Colon Cancer: Gene >> CDC20
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310955 |
| Start |
43360843:43360843(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.959A>T |
| AA Mutation |
p.Asp320Val(p.D320V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000310955 |
| Start |
43362955:43362955(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1326C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CDC20
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310955 |
| Start |
43362226:43362226(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1235A>G |
| AA Mutation |
p.Lys412Arg(p.K412R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000310955 |
| Start |
43361227:43361227(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368218162
|
| CDS Mutation |
c.1185C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|