List of variants in gene ENG reported as likely benign for not provided

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: 38

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HGVS	dbSNP	gnomAD frequency
NM_001114753.3(ENG):c.14C>T (p.Thr5Met)	rs35400405	0.04608
NM_001114753.3(ENG):c.68-256A>G	rs41505655	0.01576
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.67+254A>G	rs143016113	0.01181
NM_001114753.3(ENG):c.572G>A (p.Gly191Asp)	rs41322046	0.01000
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.523+235C>T	rs41377844	0.00329
NM_001114753.3(ENG):c.1844C>T (p.Ser615Leu)	rs148002300	0.00134
NM_001114753.3(ENG):c.617G>C (p.Gly206Ala)	rs201393380	0.00080
NM_001114753.3(ENG):c.392C>T (p.Pro131Leu)	rs139398993	0.00077
NM_001114753.3(ENG):c.219+22C>T	rs370257876	0.00073
NM_001114753.3(ENG):c.-9G>A	rs368423516	0.00040
NM_001114753.3(ENG):c.388C>T (p.Pro130Ser)	rs199840979	0.00021
NM_001114753.3(ENG):c.954G>A (p.Pro318=)	rs149590262	0.00019
NM_001114753.3(ENG):c.-188G>A	rs961480381	0.00017
NM_001114753.3(ENG):c.321G>T (p.Leu107=)	rs767907933	0.00015
NM_001114753.3(ENG):c.322C>T (p.His108Tyr)	rs756897517	0.00015
NM_001114753.3(ENG):c.850G>A (p.Glu284Lys)	rs372045549	0.00010
NM_001114753.3(ENG):c.1098C>T (p.Asp366=)	rs201497772	0.00008
NM_001114753.3(ENG):c.1762G>A (p.Val588Ile)	rs201768056	0.00007
NM_001114753.3(ENG):c.1019C>T (p.Pro340Leu)	rs772135786	0.00004
NM_001114753.3(ENG):c.705G>A (p.Thr235=)	rs755116051	0.00004
NM_001114753.3(ENG):c.405C>G (p.Thr135=)	rs773521685	0.00003
NM_001114753.3(ENG):c.1134+16C>T	rs544624587	0.00002
NM_001114753.3(ENG):c.1014C>T (p.Pro338=)	rs1057522787	0.00001
NM_001114753.3(ENG):c.179_180delinsAA (p.Ala60Glu)	rs1060504230
NM_001114753.3(ENG):c.1818C>A (p.Leu606=)	rs1588572499
NM_001114753.3(ENG):c.1853-14GCTCCC[3]	rs373296026
NM_001114753.3(ENG):c.1853-8_1853-3del
NM_001114753.3(ENG):c.195T>C (p.His65=)	rs769288237
NM_001114753.3(ENG):c.219G>A (p.Thr73=)	rs755348996
NM_001114753.3(ENG):c.319C>T (p.Leu107=)
NM_001114753.3(ENG):c.387G>A (p.Glu129=)	rs1588583668
NM_001114753.3(ENG):c.523+10C>T	rs1588583485
NM_001114753.3(ENG):c.525C>T (p.Ala175=)	rs1588583011
NM_001114753.3(ENG):c.909C>T (p.Ala303=)	rs200306464

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