ClinVar Miner

List of variants in gene CTNNA3 reported as benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_013266.4(CTNNA3):c.1128+262C>G rs4291568 0.97960
NM_013266.4(CTNNA3):c.2160-304G>A rs3780916 0.86119
NM_013266.4(CTNNA3):c.1532-279G>C rs2441719 0.64088
NM_013266.4(CTNNA3):c.2401-203A>G rs7907928 0.52026
NM_013266.4(CTNNA3):c.1787G>A (p.Ser596Asn) rs4548513 0.47526
NM_013266.4(CTNNA3):c.292+236T>C rs7089724 0.45560
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.2401-293G>T rs7922674 0.30380
NM_013266.4(CTNNA3):c.1375-199C>T rs2035602 0.23162
NM_013266.4(CTNNA3):c.293-19A>T rs1909654 0.20576
NM_013266.4(CTNNA3):c.293-291T>C rs2133696 0.20575
NM_013266.4(CTNNA3):c.460-161T>C rs7906790 0.20560
NM_013266.4(CTNNA3):c.579+306G>A rs6480263 0.20560
NM_013266.4(CTNNA3):c.460-322C>T rs6480264 0.20544
NM_013266.4(CTNNA3):c.579+105G>C rs10509289 0.18738
NM_013266.4(CTNNA3):c.843+22G>C rs4745933 0.18293
NM_013266.4(CTNNA3):c.2401-289A>G rs1670144 0.14806
NM_013266.4(CTNNA3):c.460-324T>G rs6480265 0.14691
NM_013266.4(CTNNA3):c.1047+3461C>T rs1904629 0.14268
NM_013266.4(CTNNA3):c.99+218T>C rs73270159 0.14015
NM_013266.4(CTNNA3):c.-5-1528A>G rs1582573 0.13521
NM_013266.4(CTNNA3):c.579+15T>G rs10997691 0.12289
NM_013266.4(CTNNA3):c.1281+173A>G rs74141674 0.11485
NM_013266.4(CTNNA3):c.2160-292G>A rs3780917 0.10599
NM_013266.4(CTNNA3):c.2400+206T>A rs2276158 0.10558
NM_013266.4(CTNNA3):c.100-270T>C rs55755897 0.09209
NM_013266.4(CTNNA3):c.-5-255T>G rs58825358 0.09163
NM_013266.4(CTNNA3):c.1531+178G>A rs148459048 0.09110
NM_013266.4(CTNNA3):c.1732+275A>G rs16922919 0.06468
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.459+69G>A rs11815032 0.03451
NM_013266.4(CTNNA3):c.-5-232T>G rs73270161 0.03144
NM_013266.4(CTNNA3):c.843+17A>G rs77409659 0.02787
NM_013266.4(CTNNA3):c.-5-1035G>A rs726635 0.02539
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.580-51T>A rs115482082 0.02206
NM_013266.4(CTNNA3):c.100-41dup rs142717014 0.02072
NM_013266.4(CTNNA3):c.*243G>A rs77424782 0.02067
NM_013266.4(CTNNA3):c.478T>A (p.Ser160Thr) rs61749223 0.01916
NM_013266.4(CTNNA3):c.1978-298G>A rs116317135 0.01765
NM_013266.4(CTNNA3):c.580-300G>T rs76025797 0.01714
NM_013266.4(CTNNA3):c.2265+160G>A rs111421884 0.01695
NM_013266.4(CTNNA3):c.843+323A>G rs116205388 0.01636
NM_013266.4(CTNNA3):c.1282-79A>G rs75142881 0.01598
NM_013266.4(CTNNA3):c.348A>C (p.Pro116=) rs61749224 0.01511
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.1587T>A (p.Asp529Glu) rs74141466 0.00293
NM_013266.4(CTNNA3):c.1588G>T (p.Ala530Ser) rs74141465 0.00293
NM_013266.4(CTNNA3):c.1133G>A (p.Arg378His) rs143682596 0.00240
GRCh38/hg38 10q21.3(chr10:66562861-66599677)x1
GRCh38/hg38 10q21.3(chr10:66684077-66756761)x1
GRCh38/hg38 10q21.3(chr10:66719462-66839674)x1
NM_013266.4(CTNNA3):c.1128+113dup rs5785786
NM_013266.4(CTNNA3):c.1281+197A>G rs7083123
NM_013266.4(CTNNA3):c.1374+88dup rs111590769
NM_013266.4(CTNNA3):c.1375-144_1375-141del rs145395911
NM_013266.4(CTNNA3):c.1375-267G>T rs115884777
NM_013266.4(CTNNA3):c.1532-32C>T rs12761828
NM_013266.4(CTNNA3):c.1587_1588delinsAT (p.Asp529_Ala530delinsGluSer) rs1554949356
NM_013266.4(CTNNA3):c.1732+188A>G rs9414919
NM_013266.4(CTNNA3):c.1733-217dup rs61169201
NM_013266.4(CTNNA3):c.580-225C>T rs9651325
NM_013266.4(CTNNA3):c.843+164A>T rs185707562
NM_013266.4(CTNNA3):c.99+239TA[13] rs67324505
NM_013266.4(CTNNA3):c.99+239TA[14] rs67324505
NM_013266.4(CTNNA3):c.99+239TA[16] rs67324505
NM_013266.4(CTNNA3):c.99+239TA[19] rs67324505
NM_013266.4(CTNNA3):c.99+239TA[8] rs67324505
NM_013266.4(CTNNA3):c.99+239TA[9] rs67324505

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