source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr1	40124135	AC	A	INDEL	1bp_deletion	frameshift_variant	LOC131015278	SmilChr01G002314	131015278	rna-XM_057943617.1,rna-XM_057943627.1	6	B22,B67,B70,C29,C42,C65
lof_cds	Chr1	40124137	C	CT	INDEL	1bp_insertion	frameshift_variant	LOC131015278	SmilChr01G002314	131015278	rna-XM_057943617.1,rna-XM_057943627.1	12	A10,A16,A8,B130,B137,B42,B43,B63,B79,C4,C44,C58
typical_cds_rare	Chr1	40124900	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131015278	SmilChr01G002314	131015278	rna-XM_057943617.1,rna-XM_057943627.1	1	B8
lof_cds	Chr1	40124902	TGA	T	INDEL	2bp_deletion	frameshift_variant	LOC131015278	SmilChr01G002314	131015278	rna-XM_057943617.1,rna-XM_057943627.1	3	B40,B99,C85
typical_cds_rare	Chr1	40124902	TGA	T	INDEL	2bp_deletion	CDS_variant	LOC131015278	SmilChr01G002314	131015278	rna-XM_057943617.1,rna-XM_057943627.1	3	B40,B99,C85
lof_cds	Chr1	40124962	TGA	T	INDEL	2bp_deletion	frameshift_variant	LOC131015278	SmilChr01G002314	131015278	rna-XM_057943617.1,rna-XM_057943627.1	1	B25
typical_cds_rare	Chr1	40124962	TGA	T	INDEL	2bp_deletion	CDS_variant	LOC131015278	SmilChr01G002314	131015278	rna-XM_057943617.1,rna-XM_057943627.1	1	B25
typical_cds_rare	Chr1	40125075	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131015278	SmilChr01G002314	131015278	rna-XM_057943617.1,rna-XM_057943627.1	3	B105,B119,B34
lof_cds	Chr1	40125197	TA	T	INDEL	1bp_deletion	frameshift_variant	LOC131015278	SmilChr01G002314	131015278	rna-XM_057943617.1,rna-XM_057943627.1	1	C2
typical_cds_rare	Chr1	40125197	TA	T	INDEL	1bp_deletion	CDS_variant	LOC131015278	SmilChr01G002314	131015278	rna-XM_057943617.1,rna-XM_057943627.1	1	C2