| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000287878 |
| Start |
151876511:151876511(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.110T>G |
| AA Mutation |
p.Ile37Ser(p.I37S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000287878 |
| Start |
151557213:151557213(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1698A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000287878 |
| Start |
151632084:151632084(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.739G>T |
| AA Mutation |
p.Glu247Ter(p.E247*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |