L2M (p.Leu2Met) variant of BBS2 (BBSome complex member BBS2)
L2M (p.Leu2Met) 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 Bardet-Biedl syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes published literature and structural context.
L2M (p.Leu2Met) variant details
- p.Leu2Met
- rs2144214806
- ClinGen CA395988356
- ClinVar RCV001939839
- Ensembl rs2144214806
- Uncertain significance
- Bardet-Biedl syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.608
- AlphaMissense 0.13
- MetaLR 0.77
- MetaSVM 0.42
- SIFT 0.13
- MutPred 0.54
- ClinVar: Uncertain significance (Bardet-Biedl syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- 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)