List of variants in gene EHMT1 reported by GeneReviews

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_024757.5(EHMT1):c.1413_1425del (p.Pro473fs)	rs137852715
NM_024757.5(EHMT1):c.1533_1536del (p.Asp512fs)	rs137852716
NM_024757.5(EHMT1):c.1810C>T (p.Gln604Ter)	rs137852717
NM_024757.5(EHMT1):c.1858C>T (p.Arg620Ter)	rs137852718
NM_024757.5(EHMT1):c.2028dup (p.Pro677fs)	rs1554879411
NM_024757.5(EHMT1):c.2193-1G>C	rs137852720
NM_024757.5(EHMT1):c.2863_2864del (p.Val955fs)	rs137852721
NM_024757.5(EHMT1):c.2868-1G>A	rs137852722
NM_024757.5(EHMT1):c.2877_2880del (p.Ser960fs)	rs786205129
NM_024757.5(EHMT1):c.3180+1G>T	rs137852724
NM_024757.5(EHMT1):c.3181-80_3233del	rs1554896943
NM_024757.5(EHMT1):c.3218G>A (p.Cys1073Tyr)	rs137852726
NM_024757.5(EHMT1):c.3229C>T (p.Gln1077Ter)	rs137852725
NM_024757.5(EHMT1):c.3502C>T (p.Arg1168Ter)	rs121918301
NM_024757.5(EHMT1):c.3589C>T (p.Arg1197Trp)	rs137852727
NM_024757.5(EHMT1):c.871C>T (p.Arg291Ter)	rs137852714

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