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	4972099	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	1	B106
typical_cds_rare	Chr8	4972137	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	1	B95
typical_cds_rare	Chr8	4972143	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	1	B105
lof_cds	Chr8	4972158	A	AG	INDEL	1bp_insertion	frameshift_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	6	B134,B31,B36,B89,C53,C65
typical_cds_rare	Chr8	4972350	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	1	C12
typical_cds_rare	Chr8	4972503	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	1	B106
typical_cds_rare	Chr8	4972611	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	5	B18,B19,B65,C10,C24
typical_cds_rare	Chr8	4973775	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	1	B95
lof_cds	Chr8	4973822	AGT	A	INDEL	2bp_deletion	frameshift_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	1	B79
typical_cds_rare	Chr8	4973822	AGT	A	INDEL	2bp_deletion	CDS_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	1	B79
typical_cds_rare	Chr8	4973830	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	1	B79
typical_cds_rare	Chr8	4974395	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	1	B95
lof_cds	Chr8	4974496	A	AT	INDEL	1bp_insertion	frameshift_variant	LOC131000248	SmilChr08G000671	131000248	rna-XM_057926052.1	27	A13,A5,A7,B102,B103,B127,B13,B134,B29,B3,B32,B52,B53,B6,B62,B63,B66,B88,B93,C13,C2,C24,C26,C29,C79,C81,D2