Activity
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| Fetal anomalies v4.192 | PPP2CA |
Achchuthan Shanmugasundram Tag Q3_24_promote_green was removed from gene: PPP2CA. Tag Q3_24_NHS_review was removed from gene: PPP2CA. |
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| Fetal anomalies v4.192 | PPP2CA | Achchuthan Shanmugasundram edited their review of gene: PPP2CA: Added comment: The rating of this gene has been updated to green and the mode of inheritance set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v4.191 | PPP2CA |
Achchuthan Shanmugasundram Source Expert Review Green was added to PPP2CA. Rating Changed from Amber List (moderate evidence) to Green List (high evidence) |
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| Fetal anomalies v4.83 | PPP2CA |
Achchuthan Shanmugasundram Tag Q3_24_promote_green tag was added to gene: PPP2CA. Tag Q3_24_NHS_review tag was added to gene: PPP2CA. |
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| Fetal anomalies v4.36 | PPP2CA | Achchuthan Shanmugasundram commented on gene: PPP2CA | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v4.35 | PPP2CA | Natalie Chandler reviewed gene: PPP2CA: Rating: GREEN; Mode of pathogenicity: ; Publications: 30595372; Phenotypes: Neurodevelopmental disorder and language delay with or without structural brain abnormalities, OMIM:618354; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v4.34 | PPP2CA |
Achchuthan Shanmugasundram gene: PPP2CA was added gene: PPP2CA was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: PPP2CA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: PPP2CA were set to 30595372 Phenotypes for gene: PPP2CA were set to Neurodevelopmental disorder and language delay with or without structural brain abnormalities, OMIM:618354 |
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