Annotation Detail
Information
- Associated Genes
- POLG POLGARF
- Associated Variants
-
POLG p.Pro587Leu (p.P587L)
(
ENST00000442287.6,
ENST00000636937.2,
ENST00000268124.11 )
POLG p.Pro587Leu (p.P587L) ( ENST00000268124.11, ENST00000442287.6, ENST00000636937.2 ) - Associated Disease
- mitochondrial DNA depletion syndrome 4b
- Source Database
- ClinVar
- Description
- NM_002693.3(POLG):c.1760C>T (p.Pro587Leu) AND Mitochondrial DNA depletion syndrome 4b
- Pubmed
- 12975295
- Pubmed
- 12825077
- ClinVar Allele ID
- 28544
- ClinVar RefSeq Alternation Syntax
- NM_002693.3:c.1760C>T
- ClinVar RefSeq Alternation Syntax
- NM_001126131.2:c.1760C>T
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2023-04-05
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000014456
- ClinVar Disease
- Mitochondrial DNA depletion syndrome 4b
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
- Pubmed
- 15349879
Drugs