| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361847 |
| Start |
102229574:102229574(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1065G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361847 |
| Start |
102233726:102233726(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778360894
|
| CDS Mutation |
c.654C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361847 |
| Start |
102229616:102229616(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1023A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |