| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369096 |
| Start |
106104856:106104856(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs373718206
|
| CDS Mutation |
c.696C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369096 |
| Start |
106104889:106104889(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.729C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369096 |
| Start |
106105768:106105768(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1608A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |