source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr3	44660670	A	AT	INDEL	1bp_insertion	frameshift_variant	LOC131016018	SmilChr03G002819	131016018	rna-XM_057944571.1	194	A1,A10,A11,A13,A14,A15,A18,A2,A21,A22,A23,A3,A4,A6,A7,A8,B1,B100,B102,B105,B106,B107,B11,B110,B112,B113,B114,B115,B117,B118,B119,B121,B123,B124,B125,B126,B129,B130,B131,B132,B133,B136,B137,B139,B14,B140,B15,B16,B17,B19,B2,B20,B21,B23,B24,B25,B26,B28,B29,B3,B30,B31,B32,B33,B34,B35,B36,B38,B39,B4,B40,B41,B42,B44,B45,B47,B48,B49,B5,B50,B52,B54,B55,B56,B57,B58,B60,B61,B62,B63,B64,B66,B68,B69,B7,B70,B71,B72,B73,B74,B75,B77,B78,B79,B8,B83,B84,B85,B87,B88,B89,B9,B90,B91,B92,B93,B94,B95,B96,B97,B99,C1,C10,C11,C12,C14,C16,C20,C22,C23,C25,C26,C28,C29,C3,C31,C32,C33,C34,C35,C36,C37,C39,C40,C41,C44,C47,C48,C5,C50,C51,C52,C53,C54,C56,C57,C58,C59,C60,C61,C62,C63,C64,C65,C66,C68,C69,C7,C70,C71,C72,C73,C75,C76,C77,C79,C8,C80,C81,C82,C83,C84,C85,C86,C87,D1,D10,D11,D2,D3,D5,D6,D7,D8
typical_cds_rare	Chr3	44660738	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131016018	SmilChr03G002819	131016018	rna-XM_057944571.1	1	C37
typical_cds_rare	Chr3	44660865	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131016018	SmilChr03G002819	131016018	rna-XM_057944571.1	1	B60
typical_cds_rare	Chr3	44660908	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131016018	SmilChr03G002819	131016018	rna-XM_057944571.1	3	B77,B99,C26
lof_cds	Chr3	44661068	A	AG	INDEL	1bp_insertion	frameshift_variant	LOC131016018	SmilChr03G002819	131016018	rna-XM_057944571.1	17	B16,B17,B26,B36,B47,B69,B77,B87,B90,B91,B92,C14,C26,C50,C81,D10,D6
typical_cds_rare	Chr3	44661119	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131016018	SmilChr03G002819	131016018	rna-XM_057944571.1	4	A20,B38,B39,D7
lof_cds	Chr3	44661125	C	T	SNV	EMS_canonical_SNV	stop_gained	LOC131016018	SmilChr03G002819	131016018	rna-XM_057944571.1	24	A6,B100,B107,B110,B119,B129,B133,B15,B34,B38,B41,B45,B5,B70,B83,B84,C22,C53,C59,C63,C70,C72,C76,C77
lof_cds	Chr3	44662127	AC	A	INDEL	1bp_deletion	frameshift_variant	LOC131016018	SmilChr03G002819	131016018	rna-XM_057944571.1	1	B25
typical_cds_rare	Chr3	44662127	AC	A	INDEL	1bp_deletion	CDS_variant	LOC131016018	SmilChr03G002819	131016018	rna-XM_057944571.1	1	B25
typical_cds_rare	Chr3	44662256	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131016018	SmilChr03G002819	131016018	rna-XM_057944571.1	1	D11