Syt13 Variant Search Result - Rat Genome Database

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39 records found for search term Syt13

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15190573	CV724442	single nucleotide variant	NM_020826.3(SYT13):c.471C>T (p.Asn157=)	not provided [RCV000888137]	benign	11	45254343	45254343	Human		name
15105937	CV784001	single nucleotide variant	NM_020826.3(SYT13):c.786G>A (p.Leu262=)	not provided [RCV000976537]	benign	11	45252481	45252481	Human		name
155962252	CV2200920	single nucleotide variant	NM_020826.3(SYT13):c.101A>C (p.His34Pro)	not specified [RCV004081535]	uncertain significance	11	45286107	45286107	Human		name
156074918	CV2281478	single nucleotide variant	NM_020826.3(SYT13):c.211G>C (p.Val71Leu)	not specified [RCV004153799]	uncertain significance	11	45255864	45255864	Human		name
156305516	CV2338819	single nucleotide variant	NM_020826.3(SYT13):c.169G>C (p.Gly57Arg)	not specified [RCV004182375]	likely benign	11	45286039	45286039	Human		name
156090363	CV2344659	single nucleotide variant	NM_020826.3(SYT13):c.191T>G (p.Val64Gly)	not specified [RCV004197426]	uncertain significance	11	45255884	45255884	Human		name
401730973	CV2711597	single nucleotide variant	NM_020826.3(SYT13):c.103C>A (p.Pro35Thr)	not specified [RCV004306903]	uncertain significance	11	45286105	45286105	Human		name
405727282	CV3334848	single nucleotide variant	NM_020826.3(SYT13):c.203C>T (p.Thr68Met)	not specified [RCV004463888]	uncertain significance	11	45255872	45255872	Human		name
405727290	CV3334849	single nucleotide variant	NM_020826.3(SYT13):c.269C>T (p.Thr90Met)	not specified [RCV004463889]	uncertain significance	11	45255806	45255806	Human		name
407505851	CV3478355	single nucleotide variant	NM_020826.3(SYT13):c.277G>C (p.Glu93Gln)	not specified [RCV004670949]	uncertain significance	11	45255798	45255798	Human		name
597780547	CV3618972	single nucleotide variant	NM_020826.3(SYT13):c.244A>G (p.Ile82Val)	not specified [RCV004873830]	uncertain significance	11	45255831	45255831	Human		name
156287544	CV2301246	single nucleotide variant	NM_020826.3(SYT13):c.606G>T (p.Arg202Ser)	not specified [RCV004160430]	uncertain significance	11	45252661	45252661	Human		name
156296102	CV2310373	single nucleotide variant	NM_020826.3(SYT13):c.719C>T (p.Thr240Met)	not specified [RCV004163419]	uncertain significance	11	45252548	45252548	Human		name
156392776	CV2386672	single nucleotide variant	NM_020826.3(SYT13):c.371G>T (p.Arg124Met)	not specified [RCV004231010]	uncertain significance	11	45255704	45255704	Human		name
329360710	CV2439626	single nucleotide variant	NM_020826.3(SYT13):c.361C>G (p.Arg121Gly)	not specified [RCV004255643]	uncertain significance	11	45255714	45255714	Human		name
401770590	CV2685787	single nucleotide variant	NM_020826.3(SYT13):c.787G>T (p.Asp263Tyr)	not specified [RCV004294776]	uncertain significance	11	45252480	45252480	Human		name
401728959	CV2729927	single nucleotide variant	NM_020826.3(SYT13):c.851C>A (p.Pro284Gln)	not specified [RCV004332927]	uncertain significance	11	45246508	45246508	Human		name
401779276	CV2733281	single nucleotide variant	NM_020826.3(SYT13):c.527T>C (p.Phe176Ser)	not specified [RCV004332192]	uncertain significance	11	45254287	45254287	Human		name
401879811	CV2788520	single nucleotide variant	NM_020826.3(SYT13):c.644G>C (p.Arg215Pro)	not specified [RCV004359495]	uncertain significance	11	45252623	45252623	Human		name
401882934	CV2788657	single nucleotide variant	NM_020826.3(SYT13):c.427T>A (p.Cys143Ser)	not specified [RCV004361141]	uncertain significance	11	45254387	45254387	Human		name
405727299	CV3334850	single nucleotide variant	NM_020826.3(SYT13):c.499G>A (p.Asp167Asn)	not specified [RCV004463890]	uncertain significance	11	45254315	45254315	Human		name
405742251	CV3334851	single nucleotide variant	NM_020826.3(SYT13):c.776G>A (p.Arg259His)	not specified [RCV004465874]	uncertain significance	11	45252491	45252491	Human		name
405742256	CV3334852	single nucleotide variant	NM_020826.3(SYT13):c.800T>C (p.Val267Ala)	not specified [RCV004465875]	uncertain significance	11	45252467	45252467	Human		name
405742263	CV3334853	single nucleotide variant	NM_020826.3(SYT13):c.814G>T (p.Ala272Ser)	not specified [RCV004465876]	uncertain significance	11	45252453	45252453	Human		name
405742270	CV3334854	single nucleotide variant	NM_020826.3(SYT13):c.854C>G (p.Ser285Cys)	not specified [RCV004465877]	uncertain significance	11	45246505	45246505	Human		name
597780783	CV3618965	single nucleotide variant	NM_020826.3(SYT13):c.571T>C (p.Cys191Arg)	not specified [RCV004873824]	uncertain significance	11	45252696	45252696	Human		name
597780771	CV3618968	single nucleotide variant	NM_020826.3(SYT13):c.329C>T (p.Ala110Val)	not specified [RCV004873827]	uncertain significance	11	45255746	45255746	Human		name
597780642	CV3618971	single nucleotide variant	NM_020826.3(SYT13):c.871G>A (p.Val291Ile)	not specified [RCV004873829]	uncertain significance	11	45246488	45246488	Human		name
598180990	CV3923463	single nucleotide variant	NM_020826.3(SYT13):c.842C>T (p.Ala281Val)	not specified [RCV005286636]	likely benign	11	45252425	45252425	Human		name
598264200	CV3923465	single nucleotide variant	NM_020826.3(SYT13):c.565G>A (p.Gly189Arg)	not specified [RCV005280727]	uncertain significance	11	45252702	45252702	Human		name
155905449	CV2303114	single nucleotide variant	NM_020826.3(SYT13):c.1199C>T (p.Ser400Leu)	not specified [RCV004156890]	uncertain significance	11	45244134	45244134	Human		name
156272074	CV2315873	single nucleotide variant	NM_020826.3(SYT13):c.1193A>T (p.His398Leu)	not specified [RCV004171649]	uncertain significance	11	45244140	45244140	Human		name
156358541	CV2318515	single nucleotide variant	NM_020826.3(SYT13):c.1077G>C (p.Met359Ile)	not specified [RCV004173152]	uncertain significance	11	45244256	45244256	Human		name
597780787	CV3618963	single nucleotide variant	NM_020826.3(SYT13):c.1244G>A (p.Arg415His)	not specified [RCV004873823]	uncertain significance	11	45244089	45244089	Human		name
597794685	CV3618964	single nucleotide variant	NM_020826.3(SYT13):c.1210C>T (p.Arg404Cys)	not specified [RCV004877938]	uncertain significance	11	45244123	45244123	Human		name
597780779	CV3618966	single nucleotide variant	NM_020826.3(SYT13):c.1163G>A (p.Cys388Tyr)	not specified [RCV004873825]	uncertain significance	11	45244170	45244170	Human		name
597780775	CV3618967	single nucleotide variant	NM_020826.3(SYT13):c.1099G>A (p.Asp367Asn)	not specified [RCV004873826]	uncertain significance	11	45244234	45244234	Human		name
598180984	CV3923462	single nucleotide variant	NM_020826.3(SYT13):c.1013G>A (p.Arg338Gln)	not specified [RCV005286635]	likely benign	11	45244320	45244320	Human		name
598180995	CV3923464	single nucleotide variant	NM_020826.3(SYT13):c.1182C>A (p.Ser394Arg)	not specified [RCV005286637]	uncertain significance	11	45244151	45244151	Human		name

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