| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369792 |
| Start |
110060736:110060736(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs372987570
|
| CDS Mutation |
c.1029G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000369792 |
| Start |
110061451:110061451(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.707delC |
| AA Mutation |
p.Thr236MetfsTer95(p.T236Mfs*95) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> ALX3
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369792 |
| Start |
110064710:110064710(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.471C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|