Colon Cancer: Gene >> SSB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260956 |
| Start |
169810400:169810400(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.787G>T |
| AA Mutation |
p.Asp263Tyr(p.D263Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260956 |
| Start |
169805784:169805784(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.290T>C |
| AA Mutation |
p.Leu97Pro(p.L97P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SSB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260956 |
| Start |
169811224:169811224(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1039C>A |
| AA Mutation |
p.Gln347Lys(p.Q347K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000260956 |
| Start |
169806891:169806891(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.452A>C |
| AA Mutation |
p.Lys151Thr(p.K151T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|