| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000334746 |
| Start |
93257204:93257204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1599A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000334746 |
| Start |
93253692:93253692(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1707C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000334746 |
| Start |
93248526:93248526(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2071C>T |
| AA Mutation |
p.Arg691Ter(p.R691*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |