Genename Variants
SNX25(NM_031953,sorting nexin 25,840aa) g.4:186241986G>A,c.952G>A,p.E318K
SNX25(NM_031953,sorting nexin 25,840aa) g.4:186188132C>T,c.422C>T,p.P141L
SNX25(NM_031953,sorting nexin 25,840aa) g.4:186185731C>T,c.379C>T,p.R127C
SNX22(NM_024798,sorting nexin 22,193aa) g.15:64446700T>G,c.575T>G,p.M192R
SNX22(NM_024798,sorting nexin 22,193aa) g.15:64446589C>T,c.464C>T,p.S155L
SNX22(NM_024798,sorting nexin 22,193aa) g.15:64445532A>G,c.353A>G,p.N118S
SNX21(NM_001042633,sorting nexin family member 21,158aa) g.20:44462924G>A,c.106G>A,p.A36T
SNX21(NM_001042633,sorting nexin family member 21,158aa) g.20:44462904A>G,c.86A>G,p.E29G
SNX20(NM_153337,sorting nexin 20,129aa) g.16:50711334G>A,c.104C>T,p.P35L
SNX20(NM_153337,sorting nexin 20,129aa) g.16:50709755G>A,c.208C>T,p.R70C
SNX20(NM_153337,sorting nexin 20,129aa) g.16:50703016C>T,c.326G>A,p.R109H
SNX1(NM_003099,sorting nexin 1,522aa) g.15:64428559G>A,c.1396G>A,p.D466N
SNX1(NM_003099,sorting nexin 1,522aa) g.15:64422118C>A,c.811C>A,p.P271T
SNX1(NM_003099,sorting nexin 1,522aa) g.15:64410418C>T,c.374C>T,p.S125L
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130785593C>A,c.242G>T,p.R81L
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130785386T>C,c.449A>G,p.D150G
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130784886T>C,c.949A>G,p.S317G
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130784838G>A,c.997C>T,p.H333Y
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130784754C>G,c.1081G>C,p.V361L
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130784694C>T,c.1141G>A,p.G381S
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130784647G>C,c.1188C>G,p.D396E
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130784616T>C,c.1219A>G,p.S407G
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130784589C>A,c.1246G>T,p.G416C
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130784396G>A,c.1439C>T,p.P480L
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130784168G>A,c.1667C>T,p.T556I
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130781563A>G,c.1778T>C,p.L593P
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130780225C>A,c.1854G>T,p.L618F
SNX19(NM_014758,sorting nexin 19,992aa) g.11:130780032G>T,c.1915C>A,p.Q639K
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