source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr2	3020993	AAG	A	INDEL	2bp_deletion	frameshift_variant	LOC131012643	SmilChr02G000237	131012643	rna-XM_057940628.1	1	B100
typical_cds_rare	Chr2	3020993	AAG	A	INDEL	2bp_deletion	CDS_variant	LOC131012643	SmilChr02G000237	131012643	rna-XM_057940628.1	1	B100
lof_cds	Chr2	3020995	G	GA	INDEL	1bp_insertion	frameshift_variant	LOC131012643	SmilChr02G000237	131012643	rna-XM_057940628.1	42	A21,A3,A7,A8,B108,B127,B135,B15,B23,B32,B36,B38,B39,B55,B59,B6,B65,B67,B69,B77,B83,B85,B93,C13,C15,C16,C17,C22,C33,C36,C51,C58,C62,C78,C79,C80,C81,C83,C85,C86,D11,D5
typical_cds_rare	Chr2	3021005	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131012643	SmilChr02G000237	131012643	rna-XM_057940628.1	1	B103
typical_cds_rare	Chr2	3021071	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131012643	SmilChr02G000237	131012643	rna-XM_057940628.1	2	C2,C64
typical_cds_rare	Chr2	3021531	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131012643	SmilChr02G000237	131012643	rna-XM_057940628.1	4	A8,B138,C25,C31
typical_cds_rare	Chr2	3021639	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131012643	SmilChr02G000237	131012643	rna-XM_057940628.1	4	B121,B60,C52,C69
typical_cds_rare	Chr2	3021647	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131012643	SmilChr02G000237	131012643	rna-XM_057940628.1	5	B130,B75,C46,C63,D2