Colon Cancer: Gene >> PRNP
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379440 |
| Start |
4699758:4699758(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs74315408
|
| CDS Mutation |
c.538G>A |
| AA Mutation |
p.Val180Ile(p.V180I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000379440 |
| Start |
4699643:4699643(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764920854
|
| CDS Mutation |
c.423C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PRNP
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379440 |
| Start |
4699534:4699534(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs11538758
|
| CDS Mutation |
c.314C>A |
| AA Mutation |
p.Pro105Gln(p.P105Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379440 |
| Start |
4699297:4699297(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.77C>T |
| AA Mutation |
p.Pro26Leu(p.P26L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000379440 |
| Start |
4699643:4699643(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764920854
|
| CDS Mutation |
c.423C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|