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Intellectual disability - microarray and sequencing v3.1450 NOP56 Arina Puzriakova Added comment: Comment on mode of inheritance: Lack of phenotypic relevance for SNVs - nucleotide repeat expansion mechanism
Intellectual disability - microarray and sequencing v3.1450 NOP56 Arina Puzriakova Mode of inheritance for gene: NOP56 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to Other
Intellectual disability - microarray and sequencing v3.1449 NOP56 Arina Puzriakova Phenotypes for gene: NOP56 were changed from Spinocerebellar ataxia 36, 614153 to Spinocerebellar ataxia 36, OMIM:614153
Intellectual disability - microarray and sequencing v3.1448 NOP56 Arina Puzriakova Tag nucleotide-repeat-expansion tag was added to gene: NOP56.
Tag currently-ngs-unreportable tag was added to gene: NOP56.
Intellectual disability - microarray and sequencing v3.917 NOP56 Sarah Leigh Source: Expert Review Amber was removed from gene: NOP56
Intellectual disability - microarray and sequencing NOP56 Louise Daugherty commented on NOP56
Intellectual disability - microarray and sequencing NOP56 BRIDGE consortium edited their review of NOP56
Intellectual disability - microarray and sequencing NOP56 BRIDGE consortium edited their review of NOP56
Intellectual disability - microarray and sequencing NOP56 Louise Daugherty classified NOP56 as amber
Intellectual disability - microarray and sequencing NOP56 Louise Daugherty commented on NOP56
Intellectual disability - microarray and sequencing NOP56 BRIDGE consortium reviewed NOP56