Y69C (p.Tyr69Cys) variant of BUB1B (O60566)
Y69C (p.Tyr69Cys) in BUB1B (O60566) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data, published literature, and structural context.
Y69C (p.Tyr69Cys) variant details
- p.Tyr69Cys
- rs2037144381
- ClinGen CA391678429
- ClinVar RCV002422091
- TOPMed rs2037144381
- Uncertain significance
- Inborn genetic diseases
- Missense
- Variant Prioritization Score for Impact Estimate 0.555
- REVEL 0.59
- MetaLR 0.48
- MetaSVM -0.07
- CADD 28.90
- PolyPhen-2 1.00
- SIFT 0.06
- ClinVar: Uncertain significance (Inborn genetic diseases)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Cited in: Specific guidelines for assessing and improving the methodological quality of economic evaluations of newborn screening. (PMID 22947299)
- Cited in: Including the initial newborn screening bloodspot collection device serial number on birth certificates: basis and… (PMID 23037933)