| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000302262 |
| Start |
80112928:80112928(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1941C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000302262 |
| Start |
80117019:80117019(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2241G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000302262 |
| Start |
80108381:80108381(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs138262940
|
| CDS Mutation |
c.1047C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |