Colon Cancer: Gene >> GSTO2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338595 |
| Start |
104277907:104277907(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.157A>T |
| AA Mutation |
p.Asn53Tyr(p.N53Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000338595 |
| Start |
104279451:104279451(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.448G>T |
| AA Mutation |
p.Glu150Ter(p.E150*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> GSTO2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338595 |
| Start |
104299201:104299201(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.649C>A |
| AA Mutation |
p.Leu217Ile(p.L217I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338595 |
| Start |
104278054:104278054(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.304C>A |
| AA Mutation |
p.Leu102Met(p.L102M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|