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Rasopathy v0.89 MRAS Zornitza Stark Publications for gene: MRAS were set to 28289718
Rasopathy v0.88 MRAS Zornitza Stark Phenotypes for gene: MRAS were changed from Noonan syndrome to Noonan syndrome 11, MIM#618499
Rasopathy v0.87 MRAS Zornitza Stark edited their review of gene: MRAS: Changed phenotypes: Noonan syndrome 11, MIM#618499
Rasopathy v0.30 MRAS Zornitza Stark Classified gene: MRAS as Green List (high evidence)
Rasopathy v0.30 MRAS Zornitza Stark Gene: mras has been classified as Green List (High Evidence).
Rasopathy v0.29 MRAS Zornitza Stark changed review comment from: Two unrelated individuals reported with de novo variants in this gene. Rated as LIMITED by ClinGen.
Sources: Expert list; to: Two unrelated individuals reported with de novo variants in this gene. Rated as LIMITED by ClinGen in 2018. Note 4 further individuals reported since.
Sources: Expert list
Rasopathy v0.29 MRAS Zornitza Stark edited their review of gene: MRAS: Changed publications: 28289718, 31173466, 31108500, 31173466
Rasopathy v0.29 MRAS Zornitza Stark edited their review of gene: MRAS: Changed rating: GREEN; Changed publications: 28289718, 31173466, 31108500
Rasopathy v0.28 MRAS Zornitza Stark Marked gene: MRAS as ready
Rasopathy v0.28 MRAS Zornitza Stark Gene: mras has been classified as Amber List (Moderate Evidence).
Rasopathy v0.28 MRAS Zornitza Stark Classified gene: MRAS as Amber List (moderate evidence)
Rasopathy v0.28 MRAS Zornitza Stark Gene: mras has been classified as Amber List (Moderate Evidence).
Rasopathy v0.27 MRAS Zornitza Stark gene: MRAS was added
gene: MRAS was added to Rasopathy. Sources: Expert list
Mode of inheritance for gene: MRAS was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MRAS were set to 28289718
Phenotypes for gene: MRAS were set to Noonan syndrome
Review for gene: MRAS was set to AMBER
Added comment: Two unrelated individuals reported with de novo variants in this gene. Rated as LIMITED by ClinGen.
Sources: Expert list