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	7601606	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	2	A22,B30
typical_cds_rare	Chr5	7602046	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	1	C66
typical_cds_rare	Chr5	7604811	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	2	B80,C37
typical_cds_rare	Chr5	7604852	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	3	B110,C10,C11
lof_cds	Chr5	7604892	GC	G	INDEL	1bp_deletion	frameshift_variant	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	1	C53
typical_cds_rare	Chr5	7604892	GC	G	INDEL	1bp_deletion	CDS_variant	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	1	C53
lof_cds	Chr5	7604964	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	1	B112
typical_cds_rare	Chr5	7604964	TC	T	INDEL	1bp_deletion	CDS_variant	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	1	B112
typical_cds_rare	Chr5	7604965	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	3	A7,B100,B41
lof_cds	Chr5	7605288	G	GC	INDEL	1bp_insertion	frameshift_variant	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	8	B114,B127,B28,B61,B8,C41,C49,C63
lof_cds	Chr5	7605517	C	T	SNV	EMS_canonical_SNV	stop_gained	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	1	B88
typical_cds_rare	Chr5	7605517	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130985658	SmilChr05G000942	130985658	rna-XM_057908732.1	1	B88