Colon Cancer: Gene >> UQCC2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000607484 |
| Start |
33700506:33700506(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.221G>A |
| AA Mutation |
p.Arg74His(p.R74H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000607484 |
| Start |
33700481:33700481(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.246C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> UQCC2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000607484 |
| Start |
33701386:33701386(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.173A>G |
| AA Mutation |
p.Glu58Gly(p.E58G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000607484 |
| Start |
33701359:33701359(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.200A>G |
| AA Mutation |
p.Tyr67Cys(p.Y67C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000607484 |
| Start |
33701375:33701375(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs771765075
|
| CDS Mutation |
c.184C>T |
| AA Mutation |
p.Arg62Ter(p.R62*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|