Colon Cancer: Gene >> PAEP
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000277508 |
| Start |
135564250:135564250(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.317T>C |
| AA Mutation |
p.Val106Ala(p.V106A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000277508 |
| Start |
135562326:135562326(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776119445
|
| CDS Mutation |
c.129G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PAEP
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000277508 |
| Start |
135564254:135564254(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.321G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|