Colon Cancer: Gene >> CDK4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000257904 |
| Start |
57751036:57751036(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs150281463
|
| CDS Mutation |
c.409G>A |
| AA Mutation |
p.Val137Ile(p.V137I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000257904 |
| Start |
57749302:57749302(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.699T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CDK4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000257904 |
| Start |
57749196:57749196(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs786202902
|
| CDS Mutation |
c.805G>A |
| AA Mutation |
p.Ala269Thr(p.A269T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000257904 |
| Start |
57751259:57751259(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.302G>T |
| AA Mutation |
p.Arg101Met(p.R101M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|