| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263857 |
| Start |
86099987:86099987(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.263A>T |
| AA Mutation |
p.Tyr88Phe(p.Y88F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263857 |
| Start |
86075138:86075138(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs543626300
|
| CDS Mutation |
c.1503C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263857 |
| Start |
86054278:86054278(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs545753325
|
| CDS Mutation |
c.2070G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |