極長鎖アシルCoA脱水素酵素欠損症

小児・神経疾患

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Type	Name	Gene Symbol	Clinical Significance	Chromosome	Start	Stop	Reference Allele	Alternate Allele	Review Status	Other IDs
Type	Name	Gene Symbol	Clinical Significance	Chromosome	(GRCh37)		Reference Allele	Alternate Allele	Review Status	Other IDs
single nucleotide variant	NM_000018.4(ACADVL):c.1837C>T (p.Arg613Trp)	ACADVL	Likely pathogenic	17	7128285	7128285	C	T	reviewed by expert panel	ClinGen:CA251903,UniProtKB:P49748#VAR_000365,OMIM:609575.0003
single nucleotide variant	NM_000018.4(ACADVL):c.1843C>T (p.Arg615Ter)	ACADVL	Likely pathogenic	17	7128291	7128291	C	T	reviewed by expert panel	ClinGen:CA16608642
Duplication	NM_000018.4(ACADVL):c.1908dup (p.Ile637fs)	ACADVL	Likely pathogenic	17	7128355	7128356	G	GC	criteria provided, multiple submitters, no conflicts	-