Syt5 Variant Search Result - Rat Genome Database

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37 records found for search term Syt5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155980622	CV2243984	single nucleotide variant	NM_003180.3(SYT5):c.72C>A (p.His24Gln)	not specified [RCV004108482]	uncertain significance	19	55178970	55178970	Human		name
401731476	CV2674386	single nucleotide variant	NM_003180.3(SYT5):c.61C>A (p.Arg21Ser)	not specified [RCV004289256]	uncertain significance	19	55178981	55178981	Human		name
405742594	CV3334903	single nucleotide variant	NM_003180.3(SYT5):c.62G>C (p.Arg21Pro)	not specified [RCV004465926]	uncertain significance	19	55178980	55178980	Human		name
598181181	CV3923511	single nucleotide variant	NM_003180.3(SYT5):c.61C>G (p.Arg21Gly)	not specified [RCV005286670]	uncertain significance	19	55178981	55178981	Human		name
155926671	CV2395773	single nucleotide variant	NM_003180.3(SYT5):c.122T>C (p.Leu41Pro)	not specified [RCV004235302]	uncertain significance	19	55178326	55178326	Human		name
329387615	CV2464195	single nucleotide variant	NM_003180.3(SYT5):c.164G>A (p.Cys55Tyr)	not specified [RCV004273874]	uncertain significance	19	55178284	55178284	Human		name
405742573	CV3334900	single nucleotide variant	NM_003180.3(SYT5):c.106G>A (p.Val36Met)	not specified [RCV004465923]	uncertain significance	19	55178342	55178342	Human		name
407505910	CV3478377	single nucleotide variant	NM_003180.3(SYT5):c.154C>T (p.Arg52Trp)	not specified [RCV004670965]	uncertain significance	19	55178294	55178294	Human		name
597780603	CV3619026	single nucleotide variant	NM_003180.3(SYT5):c.145T>C (p.Cys49Arg)	not specified [RCV004873879]	uncertain significance	19	55178303	55178303	Human		name
598181176	CV3923510	single nucleotide variant	NM_003180.3(SYT5):c.244A>G (p.Ile82Val)	not specified [RCV005286669]	uncertain significance	19	55178204	55178204	Human		name
598181191	CV3923513	single nucleotide variant	NM_003180.3(SYT5):c.160A>G (p.Ser54Gly)	not specified [RCV005286672]	uncertain significance	19	55178288	55178288	Human		name
598264283	CV3923514	single nucleotide variant	NM_003180.3(SYT5):c.134G>A (p.Ser45Asn)	not specified [RCV005280741]	uncertain significance	19	55178314	55178314	Human		name
156371665	CV2200879	single nucleotide variant	NM_003180.3(SYT5):c.914A>G (p.Tyr305Cys)	not specified [RCV004081501]	uncertain significance	19	55174563	55174563	Human		name
156147531	CV2212840	single nucleotide variant	NM_003180.3(SYT5):c.397A>G (p.Met133Val)	not specified [RCV004091510]	uncertain significance	19	55175852	55175852	Human		name
156346427	CV2300564	single nucleotide variant	NM_003180.3(SYT5):c.916T>C (p.Tyr306His)	not specified [RCV004155528]	uncertain significance	19	55174561	55174561	Human		name
156387511	CV2372770	single nucleotide variant	NM_003180.3(SYT5):c.306G>C (p.Gln102His)	not specified [RCV004221957]	uncertain significance	19	55176071	55176071	Human		name
329387613	CV2464196	single nucleotide variant	NM_003180.3(SYT5):c.997A>G (p.Lys333Glu)	not specified [RCV004273875]	uncertain significance	19	55173648	55173648	Human		name
405742585	CV3334902	single nucleotide variant	NM_003180.3(SYT5):c.469C>G (p.Arg157Gly)	not specified [RCV004465925]	uncertain significance	19	55175780	55175780	Human		name
405742601	CV3334904	single nucleotide variant	NM_003180.3(SYT5):c.701G>A (p.Arg234Gln)	not specified [RCV004465927]	uncertain significance	19	55175179	55175179	Human		name
405742609	CV3334905	single nucleotide variant	NM_003180.3(SYT5):c.761G>C (p.Gly254Ala)	not specified [RCV004465928]	uncertain significance	19	55174947	55174947	Human		name
405742616	CV3334906	single nucleotide variant	NM_003180.3(SYT5):c.955G>A (p.Val319Ile)	not specified [RCV004465929]	uncertain significance	19	55174522	55174522	Human		name
405743093	CV3334907	single nucleotide variant	NM_003180.3(SYT5):c.973G>A (p.Glu325Lys)	not specified [RCV004465930]	uncertain significance	19	55173672	55173672	Human		name
407505913	CV3478378	single nucleotide variant	NM_003180.3(SYT5):c.407C>G (p.Ala136Gly)	not specified [RCV004670966]	uncertain significance	19	55175842	55175842	Human		name
407505917	CV3478379	single nucleotide variant	NM_003180.3(SYT5):c.490G>C (p.Val164Leu)	not specified [RCV004670967]	uncertain significance	19	55175759	55175759	Human		name
407530353	CV3478380	single nucleotide variant	NM_003180.3(SYT5):c.835G>A (p.Val279Ile)	not specified [RCV004681867]	uncertain significance	19	55174642	55174642	Human		name
407505919	CV3478381	single nucleotide variant	NM_003180.3(SYT5):c.650T>C (p.Val217Ala)	not specified [RCV004670968]	uncertain significance	19	55175230	55175230	Human		name
597780599	CV3619025	single nucleotide variant	NM_003180.3(SYT5):c.865A>G (p.Lys289Glu)	not specified [RCV004873878]	uncertain significance	19	55174612	55174612	Human		name
597780607	CV3619027	single nucleotide variant	NM_003180.3(SYT5):c.824C>T (p.Ser275Leu)	not specified [RCV004873880]	uncertain significance	19	55174884	55174884	Human		name
597780611	CV3619028	single nucleotide variant	NM_003180.3(SYT5):c.612T>A (p.Asn204Lys)	not specified [RCV004873881]	uncertain significance	19	55175268	55175268	Human		name
597780615	CV3619029	single nucleotide variant	NM_003180.3(SYT5):c.595G>T (p.Asp199Tyr)	not specified [RCV004873882]	uncertain significance	19	55175285	55175285	Human		name
597780618	CV3619030	single nucleotide variant	NM_003180.3(SYT5):c.695C>T (p.Ala232Val)	not specified [RCV004873883]	uncertain significance	19	55175185	55175185	Human		name
598181171	CV3923509	single nucleotide variant	NM_003180.3(SYT5):c.868G>A (p.Val290Met)	not specified [RCV005286668]	uncertain significance	19	55174609	55174609	Human		name
598264289	CV3923516	single nucleotide variant	NM_003180.3(SYT5):c.544C>T (p.Pro182Ser)	not specified [RCV005280742]	uncertain significance	19	55175336	55175336	Human		name
598181200	CV3923517	single nucleotide variant	NM_003180.3(SYT5):c.529T>G (p.Phe177Val)	not specified [RCV005286674]	uncertain significance	19	55175720	55175720	Human		name
156014926	CV2301642	single nucleotide variant	NM_003180.3(SYT5):c.1088A>G (p.Asn363Ser)	not specified [RCV004162544]	uncertain significance	19	55173557	55173557	Human		name
405742580	CV3334901	single nucleotide variant	NM_003180.3(SYT5):c.1075G>T (p.Asp359Tyr)	not specified [RCV004465924]	uncertain significance	19	55173570	55173570	Human		name
598181186	CV3923512	single nucleotide variant	NM_003180.3(SYT5):c.1054G>T (p.Ala352Ser)	not specified [RCV005286671]	uncertain significance	19	55173591	55173591	Human		name

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