ClinVar Miner

List of variants in gene CTNNA3 studied for not specified

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_013266.4(CTNNA3):c.1787G>A (p.Ser596Asn) rs4548513 0.47526
NM_013266.4(CTNNA3):c.292+13A>G rs3750863 0.45524
NM_013266.4(CTNNA3):c.2266-10T>G rs2105702 0.32828
NM_013266.4(CTNNA3):c.293-19A>T rs1909654 0.20576
NM_013266.4(CTNNA3):c.579+15T>G rs10997691 0.12289
NM_013266.4(CTNNA3):c.460-13T>C rs7903421 0.05538
NM_013266.4(CTNNA3):c.1872C>A (p.Val624=) rs10997034 0.04630
NM_013266.4(CTNNA3):c.1531+16T>C rs78806593 0.03870
NM_013266.4(CTNNA3):c.843+17A>G rs77409659 0.02787
NM_013266.4(CTNNA3):c.1655C>T (p.Thr552Met) rs61737718 0.02389
NM_013266.4(CTNNA3):c.393G>A (p.Ala131=) rs80182543 0.02215
NM_013266.4(CTNNA3):c.478T>A (p.Ser160Thr) rs61749223 0.01916
NM_013266.4(CTNNA3):c.348A>C (p.Pro116=) rs61749224 0.01511
NM_013266.4(CTNNA3):c.1603C>T (p.Arg535Cys) rs41274090 0.01060
NM_013266.4(CTNNA3):c.1047C>T (p.Asn349=) rs60262757 0.00761
NM_013266.4(CTNNA3):c.2553G>A (p.Lys851=) rs115814032 0.00420
NM_013266.4(CTNNA3):c.99+11C>T rs115451937 0.00411
NM_013266.4(CTNNA3):c.2142G>A (p.Glu714=) rs115972723 0.00315
NM_013266.4(CTNNA3):c.1587T>A (p.Asp529Glu) rs74141466 0.00293
NM_013266.4(CTNNA3):c.1588G>T (p.Ala530Ser) rs74141465 0.00293
NM_013266.4(CTNNA3):c.483C>T (p.Leu161=) rs74142830 0.00255
NM_013266.4(CTNNA3):c.1133G>A (p.Arg378His) rs143682596 0.00240
NM_013266.4(CTNNA3):c.33C>T (p.Ile11=) rs61735044 0.00206
NM_013266.4(CTNNA3):c.2172A>C (p.Pro724=) rs116662854 0.00191
NM_013266.4(CTNNA3):c.1195C>A (p.Leu399Ile) rs115276158 0.00178
NM_013266.4(CTNNA3):c.429T>C (p.Asp143=) rs111880127 0.00178
NM_013266.4(CTNNA3):c.580-8C>T rs141983252 0.00170
NM_013266.4(CTNNA3):c.2158A>C (p.Arg720=) rs143867269 0.00169
NM_013266.4(CTNNA3):c.1453A>T (p.Thr485Ser) rs140913916 0.00130
NM_013266.4(CTNNA3):c.844-15G>A rs201089736 0.00098
NM_013266.4(CTNNA3):c.1929C>T (p.His643=) rs147760277 0.00055
NM_013266.4(CTNNA3):c.387G>A (p.Leu129=) rs143943926 0.00026
NM_013266.4(CTNNA3):c.2601G>A (p.Thr867=) rs575703238 0.00022
NM_013266.4(CTNNA3):c.18A>T (p.Pro6=) rs138580439 0.00018
NM_013266.4(CTNNA3):c.718A>G (p.Thr240Ala) rs367570454 0.00016
NM_013266.4(CTNNA3):c.1732+8A>G rs372686443 0.00011
NM_013266.4(CTNNA3):c.399G>A (p.Thr133=) rs150376558 0.00009
NM_013266.4(CTNNA3):c.1248G>A (p.Ala416=) rs1046657762 0.00002
NM_013266.4(CTNNA3):c.1836G>A (p.Lys612=) rs774209973
NM_013266.4(CTNNA3):c.2401-23dup rs1338241471
NM_013266.4(CTNNA3):c.660A>G (p.Ser220=)

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