Q21L (p.Gln21Leu) variant of SDHC (Q99643)
Q21L (p.Gln21Leu) in SDHC (Q99643) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes published literature and structural context.
Q21L (p.Gln21Leu) variant details
- p.Gln21Leu
- rs1670927465
- ClinGen CA343359558
- ClinVar RCV004508390
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.393
- AlphaMissense 0.07
- MetaLR 0.43
- MetaSVM -0.63
- PolyPhen-2 0.00
- SIFT 0.59
- EVE 0.12
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)