| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265512 |
| Start |
99144218:99144218(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.5G>T |
| AA Mutation |
p.Gly2Val(p.G2V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265512 |
| Start |
99141555:99141555(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs111700010
|
| CDS Mutation |
c.248C>T |
| AA Mutation |
p.Thr83Ile(p.T83I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265512 |
| Start |
99131525:99131525(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.822T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |