List of variants in gene EVC reported as uncertain significance by Natera, Inc.

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: 60

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HGVS	dbSNP	gnomAD frequency
NM_153717.3(EVC):c.1826G>A (p.Arg609Gln)	rs41269557	0.00201
NM_153717.3(EVC):c.934G>A (p.Asp312Asn)	rs115275195	0.00171
NM_153717.3(EVC):c.89C>T (p.Pro30Leu)	rs886044558	0.00121
NM_153717.3(EVC):c.2707A>G (p.Ile903Val)	rs143678893	0.00093
NM_153717.3(EVC):c.1540G>A (p.Glu514Lys)	rs141896077	0.00042
NM_153717.3(EVC):c.1892C>T (p.Thr631Met)	rs139481521	0.00041
NM_153717.3(EVC):c.2805G>A (p.Arg935=)	rs143631233	0.00037
NM_153717.3(EVC):c.1321G>A (p.Val441Ile)	rs202150959	0.00036
NM_153717.3(EVC):c.1777G>A (p.Val593Met)	rs150535483	0.00014
NM_153717.3(EVC):c.2098-10T>C	rs774109576	0.00014
NM_153717.3(EVC):c.175-10C>T	rs113406354	0.00013
NM_153717.3(EVC):c.2449+4C>T	rs753679138	0.00013
NM_153717.3(EVC):c.1707G>C (p.Leu569=)	rs575586341	0.00011
NM_153717.3(EVC):c.2341G>A (p.Val781Met)	rs370514515	0.00011
NM_153717.3(EVC):c.1744C>G (p.Leu582Val)	rs367863826	0.00009
NM_153717.3(EVC):c.2041G>A (p.Glu681Lys)	rs201877358	0.00007
NM_153717.3(EVC):c.1242C>T (p.Ser414=)	rs769206763	0.00006
NM_153717.3(EVC):c.2550G>A (p.Ala850=)	rs754053651	0.00006
NM_153717.3(EVC):c.940-150T>C	rs576076928	0.00006
NM_153717.3(EVC):c.107C>G (p.Ala36Gly)	rs1219807707	0.00005
NM_153717.3(EVC):c.312G>A (p.Pro104=)	rs763930196	0.00005
NM_153717.3(EVC):c.1269G>A (p.Thr423=)	rs551881521	0.00004
NM_153717.3(EVC):c.580C>T (p.Arg194Trp)	rs757990300	0.00004
NM_153717.3(EVC):c.1482G>A (p.Leu494=)	rs371300088	0.00003
NM_153717.3(EVC):c.1652C>T (p.Pro551Leu)	rs371682994	0.00003
NM_153717.3(EVC):c.625G>A (p.Val209Ile)	rs202026284	0.00003
NM_153717.3(EVC):c.920C>G (p.Ser307Cys)	rs372548610	0.00003
NM_153717.3(EVC):c.1448C>T (p.Pro483Leu)	rs376440801	0.00002
NM_153717.3(EVC):c.2770C>T (p.Arg924Cys)	rs772327981	0.00002
NM_153717.3(EVC):c.1693G>A (p.Ala565Thr)	rs926749491	0.00001
NM_153717.3(EVC):c.1717A>G (p.Asn573Asp)	rs1373148885	0.00001
NM_153717.3(EVC):c.2114A>G (p.Glu705Gly)	rs765248751	0.00001
NM_153717.3(EVC):c.2624A>T (p.His875Leu)	rs200403160	0.00001
NM_153717.3(EVC):c.2732G>A (p.Arg911Gln)	rs930402783	0.00001
NM_153717.3(EVC):c.339C>T (p.Phe113=)	rs750461424	0.00001
NM_153717.3(EVC):c.568C>T (p.Arg190Cys)	rs1286815295	0.00001
NM_153717.3(EVC):c.1041G>A (p.Thr347=)	rs148418233
NM_153717.3(EVC):c.104G>A (p.Gly35Asp)	rs1560259105
NM_153717.3(EVC):c.1109A>T (p.Glu370Val)	rs778032532
NM_153717.3(EVC):c.1135G>T (p.Ala379Ser)	rs760174792
NM_153717.3(EVC):c.1493G>T (p.Arg498Met)	rs1577453796
NM_153717.3(EVC):c.1564-3C>T	rs747435572
NM_153717.3(EVC):c.1603G>A (p.Val535Met)	rs753720935
NM_153717.3(EVC):c.1776+7del	rs540001390
NM_153717.3(EVC):c.1777-9C>T	rs113468936
NM_153717.3(EVC):c.1850G>T (p.Arg617Leu)	rs771110251
NM_153717.3(EVC):c.2104C>G (p.Arg702Gly)	rs545087909
NM_153717.3(EVC):c.2322G>A (p.Ala774=)	rs150373930
NM_153717.3(EVC):c.2335G>A (p.Val779Ile)	rs376396220
NM_153717.3(EVC):c.2339A>C (p.Tyr780Ser)	rs773252806
NM_153717.3(EVC):c.2395A>G (p.Arg799Gly)	rs1715095634
NM_153717.3(EVC):c.2653G>A (p.Asp885Asn)	rs1241844907
NM_153717.3(EVC):c.2782G>C (p.Glu928Gln)	rs1489027267
NM_153717.3(EVC):c.2879C>G (p.Thr960Ser)	rs780548102
NM_153717.3(EVC):c.2925A>C (p.Glu975Asp)	rs1399872123
NM_153717.3(EVC):c.2932G>T (p.Asp978Tyr)	rs150173231
NM_153717.3(EVC):c.46C>T (p.Leu16=)	rs1722990488
NM_153717.3(EVC):c.589G>T (p.Ala197Ser)	rs115507440
NM_153717.3(EVC):c.58G>C (p.Ala20Pro)	rs1359522467
NM_153717.3(EVC):c.696G>C (p.Lys232Asn)	rs371664035

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