PDLIM3[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1316633	NM_014476.6(PDLIM3):c.*188dup	PDLIM3	Duplication (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1230235	NM_014476.6(PDLIM3):c.92_125del	PDLIM3	Deletion (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1318143	NM_014476.6(PDLIM3):c.*89A>G	PDLIM3	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 639882	NC_000004.12:g.(?_185502274)_(185506672_?)del	PDLIM3	Deletion	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 1246598	NM_014476.6(PDLIM3):c.*19C>T	PDLIM3	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 138676	NM_014476.6(PDLIM3):c.*12C>T	PDLIM3	Single nucleotide variant (3 prime UTR variant +1 more)	not specified +1 more	GBenign
Select item 1488378	NM_014476.6(PDLIM3):c.1095A>G (p.Ter365=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 201955	NM_014476.6(PDLIM3):c.1082A>G (p.Tyr361Cys)	PDLIM3 (Y361C +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 198860	NM_014476.6(PDLIM3):c.1080G>C (p.Leu360=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 413246	NM_014476.6(PDLIM3):c.1078C>T (p.Leu360=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	Primary dilated cardiomyopathy +2 more	GLikely benign
Select item 201949	NM_014476.6(PDLIM3):c.1074C>A (p.Val358=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 454474	NM_014476.6(PDLIM3):c.1072G>A (p.Val358Ile)	PDLIM3 (V358I +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 1587569	NM_014476.6(PDLIM3):c.1071G>A (p.Thr357=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	Primary dilated cardiomyopathy +2 more	GLikely benign
Select item 1360818	NM_014476.6(PDLIM3):c.1070C>T (p.Thr357Met)	PDLIM3 (T269M +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +2 more	GUncertain significance
Select item 1953073	NM_014476.6(PDLIM3):c.1069A>G (p.Thr357Ala)	PDLIM3 (T269A +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 3226315	NM_014476.6(PDLIM3):c.1064A>G (p.Tyr355Cys)	PDLIM3 (Y188C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2183523	NM_014476.6(PDLIM3):c.1063T>C (p.Tyr355His)	PDLIM3 (Y188H +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 1387398	NM_014476.6(PDLIM3):c.1060G>A (p.Gly354Ser)	PDLIM3 (G187S +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 1111780	NM_014476.6(PDLIM3):c.1053C>T (p.Pro351=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GLikely benign
Select item 3416612	NM_014476.6(PDLIM3):c.1050G>A (p.Lys350=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 1366274	NM_014476.6(PDLIM3):c.1043G>T (p.Arg348Leu)	PDLIM3 (R348L +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 859330	NM_014476.6(PDLIM3):c.1043G>A (p.Arg348His)	PDLIM3 (R260H +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 1408160	NM_014476.6(PDLIM3):c.1042C>T (p.Arg348Cys)	PDLIM3 (R348C +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 451734	NM_014476.6(PDLIM3):c.1040C>T (p.Ala347Val)	PDLIM3 (A347V +3 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy +2 more	GUncertain significance
Select item 3305566	NM_014476.6(PDLIM3):c.1039G>A (p.Ala347Thr)	PDLIM3 (A347T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1381406	NM_014476.6(PDLIM3):c.1037G>A (p.Arg346Lys)	PDLIM3 (R179K +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +2 more	GUncertain significance
Select item 2923805	NM_014476.6(PDLIM3):c.1035A>G (p.Ala345=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	Primary dilated cardiomyopathy +1 more	GLikely benign
Select item 1398471	NM_014476.6(PDLIM3):c.1033G>C (p.Ala345Pro)	PDLIM3 (A345P +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 579350	NM_014476.6(PDLIM3):c.1033G>A (p.Ala345Thr)	PDLIM3 (A345T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance
Select item 706624	NM_014476.6(PDLIM3):c.1032C>T (p.His344=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GLikely benign
Select item 511207	NM_014476.6(PDLIM3):c.1029C>T (p.Thr343=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 198859	NM_014476.6(PDLIM3):c.1027A>G (p.Thr343Ala)	PDLIM3 (T343A +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 642803	NM_014476.6(PDLIM3):c.1024G>A (p.Glu342Lys)	PDLIM3 (E294K +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 452375	NM_014476.6(PDLIM3):c.1007A>G (p.Glu336Gly)	PDLIM3 (E336G +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 2513944	NM_014476.6(PDLIM3):c.1004T>C (p.Ile335Thr)	PDLIM3 (I168T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 227013	NM_014476.6(PDLIM3):c.993C>A (p.Gly331=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign/Likely benign
Select item 405205	NM_014476.6(PDLIM3):c.992G>T (p.Gly331Val)	PDLIM3 (G331V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance
Select item 2412404	NM_014476.6(PDLIM3):c.990G>C (p.Lys330Asn)	PDLIM3 (K282N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1718743	NM_014476.6(PDLIM3):c.989A>C (p.Lys330Thr)	PDLIM3 (K163T +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 1768354	NM_014476.6(PDLIM3):c.983A>G (p.Lys328Arg)	PDLIM3 (K328R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1768220	NM_014476.6(PDLIM3):c.979C>G (p.Leu327Val)	PDLIM3 (L160V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2152759	NM_014476.6(PDLIM3):c.975C>T (p.Leu325=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	Primary dilated cardiomyopathy +1 more	GLikely benign
Select item 1517141	NM_014476.6(PDLIM3):c.964G>A (p.Asp322Asn)	PDLIM3 (D155N +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 1484343	NM_014476.6(PDLIM3):c.964G>T (p.Asp322Tyr)	PDLIM3 (D322Y +3 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy +1 more	GUncertain significance
Select item 1025713	NM_014476.6(PDLIM3):c.963C>A (p.Ala321=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 701062	NM_014476.6(PDLIM3):c.963C>T (p.Ala321=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	Primary dilated cardiomyopathy +2 more	GLikely benign
Select item 1937180	NM_014476.6(PDLIM3):c.956T>C (p.Val319Ala)	PDLIM3 (V271A +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 1371493	NM_014476.6(PDLIM3):c.955G>C (p.Val319Leu)	PDLIM3 (V152L +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 640817	NM_014476.6(PDLIM3):c.955G>A (p.Val319Met)	PDLIM3 (V231M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance
Select item 1625111	NM_014476.6(PDLIM3):c.954C>T (p.Phe318=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	Primary dilated cardiomyopathy +1 more	GLikely benign
Select item 1492591	NM_014476.6(PDLIM3):c.954C>G (p.Phe318Leu)	PDLIM3 (F151L +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 3416597	NM_014476.6(PDLIM3):c.952T>G (p.Phe318Val)	PDLIM3 (F230V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495861	NM_014476.6(PDLIM3):c.949T>C (p.Cys317Arg)	PDLIM3 (C150R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2448561	NM_014476.6(PDLIM3):c.946G>A (p.Glu316Lys)	PDLIM3 (E316K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance
Select item 1766983	NM_014476.6(PDLIM3):c.944C>A (p.Pro315His)	PDLIM3 (P227H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1766959	NM_014476.6(PDLIM3):c.943C>A (p.Pro315Thr)	PDLIM3 (P315T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 577170	NM_014476.6(PDLIM3):c.938G>A (p.Arg313Gln)	PDLIM3 (R313Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance
Select item 1061382	NM_014476.6(PDLIM3):c.937C>T (p.Arg313Trp)	PDLIM3 (R146W +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 1766538	NM_014476.6(PDLIM3):c.930T>C (p.Asp310=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 1036668	NM_014476.6(PDLIM3):c.928G>A (p.Asp310Asn)	PDLIM3 (D222N +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +2 more	GUncertain significance
Select item 201954	NM_014476.6(PDLIM3):c.926G>A (p.Arg309Gln)	PDLIM3 (R309Q +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 1766359	NM_014476.6(PDLIM3):c.925C>A (p.Arg309=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 100860	NM_014476.6(PDLIM3):c.925C>T (p.Arg309Trp)	PDLIM3 (R309W +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1578813	NM_014476.6(PDLIM3):c.924G>A (p.Ala308=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	Primary dilated cardiomyopathy +2 more	GLikely benign
Select item 2937189	NM_014476.6(PDLIM3):c.923C>T (p.Ala308Val)	PDLIM3 (A220V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance
Select item 3416600	NM_014476.6(PDLIM3):c.922G>A (p.Ala308Thr)	PDLIM3 (A141T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2924532	NM_014476.6(PDLIM3):c.917T>C (p.Val306Ala)	PDLIM3 (V306A +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 1025686	NM_014476.6(PDLIM3):c.916G>A (p.Val306Met)	PDLIM3 (V139M +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 449296	NM_014476.6(PDLIM3):c.913G>A (p.Val305Met)	PDLIM3 (V305M +3 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy +2 more	GUncertain significance
Select item 1765866	NM_014476.6(PDLIM3):c.911C>G (p.Ala304Gly)	PDLIM3 (A304G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2941455	NM_014476.6(PDLIM3):c.908G>T (p.Gly303Val)	PDLIM3 (G136V +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 138675	NM_014476.6(PDLIM3):c.906C>T (p.Val302=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign
Select item 2935786	NM_014476.6(PDLIM3):c.906-2A>G	PDLIM3	Single nucleotide variant (splice acceptor variant)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 2159088	NM_014476.6(PDLIM3):c.906-4A>G	PDLIM3	Single nucleotide variant (intron variant)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 1490551	NM_014476.6(PDLIM3):c.906-7C>G	PDLIM3	Single nucleotide variant (intron variant)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 2109075	NM_014476.6(PDLIM3):c.906-8C>T	PDLIM3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy +1 more	GLikely benign
Select item 1564009	NM_014476.6(PDLIM3):c.906-17G>A	PDLIM3	Single nucleotide variant (intron variant)	Primary dilated cardiomyopathy +1 more	GLikely benign
Select item 138674	NM_014476.6(PDLIM3):c.906-18C>T	PDLIM3	Single nucleotide variant (intron variant)	Primary dilated cardiomyopathy +3 more	GBenign
Select item 671179	NM_014476.6(PDLIM3):c.906-40C>T	PDLIM3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242023	NM_014476.6(PDLIM3):c.906-99_906-98del	PDLIM3	Microsatellite (intron variant)	not provided	GBenign
Select item 1316726	NM_014476.6(PDLIM3):c.906-282T>C	PDLIM3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1296556	NM_014476.6(PDLIM3):c.905+328T>C	PDLIM3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 672898	NM_014476.6(PDLIM3):c.905+322G>A	PDLIM3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 671476	NM_014476.6(PDLIM3):c.905+58T>C	PDLIM3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1513725	NM_014476.6(PDLIM3):c.905+18C>G	PDLIM3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy +1 more	GUncertain significance
Select item 1149544	NM_014476.6(PDLIM3):c.905+10A>G	PDLIM3	Single nucleotide variant (intron variant)	Primary dilated cardiomyopathy +1 more	GLikely benign
Select item 1765600	NM_014476.6(PDLIM3):c.904G>A (p.Val302Ile)	PDLIM3 (V302I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2197429	NM_014476.6(PDLIM3):c.899G>A (p.Gly300Asp)	PDLIM3 (G212D +3 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy +1 more	GUncertain significance
Select item 201948	NM_014476.6(PDLIM3):c.896G>A (p.Ser299Asn)	PDLIM3 (S299N +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 520257	NM_014476.6(PDLIM3):c.895A>C (p.Ser299Arg)	PDLIM3 (S299R +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +2 more	GUncertain significance
Select item 1586812	NM_014476.6(PDLIM3):c.894G>C (p.Gly298=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	Primary dilated cardiomyopathy +2 more	GLikely benign
Select item 1713697	NM_014476.6(PDLIM3):c.893G>A (p.Gly298Glu)	PDLIM3 (G131E +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 659322	NM_014476.6(PDLIM3):c.890G>A (p.Cys297Tyr)	PDLIM3 (C130Y +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +1 more	GUncertain significance
Select item 2925187	NM_014476.6(PDLIM3):c.887A>T (p.Lys296Ile)	PDLIM3 (K208I +3 more)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +2 more	GUncertain significance
Select item 2929484	NM_014476.6(PDLIM3):c.882_883del (p.Cys294_Asp295delinsTer)	PDLIM3	Microsatellite (nonsense +1 more)	Hypertrophic cardiomyopathy +1 more	GUncertain significance
Select item 1089361	NM_014476.6(PDLIM3):c.879C>T (p.Leu293=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GLikely benign
Select item 1764608	NM_014476.6(PDLIM3):c.876G>T (p.Pro292=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 1764601	NM_014476.6(PDLIM3):c.876G>A (p.Pro292=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2190387	NM_014476.6(PDLIM3):c.875C>T (p.Pro292Leu)	PDLIM3 (P292L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance
Select item 1462616	NM_014476.6(PDLIM3):c.875C>G (p.Pro292Arg)	PDLIM3 (P204R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance

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