List of variants in gene ENG reported as benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_001114753.3(ENG):c.207G>A (p.Leu69=)	rs11545664	0.14184
NM_001114753.3(ENG):c.1029C>T (p.Thr343=)	rs3739817	0.06792
NM_001114753.3(ENG):c.219+25G>T	rs7847860	0.06245
NM_001114753.3(ENG):c.14C>T (p.Thr5Met)	rs35400405	0.04608
NM_001114753.3(ENG):c.1060C>T (p.Leu354=)	rs36092484	0.03618
NM_001114753.3(ENG):c.991+58A>T	rs12002508	0.01910
NM_001114753.3(ENG):c.360+21C>T	rs41355248	0.01861
NM_001114753.3(ENG):c.1794T>C (p.Gly598=)	rs41358947	0.01435
NM_001114753.3(ENG):c.524-30G>A	rs41409546	0.01314
NM_001114753.3(ENG):c.572G>A (p.Gly191Asp)	rs41322046	0.01000
NM_001114753.3(ENG):c.1932C>T (p.Ile644=)	rs181330955	0.00609
NM_001114753.3(ENG):c.120C>T (p.Gly40=)	rs41522944	0.00355
NM_001114753.3(ENG):c.1096G>C (p.Asp366His)	rs1800956	0.00353
NM_001114753.3(ENG):c.732C>T (p.Pro244=)	rs112262663	0.00124
NM_001114753.3(ENG):c.524-15C>T	rs201463582	0.00114
NM_001114753.3(ENG):c.392C>T (p.Pro131Leu)	rs139398993	0.00077
NM_001114753.3(ENG):c.991+21_991+26dup	rs148063362

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