CTNND2[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1315721	NM_001332.4(CTNND2):c.*2G>A	CTNND2	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2636444	NM_001332.4(CTNND2):c.3664G>A (p.Asp1222Asn)	CTNND2 (D1131N +4 more)	Single nucleotide variant (missense variant +1 more)	CTNND2-related disorder	GUncertain significance
Select item 709223	NM_001332.4(CTNND2):c.3663C>T (p.Pro1221=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3078695	NM_001332.4(CTNND2):c.3653C>T (p.Pro1218Leu)	CTNND2 (P1127L +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3078694	NM_001332.4(CTNND2):c.3634T>C (p.Tyr1212His)	CTNND2 (Y1212H +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1250893	NM_001332.4(CTNND2):c.3516C>T (p.Phe1172=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 724675	NM_001332.4(CTNND2):c.3462C>T (p.Tyr1154=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 2246280	NM_001332.4(CTNND2):c.3443A>T (p.Glu1148Val)	CTNND2 (E1057V +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1286931	NM_001332.4(CTNND2):c.3418-6G>A	CTNND2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 790009	NM_001332.4(CTNND2):c.3418-8C>T	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 1287782	NM_001332.4(CTNND2):c.3418-102A>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265706	NM_001332.4(CTNND2):c.3418-190C>T	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316701	NM_001332.4(CTNND2):c.3418-315G>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1277745	NM_001332.4(CTNND2):c.3418-329C>T	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286390	NM_001332.4(CTNND2):c.3417+292C>T	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271885	NM_001332.4(CTNND2):c.3417+254A>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279145	NM_001332.4(CTNND2):c.3417+234A>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1318181	NM_001332.4(CTNND2):c.3417+167GT[12]	CTNND2	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1288595	NM_001332.4(CTNND2):c.3417+167GT[15]	CTNND2	Microsatellite (intron variant)	not provided	GBenign
Select item 1253470	NM_001332.4(CTNND2):c.3417+167GT[11]	CTNND2	Microsatellite (intron variant)	not provided	GBenign
Select item 1183085	NM_001332.4(CTNND2):c.3417+167GT[13]	CTNND2	Microsatellite (intron variant)	not provided	GBenign
Select item 1254980	NM_001332.4(CTNND2):c.3417+165C>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280027	NM_001332.4(CTNND2):c.3417+114C>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316873	NM_001332.4(CTNND2):c.3417+97_3417+100del	CTNND2	Deletion (intron variant)	not provided	GLikely benign
Select item 1292997	NM_001332.4(CTNND2):c.3417+2_3417+5dup	CTNND2	Duplication (splice donor variant)	not provided	GBenign
Select item 2357630	NM_001332.4(CTNND2):c.3395C>G (p.Ala1132Gly)	CTNND2 (A1041G +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 1317592	NM_001332.4(CTNND2):c.3394G>A (p.Ala1132Thr)	CTNND2 (A1041T +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1233894	NM_001332.4(CTNND2):c.3381T>A (p.Ser1127=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2210204	NM_001332.4(CTNND2):c.3368T>C (p.Leu1123Ser)	CTNND2 (L1032S +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3078693	NM_001332.4(CTNND2):c.3350A>G (p.Asn1117Ser)	CTNND2 (N805S +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1248363	NM_001332.4(CTNND2):c.3344-11T>C	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276692	NM_001332.4(CTNND2):c.3344-176del	CTNND2	Deletion (intron variant)	not provided	GBenign
Select item 1317852	NM_001332.4(CTNND2):c.3343+86G>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1232979	NM_001332.4(CTNND2):c.3343+51A>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3054521	NM_001332.4(CTNND2):c.3343+8C>T	CTNND2	Single nucleotide variant (intron variant)	CTNND2-related disorder	GLikely benign
Select item 1317569	NM_001332.4(CTNND2):c.3343+5G>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1272437	NM_001332.4(CTNND2):c.3310G>A (p.Gly1104Ser)	CTNND2 (G1013S +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 986090	NM_001332.4(CTNND2):c.3305C>T (p.Ala1102Val)	CTNND2 (A1011V +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2688897	NM_001332.4(CTNND2):c.3271G>A (p.Glu1091Lys)	CTNND2 (E1000K +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 809732	NM_001332.4(CTNND2):c.3232C>T (p.Arg1078Trp)	CTNND2 (R766W +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3049933	NM_001332.4(CTNND2):c.3212-9T>C	CTNND2	Single nucleotide variant (intron variant)	CTNND2-related disorder	GLikely benign
Select item 1241382	NM_001332.4(CTNND2):c.3212-220A>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267963	NM_001332.4(CTNND2):c.3212-329C>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317228	NM_001332.4(CTNND2):c.3129C>T (p.Ile1043=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	CTNND2-related disorder +1 more	GLikely benign
Select item 620420	NM_001332.4(CTNND2):c.3092G>A (p.Trp1031Ter)	CTNND2 (W1031* +4 more)	Single nucleotide variant (nonsense +1 more)	not provided	GLikely pathogenic
Select item 1317568	NM_001332.4(CTNND2):c.3085-128_3085-127insCCTCTTCTGCG	CTNND2	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1275643	NM_001332.4(CTNND2):c.3085-194C>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238977	NM_001332.4(CTNND2):c.3084+134C>T	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235629	NM_001332.4(CTNND2):c.3084+16C>T	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2219559	NM_001332.4(CTNND2):c.3046A>C (p.Met1016Leu)	CTNND2 (M1016L +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2597703	NM_001332.4(CTNND2):c.3028T>A (p.Ser1010Thr)	CTNND2 (S577T +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2332433	NM_001332.4(CTNND2):c.3007C>A (p.Pro1003Thr)	CTNND2 (P1003T +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1243626	NM_001332.4(CTNND2):c.3000-217C>T	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282507	NM_001332.4(CTNND2):c.2788+283T>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274594	NM_001332.4(CTNND2):c.2788+196T>C	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248685	NM_001332.4(CTNND2):c.2788+46A>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 780517	NM_001332.4(CTNND2):c.2745G>A (p.Ala915=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	CTNND2-related disorder +1 more	GBenign
Select item 726742	NM_001332.4(CTNND2):c.2733G>A (p.Ala911=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	CTNND2-related disorder +1 more	GBenign/Likely benign
Select item 391072	NM_001332.4(CTNND2):c.2723T>C (p.Val908Ala)	CTNND2 (V908A +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3078692	NM_001332.4(CTNND2):c.2689C>T (p.Leu897Phe)	CTNND2 (L560F +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 280258	NM_001332.4(CTNND2):c.2653C>T (p.Arg885Ter)	CTNND2 (R885* +4 more)	Single nucleotide variant (nonsense +1 more)	Neurodevelopmental disorder +1 more	GConflicting classifications of pathogenicity
Select item 1318248	NM_001332.4(CTNND2):c.2638-78C>T	CTNND2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1244063	NM_001332.4(CTNND2):c.2638-323T>C	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244185	NM_001332.4(CTNND2):c.2637+218_2637+226del	CTNND2	Deletion (intron variant)	not provided	GBenign
Select item 1277959	NM_001332.4(CTNND2):c.2637+126A>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317054	NM_001332.4(CTNND2):c.2637+125A>T	CTNND2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1250713	NM_001332.4(CTNND2):c.2637+118A>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317424	NM_001332.4(CTNND2):c.2637+41T>C	CTNND2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2332178	NM_001332.4(CTNND2):c.2605G>A (p.Ala869Thr)	CTNND2 (A436T +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2688894	NM_001332.4(CTNND2):c.2464-1G>T	CTNND2	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 722905	NM_001332.4(CTNND2):c.2464-5G>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 798032	NM_001332.4(CTNND2):c.2464-6C>T	CTNND2	Single nucleotide variant (intron variant)	CTNND2-related disorder +1 more	GBenign
Select item 1253756	NM_001332.4(CTNND2):c.2464-127G>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317055	NM_001332.4(CTNND2):c.2464-214C>T	CTNND2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316757	NM_001332.4(CTNND2):c.2464-306C>T	CTNND2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1320594	NM_001332.4(CTNND2):c.2463+259A>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317889	NM_001332.4(CTNND2):c.2463+19A>C	CTNND2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2250218	NM_001332.4(CTNND2):c.2429G>T (p.Gly810Val)	CTNND2 (G377V +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 986234	NM_001332.4(CTNND2):c.2404G>A (p.Asp802Asn)	CTNND2 (D369N +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1317365	NM_001332.4(CTNND2):c.2403G>A (p.Lys801=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	CTNND2-related disorder +1 more	GLikely benign
Select item 3078688	NM_001332.4(CTNND2):c.2327C>T (p.Ala776Val)	CTNND2 (A685V +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 714949	NM_001332.4(CTNND2):c.2316G>A (p.Ser772=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 1228070	NM_001332.4(CTNND2):c.2278-98A>C	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258197	NM_001332.4(CTNND2):c.2278-189G>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286294	NM_001332.4(CTNND2):c.2277+315del	CTNND2	Deletion (intron variant)	not provided	GBenign
Select item 1262175	NM_001332.4(CTNND2):c.2277+313_2277+315del	CTNND2	Deletion (intron variant)	not provided	GBenign
Select item 1222193	NM_001332.4(CTNND2):c.2277+264G>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278555	NM_001332.4(CTNND2):c.2277+223A>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261713	NM_001332.4(CTNND2):c.2277+178T>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257049	NM_001332.4(CTNND2):c.2256G>A (p.Gly752=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2298388	NM_001332.4(CTNND2):c.2241C>G (p.Ile747Met)	CTNND2 (I410M +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2572244	NM_001332.4(CTNND2):c.2188del (p.Arg730fs)	CTNND2 (R297fs +3 more)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 731219	NM_001332.4(CTNND2):c.2175C>T (p.Ala725=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655296	NM_001332.4(CTNND2):c.2160-8C>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1254315	NM_001332.4(CTNND2):c.2160-14C>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221948	NM_001332.4(CTNND2):c.2160-25G>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241746	NM_001332.4(CTNND2):c.2159+167G>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290513	NM_001332.4(CTNND2):c.2159+31A>G	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317178	NM_001332.4(CTNND2):c.2142C>T (p.Asn714=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	CTNND2-related disorder +1 more	GLikely benign
Select item 1686608	NM_001332.4(CTNND2):c.2137C>T (p.Arg713Cys)	CTNND2 (R280C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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