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	20034360	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	1	C22
lof_cds	Chr6	20034495	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	8	B113,B132,B15,B8,C3,C46,C48,C7
typical_cds_rare	Chr6	20034506	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	1	C77
typical_cds_rare	Chr6	20034710	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	1	D10
lof_cds	Chr6	20034782	A	ATC	INDEL	2bp_insertion	frameshift_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	3	B135,B22,C25
typical_cds_rare	Chr6	20034782	A	ATC	INDEL	2bp_insertion	CDS_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	3	B135,B22,C25
lof_cds	Chr6	20034784	TGA	T	INDEL	2bp_deletion	frameshift_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	3	B135,B22,C25
typical_cds_rare	Chr6	20034784	TGA	T	INDEL	2bp_deletion	CDS_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	3	B135,B22,C25
typical_cds_rare	Chr6	20034844	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	1	B104
lof_cds	Chr6	20034911	A	AGT	INDEL	2bp_insertion	frameshift_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	22	B1,B112,B119,B22,B24,B30,B31,B32,B34,B4,B48,B69,B7,C15,C17,C21,C25,C30,C46,C53,C79,C87
typical_cds_rare	Chr6	20034929	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	1	A14
typical_cds_rare	Chr6	20035164	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990388	SmilChr06G001737	130990388	rna-XM_057914627.1	2	A20,C34