Childhood solid tumours
Gene: FANCC
As discussed at the Genomics Cancer Panel Workshop, 16th July 2019: the group agreed that there is enough evidence to rate this gene green.Created: 2 Aug 2019, 11:03 a.m. | Last Modified: 2 Aug 2019, 11:03 a.m.
Panel Version: 1.27
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Fanconi Anemia
Source NHS GMS was added to FANCC. Added phenotypes Fanconi Anemia for gene: FANCC Publications for gene FANCC were changed from to 19686080
Source Expert List was added to FANCC. Rating Changed from Green List (high evidence) to Green List (high evidence)
This gene has been classified as Green List (High Evidence).
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 Paediatric congenital malformation-dysmorphism-tumour syndromes panel. Sources: UKGTN
Model of inheritance for gene FANCC was changed to BIALLELIC, autosomal or pseudoautosomal
FANCC was added to Paediatric congenital malformation-dysmorphism-tumour syndromes panel. Sources: Illumina TruGenome Clinical Sequencing Services
FANCC was added to Paediatric congenital malformation-dysmorphism-tumour syndromes panel. Sources: Radboud University Medical Center, Nijmegen