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	45525620	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131011669	SmilChr02G002622	131011669	rna-XM_057939447.1,rna-XM_057939448.1	1	D9
typical_cds_rare	Chr2	45525732	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131011669	SmilChr02G002622	131011669	rna-XM_057939447.1,rna-XM_057939448.1	1	B71
typical_cds_rare	Chr2	45525748	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131011669	SmilChr02G002622	131011669	rna-XM_057939447.1,rna-XM_057939448.1	1	D10
typical_cds_rare	Chr2	45525786	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011669	SmilChr02G002622	131011669	rna-XM_057939447.1,rna-XM_057939448.1	4	A10,B118,C82,D4
lof_cds	Chr2	45526699	TTC	T	INDEL	2bp_deletion	frameshift_variant	LOC131011669	SmilChr02G002622	131011669	rna-XM_057939447.1,rna-XM_057939448.1	1	B48
typical_cds_rare	Chr2	45526699	TTC	T	INDEL	2bp_deletion	CDS_variant	LOC131011669	SmilChr02G002622	131011669	rna-XM_057939447.1,rna-XM_057939448.1	1	B48
lof_cds	Chr2	45526759	AT	A	INDEL	1bp_deletion	frameshift_variant	LOC131011669	SmilChr02G002622	131011669	rna-XM_057939447.1	1	B101
typical_cds_rare	Chr2	45526759	AT	A	INDEL	1bp_deletion	CDS_variant	LOC131011669	SmilChr02G002622	131011669	rna-XM_057939447.1	1	B101
lof_cds	Chr2	45526773	T	TG	INDEL	1bp_insertion	frameshift_variant	LOC131011669	SmilChr02G002622	131011669	rna-XM_057939447.1	9	B103,B121,B125,B127,B21,B52,C55,C80,D8