AXIN1 | Mutation | In-Frame | ENST00000262320.3 |
g.396700_396744del
|
c.282_326del
|
p.Asp94_Gln108del
|
damaging
| JHH7 |
AXIN1 | Mutation | Missense | ENST00000262320.3 |
g.364669C>A
|
c.893G>T
|
p.Arg298Leu
|
probably damaging
| Huh1 |
AXIN1 | Mutation | Missense | ENST00000262320.3 |
g.397011C>A
|
c.15G>T
|
p.Glu5Asp
|
benign
| JHH6 |
AXIN1 | Mutation | Truncating | ENST00000262320.3 |
g.396590G>A
|
c.436C>T
|
p.Arg146X
|
damaging
| Hep3B |
AXIN1 | Mutation | Truncating | ENST00000262320.3 |
g.360044_360056del
|
c.1033_1045del
|
p.Pro345ValfsX65
|
damaging
| SNU423 |
AXIN1 | Mutation | Truncating | ENST00000262320.3 |
g.364656_364668del
|
c.894_906del
|
p.Glu299ProfsX111
|
damaging
| Huh1 |
AXIN1 | Mutation | Truncating | ENST00000262320.3 |
g.397008_397009del
|
c.17_18del
|
p.Gln6ArgfsX22
|
damaging
| JHH5 |
AXIN1 | Mutation | Truncating | ENST00000262320.3 |
g.397010G>A
|
c.16C>T
|
p.Gln6X
|
damaging
| JHH6 |
AXIN1 | Mutation | Truncating | ENST00000262320.3 |
g.347963T>A
|
c.1543A>T
|
p.Lys515X
|
damaging
| SNU354 |
AXIN1 | Mutation | Truncating | ENST00000262320.3 |
g.396476G>A
|
c.550C>T
|
p.Gln184X
|
damaging
| SNU368 |
AXIN1 | CNA | Homozygous_Deletion | |
|
|
|
| HCC.3 |
AXIN1 | CNA | Homozygous_Deletion | |
|
|
|
| HCC.1.1 |
AXIN1 | CNA | Homozygous_Deletion | |
|
|
|
| SNU475 |
AXIN1 | CNA | Homozygous_Deletion | |
|
|
|
| PLC.PRF5 |
AXIN1 | CNA | Homozygous_Deletion | |
|
|
|
| SNU878 |