| ID |
3 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000288602 |
| Start |
140778031:140778045(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1463_1477delCAGCACCTACACCTC |
| AA Mutation |
p.Thr488_Gln493delinsLys(p.T488_Q493delinsK) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |