source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr5	7185461	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908691.1,rna-XM_057908692.1	1	D11
typical_cds_rare	Chr5	7185461	TC	T	INDEL	1bp_deletion	CDS_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908691.1,rna-XM_057908692.1	1	D11
typical_cds_rare	Chr5	7185462	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908691.1,rna-XM_057908692.1	3	A10,B22,C82
typical_cds_rare	Chr5	7185804	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908691.1,rna-XM_057908692.1	1	C71
typical_cds_rare	Chr5	7185811	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908691.1,rna-XM_057908692.1	4	A10,B136,C4,D6
lof_cds	Chr5	7185851	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908691.1,rna-XM_057908692.1	1	B13
typical_cds_rare	Chr5	7185851	TC	T	INDEL	1bp_deletion	CDS_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908691.1,rna-XM_057908692.1	1	B13
typical_cds_rare	Chr5	7185853	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908691.1,rna-XM_057908692.1	1	B13
typical_cds_rare	Chr5	7186220	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908692.1	2	A13,C13
lof_cds	Chr5	7186779	TA	T	INDEL	1bp_deletion	frameshift_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908692.1	13	A6,B104,B109,B26,B37,B59,B81,B89,C10,C29,C43,D10,D8
lof_cds	Chr5	7186783	C	T	SNV	EMS_canonical_SNV	stop_gained	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908692.1	13	A6,B104,B109,B26,B37,B59,B81,B89,C10,C29,C43,D10,D8
typical_cds_rare	Chr5	7186785	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908692.1	1	D4
lof_cds	Chr5	7186843	CA	C	INDEL	1bp_deletion	frameshift_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908692.1	9	B36,B57,C20,C34,C36,C41,C5,C72,D5
lof_cds	Chr5	7188085	TGA	T	INDEL	2bp_deletion	frameshift_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908692.1	33	A14,A2,A25,B106,B107,B118,B119,B124,B130,B33,B38,B41,B44,B47,B49,B73,B77,B90,B91,B92,C16,C21,C23,C34,C37,C39,C51,C55,C73,C82,C86,D1,D6
lof_cds	Chr5	7188099	TG	T	INDEL	1bp_deletion	frameshift_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908692.1	7	B119,B140,B73,B77,C23,C34,C37
typical_cds_rare	Chr5	7188160	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985622	SmilChr05G000908	130985622	rna-XM_057908692.1	5	B104,B26,B27,B81,C10