| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000370501 |
| Start |
62709798:62709798(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.591C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000370501 |
| Start |
62709474:62709474(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.267G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000370501 |
| Start |
62754887:62754887(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764083183
|
| CDS Mutation |
c.916+1G>A |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |