Colon Cancer: Gene >> SRGN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000242465 |
| Start |
69097176:69097176(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.172G>A |
| AA Mutation |
p.Glu58Lys(p.E58K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000242465 |
| Start |
69097119:69097119(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs557632542
|
| CDS Mutation |
c.115C>T |
| AA Mutation |
p.Arg39Cys(p.R39C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SRGN
No Mutation Annotation! |