Colon Cancer: Gene >> PDCD10
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000392750 |
| Start |
167697077:167697077(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.200T>C |
| AA Mutation |
p.Leu67Ser(p.L67S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000392750 |
| Start |
167687317:167687317(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.475-1G>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PDCD10
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000392750 |
| Start |
167695678:167695678(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs758197697
|
| CDS Mutation |
c.313G>A |
| AA Mutation |
p.Glu105Lys(p.E105K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000392750 |
| Start |
167697046:167697046(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs141664917
|
| CDS Mutation |
c.231G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|