特発性拡張型心筋症

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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_000256.3(MYBPC3):c.711C>A (p.Tyr237Ter)	MYBPC3	Pathogenic/Likely pathogenic	11	47370036	47370036	G	T	criteria provided, multiple submitters, no conflicts	-
Deletion	NM_000256.3(MYBPC3):c.342_343del (p.Gly115fs)	MYBPC3	Likely pathogenic	11	47372116	47372117	CCA	C	criteria provided, single submitter	-
Deletion	NM_000256.3(MYBPC3):c.313del (p.Ala105fs)	MYBPC3	Pathogenic	11	47372146	47372146	GC	G	criteria provided, single submitter	-
single nucleotide variant	NM_000257.4(MYH7):c.2576T>C (p.Leu859Pro)	MYH7	Likely pathogenic	14	23894081	23894081	A	G	criteria provided, single submitter	-
single nucleotide variant	NM_000257.4(MYH7):c.1400T>A (p.Ile467Asn)	MYH7	Pathogenic	14	23898171	23898171	A	T	criteria provided, single submitter	-
single nucleotide variant	NM_000257.4(MYH7):c.1325G>T (p.Arg442Leu)	MYH7	Likely pathogenic	14	23898246	23898246	C	A	criteria provided, single submitter	-
single nucleotide variant	NM_000257.4(MYH7):c.959T>A (p.Val320Glu)	MYH7	Likely pathogenic	14	23899809	23899809	A	T	criteria provided, single submitter	-
single nucleotide variant	NM_000257.4(MYH7):c.952A>C (p.Thr318Pro)	MYH7	Likely pathogenic	14	23899816	23899816	T	G	criteria provided, single submitter	-
Deletion	NM_000256.3(MYBPC3):c.3191-11_3193del	MYBPC3	Likely pathogenic	11	47354882	47354895	TTGTCTGCGGGAGAC	T	criteria provided, single submitter	-
single nucleotide variant	NM_000256.3(MYBPC3):c.2737+1G>A	MYBPC3	Pathogenic/Likely pathogenic	11	47357427	47357427	C	T	criteria provided, multiple submitters, no conflicts	-