Colon Cancer: Gene >> CGA
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000627148 |
| Start |
87085827:87085827(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.280G>A |
| AA Mutation |
p.Val94Ile(p.V94I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000627148 |
| Start |
87086431:87086431(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.92G>A |
| AA Mutation |
p.Cys31Tyr(p.C31Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CGA
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000627148 |
| Start |
87086299:87086299(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.224A>C |
| AA Mutation |
p.Lys75Thr(p.K75T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|