Colon Cancer: Gene >> UBB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302182 |
| Start |
16381972:16381972(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.65C>T |
| AA Mutation |
p.Thr22Ile(p.T22I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000302182 |
| Start |
16382471:16382471(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.570delC |
| AA Mutation |
p.Asp191ThrfsTer35(p.D191Tfs*35) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> UBB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302182 |
| Start |
16382295:16382295(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.388C>T |
| AA Mutation |
p.Arg130Cys(p.R130C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302182 |
| Start |
16382578:16382578(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.671G>A |
| AA Mutation |
p.Arg224His(p.R224H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|