Multiple Tumours
Gene: RAD51CEnsemblGeneIds (GRCh38): ENSG00000108384
EnsemblGeneIds (GRCh37): ENSG00000108384
OMIM: 602774, Gene2Phenotype
RAD51C is in 21 panels
1 review
Ellen McDonagh (Genomics England Curator)
Information from TruSight panel: Pathogenic Mutations are Inactivating.Created: 5 Feb 2016, 11:46 a.m.
Details
- Mode of Inheritance
- BOTH monoallelic and biallelic, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- TruSight Cancer Panel (Illumina)
- Phenotypes
-
- Fanconi Anemia (O) (biallelic mutations)
- Ovarian cancer (monoallelic mutations)
- Familial breast cancer
- Paediatric congenital malformation-dysmorphism-tumour syndromes
- OMIM
- 602774
- Clinvar variants
- Variants in RAD51C
- Penetrance
- Complete
- Panels with this gene
-
- Inherited ovarian cancer (without breast cancer)
- DDG2P
- Fetal anomalies
- Childhood solid tumours cancer susceptibility
- Radial dysplasia
- Haematological malignancies cancer susceptibility
- Familial breast cancer
- Ovarian cancer pertinent cancer susceptibility
- Inherited breast cancer and ovarian cancer
- Cytopenias and congenital anaemias
- Intellectual disability
- Severe microcephaly
- COVID-19 research
- Limb disorders
- Neurofibromatosis Type 1
- Childhood solid tumours
- Haematological malignancies for rare disease
- Adult solid tumours for rare disease
- Confirmed Fanconi anaemia or Bloom syndrome
- Pigmentary skin disorders
- Adult solid tumours cancer susceptibility
History Filter Activity
Added New Source
Ellen McDonagh (Genomics England Curator)RAD51C was added to Multiple Tumourspanel. Source: Expert Review Green
Created
Ellen McDonagh (Genomics England Curator)RAD51C was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)RAD51C was added to Multiple Tumourspanel. Sources: TruSight Cancer Panel (Illumina)