Colon Cancer: Gene >> CXCL1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000395761 |
| Start |
73869758:73869758(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.190T>C |
| AA Mutation |
p.Ser64Pro(p.S64P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000395761 |
| Start |
73869506:73869506(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.36T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CXCL1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000395761 |
| Start |
73869974:73869974(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.293A>G |
| AA Mutation |
p.Glu98Gly(p.E98G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|