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	8737118	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	1	B112
typical_cds_rare	Chr8	8737305	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	1	C19
typical_cds_rare	Chr8	8737410	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	1	B68
typical_cds_rare	Chr8	8737415	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	1	D10
typical_cds_rare	Chr8	8737536	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	2	C32,C68
typical_cds_rare	Chr8	8737577	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	5	A1,C19,C50,C75,C83
typical_cds_rare	Chr8	8737664	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	1	B85
typical_cds_rare	Chr8	8737674	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	4	B1,B36,C65,D6
typical_cds_rare	Chr8	8737966	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	2	A19,B1
typical_cds_rare	Chr8	8738110	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	4	B13,B41,C82,C85
typical_cds_rare	Chr8	8738377	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	3	B45,C32,C68
typical_cds_rare	Chr8	8738591	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	1	C32
lof_cds	Chr8	8738634	AAG	A	INDEL	2bp_deletion	frameshift_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	1	B101
typical_cds_rare	Chr8	8738634	AAG	A	INDEL	2bp_deletion	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	1	B101
typical_cds_rare	Chr8	8738716	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	4	B38,B39,C65,C72
lof_cds	Chr8	8738941	CTG	C	INDEL	2bp_deletion	frameshift_variant	LOC131000705	SmilChr08G001123	131000705	rna-XM_057926740.1	59	A15,A18,A3,A4,A5,A6,A9,B10,B111,B117,B125,B127,B129,B132,B134,B135,B138,B14,B140,B15,B18,B19,B22,B28,B35,B42,B43,B5,B52,B60,B61,B7,B70,B72,B78,B87,B88,B91,B97,B99,C10,C13,C22,C24,C28,C4,C55,C57,C59,C6,C62,C70,C71,C72,C76,C77,C9,D5,D6