マッカードル病

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_005609.4(PYGM):c.278G>T (p.Gly93Val)	PYGM	Likely pathogenic	11	64526142	64526142	C	A	criteria provided, single submitter	ClinGen:CA381111386
single nucleotide variant	NM_005609.4(PYGM):c.1136C>T (p.Thr379Met)	PYGM	Likely pathogenic	11	64521454	64521454	G	A	criteria provided, single submitter	ClinGen:CA381176728
single nucleotide variant	NM_005609.4(PYGM):c.1456G>A (p.Gly486Ser)	PYGM	Likely pathogenic	11	64520607	64520607	C	T	criteria provided, single submitter	ClinGen:CA223899899
Duplication	NM_005609.4(PYGM):c.1403+2dup	PYGM	Likely pathogenic	11	64520988	64520989	C	CA	criteria provided, single submitter	-
Deletion	NM_005609.4(PYGM):c.2319del (p.Val774fs)	PYGM	Likely pathogenic	11	64514453	64514453	CT	C	criteria provided, single submitter	-
Deletion	NM_005609.4(PYGM):c.219_220del (p.His74fs)	PYGM	Likely pathogenic	11	64527151	64527152	TGC	T	criteria provided, single submitter	-
single nucleotide variant	NM_005609.4(PYGM):c.1093-1G>T	PYGM	Likely pathogenic	11	64521498	64521498	C	A	criteria provided, single submitter	-
single nucleotide variant	NM_005609.4(PYGM):c.660+1G>A	PYGM	Likely pathogenic	11	64525250	64525250	C	T	criteria provided, multiple submitters, no conflicts	-
Deletion	NM_005609.4(PYGM):c.262_263del (p.Leu88fs)	PYGM	Likely pathogenic	11	64526157	64526158	TAA	T	criteria provided, single submitter	-
Deletion	NM_005609.4(PYGM):c.198del (p.Arg67fs)	PYGM	Likely pathogenic	11	64527173	64527173	GC	G	criteria provided, single submitter	-