ClinVar Miner

List of variants in gene FASTKD2 reported as likely benign for Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency

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Total variants: 5
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HGVS dbSNP
NM_001136193.2(FASTKD2):c.*557A>G rs7559712
NM_001136193.2(FASTKD2):c.*627T>C rs1048783
NM_001136193.2(FASTKD2):c.*672T>A rs61672260
NM_001136193.2(FASTKD2):c.-184C>T rs3762567
NM_001136193.2(FASTKD2):c.44G>A (p.Ser15Asn) rs3762568

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