List of variants in gene EVC reported by Department of Pathology and Laboratory Medicine, Sinai Health System

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_153717.3(EVC):c.469C>G (p.Pro157Ala)	rs146729456	0.00451
NM_153717.3(EVC):c.934G>A (p.Asp312Asn)	rs115275195	0.00176
NM_153717.3(EVC):c.1321G>A (p.Val441Ile)	rs202150959	0.00036
NM_153717.3(EVC):c.1744C>G (p.Leu582Val)	rs367863826	0.00009
NM_153717.3(EVC):c.884C>G (p.Thr295Ser)	rs754532508	0.00003
NM_153717.3(EVC):c.2624A>T (p.His875Leu)	rs200403160	0.00001
NM_153717.3(EVC):c.1075G>T (p.Asp359Tyr)
NM_153717.3(EVC):c.1124G>A (p.Arg375Gln)
NM_153717.3(EVC):c.2033G>A (p.Arg678His)
NM_153717.3(EVC):c.2311C>A (p.Leu771Met)
NM_153717.3(EVC):c.2930G>A (p.Gly977Glu)	rs749142395
NM_153717.3(EVC):c.498G>C (p.Gln166His)
NM_153717.3(EVC):c.702G>A (p.Met234Ile)
NM_153717.3(EVC):c.918C>G (p.Tyr306Ter)

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