Colon Cancer: Gene >> PRB1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000500254 |
| Start |
11355503:11355503(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.51G>T |
| AA Mutation |
p.Gln17His(p.Q17H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000500254 |
| Start |
11353129:11353129(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs761131883
|
| CDS Mutation |
c.575G>A |
| AA Mutation |
p.Arg192Lys(p.R192K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PRB1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000500254 |
| Start |
11353296:11353296(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.408C>A |
| AA Mutation |
p.Ser136Arg(p.S136R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000500254 |
| Start |
11354555:11354555(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.65-1G>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
|