| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262891 |
| Start |
45294381:45294381(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1527A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262891 |
| Start |
45280598:45280598(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1140A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000262891 |
| Start |
45287569:45287569(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1399C>T |
| AA Mutation |
p.Arg467Ter(p.R467*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |