PDCD11[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57116	GRCh38/hg38 10q23.33-25.3(chr10:95112607-116776637)x3	LOC130004500, LOC130004501 +821 more	Copy number gain	See cases	GPathogenic
Select item 59707	GRCh38/hg38 10q24.31-26.3(chr10:100194215-132432797)x3	EDRF1-AS1, EDRF1-DT +1036 more	Copy number gain	See cases	GPathogenic
Select item 148679	GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3	GSTO1, GSTO2 +1097 more	Copy number gain	See cases	GPathogenic
Select item 58780	GRCh38/hg38 10q24.32-24.33(chr10:102243341-103929730)x1	ACTR1A, ARL3 +121 more	Copy number loss	See cases	GPathogenic
Select item 3572	NC_000010.11:g.(102444036_?)_(?_104726221)del	ACTR1A, ARL3 +135 more	Deletion	Desmoplastic/nodular medulloblastoma	GPathogenic
Select item 155304	GRCh38/hg38 10q24.32-25.3(chr10:102732173-114085105)x1	LOC124416905, LOC124416906 +318 more	Copy number loss	See cases	GPathogenic
Select item 3210550	NM_014976.2(PDCD11):c.5C>T (p.Ala2Val)	PDCD11 (A2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640802	NM_014976.2(PDCD11):c.171G>A (p.Leu57=)	PDCD11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2270587	NM_014976.2(PDCD11):c.176T>C (p.Ile59Thr)	PDCD11 (I59T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400533	NM_014976.2(PDCD11):c.253C>T (p.Arg85Cys)	PDCD11 (R85C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470051	NM_014976.2(PDCD11):c.293T>C (p.Leu98Pro)	PDCD11 (L98P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535573	NM_014976.2(PDCD11):c.659C>T (p.Ala220Val)	PDCD11 (A220V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376596	NM_014976.2(PDCD11):c.684C>G (p.Asn228Lys)	PDCD11 (N228K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640803	NM_014976.2(PDCD11):c.747C>T (p.Asn249=)	PDCD11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2530522	NM_014976.2(PDCD11):c.760A>T (p.Ser254Cys)	PDCD11 (S254C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487761	NM_014976.2(PDCD11):c.839C>T (p.Pro280Leu)	PDCD11 (P280L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362539	NM_014976.2(PDCD11):c.890C>T (p.Thr297Met)	PDCD11 (T297M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353275	NM_014976.2(PDCD11):c.919G>A (p.Val307Met)	PDCD11 (V307M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210551	NM_014976.2(PDCD11):c.920T>A (p.Val307Glu)	PDCD11 (V307E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568856	NM_014976.2(PDCD11):c.1010G>C (p.Arg337Pro)	PDCD11 (R337P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210523	NM_014976.2(PDCD11):c.1024C>A (p.His342Asn)	PDCD11 (H342N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523439	NM_014976.2(PDCD11):c.1037G>A (p.Arg346His)	PDCD11 (R346H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215668	NM_014976.2(PDCD11):c.1072C>G (p.Arg358Gly)	PDCD11 (R358G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555979	NM_014976.2(PDCD11):c.1106A>G (p.Asp369Gly)	PDCD11 (D369G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262949	NM_014976.2(PDCD11):c.1108G>A (p.Asp370Asn)	PDCD11 (D370N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328021	NM_014976.2(PDCD11):c.1160A>C (p.Lys387Thr)	PDCD11 (K387T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388703	NM_014976.2(PDCD11):c.1183C>T (p.Arg395Trp)	PDCD11 (R395W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210524	NM_014976.2(PDCD11):c.1189A>C (p.Ser397Arg)	PDCD11 (S397R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387604	NM_014976.2(PDCD11):c.1199C>T (p.Ser400Phe)	PDCD11 (S400F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351897	NM_014976.2(PDCD11):c.1241G>A (p.Gly414Glu)	PDCD11 (G414E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218402	NM_014976.2(PDCD11):c.1387A>C (p.Ile463Leu)	PDCD11 (I463L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2203834	NM_014976.2(PDCD11):c.1425G>C (p.Gln475His)	PDCD11 (Q475H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314685	NM_014976.2(PDCD11):c.1431G>C (p.Arg477Ser)	PDCD11 (R477S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210525	NM_014976.2(PDCD11):c.1478C>T (p.Pro493Leu)	PDCD11 (P493L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520625	NM_014976.2(PDCD11):c.1493A>C (p.His498Pro)	PDCD11 (H498P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308840	NM_014976.2(PDCD11):c.1517G>A (p.Arg506Gln)	PDCD11 (R506Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304818	NM_014976.2(PDCD11):c.1612G>A (p.Asp538Asn)	PDCD11 (D538N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218403	NM_014976.2(PDCD11):c.1619A>G (p.Lys540Arg)	PDCD11 (K540R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291129	NM_014976.2(PDCD11):c.1634C>G (p.Thr545Arg)	PDCD11 (T545R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592100	NM_014976.2(PDCD11):c.1745C>T (p.Pro582Leu)	PDCD11 (P582L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337896	NM_014976.2(PDCD11):c.1819C>T (p.Leu607Phe)	PDCD11 (L607F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210526	NM_014976.2(PDCD11):c.1871G>A (p.Gly624Glu)	PDCD11 (G624E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289149	NM_014976.2(PDCD11):c.1880A>G (p.Gln627Arg)	PDCD11 (Q627R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495779	NM_014976.2(PDCD11):c.1918G>A (p.Asp640Asn)	PDCD11 (D640N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210527	NM_014976.2(PDCD11):c.1996A>T (p.Thr666Ser)	PDCD11 (T666S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507647	NM_014976.2(PDCD11):c.2062A>G (p.Ile688Val)	PDCD11 (I688V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527302	NM_014976.2(PDCD11):c.2065C>T (p.Leu689Phe)	PDCD11 (L689F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600402	NM_014976.2(PDCD11):c.2072G>A (p.Arg691Gln)	PDCD11 (R691Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640804	NM_014976.2(PDCD11):c.2095G>A (p.Glu699Lys)	PDCD11 (E699K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2269762	NM_014976.2(PDCD11):c.2126C>G (p.Ala709Gly)	PDCD11 (A709G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314574	NM_014976.2(PDCD11):c.2156A>T (p.Asp719Val)	PDCD11 (D719V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210528	NM_014976.2(PDCD11):c.2260G>A (p.Gly754Arg)	PDCD11 (G754R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597700	NM_014976.2(PDCD11):c.2267C>T (p.Ala756Val)	PDCD11 (A756V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210529	NM_014976.2(PDCD11):c.2314C>T (p.His772Tyr)	PDCD11 (H772Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486867	NM_014976.2(PDCD11):c.2354A>G (p.Asn785Ser)	PDCD11 (N785S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357973	NM_014976.2(PDCD11):c.2370G>C (p.Lys790Asn)	PDCD11 (K790N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640805	NM_014976.2(PDCD11):c.2400G>A (p.Ser800=)	PDCD11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3210530	NM_014976.2(PDCD11):c.2416G>T (p.Asp806Tyr)	PDCD11 (D806Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555351	NM_014976.2(PDCD11):c.2435T>G (p.Leu812Arg)	PDCD11 (L812R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241086	NM_014976.2(PDCD11):c.2518C>G (p.Leu840Val)	PDCD11 (L840V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210531	NM_014976.2(PDCD11):c.2522C>A (p.Ala841Asp)	PDCD11 (A841D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476029	NM_014976.2(PDCD11):c.2534C>T (p.Pro845Leu)	PDCD11 (P845L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460166	NM_014976.2(PDCD11):c.2541G>A (p.Met847Ile)	PDCD11 (M847I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393563	NM_014976.2(PDCD11):c.2594G>A (p.Ser865Asn)	PDCD11 (S865N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210532	NM_014976.2(PDCD11):c.2722G>A (p.Val908Ile)	PDCD11 (V908I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210533	NM_014976.2(PDCD11):c.2764C>G (p.Leu922Val)	PDCD11 (L922V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492378	NM_014976.2(PDCD11):c.2840C>T (p.Thr947Met)	PDCD11 (T947M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343389	NM_014976.2(PDCD11):c.2857T>C (p.Phe953Leu)	PDCD11 (F953L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523073	NM_014976.2(PDCD11):c.3239C>T (p.Thr1080Ile)	PDCD11 (T1080I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596684	NM_014976.2(PDCD11):c.3272G>T (p.Arg1091Leu)	PDCD11 (R1091L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318896	NM_014976.2(PDCD11):c.3308A>G (p.Tyr1103Cys)	PDCD11 (Y1103C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394330	NM_014976.2(PDCD11):c.3316A>G (p.Ile1106Val)	PDCD11 (I1106V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210535	NM_014976.2(PDCD11):c.3347C>T (p.Pro1116Leu)	PDCD11 (P1116L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338113	NM_014976.2(PDCD11):c.3362G>A (p.Arg1121Gln)	PDCD11 (R1121Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339144	NM_014976.2(PDCD11):c.3484G>A (p.Val1162Met)	PDCD11 (V1162M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454340	NM_014976.2(PDCD11):c.3524G>A (p.Arg1175Gln)	PDCD11 (R1175Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261634	NM_014976.2(PDCD11):c.3545T>G (p.Leu1182Arg)	PDCD11 (L1182R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210536	NM_014976.2(PDCD11):c.3548C>G (p.Thr1183Ser)	PDCD11 (T1183S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210537	NM_014976.2(PDCD11):c.3593G>A (p.Arg1198Gln)	PDCD11 (R1198Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2537754	NM_014976.2(PDCD11):c.3689G>A (p.Gly1230Glu)	PDCD11 (G1230E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210538	NM_014976.2(PDCD11):c.3809C>T (p.Thr1270Met)	PDCD11 (T1270M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2251326	NM_014976.2(PDCD11):c.3868G>A (p.Asp1290Asn)	PDCD11 (D1290N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210539	NM_014976.2(PDCD11):c.4147C>T (p.Arg1383Cys)	PDCD11 (R1383C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210540	NM_014976.2(PDCD11):c.4213G>A (p.Val1405Met)	PDCD11 (V1405M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467235	NM_014976.2(PDCD11):c.4258A>T (p.Arg1420Trp)	PDCD11 (R1420W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338168	NM_014976.2(PDCD11):c.4280G>A (p.Arg1427Lys)	PDCD11 (R1427K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370751	NM_014976.2(PDCD11):c.4406G>A (p.Gly1469Asp)	PDCD11 (G1469D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210542	NM_014976.2(PDCD11):c.4408G>T (p.Gly1470Trp)	PDCD11 (G1470W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210543	NM_014976.2(PDCD11):c.4420C>T (p.Arg1474Trp)	PDCD11 (R1474W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210544	NM_014976.2(PDCD11):c.4442A>G (p.Glu1481Gly)	PDCD11 (E1481G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459346	NM_014976.2(PDCD11):c.4513C>T (p.Arg1505Trp)	PDCD11 (R1505W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401310	NM_014976.2(PDCD11):c.4523A>G (p.Lys1508Arg)	PDCD11 (K1508R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245970	NM_014976.2(PDCD11):c.4544A>G (p.Asn1515Ser)	PDCD11 (N1515S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2640806	NM_014976.2(PDCD11):c.4570A>C (p.Lys1524Gln)	PDCD11 (K1524Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3210545	NM_014976.2(PDCD11):c.4576G>A (p.Ala1526Thr)	PDCD11 (A1526T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325755	NM_014976.2(PDCD11):c.4577C>G (p.Ala1526Gly)	PDCD11 (A1526G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592428	NM_014976.2(PDCD11):c.4640C>T (p.Thr1547Ile)	PDCD11 (T1547I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295206	NM_014976.2(PDCD11):c.4661C>G (p.Ala1554Gly)	PDCD11 (A1554G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3210546	NM_014976.2(PDCD11):c.4768C>T (p.Arg1590Cys)	PDCD11 (R1590C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469016	NM_014976.2(PDCD11):c.4813G>A (p.Ala1605Thr)	PDCD11 (A1605T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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