| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000244745 |
| Start |
21595908:21595908(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1374C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000244745 |
| Start |
21594771:21594771(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs773518535
|
| CDS Mutation |
c.237G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SOX4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000244745 |
| Start |
21594771:21594771(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.237G>T |
| AA Mutation |
p.Glu79Asp(p.E79D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000244745 |
| Start |
21595737:21595737(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145209759
|
| CDS Mutation |
c.1203C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|