source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr8	4088853	C	CA	INDEL	1bp_insertion	frameshift_variant	LOC131000153	SmilChr08G000564	131000153	rna-XM_057925933.1	65	A11,A16,A2,A24,A3,A4,A7,A8,A9,B101,B107,B110,B119,B120,B125,B127,B128,B134,B135,B136,B138,B14,B18,B19,B3,B33,B34,B41,B47,B60,B77,B81,B86,B9,B91,B95,B97,B98,C20,C25,C27,C3,C35,C37,C42,C43,C49,C55,C57,C58,C6,C60,C63,C65,C67,C7,C73,C74,C76,C79,C82,D11,D6,D8,D9
typical_cds_rare	Chr8	4089173	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000153	SmilChr08G000564	131000153	rna-XM_057925933.1	1	B60
typical_cds_rare	Chr8	4089202	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000153	SmilChr08G000564	131000153	rna-XM_057925933.1	1	C6
typical_cds_rare	Chr8	4089229	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000153	SmilChr08G000564	131000153	rna-XM_057925933.1	1	B26
lof_cds	Chr8	4089321	GC	G	INDEL	1bp_deletion	frameshift_variant	LOC131000153	SmilChr08G000564	131000153	rna-XM_057925933.1	1	B7
typical_cds_rare	Chr8	4089321	GC	G	INDEL	1bp_deletion	CDS_variant	LOC131000153	SmilChr08G000564	131000153	rna-XM_057925933.1	1	B7
lof_cds	Chr8	4089323	GGC	G	INDEL	2bp_deletion	frameshift_variant	LOC131000153	SmilChr08G000564	131000153	rna-XM_057925933.1	1	B7
typical_cds_rare	Chr8	4089323	GGC	G	INDEL	2bp_deletion	CDS_variant	LOC131000153	SmilChr08G000564	131000153	rna-XM_057925933.1	1	B7