Colon Cancer: Gene >> GPX3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000388825 |
| Start |
151028057:151028057(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs560735748
|
| CDS Mutation |
c.608C>T |
| AA Mutation |
p.Thr203Met(p.T203M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000388825 |
| Start |
151028080:151028080(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.631A>G |
| AA Mutation |
p.Ile211Val(p.I211V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> GPX3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000388825 |
| Start |
151028015:151028015(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.566G>T |
| AA Mutation |
p.Gly189Val(p.G189V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000388825 |
| Start |
151027988:151027988(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.539G>A |
| AA Mutation |
p.Arg180His(p.R180H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|