| Mutation ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000353379 |
| Start |
89690582:89690582(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.190A>G |
| AA Mutation |
p.Ile64Val(p.I64V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000353379 |
| Start |
89691498:89691498(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs772182758
|
| CDS Mutation |
c.288G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CDK10
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000353379 |
| Start |
89694689:89694689(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750772459
|
| CDS Mutation |
c.693G>C |
| AA Mutation |
p.Glu231Asp(p.E231D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|