| ID |
4 |
| Mutation Consequence |
splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID |
ENST00000316099 |
| Start |
44419855:44419883(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.873_892+9delCATCATCTTCTTTGACCCAGGTACAGTGC |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |