| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376414 |
| Start |
99295642:99295642(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763839031
|
| CDS Mutation |
c.504C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376414 |
| Start |
99295978:99295978(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.168T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376414 |
| Start |
99295120:99295120(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1026T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |