source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
typical_cds_rare	Chr4	11275108	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022709	SmilChr04G000884	131022709	rna-XM_057952224.1	2	C39,C75
lof_cds	Chr4	11276316	TG	T	INDEL	1bp_deletion	frameshift_variant	LOC131022709	SmilChr04G000884	131022709	rna-XM_057952224.1	1	B130
typical_cds_rare	Chr4	11276316	TG	T	INDEL	1bp_deletion	CDS_variant	LOC131022709	SmilChr04G000884	131022709	rna-XM_057952224.1	1	B130
typical_cds_rare	Chr4	11276364	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131022709	SmilChr04G000884	131022709	rna-XM_057952224.1	2	B124,B79
typical_cds_rare	Chr4	11276402	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022709	SmilChr04G000884	131022709	rna-XM_057952224.1	3	B25,B64,C84
typical_cds_rare	Chr4	11276626	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC131022709	SmilChr04G000884	131022709	rna-XM_057952224.1	2	C8,D4
typical_cds_rare	Chr4	11276843	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022709	SmilChr04G000884	131022709	rna-XM_057952224.1	1	B122
lof_cds	Chr4	11277677	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC131022709	SmilChr04G000884	131022709	rna-XM_057952224.1	2	B120,B62
typical_cds_rare	Chr4	11277677	TC	T	INDEL	1bp_deletion	CDS_variant	LOC131022709	SmilChr04G000884	131022709	rna-XM_057952224.1	2	B120,B62
typical_cds_rare	Chr4	11277695	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC131022709	SmilChr04G000884	131022709	rna-XM_057952224.1	2	B124,B79