ClinVar Miner

List of variants in gene CTNNA3 studied for arrhythmogenic right ventricular dysplasia 13

Included ClinVar conditions (1):
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Gene type:
ClinVar version:
Total variants: 108
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HGVS dbSNP
NC_000010.10:g.(?_67726350)_(67748575_?)del
NC_000010.10:g.(?_68381430)_(68526194_?)del
NC_000010.11:g.(?_66280450)_(66280641_?)del
NC_000010.11:g.(?_66280450)_(66621804_?)dup
NC_000010.11:g.(?_66379132)_(66379372_?)del
NC_000010.11:g.(?_66520597)_(66520793_?)del
NC_000010.11:g.(?_66520597)_(66520793_?)dup
NC_000010.11:g.(?_66520597)_(66621804_?)del
NC_000010.11:g.(?_66520597)_(66775544_?)dup
NC_000010.11:g.(?_66621672)_(66621804_?)del
NC_000010.11:g.(?_66766244)_(66775544_?)del
NC_000010.11:g.(?_66775424)_(66775544_?)del
NC_000010.11:g.(?_67180297)_(67180540_?)dup
NM_001127384.2(CTNNA3):c.1532-1G>A rs756034227
NM_013266.3(CTNNA3):c.1007G>A (p.Arg336His) rs372482202
NM_013266.3(CTNNA3):c.1047C>T (p.Asn349=) rs60262757
NM_013266.3(CTNNA3):c.1064G>A (p.Arg355Lys) rs375610128
NM_013266.3(CTNNA3):c.1073C>A (p.Thr358Asn) rs751471841
NM_013266.3(CTNNA3):c.1120C>T (p.Arg374Cys) rs370981751
NM_013266.3(CTNNA3):c.1128+2T>A
NM_013266.3(CTNNA3):c.1128+7G>T rs200113495
NM_013266.3(CTNNA3):c.1132C>T (p.Arg378Cys) rs187752783
NM_013266.3(CTNNA3):c.1133G>A (p.Arg378His) rs143682596
NM_013266.3(CTNNA3):c.1175C>T (p.Thr392Met) rs146777494
NM_013266.3(CTNNA3):c.1183C>A (p.Pro395Thr) rs1554848924
NM_013266.3(CTNNA3):c.1186C>G (p.Leu396Val)
NM_013266.3(CTNNA3):c.1195C>A (p.Leu399Ile) rs115276158
NM_013266.3(CTNNA3):c.1215T>C (p.Asn405=) rs775938724
NM_013266.3(CTNNA3):c.1231A>G (p.Ile411Val) rs372808360
NM_013266.3(CTNNA3):c.1233A>G (p.Ile411Met) rs1554848898
NM_013266.3(CTNNA3):c.1247C>T (p.Ala416Val) rs1032740164
NM_013266.3(CTNNA3):c.1303A>G (p.Met435Val) rs377404952
NM_013266.3(CTNNA3):c.1402G>A (p.Ala468Thr)
NM_013266.3(CTNNA3):c.1450C>T (p.Arg484Cys) rs200182913
NM_013266.3(CTNNA3):c.1453A>T (p.Thr485Ser) rs140913916
NM_013266.3(CTNNA3):c.1507A>C (p.Ile503Leu) rs147802834
NM_013266.3(CTNNA3):c.1536C>T (p.Ser512=) rs1060504519
NM_013266.3(CTNNA3):c.155C>T (p.Ser52Leu) rs139105272
NM_013266.3(CTNNA3):c.156G>C (p.Ser52=) rs61759502
NM_013266.3(CTNNA3):c.1587_1588delTGinsAT (p.Asp529_Ala530delinsGluSer) rs1554949356
NM_013266.3(CTNNA3):c.1603C>T (p.Arg535Cys) rs41274090
NM_013266.3(CTNNA3):c.1604G>A (p.Arg535His) rs139378888
NM_013266.3(CTNNA3):c.1611G>A (p.Ala537=) rs146900023
NM_013266.3(CTNNA3):c.1627C>T (p.Arg543Trp) rs372758887
NM_013266.3(CTNNA3):c.1655C>T (p.Thr552Met) rs61737718
NM_013266.3(CTNNA3):c.1669A>G (p.Ser557Gly) rs768735520
NM_013266.3(CTNNA3):c.1733-1G>C rs193155648
NM_013266.3(CTNNA3):c.1790C>T (p.Ser597Leu) rs780346090
NM_013266.3(CTNNA3):c.1819G>A (p.Val607Met)
NM_013266.3(CTNNA3):c.1823A>T (p.Asp608Val) rs138314889
NM_013266.3(CTNNA3):c.1841A>G (p.Tyr614Cys) rs770893892
NM_013266.3(CTNNA3):c.1865G>A (p.Cys622Tyr) rs367616357
NM_013266.3(CTNNA3):c.1872C>A (p.Val624=) rs10997034
NM_013266.3(CTNNA3):c.1883G>A (p.Arg628Gln) rs754792055
NM_013266.3(CTNNA3):c.1894G>A (p.Glu632Lys) rs1060502222
NM_013266.3(CTNNA3):c.1900G>A (p.Glu634Lys) rs77165728
NM_013266.3(CTNNA3):c.1929C>T (p.His643=) rs147760277
NM_013266.3(CTNNA3):c.1949G>A (p.Ser650Asn) rs1060502223
NM_013266.3(CTNNA3):c.1959C>T (p.Thr653=) rs556623128
NM_013266.3(CTNNA3):c.1978-9_1978-8delAT rs750667259
NM_013266.3(CTNNA3):c.1979C>T (p.Ala660Val) rs778640435
NM_013266.3(CTNNA3):c.213C>G (p.Asp71Glu) rs771791661
NM_013266.3(CTNNA3):c.2142G>A (p.Glu714=) rs115972723
NM_013266.3(CTNNA3):c.2158A>C (p.Arg720=) rs143867269
NM_013266.3(CTNNA3):c.2172A>C (p.Pro724=) rs116662854
NM_013266.3(CTNNA3):c.2278T>C (p.Ser760Pro)
NM_013266.3(CTNNA3):c.2296_2298delTTG (p.Leu766del) rs587777135
NM_013266.3(CTNNA3):c.2368C>G (p.Gln790Glu)
NM_013266.3(CTNNA3):c.2501G>A (p.Arg834Gln) rs373081692
NM_013266.3(CTNNA3):c.2524C>T (p.Arg842Trp) rs199852825
NM_013266.3(CTNNA3):c.2528A>G (p.His843Arg) rs540211204
NM_013266.3(CTNNA3):c.2553G>A (p.Lys851=) rs115814032
NM_013266.3(CTNNA3):c.2630A>C (p.Lys877Thr) rs781167292
NM_013266.3(CTNNA3):c.2638dupA (p.Ile880Asnfs) rs761152565
NM_013266.3(CTNNA3):c.264G>A (p.Thr88=) rs752481842
NM_013266.3(CTNNA3):c.281T>A (p.Val94Asp) rs587777134
NM_013266.3(CTNNA3):c.33C>T (p.Ile11=) rs61735044
NM_013266.3(CTNNA3):c.348A>C (p.Pro116=) rs61749224
NM_013266.3(CTNNA3):c.392C>T (p.Ala131Val) rs774544494
NM_013266.3(CTNNA3):c.393G>A (p.Ala131=) rs80182543
NM_013266.3(CTNNA3):c.398C>T (p.Thr133Met)
NM_013266.3(CTNNA3):c.399G>A (p.Thr133=) rs150376558
NM_013266.3(CTNNA3):c.412C>A (p.Leu138Ile) rs899335202
NM_013266.3(CTNNA3):c.417G>A (p.Ala139=)
NM_013266.3(CTNNA3):c.429T>C (p.Asp143=) rs111880127
NM_013266.3(CTNNA3):c.452T>G (p.Val151Gly) rs756167695
NM_013266.3(CTNNA3):c.457G>C (p.Ala153Pro) rs147116577
NM_013266.3(CTNNA3):c.478T>A (p.Ser160Thr) rs61749223
NM_013266.3(CTNNA3):c.483C>T (p.Leu161=) rs74142830
NM_013266.3(CTNNA3):c.578A>G (p.Gln193Arg) rs373233387
NM_013266.3(CTNNA3):c.580-8C>T rs141983252
NM_013266.3(CTNNA3):c.649C>T (p.Leu217Phe) rs374834298
NM_013266.3(CTNNA3):c.654G>T (p.Leu218Phe)
NM_013266.3(CTNNA3):c.674G>T (p.Cys225Phe)
NM_013266.3(CTNNA3):c.742G>T (p.Ala248Ser) rs192093851
NM_013266.3(CTNNA3):c.779A>G (p.Gln260Arg) rs190073606
NM_013266.3(CTNNA3):c.78A>T (p.Leu26=) rs1250437620
NM_013266.3(CTNNA3):c.843+1G>T
NM_013266.3(CTNNA3):c.856C>A (p.Leu286Met) rs1554939194
NM_013266.3(CTNNA3):c.880G>A (p.Glu294Lys) rs146475470
NM_013266.3(CTNNA3):c.904A>G (p.Lys302Glu) rs970349800
NM_013266.3(CTNNA3):c.945G>A (p.Ala315=) rs375992799
NM_013266.3(CTNNA3):c.952T>C (p.Ser318Pro)
NM_013266.3(CTNNA3):c.974G>A (p.Arg325Gln)
NM_013266.3(CTNNA3):c.974G>C (p.Arg325Pro) rs773609785
NM_013266.3(CTNNA3):c.986T>C (p.Ile329Thr) rs181929603
NM_013266.3(CTNNA3):c.999C>A (p.Asn333Lys) rs146754105
NM_013266.3(CTNNA3):c.999C>T (p.Asn333=) rs146754105

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