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
Deletion	NM_000256.3(MYBPC3):c.1755del (p.Asp587fs)	MYBPC3	Pathogenic	11	47363577	47363577	GC	G	criteria provided, single submitter	-
Indel	NM_000256.3(MYBPC3):c.1440_1441delinsC (p.Glu480fs)	MYBPC3	Pathogenic	11	47364397	47364398	CC	G	criteria provided, single submitter	-
Deletion	NM_000256.3(MYBPC3):c.1319_1328del (p.Gly440fs)	MYBPC3	Pathogenic	11	47364595	47364604	ACACTTCTCGC	A	criteria provided, single submitter	-
Deletion	NM_000256.3(MYBPC3):c.440del (p.Pro147fs)	MYBPC3	Pathogenic	11	47371630	47371630	AG	A	criteria provided, single submitter	-
single nucleotide variant	NM_000257.4(MYH7):c.5594A>C (p.Gln1865Pro)	MYH7	Pathogenic	14	23883277	23883277	T	G	criteria provided, single submitter	-
single nucleotide variant	NM_000257.4(MYH7):c.4358T>C (p.Leu1453Pro)	MYH7	Pathogenic	14	23886523	23886523	A	G	criteria provided, single submitter	-
single nucleotide variant	NM_000257.4(MYH7):c.2459C>A (p.Ala820Asp)	MYH7	Pathogenic	14	23894198	23894198	G	T	criteria provided, single submitter	-
single nucleotide variant	NM_000257.4(MYH7):c.2200C>G (p.Gln734Glu)	MYH7	Likely pathogenic	14	23894990	23894990	G	C	criteria provided, single submitter	-
single nucleotide variant	NM_000257.4(MYH7):c.1751G>T (p.Gly584Val)	MYH7	Likely pathogenic	14	23896931	23896931	C	A	criteria provided, single submitter	-
single nucleotide variant	NM_000257.4(MYH7):c.1711G>C (p.Gly571Arg)	MYH7	Pathogenic	14	23896971	23896971	C	G	criteria provided, single submitter	-