| Mutation ID |
12 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262291 |
| Start |
59839905:59839905(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1215T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
13 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262291 |
| Start |
59735411:59735411(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768887557
|
| CDS Mutation |
c.150G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> VMP1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262291 |
| Start |
59735366:59735366(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.105G>T |
| AA Mutation |
p.Arg35Ser(p.R35S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262291 |
| Start |
59731511:59731511(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.65G>A |
| AA Mutation |
p.Gly22Glu(p.G22E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|