| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Haematological malignancies v0.103 | Bryony Thompson Added reviews for gene SAMD9L from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Haematological malignancies v0.102 | Bryony Thompson Copied gene SAMD9 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Haematological malignancies v0.102 | SAMD9 |
Bryony Thompson gene: SAMD9 was added gene: SAMD9 was added to Haematological malignancies. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: SAMD9 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: SAMD9 were set to 33237688; 32619790; 16960814; 18094730 Phenotypes for gene: SAMD9 were set to MIRAGE syndrome, MIM#617053; Tumoral calcinosis, familial, normophosphatemic, MIM#610455; Monosomy 7 myelodysplasia and leukemia syndrome 2, MIM# 619041 |
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| Haematological malignancies v0.0 | SAMD9L |
Bryony Thompson gene: SAMD9L was added gene: SAMD9L was added to Haematological malignancies cancer susceptibility. Sources: Curated sources,Expert Review Green Mode of inheritance for gene: SAMD9L was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: SAMD9L were set to 28297620 Phenotypes for gene: SAMD9L were set to MDS, AML; Class: miscellaneous; Ataxia Pancytopenia Syndrome |
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