source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr2	62066458	C	T	SNV	EMS_canonical_SNV	stop_gained	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	160	A1,A10,A11,A13,A16,A18,A19,A2,A21,A22,A24,A4,A6,A7,A9,B101,B103,B106,B108,B109,B11,B110,B111,B112,B114,B115,B118,B119,B12,B120,B122,B123,B124,B127,B129,B13,B131,B132,B133,B135,B136,B138,B139,B16,B17,B18,B19,B2,B20,B21,B22,B23,B27,B28,B30,B31,B33,B34,B35,B36,B4,B42,B43,B44,B45,B53,B54,B55,B56,B57,B59,B6,B60,B62,B64,B65,B66,B67,B68,B69,B70,B71,B72,B74,B75,B79,B80,B82,B84,B88,B89,B9,B90,B91,B92,B93,B94,B96,B97,B98,C10,C11,C13,C14,C2,C20,C22,C23,C24,C26,C27,C29,C30,C31,C32,C33,C36,C38,C4,C40,C42,C43,C44,C47,C48,C5,C51,C55,C56,C57,C6,C60,C61,C63,C67,C69,C7,C70,C71,C72,C73,C74,C75,C76,C77,C78,C79,C80,C82,C83,C84,C85,C87,C9,D1,D10,D11,D2,D3,D4
typical_cds_rare	Chr2	62066487	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	5	B107,B59,C10,D4,D9
typical_cds_rare	Chr2	62066508	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	4	A20,B59,C62,D10
lof_cds	Chr2	62066657	G	A	SNV	EMS_canonical_SNV	stop_gained	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	2	B131,C49
typical_cds_rare	Chr2	62066657	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	2	B131,C49
typical_cds_rare	Chr2	62066773	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	3	A21,B40,C8
lof_cds	Chr2	62066790	AAG	A	INDEL	2bp_deletion	frameshift_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	42	A11,A18,A2,A23,A25,A4,A8,A9,B1,B101,B102,B110,B130,B131,B33,B37,B44,B49,B54,B57,B60,B62,B79,B88,B9,B91,B98,C12,C18,C20,C27,C33,C51,C60,C64,C66,C67,C75,C79,C84,D1,D7
lof_cds	Chr2	62066826	G	GT	INDEL	1bp_insertion	frameshift_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	1	B140
typical_cds_rare	Chr2	62066826	G	GT	INDEL	1bp_insertion	CDS_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	1	B140
lof_cds	Chr2	62066943	GT	G	INDEL	1bp_deletion	frameshift_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	2	A10,B26
typical_cds_rare	Chr2	62066943	GT	G	INDEL	1bp_deletion	CDS_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	2	A10,B26
typical_cds_rare	Chr2	62066951	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	1	B78
lof_cds	Chr2	62066968	G	GT	INDEL	1bp_insertion	frameshift_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	1	B140
typical_cds_rare	Chr2	62066968	G	GT	INDEL	1bp_insertion	CDS_variant	LOC131010920	SmilChr02G003981	131010920	rna-XM_057938628.1	1	B140