| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268150 |
| Start |
88909858:88909858(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs148213281
|
| CDS Mutation |
c.139G>C |
| AA Mutation |
p.Gly47Arg(p.G47R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268150 |
| Start |
88899796:88899796(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.886T>A |
| AA Mutation |
p.Ser296Thr(p.S296T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000268150 |
| Start |
88907312:88907312(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.270T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |