source	chrom	pos	ref	alt	variant_type	ems_class	effect	gene_id	standard_gene_id	ncbi_geneid	transcripts	carrier_n	carriers
lof_cds	Chr6	15498627	T	TAA	INDEL	2bp_insertion	frameshift_variant	LOC130990560	SmilChr06G001464	130990560	rna-XM_057914783.1	10	A19,B24,B40,B47,B59,C40,C46,C48,C8,D2
lof_cds	Chr6	15498628	CAG	C	INDEL	2bp_deletion	frameshift_variant	LOC130990560	SmilChr06G001464	130990560	rna-XM_057914783.1	119	A13,A15,A16,A18,A21,A4,A5,A8,A9,B1,B103,B106,B107,B108,B110,B111,B112,B114,B117,B118,B119,B12,B120,B121,B122,B123,B124,B125,B127,B128,B129,B13,B130,B133,B137,B139,B14,B18,B19,B21,B22,B23,B28,B30,B31,B33,B34,B35,B38,B39,B45,B48,B49,B5,B50,B52,B53,B54,B55,B6,B60,B62,B63,B64,B68,B7,B75,B77,B79,B80,B82,B83,B85,B87,B9,B97,B98,C1,C11,C12,C13,C14,C15,C17,C20,C21,C23,C25,C27,C28,C30,C38,C39,C43,C49,C5,C50,C52,C54,C56,C58,C6,C62,C64,C65,C66,C67,C69,C76,C77,C78,C82,C84,D10,D11,D3,D4,D5,D8
lof_cds	Chr6	15498629	A	AGT	INDEL	2bp_insertion	frameshift_variant	LOC130990560	SmilChr06G001464	130990560	rna-XM_057914783.1	67	A13,A16,A4,A5,B1,B107,B108,B110,B112,B114,B119,B12,B125,B13,B139,B14,B19,B22,B30,B34,B38,B39,B45,B48,B50,B52,B53,B60,B62,B63,B64,B68,B7,B75,B77,B79,B82,B83,B88,B97,C1,C11,C12,C13,C15,C17,C20,C21,C23,C25,C28,C30,C39,C43,C49,C5,C50,C52,C56,C6,C69,C77,C82,D11,D3,D4,D5
lof_cds	Chr6	15498650	GT	G	INDEL	1bp_deletion	frameshift_variant	LOC130990560	SmilChr06G001464	130990560	rna-XM_057914783.1	3	B103,B117,C45
typical_cds_rare	Chr6	15498650	GT	G	INDEL	1bp_deletion	CDS_variant	LOC130990560	SmilChr06G001464	130990560	rna-XM_057914783.1	3	B103,B117,C45
typical_cds_rare	Chr6	15498660	C	T	SNV	EMS_canonical_SNV	CDS_variant	LOC130990560	SmilChr06G001464	130990560	rna-XM_057914783.1	3	B26,B30,B72
typical_cds_rare	Chr6	15498697	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990560	SmilChr06G001464	130990560	rna-XM_057914783.1	1	B100
typical_cds_rare	Chr6	15498783	G	A	SNV	EMS_canonical_SNV	CDS_variant	LOC130990560	SmilChr06G001464	130990560	rna-XM_057914783.1	2	B44,C79
lof_cds	Chr6	15498863	G	GT	INDEL	1bp_insertion	frameshift_variant	LOC130990560	SmilChr06G001464	130990560	rna-XM_057914783.1	2	B14,C75
typical_cds_rare	Chr6	15498863	G	GT	INDEL	1bp_insertion	CDS_variant	LOC130990560	SmilChr06G001464	130990560	rna-XM_057914783.1	2	B14,C75