| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000196061 |
| Start |
11948013:11948013(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs11553679
|
| CDS Mutation |
c.114C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000196061 |
| Start |
11949817:11949817(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769238622
|
| CDS Mutation |
c.213G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000196061 |
| Start |
11957002:11957002(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs567164584
|
| CDS Mutation |
c.729C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |