| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376670 |
| Start |
48791214:48791214(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.105C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376670 |
| Start |
48794083:48794083(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1161G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000376670 |
| Start |
48791888:48791888(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.269delG |
| AA Mutation |
p.Gly90AlafsTer47(p.G90Afs*47) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |