source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr5	1247950	C	CT	INDEL	1bp_insertion	frameshift_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	3	B78,C8,D7
typical_cds_rare	Chr5	1247950	C	CT	INDEL	1bp_insertion	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	3	B78,C8,D7
typical_cds_rare	Chr5	1247962	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	1	C82
typical_cds_rare	Chr5	1247987	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	3	B113,C22,C8
lof_cds	Chr5	1248017	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	1	C86
typical_cds_rare	Chr5	1248017	TC	T	INDEL	1bp_deletion	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	1	C86
typical_cds_rare	Chr5	1248165	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	1	B104
typical_cds_rare	Chr5	1248201	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	1	B67
typical_cds_rare	Chr5	1249114	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	1	B65
lof_cds	Chr5	1249117	G	GCT	INDEL	2bp_insertion	frameshift_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	2	B99,C87
typical_cds_rare	Chr5	1249117	G	GCT	INDEL	2bp_insertion	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	2	B99,C87
typical_cds_rare	Chr5	1249343	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	2	B104,B93
typical_cds_rare	Chr5	1249358	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	4	A3,B137,B79,C87
typical_cds_rare	Chr5	1249400	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	5	A3,B47,B79,C46,C87
lof_cds	Chr5	1249439	GT	G	INDEL	1bp_deletion	frameshift_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	3	A3,B113,C46
typical_cds_rare	Chr5	1249439	GT	G	INDEL	1bp_deletion	CDS_variant	LOC130984929	SmilChr05G000154	130984929	rna-XM_057907641.1	3	A3,B113,C46