source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr8	4371707	CGT	C	INDEL	2bp_deletion	frameshift_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	52	A10,A22,A23,A24,A25,B11,B112,B114,B122,B129,B130,B139,B38,B41,B47,B55,B58,B65,B73,B74,B75,B76,B77,B79,B82,B91,B93,C11,C13,C17,C18,C27,C3,C30,C32,C37,C38,C39,C41,C44,C5,C61,C62,C64,C66,C75,C8,C83,C86,C87,D1,D3
lof_cds	Chr8	4372225	GCC	G	INDEL	2bp_deletion	frameshift_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	D6
typical_cds_rare	Chr8	4372225	GCC	G	INDEL	2bp_deletion	CDS_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	D6
lof_cds	Chr8	4372758	TC	T	INDEL	1bp_deletion	frameshift_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	32	A16,A20,A25,A7,A8,B10,B112,B17,B23,B28,B3,B49,B75,B77,B79,B82,B94,B99,C1,C16,C17,C34,C37,C39,C43,C56,C66,C69,C78,C86,C87,D4
typical_cds_rare	Chr8	4374078	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	C80
lof_cds	Chr8	4374101	A	AAG	INDEL	2bp_insertion	frameshift_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	C80
typical_cds_rare	Chr8	4374101	A	AAG	INDEL	2bp_insertion	CDS_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	C80
typical_cds_rare	Chr8	4374127	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	C80
typical_cds_rare	Chr8	4374151	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	C80
typical_cds_rare	Chr8	4374158	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	C80
typical_cds_rare	Chr8	4374173	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	C23
typical_cds_rare	Chr8	4374192	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	C80
typical_cds_rare	Chr8	4374206	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	C23
lof_cds	Chr8	4374217	GT	G	INDEL	1bp_deletion	frameshift_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	C23
typical_cds_rare	Chr8	4374217	GT	G	INDEL	1bp_deletion	CDS_variant	LOC130997967	SmilChr08G000588	130997967	rna-XM_057923405.1	1	C23