ClinVar Miner

List of variants in gene CTNNA3 reported as uncertain significance for arrhythmogenic right ventricular dysplasia 13

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 92
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HGVS dbSNP
NC_000010.10:g.(?_67726350)_(67748575_?)del
NC_000010.10:g.(?_68040208)_(68040399_?)del
NC_000010.10:g.(?_68040208)_(68381562_?)dup
NC_000010.10:g.(?_68138890)_(68139130_?)del
NC_000010.10:g.(?_68138900)_(68139120_?)del
NC_000010.10:g.(?_68280355)_(68280551_?)del
NC_000010.10:g.(?_68280355)_(68280551_?)dup
NC_000010.10:g.(?_68280355)_(68381562_?)del
NC_000010.10:g.(?_68280355)_(68535302_?)dup
NC_000010.10:g.(?_68280365)_(68280541_?)del
NC_000010.10:g.(?_68381430)_(68381562_?)del
NC_000010.10:g.(?_68381430)_(68526194_?)del
NC_000010.10:g.(?_68381440)_(68381552_?)del
NC_000010.10:g.(?_68526002)_(68535302_?)del
NC_000010.10:g.(?_68526012)_(68535292_?)del
NC_000010.10:g.(?_68535182)_(68535302_?)del
NC_000010.10:g.(?_69366605)_(69407286_?)dup
NM_013266.4(CTNNA3):c.100-7A>G
NM_013266.4(CTNNA3):c.1000G>A (p.Ala334Thr)
NM_013266.4(CTNNA3):c.1007G>A (p.Arg336His) rs372482202
NM_013266.4(CTNNA3):c.1064G>A (p.Arg355Lys) rs375610128
NM_013266.4(CTNNA3):c.1073C>A (p.Thr358Asn) rs751471841
NM_013266.4(CTNNA3):c.1120C>T (p.Arg374Cys) rs370981751
NM_013266.4(CTNNA3):c.1128+2T>A rs1564675010
NM_013266.4(CTNNA3):c.1128+7G>T rs200113495
NM_013266.4(CTNNA3):c.1132C>T (p.Arg378Cys) rs187752783
NM_013266.4(CTNNA3):c.1175C>T (p.Thr392Met) rs146777494
NM_013266.4(CTNNA3):c.1183C>A (p.Pro395Thr) rs1554848924
NM_013266.4(CTNNA3):c.1186C>G (p.Leu396Val)
NM_013266.4(CTNNA3):c.1219C>T (p.Arg407Trp)
NM_013266.4(CTNNA3):c.1231A>G (p.Ile411Val) rs372808360
NM_013266.4(CTNNA3):c.1233A>G (p.Ile411Met) rs1554848898
NM_013266.4(CTNNA3):c.1247C>T (p.Ala416Val) rs1032740164
NM_013266.4(CTNNA3):c.1303A>G (p.Met435Val) rs377404952
NM_013266.4(CTNNA3):c.1402G>A (p.Ala468Thr)
NM_013266.4(CTNNA3):c.1451G>A (p.Arg484His)
NM_013266.4(CTNNA3):c.1507A>C (p.Ile503Leu) rs147802834
NM_013266.4(CTNNA3):c.1508T>C (p.Ile503Thr)
NM_013266.4(CTNNA3):c.1532-1G>A rs756034227
NM_013266.4(CTNNA3):c.155C>T (p.Ser52Leu) rs139105272
NM_013266.4(CTNNA3):c.1571C>G (p.Ala524Gly)
NM_013266.4(CTNNA3):c.1604G>A (p.Arg535His) rs139378888
NM_013266.4(CTNNA3):c.1610C>T (p.Ala537Val)
NM_013266.4(CTNNA3):c.1627C>T (p.Arg543Trp) rs372758887
NM_013266.4(CTNNA3):c.1669A>G (p.Ser557Gly) rs768735520
NM_013266.4(CTNNA3):c.1733-1G>C rs193155648
NM_013266.4(CTNNA3):c.1790C>T (p.Ser597Leu) rs780346090
NM_013266.4(CTNNA3):c.1819G>A (p.Val607Met) rs1564836430
NM_013266.4(CTNNA3):c.1823A>T (p.Asp608Val) rs138314889
NM_013266.4(CTNNA3):c.1841A>G (p.Tyr614Cys) rs770893892
NM_013266.4(CTNNA3):c.1865G>A (p.Cys622Tyr) rs367616357
NM_013266.4(CTNNA3):c.1883G>A (p.Arg628Gln) rs754792055
NM_013266.4(CTNNA3):c.1894G>A (p.Glu632Lys) rs1060502222
NM_013266.4(CTNNA3):c.1900G>A (p.Glu634Lys) rs77165728
NM_013266.4(CTNNA3):c.1949G>A (p.Ser650Asn) rs1060502223
NM_013266.4(CTNNA3):c.1979C>T (p.Ala660Val) rs778640435
NM_013266.4(CTNNA3):c.2122A>G (p.Met708Val)
NM_013266.4(CTNNA3):c.213C>G (p.Asp71Glu) rs771791661
NM_013266.4(CTNNA3):c.2211G>C (p.Met737Ile)
NM_013266.4(CTNNA3):c.2265+1G>C
NM_013266.4(CTNNA3):c.2278T>C (p.Ser760Pro)
NM_013266.4(CTNNA3):c.2368C>G (p.Gln790Glu)
NM_013266.4(CTNNA3):c.2501G>A (p.Arg834Gln) rs373081692
NM_013266.4(CTNNA3):c.2501G>T (p.Arg834Leu)
NM_013266.4(CTNNA3):c.2524C>T (p.Arg842Trp) rs199852825
NM_013266.4(CTNNA3):c.2528A>G (p.His843Arg) rs540211204
NM_013266.4(CTNNA3):c.2630A>C (p.Lys877Thr) rs781167292
NM_013266.4(CTNNA3):c.2638dup (p.Ile880fs) rs761152565
NM_013266.4(CTNNA3):c.392C>T (p.Ala131Val) rs774544494
NM_013266.4(CTNNA3):c.398C>T (p.Thr133Met)
NM_013266.4(CTNNA3):c.40C>T (p.Gln14Ter)
NM_013266.4(CTNNA3):c.412C>A (p.Leu138Ile) rs899335202
NM_013266.4(CTNNA3):c.417G>A (p.Ala139=) rs1204895034
NM_013266.4(CTNNA3):c.452T>G (p.Val151Gly) rs756167695
NM_013266.4(CTNNA3):c.457G>C (p.Ala153Pro) rs147116577
NM_013266.4(CTNNA3):c.578A>G (p.Gln193Arg) rs373233387
NM_013266.4(CTNNA3):c.649C>T (p.Leu217Phe) rs374834298
NM_013266.4(CTNNA3):c.654G>T (p.Leu218Phe)
NM_013266.4(CTNNA3):c.670G>C (p.Ala224Pro)
NM_013266.4(CTNNA3):c.674G>T (p.Cys225Phe)
NM_013266.4(CTNNA3):c.843+1G>T rs1256726247
NM_013266.4(CTNNA3):c.856C>A (p.Leu286Met) rs1554939194
NM_013266.4(CTNNA3):c.880G>A (p.Glu294Lys) rs146475470
NM_013266.4(CTNNA3):c.904A>G (p.Lys302Glu) rs970349800
NM_013266.4(CTNNA3):c.952T>C (p.Ser318Pro) rs1564948470
NM_013266.4(CTNNA3):c.973C>T (p.Arg325Ter)
NM_013266.4(CTNNA3):c.974G>A (p.Arg325Gln)
NM_013266.4(CTNNA3):c.974G>C (p.Arg325Pro) rs773609785
NM_013266.4(CTNNA3):c.986T>C (p.Ile329Thr) rs181929603
NM_013266.4(CTNNA3):c.99+5T>C
NM_013266.4(CTNNA3):c.999C>A (p.Asn333Lys) rs146754105
Single allele

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