URB2 | Mutation | Missense | ENST00000258243.2 |
g.229770779C>T
|
c.419C>T
|
p.Thr140Met
|
probably damaging
| Hep3B |
URB2 | Mutation | Missense | ENST00000258243.2 |
g.229773866C>T
|
c.3506C>T
|
p.Ala1169Val
|
benign
| SNU387 |
URB2 | Mutation | Missense | ENST00000258243.2 |
g.229773407A>T
|
c.3047A>T
|
p.Lys1016Met
|
probably damaging
| PLC.PRF5 |
URB2 | Mutation | Missense | ENST00000258243.2 |
g.229773793A>G
|
c.3433A>G
|
p.Arg1145Gly
|
benign
| SNU368 |
URB2 | Mutation | Missense | ENST00000258243.2 |
g.229770731G>A
|
c.371G>A
|
p.Arg124Gln
|
benign
| SNU761 |