LAMC2 | Mutation | Missense | ENST00000264144.4 |
g.183194828C>T
|
c.1039C>T
|
p.Arg347Cys
|
probably damaging
| SNU398 |
LAMC2 | Mutation | Missense | ENST00000264144.4 |
g.183206565C>T
|
c.2680C>T
|
p.Arg894Cys
|
probably damaging
| PLC.PRF5 |
LAMC2 | Mutation | Missense | ENST00000264144.4 |
g.183200111C>T
|
c.1730C>T
|
p.Pro577Leu
|
probably damaging
| HLE |
LAMC2 | Mutation | Missense | ENST00000264144.4 |
g.183200111C>T
|
c.1730C>T
|
p.Pro577Leu
|
probably damaging
| HLF |
LAMC2 | Mutation | Missense | ENST00000264144.4 |
g.183204775C>G
|
c.2366C>G
|
p.Ala789Gly
|
possibly damaging
| Li7 |