ClinVar Miner

List of variants in gene CTSD reported as uncertain significance for Seizures

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Total variants: 11
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HGVS dbSNP
NM_001909.5(CTSD):c.100C>T (p.Arg34Trp) rs779278368
NM_001909.5(CTSD):c.1036G>C (p.Gly346Arg) rs1565018716
NM_001909.5(CTSD):c.1170C>G (p.Ile390Met) rs370985523
NM_001909.5(CTSD):c.410C>T (p.Ser137Leu) rs777645484
NM_001909.5(CTSD):c.431C>G (p.Ser144Trp) rs754147413
NM_001909.5(CTSD):c.471G>A (p.Ser157=) rs760318745
NM_001909.5(CTSD):c.505C>G (p.Leu169Val) rs768487717
NM_001909.5(CTSD):c.52G>C (p.Ala18Pro) rs796052403
NM_001909.5(CTSD):c.828-5C>T rs762444592
NM_001909.5(CTSD):c.926G>A (p.Arg309His) rs374540411
NM_001909.5(CTSD):c.977T>C (p.Met326Thr) rs1565018786

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