| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000257068 |
| Start |
92982288:92982288(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1065G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000257068 |
| Start |
92969755:92969755(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.30C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000257068 |
| Start |
92982289:92982289(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs748364564
|
| CDS Mutation |
c.1066C>T |
| AA Mutation |
p.Gln356Ter(p.Q356*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |