source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
typical_cds_rare	Chr2	11914738	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011218	SmilChr02G000735	131011218	rna-XM_057939007.1	3	A22,B76,C49
lof_cds	Chr2	11914757	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC131011218	SmilChr02G000735	131011218	rna-XM_057939007.1	59	A16,A18,A3,A6,B10,B100,B103,B107,B109,B110,B119,B12,B126,B134,B140,B17,B30,B38,B39,B42,B43,B45,B46,B47,B5,B51,B52,B58,B6,B68,B71,B82,B85,B86,B87,B88,B89,B9,B90,B99,C1,C16,C19,C2,C22,C25,C37,C39,C40,C42,C45,C47,C5,C53,C55,C56,D6,D7,D9
typical_cds_rare	Chr2	11915226	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011218	SmilChr02G000735	131011218	rna-XM_057939007.1	2	B129,C29
lof_cds	Chr2	11915921	AG	A	INDEL	1bp_deletion	frameshift_variant	LOC131011218	SmilChr02G000735	131011218	rna-XM_057939007.1	2	B129,B2
typical_cds_rare	Chr2	11915921	AG	A	INDEL	1bp_deletion	CDS_variant	LOC131011218	SmilChr02G000735	131011218	rna-XM_057939007.1	2	B129,B2
typical_cds_rare	Chr2	11915927	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011218	SmilChr02G000735	131011218	rna-XM_057939007.1	1	B9
lof_cds	Chr2	11915957	C	T	SNV	EMS_canonical_SNV	stop_gained	LOC131011218	SmilChr02G000735	131011218	rna-XM_057939007.1	2	B93,D11
typical_cds_rare	Chr2	11915957	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131011218	SmilChr02G000735	131011218	rna-XM_057939007.1	2	B93,D11
lof_cds	Chr2	11915974	T	TTG	INDEL	2bp_insertion	frameshift_variant	LOC131011218	SmilChr02G000735	131011218	rna-XM_057939007.1	5	A9,B10,B112,B26,B82
typical_cds_rare	Chr2	11915974	T	TTG	INDEL	2bp_insertion	CDS_variant	LOC131011218	SmilChr02G000735	131011218	rna-XM_057939007.1	5	A9,B10,B112,B26,B82
typical_cds_rare	Chr2	11916398	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011218	SmilChr02G000735	131011218	rna-XM_057939007.1	2	B105,D1