不整脈原性右室心筋症

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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_170707.4(LMNA):c.928C>T (p.Gln310Ter)	LMNA	Pathogenic	1	156105095	156105095	C	T	criteria provided, single submitter	ClinGen:CA10581728
single nucleotide variant	NM_001927.4(DES):c.1013T>C (p.Leu338Pro)	DES	Likely pathogenic	2	220285665	220285665	T	C	criteria provided, single submitter	ClinGen:CA10581950
Indel	NM_001005242.3(PKP2):c.2066_2071delinsG (p.His689fs)	PKP2	Pathogenic	12	32955433	32955438	GGGTGT	C	criteria provided, single submitter	ClinGen:CA10583044
single nucleotide variant	NM_170707.4(LMNA):c.3G>C (p.Met1Ile)	LMNA	Pathogenic	1	156084712	156084712	G	C	criteria provided, single submitter	ClinGen:CA10584109
Deletion	NM_170707.4(LMNA):c.162_163del (p.Asn56fs)	LMNA	Pathogenic	1	156084871	156084872	CGG	C	criteria provided, multiple submitters, no conflicts	ClinGen:CA10584112
single nucleotide variant	NM_170707.4(LMNA):c.443T>C (p.Leu148Pro)	LMNA	Likely pathogenic	1	156100494	156100494	T	C	criteria provided, single submitter	ClinGen:CA10584118
single nucleotide variant	NM_170707.4(LMNA):c.513+1G>A	LMNA	Pathogenic/Likely pathogenic	1	156100565	156100565	G	A	criteria provided, multiple submitters, no conflicts	ClinGen:CA10584120
single nucleotide variant	NM_170707.4(LMNA):c.917T>C (p.Leu306Pro)	LMNA	Likely pathogenic	1	156105084	156105084	T	C	criteria provided, multiple submitters, no conflicts	ClinGen:CA10584123
Deletion	NM_170707.4(LMNA):c.1150del (p.Glu384fs)	LMNA	Pathogenic	1	156105904	156105904	AG	A	criteria provided, single submitter	ClinGen:CA10584127
single nucleotide variant	NM_170707.4(LMNA):c.1157+1G>T	LMNA	Pathogenic/Likely pathogenic	1	156105913	156105913	G	T	criteria provided, multiple submitters, no conflicts	ClinGen:CA10584128