| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000392977 |
| Start |
101094285:101094285(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752244271
|
| CDS Mutation |
c.1731G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000392977 |
| Start |
101111624:101111624(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2364C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000392977 |
| Start |
101116745:101116745(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2517T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |