R13S (p.Arg13Ser) variant of PTCH1 (Protein patched homolog 1)
R13S (p.Arg13Ser) in PTCH1 (Protein patched homolog 1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Gorlin syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
R13S (p.Arg13Ser) variant details
- p.Arg13Ser
- rs779791579
- ClinGen CA374121584
- ClinVar RCV003080054
- Uncertain significance
- Gorlin syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.248
- REVEL 0.23
- CADD 14.70
- PolyPhen-2 0.00
- SIFT 0.58
- ClinVar: Uncertain significance (Gorlin syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available
- Cited in: Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. (PMID 15604628)
- Cited in: Nevoid Basal Cell Carcinoma Syndrome. (PMID 20301330)