| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Transplant Co-Morbidity v1.0 | TTR | Gene migrated from ENSG00000118271 to ENSG00000118271 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Transplant Co-Morbidity v0.0 | TTR |
Bryony Thompson gene: TTR was added gene: TTR was added to Transplant Co-Morbidity Superpanel. Sources: Victorian Clinical Genetics Services,Expert Review Green Mode of inheritance for gene: TTR was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: TTR were set to 28475415; 35802134; 31554435 Phenotypes for gene: TTR were set to Amyloidosis, hereditary, transthyretin-related MIM#105210 |
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