| Mutation ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000280200 |
| Start |
69895777:69895777(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs207476919
|
| CDS Mutation |
c.651G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
8 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000280200 |
| Start |
69947390:69947390(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.17T>G |
| AA Mutation |
p.Leu6Ter(p.L6*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CD226
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000280200 |
| Start |
69895734:69895734(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.694G>A |
| AA Mutation |
p.Glu232Lys(p.E232K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000280200 |
| Start |
69895927:69895927(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.501G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|