Colon Cancer: Gene >> CXCL2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000508487 |
| Start |
74098612:74098612(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.297G>T |
| AA Mutation |
p.Lys99Asn(p.K99N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant;splice_region_variant |
| Transcription ID |
ENST00000508487 |
| Start |
74098601:74098601(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
rs745343380
|
| CDS Mutation |
c.308delA |
| AA Mutation |
p.Asn103MetfsTer50(p.N103Mfs*50) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CXCL2
No Mutation Annotation! |