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Confirmed Fanconi anaemia or Bloom syndrome v0.20 FANCG Louise Daugherty commented on gene: FANCG: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: FANCG; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Fanconi Anemia;Fanconi anemia, complementation group G, 614082; PMID(s): none submitted
Confirmed Fanconi anaemia or Bloom syndrome v0.19 FANCG Steve Keeney reviewed gene: FANCG: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Fanconi Anemia, Fanconi anemia, complementation group G, 614082; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Confirmed Fanconi anaemia or Bloom syndrome v0.18 FANCG Louise Daugherty Added phenotypes Fanconi Anemia; Fanconi anemia, complementation group G, 614082 for gene: FANCG
Confirmed Fanconi anaemia or Bloom syndrome v0.16 FANCG Louise Daugherty Source North West GLH was added to FANCG.
Confirmed Fanconi anaemia or Bloom syndrome v0.11 FANCG Louise Daugherty commented on gene: FANCG: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: FANCG; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 614082 Fanconi anemia, complementation group G; PMID(s): none submitted
Confirmed Fanconi anaemia or Bloom syndrome v0.10 FANCG Mandy nesbitt reviewed gene: FANCG: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 614082 Fanconi anemia, complementation group G; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Confirmed Fanconi anaemia or Bloom syndrome v0.9 FANCG Louise Daugherty Added phenotypes 614082 Fanconi anemia, complementation group G for gene: FANCG
Confirmed Fanconi anaemia or Bloom syndrome v0.7 FANCG Louise Daugherty Source Yorkshire and North East GLH was added to FANCG.
Confirmed Fanconi anaemia or Bloom syndrome v0.6 FANCG Louise Daugherty reviewed gene: FANCG: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Confirmed Fanconi anaemia or Bloom syndrome v0.5 FANCG Carl Fratter reviewed gene: FANCG: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Confirmed Fanconi anaemia or Bloom syndrome v0.4 FANCG Louise Daugherty Source NHS GMS was added to FANCG.
Confirmed Fanconi anaemia or Bloom syndrome v0.3 FANCG Louise Daugherty Source Expert Review Green was added to FANCG.
Mode of inheritance for gene FANCG was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Fanconi Anemia; Fanconi anemia, complementation group G, 614082 for gene: FANCG
Publications for gene FANCG were changed from to 9806548
Rating Changed from Red List (low evidence) to Green List (high evidence)
Confirmed Fanconi anaemia or Bloom syndrome v0.2 FANCG Louise Daugherty gene: FANCG was added
gene: FANCG was added to Confirmed Fanconi anaemia or Bloom syndrome. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: FANCG was set to