| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361866 |
| Start |
46002248:46002248(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs537366421
|
| CDS Mutation |
c.2097C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361866 |
| Start |
46003710:46003710(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775569169
|
| CDS Mutation |
c.2784C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361866 |
| Start |
46003494:46003494(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs771446601
|
| CDS Mutation |
c.2568C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |