| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357360 |
| Start |
154478328:154478328(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.272G>T |
| AA Mutation |
p.Arg91Met(p.R91M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000357360 |
| Start |
154477956:154477956(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.420delC |
| AA Mutation |
p.Val141PhefsTer20(p.V141Ffs*20) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> LAGE3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357360 |
| Start |
154478376:154478376(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.224C>T |
| AA Mutation |
p.Ala75Val(p.A75V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|