Y11C (p.Tyr11Cys) variant of POT1 (Q9NUX5)
Y11C (p.Tyr11Cys) in POT1 (Q9NUX5) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Tumor predisposition syndrome 3; not sp. The available variant effect predictions contribute to a CATVariant prioritization score of 0.76 / 1. The record also includes population frequency data, published literature, and structural context.
Y11C (p.Tyr11Cys) variant details
- p.Tyr11Cys
- rs1796392612
- ClinGen CA369066256
- ClinVar RCV002628435
- ClinVar RCV004070588
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Tumor predisposition syndrome 3; not sp
- Missense
- Variant Prioritization Score for Impact Estimate 0.762
- REVEL 0.85
- CADD 27.60
- PolyPhen-2 1.00
- SIFT 0.00
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Tumor predisposition sy)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9.5e-07)
- 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)
- Cited in: POT1 Tumor Predisposition. (PMID 33119245)