| Mutation ID |
8 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000234111 |
| Start |
10443275:10443275(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs11538363
|
| CDS Mutation |
c.705C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
9 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000234111 |
| Start |
10444228:10444228(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.316G>T |
| AA Mutation |
p.Glu106Ter(p.E106*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> ODC1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000234111 |
| Start |
10442134:10442134(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.791C>T |
| AA Mutation |
p.Pro264Leu(p.P264L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000234111 |
| Start |
10444154:10444154(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.390G>T |
| AA Mutation |
p.Met130Ile(p.M130I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|