シャルコー・マリー・トゥース病

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
Deletion	NM_170707.4(LMNA):c.329del (p.Arg110fs)	LMNA	Likely pathogenic	1	156085038	156085038	CG	C	criteria provided, single submitter	ClinGen:CA017885
Duplication	NM_170707.4(LMNA):c.339dup (p.Lys114Ter)	LMNA	Likely pathogenic	1	156085045	156085046	G	GT	criteria provided, single submitter	ClinGen:CA306281
single nucleotide variant	NM_170707.4(LMNA):c.356+1G>A	LMNA	Pathogenic	1	156085066	156085066	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA017954
Indel	NM_170707.4(LMNA):c.381_383delinsTGGTCACCTGAGAG (p.Ile128fs)	LMNA	Pathogenic	1	156100432	156100434	GAT	TGGTCACCTGAGAG	criteria provided, single submitter	ClinGen:CA018019
Deletion	NM_170707.4(LMNA):c.522del (p.Ala175fs)	LMNA	Pathogenic	1	156104202	156104202	CA	C	criteria provided, single submitter	ClinGen:CA018211
Deletion	NM_170707.4(LMNA):c.586_596del (p.Arg196fs)	LMNA	Pathogenic	1	156104264	156104274	AACAGGCTGCAG	A	criteria provided, single submitter	ClinGen:CA018281
single nucleotide variant	NM_170707.4(LMNA):c.768G>A (p.Val256=)	LMNA	Pathogenic	1	156104724	156104724	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA018593
Deletion	NM_170707.4(LMNA):c.859del (p.Ala287fs)	LMNA	Pathogenic/Likely pathogenic	1	156105022	156105022	TG	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA018752
single nucleotide variant	NM_170707.4(LMNA):c.871G>A (p.Glu291Lys)	LMNA	Pathogenic	1	156105038	156105038	G	A	criteria provided, single submitter	ClinGen:CA018791
Duplication	NM_170707.4(LMNA):c.973dup (p.Asp325fs)	LMNA	Pathogenic	1	156105726	156105727	A	AG	criteria provided, single submitter	ClinGen:CA306282