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	44763797	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011634	SmilChr02G002575	131011634	rna-XM_057939406.1	1	D10
typical_cds_rare	Chr2	44763970	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011634	SmilChr02G002575	131011634	rna-XM_057939406.1	1	B87
typical_cds_rare	Chr2	44763988	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011634	SmilChr02G002575	131011634	rna-XM_057939406.1	1	B87
typical_cds_rare	Chr2	44764111	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131011634	SmilChr02G002575	131011634	rna-XM_057939406.1	2	A3,B60
typical_cds_rare	Chr2	44764660	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011634	SmilChr02G002575	131011634	rna-XM_057939406.1	1	B104
typical_cds_rare	Chr2	44764747	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011634	SmilChr02G002575	131011634	rna-XM_057939406.1	5	A10,B1,B118,B2,D4
lof_cds	Chr2	44764815	GC	G	INDEL	1bp_deletion	frameshift_variant	LOC131011634	SmilChr02G002575	131011634	rna-XM_057939406.1	13	A21,A7,B101,B13,B130,B2,B28,B54,B7,C16,C42,C79,C81
lof_cds	Chr2	44764817	TGC	T	INDEL	2bp_deletion	frameshift_variant	LOC131011634	SmilChr02G002575	131011634	rna-XM_057939406.1	13	A21,A7,B101,B13,B130,B2,B28,B54,B7,C16,C42,C79,C81