Colon Cancer: Gene >> HSD11B2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000326152 |
| Start |
67436322:67436322(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.738C>G |
| AA Mutation |
p.Phe246Leu(p.F246L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000326152 |
| Start |
67436064:67436064(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs560632514
|
| CDS Mutation |
c.586G>A |
| AA Mutation |
p.Ala196Thr(p.A196T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> HSD11B2
No Mutation Annotation! |