Annotation Detail
Information
- Associated Genes
- PBX4 LOC130064083
- Associated Variants
-
PBX4 p.Pro4Ala (p.P4A)
(
ENST00000251203.14 )
PBX4 p.Pro4Ala (p.P4A) ( ENST00000251203.14 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_025245.3(PBX4):c.10C>G (p.Pro4Ala) AND not specified
- ClinVar Allele ID
- 3374871
- ClinVar RefSeq Alternation Syntax
- NR_038198.2:n.68C>G
- ClinVar RefSeq Alternation Syntax
- NM_025245.3:c.10C>G
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2024-02-28
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004504910
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs