SVIL | Mutation | Missense | ENST00000355867.4 |
g.29821019G>A
|
c.1921C>T
|
p.Arg641Cys
|
probably damaging
| HCC.1.2 |
SVIL | Mutation | Missense | ENST00000355867.4 |
g.29839748A>G
|
c.605T>C
|
p.Ile202Thr
|
benign
| SNU423 |
SVIL | Mutation | Missense | ENST00000355867.4 |
g.29818702C>A
|
c.2178G>T
|
p.Arg726Ser
|
probably damaging
| PLC.PRF5 |
SVIL | Mutation | Missense | ENST00000355867.4 |
g.29747415T>G
|
c.6506A>C
|
p.Glu2169Ala
|
possibly damaging
| JHH2 |
SVIL | Mutation | Missense | ENST00000355867.4 |
g.29747213T>C
|
c.6608A>G
|
p.Lys2203Arg
|
probably damaging
| JHH7 |
SVIL | Mutation | Truncating | ENST00000375400.3 |
g.29773582T>A
|
c.3677+3A>T
|
p.?
|
damaging
| MHCC97H |