CTNNB1 | Mutation | In-Frame | ENST00000349496.5 |
g.41265568_41266630del
|
c.9_427del
|
p.Ala5_Gln143del
|
damaging
| HepG2 |
CTNNB1 | Mutation | In-Frame | ENST00000349496.5 |
g.41266101_41266358del
|
c.98_242-87del
|
p.Ser33_Asp81delinsTyr
|
damaging
| MHCC97H |
CTNNB1 | Mutation | Missense | ENST00000349496.5 |
g.41266124A>G
|
c.121A>G
|
p.Thr41Ala
|
possibly damaging
| B1 |
CTNNB1 | Mutation | Missense | ENST00000349496.5 |
g.41266113C>G
|
c.110C>G
|
p.Ser37Cys
|
probably damaging
| SNU398 |
CTNNB1 | Mutation | Missense | ENST00000349496.5 |
g.41266104G>T
|
c.101G>T
|
p.Gly34Val
|
probably damaging
| Huh6 |