| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000524993 |
| Start |
117918452:117918452(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.408T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000524993 |
| Start |
117918758:117918758(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.102A>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000524993 |
| Start |
117913809:117913809(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs758103334
|
| CDS Mutation |
c.777A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |