List of variants in gene ENG reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001114753.3(ENG):c.572G>A (p.Gly191Asp)	rs41322046	0.01000
NM_001114753.3(ENG):c.1844C>T (p.Ser615Leu)	rs148002300	0.00134
NM_001114753.3(ENG):c.392C>T (p.Pro131Leu)	rs139398993	0.00077
NM_001114753.3(ENG):c.219+23G>A	rs200726108	0.00037
NM_001114753.3(ENG):c.-70C>T	rs562538400	0.00020
NM_001114753.3(ENG):c.596G>A (p.Arg199His)	rs548424658	0.00004
NM_001114753.3(ENG):c.*431T>G	rs549011956	0.00001
NM_001114753.3(ENG):c.909C>T (p.Ala303=)	rs200306464

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