| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000344722 |
| Start |
160430617:160430617(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2814A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000344722 |
| Start |
160430626:160430626(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2823C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000344722 |
| Start |
160416326:160416326(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1348G>T |
| AA Mutation |
p.Glu450Ter(p.E450*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |