| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000432109 |
| Start |
201285201:201285201(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776243948
|
| CDS Mutation |
c.1188G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000432109 |
| Start |
201285307:201285307(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1294C>T |
| AA Mutation |
p.Arg432Ter(p.R432*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000432109 |
| Start |
201266592:201266592(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.106G>T |
| AA Mutation |
p.Glu36Ter(p.E36*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |