ClinVar Miner

List of variants reported as uncertain significance for Ceroid lipofuscinosis neuronal 2; Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia by Fulgent Genetics,Fulgent Genetics

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Total variants: 6
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HGVS dbSNP
NM_000391.4(TPP1):c.101G>A (p.Gly34Asp) rs138448968
NM_000391.4(TPP1):c.1138G>A (p.Ala380Thr) rs190013230
NM_000391.4(TPP1):c.1280C>T (p.Thr427Met) rs201034755
NM_000391.4(TPP1):c.1526A>G (p.Gln509Arg) rs149529997
NM_000391.4(TPP1):c.319G>A (p.Gly107Arg) rs201613668
NM_000391.4(TPP1):c.776G>A (p.Arg259His) rs140176031

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