CUBN | Mutation | Missense | ENST00000377833.4 |
g.16916460C>T
|
c.9149G>A
|
p.Ser3050Asn
|
possibly damaging
| HepG2 |
CUBN | Mutation | Missense | ENST00000377833.4 |
g.16982150C>T
|
c.5429G>A
|
p.Arg1810Gln
|
probably damaging
| HCC.1.2 |
CUBN | Mutation | Missense | ENST00000377833.4 |
g.16916380C>T
|
c.9229G>A
|
p.Glu3077Lys
|
benign
| Huh6 |
CUBN | Mutation | Missense | ENST00000377833.4 |
g.16873384T>A
|
c.10395A>T
|
p.Leu3465Phe
|
probably damaging
| SNU878 |