Colon Cancer: Gene >> HPGDS
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000295256 |
| Start |
94308667:94308667(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.303T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> HPGDS
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295256 |
| Start |
94317950:94317950(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.149A>G |
| AA Mutation |
p.Lys50Arg(p.K50R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000295256 |
| Start |
94302161:94302161(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.420G>A |
| AA Mutation |
p.Trp140Ter(p.W140*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|