List of variants in gene ENG reported as likely pathogenic by Mayo Clinic Laboratories, Mayo Clinic

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001114753.3(ENG):c.-10C>T	rs756994701	0.00001
NM_001114753.3(ENG):c.1833G>A (p.Trp611Ter)
NM_001114753.3(ENG):c.23T>C (p.Leu8Pro)	rs1564466414
NM_001114753.3(ENG):c.360+5G>A	rs1060501417
NM_001114753.3(ENG):c.67+2del
NM_001114753.3(ENG):c.694_699del (p.Arg232_Thr233del)	rs2131888057
NM_001114753.3(ENG):c.713T>A (p.Val238Glu)	rs1060501415
NM_001114753.3(ENG):c.885_886del (p.Pro296fs)	rs2539073079
NM_001114753.3(ENG):c.899T>C (p.Leu300Pro)	rs1335718486

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