Gene >> USP5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229268 |
| Start |
6861082:6861082(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs781900287
|
| CDS Mutation |
c.1474C>T |
| AA Mutation |
p.Pro492Ser(p.P492S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000229268 |
| Start |
6861570:6861570(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs782540537
|
| CDS Mutation |
c.1626C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |