Colon Cancer: Gene >> NPL
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000258317 |
| Start |
182803764:182803764(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.135C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> NPL
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000258317 |
| Start |
182818652:182818652(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs780412696
|
| CDS Mutation |
c.569G>A |
| AA Mutation |
p.Arg190His(p.R190H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000258317 |
| Start |
182828865:182828865(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.920C>A |
| AA Mutation |
p.Ser307Tyr(p.S307Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000258317 |
| Start |
182806192:182806192(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.190C>T |
| AA Mutation |
p.Arg64Cys(p.R64C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000258317 |
| Start |
182822132:182822133(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
null
|
| CDS Mutation |
c.677dupA |
| AA Mutation |
p.Thr227AspfsTer9(p.T227Dfs*9) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
|