| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000395863 |
| Start |
57265839:57265839(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.284G>A |
| AA Mutation |
p.Gly95Asp(p.G95D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000395863 |
| Start |
57265838:57265838(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.285C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000395863 |
| Start |
57202482:57202482(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.753G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |