| Mutation ID |
2 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000294984 |
| Start |
206901650:206901650(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.460A>T |
| AA Mutation |
p.Ser154Cys(p.S154C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000294984 |
| Start |
206900314:206900314(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs144126009
|
| CDS Mutation |
c.260C>T |
| AA Mutation |
p.Thr87Met(p.T87M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000294984 |
| Start |
206897859:206897859(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.27C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> IL24
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000294984 |
| Start |
206901606:206901606(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.416C>A |
| AA Mutation |
p.Thr139Asn(p.T139N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|