| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379638 |
| Start |
112887110:112887110(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs755142860
|
| CDS Mutation |
c.425G>A |
| AA Mutation |
p.Arg142His(p.R142H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000379638 |
| Start |
112887154:112887154(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs745340401
|
| CDS Mutation |
c.381G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000379638 |
| Start |
112922098:112922098(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370119424
|
| CDS Mutation |
c.93C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |