| Mutation ID |
5 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000369406 |
| Start |
119759139:119759139(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.829delA |
| AA Mutation |
p.Ile277SerfsTer22(p.I277Sfs*22) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000369406 |
| Start |
119753304:119753304(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs137852637
|
| CDS Mutation |
c.1270C>T |
| AA Mutation |
p.Arg424Ter(p.R424*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> HMGCS2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369406 |
| Start |
119768765:119768765(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757169217
|
| CDS Mutation |
c.80G>A |
| AA Mutation |
p.Arg27His(p.R27H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|