| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000394836 |
| Start |
61908276:61908276(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs751497624
|
| CDS Mutation |
c.42G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000394836 |
| Start |
61902501:61902501(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.940C>T |
| AA Mutation |
p.Arg314Ter(p.R314*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RAB3IL1
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000394836 |
| Start |
61906475:61906475(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.648G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000394836 |
| Start |
61907452:61907452(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.379C>T |
| AA Mutation |
p.Arg127Ter(p.R127*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|