TRIP11 | Mutation | Missense | ENST00000267622.4 |
g.92460245T>A
|
c.5068A>T
|
p.Met1690Leu
|
benign
| SNU398 |
TRIP11 | Mutation | Missense | ENST00000267622.4 |
g.92470786C>G
|
c.3534G>C
|
p.Gln1178His
|
probably damaging
| PLC.PRF5 |
TRIP11 | Mutation | Missense | ENST00000267622.4 |
g.92472014T>G
|
c.2306A>C
|
p.Gln769Pro
|
probably damaging
| PLC.PRF5 |
TRIP11 | Mutation | Missense | ENST00000267622.4 |
g.92470258T>G
|
c.4062A>C
|
p.Lys1354Asn
|
benign
| Huh6 |
TRIP11 | Mutation | Missense | ENST00000267622.4 |
g.92471457T>C
|
c.2863A>G
|
p.Thr955Ala
|
benign
| JHH2 |
TRIP11 | Mutation | Missense | ENST00000267622.4 |
g.92471907G>T
|
c.2413C>A
|
p.Gln805Lys
|
possibly damaging
| JHH5 |