| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000357134 |
| Start |
21113657:21113657(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs561468649
|
| CDS Mutation |
c.1369T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000357134 |
| Start |
20677972:20677972(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.96C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000357134 |
| Start |
21534372:21534372(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1646-2A>G |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |