I37N (p.Ile37Asn) variant of SUFU (Suppressor of fused homolog)
I37N (p.Ile37Asn) in SUFU (Suppressor of fused homolog) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes published literature and structural context.
I37N (p.Ile37Asn) variant details
- p.Ile37Asn
- rs2544831254
- ClinGen CA377886501
- ClinVar RCV002428957
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance (in dbSNP:rs745793517)
- UniProt: Uncertain significance (in dbSNP:rs745793517)
- 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)