Non-Fanconi anaemia
Gene: FANCC
Variants in this GENE are reported as part of current diagnostic practice
~25% of patients show evidence of mosaicismCreated: 26 Jan 2016, 10:57 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Fanconi anemia complementation group C
FANCC was added to Non-Fanconi anaemiapanel. Source: Expert list
Model of inheritance for gene FANCC was set to BIALLELIC, autosomal or pseudoautosomal
FANCC was added to Non-Fanconi anaemiapanel. Source: UKGTN
Model of inheritance for gene FANCC was set to BIALLELIC, autosomal or pseudoautosomal
FANCC was added to Non-Fanconi anaemiapanel. Source: Radboud University Medical Center, Nijmegen
Model of inheritance for gene FANCC was set to BIALLELIC, autosomal or pseudoautosomal
FANCC was added to Non-Fanconi anaemiapanel. Source: Illumina TruGenome Clinical Sequencing Services
Model of inheritance for gene FANCC was set to BIALLELIC, autosomal or pseudoautosomal
FANCC was added to Non-Fanconi anaemiapanel. Source: UKGTN
Model of inheritance for gene FANCC was set to BIALLELIC, autosomal or pseudoautosomal
FANCC was added to Non-Fanconi anaemiapanel. Source: Radboud University Medical Center, Nijmegen
Model of inheritance for gene FANCC was set to BIALLELIC, autosomal or pseudoautosomal
FANCC was added to Non-Fanconi anaemiapanel. Source: Illumina TruGenome Clinical Sequencing Services
Model of inheritance for gene FANCC was changed to BIALLELIC, autosomal or pseudoautosomal
Model of inheritance for gene FANCC was changed to BIALLELIC, autosomal or pseudoautosomal
Model of inheritance for gene FANCC was changed to BIALLELIC, autosomal or pseudoautosomal
Model of inheritance for gene FANCC was changed to BIALLELIC, autosomal or pseudoautosomal
Model of inheritance for gene FANCC was changed to BIALLELIC, autosomal or pseudoautosomal
Model of inheritance for gene FANCC was changed to BIALLELIC, autosomal or pseudoautosomal
Model of inheritance for gene FANCC was changed to BIALLELIC, autosomal or pseudoautosomal
FANCC was added to Non-Fanconi anaemiapanel. Sources: Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN
Model of inheritance for gene FANCC was changed to BIALLELIC, autosomal or pseudoautosomal
FANCC was added to Non-Fanconi anaemiapanel. Sources: Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN
FANCC was added to Non-Fanconi anaemiapanel. Sources: Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN