source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr5	4771833	C	T	SNV	EMS_canonical_SNV	stop_gained	LOC130985308	SmilChr05G000632	130985308	rna-XM_057908223.1,rna-XM_057908224.1	56	A10,A13,A15,A20,A22,A23,A3,B1,B101,B103,B106,B110,B115,B117,B125,B129,B131,B139,B17,B25,B42,B43,B46,B47,B55,B58,B59,B62,B63,B7,B76,B83,B95,C11,C13,C17,C21,C22,C27,C28,C31,C38,C43,C45,C49,C52,C56,C57,C69,C70,C71,C76,C81,C83,C84,D2
typical_cds_rare	Chr5	4771839	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985308	SmilChr05G000632	130985308	rna-XM_057908223.1,rna-XM_057908224.1	2	C64,C66
typical_cds_rare	Chr5	4771896	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985308	SmilChr05G000632	130985308	rna-XM_057908223.1,rna-XM_057908224.1	3	B13,B40,D11
lof_cds	Chr5	4775100	TGA	T	INDEL	2bp_deletion	frameshift_variant	LOC130985308	SmilChr05G000632	130985308	rna-XM_057908223.1,rna-XM_057908224.1	4	B104,B29,B72,C79
typical_cds_rare	Chr5	4775100	TGA	T	INDEL	2bp_deletion	CDS_variant	LOC130985308	SmilChr05G000632	130985308	rna-XM_057908223.1,rna-XM_057908224.1	4	B104,B29,B72,C79
typical_cds_rare	Chr5	4775633	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985308	SmilChr05G000632	130985308	rna-XM_057908223.1,rna-XM_057908224.1	1	C60
typical_cds_rare	Chr5	4775691	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130985308	SmilChr05G000632	130985308	rna-XM_057908223.1,rna-XM_057908224.1	1	B104
typical_cds_rare	Chr5	4775721	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130985308	SmilChr05G000632	130985308	rna-XM_057908223.1,rna-XM_057908224.1	1	D11
typical_cds_rare	Chr5	4775938	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985308	SmilChr05G000632	130985308	rna-XM_057908223.1,rna-XM_057908224.1	5	B124,B30,B86,C34,C54