| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000025008 |
| Start |
52673983:52673983(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs747652097
|
| CDS Mutation |
c.864G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000025008 |
| Start |
52642425:52642425(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4263A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000025008 |
| Start |
52657453:52657453(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2376T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |