V19M (p.Val19Met) variant of BBS2 (BBSome complex member BBS2)
V19M (p.Val19Met) in BBS2 (BBSome complex member BBS2) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Inborn genetic diseases; Bardet-Biedl syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data, published literature, and structural context.
V19M (p.Val19Met) variant details
- p.Val19Met
- rs1158566793
- ClinGen CA395988155
- ClinVar RCV001303734
- ClinVar RCV001830201
- Uncertain significance
- Inborn genetic diseases; Bardet-Biedl syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.524
- REVEL 0.40
- CADD 28.30
- PolyPhen-2 0.91
- SIFT 0.00
- ClinVar: Uncertain significance (Inborn genetic diseases; Bardet-Biedl syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the African/African-American population (allele frequency 0.00031)
- Structural context available
- Cited in: Bardet-Biedl Syndrome Overview. (PMID 20301537)
- Cited in: Pediatric Obesity-Assessment, Treatment, and Prevention: An Endocrine Society Clinical Practice Guideline. (PMID 28359099)