| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000396923 |
| Start |
43558826:43558826(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3354C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000396923 |
| Start |
43535211:43535211(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3765C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PPIP5K1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000396923 |
| Start |
43539491:43539491(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs202101760
|
| CDS Mutation |
c.3478C>T |
| AA Mutation |
p.Arg1160Cys(p.R1160C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|