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Date	Panel	Item	Activity
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14 Jan 2020	Ataxia - adult onset v0.3	SPTBN2	Bryony Thompson Marked gene: SPTBN2 as ready
14 Jan 2020	Ataxia - adult onset v0.3	SPTBN2	Bryony Thompson Gene: sptbn2 has been classified as Green List (High Evidence).
14 Jan 2020	Ataxia - adult onset v0.3	SPTBN2	Bryony Thompson Phenotypes for gene: SPTBN2 were changed from SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14; Spinocerebellar ataxia 5; Spinocerebellar ataxia 5, 600224; SPINOCEREBELLAR ATAXIA 5 (autosomal dominant); Spinocerebellar ataxia, autosomal recessive 14; Spinocerebellar Ataxia, Dominant; Autosomal recessive spinocerebellar ataxia 14, 615386 to Spinocerebellar ataxia 5, 600224; Spinocerebellar ataxia, autosomal recessive 14, 615386
19 Dec 2019	Ataxia - adult onset v0.0	SPTBN2	Bryony Thompson gene: SPTBN2 was added gene: SPTBN2 was added to Ataxia - adult onset_RMH. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: SPTBN2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Phenotypes for gene: SPTBN2 were set to SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14; Spinocerebellar ataxia 5; Spinocerebellar ataxia 5, 600224; SPINOCEREBELLAR ATAXIA 5 (autosomal dominant); Spinocerebellar ataxia, autosomal recessive 14; Spinocerebellar Ataxia, Dominant; Autosomal recessive spinocerebellar ataxia 14, 615386