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	29236280	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131026357	SmilChr05G002604	131026357	rna-XM_057956223.1	1	C15
typical_cds_rare	Chr5	29236320	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131026357	SmilChr05G002604	131026357	rna-XM_057956223.1	1	C20
typical_cds_rare	Chr5	29236727	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131026357	SmilChr05G002604	131026357	rna-XM_057956223.1	2	A15,D1
typical_cds_rare	Chr5	29236766	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131026357	SmilChr05G002604	131026357	rna-XM_057956223.1	4	B130,B136,B140,C33
typical_cds_rare	Chr5	29237817	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131026357	SmilChr05G002604	131026357	rna-XM_057956223.1	1	D11
typical_cds_rare	Chr5	29237873	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131026357	SmilChr05G002604	131026357	rna-XM_057956223.1	2	C76,C9
typical_cds_rare	Chr5	29237897	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131026357	SmilChr05G002604	131026357	rna-XM_057956223.1	1	B112
lof_cds	Chr5	29238751	TCG	T	INDEL	2bp_deletion	frameshift_variant	LOC131026357	SmilChr05G002604	131026357	rna-XM_057956223.1	1	C27
typical_cds_rare	Chr5	29238751	TCG	T	INDEL	2bp_deletion	CDS_variant	LOC131026357	SmilChr05G002604	131026357	rna-XM_057956223.1	1	C27
typical_cds_rare	Chr5	29238865	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131026357	SmilChr05G002604	131026357	rna-XM_057956223.1	4	B49,C22,C47,C6
typical_cds_rare	Chr5	29238921	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131026357	SmilChr05G002604	131026357	rna-XM_057956223.1	1	C65