| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000292123 |
| Start |
5653388:5653388(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs749049469
|
| CDS Mutation |
c.1494C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000292123 |
| Start |
5661728:5661728(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2073C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000292123 |
| Start |
5641925:5641925(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs758696281
|
| CDS Mutation |
c.525G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |