| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000309958 |
| Start |
51014869:51014869(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.762G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000309958 |
| Start |
51017166:51017166(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.213C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000309958 |
| Start |
51014827:51014827(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.804G>A |
| AA Mutation |
p.Trp268Ter(p.W268*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |