| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000452722 |
| Start |
115217948:115217948(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.765C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000452722 |
| Start |
115229141:115229141(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.693G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000452722 |
| Start |
115176555:115176555(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750612978
|
| CDS Mutation |
c.1248C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |