Colon Cancer: Gene >> CD8A
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000283635 |
| Start |
86788530:86788530(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs138963205
|
| CDS Mutation |
c.656G>A |
| AA Mutation |
p.Arg219Gln(p.R219Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000283635 |
| Start |
86790596:86790596(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.135G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CD8A
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000283635 |
| Start |
86790415:86790415(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200418942
|
| CDS Mutation |
c.316C>T |
| AA Mutation |
p.Arg106Cys(p.R106C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000283635 |
| Start |
86788549:86788549(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.637C>T |
| AA Mutation |
p.Arg213Cys(p.R213C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|