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Variants search result for Homo sapiens
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42 records found for search term Syt9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8653189CV129764single nucleotide variantNM_175733.3(SYT9):c.1044+22478C>GLung cancer [RCV000110251]uncertain significance1173364197336419Humanname
8653194CV129769single nucleotide variantNM_175733.3(SYT9):c.1468-22747A>TLung cancer [RCV000110256]uncertain significance1174440457444045Humanname
401874096CV2757828single nucleotide variantNM_175733.4(SYT9):c.10G>A (p.Ala4Thr)not specified [RCV004336975]uncertain significance1172521967252196Humanname
155929419CV2389155single nucleotide variantNM_175733.4(SYT9):c.50C>T (p.Ala17Val)not specified [RCV004235483]uncertain significance1172522367252236Humanname
156384292CV2231044single nucleotide variantNM_175733.4(SYT9):c.217G>A (p.Val73Ile)not specified [RCV004094276]uncertain significance1173031107303110Humanname
401760744CV2695145single nucleotide variantNM_175733.4(SYT9):c.149T>C (p.Ile50Thr)not specified [RCV004303299]uncertain significance1173030427303042Humanname
405742629CV3334932single nucleotide variantNM_175733.4(SYT9):c.109C>G (p.Leu37Val)not specified [RCV004465955]uncertain significance1172522957252295Humanname
407530367CV3478395single nucleotide variantNM_175733.4(SYT9):c.274A>G (p.Lys92Glu)not specified [RCV004681874]uncertain significance1173031677303167Humanname
407505951CV3478399single nucleotide variantNM_175733.4(SYT9):c.119G>A (p.Arg40His)not specified [RCV004670977]uncertain significance1172523057252305Humanname
597780702CV3619052single nucleotide variantNM_175733.4(SYT9):c.103T>G (p.Tyr35Asp)not specified [RCV004873905]uncertain significance1172522897252289Humanname
597780709CV3619054single nucleotide variantNM_175733.4(SYT9):c.187G>C (p.Gly63Arg)not specified [RCV004873907]uncertain significance1173030807303080Humanname
156184305CV2195478single nucleotide variantNM_175733.4(SYT9):c.944G>A (p.Arg315His)not specified [RCV004082703]uncertain significance1173138417313841Humanname
156177824CV2201541single nucleotide variantNM_175733.4(SYT9):c.454G>A (p.Val152Ile)not specified [RCV004080032]likely benign1173033477303347Humanname
155931249CV2297292single nucleotide variantNM_175733.4(SYT9):c.564A>C (p.Lys188Asn)not specified [RCV004152955]uncertain significance1173134617313461Humanname
401723389CV2674935single nucleotide variantNM_175733.4(SYT9):c.302A>G (p.Tyr101Cys)not specified [RCV004296247]uncertain significance1173031957303195Humanname
401758663CV2700680single nucleotide variantNM_175733.4(SYT9):c.802C>T (p.Arg268Trp)not specified [RCV004313395]uncertain significance1173136997313699Humanname
401862550CV2768379single nucleotide variantNM_175733.4(SYT9):c.847C>G (p.Pro283Ala)not specified [RCV004350631]uncertain significance1173137447313744Humanname
401870619CV2769253single nucleotide variantNM_175733.4(SYT9):c.457C>T (p.Arg153Cys)not specified [RCV004357267]uncertain significance1173033507303350Humanname
401894792CV2785285single nucleotide variantNM_175733.4(SYT9):c.319A>G (p.Asn107Asp)not specified [RCV004357047]uncertain significance1173032127303212Humanname
405742649CV3334935single nucleotide variantNM_175733.4(SYT9):c.339G>C (p.Glu113Asp)not specified [RCV004465958]uncertain significance1173032327303232Humanname
405742670CV3334938single nucleotide variantNM_175733.4(SYT9):c.343T>C (p.Phe115Leu)not specified [RCV004465961]uncertain significance1173032367303236Humanname
405742677CV3334939single nucleotide variantNM_175733.4(SYT9):c.637G>A (p.Gly213Arg)not specified [RCV004465962]uncertain significance1173135347313534Humanname
405742682CV3334940single nucleotide variantNM_175733.4(SYT9):c.644G>A (p.Arg215Gln)not specified [RCV004465963]likely benign1173135417313541Humanname
407530369CV3478396single nucleotide variantNM_175733.4(SYT9):c.359C>T (p.Thr120Met)not specified [RCV004681875]uncertain significance1173032527303252Humanname
407505948CV3478397single nucleotide variantNM_175733.4(SYT9):c.708G>C (p.Gln236His)not specified [RCV004670976]uncertain significance1173136057313605Humanname
597780706CV3619053single nucleotide variantNM_175733.4(SYT9):c.698A>T (p.Asp233Val)not specified [RCV004873906]uncertain significance1173135957313595Humanname
598181261CV3923531single nucleotide variantNM_175733.4(SYT9):c.753C>G (p.Asp251Glu)not specified [RCV005286686]uncertain significance1173136507313650Humanname
8634365CV89585single nucleotide variantNM_175733.3(SYT9):c.733G>A (p.Val245Ile)Malignant melanoma [RCV000069682]not provided1173136307313630Humanname
156399498CV2205155single nucleotide variantNM_175733.4(SYT9):c.1339G>A (p.Val447Ile)not specified [RCV004077751]uncertain significance1174205077420507Humanname
156228806CV2234925single nucleotide variantNM_175733.4(SYT9):c.1336C>T (p.Arg446Cys)not specified [RCV004113129]uncertain significance1174181277418127Humanname
155921296CV2240505single nucleotide variantNM_175733.4(SYT9):c.1462G>C (p.Val488Leu)not specified [RCV004119170]uncertain significance1174206307420630Humanname
156022864CV2273702single nucleotide variantNM_175733.4(SYT9):c.1302A>T (p.Gln434His)not specified [RCV004132356]uncertain significance1174180937418093Humanname
156153028CV2374810single nucleotide variantNM_175733.4(SYT9):c.1432C>T (p.Arg478Trp)not specified [RCV004227846]uncertain significance1174206007420600Humanname
329355936CV2434397single nucleotide variantNM_175733.4(SYT9):c.1351G>A (p.Glu451Lys)not specified [RCV004252063]uncertain significance1174205197420519Humanname
329368796CV2450420single nucleotide variantNM_175733.4(SYT9):c.1063G>A (p.Glu355Lys)not specified [RCV004265348]uncertain significance1174160607416060Humanname
405742638CV3334933single nucleotide variantNM_175733.4(SYT9):c.1117A>G (p.Ile373Val)not specified [RCV004465956]uncertain significance1174161147416114Humanname
405742642CV3334934single nucleotide variantNM_175733.4(SYT9):c.1406A>T (p.His469Leu)not specified [RCV004465957]uncertain significance1174205747420574Humanname
407530371CV3478398single nucleotide variantNM_175733.4(SYT9):c.1288G>A (p.Glu430Lys)not specified [RCV004681876]uncertain significance1174180797418079Humanname
597780698CV3619051single nucleotide variantNM_175733.4(SYT9):c.1381G>A (p.Glu461Lys)not specified [RCV004873904]uncertain significance1174205497420549Humanname
597780713CV3619055single nucleotide variantNM_175733.4(SYT9):c.1030G>A (p.Glu344Lys)not specified [RCV004873908]uncertain significance1173139277313927Humanname
598181256CV3923530single nucleotide variantNM_175733.4(SYT9):c.1049A>G (p.Asn350Ser)not specified [RCV005286685]uncertain significance1174160467416046Humanname
8634370CV89590single nucleotide variantNM_175733.3(SYT9):c.1205G>A (p.Arg402Gln)Malignant melanoma [RCV000069687]not provided1174179967417996Humanname