source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
typical_cds_rare	Chr6	45477921	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	5	B104,B16,B46,B76,D2
typical_cds_rare	Chr6	45477970	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	1	B16
typical_cds_rare	Chr6	45478116	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	4	B104,B46,B76,D2
typical_cds_rare	Chr6	45478124	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	1	C8
lof_cds	Chr6	45478199	T	TG	INDEL	1bp_insertion	frameshift_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	12	A1,B12,B125,B22,B27,B6,C18,C55,C63,C67,C74,C87
lof_cds	Chr6	45478201	ACT	A	INDEL	2bp_deletion	frameshift_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	2	A24,C42
typical_cds_rare	Chr6	45478201	ACT	A	INDEL	2bp_deletion	CDS_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	2	A24,C42
typical_cds_rare	Chr6	45478227	TC	*	INDEL	1bp_deletion	CDS_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	2	B2,C42
typical_cds_rare	Chr6	45478329	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	2	B71,C78
typical_cds_rare	Chr6	45478469	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	1	C8
typical_cds_rare	Chr6	45478545	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	1	C8
typical_cds_rare	Chr6	45478564	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	2	B117,B49
typical_cds_rare	Chr6	45478877	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130990007	SmilChr06G003293	130990007	rna-XM_057914192.1	1	B65