| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000269080 |
| Start |
68924756:68924756(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1387T>G |
| AA Mutation |
p.Phe463Val(p.F463V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000269080 |
| Start |
68877611:68877611(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3987G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000269080 |
| Start |
68869767:68869767(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4524G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |