| ID |
4 |
| Mutation Consequence |
splice_acceptor_variant;coding_sequence_variant;intron_variant |
| Transcription ID |
ENST00000281172 |
| Start |
15631661:15631698(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1822-34_1825delTTAAATTTTAAGTTAATTATTTGTCTTTTTATAGAAAC |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |