| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000225831 |
| Start |
34256294:34256294(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.149G>T |
| AA Mutation |
p.Ser50Ile(p.S50I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000225831 |
| Start |
34256740:34256740(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.213C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CCL2
| Mutation ID |
1 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000225831 |
| Start |
34256786:34256786(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.259delA |
| AA Mutation |
p.Met87TrpfsTer25(p.M87Wfs*25) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
|