| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000255390 |
| Start |
10695747:10695747(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.358G>A |
| AA Mutation |
p.Ala120Thr(p.A120T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000255390 |
| Start |
10686774:10686774(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs761217696
|
| CDS Mutation |
c.724A>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SCO1
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000255390 |
| Start |
10691888:10691888(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs144621417
|
| CDS Mutation |
c.639C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|