain significance	6	10956154	10956154	Human		name
597770869	CV3609075	single nucleotide variant	NM_001040274.3(SYCP2L):c.1517C>G (p.Ser506Cys)	not specified [RCV004871530]	uncertain significance	6	10930398	10930398	Human		name
598263814	CV3912785	single nucleotide variant	NM_001040274.3(SYCP2L):c.1147A>G (p.Ile383Val)	not specified [RCV005280620]	uncertain significance	6	10924570	10924570	Human		name
598223130	CV3912787	single nucleotide variant	NM_001040274.3(SYCP2L):c.1400C>G (p.Ser467Cys)	not specified [RCV005293905]	uncertain significance	6	10927327	10927327	Human		name
598223140	CV3912789	single nucleotide variant	NM_001040274.3(SYCP2L):c.2375C>G (p.Ser792Cys)	not specified [RCV005293907]	uncertain significance	6	10961519	10961519	Human		name
598223151	CV3912791	single nucleotide variant	NM_001040274.3(SYCP2L):c.1699C>A (p.Pro567Thr)	not specified [RCV005293909]	uncertain significance	6	10935073	10935073	Human		name
405852608	CV3396275	microsatellite	NM_001040274.3(SYCP2L):c.154_155del (p.Ser52fs)	Premature ovarian failure 24 [RCV004557228]	pathogenic	6	10893938	10893939	Human		name

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