| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263277 |
| Start |
47741162:47741162(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs138874482
|
| CDS Mutation |
c.1362C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263277 |
| Start |
47718581:47718581(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs369297316
|
| CDS Mutation |
c.477G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263277 |
| Start |
47736473:47736473(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs536783884
|
| CDS Mutation |
c.1020G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |