| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000452722 |
| Start |
115240319:115240319(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752868486
|
| CDS Mutation |
c.226C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000452722 |
| Start |
115214723:115214723(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.879G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_lost |
| Transcription ID |
ENST00000452722 |
| Start |
115176475:115176475(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1328A>T |
| AA Mutation |
p.Ter443LeuextTer15(p.*443Lext*15) |
| Mutation Classification |
Nonstop_Mutation |
| Feature Type |
Transcript |