| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000027335 |
| Start |
94176598:94176598(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.367C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000027335 |
| Start |
94170440:94170440(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs765227677
|
| CDS Mutation |
c.1023G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000027335 |
| Start |
94162113:94162113(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1332T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |