WDR11 | Mutation | Missense | ENST00000263461.6 |
g.122630836G>C
|
c.1449G>C
|
p.M483I
|
benign
| HCC.1.2 |
WDR11 | Mutation | Missense | ENST00000263461.6 |
g.122662613C>T
|
c.2800C>T
|
p.H934Y
|
possibly damaging
| SNU182 |
WDR11 | Mutation | Missense | ENST00000263461.6 |
g.122664863G>A
|
c.3226G>A
|
p.A1076T
|
probably damaging
| Li7 |
WDR11 | Mutation | Missense | ENST00000263461.6 |
g.122650283A>C
|
c.2399A>C
|
p.D800A
|
probably damaging
| JHH7 |