source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
typical_cds_rare	Chr5	15011172	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	C3
typical_cds_rare	Chr5	15011197	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	B103
typical_cds_rare	Chr5	15011715	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	B54
lof_cds	Chr5	15011719	A	AT	INDEL	1bp_insertion	frameshift_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	B54
typical_cds_rare	Chr5	15011719	A	AT	INDEL	1bp_insertion	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	B54
typical_cds_rare	Chr5	15012441	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	3	A5,B101,B70
typical_cds_rare	Chr5	15013489	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	B45
typical_cds_rare	Chr5	15014305	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	2	B38,B39
typical_cds_rare	Chr5	15014688	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	B24
typical_cds_rare	Chr5	15017657	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	2	B120,B44
typical_cds_rare	Chr5	15017733	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	4	A16,A24,C42,D10
typical_cds_rare	Chr5	15017989	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	4	A24,B118,B74,C23
typical_cds_rare	Chr5	15018281	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	B104
lof_cds	Chr5	15019891	TCA	T	INDEL	2bp_deletion	frameshift_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	B103
typical_cds_rare	Chr5	15019891	TCA	T	INDEL	2bp_deletion	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	B103
typical_cds_rare	Chr5	15019966	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	4	A24,B118,B74,C23
typical_cds_rare	Chr5	15020155	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	B49
typical_cds_rare	Chr5	15020331	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	B49
typical_cds_rare	Chr5	15020774	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130986302	SmilChr05G001622	130986302	rna-XM_057909678.1	1	D10
