F419L (p.Phe419Leu) variant of ALDH5A1 (P51649)
F419L (p.Phe419Leu) in ALDH5A1 (P51649) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as pathogenic in the context of Succinate-semialdehyde dehydrogenase deficiency. The available variant effect predictions contribute to a CATVariant prioritization score of 0.72 / 1. The record also includes population frequency data, published literature, and structural context.
F419L (p.Phe419Leu) variant details
- p.Phe419Leu
- rs765595608
- ClinGen CA3656891
- cosmic curated COSV62374
- ClinVar RCV002510532
- Pathogenic
- Succinate-semialdehyde dehydrogenase deficiency
- Missense
- Variant Prioritization Score for Impact Estimate 0.718
- REVEL 0.75
- CADD 25.90
- PolyPhen-2 0.97
- SIFT 0.00
- ClinVar: Pathogenic (Succinate-semialdehyde dehydrogenase deficiency)
- EBI: Pathogenic
- UniProt: Pathogenic
- Population evidence available
- Structural context available
- Cited in: Succinic Semialdehyde Dehydrogenase Deficiency. (PMID 20301374)
- Cited in: Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions. (PMID 23519317)