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	31671664	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130997722	SmilChr08G003132	130997722	rna-XM_057923133.1	5	A10,A11,A13,A3,C65
lof_cds	Chr8	31671669	TG	T	INDEL	1bp_deletion	frameshift_variant	LOC130997722	SmilChr08G003132	130997722	rna-XM_057923133.1	1	C53
typical_cds_rare	Chr8	31671669	TG	T	INDEL	1bp_deletion	CDS_variant	LOC130997722	SmilChr08G003132	130997722	rna-XM_057923133.1	1	C53
typical_cds_rare	Chr8	31671684	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130997722	SmilChr08G003132	130997722	rna-XM_057923133.1	1	B73
typical_cds_rare	Chr8	31671738	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130997722	SmilChr08G003132	130997722	rna-XM_057923133.1	4	A10,A11,A13,A3
typical_cds_rare	Chr8	31671839	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130997722	SmilChr08G003132	130997722	rna-XM_057923133.1	1	B88
typical_cds_rare	Chr8	31672116	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130997722	SmilChr08G003132	130997722	rna-XM_057923133.1	1	C53
lof_cds	Chr8	31672668	GC	G	INDEL	1bp_deletion	frameshift_variant	LOC130997722	SmilChr08G003132	130997722	rna-XM_057923133.1	1	B127
typical_cds_rare	Chr8	31672668	GC	G	INDEL	1bp_deletion	CDS_variant	LOC130997722	SmilChr08G003132	130997722	rna-XM_057923133.1	1	B127
typical_cds_rare	Chr8	31672672	GT	*	INDEL	1bp_deletion	CDS_variant	LOC130997722	SmilChr08G003132	130997722	rna-XM_057923133.1	1	A25
typical_cds_rare	Chr8	31672782	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130997722	SmilChr08G003132	130997722	rna-XM_057923133.1	3	B16,C8,D11