Annotation Detail
Information
- Associated Genes
- MDN1 MDN1-AS1 LOC126859739
- Associated Variants
-
MDN1 p.Pro4908Thr (p.P4908T)
(
ENST00000369393.8 )
MDN1 p.Pro4908Thr (p.P4908T) ( ENST00000369393.8 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_014611.3(MDN1):c.14722C>A (p.Pro4908Thr) AND not specified
- ClinVar Allele ID
- 2340928
- ClinVar RefSeq Alternation Syntax
- NM_014611.3:c.14722C>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2022-06-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004181422
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs