| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000283268 |
| Start |
62372542:62372542(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.327C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000283268 |
| Start |
62372056:62372056(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.813T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000283268 |
| Start |
62371247:62371247(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1090G>T |
| AA Mutation |
p.Glu364Ter(p.E364*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |