| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000524377 |
| Start |
156880153:156880153(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs755323716
|
| CDS Mutation |
c.2201C>T |
| AA Mutation |
p.Thr734Met(p.T734M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000524377 |
| Start |
156880056:156880056(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs374918502
|
| CDS Mutation |
c.2104C>T |
| AA Mutation |
p.Arg702Cys(p.R702C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000524377 |
| Start |
156875638:156875638(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs373181158
|
| CDS Mutation |
c.1473C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |