G26D (p.Gly26Asp) variant of NF1 (Neurofibromin)
G26D (p.Gly26Asp) in NF1 (Neurofibromin) is a missense change. Clinical records from EBI and UniProt describe it as pathogenic. The record also includes published literature and structural context.
G26D (p.Gly26Asp) variant details
- p.Gly26Asp
- rs2143625360
- ClinGen CA2573153519
- ClinVar RCV001916555
- Pathogenic
- Missense
- EBI: Pathogenic
- UniProt: Pathogenic
- Structural context available
- Cited in: Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. (PMID 15604628)
- Cited in: Neurofibromatosis type 1 in genetic counseling practice: recommendations of the National Society of Genetic Counselors. (PMID 17636453)