Gene >> UCN3
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380433 |
| Start |
5374096:5374096(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs186863985
|
| CDS Mutation |
c.376G>A |
| AA Mutation |
p.Val126Ile(p.V126I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380433 |
| Start |
5373731:5373731(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.11C>T |
| AA Mutation |
p.Pro4Leu(p.P4L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |