NM_021625.5(TRPV4):c.55C>T (p.Pro19Ser)
|
rs3742030
|
0.03470
|
NM_021625.5(TRPV4):c.805C>T (p.Arg269Cys)
|
rs267607146
|
0.00001
|
NM_021625.5(TRPV4):c.943C>T (p.Arg315Trp)
|
rs267607143
|
0.00001
|
NM_021625.4(TRPV4):c.[2481_2484delCCGC;2486T>A]
|
|
|
NM_021625.5(TRPV4):c.1412_1414del (p.Phe471del)
|
rs515726154
|
|
NM_021625.5(TRPV4):c.1625C>A (p.Ser542Tyr)
|
rs387906902
|
|
NM_021625.5(TRPV4):c.1781G>A (p.Arg594His)
|
rs77975504
|
|
NM_021625.5(TRPV4):c.1805A>G (p.Tyr602Cys)
|
rs267607150
|
|
NM_021625.5(TRPV4):c.1847G>A (p.Arg616Gln)
|
rs121912632
|
|
NM_021625.5(TRPV4):c.1853T>C (p.Leu618Pro)
|
rs515726163
|
|
NM_021625.5(TRPV4):c.1858G>A (p.Val620Ile)
|
rs121912633
|
|
NM_021625.5(TRPV4):c.2146G>T (p.Ala716Ser)
|
rs121912635
|
|
NM_021625.5(TRPV4):c.2219C>T (p.Thr740Ile)
|
rs387906906
|
|
NM_021625.5(TRPV4):c.232G>T (p.Gly78Trp)
|
rs397514474
|
|
NM_021625.5(TRPV4):c.2389G>A (p.Glu797Lys)
|
rs267607149
|
|
NM_021625.5(TRPV4):c.2395C>G (p.Pro799Ala)
|
rs267607147
|
|
NM_021625.5(TRPV4):c.2395C>T (p.Pro799Ser)
|
rs267607147
|
|
NM_021625.5(TRPV4):c.2396C>G (p.Pro799Arg)
|
rs121912637
|
|
NM_021625.5(TRPV4):c.2396C>T (p.Pro799Leu)
|
rs121912637
|
|
NM_021625.5(TRPV4):c.2396_2412del (p.Pro799fs)
|
rs515726166
|
|
NM_021625.5(TRPV4):c.266C>T (p.Thr89Ile)
|
rs397514473
|
|
NM_021625.5(TRPV4):c.547G>A (p.Glu183Lys)
|
rs387906324
|
|
NM_021625.5(TRPV4):c.557G>A (p.Arg186Gln)
|
rs397514494
|
|
NM_021625.5(TRPV4):c.590A>G (p.Lys197Arg)
|
rs387906903
|
|
NM_021625.5(TRPV4):c.694C>T (p.Arg232Cys)
|
rs387906904
|
|
NM_021625.5(TRPV4):c.806G>A (p.Arg269His)
|
rs267607144
|
|
NM_021625.5(TRPV4):c.809G>T (p.Gly270Val)
|
rs387907220
|
|
NM_021625.5(TRPV4):c.812G>C (p.Arg271Pro)
|
rs387907219
|
|
NM_021625.5(TRPV4):c.819C>G (p.Phe273Leu)
|
rs515726170
|
|
NM_021625.5(TRPV4):c.826A>G (p.Lys276Glu)
|
rs387906907
|
|
NM_021625.5(TRPV4):c.832G>A (p.Glu278Lys)
|
rs267607148
|
|
NM_021625.5(TRPV4):c.946C>T (p.Arg316Cys)
|
rs267607145
|
|
NM_021625.5(TRPV4):c.947G>A (p.Arg316His)
|
rs387906905
|
|
NM_021625.5(TRPV4):c.991A>T (p.Ile331Phe)
|
rs121912636
|
|
NM_021625.5(TRPV4):c.998A>G (p.Asp333Gly)
|
rs121912634
|
|