PTPRU | Mutation | Missense | ENST00000345512.3 |
g.29650270G>A
|
c.4112G>A
|
p.Ser1371Asn
|
benign
| SNU398 |
PTPRU | Mutation | Missense | ENST00000323874.8 |
g.29606134A>G
|
c.1730A>G
|
p.Gln577Arg
|
probably damaging
| JHH2 |
PTPRU | Mutation | Missense | ENST00000323874.8 |
g.29581862A>T
|
c.149A>T
|
p.Gln50Leu
|
possibly damaging
| SNU739 |
PTPRU | Mutation | Missense | ENST00000345512.3 |
g.29631305A>G
|
c.2717A>G
|
p.Asp906Gly
|
probably damaging
| SNU761 |