ClinVar Miner

List of variants in gene NEXN reported as likely benign for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 115
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HGVS dbSNP gnomAD frequency
NM_144573.4(NEXN):c.1659+18C>G rs147422621 0.00228
NM_144573.4(NEXN):c.1785C>T (p.Asp595=) rs182998780 0.00041
NM_144573.4(NEXN):c.1788T>G (p.Ser596Arg) rs199738750 0.00029
NM_144573.4(NEXN):c.1029G>A (p.Ala343=) rs374260457 0.00023
NM_144573.4(NEXN):c.1252-11T>G rs781115798 0.00017
NM_144573.4(NEXN):c.865-17A>G rs201771600 0.00016
NM_144573.4(NEXN):c.893C>G (p.Thr298Arg) rs200753280 0.00016
NM_144573.4(NEXN):c.1806G>A (p.Thr602=) rs373102543 0.00014
NM_144573.4(NEXN):c.1582G>C (p.Glu528Gln) rs200071700 0.00011
NM_144573.4(NEXN):c.688-10G>A rs370574269 0.00011
NM_144573.4(NEXN):c.856C>T (p.Arg286Trp) rs199917913 0.00009
NM_144573.4(NEXN):c.949A>C (p.Met317Leu) rs559464457 0.00009
NM_144573.4(NEXN):c.1488T>C (p.Asp496=) rs754485056 0.00008
NM_144573.4(NEXN):c.865-9T>C rs182083204 0.00007
NM_144573.4(NEXN):c.1422G>A (p.Arg474=) rs775204901 0.00006
NM_144573.4(NEXN):c.222T>C (p.Ile74=) rs767610015 0.00005
NM_144573.4(NEXN):c.865-5G>A rs727505353 0.00005
NM_144573.4(NEXN):c.1252-20C>A rs776869661 0.00004
NM_144573.4(NEXN):c.1450C>A (p.Arg484=) rs767792289 0.00004
NM_144573.4(NEXN):c.249G>A (p.Glu83=) rs372532824 0.00004
NM_144573.4(NEXN):c.739T>C (p.Leu247=) rs781118443 0.00004
NM_144573.4(NEXN):c.1662A>G (p.Lys554=) rs752270974 0.00003
NM_144573.4(NEXN):c.216G>A (p.Gln72=) rs531315786 0.00003
NM_144573.4(NEXN):c.468G>A (p.Thr156=) rs199988442 0.00003
NM_144573.4(NEXN):c.1368A>C (p.Gly456=) rs397517845 0.00002
NM_144573.4(NEXN):c.1651C>T (p.Leu551=) rs1346328853 0.00002
NM_144573.4(NEXN):c.507A>G (p.Leu169=) rs776106290 0.00002
NM_144573.4(NEXN):c.1083T>C (p.Tyr361=) rs1060504549 0.00001
NM_144573.4(NEXN):c.1251+10T>C rs1397556067 0.00001
NM_144573.4(NEXN):c.1266T>C (p.Asn422=) rs1200707526 0.00001
NM_144573.4(NEXN):c.1332A>G (p.Gln444=) rs1385609119 0.00001
NM_144573.4(NEXN):c.1401A>T (p.Ile467=) rs1571157558 0.00001
NM_144573.4(NEXN):c.1413A>G (p.Arg471=) rs780858511 0.00001
NM_144573.4(NEXN):c.1419A>G (p.Arg473=) rs140900323 0.00001
NM_144573.4(NEXN):c.1474-10T>C rs374541562 0.00001
NM_144573.4(NEXN):c.1605A>G (p.Gln535=) rs778477679 0.00001
NM_144573.4(NEXN):c.1653A>G (p.Leu551=) rs794727078 0.00001
NM_144573.4(NEXN):c.1683A>G (p.Glu561=) rs1403473507 0.00001
NM_144573.4(NEXN):c.1704C>T (p.Gly568=) rs397517850 0.00001
NM_144573.4(NEXN):c.1731C>G (p.Thr577=) rs371743669 0.00001
NM_144573.4(NEXN):c.1743T>G (p.Ala581=) rs772313224 0.00001
NM_144573.4(NEXN):c.1899G>A (p.Arg633=) rs374467054 0.00001
NM_144573.4(NEXN):c.1995T>C (p.Ser665=) rs757311272 0.00001
NM_144573.4(NEXN):c.207G>A (p.Arg69=) rs1414407444 0.00001
NM_144573.4(NEXN):c.237T>C (p.Ala79=) rs727504549 0.00001
NM_144573.4(NEXN):c.448-10C>T rs773027207 0.00001
NM_144573.4(NEXN):c.456C>T (p.Asp152=) rs760312569 0.00001
NM_144573.4(NEXN):c.579A>G (p.Glu193=) rs1476054611 0.00001
NM_144573.4(NEXN):c.669G>A (p.Lys223=) rs767747207 0.00001
NM_144573.4(NEXN):c.66T>C (p.Tyr22=) rs749182975 0.00001
NM_144573.4(NEXN):c.711A>C (p.Ala237=) rs754009978 0.00001
NM_144573.4(NEXN):c.987A>C (p.Ala329=) rs1270187994 0.00001
NM_144573.4(NEXN):c.*418dup rs368295679
NM_144573.4(NEXN):c.1089A>C (p.Thr363=) rs878855209
NM_144573.4(NEXN):c.1137A>G (p.Glu379=) rs1553240026
NM_144573.4(NEXN):c.1140A>G (p.Glu380=)
NM_144573.4(NEXN):c.1144T>C (p.Leu382=)
NM_144573.4(NEXN):c.1179A>C (p.Thr393=) rs1650467406
NM_144573.4(NEXN):c.1182G>A (p.Glu394=)
NM_144573.4(NEXN):c.1200G>A (p.Lys400=)
NM_144573.4(NEXN):c.1231C>T (p.Leu411=)
NM_144573.4(NEXN):c.1252-12T>A rs1400355724
NM_144573.4(NEXN):c.1252-14_1252-11del rs935328552
NM_144573.4(NEXN):c.1252-19_1252-18del
NM_144573.4(NEXN):c.1252-6T>C rs1571156994
NM_144573.4(NEXN):c.1257G>A (p.Glu419=) rs1557990801
NM_144573.4(NEXN):c.133A>C (p.Arg45=) rs2102092028
NM_144573.4(NEXN):c.1368A>G (p.Gly456=) rs397517845
NM_144573.4(NEXN):c.1372T>C (p.Leu458=) rs1356476468
NM_144573.4(NEXN):c.1377T>A (p.Ser459=) rs2102155734
NM_144573.4(NEXN):c.1383A>G (p.Lys461=)
NM_144573.4(NEXN):c.1411C>A (p.Arg471=)
NM_144573.4(NEXN):c.1437T>G (p.Leu479=) rs2102156211
NM_144573.4(NEXN):c.1473+15del
NM_144573.4(NEXN):c.1473+7dup
NM_144573.4(NEXN):c.1474-18T>C
NM_144573.4(NEXN):c.1509C>T (p.Ser503=)
NM_144573.4(NEXN):c.1527C>T (p.His509=)
NM_144573.4(NEXN):c.1533G>T (p.Val511=) rs765353395
NM_144573.4(NEXN):c.15C>T (p.Ser5=)
NM_144573.4(NEXN):c.1638A>G (p.Glu546=)
NM_144573.4(NEXN):c.1659+8G>A
NM_144573.4(NEXN):c.1659+9C>T
NM_144573.4(NEXN):c.1660-11_1660-7del rs727503344
NM_144573.4(NEXN):c.1660-16A>C
NM_144573.4(NEXN):c.1671GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.4(NEXN):c.1674G>A (p.Glu558=) rs937473668
NM_144573.4(NEXN):c.1752C>T (p.Phe584=)
NM_144573.4(NEXN):c.1779T>G (p.Val593=)
NM_144573.4(NEXN):c.1794A>G (p.Pro598=) rs1651468941
NM_144573.4(NEXN):c.1839T>C (p.Ile613=)
NM_144573.4(NEXN):c.1921T>C (p.Leu641=) rs1321925816
NM_144573.4(NEXN):c.1950A>G (p.Gly650=) rs2102182136
NM_144573.4(NEXN):c.195A>G (p.Arg65=) rs2102092422
NM_144573.4(NEXN):c.220-13_220-10del rs751831143
NM_144573.4(NEXN):c.220-17T>C
NM_144573.4(NEXN):c.220-19_220-16del rs780428399
NM_144573.4(NEXN):c.27+7C>T rs2102087424
NM_144573.4(NEXN):c.28-12C>A
NM_144573.4(NEXN):c.490-14A>G
NM_144573.4(NEXN):c.490-15T>A
NM_144573.4(NEXN):c.490-21_490-18del rs775189174
NM_144573.4(NEXN):c.492A>G (p.Glu164=) rs1571134764
NM_144573.4(NEXN):c.522A>C (p.Val174=)
NM_144573.4(NEXN):c.591A>G (p.Glu197=) rs2102123700
NM_144573.4(NEXN):c.612C>T (p.Tyr204=)
NM_144573.4(NEXN):c.651A>G (p.Pro217=)
NM_144573.4(NEXN):c.666A>G (p.Ala222=)
NM_144573.4(NEXN):c.732C>T (p.Pro244=) rs201171783
NM_144573.4(NEXN):c.789G>A (p.Lys263=)
NM_144573.4(NEXN):c.826G>A (p.Glu276Lys) rs1649891198
NM_144573.4(NEXN):c.855G>A (p.Arg285=) rs753748512
NM_144573.4(NEXN):c.864+11A>G
NM_144573.4(NEXN):c.930C>T (p.Leu310=)
NM_144573.4(NEXN):c.972T>C (p.Asp324=)

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