T18P (p.Thr18Pro) variant of FLCN (Folliculin)
T18P (p.Thr18Pro) in FLCN (Folliculin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Birt-Hogg-Dube syndrome; not provided. The record also includes published literature and structural context.
T18P (p.Thr18Pro) variant details
- p.Thr18Pro
- rs761993256
- ClinGen CA398535428
- ClinVar RCV001221879
- ClinVar RCV001776150
- Uncertain significance
- Birt-Hogg-Dube syndrome; not provided
- Missense
- ClinVar: Uncertain significance (Birt-Hogg-Dube syndrome; not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Birt-Hogg-Dubé Syndrome. (PMID 20301695)
- Cited in: Canadian guideline on genetic screening for hereditary renal cell cancers. (PMID 24319509)