Colon Cancer: Gene >> PTH
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282091 |
| Start |
13492509:13492509(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.244C>T |
| AA Mutation |
p.Pro82Ser(p.P82S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> PTH
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282091 |
| Start |
13492610:13492610(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762100011
|
| CDS Mutation |
c.143C>T |
| AA Mutation |
p.Ser48Leu(p.S48L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282091 |
| Start |
13492791:13492791(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.65A>C |
| AA Mutation |
p.Lys22Thr(p.K22T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|