| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296140 |
| Start |
46203881:46203881(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs777872590
|
| CDS Mutation |
c.433C>T |
| AA Mutation |
p.Arg145Trp(p.R145W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000296140 |
| Start |
46203903:46203903(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768750994
|
| CDS Mutation |
c.411C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000296140 |
| Start |
46203876:46203876(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs146268408
|
| CDS Mutation |
c.438C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |