| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000479077 |
| Start |
218263657:218263657(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.933C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000479077 |
| Start |
218263285:218263285(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs760312764
|
| CDS Mutation |
c.561C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000479077 |
| Start |
218263177:218263177(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.453T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |