| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000266970 |
| Start |
55968104:55968104(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.250C>T |
| AA Mutation |
p.His84Tyr(p.H84Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000266970 |
| Start |
55968801:55968801(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.339G>T |
| AA Mutation |
p.Gln113His(p.Q113H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CDK2
| Mutation ID |
1 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000266970 |
| Start |
55967126:55967126(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.116+2T>C |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
|