source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr1	27263085	CAG	C	INDEL	2bp_deletion	frameshift_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	26	A23,B110,B112,B120,B125,B134,B138,B27,B41,B45,B63,B88,B90,B92,B99,C2,C22,C34,C46,C61,C7,C72,C76,D6,D8,D9
lof_cds	Chr1	27263089	G	GCA	INDEL	2bp_insertion	frameshift_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	25	A23,B110,B112,B120,B125,B134,B138,B27,B41,B45,B88,B90,B92,B99,C2,C22,C34,C46,C61,C7,C72,C76,D6,D8,D9
typical_cds_rare	Chr1	27263119	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	2	A10,B63
typical_cds_rare	Chr1	27263138	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	2	B129,C75
typical_cds_rare	Chr1	27263170	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	3	A10,B32,B75
typical_cds_rare	Chr1	27263209	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	2	B140,C3
typical_cds_rare	Chr1	27263542	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	1	C27
typical_cds_rare	Chr1	27263641	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	1	B21
lof_cds	Chr1	27263701	GTT	G	INDEL	2bp_deletion	frameshift_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	1	B131
typical_cds_rare	Chr1	27263701	GTT	G	INDEL	2bp_deletion	CDS_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	1	B131
lof_cds	Chr1	27263742	G	A	SNV	EMS_canonical_SNV	stop_gained	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	20	A21,B103,B109,B22,B34,B38,B47,B54,B56,B59,B72,B83,B96,C11,C54,C63,C67,C69,C71,C83
typical_cds_rare	Chr1	27263788	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	4	C10,C3,C79,D8
lof_cds	Chr1	27264541	CGT	C	INDEL	2bp_deletion	frameshift_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	10	B113,B123,B124,B28,B48,B71,C53,C78,C8,D2
typical_cds_rare	Chr1	27264578	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131017670	SmilChr01G001386	131017670	rna-XM_057946443.1	4	B121,B122,B33,C61