Colon Cancer: Gene >> CSH1
No Mutation Annotation! |
Rectum Cancer: Gene >> CSH1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000316193 |
| Start |
63895580:63895580(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368663907
|
| CDS Mutation |
c.349C>T |
| AA Mutation |
p.Arg117Trp(p.R117W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000316193 |
| Start |
63895537:63895537(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.392C>G |
| AA Mutation |
p.Thr131Ser(p.T131S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000316193 |
| Start |
63896507:63896507(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.5C>A |
| AA Mutation |
p.Ala2Asp(p.A2D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000316193 |
| Start |
63895491:63895491(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.438C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|