source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr1	50031965	AT	A	INDEL	1bp_deletion	frameshift_variant	LOC130990145	SmilChr01G003121	130990145	rna-XM_057914352.1	28	A13,A20,A21,A3,B128,B132,B15,B17,B22,B25,B31,B47,B63,B67,B69,B86,B88,C19,C34,C44,C46,C54,C60,C62,C79,D1,D2,D3
lof_cds	Chr1	50032113	G	A	SNV	EMS_canonical_SNV	stop_gained	LOC130990145	SmilChr01G003121	130990145	rna-XM_057914352.1	18	A14,A6,B100,B102,B112,B117,B12,B123,B125,B3,B84,B90,B92,C14,C38,C65,C75,C83
typical_cds_rare	Chr1	50032158	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130990145	SmilChr01G003121	130990145	rna-XM_057914352.1	1	B85
typical_cds_rare	Chr1	50032204	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130990145	SmilChr01G003121	130990145	rna-XM_057914352.1	4	B28,B55,C60,D11
typical_cds_rare	Chr1	50032352	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990145	SmilChr01G003121	130990145	rna-XM_057914352.1	2	B78,C2
lof_cds	Chr1	50032945	C	CT	INDEL	1bp_insertion	frameshift_variant	LOC130990145	SmilChr01G003121	130990145	rna-XM_057914352.1	1	B10
typical_cds_rare	Chr1	50032945	C	CT	INDEL	1bp_insertion	CDS_variant	LOC130990145	SmilChr01G003121	130990145	rna-XM_057914352.1	1	B10
typical_cds_rare	Chr1	50033273	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990145	SmilChr01G003121	130990145	rna-XM_057914352.1	1	C51