NM_001291303.3(FAT4):c.10810A>C (p.Ile3604Leu)
|
rs76491994
|
0.00978
|
NM_001291303.3(FAT4):c.12986A>G (p.Asp4329Gly)
|
rs114234553
|
0.00519
|
NM_001291303.3(FAT4):c.10853C>T (p.Thr3618Met)
|
rs111423173
|
0.00407
|
NM_001291303.3(FAT4):c.12855T>C (p.Asp4285=)
|
rs78040862
|
0.00365
|
NM_001291303.3(FAT4):c.7358G>T (p.Ser2453Ile)
|
rs72914988
|
0.00327
|
NM_001291303.3(FAT4):c.4303A>G (p.Ile1435Val)
|
rs142747281
|
0.00288
|
NM_001291303.3(FAT4):c.14666G>A (p.Arg4889Lys)
|
rs35845544
|
0.00261
|
NM_001291303.3(FAT4):c.7935C>T (p.Asp2645=)
|
rs146157250
|
0.00244
|
NM_001291303.3(FAT4):c.524G>T (p.Arg175Leu)
|
rs143534324
|
0.00217
|
NM_001291303.3(FAT4):c.5921-14C>T
|
rs190218898
|
0.00151
|
NM_001291303.3(FAT4):c.9810G>A (p.Val3270=)
|
rs139518045
|
0.00062
|
NM_001291303.3(FAT4):c.12769G>A (p.Glu4257Lys)
|
rs143513466
|
0.00056
|
NM_001291303.3(FAT4):c.3768A>G (p.Arg1256=)
|
rs114652326
|
0.00042
|
NM_001291303.3(FAT4):c.1698C>T (p.Ala566=)
|
rs370653820
|
0.00033
|
NM_001291303.3(FAT4):c.14718C>T (p.Gly4906=)
|
rs147617723
|
0.00030
|
NM_001291303.3(FAT4):c.1959C>T (p.Ala653=)
|
rs191491571
|
0.00021
|
NM_001291303.3(FAT4):c.7131A>G (p.Ala2377=)
|
rs138403046
|
0.00014
|
NM_001291303.3(FAT4):c.11358A>G (p.Glu3786=)
|
rs369625076
|
0.00007
|
NM_001291303.3(FAT4):c.12381G>A (p.Val4127=)
|
rs377051363
|
0.00007
|
NM_001291303.3(FAT4):c.3351G>A (p.Ser1117=)
|
rs769768427
|
0.00004
|
NM_001291303.3(FAT4):c.12870G>C (p.Gly4290=)
|
rs779040505
|
0.00003
|
NM_001291303.3(FAT4):c.4530T>C (p.Tyr1510=)
|
rs368207419
|
0.00003
|
NM_001291303.3(FAT4):c.4542C>T (p.Asn1514=)
|
rs199793434
|
0.00003
|
NM_001291303.3(FAT4):c.9696G>A (p.Ala3232=)
|
rs142877205
|
0.00002
|
NM_001291303.3(FAT4):c.10395C>T (p.Thr3465=)
|
rs768300702
|
0.00001
|
NM_001291303.3(FAT4):c.12299+6G>C
|
rs541775780
|
0.00001
|
NM_001291303.3(FAT4):c.5308-19G>A
|
rs1369164587
|
0.00001
|
NM_001291303.3(FAT4):c.5424C>G (p.Ser1808=)
|
rs200354953
|
0.00001
|
NM_001291303.3(FAT4):c.960G>A (p.Ser320=)
|
rs1057523940
|
0.00001
|
NM_001291303.3(FAT4):c.10155T>A (p.Gly3385=)
|
rs780130895
|
|
NM_001291303.3(FAT4):c.12927T>C (p.Phe4309=)
|
rs146058039
|
|
NM_001291303.3(FAT4):c.4944G>A (p.Val1648=)
|
|
|
NM_001291303.3(FAT4):c.5322C>T (p.Leu1774=)
|
|
|
NM_001291303.3(FAT4):c.5921-18dup
|
rs535120107
|
|
NM_001291303.3(FAT4):c.738C>T (p.Asn246=)
|
|
|
NM_001291303.3(FAT4):c.7466C>T (p.Ala2489Val)
|
rs144853732
|
|
NM_001291303.3(FAT4):c.7593C>T (p.Asn2531=)
|
rs367971071
|
|
NM_001291303.3(FAT4):c.8985C>T (p.Thr2995=)
|
rs1057521481
|
|