| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000217131 |
| Start |
59001534:59001534(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs748740856
|
| CDS Mutation |
c.418G>A |
| AA Mutation |
p.Val140Met(p.V140M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000217131 |
| Start |
58996722:58996722(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.718A>C |
| AA Mutation |
p.Asn240His(p.N240H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CTSZ
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000217131 |
| Start |
58997656:58997656(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.585C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|