CELSR2 | Mutation | Missense | ENST00000271332.3 |
g.109794206C>T
|
c.1505C>T
|
p.Ala502Val
|
possibly damaging
| HepaRG |
CELSR2 | Mutation | Missense | ENST00000271332.3 |
g.109793822G>A
|
c.1121G>A
|
p.Arg374Gln
|
possibly damaging
| Huh1 |
CELSR2 | Mutation | Missense | ENST00000271332.3 |
g.109792780C>T
|
c.79C>T
|
p.Pro27Ser
|
benign
| JHH2 |
CELSR2 | Mutation | Missense | ENST00000271332.3 |
g.109816144C>T
|
c.8596C>T
|
p.Arg2866Trp
|
probably damaging
| SNU354 |
CELSR2 | Mutation | Missense | ENST00000271332.3 |
g.109814294C>T
|
c.7876C>T
|
p.Arg2626Cys
|
probably damaging
| SNU886 |
CELSR2 | Mutation | Truncating | ENST00000271332.3 |
g.109807487C>T
|
c.5465-3C>T
|
p.?
|
damaging
| Huh1 |