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_001267550.2(TTN):c.99063del (p.Lys33021fs)	TTN	Pathogenic/Likely pathogenic	2	179403493	179403493	GT	G	criteria provided, multiple submitters, no conflicts	-
single nucleotide variant	NM_001267550.2(TTN):c.54418C>T (p.Arg18140Ter)	TTN	Likely pathogenic	2	179468996	179468996	G	A	criteria provided, multiple submitters, no conflicts	-
Duplication	NM_001267550.2(TTN):c.90994_90997dup (p.Ile30333fs)	TTN	Likely pathogenic	2	179416629	179416630	A	ATAAC	criteria provided, single submitter	-
single nucleotide variant	NM_001267550.2(TTN):c.90195T>A (p.Tyr30065Ter)	TTN	Likely pathogenic	2	179417432	179417432	A	T	criteria provided, single submitter	-
single nucleotide variant	NM_001267550.2(TTN):c.52512C>G (p.Tyr17504Ter)	TTN	Likely pathogenic	2	179473098	179473098	G	C	criteria provided, single submitter	-
Duplication	NM_001267550.2(TTN):c.86003dup (p.Thr28669fs)	TTN	Likely pathogenic	2	179424855	179424856	T	TA	criteria provided, single submitter	-
Indel	NM_001267550.2(TTN):c.52499_52504delinsAGTAA (p.Pro17500_Leu17502delinsGlnTer)	TTN	Likely pathogenic	2	179473106	179473111	AAATGG	TTACT	criteria provided, single submitter	-
single nucleotide variant	NM_001267550.2(TTN):c.79298G>A (p.Trp26433Ter)	TTN	Likely pathogenic	2	179431561	179431561	C	T	criteria provided, single submitter	-
Duplication	NM_001267550.2(TTN):c.77906dup (p.Asn25969fs)	TTN	Likely pathogenic	2	179432952	179432953	G	GT	criteria provided, single submitter	-
Deletion	NM_001267550.2(TTN):c.76540del (p.Asp25513_Leu25514insTer)	TTN	Likely pathogenic	2	179434319	179434319	AG	A	criteria provided, single submitter	-