ClinVar Miner

List of variants in gene NEXN studied for Cardiovascular phenotype

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Total variants: 48
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HGVS dbSNP
NM_144573.3(NEXN):c.1029G>A (p.Ala343=) rs374260457
NM_144573.3(NEXN):c.1332A>G (p.Gln444=) rs1385609119
NM_144573.3(NEXN):c.1400T>C (p.Ile467Thr) rs370195451
NM_144573.3(NEXN):c.1401_1403AGA[2] (p.Glu470del) rs397517846
NM_144573.3(NEXN):c.1408G>C (p.Glu470Gln) rs35366555
NM_144573.3(NEXN):c.1416_1418AAG[1] (p.Arg475del) rs794729091
NM_144573.3(NEXN):c.141A>G (p.Gln47=) rs1459232585
NM_144573.3(NEXN):c.1432G>A (p.Asp478Asn) rs1309129145
NM_144573.3(NEXN):c.1435C>T (p.Leu479Phe) rs181520023
NM_144573.3(NEXN):c.1477G>A (p.Asp493Asn) rs1553241790
NM_144573.3(NEXN):c.1481A>T (p.Asp494Val) rs750183004
NM_144573.3(NEXN):c.1488T>C (p.Asp496=) rs754485056
NM_144573.3(NEXN):c.156C>T (p.Asp52=) rs371431782
NM_144573.3(NEXN):c.157G>A (p.Glu53Lys) rs373778361
NM_144573.3(NEXN):c.1618A>G (p.Met540Val) rs201390657
NM_144573.3(NEXN):c.1640T>C (p.Ile547Thr) rs753636624
NM_144573.3(NEXN):c.1671_1673GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.3(NEXN):c.1671_1673GGA[5] (p.Glu562dup) rs397517848
NM_144573.3(NEXN):c.1672G>A (p.Glu558Lys) rs927477236
NM_144573.3(NEXN):c.1704C>G (p.Gly568=) rs397517850
NM_144573.3(NEXN):c.1771A>G (p.Thr591Ala) rs369019618
NM_144573.3(NEXN):c.1785C>T (p.Asp595=) rs182998780
NM_144573.3(NEXN):c.1918_1922del (p.Tyr640fs) rs1222794437
NM_144573.3(NEXN):c.1946_1948GAG[1] (p.Gly650del) rs397517853
NM_144573.3(NEXN):c.1950_1951AG[1] (p.Glu651fs) rs1553242326
NM_144573.3(NEXN):c.1955A>G (p.Tyr652Cys) rs137853197
NM_144573.3(NEXN):c.1A>C (p.Met1Leu) rs749167943
NM_144573.3(NEXN):c.2012T>C (p.Ile671Thr) rs747781785
NM_144573.3(NEXN):c.237T>C (p.Ala79=) rs727504549
NM_144573.3(NEXN):c.363G>A (p.Thr121=) rs35117963
NM_144573.3(NEXN):c.374G>A (p.Arg125Gln) rs747265816
NM_144573.3(NEXN):c.392A>C (p.Gln131Pro) rs397517858
NM_144573.3(NEXN):c.512T>C (p.Ile171Thr) rs372065024
NM_144573.3(NEXN):c.616G>A (p.Glu206Lys) rs370428679
NM_144573.3(NEXN):c.620A>G (p.Asp207Gly) rs570946423
NM_144573.3(NEXN):c.626G>T (p.Arg209Ile) rs1433269866
NM_144573.3(NEXN):c.634T>A (p.Tyr212Asn) rs769549962
NM_144573.3(NEXN):c.732C>A (p.Pro244=) rs201171783
NM_144573.3(NEXN):c.733G>A (p.Gly245Arg) rs1166698
NM_144573.3(NEXN):c.739T>C (p.Leu247=) rs781118443
NM_144573.3(NEXN):c.777A>G (p.Gln259=) rs375544798
NM_144573.3(NEXN):c.784C>T (p.Arg262Ter) rs1002648603
NM_144573.3(NEXN):c.78T>C (p.Leu26=) rs376535223
NM_144573.3(NEXN):c.7_9del (p.Asp3del) rs760463744
NM_144573.3(NEXN):c.817C>T (p.Arg273Cys) rs757571525
NM_144573.3(NEXN):c.856C>T (p.Arg286Trp) rs199917913
NM_144573.3(NEXN):c.893C>G (p.Thr298Arg) rs200753280
NM_144573.3(NEXN):c.995A>C (p.Glu332Ala) rs201763096

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