| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000217289 |
| Start |
6097610:6097610(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.871C>G |
| AA Mutation |
p.Gln291Glu(p.Q291E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000217289 |
| Start |
6096931:6096931(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1060C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000217289 |
| Start |
6110512:6110512(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.533-1G>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |