| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000344895 |
| Start |
111073519:111073519(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.225C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000344895 |
| Start |
111073567:111073567(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.273G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000344895 |
| Start |
111073526:111073526(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.232G>T |
| AA Mutation |
p.Glu78Ter(p.E78*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |