FAT4 | Mutation | Missense | ENST00000394329.3 |
g.126412333G>A
|
c.14356G>A
|
p.Gly4786Arg
|
probably damaging
| HepG2 |
FAT4 | Mutation | Missense | ENST00000394329.3 |
g.126336222C>A
|
c.6104C>A
|
p.Ala2035Asp
|
probably damaging
| SNU387 |
FAT4 | Mutation | Missense | ENST00000394329.3 |
g.126373318G>A
|
c.11147G>A
|
p.Arg3716His
|
probably damaging
| Li7 |
FAT4 | Mutation | Missense | ENST00000394329.3 |
g.126242209C>A
|
c.4643C>A
|
p.Thr1548Lys
|
probably damaging
| JHH2 |