| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000294728 |
| Start |
100724802:100724802(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201887131
|
| CDS Mutation |
c.840T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000294728 |
| Start |
100729144:100729144(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.966G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000294728 |
| Start |
100729309:100729309(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs372051353
|
| CDS Mutation |
c.1131C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |