Colon Cancer: Gene >> YBX3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000228251 |
| Start |
10704066:10704066(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs745797213
|
| CDS Mutation |
c.863G>A |
| AA Mutation |
p.Arg288His(p.R288H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000228251 |
| Start |
10710104:10710104(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs749620675
|
| CDS Mutation |
c.584A>G |
| AA Mutation |
p.Glu195Gly(p.E195G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> YBX3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000228251 |
| Start |
10702066:10702066(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.947C>G |
| AA Mutation |
p.Ala316Gly(p.A316G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000228251 |
| Start |
10709956:10709956(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.732G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|