source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
typical_cds_rare	Chr2	56224763	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131010469	SmilChr02G003503	131010469	rna-XM_057938006.1	2	B28,B99
lof_cds	Chr2	56224955	AG	A	INDEL	1bp_deletion	frameshift_variant	LOC131010469	SmilChr02G003503	131010469	rna-XM_057938006.1	3	B70,C23,C74
typical_cds_rare	Chr2	56224955	AG	A	INDEL	1bp_deletion	CDS_variant	LOC131010469	SmilChr02G003503	131010469	rna-XM_057938006.1	3	B70,C23,C74
lof_cds	Chr2	56225099	TG	T	INDEL	1bp_deletion	frameshift_variant	LOC131010469	SmilChr02G003503	131010469	rna-XM_057938006.1	9	A7,B108,B109,B20,B75,C33,C35,C42,C76
lof_cds	Chr2	56225156	A	ATT	INDEL	2bp_insertion	frameshift_variant	LOC131010469	SmilChr02G003503	131010469	rna-XM_057938006.1	5	B102,B110,B7,B80,C51
typical_cds_rare	Chr2	56225156	A	ATT	INDEL	2bp_insertion	CDS_variant	LOC131010469	SmilChr02G003503	131010469	rna-XM_057938006.1	5	B102,B110,B7,B80,C51
lof_cds	Chr2	56225276	CG	C	INDEL	1bp_deletion	frameshift_variant	LOC131010469	SmilChr02G003503	131010469	rna-XM_057938006.1	1	B62
typical_cds_rare	Chr2	56225276	CG	C	INDEL	1bp_deletion	CDS_variant	LOC131010469	SmilChr02G003503	131010469	rna-XM_057938006.1	1	B62