Colon Cancer: Gene >> HMGA1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000311487 |
| Start |
34240898:34240898(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.118G>A |
| AA Mutation |
p.Ala40Thr(p.A40T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_lost |
| Transcription ID |
ENST00000311487 |
| Start |
34244882:34244882(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.322T>C |
| AA Mutation |
p.Ter108ArgextTer66(p.*108Rext*66) |
| Mutation Classification |
Nonstop_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> HMGA1
No Mutation Annotation! |