source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr7	1179111	TG	T	INDEL	1bp_deletion	frameshift_variant	LOC130991378	SmilChr07G000186	130991378	rna-XM_057915556.1	11	A9,B132,B37,B42,B43,B73,B74,B77,C20,C22,C52
typical_cds_rare	Chr7	1180131	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130991378	SmilChr07G000186	130991378	rna-XM_057915556.1	2	C55,C85
typical_cds_rare	Chr7	1180178	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130991378	SmilChr07G000186	130991378	rna-XM_057915556.1	5	B48,B53,B58,B66,B78
typical_cds_rare	Chr7	1180212	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130991378	SmilChr07G000186	130991378	rna-XM_057915556.1	2	B114,D10
lof_cds	Chr7	1180239	GC	G	INDEL	1bp_deletion	frameshift_variant	LOC130991378	SmilChr07G000186	130991378	rna-XM_057915556.1	1	B2
typical_cds_rare	Chr7	1180239	GC	G	INDEL	1bp_deletion	CDS_variant	LOC130991378	SmilChr07G000186	130991378	rna-XM_057915556.1	1	B2
typical_cds_rare	Chr7	1180242	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130991378	SmilChr07G000186	130991378	rna-XM_057915556.1	3	B128,B2,B20
lof_cds	Chr7	1180270	T	TCG	INDEL	2bp_insertion	frameshift_variant	LOC130991378	SmilChr07G000186	130991378	rna-XM_057915556.1	1	D3
typical_cds_rare	Chr7	1180270	T	TCG	INDEL	2bp_insertion	CDS_variant	LOC130991378	SmilChr07G000186	130991378	rna-XM_057915556.1	1	D3
typical_cds_rare	Chr7	1180420	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130991378	SmilChr07G000186	130991378	rna-XM_057915556.1	1	B68