source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr5	12267584	CG	C	INDEL	1bp_deletion	frameshift_variant	LOC130986067	SmilChr05G001375	130986067	rna-XM_057909346.1	137	A1,A10,A14,A18,A19,A2,A21,A22,A25,A7,A8,A9,B1,B103,B106,B107,B109,B110,B113,B115,B117,B118,B12,B122,B123,B124,B127,B128,B129,B131,B133,B135,B139,B140,B16,B19,B2,B20,B23,B25,B26,B29,B3,B32,B36,B37,B38,B39,B44,B46,B47,B48,B50,B56,B57,B59,B6,B61,B64,B66,B68,B69,B7,B73,B76,B78,B79,B8,B80,B84,B85,B87,B89,B90,B91,B92,B96,B98,B99,C1,C11,C17,C18,C19,C2,C21,C23,C25,C27,C28,C29,C3,C31,C33,C34,C35,C36,C37,C38,C39,C41,C42,C43,C45,C47,C49,C5,C53,C55,C56,C58,C6,C60,C61,C63,C64,C65,C67,C69,C70,C72,C74,C75,C76,C77,C78,C81,C83,C87,D1,D10,D11,D2,D5,D6,D7,D8
typical_cds_rare	Chr5	12267914	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986067	SmilChr05G001375	130986067	rna-XM_057909346.1	1	B126
typical_cds_rare	Chr5	12270011	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986067	SmilChr05G001375	130986067	rna-XM_057909346.1	4	B103,C32,C68,D5
typical_cds_rare	Chr5	12270016	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130986067	SmilChr05G001375	130986067	rna-XM_057909346.1	2	C22,D10