基因名 突变
PLXNB2(NM_012401,plexin B2,1838aa) g.22:50720671G>A,c.3059C>T,p.A1020V
PLXNB2(NM_012401,plexin B2,1838aa) g.22:50720408C>T,c.3220G>A,p.E1074K
PLXNB2(NM_012401,plexin B2,1838aa) g.22:50719246G>A,c.3920C>T,p.P1307L
PLXNB2(NM_012401,plexin B2,1838aa) g.22:50719238G>T,c.3928C>A,p.P1310T
PLXNB2(NM_012401,plexin B2,1838aa) g.22:50719174T>C,c.3992A>G,p.N1331S
PLXNB2(NM_012401,plexin B2,1838aa) g.22:50717060G>A,c.4612C>T,p.R1538W
PLXNB2(NM_012401,plexin B2,1838aa) g.22:50716384G>A,c.4946C>T,p.A1649V
PLXNB2(NM_012401,plexin B2,1838aa) g.22:50714389G>A,c.5341C>T,p.H1781Y
PLXNB2(NM_012401,plexin B2,1838aa) g.22:50714320C>T,c.5410G>A,p.E1804K
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48465278A>C,c.743T>G,p.V248G
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48465206C>T,c.815G>A,p.R272H
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48465168T>C,c.853A>G,p.R285G
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48465113G>C,c.908C>G,p.P303R
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48465030G>A,c.991C>T,p.R331W
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48464338G>A,c.1126C>T,p.P376S
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48464292G>A,c.1172C>T,p.P391L
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48463856G>A,c.1303C>T,p.P435S
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48463799T>G,c.1360A>C,p.S454R
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48462318C>T,c.1858G>A,p.A620T
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48461627G>C,c.2068C>G,p.P690A
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48461530G>A,c.2165C>T,p.S722L
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48461192C>T,c.2503G>A,p.V835M
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48461187C>G,c.2508G>C,p.K836N
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48461135C>T,c.2560G>A,p.E854K
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48460382C>T,c.2899G>A,p.V967I
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48459873C>T,c.3034G>A,p.A1012T
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48459730C>T,c.3092G>A,p.R1031H
PLXNB1(NM_002673,plexin B1,2135aa) g.3:48459661C>T,c.3161G>A,p.R1054Q
注意:这是数据表的摘录,包括在我们的研究中观察到的已发表的多态性位点。 如需完整的变体列表和潜在合作,请联系 huh@cougarlab.org