| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274026 |
| Start |
121819448:121819448(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.926C>G |
| AA Mutation |
p.Pro309Arg(p.P309R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000274026 |
| Start |
121819556:121819556(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.818delC |
| AA Mutation |
p.Pro273GlnfsTer3(p.P273Qfs*3) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CCNA2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274026 |
| Start |
121822616:121822616(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.244G>T |
| AA Mutation |
p.Asp82Tyr(p.D82Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|