source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr2	64511407	AAT	A	INDEL	2bp_deletion	frameshift_variant	LOC131012977	SmilChr02G004233	131012977	rna-XM_057940966.1	136	A10,A11,A13,A14,A16,A18,A19,A2,A20,A22,A24,A7,A8,A9,B10,B101,B104,B105,B107,B108,B109,B11,B110,B115,B117,B12,B120,B128,B132,B133,B136,B14,B140,B18,B19,B2,B21,B22,B23,B25,B26,B27,B28,B3,B31,B35,B37,B38,B4,B40,B42,B43,B44,B46,B49,B50,B51,B52,B55,B58,B59,B63,B67,B70,B72,B73,B74,B75,B76,B77,B78,B79,B8,B81,B82,B83,B84,B86,B9,B91,B99,C1,C10,C13,C18,C20,C21,C23,C24,C26,C29,C3,C30,C33,C35,C37,C39,C4,C40,C41,C43,C45,C49,C5,C53,C56,C57,C58,C59,C60,C61,C62,C64,C66,C70,C71,C73,C76,C77,C79,C82,C83,C84,C85,C86,C9,D1,D10,D11,D2,D4,D5,D6,D7,D8,D9
lof_cds	Chr2	64511427	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC131012977	SmilChr02G004233	131012977	rna-XM_057940966.1	1	B78
typical_cds_rare	Chr2	64511427	TC	T	INDEL	1bp_deletion	CDS_variant	LOC131012977	SmilChr02G004233	131012977	rna-XM_057940966.1	1	B78
typical_cds_rare	Chr2	64511520	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131012977	SmilChr02G004233	131012977	rna-XM_057940966.1	1	D3
typical_cds_rare	Chr2	64511685	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131012977	SmilChr02G004233	131012977	rna-XM_057940966.1	2	B107,B140
typical_cds_rare	Chr2	64511802	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131012977	SmilChr02G004233	131012977	rna-XM_057940966.1	1	B135
typical_cds_rare	Chr2	64512030	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131012977	SmilChr02G004233	131012977	rna-XM_057940966.1	2	B107,B140
typical_cds_rare	Chr2	64512129	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131012977	SmilChr02G004233	131012977	rna-XM_057940966.1	2	B107,B140
typical_cds_rare	Chr2	64512156	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131012977	SmilChr02G004233	131012977	rna-XM_057940966.1	4	B120,B77,C49,C71
typical_cds_rare	Chr2	64512168	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131012977	SmilChr02G004233	131012977	rna-XM_057940966.1	4	B120,B77,C49,C71
typical_cds_rare	Chr2	64512179	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131012977	SmilChr02G004233	131012977	rna-XM_057940966.1	3	B108,B50,C23