| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000404816 |
| Start |
33020934:33020934(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.591T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000404816 |
| Start |
33134815:33134815(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1056C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
8 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000404816 |
| Start |
33273675:33273675(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2637G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |