source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr7	28978157	AC	A	INDEL	1bp_deletion	frameshift_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	1	B121
typical_cds_rare	Chr7	28978157	AC	A	INDEL	1bp_deletion	CDS_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	1	B121
typical_cds_rare	Chr7	28978530	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	3	B22,B41,D9
typical_cds_rare	Chr7	28979071	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	1	D11
typical_cds_rare	Chr7	28979324	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	1	A19
typical_cds_rare	Chr7	28979532	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	2	B71,C60
typical_cds_rare	Chr7	28979724	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	4	B42,B43,B72,B95
lof_cds	Chr7	28980063	G	GC	INDEL	1bp_insertion	frameshift_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	2	B101,B18
typical_cds_rare	Chr7	28980063	G	GC	INDEL	1bp_insertion	CDS_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	2	B101,B18
typical_cds_rare	Chr7	28980389	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	2	B42,B72
typical_cds_rare	Chr7	28980667	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	2	D10,D11
typical_cds_rare	Chr7	28980671	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130995889	SmilChr07G002877	130995889	rna-XM_057921382.1	5	B136,B34,C38,C71,C83