| Mutation ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000370759 |
| Start |
78095080:78095080(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.560delA |
| AA Mutation |
p.Lys187ArgfsTer7(p.K187Rfs*7) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000370759 |
| Start |
78125947:78125947(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774818269
|
| CDS Mutation |
c.781C>T |
| AA Mutation |
p.Arg261Ter(p.R261*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> GIPC2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370759 |
| Start |
78080777:78080777(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs758543783
|
| CDS Mutation |
c.343G>A |
| AA Mutation |
p.Glu115Lys(p.E115K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000370759 |
| Start |
78119431:78119431(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs140087680
|
| CDS Mutation |
c.646G>T |
| AA Mutation |
p.Glu216Ter(p.E216*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|