source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr2	54710657	CAT	C	INDEL	2bp_deletion	frameshift_variant	LOC131010371	SmilChr02G003352	131010371	rna-XM_057937868.1	1	B94
typical_cds_rare	Chr2	54710657	CAT	C	INDEL	2bp_deletion	CDS_variant	LOC131010371	SmilChr02G003352	131010371	rna-XM_057937868.1	1	B94
lof_cds	Chr2	54710729	G	GAA	INDEL	2bp_insertion	frameshift_variant	LOC131010371	SmilChr02G003352	131010371	rna-XM_057937868.1	16	A24,B106,B108,B112,B114,B3,B38,B39,B5,B73,B97,C13,C30,C59,C83,C84
lof_cds	Chr2	54710774	A	AT	INDEL	1bp_insertion	frameshift_variant	LOC131010371	SmilChr02G003352	131010371	rna-XM_057937868.1	19	B123,B137,B139,B29,B30,B37,B4,B51,B6,B62,B66,B72,B97,C35,C37,C4,C52,C67,D3
lof_cds	Chr2	54710904	G	A	SNV	EMS_canonical_SNV	stop_gained	LOC131010371	SmilChr02G003352	131010371	rna-XM_057937868.1,rna-XM_057937869.1	2	C29,C6
typical_cds_rare	Chr2	54710904	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131010371	SmilChr02G003352	131010371	rna-XM_057937868.1,rna-XM_057937869.1	2	C29,C6
typical_cds_rare	Chr2	54711597	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131010371	SmilChr02G003352	131010371	rna-XM_057937868.1,rna-XM_057937869.1	1	A21
typical_cds_rare	Chr2	54711634	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131010371	SmilChr02G003352	131010371	rna-XM_057937868.1,rna-XM_057937869.1	1	A21