| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000200457 |
| Start |
100868761:100868761(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs781538629
|
| CDS Mutation |
c.630G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000200457 |
| Start |
100872741:100872741(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs746411837
|
| CDS Mutation |
c.1296C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000200457 |
| Start |
100867860:100867860(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.110-1G>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |