source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
typical_cds_rare	Chr4	2305356	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	4	B27,B55,C17,C43
typical_cds_rare	Chr4	2305590	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	1	D10
typical_cds_rare	Chr4	2305716	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	1	B15
typical_cds_rare	Chr4	2305832	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	1	B58
typical_cds_rare	Chr4	2305896	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	1	B41
typical_cds_rare	Chr4	2305902	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	4	B4,B50,C52,C85
typical_cds_rare	Chr4	2306008	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	1	B117
typical_cds_rare	Chr4	2306096	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	2	B47,C7
typical_cds_rare	Chr4	2306218	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	2	A24,B33
typical_cds_rare	Chr4	2306385	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	1	C79
typical_cds_rare	Chr4	2306418	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	1	B62
lof_cds	Chr4	2306689	GC	G	INDEL	1bp_deletion	frameshift_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	72	A18,A2,A21,A23,A25,A3,A5,A7,A9,B104,B105,B107,B108,B11,B110,B115,B118,B119,B12,B13,B131,B132,B135,B136,B137,B138,B21,B22,B23,B24,B28,B29,B4,B40,B42,B5,B61,B63,B65,B67,B69,B7,B72,B73,B77,B8,B84,B87,B90,B92,B96,B98,C2,C24,C29,C3,C30,C33,C41,C48,C5,C51,C55,C59,C61,C63,C73,C77,C84,C87,D8,D9
lof_cds	Chr4	2306695	C	CT	INDEL	1bp_insertion	frameshift_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	71	A18,A2,A21,A23,A25,A3,A5,A7,A9,B104,B105,B107,B108,B11,B110,B115,B118,B119,B12,B13,B131,B132,B135,B136,B137,B138,B21,B22,B24,B28,B29,B4,B40,B42,B5,B61,B63,B65,B67,B69,B7,B72,B73,B77,B8,B84,B87,B90,B92,B96,B98,C2,C24,C29,C3,C30,C33,C41,C48,C5,C51,C55,C59,C61,C63,C73,C77,C84,C87,D8,D9
typical_cds_rare	Chr4	2306742	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022177	SmilChr04G000253	131022177	rna-XM_057951605.1	3	B67,B7,B96