| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000329797 |
| Start |
105052097:105052097(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778976347
|
| CDS Mutation |
c.40G>A |
| AA Mutation |
p.Ala14Thr(p.A14T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000329797 |
| Start |
105051105:105051105(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778680528
|
| CDS Mutation |
c.1032C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000329797 |
| Start |
105051438:105051438(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs75775050
|
| CDS Mutation |
c.699C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |