| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265713 |
| Start |
41955379:41955379(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1515A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265713 |
| Start |
41941295:41941295(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2586A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000265713 |
| Start |
41941096:41941096(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2785C>T |
| AA Mutation |
p.Gln929Ter(p.Q929*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |