Colon Cancer: Gene >> TMEM9
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367330 |
| Start |
201135766:201135766(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.449C>A |
| AA Mutation |
p.Ala150Glu(p.A150E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367330 |
| Start |
201135695:201135695(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776119463
|
| CDS Mutation |
c.520A>G |
| AA Mutation |
p.Thr174Ala(p.T174A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TMEM9
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367330 |
| Start |
201143826:201143826(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.393G>T |
| AA Mutation |
p.Glu131Asp(p.E131D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|