Colon Cancer: Gene >> DESI2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302550 |
| Start |
244705778:244705778(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.574A>C |
| AA Mutation |
p.Thr192Pro(p.T192P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained;splice_region_variant |
| Transcription ID |
ENST00000302550 |
| Start |
244686669:244686669(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.115G>T |
| AA Mutation |
p.Glu39Ter(p.E39*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> DESI2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302550 |
| Start |
244705559:244705559(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.355C>A |
| AA Mutation |
p.Leu119Ile(p.L119I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000302550 |
| Start |
244689326:244689326(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.193G>T |
| AA Mutation |
p.Glu65Ter(p.E65*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000302550 |
| Start |
244691977:244691977(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.308T>G |
| AA Mutation |
p.Leu103Ter(p.L103*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|