source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
typical_cds_rare	Chr5	54900965	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131025165	SmilChr05G004104	131025165	rna-XM_057954793.1	3	B10,B137,B35
lof_cds	Chr5	54901021	T	TA	INDEL	1bp_insertion	frameshift_variant	LOC131025165	SmilChr05G004104	131025165	rna-XM_057954793.1	1	B48
typical_cds_rare	Chr5	54901021	T	TA	INDEL	1bp_insertion	CDS_variant	LOC131025165	SmilChr05G004104	131025165	rna-XM_057954793.1	1	B48
typical_cds_rare	Chr5	54901356	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131025165	SmilChr05G004104	131025165	rna-XM_057954793.1	2	B121,B127
typical_cds_rare	Chr5	54901414	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131025165	SmilChr05G004104	131025165	rna-XM_057954793.1	1	B83
lof_cds	Chr5	54901757	T	TG	INDEL	1bp_insertion	frameshift_variant	LOC131025165	SmilChr05G004104	131025165	rna-XM_057954793.1	1	C55
typical_cds_rare	Chr5	54901757	T	TG	INDEL	1bp_insertion	CDS_variant	LOC131025165	SmilChr05G004104	131025165	rna-XM_057954793.1	1	C55
typical_cds_rare	Chr5	54902071	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131025165	SmilChr05G004104	131025165	rna-XM_057954793.1	1	B91
lof_cds	Chr5	54902565	AAG	A	INDEL	2bp_deletion	frameshift_variant	LOC131025165	SmilChr05G004104	131025165	rna-XM_057954793.1	1	B138
typical_cds_rare	Chr5	54902565	AAG	A	INDEL	2bp_deletion	CDS_variant	LOC131025165	SmilChr05G004104	131025165	rna-XM_057954793.1	1	B138
