| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000370350 |
| Start |
151716170:151716170(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.51A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000370350 |
| Start |
151721458:151721458(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.298G>T |
| AA Mutation |
p.Glu100Ter(p.E100*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000370350 |
| Start |
151722741:151722741(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.534G>A |
| AA Mutation |
p.Trp178Ter(p.W178*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |