ClinVar Miner

List of variants in gene SYT3

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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_001160329.2(SYT3):c.1063-9C>G rs182688683 0.01025
NM_001160329.2(SYT3):c.676T>C (p.Tyr226His) rs188199665 0.00273
NM_001160329.2(SYT3):c.529G>A (p.Ala177Thr) rs141570463 0.00060
NM_001160329.2(SYT3):c.1353C>T (p.Thr451=) rs368077148 0.00017
NM_001160329.2(SYT3):c.1663G>A (p.Ala555Thr) rs569101828 0.00015
NM_001160329.2(SYT3):c.385G>A (p.Gly129Ser) rs747211137 0.00009
NM_001160329.2(SYT3):c.1267G>A (p.Val423Met) rs796357681 0.00007
NM_001160329.2(SYT3):c.289C>T (p.Arg97Cys) rs769285279 0.00007
NM_001160329.2(SYT3):c.862G>A (p.Gly288Ser) rs150387707 0.00007
NM_001160329.2(SYT3):c.745C>T (p.Arg249Trp) rs200843293 0.00004
NM_001160329.2(SYT3):c.1250C>T (p.Pro417Leu) rs768170643 0.00002
NM_001160329.2(SYT3):c.263G>T (p.Gly88Val) rs202245277 0.00002
NM_001160329.2(SYT3):c.32G>A (p.Arg11Gln) rs768504157 0.00002
NM_001160329.2(SYT3):c.746G>A (p.Arg249Gln) rs761715733 0.00002
NM_001160329.2(SYT3):c.122G>A (p.Arg41Gln) rs929145527 0.00001
NM_001160329.2(SYT3):c.1768G>A (p.Glu590Lys) rs760966257 0.00001
NM_001160329.2(SYT3):c.220G>A (p.Val74Met) rs753480602 0.00001
NM_001160329.2(SYT3):c.334G>A (p.Gly112Arg) rs751492794 0.00001
NM_001160329.2(SYT3):c.599T>A (p.Leu200Gln) rs749021783 0.00001
NM_001160329.2(SYT3):c.730C>T (p.Pro244Ser) rs762468525 0.00001
NM_001160329.2(SYT3):c.995A>G (p.Asn332Ser) rs775248622 0.00001
NM_001160329.2(SYT3):c.105G>C (p.Glu35Asp) rs1170440958
NM_001160329.2(SYT3):c.1087G>A (p.Val363Ile)
NM_001160329.2(SYT3):c.1126G>C (p.Glu376Gln)
NM_001160329.2(SYT3):c.1195G>A (p.Gly399Ser) rs2513824763
NM_001160329.2(SYT3):c.1195G>T (p.Gly399Cys)
NM_001160329.2(SYT3):c.1519G>A (p.Ala507Thr)
NM_001160329.2(SYT3):c.1530C>T (p.Ser510=)
NM_001160329.2(SYT3):c.1555G>T (p.Ala519Ser) rs754747321
NM_001160329.2(SYT3):c.1621G>A (p.Ala541Thr)
NM_001160329.2(SYT3):c.1636G>A (p.Gly546Ser)
NM_001160329.2(SYT3):c.22G>A (p.Asp8Asn) rs2513838641
NM_001160329.2(SYT3):c.250C>T (p.Arg84Trp) rs185774466
NM_001160329.2(SYT3):c.263G>C (p.Gly88Ala) rs202245277
NM_001160329.2(SYT3):c.272T>C (p.Val91Ala) rs2513832605
NM_001160329.2(SYT3):c.277G>A (p.Gly93Ser)
NM_001160329.2(SYT3):c.367G>A (p.Gly123Ser)
NM_001160329.2(SYT3):c.371A>T (p.His124Leu)
NM_001160329.2(SYT3):c.398A>G (p.His133Arg)
NM_001160329.2(SYT3):c.401C>T (p.Ala134Val)
NM_001160329.2(SYT3):c.439G>A (p.Glu147Lys)
NM_001160329.2(SYT3):c.443C>T (p.Pro148Leu) rs1018064840
NM_001160329.2(SYT3):c.461C>A (p.Ser154Tyr)
NM_001160329.2(SYT3):c.574G>C (p.Gly192Arg)
NM_001160329.2(SYT3):c.574G>T (p.Gly192Trp) rs376869372
NM_001160329.2(SYT3):c.575G>A (p.Gly192Glu) rs771656522
NM_001160329.2(SYT3):c.58C>T (p.Leu20Phe)
NM_001160329.2(SYT3):c.631G>C (p.Ala211Pro)
NM_001160329.2(SYT3):c.649G>T (p.Val217Phe)
NM_001160329.2(SYT3):c.664C>A (p.Pro222Thr) rs773437586
NM_001160329.2(SYT3):c.683C>T (p.Ala228Val)
NM_001160329.2(SYT3):c.689C>T (p.Pro230Leu) rs1235455746
NM_001160329.2(SYT3):c.88A>C (p.Asn30His) rs2513838476
NM_001160329.2(SYT3):c.923G>A (p.Arg308Gln)
NM_001160329.2(SYT3):c.938C>T (p.Ser313Leu)
NM_001160329.2(SYT3):c.949G>A (p.Val317Met) rs1405371056
NM_001160329.2(SYT3):c.997G>A (p.Gly333Ser)

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