| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000276943 |
| Start |
27524757:27524757(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.421G>T |
| AA Mutation |
p.Glu141Ter(p.E141*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000276943 |
| Start |
27524536:27524537(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.200_201insATCATATCAG |
| AA Mutation |
p.Leu68SerfsTer25(p.L68Sfs*25) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> IFNK
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000276943 |
| Start |
27524679:27524679(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.343C>A |
| AA Mutation |
p.Gln115Lys(p.Q115K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000276943 |
| Start |
27524859:27524859(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.523G>T |
| AA Mutation |
p.Glu175Ter(p.E175*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|