List of variants in gene combination DCLRE1C, SUV39H2

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001193424.2(SUV39H2):c.850-483T>G	rs7896464	0.41115
NM_001193424.2(SUV39H2):c.850-305C>T	rs60006238	0.08419
NM_001193424.2(SUV39H2):c.850-6G>C	rs112796645	0.00773
NM_001350965.2(DCLRE1C):c.*44C>G	rs76797003	0.00298
NM_001350965.2(DCLRE1C):c.1812C>T (p.Cys604=)	rs904972641	0.00029
NM_001193424.2(SUV39H2):c.781C>T (p.Arg261Cys)	rs375736366	0.00010
NM_001193424.2(SUV39H2):c.850-295C>G	rs978587789	0.00004
NM_001193424.2(SUV39H2):c.899A>G (p.Lys300Arg)	rs1212027801	0.00001
GRCh37/hg19 10p13(chr10:14945105-14954010)x3
NC_000010.11:g.(?_14903611)_(14955432_?)dup
NM_001193424.2(SUV39H2):c.1022A>T (p.Asn341Ile)
NM_001193424.2(SUV39H2):c.1139T>C (p.Ile380Thr)
NM_001193424.2(SUV39H2):c.1159C>G (p.His387Asp)	rs2491559996
NM_001193424.2(SUV39H2):c.719C>G (p.Pro240Arg)
NM_001193424.2(SUV39H2):c.850-352G>A	rs148343292

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