source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr5	13150671	G	GT	INDEL	1bp_insertion	frameshift_variant	LOC130986131	SmilChr05G001440	130986131	rna-XM_057909416.1	1	D6
typical_cds_rare	Chr5	13150671	G	GT	INDEL	1bp_insertion	CDS_variant	LOC130986131	SmilChr05G001440	130986131	rna-XM_057909416.1	1	D6
lof_cds	Chr5	13150702	TTG	T	INDEL	2bp_deletion	frameshift_variant	LOC130986131	SmilChr05G001440	130986131	rna-XM_057909416.1	1	B61
typical_cds_rare	Chr5	13150702	TTG	T	INDEL	2bp_deletion	CDS_variant	LOC130986131	SmilChr05G001440	130986131	rna-XM_057909416.1	1	B61
lof_cds	Chr5	13150784	T	TA	INDEL	1bp_insertion	frameshift_variant	LOC130986131	SmilChr05G001440	130986131	rna-XM_057909416.1	42	A11,A14,A15,A23,A3,A4,A9,B105,B121,B123,B133,B134,B135,B16,B5,B69,B81,B87,B89,C1,C12,C14,C16,C17,C23,C26,C27,C30,C45,C47,C5,C53,C64,C66,C67,C73,C76,C86,C87,D3,D4,D6
typical_cds_rare	Chr5	13150855	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130986131	SmilChr05G001440	130986131	rna-XM_057909416.1	1	A6
typical_cds_rare	Chr5	13151079	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986131	SmilChr05G001440	130986131	rna-XM_057909416.1	5	A11,B24,B33,B68,C48