source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr1	28572730	C	CG	INDEL	1bp_insertion	frameshift_variant	LOC131018432	SmilChr01G001480	131018432	rna-XM_057947158.1	116	A10,A11,A16,A18,A2,A21,A23,A24,A3,A7,A9,B101,B103,B104,B106,B108,B113,B115,B117,B120,B126,B127,B128,B13,B130,B132,B134,B136,B138,B139,B14,B15,B2,B24,B28,B30,B33,B34,B39,B4,B41,B44,B46,B51,B52,B56,B58,B59,B64,B65,B79,B8,B81,B82,B83,B88,B89,B90,B92,B93,B95,B96,B98,C10,C11,C13,C16,C17,C18,C2,C20,C22,C23,C26,C27,C3,C30,C33,C34,C35,C36,C38,C39,C4,C40,C43,C44,C46,C48,C5,C51,C52,C53,C54,C56,C59,C6,C60,C61,C62,C64,C65,C66,C69,C71,C74,C76,C77,C78,C79,C8,C83,C86,D2,D3,D8
lof_cds	Chr1	28572759	CTT	C	INDEL	2bp_deletion	frameshift_variant	LOC131018432	SmilChr01G001480	131018432	rna-XM_057947158.1	1	B20
typical_cds_rare	Chr1	28572759	CTT	C	INDEL	2bp_deletion	CDS_variant	LOC131018432	SmilChr01G001480	131018432	rna-XM_057947158.1	1	B20
typical_cds_rare	Chr1	28573085	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131018432	SmilChr01G001480	131018432	rna-XM_057947158.1	4	A22,B118,B80,C40
typical_cds_rare	Chr1	28573105	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131018432	SmilChr01G001480	131018432	rna-XM_057947158.1	2	C13,C7