| Mutation ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000314531 |
| Start |
2936658:2936658(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs770342384
|
| CDS Mutation |
c.177C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
8 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000314531 |
| Start |
2933761:2933761(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768214682
|
| CDS Mutation |
c.1366C>T |
| AA Mutation |
p.Arg456Ter(p.R456*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> ZNF77
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000314531 |
| Start |
2933871:2933871(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1256T>G |
| AA Mutation |
p.Phe419Cys(p.F419C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000314531 |
| Start |
2934715:2934715(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.412G>A |
| AA Mutation |
p.Glu138Lys(p.E138K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000314531 |
| Start |
2936572:2936572(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.263G>T |
| AA Mutation |
p.Arg88Ile(p.R88I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|