Colon Cancer: Gene >> CARD18
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000530950 |
| Start |
105139015:105139015(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.71C>A |
| AA Mutation |
p.Ala24Asp(p.A24D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000530950 |
| Start |
105139016:105139016(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.70G>A |
| AA Mutation |
p.Ala24Thr(p.A24T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CARD18
| Mutation ID |
1 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000530950 |
| Start |
105138923:105138923(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs377022898
|
| CDS Mutation |
c.163C>T |
| AA Mutation |
p.Arg55Ter(p.R55*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|