先天性筋無力症候群 - MGenReviews

先天性筋無力症候群

小児・神経疾患

疾患の紹介

病的バリアントリスト

Excelでダウンロード

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最新の情報は下記 URL でご確認いただけます (外部サイトへ移動します) 。

https://ftp.ncbi.nlm.nih.gov/pub/clinvar/tab_delimited/archive/

表のタイトル行が青色の項目は、クリックすることでソートすることができます。

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_173660.5(DOK7):c.514G>A (p.Gly172Arg)	DOK7	Pathogenic/Likely pathogenic	4	3478251	3478251	G	A	criteria provided, multiple submitters, no conflicts	-
Deletion	NM_198576.4(AGRN):c.914_947del (p.Arg305fs)	AGRN	Pathogenic	1	976735	976768	CGCCCGCCAGGAGAATGTCTTCAAGAAGTTCGACG	C	criteria provided, single submitter	-
Deletion	NC_000002.12:g.(?_44280716)_(44346390_?)del	PREPL	Pathogenic	2	44507855	44573529	na	na	criteria provided, single submitter	-
single nucleotide variant	NM_001171613.2(PREPL):c.1262+1G>A	PREPL	Pathogenic/Likely pathogenic	2	44556075	44556075	C	T	criteria provided, multiple submitters, no conflicts	-
single nucleotide variant	NM_001244710.2(GFPT1):c.982C>T (p.Gln328Ter)	GFPT1	Pathogenic	2	69575330	69575330	G	A	criteria provided, single submitter	-
single nucleotide variant	NM_001171613.2(PREPL):c.427C>T (p.Arg143Ter)	PREPL	Pathogenic	2	44569614	44569614	G	A	criteria provided, single submitter	-
Deletion	NM_001171613.2(PREPL):c.167del (p.Leu56fs)	PREPL	Pathogenic/Likely pathogenic	2	44571066	44571066	TA	T	criteria provided, multiple submitters, no conflicts	-
Deletion	NM_001244710.2(GFPT1):c.197_201del (p.Val66fs)	GFPT1	Pathogenic	2	69597155	69597159	CCTTAA	C	criteria provided, single submitter	-
Deletion	NC_000002.12:g.(?_44321336)_(44346410_?)del	PREPL	Pathogenic	2	44548475	44573549	na	na	criteria provided, single submitter	-
Duplication	NM_005677.4(COLQ):c.1225dup (p.His409fs)	COLQ	Pathogenic	3	15495408	15495409	T	TG	criteria provided, single submitter	-

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