| Mutation ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000313961 |
| Start |
163168324:163168325(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.88_89insTA |
| AA Mutation |
p.Pro30LeufsTer54(p.P30Lfs*54) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000313961 |
| Start |
163168325:163168326(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.87_88insTT |
| AA Mutation |
p.Pro30PhefsTer54(p.P30Ffs*54) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RGS5
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000313961 |
| Start |
163168329:163168329(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.84G>T |
| AA Mutation |
p.Gln28His(p.Q28H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000313961 |
| Start |
163202826:163202826(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.10G>T |
| AA Mutation |
p.Gly4Ter(p.G4*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|