| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361735 |
| Start |
171784059:171784059(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.473G>T |
| AA Mutation |
p.Cys158Phe(p.C158F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361735 |
| Start |
171790516:171790516(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1374A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361735 |
| Start |
171792108:171792108(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1566T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |