| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000576479 |
| Start |
14075381:14075381(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.516A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000576479 |
| Start |
14259395:14259395(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1608C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000576479 |
| Start |
14243397:14243397(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.890+1G>A |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |