CSMD2 | Mutation | Missense | ENST00000241312.4 |
g.33985512G>A
|
c.10204C>T
|
p.Arg3546Cys
|
benign
| HCC.1.1 |
CSMD2 | Mutation | Missense | ENST00000241312.4 |
g.34128652C>T
|
c.3973G>A
|
p.Val238Met
|
probably damaging
| Huh6 |
CSMD2 | Mutation | Missense | ENST00000373381.4 |
g.34025043A>G
|
c.8411T>C
|
p.V2804A
|
benign
| Huh1 |
CSMD2 | Mutation | Missense | ENST00000241312.4 |
g.33985195C>T
|
c.10387G>A
|
p.Asp3607Asn
|
probably damaging
| JHH2 |
CSMD2 | Mutation | Missense | ENST00000373381.4 |
g.34023460G>A
|
c.8617C>T
|
p.P2873S
|
benign
| SNU368 |
CSMD2 | Mutation | Missense | ENST00000241312.4 |
g.34090222G>T
|
c.5402C>A
|
p.Thr1801Lys
|
probably damaging
| MHCC97H |