| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376259 |
| Start |
12191865:12191865(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.399G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376259 |
| Start |
12192911:12192911(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.600C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376259 |
| Start |
12206786:12206786(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs765379693
|
| CDS Mutation |
c.1152C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |