| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303538 |
| Start |
39904096:39904096(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs766740882
|
| CDS Mutation |
c.1329C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000303538 |
| Start |
39890310:39890310(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1825G>T |
| AA Mutation |
p.Glu609Ter(p.E609*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000303538 |
| Start |
39913628:39913628(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.975G>A |
| AA Mutation |
p.Trp325Ter(p.W325*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |