| Mutation ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000311604 |
| Start |
1881556:1881556(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.322delC |
| AA Mutation |
p.Gln108SerfsTer31(p.Q108Sfs*31) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000311604 |
| Start |
1881469:1881469(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.229G>T |
| AA Mutation |
p.Glu77Ter(p.E77*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000311604 |
| Start |
1881555:1881556(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
rs752018434
|
| CDS Mutation |
c.322dupC |
| AA Mutation |
p.Gln108ProfsTer6(p.Q108Pfs*6) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> LSP1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000311604 |
| Start |
1883989:1883989(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs149086047
|
| CDS Mutation |
c.556G>A |
| AA Mutation |
p.Glu186Lys(p.E186K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|