source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr8	8924329	A	AAT	INDEL	2bp_insertion	stop_gained,frameshift_variant	LOC130998032	SmilChr08G001136	130998032	rna-XM_057923467.1	111	A1,A11,A15,A18,A20,A23,A6,A8,A9,B1,B10,B103,B104,B105,B107,B108,B109,B114,B120,B122,B128,B131,B132,B133,B136,B14,B2,B22,B23,B24,B26,B28,B3,B30,B31,B33,B35,B38,B39,B4,B41,B46,B49,B5,B57,B58,B61,B63,B64,B65,B66,B68,B69,B7,B70,B73,B74,B76,B79,B82,B86,B88,B89,B91,B93,B94,B95,B98,B99,C10,C14,C15,C16,C17,C20,C22,C23,C27,C3,C30,C32,C35,C36,C41,C45,C46,C49,C50,C51,C53,C55,C61,C63,C64,C65,C66,C67,C68,C72,C73,C75,C76,C79,C8,C84,C87,C9,D1,D11,D7,D9
typical_cds_rare	Chr8	8924346	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130998032	SmilChr08G001136	130998032	rna-XM_057923467.1	1	C28
typical_cds_rare	Chr8	8924528	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130998032	SmilChr08G001136	130998032	rna-XM_057923467.1	1	C57
lof_cds	Chr8	8924705	GGA	G	INDEL	2bp_deletion	frameshift_variant	LOC130998032	SmilChr08G001136	130998032	rna-XM_057923467.1	4	A23,B24,C13,C57
typical_cds_rare	Chr8	8924705	GGA	G	INDEL	2bp_deletion	CDS_variant	LOC130998032	SmilChr08G001136	130998032	rna-XM_057923467.1	4	A23,B24,C13,C57