List of variants in gene EVC reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 37

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HGVS	dbSNP	gnomAD frequency
NM_153717.3(EVC):c.2505G>A (p.Ser835=)	rs115976359	0.00969
NM_153717.3(EVC):c.284A>G (p.Asp95Gly)	rs41269547	0.00561
NM_153717.3(EVC):c.1855G>A (p.Val619Ile)	rs111293777	0.00354
NM_153717.3(EVC):c.1127C>T (p.Ala376Val)	rs142535134	0.00309
NM_153717.3(EVC):c.1636A>G (p.Met546Val)	rs112608085	0.00209
NM_153717.3(EVC):c.1826G>A (p.Arg609Gln)	rs41269557	0.00201
NM_153717.3(EVC):c.550G>A (p.Asp184Asn)	rs41269549	0.00194
NM_153717.3(EVC):c.93C>G (p.Ala31=)	rs866226288	0.00194
NM_153717.3(EVC):c.1369G>A (p.Glu457Lys)	rs141859946	0.00188
NM_153717.3(EVC):c.934G>A (p.Asp312Asn)	rs115275195	0.00171
NM_153717.3(EVC):c.1500G>A (p.Met500Ile)	rs149898884	0.00163
NM_153717.3(EVC):c.1333A>C (p.Lys445Gln)	rs116952023	0.00150
NM_153717.3(EVC):c.1040C>T (p.Thr347Met)	rs34947207	0.00127
NM_153717.3(EVC):c.89C>T (p.Pro30Leu)	rs886044558	0.00121
NM_153717.3(EVC):c.1770C>T (p.Asp590=)	rs141755737	0.00079
NM_153717.3(EVC):c.1995G>A (p.Ser665=)	rs142897994	0.00038
NM_153717.3(EVC):c.2276G>A (p.Ser759Asn)	rs201776972	0.00025
NM_153717.3(EVC):c.442T>C (p.Leu148=)	rs139931919	0.00022
NM_153717.3(EVC):c.2098-10T>C	rs774109576	0.00014
NM_153717.3(EVC):c.2241G>A (p.Ala747=)	rs142094016	0.00014
NM_153717.3(EVC):c.175-10C>T	rs113406354	0.00013
NM_153717.3(EVC):c.1707G>C (p.Leu569=)	rs575586341	0.00011
NM_153717.3(EVC):c.2298C>T (p.Asp766=)	rs140546984	0.00011
NM_153717.3(EVC):c.107C>G (p.Ala36Gly)	rs1219807707	0.00005
NM_153717.3(EVC):c.717T>A (p.Ile239=)	rs372312182	0.00004
NM_153717.3(EVC):c.1313G>A (p.Arg438Gln)	rs373718642	0.00002
NM_153717.3(EVC):c.1872C>T (p.Gly624=)	rs374432399	0.00002
NM_153717.3(EVC):c.2376G>A (p.Ala792=)	rs1005244629	0.00001
NM_153717.3(EVC):c.876G>A (p.Glu292=)	rs902304992	0.00001
NM_153717.3(EVC):c.*3T>G	rs368249789
NM_153717.3(EVC):c.1018C>A (p.Arg340=)	rs121908425
NM_153717.3(EVC):c.1219C>T (p.Leu407=)
NM_153717.3(EVC):c.1464+20T>C	rs886038740
NM_153717.3(EVC):c.1528G>A (p.Val510Ile)	rs143971158
NM_153717.3(EVC):c.1776+4C>T
NM_153717.3(EVC):c.1940G>A (p.Arg647Gln)	rs35401386
NM_153717.3(EVC):c.2449+15del	rs398092136

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