source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr7	2137800	G	GC	INDEL	1bp_insertion	frameshift_variant	LOC130991513	SmilChr07G000318	130991513	rna-XM_057915772.1	2	B104,D10
typical_cds_rare	Chr7	2137800	G	GC	INDEL	1bp_insertion	CDS_variant	LOC130991513	SmilChr07G000318	130991513	rna-XM_057915772.1	2	B104,D10
lof_cds	Chr7	2137848	G	GC	INDEL	1bp_insertion	frameshift_variant	LOC130991513	SmilChr07G000318	130991513	rna-XM_057915772.1	42	A13,A23,A4,B106,B110,B111,B128,B130,B140,B17,B18,B25,B37,B40,B48,B49,B51,B54,B68,B7,B77,B79,B83,B99,C14,C16,C18,C19,C27,C29,C3,C40,C47,C54,C57,C58,C7,C70,C78,C84,D4,D8
lof_cds	Chr7	2137867	GT	G	INDEL	1bp_deletion	frameshift_variant	LOC130991513	SmilChr07G000318	130991513	rna-XM_057915772.1	1	B29
typical_cds_rare	Chr7	2137867	GT	G	INDEL	1bp_deletion	CDS_variant	LOC130991513	SmilChr07G000318	130991513	rna-XM_057915772.1	1	B29
typical_cds_rare	Chr7	2137869	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130991513	SmilChr07G000318	130991513	rna-XM_057915772.1	1	B29
typical_cds_rare	Chr7	2138178	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130991513	SmilChr07G000318	130991513	rna-XM_057915772.1	1	D9
typical_cds_rare	Chr7	2138224	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130991513	SmilChr07G000318	130991513	rna-XM_057915772.1	1	B100
lof_cds	Chr7	2138288	GAC	G	INDEL	2bp_deletion	frameshift_variant	LOC130991513	SmilChr07G000318	130991513	rna-XM_057915772.1	18	A16,A4,B101,B128,B55,B87,C10,C14,C17,C20,C47,C52,C55,C66,C73,C74,C80,C87
typical_cds_rare	Chr7	2138299	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130991513	SmilChr07G000318	130991513	rna-XM_057915772.1	3	B137,B72,C71