source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr2	45684170	T	TA	INDEL	1bp_insertion	stop_gained,frameshift_variant	LOC131009602	SmilChr02G002630	131009602	rna-XM_057937017.1	2	C20,C72
typical_cds_rare	Chr2	45684170	T	TA	INDEL	1bp_insertion	CDS_variant	LOC131009602	SmilChr02G002630	131009602	rna-XM_057937017.1	2	C20,C72
lof_cds	Chr2	45684193	A	AG	INDEL	1bp_insertion	frameshift_variant	LOC131009602	SmilChr02G002630	131009602	rna-XM_057937017.1	53	A14,A20,A4,A7,A9,B1,B100,B102,B104,B114,B124,B125,B127,B131,B14,B15,B16,B22,B23,B37,B38,B60,B64,B71,B78,B81,B82,B90,B92,C16,C17,C19,C22,C27,C30,C31,C32,C35,C36,C45,C46,C48,C53,C54,C56,C59,C6,C61,C67,C70,C74,D11,D8
typical_cds_rare	Chr2	45684238	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131009602	SmilChr02G002630	131009602	rna-XM_057937017.1	4	B128,B18,B38,C70
typical_cds_rare	Chr2	45684262	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131009602	SmilChr02G002630	131009602	rna-XM_057937017.1	5	B102,B14,B15,B38,C70
typical_cds_rare	Chr2	45684402	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131009602	SmilChr02G002630	131009602	rna-XM_057937017.1	1	B19
typical_cds_rare	Chr2	45684555	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131009602	SmilChr02G002630	131009602	rna-XM_057937017.1	2	B118,C51
typical_cds_rare	Chr2	45685479	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131009602	SmilChr02G002630	131009602	rna-XM_057937017.1	3	B21,B28,C26
typical_cds_rare	Chr2	45685579	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131009602	SmilChr02G002630	131009602	rna-XM_057937017.1	4	B105,B4,B78,B97