Colon Cancer: Gene >> STOM
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000286713 |
| Start |
121348103:121348103(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763192503
|
| CDS Mutation |
c.572G>A |
| AA Mutation |
p.Arg191His(p.R191H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000286713 |
| Start |
121349214:121349214(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.431G>A |
| AA Mutation |
p.Arg144His(p.R144H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> STOM
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000286713 |
| Start |
121353242:121353242(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.299C>T |
| AA Mutation |
p.Ser100Leu(p.S100L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000286713 |
| Start |
121341396:121341396(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201671242
|
| CDS Mutation |
c.673G>A |
| AA Mutation |
p.Glu225Lys(p.E225K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000286713 |
| Start |
121341212:121341212(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.857A>G |
| AA Mutation |
p.His286Arg(p.H286R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|