source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
typical_cds_rare	Chr8	3840988	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	1	B105
lof_cds	Chr8	3841094	GCA	G	INDEL	2bp_deletion	frameshift_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	22	A14,A5,B123,B126,B134,B33,B46,B48,B67,B80,B82,B84,B91,B99,C11,C16,C23,C33,C57,C69,C77,C79
typical_cds_rare	Chr8	3841130	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	3	B111,B75,C35
typical_cds_rare	Chr8	3841174	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	1	D11
typical_cds_rare	Chr8	3841240	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	2	B140,D11
typical_cds_rare	Chr8	3841260	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	1	D11
lof_cds	Chr8	3841448	GC	G	INDEL	1bp_deletion	frameshift_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	1	A10
typical_cds_rare	Chr8	3841448	GC	G	INDEL	1bp_deletion	CDS_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	1	A10
lof_cds	Chr8	3841486	GC	G	INDEL	1bp_deletion	frameshift_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	4	B32,B85,C50,C82
typical_cds_rare	Chr8	3841486	GC	G	INDEL	1bp_deletion	CDS_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	4	B32,B85,C50,C82
typical_cds_rare	Chr8	3841494	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	1	B53
typical_cds_rare	Chr8	3841516	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000117	SmilChr08G000527	131000117	rna-XM_057925886.1	1	B53