α1-アンチトリプシン欠乏症

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
Deletion	NM_000295.5(SERPINA1):c.1158del (p.Glu387fs)	SERPINA1	Likely pathogenic	14	94844885	94844885	CG	C	criteria provided, single submitter	ClinGen:CA7327257,LOVD 3:SERPINA1_000014,OMIM:107400.0025
single nucleotide variant	NM_000295.5(SERPINA1):c.1A>G (p.Met1Val)	SERPINA1	Likely pathogenic	14	94849574	94849574	T	C	criteria provided, single submitter	ClinGen:CA16041711
single nucleotide variant	NM_000295.5(SERPINA1):c.21G>A (p.Trp7Ter)	SERPINA1	Likely pathogenic	14	94849554	94849554	C	T	criteria provided, single submitter	ClinGen:CA16041710
single nucleotide variant	NM_000295.5(SERPINA1):c.186C>A (p.Tyr62Ter)	SERPINA1	Likely pathogenic	14	94849389	94849389	G	T	criteria provided, single submitter	ClinGen:CA7327531
single nucleotide variant	NM_000295.5(SERPINA1):c.646+2T>C	SERPINA1	Likely pathogenic	14	94848927	94848927	A	G	criteria provided, single submitter	ClinGen:CA7327455
Deletion	NM_000295.5(SERPINA1):c.714del (p.Thr239fs)	SERPINA1	Likely pathogenic	14	94847411	94847411	TG	T	criteria provided, single submitter	ClinGen:CA16041709
Deletion	NM_000295.5(SERPINA1):c.1018del (p.Ala340fs)	SERPINA1	Likely pathogenic	14	94845848	94845848	GC	G	criteria provided, single submitter	ClinGen:CA16041708
single nucleotide variant	NM_000295.5(SERPINA1):c.745G>C (p.Gly249Arg)	SERPINA1	Likely pathogenic	14	94847380	94847380	C	G	criteria provided, single submitter	ClinGen:CA274265