| Mutation ID |
3 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000274255 |
| Start |
36166661:36166661(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752559772
|
| CDS Mutation |
c.535A>G |
| AA Mutation |
p.Ser179Gly(p.S179G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000274255 |
| Start |
36168343:36168343(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs137857862
|
| CDS Mutation |
c.567G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SKP2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274255 |
| Start |
36168320:36168320(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750556105
|
| CDS Mutation |
c.544C>T |
| AA Mutation |
p.Arg182Cys(p.R182C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|