ADAMTS4 | Mutation | Missense | ENST00000367995.3 |
g.161168120A>G
|
c.298T>C
|
p.Ser100Pro
|
benign
| HCC.3 |
ADAMTS4 | Mutation | Missense | ENST00000367996.5 |
g.161163477C>T
|
c.1688G>A
|
p.Arg563His
|
possibly damaging
| PLC.PRF5 |
ADAMTS4 | Mutation | Missense | ENST00000367996.5 |
g.161163805C>A
|
c.1468G>T
|
p.Ala490Ser
|
probably damaging
| PLC.PRF5 |
ADAMTS4 | Mutation | Missense | ENST00000367995.3 |
g.161168167C>T
|
c.251G>A
|
p.Arg84His
|
probably damaging
| MHCC97H |
ADAMTS4 | CNA | Focal_Amplification | |
|
|
|
| SNU368 |