Colon Cancer: Gene >> OPN1MW
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000595290 |
| Start |
154193528:154193528(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.865T>A |
| AA Mutation |
p.Cys289Ser(p.C289S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000595290 |
| Start |
154193597:154193597(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.937delA |
| AA Mutation |
p.Ser313ValfsTer13(p.S313Vfs*13) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> OPN1MW
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000595290 |
| Start |
154188007:154188007(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.350G>A |
| AA Mutation |
p.Gly117Asp(p.G117D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000595290 |
| Start |
154193452:154193452(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.789G>T |
| AA Mutation |
p.Glu263Asp(p.E263D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|