| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000255189 |
| Start |
79026458:79026458(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2156G>A |
| AA Mutation |
p.Arg719His(p.R719H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000255189 |
| Start |
79024297:79024297(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757937639
|
| CDS Mutation |
c.2224C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000255189 |
| Start |
79026472:79026472(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2142C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |