| Mutation ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339252 |
| Start |
157052573:157052573(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201270450
|
| CDS Mutation |
c.461C>T |
| AA Mutation |
p.Thr154Met(p.T154M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
stop_lost |
| Transcription ID |
ENST00000339252 |
| Start |
157029735:157029735(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776039147
|
| CDS Mutation |
c.1093T>C |
| AA Mutation |
p.Ter365GlnextTer12(p.*365Qext*12) |
| Mutation Classification |
Nonstop_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> HAVCR1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339252 |
| Start |
157052600:157052600(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs369837589
|
| CDS Mutation |
c.434G>A |
| AA Mutation |
p.Arg145Gln(p.R145Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339252 |
| Start |
157032880:157032880(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.960C>G |
| AA Mutation |
p.Phe320Leu(p.F320L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|