Colon Cancer: Gene >> NFKBIE
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000275015 |
| Start |
44260477:44260477(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1171C>T |
| AA Mutation |
p.Arg391Trp(p.R391W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000275015 |
| Start |
44265532:44265532(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.232delT |
| AA Mutation |
p.Trp78GlyfsTer167(p.W78Gfs*167) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> NFKBIE
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000275015 |
| Start |
44260240:44260240(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1240A>G |
| AA Mutation |
p.Thr414Ala(p.T414A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000275015 |
| Start |
44260260:44260260(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145497659
|
| CDS Mutation |
c.1220C>T |
| AA Mutation |
p.Ala407Val(p.A407V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000275015 |
| Start |
44265656:44265656(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.108C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|