| Panel | Mode of inheritance | Details |
|---|---|---|
10 panels | ||
Signed-off version 2.2 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Li Fraumeni Syndrome |
Signed-off version 1.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Adult Glioma |
Signed-off version 2.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Breast cancer |
Green in Childhood solid tumoursSigned-off version 5.11 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Adrenocortical carcinoma, Li Fraumeni Syndrome |
R-numbers: R456 Signed-off version 1.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes {Colorectal cancer}, OMIM:114500, {Adrenocortical carcinoma, pediatric}, OMIM:202300, choroid plexus papilloma, MONDO:0009837, {Choroid plexus papilloma}, OMIM:260500, Li-Fraumeni syndrome, MONDO:0018875, nasopharyngeal carcinoma, susceptibility to, 1, MONDO:0011775, {Basal cell carcinoma 7}, OMIM:614740, Li-Fraumeni syndrome, OMIM:151623, basal cell carcinoma, susceptibility to, 7, MONDO:0013876, {Glioma susceptibility 1}, OMIM:137800, adrenocortical carcinoma, hereditary, MONDO:0008734 |
Signed-off version 5.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Class: Familial cancer syndrome, Li-Fraumeni syndrome, ALL, AML, MDS, Adrenal, breast, brain, and lung sarcoma, gastrointestinal cancers, Breast cancer, osteosarcoma, soft tissue sarcomas, brain tumors, adrenocortical carcinoma |
R-numbers: R347 Signed-off version 3.5 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Li-Fraumeni syndrome, OMIM:151623, Li-Fraumeni syndrome 1, MONDO:0007903 |
Green in Li Fraumeni SyndromeR-numbers: R216 Signed-off version 1.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes |
Green in Sarcoma of possible germline originR-numbers: R457 Signed-off version 1.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes {Colorectal cancer}, OMIM:114500, basal cell carcinoma, susceptibility to, 7, MONDO:0013876, adrenocortical carcinoma, hereditary, MONDO:0008734, {Glioma susceptibility 1}, OMIM:137800, nasopharyngeal carcinoma, susceptibility to, 1, MONDO:0011775, Li-Fraumeni syndrome, OMIM:151623, Li-Fraumeni syndrome, MONDO:0018875, {Basal cell carcinoma 7}, OMIM:614740, choroid plexus papilloma, MONDO:0009837, {Adrenocortical carcinoma, pediatric}, OMIM:202300, {Choroid plexus papilloma}, OMIM:260500 |
Green in Sarcoma susceptibilitySigned-off version 1.2 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Sarcoma, Li-Fraumeni syndrome, 151623 |