| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367265 |
| Start |
202735516:202735516(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3336G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367265 |
| Start |
202741543:202741543(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2769G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000367265 |
| Start |
202756482:202756482(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1232G>A |
| AA Mutation |
p.Trp411Ter(p.W411*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |