| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000390649 |
| Start |
56053767:56053767(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764666206
|
| CDS Mutation |
c.3258C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000390649 |
| Start |
56027643:56027643(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1410G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000390649 |
| Start |
56027145:56027145(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368367207
|
| CDS Mutation |
c.912G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |