| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000222330 |
| Start |
42232662:42232662(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201146173
|
| CDS Mutation |
c.1119G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000222330 |
| Start |
42234616:42234616(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs199858279
|
| CDS Mutation |
c.729C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000222330 |
| Start |
42232684:42232684(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1099-2A>G |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |