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| Wilms Tumour v0.40 | FBXW7 | Zornitza Stark Marked gene: FBXW7 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wilms Tumour v0.40 | FBXW7 | Zornitza Stark Gene: fbxw7 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wilms Tumour v0.31 | FBXW7 |
Chirag Patel changed review comment from: Some evidence for gene-disease association for Wilms tumour. Few cases of monoallelic truncating variants associated with sporadic Wilms tumour (possible incomplete penetrance). Sources: Expert list, Expert Review, Literature; to: Some evidence for gene-disease association for Wilms tumour. Four cases of monoallelic truncating variants associated with sporadic Wilms tumour (possible incomplete penetrance). Sources: Expert list, Expert Review, Literature |
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| Wilms Tumour v0.31 | FBXW7 | Chirag Patel Classified gene: FBXW7 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wilms Tumour v0.31 | FBXW7 | Chirag Patel Gene: fbxw7 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wilms Tumour v0.30 | FBXW7 |
Chirag Patel gene: FBXW7 was added gene: FBXW7 was added to Wilms Tumour. Sources: Expert list,Expert Review,Literature Mode of inheritance for gene: FBXW7 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: FBXW7 were set to PMID: 30885698 Phenotypes for gene: FBXW7 were set to Wilms tumor, MONDO:0006058; Wilms tumour, no MIM# Review for gene: FBXW7 was set to AMBER Added comment: Some evidence for gene-disease association for Wilms tumour. Few cases of monoallelic truncating variants associated with sporadic Wilms tumour (possible incomplete penetrance). Sources: Expert list, Expert Review, Literature |
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