FAT3 | Mutation | Missense | ENST00000298047.6 |
g.92534220G>T
|
c.8041G>T
|
p.Val2681Leu
|
benign
| HCC.3 |
FAT3 | Mutation | Missense | ENST00000298047.6 |
g.92088388A>G
|
c.3110A>G
|
p.Asn1037Ser
|
probably damaging
| HCC.1.1 |
FAT3 | Mutation | Missense | ENST00000298047.6 |
g.92088189G>C
|
c.2911G>C
|
p.Val971Leu
|
probably damaging
| SNU475 |
FAT3 | Mutation | Missense | ENST00000298047.6 |
g.92600259G>A
|
c.12011G>A
|
p.Ser4004Asn
|
possibly damaging
| PLC.PRF5 |
FAT3 | Mutation | Missense | ENST00000298047.6 |
g.92533669C>T
|
c.7490C>T
|
p.Ser2497Leu
|
probably damaging
| Huh6 |
FAT3 | Mutation | Missense | ENST00000298047.6 |
g.92615933G>C
|
c.12311G>C
|
p.Arg4104Pro
|
possibly damaging
| Huh6 |
FAT3 | Mutation | Missense | ENST00000298047.6 |
g.92088460G>T
|
c.3182G>T
|
p.Ser1061Ile
|
probably damaging
| Huh1 |
FAT3 | Mutation | Missense | ENST00000298047.6 |
g.92533002T>G
|
c.6823T>G
|
p.Leu2275Val
|
benign
| SNU354 |
FAT3 | Mutation | Truncating | ENST00000298047.6 |
g.92430546A>G
|
c.3608-4A>G
|
p.?
|
damaging
| JHH7 |