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Ataxia and cerebellar anomalies - narrow panel v4.38 NFASC Achchuthan Shanmugasundram Tag Q2_23_promote_green was removed from gene: NFASC.
Ataxia and cerebellar anomalies - narrow panel v4.37 NFASC Eleanor Williams reviewed gene: NFASC: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ataxia and cerebellar anomalies - narrow panel v4.35 NFASC Achchuthan Shanmugasundram Source Expert Review Green was added to NFASC.
Source NHS GMS was added to NFASC.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Ataxia and cerebellar anomalies - narrow panel v4.4 NFASC Sarah Leigh Deleted their comment
Ataxia and cerebellar anomalies - narrow panel v4.4 NFASC Sarah Leigh Deleted their comment
Ataxia and cerebellar anomalies - narrow panel v4.4 NFASC Sarah Leigh Classified gene: NFASC as Amber List (moderate evidence)
Ataxia and cerebellar anomalies - narrow panel v4.4 NFASC Sarah Leigh Added comment: Comment on list classification: There is enough evidence for this gene to be rated GREEN at the next major review.
Ataxia and cerebellar anomalies - narrow panel v4.4 NFASC Sarah Leigh Gene: nfasc has been classified as Amber List (Moderate Evidence).
Ataxia and cerebellar anomalies - narrow panel v4.3 NFASC Sarah Leigh Tag Q2_23_promote_green tag was added to gene: NFASC.
Ataxia and cerebellar anomalies - narrow panel v4.3 NFASC Sarah Leigh Classified gene: NFASC as Amber List (moderate evidence)
Ataxia and cerebellar anomalies - narrow panel v4.3 NFASC Sarah Leigh Added comment: Comment on list classification: There is enough evidence for this gene to be rated GREEN at the next major review.
Ataxia and cerebellar anomalies - narrow panel v4.3 NFASC Sarah Leigh Gene: nfasc has been classified as Amber List (Moderate Evidence).
Ataxia and cerebellar anomalies - narrow panel v4.2 NFASC Sarah Leigh Entity copied from Hereditary ataxia v1.317
Ataxia and cerebellar anomalies - narrow panel v4.2 NFASC Sarah Leigh gene: NFASC was added
gene: NFASC was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Literature,Expert Review Green
Mode of inheritance for gene: NFASC was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NFASC were set to 30850329; 31608123; 31501903
Phenotypes for gene: NFASC were set to Neurodevelopmental disorder with central and peripheral motor dysfunction, OMIM:618356; neurodevelopmental disorder with central and peripheral motor dysfunction, MONDO:0032698
Penetrance for gene: NFASC were set to Complete