家族性胸部大動脈瘤・解離

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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_001613.4(ACTA2):c.445C>T (p.Arg149Cys)	ACTA2	Pathogenic	10	90701551	90701551	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA006936,UniProtKB:P62736#VAR_045918,OMIM:102620.0001
single nucleotide variant	NM_001613.4(ACTA2):c.773G>A (p.Arg258His)	ACTA2	Pathogenic/Likely pathogenic	10	90699299	90699299	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA007026,UniProtKB:P62736#VAR_045921,OMIM:102620.0002
single nucleotide variant	NM_001613.4(ACTA2):c.772C>T (p.Arg258Cys)	ACTA2	Pathogenic	10	90699300	90699300	G	A	criteria provided, multiple submitters, no conflicts	UniProtKB:P62736#VAR_045920,OMIM:102620.0003,ClinGen:CA007017
single nucleotide variant	NM_001613.4(ACTA2):c.536G>A (p.Arg179His)	ACTA2	Pathogenic	10	90701066	90701066	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA006970,UniProtKB:P62736#VAR_064516,OMIM:102620.0004
single nucleotide variant	NM_001613.4(ACTA2):c.635G>A (p.Arg212Gln)	ACTA2	Pathogenic/Likely pathogenic	10	90699437	90699437	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA006985,UniProtKB:P62736#VAR_062580
single nucleotide variant	NM_001613.4(ACTA2):c.115C>T (p.Arg39Cys)	ACTA2	Pathogenic/Likely pathogenic	10	90708573	90708573	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA006817,OMIM:102620.0005
single nucleotide variant	NM_001613.4(ACTA2):c.991-1G>C	ACTA2	Likely pathogenic	10	90695124	90695124	C	G	criteria provided, single submitter	ClinGen:CA007075
single nucleotide variant	NM_001613.4(ACTA2):c.446G>T (p.Arg149Leu)	ACTA2	Likely pathogenic	10	90701550	90701550	C	A	criteria provided, single submitter	ClinGen:CA006944
single nucleotide variant	NM_001613.4(ACTA2):c.353G>A (p.Arg118Gln)	ACTA2	Pathogenic/Likely pathogenic	10	90703570	90703570	C	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA006909,UniProtKB:P62736#VAR_045916
single nucleotide variant	NM_001613.4(ACTA2):c.116G>A (p.Arg39His)	ACTA2	Pathogenic/Likely pathogenic	10	90708572	90708572	C	T	criteria provided, multiple submitters, no conflicts	UniProtKB:P62736#VAR_062577,ClinGen:CA006825