Gene >> USP10
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000219473 |
| Start |
84772610:84772610(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774568908
|
| CDS Mutation |
c.2068G>A |
| AA Mutation |
p.Val690Ile(p.V690I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000219473 |
| Start |
84764240:84764240(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370164533
|
| CDS Mutation |
c.1809C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |