INSRR | Mutation | Missense | ENST00000368195.3 |
g.156823861G>A
|
c.320C>T
|
p.Thr107Met
|
possibly damaging
| HepG2 |
INSRR | Mutation | Missense | ENST00000368195.3 |
g.156816453C>G
|
c.1668G>C
|
p.Gln556His
|
probably damaging
| SNU475 |
INSRR | Mutation | Missense | ENST00000368195.3 |
g.156810796G>T
|
c.3763C>A
|
p.Arg1255Ser
|
benign
| PLC.PRF5 |
INSRR | Mutation | Missense | ENST00000368195.3 |
g.156811545G>A
|
c.3439C>T
|
p.Arg1147Cys
|
probably damaging
| SNU886 |
INSRR | CNA | Focal_Amplification | |
|
|
|
| MHCC97H |