source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr2	64558399	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC131012982	SmilChr02G004238	131012982	rna-XM_057940972.1	1	B101
typical_cds_rare	Chr2	64558399	TC	T	INDEL	1bp_deletion	CDS_variant	LOC131012982	SmilChr02G004238	131012982	rna-XM_057940972.1	1	B101
lof_cds	Chr2	64558401	AT	A	INDEL	1bp_deletion	frameshift_variant	LOC131012982	SmilChr02G004238	131012982	rna-XM_057940972.1	1	B101
typical_cds_rare	Chr2	64558401	AT	A	INDEL	1bp_deletion	CDS_variant	LOC131012982	SmilChr02G004238	131012982	rna-XM_057940972.1	1	B101
typical_cds_rare	Chr2	64559938	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131012982	SmilChr02G004238	131012982	rna-XM_057940972.1	1	B69
lof_cds	Chr2	64560328	TGG	T	INDEL	2bp_deletion	frameshift_variant	LOC131012982	SmilChr02G004238	131012982	rna-XM_057940972.1	1	C70
typical_cds_rare	Chr2	64560328	TGG	T	INDEL	2bp_deletion	CDS_variant	LOC131012982	SmilChr02G004238	131012982	rna-XM_057940972.1	1	C70
lof_cds	Chr2	64560331	TG	T	INDEL	1bp_deletion	frameshift_variant	LOC131012982	SmilChr02G004238	131012982	rna-XM_057940972.1	1	C70
typical_cds_rare	Chr2	64560331	TG	T	INDEL	1bp_deletion	CDS_variant	LOC131012982	SmilChr02G004238	131012982	rna-XM_057940972.1	1	C70
lof_cds	Chr2	64560334	T	TGG	INDEL	2bp_insertion	frameshift_variant	LOC131012982	SmilChr02G004238	131012982	rna-XM_057940972.1	16	A13,B18,B26,B49,B52,B73,B78,B8,B91,B93,C38,C46,C50,C60,C63,C72