| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263801 |
| Start |
43457213:43457213(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1380T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263801 |
| Start |
43432482:43432482(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3372G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000263801 |
| Start |
43420434:43420436(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4535_4537delCTG |
| AA Mutation |
p.Ala1512del(p.A1512del) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |