source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
typical_cds_rare	Chr4	53995061	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	1	D11
typical_cds_rare	Chr4	53995146	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	1	D11
typical_cds_rare	Chr4	53995200	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	3	B138,B25,B75
typical_cds_rare	Chr4	53995261	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	2	C11,C69
typical_cds_rare	Chr4	53995574	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	1	B52
typical_cds_rare	Chr4	53995842	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	1	B104
typical_cds_rare	Chr4	53995990	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	5	B16,B2,B20,B82,C80
typical_cds_rare	Chr4	53996181	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	1	B16
lof_cds	Chr4	53996515	A	AT	INDEL	1bp_insertion	frameshift_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	29	A15,A19,B110,B12,B131,B21,B4,B59,B68,B70,B72,B87,C1,C10,C12,C26,C27,C36,C47,C5,C55,C60,C61,C71,C76,C78,D5,D6,D8
typical_cds_rare	Chr4	53996520	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	1	B104
typical_cds_rare	Chr4	53996867	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	1	B104
typical_cds_rare	Chr4	53996921	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	5	B26,B31,B37,B47,B8
typical_cds_rare	Chr4	53996947	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	2	B91,C1
lof_cds	Chr4	53997011	TGG	T	INDEL	2bp_deletion	frameshift_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	1	B111
typical_cds_rare	Chr4	53997011	TGG	T	INDEL	2bp_deletion	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	1	B111
typical_cds_rare	Chr4	53997239	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	5	A11,B124,B60,C64,C66
lof_cds	Chr4	53997253	GTC	G	INDEL	2bp_deletion	frameshift_variant	LOC131020663	SmilChr04G003782	131020663	rna-XM_057949633.1	6	B18,B46,B58,C37,C4,C74