List of variants reported as benign for childhood encephalopathy due to thiamine pyrophosphokinase deficiency

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_022445.4(TPK1):c.98G>A (p.Arg33His)	rs77358162	0.00512
NM_022445.4(TPK1):c.663C>T (p.Tyr221=)	rs113536847	0.00234
NM_022445.4(TPK1):c.259-20dup	rs771212575
NM_022445.4(TPK1):c.614-13del	rs539336947

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