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	44671509	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	5	B42,B43,B70,C57,C58
typical_cds_rare	Chr2	44673251	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	1	D11
typical_cds_rare	Chr2	44673518	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	2	C53,D3
typical_cds_rare	Chr2	44673671	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	1	C30
typical_cds_rare	Chr2	44673700	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	1	B35
lof_cds	Chr2	44673748	TCA	T	INDEL	2bp_deletion	frameshift_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	1	B28
typical_cds_rare	Chr2	44673748	TCA	T	INDEL	2bp_deletion	CDS_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	1	B28
lof_cds	Chr2	44674729	GA	G	INDEL	1bp_deletion	frameshift_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	1	B127
typical_cds_rare	Chr2	44674729	GA	G	INDEL	1bp_deletion	CDS_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	1	B127
typical_cds_rare	Chr2	44674872	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	2	C30,C40
typical_cds_rare	Chr2	44674918	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	1	B84
typical_cds_rare	Chr2	44675008	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	1	C41
typical_cds_rare	Chr2	44675019	AGT	A	INDEL	2bp_deletion	CDS_variant	LOC131011632	SmilChr02G002567	131011632	rna-XM_057939404.1	1	B95