Entity rating | Entity | Mode of inheritance | Mode of pathogenicity | Tags |
---|---|---|---|---|
Green | BIALLELIC, autosomal or pseudoautosomal | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments | N/A | |
Green | BIALLELIC, autosomal or pseudoautosomal | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | BIALLELIC, autosomal or pseudoautosomal | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments | N/A | |
Green | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments | N/A | |
Green | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | N/A | Q4_21_MOI | |
Green | BIALLELIC, autosomal or pseudoautosomal | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Other | N/A | |
Green | BIALLELIC, autosomal or pseudoautosomal | N/A | watchlist | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype -please provide details in the comments | N/A | |
Green | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A | |
Green | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | N/A | N/A |