"GeneDx"[submitter] AND "CTNNA3"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152646	GRCh38/hg38 10q21.1-21.3(chr10:55287177-67558442)x3	ADO, ANK3 +227 more	Copy number gain	See cases	GPathogenic
Select item 58726	GRCh38/hg38 10q21.1-22.2(chr10:58436466-74415216)x1	LOC129390190, LOC129390191 +610 more	Copy number loss	See cases	GPathogenic
Select item 1257910	NM_013266.4(CTNNA3):c.*243G>A	CTNNA3	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 155780	NM_013266.4(CTNNA3):c.2573T>C (p.Leu858Ser)	CTNNA3 (L858S)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13 +1 more	GConflicting classifications of pathogenicity
Select item 240869	NM_013266.4(CTNNA3):c.2553G>A (p.Lys851=)	CTNNA3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 541664	NM_013266.4(CTNNA3):c.2524C>T (p.Arg842Trp)	CTNNA3 (R842W)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1318271	NM_013266.4(CTNNA3):c.2401-86C>T	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316238	NM_013266.4(CTNNA3):c.2401-166C>T	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1264448	NM_013266.4(CTNNA3):c.2401-203A>G	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229121	NM_013266.4(CTNNA3):c.2401-289A>G	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267896	NM_013266.4(CTNNA3):c.2401-293G>T	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1269267	NM_013266.4(CTNNA3):c.2400+206T>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 696072	NM_013266.4(CTNNA3):c.2378G>A (p.Gly793Glu)	CTNNA3 (G793E)	Single nucleotide variant (missense variant)	not specified +2 more	GLikely benign
Select item 516743	NM_013266.4(CTNNA3):c.2266-10T>G	CTNNA3	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1316643	NM_013266.4(CTNNA3):c.2266-98T>C	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316312	NM_013266.4(CTNNA3):c.2266-206T>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1221594	NM_013266.4(CTNNA3):c.2265+160G>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 474823	NM_013266.4(CTNNA3):c.2172A>C (p.Pro724=)	CTNNA3	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 13 +2 more	GBenign/Likely benign
Select item 1287523	NM_013266.4(CTNNA3):c.2160-292G>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294045	NM_013266.4(CTNNA3):c.2160-304G>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 474822	NM_013266.4(CTNNA3):c.2158A>C (p.Arg720=)	CTNNA3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 474821	NM_013266.4(CTNNA3):c.2142G>A (p.Glu714=)	CTNNA3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 240867	NM_013266.4(CTNNA3):c.1978-9_1978-8del	CTNNA3	Deletion (intron variant)	Arrhythmogenic right ventricular dysplasia 13 +1 more	GLikely benign
Select item 1230191	NM_013266.4(CTNNA3):c.1978-298G>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 415362	NM_013266.4(CTNNA3):c.1959C>T (p.Thr653=)	CTNNA3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 695631	NM_013266.4(CTNNA3):c.1936C>T (p.Arg646Cys)	CTNNA3 (R646C)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13 +2 more	GConflicting classifications of pathogenicity
Select item 415369	NM_013266.4(CTNNA3):c.1929C>T (p.His643=)	CTNNA3	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 13 +2 more	GBenign/Likely benign
Select item 1081803	NM_013266.4(CTNNA3):c.1885-9T>C	CTNNA3	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1316311	NM_013266.4(CTNNA3):c.1885-122G>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 145818	GRCh38/hg38 10q21.3(chr10:66203935-66312974)x1	CTNNA3, LOC132089817 +1 more	Copy number loss	See cases	GLikely benign
Select item 1317619	NM_013266.4(CTNNA3):c.1884+242A>G	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 415368	NM_013266.4(CTNNA3):c.1872C>A (p.Val624=)	CTNNA3	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 13 +2 more	GBenign
Select item 1169338	NM_013266.4(CTNNA3):c.1787G>A (p.Ser596Asn)	CTNNA3 (S596N)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 1223049	NM_013266.4(CTNNA3):c.1733-217dup	CTNNA3	Duplication (intron variant)	not provided	GBenign
Select item 152654	GRCh38/hg38 10q21.3(chr10:66312974-66491777)x1	CTNNA3, LOC126860948 +1 more	Copy number loss	See cases	GBenign
Select item 152647	GRCh38/hg38 10q21.3(chr10:66312974-66394729)x1	CTNNA3, LOC132089819	Copy number loss	See cases	GBenign
Select item 1240767	NM_013266.4(CTNNA3):c.1732+275A>G	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1296290	NM_013266.4(CTNNA3):c.1732+188A>G	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 415374	NM_013266.4(CTNNA3):c.1655C>T (p.Thr552Met)	CTNNA3 (T552M)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13 +2 more	GBenign/Likely benign
Select item 474818	NM_013266.4(CTNNA3):c.1611G>A (p.Ala537=)	CTNNA3	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 13 +2 more	GBenign/Likely benign
Select item 240864	NM_013266.4(CTNNA3):c.1603C>T (p.Arg535Cys)	CTNNA3 (R535C)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 714456	NM_013266.4(CTNNA3):c.1588G>T (p.Ala530Ser)	CTNNA3 (A530S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 474817	NM_013266.4(CTNNA3):c.1587_1588delinsAT (p.Asp529_Ala530delinsGluSer)	CTNNA3	Indel (missense variant)	not provided +1 more	GBenign
Select item 714482	NM_013266.4(CTNNA3):c.1587T>A (p.Asp529Glu)	CTNNA3 (D529E)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1270611	NM_013266.4(CTNNA3):c.1532-32C>T	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259972	NM_013266.4(CTNNA3):c.1532-279G>C	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 152659	GRCh38/hg38 10q21.3(chr10:66394729-66599677)x1	CTNNA3, LOC126860948 +2 more	Copy number loss	See cases	GBenign
Select item 1296289	NM_013266.4(CTNNA3):c.1531+178G>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1318128	NM_013266.4(CTNNA3):c.1531+163C>T	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316171	NM_013266.4(CTNNA3):c.1531+114G>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1284061	NM_013266.4(CTNNA3):c.1531+16T>C	CTNNA3	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 415361	NM_013266.4(CTNNA3):c.1453A>T (p.Thr485Ser)	CTNNA3 (T485S)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 848166	NM_013266.4(CTNNA3):c.1421C>T (p.Ala474Val)	CTNNA3 (A474V)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1296287	NM_013266.4(CTNNA3):c.1375-144_1375-141del	CTNNA3	Microsatellite (intron variant)	not provided	GBenign
Select item 1318190	NM_013266.4(CTNNA3):c.1375-168T>G	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1228619	NM_013266.4(CTNNA3):c.1375-199C>T	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275123	NM_013266.4(CTNNA3):c.1375-267G>T	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 145858	GRCh38/hg38 10q21.3(chr10:66523779-66684077)x1	CTNNA3, LOC132089820 +1 more	Copy number loss	See cases	GLikely benign
Select item 59399	GRCh38/hg38 10q21.3(chr10:66544198-66756820)x1	CTNNA3	Copy number loss	See cases	GUncertain significance
Select item 152648	GRCh38/hg38 10q21.3(chr10:66562861-66599677)x1	CTNNA3	Copy number loss	See cases	GBenign
Select item 145870	GRCh38/hg38 10q21.3(chr10:66562861-66684077)x1	CTNNA3	Copy number loss	See cases	GLikely benign
Select item 1317539	NM_013266.4(CTNNA3):c.1374+284C>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317612	NM_013266.4(CTNNA3):c.1374+247C>T	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1296288	NM_013266.4(CTNNA3):c.1374+88dup	CTNNA3	Duplication (intron variant)	not provided	GBenign
Select item 220977	NM_013266.4(CTNNA3):c.1303A>G (p.Met435Val)	CTNNA3 (M435V)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13 +1 more	GConflicting classifications of pathogenicity
Select item 1239169	NM_013266.4(CTNNA3):c.1282-79A>G	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 145216	GRCh38/hg38 10q21.3(chr10:66684077-66756761)x1	CTNNA3	Copy number loss	See cases	GBenign
Select item 144976	GRCh38/hg38 10q21.3(chr10:66719462-66839674)x1	CTNNA3	Copy number loss	See cases	GBenign
Select item 1318432	NM_013266.4(CTNNA3):c.1281+291T>C	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1296286	NM_013266.4(CTNNA3):c.1281+197A>G	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230959	NM_013266.4(CTNNA3):c.1281+173A>G	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317629	NM_013266.4(CTNNA3):c.1281+4A>G	CTNNA3	Single nucleotide variant (intron variant)	Arrhythmogenic right ventricular dysplasia 13 +1 more	GConflicting classifications of pathogenicity
Select item 220976	NM_013266.4(CTNNA3):c.1231A>G (p.Ile411Val)	CTNNA3 (I411V)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13 +1 more	GConflicting classifications of pathogenicity
Select item 415371	NM_013266.4(CTNNA3):c.1195C>A (p.Leu399Ile)	CTNNA3 (L399I)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13 +1 more	GBenign/Likely benign
Select item 1144273	NM_013266.4(CTNNA3):c.1192G>A (p.Val398Ile)	CTNNA3 (V398I)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 415363	NM_013266.4(CTNNA3):c.1133G>A (p.Arg378His)	CTNNA3 (R378H)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 409017	NM_013266.4(CTNNA3):c.1132C>T (p.Arg378Cys)	CTNNA3 (R378C)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13 +2 more	GConflicting classifications of pathogenicity
Select item 1318023	NM_013266.4(CTNNA3):c.1129-22T>C	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1318288	NM_013266.4(CTNNA3):c.1129-44T>C	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1294050	NM_013266.4(CTNNA3):c.1128+262C>G	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250768	NM_013266.4(CTNNA3):c.1128+113dup	CTNNA3	Duplication (intron variant)	not provided	GBenign
Select item 1315808	NM_013266.4(CTNNA3):c.1128+38G>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316900	NM_013266.4(CTNNA3):c.1047+3683G>C	CTNNA3	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1317924	NM_013266.4(CTNNA3):c.1047+3462C>T	CTNNA3	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1260265	NM_013266.4(CTNNA3):c.1047+3461C>T	CTNNA3	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 240863	NM_013266.4(CTNNA3):c.1047C>T (p.Asn349=)	CTNNA3	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 1294049	NM_013266.4(CTNNA3):c.843+323A>G	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235898	NM_013266.4(CTNNA3):c.843+164A>T	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1296388	NM_013266.4(CTNNA3):c.843+22G>C	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281398	NM_013266.4(CTNNA3):c.843+17A>G	CTNNA3	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 474826	NM_013266.4(CTNNA3):c.779A>G (p.Gln260Arg)	CTNNA3 (Q260R +1 more)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13 +2 more	GConflicting classifications of pathogenicity
Select item 240874	NM_013266.4(CTNNA3):c.580-8C>T	CTNNA3	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 1297365	NM_013266.4(CTNNA3):c.580-51T>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295208	NM_013266.4(CTNNA3):c.580-225C>T	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268420	NM_013266.4(CTNNA3):c.580-300G>T	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271665	NM_013266.4(CTNNA3):c.579+306G>A	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182394	NM_013266.4(CTNNA3):c.579+105G>C	CTNNA3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248579	NM_013266.4(CTNNA3):c.579+15T>G	CTNNA3	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 415377	NM_013266.4(CTNNA3):c.483C>T (p.Leu161=)	CTNNA3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 240872	NM_013266.4(CTNNA3):c.478T>A (p.Ser160Thr)	CTNNA3 (S160T +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign

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