Colon Cancer: Gene >> CST5
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000304710 |
| Start |
23876198:23876198(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs146272783
|
| CDS Mutation |
c.419G>A |
| AA Mutation |
p.Arg140Gln(p.R140Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000304710 |
| Start |
23877576:23877576(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs572646770
|
| CDS Mutation |
c.274C>T |
| AA Mutation |
p.Arg92Ter(p.R92*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CST5
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000304710 |
| Start |
23879657:23879657(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs756477706
|
| CDS Mutation |
c.20C>T |
| AA Mutation |
p.Thr7Ile(p.T7I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|