MAST4 | Mutation | In-Frame | ENST00000403625.2 |
g.66461184_66461186del
|
c.6177_6179del
|
p.Ser2060del
|
damaging
| JHH6 |
MAST4 | Mutation | Missense | ENST00000403625.2 |
g.66440591A>G
|
c.2825A>G
|
p.Glu942Gly
|
benign
| Hep3B |
MAST4 | Mutation | Missense | ENST00000403625.2 |
g.66459919C>T
|
c.4912C>T
|
p.Arg1638Trp
|
probably damaging
| SNU387 |
MAST4 | Mutation | Missense | ENST00000403625.2 |
g.66461680A>G
|
c.6673A>G
|
p.Lys2225Glu
|
benign
| PLC.PRF5 |
MAST4 | Mutation | Missense | ENST00000403625.2 |
g.66398371C>T
|
c.1078C>T
|
p.Arg360Cys
|
probably damaging
| JHH6 |
MAST4 | Mutation | Missense | ENST00000403625.2 |
g.66460561G>C
|
c.5554G>C
|
p.Asp1852His
|
possibly damaging
| SNU878 |
MAST4 | Mutation | Missense | ENST00000403625.2 |
g.66459743A>C
|
c.4736A>C
|
p.Lys1579Thr
|
benign
| SNU886 |
MAST4 | Mutation | Truncating | ENST00000403625.2 |
g.66458971A>C
|
c.3968-4A>C
|
p.?
|
damaging
| JHH4 |
MAST4 | Mutation | Truncating | ENST00000403625.2 |
g.66462583dup
|
c.7576dup
|
p.Val2526GlyfsX49
|
damaging
| SNU886 |