Colon Cancer: Gene >> CCL25
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000390669 |
| Start |
8056464:8056464(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.290T>G |
| AA Mutation |
p.Phe97Cys(p.F97C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000390669 |
| Start |
8056243:8056243(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769251313
|
| CDS Mutation |
c.165C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CCL25
No Mutation Annotation! |