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	7156072	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130998002	SmilChr08G000960	130998002	rna-XM_057923441.1	2	B58,C31	560892	continuous_repair_20261008_165818_r68	nuclear_20260923	8
typical_cds_rare	Chr8	7156080	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130998002	SmilChr08G000960	130998002	rna-XM_057923441.1	2	B58,C31	560893	continuous_repair_20261008_165818_r68	nuclear_20260923	8
typical_cds_rare	Chr8	7156083	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130998002	SmilChr08G000960	130998002	rna-XM_057923441.1	2	B58,C31	560894	continuous_repair_20261008_165818_r68	nuclear_20260923	8
lof_cds	Chr8	7156288	T	TC	INDEL	1bp_insertion	frameshift_variant	LOC130998002	SmilChr08G000960	130998002	rna-XM_057923441.1	16	A1,A23,B113,B123,B2,B22,B25,B46,C12,C44,C65,C74,C77,C8,C9,D3	755063	continuous_repair_20261008_165818_r68	nuclear_20260923	8
lof_cds	Chr8	7156401	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC130998002	SmilChr08G000960	130998002	rna-XM_057923441.1	1	A23	755064	continuous_repair_20261008_165818_r68	nuclear_20260923	8
typical_cds_rare	Chr8	7156401	TC	T	INDEL	1bp_deletion	CDS_variant	LOC130998002	SmilChr08G000960	130998002	rna-XM_057923441.1	1	A23	560895	continuous_repair_20261008_165818_r68	nuclear_20260923	8
typical_cds_rare	Chr8	7156546	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130998002	SmilChr08G000960	130998002	rna-XM_057923441.1	3	B100,B13,B68	560896	continuous_repair_20261008_165818_r68	nuclear_20260923	8
lof_cds	Chr8	7156831	GT	G	INDEL	1bp_deletion	frameshift_variant	LOC130998002	SmilChr08G000960	130998002	rna-XM_057923441.1	21	A2,A9,B101,B114,B137,B24,B41,B56,B59,B7,B71,B78,B96,B99,C13,C61,C63,C67,C75,C85,D8	755065	continuous_repair_20261008_165818_r68	nuclear_20260923	8