| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000366756 |
| Start |
170283398:170283398(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201096307
|
| CDS Mutation |
c.1881C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000366756 |
| Start |
170283788:170283788(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs777888615
|
| CDS Mutation |
c.1491C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000366756 |
| Start |
170288342:170288342(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.567C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |