遺伝性圧脆弱性ニューロパチー

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
Duplication	NC_000017.10:g.(?_15142778)_(15164054_?)dup	PMP22	Pathogenic	17	15142778	15164054	na	na	criteria provided, single submitter	-
Deletion	NC_000017.11:g.(?_15239461)_(15260737_?)del	PMP22	Pathogenic	17	15142778	15164054	na	na	criteria provided, single submitter	-
Deletion	NC_000017.11:g.(?_15239451)_(15239631_?)del	PMP22	Pathogenic	17	15142768	15142948	na	na	criteria provided, single submitter	-
single nucleotide variant	NM_000304.4(PMP22):c.320G>T (p.Gly107Val)	PMP22	Pathogenic/Likely pathogenic	17	15134397	15134397	C	A	criteria provided, multiple submitters, no conflicts	-
single nucleotide variant	NM_000304.4(PMP22):c.327C>A (p.Cys109Ter)	PMP22	Pathogenic	17	15134390	15134390	G	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA279101
single nucleotide variant	NM_000304.4(PMP22):c.372G>A (p.Trp124Ter)	PMP22	Pathogenic	17	15134345	15134345	C	T	criteria provided, single submitter	-
single nucleotide variant	NM_000304.4(PMP22):c.390C>G (p.Tyr130Ter)	PMP22	Likely pathogenic	17	15134327	15134327	G	C	criteria provided, multiple submitters, no conflicts	ClinGen:CA398739656
single nucleotide variant	NM_000304.4(PMP22):c.418T>A (p.Trp140Arg)	PMP22	Likely pathogenic	17	15134299	15134299	A	T	criteria provided, multiple submitters, no conflicts	-
single nucleotide variant	NM_000304.4(PMP22):c.419G>A (p.Trp140Ter)	PMP22	Pathogenic	17	15134298	15134298	C	T	criteria provided, single submitter	-
single nucleotide variant	NM_000304.4(PMP22):c.420G>A (p.Trp140Ter)	PMP22	Pathogenic/Likely pathogenic	17	15134297	15134297	C	T	criteria provided, multiple submitters, no conflicts	-