source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
typical_cds_rare	Chr8	6566016	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	3	B103,B132,D2
typical_cds_rare	Chr8	6566405	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	1	C36
typical_cds_rare	Chr8	6566659	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	2	B26,C19
typical_cds_rare	Chr8	6567167	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	3	B138,B19,C65
typical_cds_rare	Chr8	6567180	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	2	B31,C56
lof_cds	Chr8	6567253	CG	C	INDEL	1bp_deletion	frameshift_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	39	A20,A24,A25,A7,B112,B124,B127,B130,B39,B4,B42,B43,B46,B54,B60,B70,B75,B78,B8,B80,B86,B99,C18,C27,C34,C46,C47,C48,C49,C54,C57,C58,C70,C72,C74,C84,D3,D5,D6
typical_cds_rare	Chr8	6567401	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	2	B42,B43
typical_cds_rare	Chr8	6567410	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	1	C22
typical_cds_rare	Chr8	6567416	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	1	D11
typical_cds_rare	Chr8	6567530	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	1	D11
lof_cds	Chr8	6567562	TG	T	INDEL	1bp_deletion	frameshift_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	1	B28
typical_cds_rare	Chr8	6567562	TG	T	INDEL	1bp_deletion	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	1	B28
typical_cds_rare	Chr8	6567575	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	1	C4
typical_cds_rare	Chr8	6567708	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	1	B112
lof_cds	Chr8	6567787	GC	G	INDEL	1bp_deletion	frameshift_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	4	B2,B29,B61,C74
typical_cds_rare	Chr8	6567787	GC	G	INDEL	1bp_deletion	CDS_variant	LOC131000473	SmilChr08G000886	131000473	rna-XM_057926392.1	4	B2,B29,B61,C74