| Mutation ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000329608 |
| Start |
109923833:109923833(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1212G>T |
| AA Mutation |
p.Arg404Ser(p.R404S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000329608 |
| Start |
109923339:109923339(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.721delC |
| AA Mutation |
p.Leu241CysfsTer122(p.L241Cfs*122) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CSF1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000329608 |
| Start |
109924041:109924041(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs548942397
|
| CDS Mutation |
c.1420G>A |
| AA Mutation |
p.Val474Ile(p.V474I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|