source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers	variant_id	portal_version	data_version	query_total
typical_cds_rare	Chr8	37576608	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130996618	SmilChr08G003501	130996618	rna-XM_057921916.1	1	D11	591925	continuous_repair_20261008_165818_r68	nuclear_20260923	8
typical_cds_rare	Chr8	37576644	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130996618	SmilChr08G003501	130996618	rna-XM_057921916.1	3	B122,B16,B31	591926	continuous_repair_20261008_165818_r68	nuclear_20260923	8
typical_cds_rare	Chr8	37576677	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130996618	SmilChr08G003501	130996618	rna-XM_057921916.1	3	B56,B59,B96	591927	continuous_repair_20261008_165818_r68	nuclear_20260923	8
lof_cds	Chr8	37576682	CT	C	INDEL	1bp_deletion	frameshift_variant	LOC130996618	SmilChr08G003501	130996618	rna-XM_057921916.1	7	A8,B122,B53,B57,C11,C26,C69	762118	continuous_repair_20261008_165818_r68	nuclear_20260923	8
lof_cds	Chr8	37576834	A	ATG	INDEL	2bp_insertion	frameshift_variant	LOC130996618	SmilChr08G003501	130996618	rna-XM_057921916.1	3	B46,B70,C62	762119	continuous_repair_20261008_165818_r68	nuclear_20260923	8
typical_cds_rare	Chr8	37576834	A	ATG	INDEL	2bp_insertion	CDS_variant	LOC130996618	SmilChr08G003501	130996618	rna-XM_057921916.1	3	B46,B70,C62	591928	continuous_repair_20261008_165818_r68	nuclear_20260923	8
typical_cds_rare	Chr8	37576854	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130996618	SmilChr08G003501	130996618	rna-XM_057921916.1	3	B30,B69,C19	591929	continuous_repair_20261008_165818_r68	nuclear_20260923	8
typical_cds_rare	Chr8	37577829	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130996618	SmilChr08G003501	130996618	rna-XM_057921916.1	1	B25	591930	continuous_repair_20261008_165818_r68	nuclear_20260923	8