RAD51C

RAD51 paralog C
OMIM: 602774, ClinGen, DECIPHER

12 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 12 panels
Amber RAD51C in Bone Marrow Failure Level 2: Haematological disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Fanconi anemia, complementation group O, MIM# 613390
Green RAD51C in Chromosome Breakage Disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Fanconi anemia, complementation group O, MIM# 613390
Green RAD51C in Mendeliome Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group O (MIM#613390)
Red RAD51C in Cancer Predisposition_Paediatric Level 2: Cancer Version 1.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Fanconi anemia, complementation group O, MIM# 613390
Green RAD51C in Radial Ray Abnormalities Level 2: Dysmorphic and congenital abnormality syndromes Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Fanconi anemia, complementation group O, MIM# 613390
Green RAD51C in Additional findings_Adult Level 2: Screening Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes Fanconi anaemia, complementation group O, MIM# 613390
Green RAD51C in Homologous_recombination_deficiency_WTS_UMCCR Level 2: Cancer Version 1.0	0 reviews	Unknown	Sources Expert list Expert Review Green Tags umccr
Green RAD51C in Growth failure Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes Fanconi anaemia, complementation group O, MIM# 613390
Green RAD51C in Fetal anomalies Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Fanconi anemia, complementation group O, MIM# 613390
Green RAD51C in IBMDx study Version 1.0	1 review	Unknown	Sources Expert Review Green IBMDx Study Expert Review Green Victorian Clinical Genetics Services Phenotypes Fanconi anemia, complementation group O, MIM# 613390
Green RAD51C in Ovarian Cancer Level 2: Cancer Predisposition Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Ovarian cancer, MONDO:0008170 RAD51C-related cancer predisposition, MONDO:0700273 Breast-ovarian cancer, familial, susceptibility to, 3, MONDO:0013253 Breast-ovarian cancer, familial, susceptibility to, 3, MIM#613399
Green RAD51C in Breast Cancer Level 2: Cancer Predisposition Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Breast cancer, MONDO:0007254 RAD51C-related cancer predisposition, MONDO:0700273 Breast-ovarian cancer, familial, susceptibility to, 3, MONDO:0013253 Breast-ovarian cancer, familial, susceptibility to, 3, MIM#613399