NM_001110556.2(FLNA):c.65A>G (p.Asp22Gly)
|
rs782598729
|
0.00032
|
NM_001110556.2(FLNA):c.2954T>C (p.Val985Ala)
|
rs782804253
|
0.00018
|
NM_001110556.2(FLNA):c.3995A>G (p.Asp1332Gly)
|
rs200615848
|
0.00018
|
NM_001110556.2(FLNA):c.5764G>A (p.Val1922Met)
|
rs371366175
|
0.00011
|
NM_001110556.2(FLNA):c.4075C>T (p.Arg1359Cys)
|
rs369768801
|
0.00009
|
NM_001110556.2(FLNA):c.7066A>C (p.Ser2356Arg)
|
rs781823700
|
0.00009
|
NM_001110556.2(FLNA):c.5911A>T (p.Ile1971Phe)
|
rs190712778
|
0.00008
|
NM_001110556.2(FLNA):c.3106C>T (p.Arg1036Cys)
|
rs781844419
|
0.00007
|
NM_001110556.2(FLNA):c.7205T>C (p.Ile2402Thr)
|
rs202152952
|
0.00007
|
NM_001110556.2(FLNA):c.4060G>A (p.Asp1354Asn)
|
rs377390031
|
0.00006
|
NM_001110556.2(FLNA):c.5710G>A (p.Gly1904Ser)
|
rs782549964
|
0.00006
|
NM_001110556.2(FLNA):c.1621G>A (p.Glu541Lys)
|
rs743546
|
0.00004
|
NM_001110556.2(FLNA):c.6175G>A (p.Glu2059Lys)
|
rs782779958
|
0.00004
|
NM_001110556.2(FLNA):c.2925G>C (p.Lys975Asn)
|
rs375495397
|
0.00003
|
NM_001110556.2(FLNA):c.6871G>A (p.Gly2291Ser)
|
rs797044739
|
0.00003
|
NM_001110556.2(FLNA):c.1580G>A (p.Arg527His)
|
rs782450368
|
0.00002
|
NM_001110556.2(FLNA):c.1991G>A (p.Arg664His)
|
rs1271495778
|
0.00002
|
NM_001110556.2(FLNA):c.1096G>A (p.Ala366Thr)
|
rs781805670
|
0.00001
|
NM_001110556.2(FLNA):c.1114G>T (p.Val372Leu)
|
rs781848457
|
0.00001
|
NM_001110556.2(FLNA):c.1439C>T (p.Pro480Leu)
|
rs782168634
|
0.00001
|
NM_001110556.2(FLNA):c.2186G>A (p.Gly729Asp)
|
rs782330533
|
0.00001
|
NM_001110556.2(FLNA):c.2254G>A (p.Val752Ile)
|
rs1297013254
|
0.00001
|
NM_001110556.2(FLNA):c.3172C>T (p.Pro1058Ser)
|
rs1455557557
|
0.00001
|
NM_001110556.2(FLNA):c.4726G>A (p.Gly1576Arg)
|
rs797045044
|
0.00001
|
NM_001110556.2(FLNA):c.6719A>G (p.Lys2240Arg)
|
rs797045581
|
0.00001
|
NM_001110556.2(FLNA):c.7463C>A (p.Thr2488Asn)
|
rs909387820
|
0.00001
|
NM_001110556.2(FLNA):c.1208A>C (p.Tyr403Ser)
|
|
|
NM_001110556.2(FLNA):c.149C>G (p.Thr50Arg)
|
rs1557180204
|
|
NM_001110556.2(FLNA):c.1691+6G>A
|
rs1557178889
|
|
NM_001110556.2(FLNA):c.2588G>A (p.Arg863Gln)
|
|
|
NM_001110556.2(FLNA):c.2827G>A (p.Gly943Ser)
|
|
|
NM_001110556.2(FLNA):c.4122C>G (p.Asn1374Lys)
|
rs2148111433
|
|
NM_001110556.2(FLNA):c.4255G>A (p.Ala1419Thr)
|
|
|
NM_001110556.2(FLNA):c.6146G>A (p.Arg2049His)
|
rs1557176118
|
|
NM_001110556.2(FLNA):c.7370C>T (p.Ala2457Val)
|
|
|