NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val)
|
rs145639192
|
0.00145
|
NM_001291303.3(FAT4):c.7103C>A (p.Ala2368Glu)
|
rs116568645
|
0.00066
|
NM_001291303.3(FAT4):c.11260A>G (p.Ser3754Gly)
|
rs79909102
|
0.00061
|
NM_001291303.3(FAT4):c.185G>C (p.Gly62Ala)
|
rs201009019
|
0.00045
|
NM_001291303.3(FAT4):c.12647G>A (p.Arg4216His)
|
rs148170326
|
0.00041
|
NM_001291303.3(FAT4):c.5597C>T (p.Thr1866Met)
|
rs141773516
|
0.00033
|
NM_001291303.3(FAT4):c.8821A>G (p.Thr2941Ala)
|
rs151209952
|
0.00019
|
NM_001291303.3(FAT4):c.10643A>G (p.Tyr3548Cys)
|
rs79726583
|
0.00015
|
NM_001291303.3(FAT4):c.6094A>G (p.Thr2032Ala)
|
rs147314754
|
0.00015
|
NM_001291303.3(FAT4):c.8313T>C (p.Asn2771=)
|
rs148344513
|
0.00012
|
NM_001291303.3(FAT4):c.9451G>A (p.Ala3151Thr)
|
rs200702071
|
0.00011
|
NM_001291303.3(FAT4):c.12085G>A (p.Ala4029Thr)
|
rs140544054
|
0.00009
|
NM_001291303.3(FAT4):c.7312G>T (p.Val2438Phe)
|
rs376545643
|
0.00009
|
NM_001291303.3(FAT4):c.4543G>A (p.Val1515Met)
|
rs773912269
|
0.00006
|
NM_001291303.3(FAT4):c.4081G>A (p.Gly1361Arg)
|
rs200361960
|
0.00004
|
NM_001291303.3(FAT4):c.11134G>T (p.Asp3712Tyr)
|
rs769490380
|
0.00001
|
NM_001291303.3(FAT4):c.14273C>T (p.Pro4758Leu)
|
rs1405492776
|
0.00001
|
NM_001291303.3(FAT4):c.2290G>A (p.Val764Ile)
|
rs746714727
|
0.00001
|
NM_001291303.3(FAT4):c.8216C>A (p.Ser2739Tyr)
|
rs748854090
|
0.00001
|
NM_001291303.3(FAT4):c.8753A>G (p.Glu2918Gly)
|
rs762206992
|
0.00001
|
NM_001291303.3(FAT4):c.9152C>A (p.Ser3051Tyr)
|
rs866162018
|
0.00001
|
NM_001291303.3(FAT4):c.11706T>G (p.Asp3902Glu)
|
rs774612831
|
|
NM_001291303.3(FAT4):c.12479+3A>G
|
rs2126083898
|
|
NM_001291303.3(FAT4):c.13399G>A (p.Val4467Met)
|
rs1215405311
|
|
NM_001291303.3(FAT4):c.14404C>T (p.Pro4802Ser)
|
rs1727627190
|
|
NM_001291303.3(FAT4):c.3808A>C (p.Ile1270Leu)
|
|
|
NM_001291303.3(FAT4):c.4143A>T (p.Glu1381Asp)
|
|
|
NM_001291303.3(FAT4):c.4432A>G (p.Ile1478Val)
|
rs200565115
|
|
NM_001291303.3(FAT4):c.5161A>G (p.Thr1721Ala)
|
rs904769252
|
|
NM_001291303.3(FAT4):c.5355T>G (p.Asp1785Glu)
|
rs778606448
|
|
NM_001291303.3(FAT4):c.5944A>G (p.Ser1982Gly)
|
rs746510253
|
|
NM_001291303.3(FAT4):c.6515A>C (p.Asp2172Ala)
|
rs1328569048
|
|
NM_001291303.3(FAT4):c.7466C>A (p.Ala2489Glu)
|
rs144853732
|
|
NM_001291303.3(FAT4):c.913A>T (p.Ile305Phe)
|
rs1553958385
|
|
NM_001291303.3(FAT4):c.9517T>G (p.Trp3173Gly)
|
|
|