Genename Variants
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6128632C>T,c.3952G>A,p.V1318M
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6128509C>T,c.4075G>A,p.E1359K
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6128446T>C,c.4138A>G,p.I1380V
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6128443T>C,c.4141A>G,p.T1381A
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6128438C>A,c.4146G>T,p.L1382L
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6128388C>T,c.4196G>A,p.R1399H
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6128170C>G,c.4414G>C,p.D1472H
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6128076A>G,c.4508T>C,p.L1503P
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6128067G>A,c.4517C>T,p.S1506L
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6127891C>A,c.4693G>T,p.V1565L
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6127833T>C,c.4751A>G,p.Y1584C
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6127570C>T,c.5014G>A,p.G1672R
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6125802A>T,c.5191T>A,p.S1731T
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6125715C>T,c.5278G>A,p.V1760I
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6122734C>T,c.5533G>A,p.D1845N
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6105380T>C,c.5851A>G,p.T1951A
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6103733C>T,c.6104G>A,p.G2035D
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6103650G>A,c.6187C>T,p.P2063S
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6103202G>A,c.6424C>T,p.L2142F
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6103193G>A,c.6433C>T,p.P2145S
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6103094C>A,c.6532G>T,p.A2178S
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6103072C>T,c.6554G>A,p.R2185Q
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6094279G>A,c.6908C>T,p.T2303M
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6092390G>A,c.7007C>T,p.P2336L
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6085353G>T,c.7361C>A,p.T2454N
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6085324G>A,c.7390C>T,p.R2464C
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6080794G>A,c.7519C>T,p.R2507W
VWF(NM_000552,von Willebrand factor,2813aa) g.12:6078535G>A,c.7571C>T,p.P2524L
This is an excerpt of data-sheet including the published polymorphism sites observed in our studies. For the complete variant lists and potential collaboration, please contact huh@cougarlab.org