海綿状血管腫 - MGenReviews

海綿状血管腫

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_031443.4(CCM2):c.169A>T (p.Arg57Ter)	CCM2	Pathogenic/Likely pathogenic	7	45077990	45077990	A	T	criteria provided, multiple submitters, no conflicts	-
Deletion	NM_031443.4(CCM2):c.289-19_352del	CCM2	Likely pathogenic	7	45104042	45104124	ATGCCCTGTGGTTCCTTCCAGAGAGCCCACCAGCTTCCGGGACACTTGACTCAGGAGCACGATGCTGTGCTCAGCCTGTCTGCG	A	criteria provided, single submitter	-
single nucleotide variant	NM_031443.4(CCM2):c.289-1G>A	CCM2	Pathogenic/Likely pathogenic	7	45104061	45104061	G	A	criteria provided, multiple submitters, no conflicts	-
single nucleotide variant	NM_031443.4(CCM2):c.289-1G>T	CCM2	Pathogenic	7	45104061	45104061	G	T	criteria provided, single submitter	-
Deletion	NM_031443.4(CCM2):c.298del (p.Gln100fs)	CCM2	Likely pathogenic	7	45104070	45104070	AC	A	criteria provided, single submitter	-
Deletion	NM_031443.4(CCM2):c.314del (p.His104_Leu105insTer)	CCM2	Pathogenic	7	45104086	45104086	CT	C	criteria provided, single submitter	-
Deletion	NM_031443.4(CCM2):c.586del (p.Val196fs)	CCM2	Likely pathogenic	7	45108154	45108154	TG	T	criteria provided, single submitter	-
single nucleotide variant	NM_031443.4(CCM2):c.609G>A (p.Lys203=)	CCM2	Likely pathogenic	7	45108178	45108178	G	A	criteria provided, single submitter	-
single nucleotide variant	NM_031443.4(CCM2):c.610-1G>A	CCM2	Pathogenic	7	45109424	45109424	G	A	criteria provided, single submitter	OMIM:607929.0003
Deletion	NM_031443.4(CCM2):c.790del (p.Glu264fs)	CCM2	Likely pathogenic	7	45112368	45112368	TG	T	criteria provided, single submitter	-