| Mutation ID |
7 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000232892 |
| Start |
151827730:151827730(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.758delA |
| AA Mutation |
p.Tyr253PhefsTer40(p.Y253Ffs*40) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| Mutation ID |
8 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000232892 |
| Start |
151827905:151827905(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.933T>A |
| AA Mutation |
p.Tyr311Ter(p.Y311*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> AADAC
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000232892 |
| Start |
151827796:151827796(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.824G>T |
| AA Mutation |
p.Ser275Ile(p.S275I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000232892 |
| Start |
151827743:151827743(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs756745068
|
| CDS Mutation |
c.771T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000232892 |
| Start |
151828145:151828145(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1173T>G |
| AA Mutation |
p.Tyr391Ter(p.Y391*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|