Colon Cancer: Gene >> SAA2
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000256733 |
| Start |
18245464:18245464(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs369541409
|
| CDS Mutation |
c.282G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> SAA2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256733 |
| Start |
18246003:18246003(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.137A>C |
| AA Mutation |
p.Asn46Thr(p.N46T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256733 |
| Start |
18247926:18247926(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.86T>G |
| AA Mutation |
p.Phe29Cys(p.F29C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|