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Inherited renal cancer v1.27 BAP1 Arina Puzriakova Phenotypes for gene: BAP1 were changed from Tumor predisposition syndrome, OMIM:614327; BAP1-related tumor predisposition syndrome, MONDO:0013692; Renal cell carcinoma (disease), MONDO:0005086; Clear cell renal carcinoma, MONDO:0005005 to Tumor predisposition syndrome 1, OMIM:614327; {Uveal melanoma, susceptibility to, 2}, OMIM:606661
Inherited renal cancer v1.6 BAP1 Arina Puzriakova Phenotypes for gene: BAP1 were changed from Malignant mesothelioma after asbestos exposure; Uveal melanoma; Cutaneous melanoma; Meningioma; Renal cell carcinoma, usually clear cell type to Tumor predisposition syndrome, OMIM:614327; BAP1-related tumor predisposition syndrome, MONDO:0013692; Renal cell carcinoma (disease), MONDO:0005086; Clear cell renal carcinoma, MONDO:0005005
Inherited renal cancer v1.5 BAP1 Arina Puzriakova Publications for gene: BAP1 were set to
Inherited renal cancer v0.38 BAP1 Ivone Leong commented on gene: BAP1
Inherited renal cancer v0.29 BAP1 Ivone Leong Classified gene: BAP1 as Green List (high evidence)
Inherited renal cancer v0.29 BAP1 Ivone Leong Gene: bap1 has been classified as Green List (High Evidence).
Inherited renal cancer v0.3 BAP1 Lara Hawkes reviewed gene: BAP1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Inherited renal cancer v0.2 BAP1 Ivone Leong Source Expert List was added to BAP1.
Rating Changed from No List (delete) to Red List (low evidence)
Inherited renal cancer v0.1 BAP1 Rachel Robinson gene: BAP1 was added
gene: BAP1 was added to Inherited renal cancer. Sources: UKGTN
Mode of inheritance for gene: BAP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: BAP1 were set to Malignant mesothelioma after asbestos exposure; Uveal melanoma; Cutaneous melanoma; Meningioma; Renal cell carcinoma, usually clear cell type
Penetrance for gene: BAP1 were set to Incomplete
Review for gene: BAP1 was set to GREEN
gene: BAP1 was marked as current diagnostic
Added comment: Sources: UKGTN