| Mutation ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000449934 |
| Start |
31412384:31412384(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
rs67841474
|
| CDS Mutation |
c.953delG |
| AA Mutation |
p.Gly318AlafsTer68(p.G318Afs*68) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000449934 |
| Start |
31412401:31412403(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.977_979delATT |
| AA Mutation |
p.Tyr326del(p.Y326del) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> MICA
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000449934 |
| Start |
31410545:31410545(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.73C>T |
| AA Mutation |
p.Pro25Ser(p.P25S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000449934 |
| Start |
31412414:31412414(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.982C>A |
| AA Mutation |
p.Leu328Ile(p.L328I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|