source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr5	14441052	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC130986260	SmilChr05G001577	130986260	rna-XM_057909614.1	1	B9
typical_cds_rare	Chr5	14441052	TC	T	INDEL	1bp_deletion	CDS_variant	LOC130986260	SmilChr05G001577	130986260	rna-XM_057909614.1	1	B9
typical_cds_rare	Chr5	14441409	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130986260	SmilChr05G001577	130986260	rna-XM_057909614.1	3	A18,B27,C43
typical_cds_rare	Chr5	14441471	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986260	SmilChr05G001577	130986260	rna-XM_057909614.1	4	B21,B41,B71,D9
typical_cds_rare	Chr5	14441930	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986260	SmilChr05G001577	130986260	rna-XM_057909614.1	1	D10
typical_cds_rare	Chr5	14441960	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986260	SmilChr05G001577	130986260	rna-XM_057909614.1	1	D10
typical_cds_rare	Chr5	14443666	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986260	SmilChr05G001577	130986260	rna-XM_057909614.1	4	B124,B66,B94,D5
lof_cds	Chr5	14443864	TGG	T	INDEL	2bp_deletion	frameshift_variant	LOC130986260	SmilChr05G001577	130986260	rna-XM_057909614.1	1	A13
typical_cds_rare	Chr5	14443864	TGG	T	INDEL	2bp_deletion	CDS_variant	LOC130986260	SmilChr05G001577	130986260	rna-XM_057909614.1	1	A13
typical_cds_rare	Chr5	14443959	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986260	SmilChr05G001577	130986260	rna-XM_057909614.1	3	A16,A24,C42