BAI2 | Mutation | Missense | ENST00000257070.4 |
g.32203866G>A
|
c.2707C>T
|
p.His903Tyr
|
probably damaging
| HepG2 |
BAI2 | Mutation | Missense | ENST00000257070.4 |
g.32205768C>G
|
c.2001G>C
|
p.Gln667His
|
possibly damaging
| Huh7 |
BAI2 | Mutation | Missense | ENST00000257070.4 |
g.32208558C>T
|
c.1133G>A
|
p.Arg378His
|
probably damaging
| JHH7 |
BAI2 | Mutation | Missense | ENST00000373658.3 |
g.32193079C>T
|
c.4700G>A
|
p.Arg1567Gln
|
possibly damaging
| SNU886 |
BAI2 | Mutation | Truncating | ENST00000257070.4 |
g.32203929T>G
|
c.2646-2A>C
|
p.A882_splice
|
damaging
| Mahlavu |