Colon Cancer: Gene >> SBSPON
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000297354 |
| Start |
73092870:73092870(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.198C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> SBSPON
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000297354 |
| Start |
73081132:73081132(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs758346150
|
| CDS Mutation |
c.296G>A |
| AA Mutation |
p.Arg99His(p.R99H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000297354 |
| Start |
73067444:73067444(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.692A>G |
| AA Mutation |
p.His231Arg(p.H231R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000297354 |
| Start |
73067354:73067354(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767468598
|
| CDS Mutation |
c.782T>C |
| AA Mutation |
p.Phe261Ser(p.F261S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|