| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Proteinuria v1.0 | AVIL | Gene migrated from ENSG00000135407 to ENSG00000135407 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Proteinuria v0.235 | Bryony Thompson Copied gene AVIL from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Proteinuria v0.235 | AVIL |
Bryony Thompson gene: AVIL was added gene: AVIL was added to Proteinuria. Sources: Expert Review Green,Literature Mode of inheritance for gene: AVIL was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: AVIL were set to 29058690 Phenotypes for gene: AVIL were set to Nephrotic syndrome, type 21 MONDO:0032826 |
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